LGMDR4
MCID: MSC176
MIFTS: 29

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 (LGMDR4)

Categories: Genetic diseases, Metabolic diseases, Muscle diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

MalaCards integrated aliases for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

Name: Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 58 76
Lgmd2e 58 60 76 56
Muscular Dystrophy, Limb-Girdle, Type 2e 58 76 13
Lgmdr4 58 76
Limb-Girdle Muscular Dystrophy Due to Beta-Sarcoglycan Deficiency 60
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e 60
Muscular Dystrophy, Limb-Girdle, Type 2e; Lgmd2e 58
Limb-Girdle Muscular Dystrophy 2e 76
Beta-Sarcoglycanopathy 60

Characteristics:

Orphanet epidemiological data:

60
autosomal recessive limb-girdle muscular dystrophy type 2e
Inheritance: Autosomal recessive; Prevalence: <1/1000000 (United Kingdom),<1/1000000 (Europe); Age of onset: Adolescent,Childhood; Age of death: adult;

OMIM:

58
Inheritance:
autosomal recessive

Miscellaneous:
intrafamilial variability
variable progression
onset in childhood (range 4 to 12 years)
most patients become wheelchair-bound in the second to fourth decades


HPO:

33
muscular dystrophy, limb-girdle, autosomal recessive 4:
Onset and clinical course juvenile onset
Inheritance autosomal recessive inheritance


Classifications:

Orphanet: 60  
Rare neurological diseases


External Ids:

OMIM 58 604286
MeSH 45 D049288
ICD10 via Orphanet 35 G71.0
UMLS via Orphanet 75 C1858593 C2930900
Orphanet 60 ORPHA119
MedGen 43 C1858593

Summaries for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

UniProtKB/Swiss-Prot : 76 Muscular dystrophy, limb-girdle, autosomal recessive 4: An autosomal recessive degenerative myopathy characterized by pelvic and shoulder muscle wasting, onset usually in childhood and variable progression rate.

MalaCards based summary : Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4, also known as lgmd2e, is related to muscular dystrophy, limb-girdle, autosomal recessive 2 and muscular dystrophy, limb-girdle, autosomal recessive 1. An important gene associated with Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 is SGCB (Sarcoglycan Beta). Affiliated tissues include skeletal muscle, and related phenotypes are dilated cardiomyopathy and delayed speech and language development

Description from OMIM: 604286

Related Diseases for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Diseases in the Limb-Girdle Muscular Dystrophy family:

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 12 Muscular Dystrophy, Limb-Girdle, Type 1h
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 17 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 18
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 25 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 21
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 4 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 23
Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2q
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2w Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x
Limb-Girdle Muscular Dystrophy Type 1a Limb-Girdle Muscular Dystrophy Type 1b
Limb-Girdle Muscular Dystrophy Type 1c

Diseases related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 7, show less)
# Related Disease Score Top Affiliating Genes
1 muscular dystrophy, limb-girdle, autosomal recessive 2 11.7
2 muscular dystrophy, limb-girdle, autosomal recessive 1 11.1
3 muscular dystrophy 10.4
4 maternal uniparental disomy of chromosome 4 10.4
5 dilated cardiomyopathy 10.1
6 myoglobinuria 10.1
7 limb-girdle muscular dystrophy 10.1

Graphical network of the top 20 diseases related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:



Diseases related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Symptoms & Phenotypes for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Human phenotypes related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

33 60 (showing 22, show less)
# Description HPO Frequency Orphanet Frequency HPO Source Accession
1 dilated cardiomyopathy 33 occasional (7.5%) HP:0001644
2 delayed speech and language development 60 Frequent (79-30%)
3 myopathy 60 Frequent (79-30%)
4 elevated serum creatine phosphokinase 60 Frequent (79-30%)
5 cardiomyopathy 60 Occasional (29-5%)
6 waddling gait 60 Frequent (79-30%)
7 scapular winging 33 HP:0003691
8 pelvic girdle muscle weakness 60 Frequent (79-30%)
9 difficulty walking 60 Frequent (79-30%)
10 myopathic facies 60 Frequent (79-30%)
11 limb-girdle muscle weakness 33 HP:0003325
12 increased variability in muscle fiber diameter 60 Frequent (79-30%)
13 muscular dystrophy 33 HP:0003560
14 proximal amyotrophy 33 HP:0007126
15 gowers sign 60 Frequent (79-30%)
16 calf muscle hypertrophy 60 Frequent (79-30%)
17 calf muscle pseudohypertrophy 33 HP:0003707
18 myoglobinuria 60 Occasional (29-5%)
19 broad-based gait 60 Frequent (79-30%)
20 pelvic girdle muscle atrophy 33 HP:0008988
21 shoulder girdle muscle atrophy 33 HP:0003724
22 elevated serum creatine kinase 33 HP:0003236

Symptoms via clinical synopsis from OMIM:

58
Chest Ribs Sternum Clavicles And Scapulae:
scapular winging

Muscle Soft Tissue:
proximal muscle atrophy
muscle weakness, proximal, limb-girdle
trunk muscle atrophy
calf pseudohypertrophy
skeletal muscle shows dystrophic changes
more
Laboratory Abnormalities:
increased serum creatine kinase

Cardiovascular Heart:
dilated cardiomyopathy (rare)

Clinical features from OMIM:

604286

Drugs & Therapeutics for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Interventional clinical trials:

(showing 2, show less)
# Name Status NCT ID Phase Drugs
1 Gene Transfer Clinical Trial for LGMD2E (Beta-sarcoglycan Deficiency) Using scAAVrh74.MHCK7.hSGCB Recruiting NCT03652259 Phase 1, Phase 2 scAAVrh74.MHCK7.hSGCB
2 Limb Girdle Muscular Dystrophy Type 2E Recruitment Study Recruiting NCT03492346

Search NIH Clinical Center for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Genetic Tests for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Anatomical Context for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

MalaCards organs/tissues related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

42
Skeletal Muscle

Publications for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Articles related to Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

(showing 6, show less)
# Title Authors Year
1
Systemic AAV-Mediated β-Sarcoglycan Delivery Targeting Cardiac and Skeletal Muscle Ameliorates Histological and Functional Deficits in LGMD2E Mice. ( 28284983 )
2017
2
LGMD2E is the most common type of sarcoglycanopathies in the Iranian population. ( 28687063 )
2017
3
β-Sarcoglycan gene transfer decreases fibrosis and restores force in LGMD2E mice. ( 26214262 )
2016
4
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technology. ( 21480868 )
2012
5
LGMD2E patients risk developing dilated cardiomyopathy. ( 12868499 )
2003
6
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. ( 9565988 )
1998

Variations for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

UniProtKB/Swiss-Prot genetic disease variations for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

76 (showing 12, show less)
# Symbol AA change Variation ID SNP ID
1 SGCB p.Arg91Leu VAR_010391 rs104893869
2 SGCB p.Arg91Pro VAR_010392 rs104893869
3 SGCB p.Met100Lys VAR_010393 rs104893871
4 SGCB p.Leu108Arg VAR_010394 rs104893870
5 SGCB p.Thr151Arg VAR_010395 rs28936383
6 SGCB p.Gln11Glu VAR_010421 rs752492870
7 SGCB p.Arg91Cys VAR_010422 rs555514820
8 SGCB p.Ser114Phe VAR_010423 rs150518260
9 SGCB p.Ile119Phe VAR_010424 rs762412447
10 SGCB p.Gly139Asp VAR_010425
11 SGCB p.Gly167Ser VAR_010426 rs779516489
12 SGCB p.Thr182Ala VAR_010427

ClinVar genetic disease variations for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4:

6 (showing 139, show less)
# Gene Variation Type Significance SNP ID Assembly Location
1 SGCB SGCB, 2-BP DEL, NT465 deletion Pathogenic
2 SGCB SGCB, 8-BP DUP, NT383 duplication Pathogenic
3 SGCB NM_000232.4(SGCB): c.452C> G (p.Thr151Arg) single nucleotide variant Pathogenic/Likely pathogenic rs28936383 GRCh37 Chromosome 4, 52895065: 52895065
4 SGCB NM_000232.4(SGCB): c.452C> G (p.Thr151Arg) single nucleotide variant Pathogenic/Likely pathogenic rs28936383 GRCh38 Chromosome 4, 52028899: 52028899
5 SGCB NM_000232.4(SGCB): c.552T> G (p.Tyr184Ter) single nucleotide variant Likely pathogenic rs104893868 GRCh37 Chromosome 4, 52894965: 52894965
6 SGCB NM_000232.4(SGCB): c.552T> G (p.Tyr184Ter) single nucleotide variant Likely pathogenic rs104893868 GRCh38 Chromosome 4, 52028799: 52028799
7 SGCB NM_000232.4(SGCB): c.272G> C (p.Arg91Pro) single nucleotide variant Pathogenic rs104893869 GRCh37 Chromosome 4, 52896001: 52896001
8 SGCB NM_000232.4(SGCB): c.272G> C (p.Arg91Pro) single nucleotide variant Pathogenic rs104893869 GRCh38 Chromosome 4, 52029835: 52029835
9 SGCB NM_000232.4(SGCB): c.323T> G (p.Leu108Arg) single nucleotide variant Pathogenic rs104893870 GRCh37 Chromosome 4, 52895950: 52895950
10 SGCB NM_000232.4(SGCB): c.323T> G (p.Leu108Arg) single nucleotide variant Pathogenic rs104893870 GRCh38 Chromosome 4, 52029784: 52029784
11 SGCB NM_000232.4(SGCB): c.299T> A (p.Met100Lys) single nucleotide variant Likely pathogenic rs104893871 GRCh37 Chromosome 4, 52895974: 52895974
12 SGCB NM_000232.4(SGCB): c.299T> A (p.Met100Lys) single nucleotide variant Likely pathogenic rs104893871 GRCh38 Chromosome 4, 52029808: 52029808
13 SGCB NM_000232.4(SGCB): c.272G> T (p.Arg91Leu) single nucleotide variant Likely pathogenic rs104893869 GRCh37 Chromosome 4, 52896001: 52896001
14 SGCB NM_000232.4(SGCB): c.272G> T (p.Arg91Leu) single nucleotide variant Likely pathogenic rs104893869 GRCh38 Chromosome 4, 52029835: 52029835
15 SGCB SGCB, 4-BP DEL, 243+3GAGT deletion Pathogenic
16 SGCB NM_000232.4(SGCB): c.341C> T (p.Ser114Phe) single nucleotide variant Pathogenic/Likely pathogenic rs150518260 GRCh37 Chromosome 4, 52895932: 52895932
17 SGCB NM_000232.4(SGCB): c.341C> T (p.Ser114Phe) single nucleotide variant Pathogenic/Likely pathogenic rs150518260 GRCh38 Chromosome 4, 52029766: 52029766
18 SGCB NM_000232.4(SGCB): c.1A> G (p.Met1Val) single nucleotide variant Pathogenic rs398123262 GRCh37 Chromosome 4, 52904425: 52904425
19 SGCB NM_000232.4(SGCB): c.151C> T (p.Arg51Cys) single nucleotide variant Uncertain significance rs144743676 GRCh37 Chromosome 4, 52899689: 52899689
20 SGCB NM_000232.4(SGCB): c.151C> T (p.Arg51Cys) single nucleotide variant Uncertain significance rs144743676 GRCh38 Chromosome 4, 52033523: 52033523
21 SGCB NM_000232.4(SGCB): c.1A> G (p.Met1Val) single nucleotide variant Pathogenic rs398123262 GRCh38 Chromosome 4, 52038259: 52038259
22 SGCB NM_000232.4(SGCB): c.92G> T (p.Ser31Ile) single nucleotide variant Benign/Likely benign rs115928999 GRCh37 Chromosome 4, 52899748: 52899748
23 SGCB NM_000232.4(SGCB): c.92G> T (p.Ser31Ile) single nucleotide variant Benign/Likely benign rs115928999 GRCh38 Chromosome 4, 52033582: 52033582
24 SGCB NM_000232.4(SGCB): c.21_23dupGGC (p.Ala9_Glu10insAla) duplication Uncertain significance rs768838951 GRCh37 Chromosome 4, 52904403: 52904405
25 SGCB NM_000232.4(SGCB): c.21_23dupGGC (p.Ala9_Glu10insAla) duplication Uncertain significance rs768838951 GRCh38 Chromosome 4, 52038237: 52038239
26 SGCB NM_000232.4(SGCB): c.32dupA (p.Gln12Alafs) duplication Pathogenic rs796065319 GRCh37 Chromosome 4, 52904394: 52904394
27 SGCB NM_000232.4(SGCB): c.32dupA (p.Gln12Alafs) duplication Pathogenic rs796065319 GRCh38 Chromosome 4, 52038228: 52038228
28 SGCB NM_000232.4(SGCB): c.794C> T (p.Thr265Ile) single nucleotide variant Uncertain significance rs116214830 GRCh37 Chromosome 4, 52890286: 52890286
29 SGCB NM_000232.4(SGCB): c.794C> T (p.Thr265Ile) single nucleotide variant Uncertain significance rs116214830 GRCh38 Chromosome 4, 52024120: 52024120
30 SGCB NM_000232.4(SGCB): c.31C> G (p.Gln11Glu) single nucleotide variant Uncertain significance rs752492870 GRCh37 Chromosome 4, 52904395: 52904395
31 SGCB NM_000232.4(SGCB): c.31C> G (p.Gln11Glu) single nucleotide variant Uncertain significance rs752492870 GRCh38 Chromosome 4, 52038229: 52038229
32 SGCB NM_000232.4(SGCB): c.355A> T (p.Ile119Phe) single nucleotide variant Uncertain significance rs762412447 GRCh37 Chromosome 4, 52895918: 52895918
33 SGCB NM_000232.4(SGCB): c.355A> T (p.Ile119Phe) single nucleotide variant Uncertain significance rs762412447 GRCh38 Chromosome 4, 52029752: 52029752
34 SGCB NM_000232.4(SGCB): c.799C> T (p.Arg267Cys) single nucleotide variant Conflicting interpretations of pathogenicity rs200761715 GRCh37 Chromosome 4, 52890281: 52890281
35 SGCB NM_000232.4(SGCB): c.799C> T (p.Arg267Cys) single nucleotide variant Conflicting interpretations of pathogenicity rs200761715 GRCh38 Chromosome 4, 52024115: 52024115
36 SGCB NM_000232.4(SGCB): c.838G> A (p.Gly280Ser) single nucleotide variant Uncertain significance rs879945095 GRCh37 Chromosome 4, 52890242: 52890242
37 SGCB NM_000232.4(SGCB): c.838G> A (p.Gly280Ser) single nucleotide variant Uncertain significance rs879945095 GRCh38 Chromosome 4, 52024076: 52024076
38 SGCB NM_000232.4(SGCB): c.392G> A (p.Arg131Gln) single nucleotide variant Uncertain significance rs201439705 GRCh37 Chromosome 4, 52895881: 52895881
39 SGCB NM_000232.4(SGCB): c.392G> A (p.Arg131Gln) single nucleotide variant Uncertain significance rs201439705 GRCh38 Chromosome 4, 52029715: 52029715
40 SGCB NM_000232.4(SGCB): c.502A> G (p.Met168Val) single nucleotide variant Uncertain significance rs754465904 GRCh37 Chromosome 4, 52895015: 52895015
41 SGCB NM_000232.4(SGCB): c.502A> G (p.Met168Val) single nucleotide variant Uncertain significance rs754465904 GRCh38 Chromosome 4, 52028849: 52028849
42 SGCB NM_000232.4(SGCB): c.496A> G (p.Ile166Val) single nucleotide variant Uncertain significance rs138877636 GRCh37 Chromosome 4, 52895021: 52895021
43 SGCB NM_000232.4(SGCB): c.496A> G (p.Ile166Val) single nucleotide variant Uncertain significance rs138877636 GRCh38 Chromosome 4, 52028855: 52028855
44 SGCB NM_000232.4(SGCB): c.699_702delCATT (p.Phe233Leufs) deletion Likely pathogenic rs1057516515 GRCh38 Chromosome 4, 52028019: 52028022
45 SGCB NM_000232.4(SGCB): c.699_702delCATT (p.Phe233Leufs) deletion Likely pathogenic rs1057516515 GRCh37 Chromosome 4, 52894185: 52894188
46 SGCB NM_000232.4(SGCB): c.622-2A> G single nucleotide variant Likely pathogenic rs780596734 GRCh37 Chromosome 4, 52894267: 52894267
47 SGCB NM_000232.4(SGCB): c.622-2A> G single nucleotide variant Likely pathogenic rs780596734 GRCh38 Chromosome 4, 52028101: 52028101
48 SGCB NM_000232.4(SGCB): c.551_552delAT (p.Tyr184Terfs) deletion Likely pathogenic rs1057517051 GRCh38 Chromosome 4, 52028799: 52028800
49 SGCB NM_000232.4(SGCB): c.551_552delAT (p.Tyr184Terfs) deletion Likely pathogenic rs1057517051 GRCh37 Chromosome 4, 52894965: 52894966
50 SGCB NM_000232.4(SGCB): c.216_219delGTTT (p.Phe73Serfs) deletion Likely pathogenic rs1057516360 GRCh37 Chromosome 4, 52899621: 52899624
51 SGCB NM_000232.4(SGCB): c.216_219delGTTT (p.Phe73Serfs) deletion Likely pathogenic rs1057516360 GRCh38 Chromosome 4, 52033455: 52033458
52 SGCB NM_000232.4(SGCB): c.85A> T (p.Arg29Ter) single nucleotide variant Likely pathogenic rs747809412 GRCh38 Chromosome 4, 52033589: 52033589
53 SGCB NM_000232.4(SGCB): c.85A> T (p.Arg29Ter) single nucleotide variant Likely pathogenic rs747809412 GRCh37 Chromosome 4, 52899755: 52899755
54 SGCB NM_000232.4(SGCB): c.29_33del5 (p.Glu10Alafs) deletion Pathogenic/Likely pathogenic rs1057517064 GRCh38 Chromosome 4, 52038227: 52038231
55 SGCB NM_000232.4(SGCB): c.29_33del5 (p.Glu10Alafs) deletion Pathogenic/Likely pathogenic rs1057517064 GRCh37 Chromosome 4, 52904393: 52904397
56 SGCB NM_000232.4(SGCB): c.-15_8del23 deletion Likely pathogenic rs1057517205 GRCh37 Chromosome 4, 52904418: 52904440
57 SGCB NM_000232.4(SGCB): c.-15_8del23 deletion Likely pathogenic rs1057517205 GRCh38 Chromosome 4, 52038252: 52038274
58 SGCB NM_000232.4(SGCB): c.9_14dupAGCGGC (p.Ala9_Glu10insAlaAla) duplication Conflicting interpretations of pathogenicity rs886044103 GRCh38 Chromosome 4, 52038246: 52038251
59 SGCB NM_000232.4(SGCB): c.9_14dupAGCGGC (p.Ala9_Glu10insAlaAla) duplication Conflicting interpretations of pathogenicity rs886044103 GRCh37 Chromosome 4, 52904412: 52904417
60 SGCB NM_000232.4(SGCB): c.244A> G (p.Ile82Val) single nucleotide variant Uncertain significance rs143106297 GRCh37 Chromosome 4, 52896029: 52896029
61 SGCB NM_000232.4(SGCB): c.244A> G (p.Ile82Val) single nucleotide variant Uncertain significance rs143106297 GRCh38 Chromosome 4, 52029863: 52029863
62 SGCB NC_000004.12: g.(?_52038207)_(52038279_?)del deletion Pathogenic GRCh37 Chromosome 4, 52904373: 52904445
63 SGCB NC_000004.12: g.(?_52038207)_(52038279_?)del deletion Pathogenic GRCh38 Chromosome 4, 52038207: 52038279
64 SGCB NM_000232.4(SGCB): c.707G> A (p.Gly236Asp) single nucleotide variant Uncertain significance rs1553940073 GRCh37 Chromosome 4, 52894180: 52894180
65 SGCB NM_000232.4(SGCB): c.707G> A (p.Gly236Asp) single nucleotide variant Uncertain significance rs1553940073 GRCh38 Chromosome 4, 52028014: 52028014
66 SGCB NM_000232.4(SGCB): c.82_86delGAGAG (p.Glu28Lysfs) deletion Pathogenic rs1553940687 GRCh37 Chromosome 4, 52899754: 52899758
67 SGCB NM_000232.4(SGCB): c.82_86delGAGAG (p.Glu28Lysfs) deletion Pathogenic rs1553940687 GRCh38 Chromosome 4, 52033588: 52033592
68 SGCB NM_000232.4(SGCB): c.-10_22dup duplication Conflicting interpretations of pathogenicity rs1553940963 GRCh37 Chromosome 4, 52904404: 52904435
69 SGCB NM_000232.4(SGCB): c.-10_22dup duplication Conflicting interpretations of pathogenicity rs1553940963 GRCh38 Chromosome 4, 52038238: 52038269
70 SGCB NM_000232.4(SGCB): c.940T> C (p.Cys314Arg) single nucleotide variant Uncertain significance rs573919387 GRCh38 Chromosome 4, 52023974: 52023974
71 SGCB NM_000232.4(SGCB): c.940T> C (p.Cys314Arg) single nucleotide variant Uncertain significance rs573919387 GRCh37 Chromosome 4, 52890140: 52890140
72 SGCB NM_000232.4(SGCB): c.753+10_753+12delCTT deletion Benign rs138604476 GRCh37 Chromosome 4, 52894122: 52894124
73 SGCB NM_000232.4(SGCB): c.753+10_753+12delCTT deletion Benign rs138604476 GRCh38 Chromosome 4, 52027956: 52027958
74 SGCB NM_000232.4(SGCB): c.725A> C (p.His242Pro) single nucleotide variant Uncertain significance rs1553940064 GRCh37 Chromosome 4, 52894162: 52894162
75 SGCB NM_000232.4(SGCB): c.725A> C (p.His242Pro) single nucleotide variant Uncertain significance rs1553940064 GRCh38 Chromosome 4, 52027996: 52027996
76 SGCB NM_000232.4(SGCB): c.656_657delAA (p.Lys219Serfs) deletion Pathogenic/Likely pathogenic rs775458201 GRCh37 Chromosome 4, 52894230: 52894231
77 SGCB NM_000232.4(SGCB): c.656_657delAA (p.Lys219Serfs) deletion Pathogenic/Likely pathogenic rs775458201 GRCh38 Chromosome 4, 52028064: 52028065
78 SGCB NM_000232.4(SGCB): c.544A> C (p.Thr182Pro) single nucleotide variant Uncertain significance rs751427686 GRCh37 Chromosome 4, 52894973: 52894973
79 SGCB NM_000232.4(SGCB): c.544A> C (p.Thr182Pro) single nucleotide variant Uncertain significance rs751427686 GRCh38 Chromosome 4, 52028807: 52028807
80 SGCB NM_000232.4(SGCB): c.253_254delGT (p.Val85Tyrfs) deletion Pathogenic rs1553940274 GRCh37 Chromosome 4, 52896019: 52896020
81 SGCB NM_000232.4(SGCB): c.253_254delGT (p.Val85Tyrfs) deletion Pathogenic rs1553940274 GRCh38 Chromosome 4, 52029853: 52029854
82 SGCB NM_000232.4(SGCB): c.752C> T (p.Ala251Val) single nucleotide variant Uncertain significance rs146111013 GRCh37 Chromosome 4, 52894135: 52894135
83 SGCB NM_000232.4(SGCB): c.752C> T (p.Ala251Val) single nucleotide variant Uncertain significance rs146111013 GRCh38 Chromosome 4, 52027969: 52027969
84 SGCB NC_000004.12: g.(?_52033411)_(52033660_?)dup duplication Uncertain significance GRCh38 Chromosome 4, 52033411: 52033660
85 SGCB NC_000004.12: g.(?_52033411)_(52033660_?)dup duplication Uncertain significance GRCh37 Chromosome 4, 52899577: 52899826
86 SGCB NM_000232.4(SGCB): c.785T> C (p.Met262Thr) single nucleotide variant Uncertain significance rs201923065 GRCh38 Chromosome 4, 52024129: 52024129
87 SGCB NM_000232.4(SGCB): c.785T> C (p.Met262Thr) single nucleotide variant Uncertain significance rs201923065 GRCh37 Chromosome 4, 52890295: 52890295
88 SGCB NM_000232.4(SGCB): c.859delC (p.Leu287Serfs) deletion Uncertain significance rs1553939675 GRCh38 Chromosome 4, 52024055: 52024055
89 SGCB NM_000232.4(SGCB): c.859delC (p.Leu287Serfs) deletion Uncertain significance rs1553939675 GRCh37 Chromosome 4, 52890221: 52890221
90 SGCB NM_000232.4(SGCB): c.551A> G (p.Tyr184Cys) single nucleotide variant Uncertain significance rs1365923535 GRCh37 Chromosome 4, 52894966: 52894966
91 SGCB NM_000232.4(SGCB): c.551A> G (p.Tyr184Cys) single nucleotide variant Uncertain significance rs1365923535 GRCh38 Chromosome 4, 52028800: 52028800
92 SGCB NM_000232.4(SGCB): c.156C> T (p.Leu52=) single nucleotide variant Likely benign rs1553940675 GRCh37 Chromosome 4, 52899684: 52899684
93 SGCB NM_000232.4(SGCB): c.156C> T (p.Leu52=) single nucleotide variant Likely benign rs1553940675 GRCh38 Chromosome 4, 52033518: 52033518
94 SGCB NM_000232.4(SGCB): c.28G> T (p.Glu10Ter) single nucleotide variant Pathogenic rs1448040082 GRCh37 Chromosome 4, 52904398: 52904398
95 SGCB NM_000232.4(SGCB): c.28G> T (p.Glu10Ter) single nucleotide variant Pathogenic rs1448040082 GRCh38 Chromosome 4, 52038232: 52038232
96 SGCB NM_000232.4(SGCB): c.621+1G> T single nucleotide variant Likely pathogenic rs1264362642 GRCh37 Chromosome 4, 52894895: 52894895
97 SGCB NM_000232.4(SGCB): c.621+1G> T single nucleotide variant Likely pathogenic rs1264362642 GRCh38 Chromosome 4, 52028729: 52028729
98 SGCB NM_000232.4(SGCB): c.124_125insTTA (p.Ala42delinsValThr) insertion Uncertain significance rs1553940680 GRCh37 Chromosome 4, 52899715: 52899715
99 SGCB NM_000232.4(SGCB): c.124_125insTTA (p.Ala42delinsValThr) insertion Uncertain significance rs1553940680 GRCh38 Chromosome 4, 52033549: 52033550
100 SGCB NM_000232.4(SGCB): c.9_23dup (p.Ala9_Glu10insAlaAlaAlaAlaAla) duplication Uncertain significance rs781364428 GRCh37 Chromosome 4, 52904402: 52904402
101 SGCB NM_000232.4(SGCB): c.9_23dup (p.Ala9_Glu10insAlaAlaAlaAlaAla) duplication Uncertain significance rs781364428 GRCh38 Chromosome 4, 52038237: 52038251
102 SGCB NM_000232.4(SGCB): c.9_17dup (p.Ala9_Glu10insAlaAlaAla) duplication Uncertain significance rs1410190129 GRCh37 Chromosome 4, 52904408: 52904408
103 SGCB NM_000232.4(SGCB): c.9_17dup (p.Ala9_Glu10insAlaAlaAla) duplication Uncertain significance rs1410190129 GRCh38 Chromosome 4, 52038243: 52038251
104 SGCB NM_000232.4(SGCB): c.*18C> G single nucleotide variant Uncertain significance rs191486389 GRCh37 Chromosome 4, 52890105: 52890105
105 SGCB NM_000232.4(SGCB): c.*18C> G single nucleotide variant Uncertain significance rs191486389 GRCh38 Chromosome 4, 52023939: 52023939
106 SGCB NM_000232.4(SGCB): c.429+24G> T single nucleotide variant Likely benign rs367761233 GRCh37 Chromosome 4, 52895820: 52895820
107 SGCB NM_000232.4(SGCB): c.429+24G> T single nucleotide variant Likely benign rs367761233 GRCh38 Chromosome 4, 52029654: 52029654
108 SGCB NM_000232.4(SGCB): c.334C> T (p.Gln112Ter) single nucleotide variant Likely pathogenic rs1553940262 GRCh37 Chromosome 4, 52895939: 52895939
109 SGCB NM_000232.4(SGCB): c.334C> T (p.Gln112Ter) single nucleotide variant Likely pathogenic rs1553940262 GRCh38 Chromosome 4, 52029773: 52029773
110 SGCB NM_000232.4(SGCB): c.650delA (p.Asn217Ilefs) deletion Likely pathogenic rs1553940079 GRCh37 Chromosome 4, 52894236: 52894237
111 SGCB NM_000232.4(SGCB): c.650delA (p.Asn217Ilefs) deletion Likely pathogenic rs1553940079 GRCh38 Chromosome 4, 52028071: 52028071
112 SGCB NM_000232.4(SGCB): c.499G> A (p.Gly167Ser) single nucleotide variant Uncertain significance rs779516489 GRCh37 Chromosome 4, 52895018: 52895018
113 SGCB NM_000232.4(SGCB): c.499G> A (p.Gly167Ser) single nucleotide variant Uncertain significance rs779516489 GRCh38 Chromosome 4, 52028852: 52028852
114 SGCB NM_000232.4(SGCB): c.265G> A (p.Val89Met) single nucleotide variant Uncertain significance rs762652676 GRCh37 Chromosome 4, 52896008: 52896008
115 SGCB NM_000232.4(SGCB): c.265G> A (p.Val89Met) single nucleotide variant Uncertain significance rs762652676 GRCh38 Chromosome 4, 52029842: 52029842
116 SGCB NM_000232.4(SGCB): c.243+3_243+6delGAGT deletion Uncertain significance rs1553940660 GRCh37 Chromosome 4, 52899590: 52899594
117 SGCB NM_000232.4(SGCB): c.243+3_243+6delGAGT deletion Uncertain significance rs1553940660 GRCh38 Chromosome 4, 52033425: 52033428
118 SGCB NM_000232.4(SGCB): c.243+2T> G single nucleotide variant Likely pathogenic rs1553940661 GRCh37 Chromosome 4, 52899595: 52899595
119 SGCB NM_000232.4(SGCB): c.243+2T> G single nucleotide variant Likely pathogenic rs1553940661 GRCh38 Chromosome 4, 52033429: 52033429
120 SGCB NM_000232.4(SGCB): c.243+1G> T single nucleotide variant Likely pathogenic rs1553940663 GRCh37 Chromosome 4, 52899596: 52899596
121 SGCB NM_000232.4(SGCB): c.243+1G> T single nucleotide variant Likely pathogenic rs1553940663 GRCh38 Chromosome 4, 52033430: 52033430
122 SGCB NM_000232.4(SGCB): c.33+1G> A single nucleotide variant Likely pathogenic rs1553940957 GRCh37 Chromosome 4, 52904392: 52904392
123 SGCB NM_000232.4(SGCB): c.33+1G> A single nucleotide variant Likely pathogenic rs1553940957 GRCh38 Chromosome 4, 52038226: 52038226
124 SGCB NM_000232.4(SGCB): c.857delA (p.Lys286Serfs) deletion Uncertain significance rs1553939681 GRCh37 Chromosome 4, 52890222: 52890223
125 SGCB NM_000232.4(SGCB): c.857delA (p.Lys286Serfs) deletion Uncertain significance rs1553939681 GRCh38 Chromosome 4, 52024057: 52024057
126 SGCB NM_000232.4(SGCB): c.595_598delAATG (p.Asn199Phefs) deletion Likely pathogenic rs762114570 GRCh37 Chromosome 4, 52894918: 52894922
127 SGCB NM_000232.4(SGCB): c.595_598delAATG (p.Asn199Phefs) deletion Likely pathogenic rs762114570 GRCh38 Chromosome 4, 52028753: 52028756
128 SGCB NM_000232.4(SGCB): c.602A> C (p.Gln201Pro) single nucleotide variant Uncertain significance GRCh37 Chromosome 4, 52894915: 52894915
129 SGCB NM_000232.4(SGCB): c.602A> C (p.Gln201Pro) single nucleotide variant Uncertain significance GRCh38 Chromosome 4, 52028749: 52028749
130 SGCB NM_000232.4(SGCB): c.343G> C (p.Asp115His) single nucleotide variant Uncertain significance GRCh37 Chromosome 4, 52895930: 52895930
131 SGCB NM_000232.4(SGCB): c.343G> C (p.Asp115His) single nucleotide variant Uncertain significance GRCh38 Chromosome 4, 52029764: 52029764
132 SGCB NC_000004.12: g.(?_52023937)_(52038279_?)dup duplication Uncertain significance GRCh37 Chromosome 4, 52890103: 52904445
133 SGCB NC_000004.12: g.(?_52023937)_(52038279_?)dup duplication Uncertain significance GRCh38 Chromosome 4, 52023937: 52038279
134 SGCB NM_000232.4(SGCB): c.892G> A (p.Val298Met) single nucleotide variant Uncertain significance GRCh37 Chromosome 4, 52890188: 52890188
135 SGCB NM_000232.4(SGCB): c.892G> A (p.Val298Met) single nucleotide variant Uncertain significance GRCh38 Chromosome 4, 52024022: 52024022
136 SGCB NM_000232.4(SGCB): c.44A> G (p.Asn15Ser) single nucleotide variant Uncertain significance GRCh37 Chromosome 4, 52899796: 52899796
137 SGCB NM_000232.4(SGCB): c.44A> G (p.Asn15Ser) single nucleotide variant Uncertain significance GRCh38 Chromosome 4, 52033630: 52033630
138 SGCB NM_000232.4(SGCB): c.29A> G (p.Glu10Gly) single nucleotide variant Uncertain significance GRCh37 Chromosome 4, 52904397: 52904397
139 SGCB NM_000232.4(SGCB): c.29A> G (p.Glu10Gly) single nucleotide variant Uncertain significance GRCh38 Chromosome 4, 52038231: 52038231

Expression for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Search GEO for disease gene expression data for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4.

Pathways for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

GO Terms for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

Sources for Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4

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