AKU
MCID: ALK013
MIFTS: 54

Alkaptonuria (AKU) malady

Categories: Genetic diseases, Rare diseases, Eye diseases, Skin diseases, Metabolic diseases

Aliases & Classifications for Alkaptonuria

Aliases & Descriptions for Alkaptonuria:

Name: Alkaptonuria 54 12 71 23 50 24 25 56 66 29 13 52 42 14 69
Alcaptonuria 12 23 50 24 25
Homogentisic Acid Oxidase Deficiency 50 25 56 66
Aku 50 25 66
Alkaptonuric Ochronosis 50 69
Ochronosis, Hereditary 50 69
Homogentisic Acidura 50 25
Homogentisate 1,2-Dioxygenase Deficiency 12
Deficiency of Homogentisicase 12
Homogentisate 1,2-Dioxygenase 13
Hereditary Ochronosis 56

Characteristics:

Orphanet epidemiological data:

56
alkaptonuria
Inheritance: Autosomal recessive; Prevalence: 1-9/1000000 (Worldwide),1-9/1000000 (Europe),1-9/1000000 (France),1-9/100000 (Slovakia); Age of onset: Adult,Infancy; Age of death: normal life expectancy;

GeneReviews:

23
alkaptonuria:
Inheritance autosomal recessive inheritance


GeneReviews:

23
Penetrance Elevated urinary hga and ochronotic arthritis occur in all individuals who are homozygous or compound heterozygous for pathogenic variants in hgd...

Classifications:



External Ids:

OMIM 54 203500
Disease Ontology 12 DOID:9270
ICD10 33 E70.29
MeSH 42 D000474
NCIt 47 C84546
Orphanet 56 ORPHA56
UMLS via Orphanet 70 C0002066 C2931645
ICD10 via Orphanet 34 E70.2
MESH via Orphanet 43 C537862 D000474
MedGen 40 C0002066
UMLS 69 C0002066

Summaries for Alkaptonuria

NIH Rare Diseases : 50 alkaptonuria is an inherited condition that causes urine to turn black when exposed to air. the three major features of alkaptonuria are the presence of dark urine, ochronosis, a buildup of dark pigment in connective tissues such as cartilage and skin, and arthritis of the spine and larger joints. ochronosis starts after age 30 and arthritis in early adulthood. other features of this condition can include heart problems, kidney stones, and prostate stones. alkaptonuria is caused by mutations in the hgd gene. it is inherited in an autosomal recessive fashion. there is still no cure for this disease. treatment includes the management of joint pain, physical and occupational therapy, joint replacements and surgery when needed. last updated: 3/18/2016

MalaCards based summary : Alkaptonuria, also known as alcaptonuria, is related to ochronosis and exogenous ochronosis, and has symptoms including arthralgia, joint swelling and joint stiffness. An important gene associated with Alkaptonuria is HGD (Homogentisate 1,2-Dioxygenase), and among its related pathways/superpathways are Metabolism and Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism. The drugs Nitisinone and tyrosine have been mentioned in the context of this disorder. Affiliated tissues include heart, kidney and skin, and related phenotype is renal/urinary system.

Disease Ontology : 12 An amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct.

Genetics Home Reference : 25 Alkaptonuria is an inherited condition that causes urine to turn black when exposed to air. Ochronosis, a buildup of dark pigment in connective tissues such as cartilage and skin, is also characteristic of the disorder. This blue-black pigmentation usually appears after age 30. People with alkaptonuria typically develop arthritis, particularly in the spine and large joints, beginning in early adulthood. Other features of this condition can include heart problems, kidney stones, and prostate stones.

OMIM : 54 Alkaptonuria is an autosomal recessive metabolic disorder characterized by accumulation of homogentisic acid, leading... (203500) more...

UniProtKB/Swiss-Prot : 66 Alkaptonuria: An autosomal recessive error of metabolism characterized by an increase in the level of homogentisic acid. The clinical manifestations are urine that turns dark on standing and alkalinization, black ochronotic pigmentation of cartilage and collagenous tissues, and spine arthritis.

Wikipedia : 71 Alkaptonuria (black urine disease, black bone disease, or alcaptonuria) is a rare inherited genetic... more...

GeneReviews: NBK1454

Related Diseases for Alkaptonuria

Diseases related to Alkaptonuria via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 38)
id Related Disease Score Top Affiliating Genes
1 ochronosis 11.5
2 exogenous ochronosis 10.8
3 vaginal squamous papilloma 10.1 HGD HPD
4 azoospermia 10.0 HGD HPD
5 myopathy with lactic acidosis, hereditary 10.0 FAH HPD
6 cataract 20, multiple types 10.0 FAH HGD
7 arthropathy 10.0
8 intravascular fasciitis 10.0 HGD HPD
9 borderline glaucoma 9.9 FAH HGD
10 arthritis 9.8
11 central neurocytoma 9.8
12 prostatitis 9.8
13 amyloidosis 9.8
14 back pain 9.8
15 spondyloarthropathy 9.8
16 weill-marchesani-like syndrome 9.7 FAH GSTZ1 HPD
17 myocardium cancer 9.7 FAH GSTZ1 HPD
18 gout 9.6
19 hyperparathyroidism 9.6
20 neuroblastoma 9.6
21 cystinuria 9.6
22 pentosuria 9.6
23 spondylosis 9.6
24 chronic kidney failure 9.6
25 hepatitis 9.6
26 mediastinitis 9.6
27 hepatitis b 9.6
28 keratopathy 9.6
29 albinism 9.6
30 osteoarthritis 9.6
31 anterior uveitis 9.6
32 familial hypocalciuric hypercalcemia 9.6
33 methemoglobinemia 9.6
34 foot drop 9.6
35 nephrocalcinosis 9.6
36 acquired methemoglobinemia 9.6
37 uveitis 9.6
38 dowling-degos disease 4 9.1 ARL13B DCXR FAH GSTZ1 HGD HPD

Graphical network of the top 20 diseases related to Alkaptonuria:



Diseases related to Alkaptonuria

Symptoms & Phenotypes for Alkaptonuria

Symptoms by clinical synopsis from OMIM:

203500

Clinical features from OMIM:

203500

Human phenotypes related to Alkaptonuria:

56 32 (show all 41)
id Description HPO Frequency Orphanet Frequency HPO Source Accession
1 arthralgia 56 32 Very frequent (99-80%) HP:0002829
2 joint swelling 56 32 Very frequent (99-80%) HP:0001386
3 joint stiffness 56 32 Very frequent (99-80%) HP:0001387
4 joint dislocation 56 32 Very frequent (99-80%) HP:0001373
5 osteoarthritis 56 32 Very frequent (99-80%) HP:0002758
6 hypertension 56 32 Occasional (29-5%) HP:0000822
7 arthritis 56 32 Very frequent (99-80%) HP:0001369
8 aminoaciduria 56 32 Very frequent (99-80%) HP:0003355
9 abnormality of vision 56 32 Very frequent (99-80%) HP:0000504
10 abnormality of the nail 56 32 Frequent (79-30%) HP:0001597
11 myocardial infarction 56 32 Occasional (29-5%) HP:0001658
12 hearing abnormality 56 32 Very frequent (99-80%) HP:0000364
13 reduced bone mineral density 56 32 Occasional (29-5%) HP:0004349
14 mitral valve calcification 56 32 Frequent (79-30%) HP:0004382
15 irregular hyperpigmentation 56 32 Very frequent (99-80%) HP:0007400
16 nephrolithiasis 56 32 Frequent (79-30%) HP:0000787
17 blue sclerae 56 32 Very frequent (99-80%) HP:0000592
18 abnormality of the nose 56 32 Frequent (79-30%) HP:0000366
19 prostatitis 56 32 Frequent (79-30%) HP:0000024
20 coronary artery calcification 56 32 Very frequent (99-80%) HP:0001717
21 aortic valve calcification 56 32 Frequent (79-30%) HP:0004380
22 thickened achilles tendon 56 32 Frequent (79-30%) HP:0004690
23 intervertebral disk calcification 56 32 Very frequent (99-80%) HP:0005645
24 tendon rupture 56 32 Frequent (79-30%) HP:0100550
25 calcification of cartilage 56 32 Very frequent (99-80%) HP:0100593
26 cartilage destruction 56 32 Frequent (79-30%) HP:0100773
27 back pain 32 HP:0003418
28 kyphosis 32 HP:0002808
29 abnormality of the eye 56 Very frequent (99-80%)
30 abnormality of metabolism/homeostasis 32 HP:0001939
31 abnormality of the heart valves 56 Frequent (79-30%)
32 aortic dilatation 32 HP:0001724
33 vertebral fusion 32 HP:0002948
34 abnormality of skin pigmentation 56 Very frequent (99-80%)
35 abnormality of the urinary system 32 HP:0000079
36 atherosclerosis 56 Occasional (29-5%)
37 abnormality of the ear 32 HP:0000598
38 intervertebral disc degeneration 32 HP:0008419
39 arthropathy 32 HP:0003040
40 growth abnormality 32 HP:0001507
41 pigmentation of the sclera 32 HP:0007832

UMLS symptoms related to Alkaptonuria:


back pain

MGI Mouse Phenotypes related to Alkaptonuria:

44
id Description MGI Source Accession Score Top Affiliating Genes
1 renal/urinary system MP:0005367 8.92 FAH GSTZ1 HGD HPD

Drugs & Therapeutics for Alkaptonuria

Drugs for Alkaptonuria (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):


id Name Status Phase Clinical Trials Cas Number PubChem Id
1
Nitisinone Approved, Investigational Phase 3,Phase 2 104206-65-7 115355
2 tyrosine Nutraceutical Phase 2

Interventional clinical trials:


id Name Status NCT ID Phase
1 Suitability of Nitisinone in Alkaptonuria 2 Active, not recruiting NCT01916382 Phase 3
2 Nitisinone (NTBC) In Different Age Groups Of Patients With Alkaptonuria Active, not recruiting NCT01390077 Phase 2, Phase 3
3 Long-Term Study of Nitisinone to Treat Alkaptonuria Completed NCT00107783 Phase 2
4 Dose Response Study of Nitisinone in Alkaptonuria Completed NCT01828463 Phase 2
5 Study of Alkaptonuria Recruiting NCT00005909

Search NIH Clinical Center for Alkaptonuria

Cochrane evidence based reviews: alkaptonuria

Genetic Tests for Alkaptonuria

Genetic tests related to Alkaptonuria:

id Genetic test Affiliating Genes
1 Alkaptonuria 29 24 HGD

Anatomical Context for Alkaptonuria

MalaCards organs/tissues related to Alkaptonuria:

39
Heart, Kidney, Skin, Prostate, Bone, Eye, Brain

Publications for Alkaptonuria

Articles related to Alkaptonuria:

(show top 50) (show all 167)
id Title Authors Year
1
Cartilage biomarkers in the osteoarthropathy of alkaptonuria reveal low turnover and accelerated ageing. ( 28028161 )
2017
2
Reduced primary cilia length and altered Arl13b expression are associated with deregulated chondrocyte Hedgehog signaling in alkaptonuria. ( 28158906 )
2017
3
ANNALS EXPRESS: The effect of nitisinone on homogentisic acid and tyrosine: A two-year survey of patients attending the National Alkaptonuria Centre, Liverpool. ( 28081634 )
2017
4
A new light on Alkaptonuria: A Fourier-transform infrared microscopy (FTIRM) and low energy X-ray fluorescence (LEXRF) microscopy correlative study on a rare disease. ( 28192171 )
2017
5
Aortic Valve Stenosis in Alkaptonuria. ( 28528068 )
2017
6
Alkaptonuria: A Case of Familial Inheritance from Hangarki Village in Dharwad District of Karnataka. ( 27382210 )
2016
7
Alkaptonuria Presenting with Impressive Osteoarticular Changes and Severe Aortic Stenosis. ( 27169295 )
2016
8
Alkaptonuria: a disease with dark brown urine. ( 27026014 )
2016
9
Smoothened-Antagonists Reverse Homogentisic Acid-Induced Alterations of Hedgehog Signalling and Primary Cilium Length in Alkaptonuria. ( 28019670 )
2016
10
Alkaptonuria: An example of a "fundamental disease"-A rare disease with important lessons for more common disorders. ( 26891864 )
2016
11
Inhibition of para-Hydroxyphenylpyruvate Dioxygenase by Analogues of the Herbicide Nitisinone As a Strategy to Decrease Homogentisic Acid Levels, the Causative Agent of Alkaptonuria. ( 26947423 )
2016
12
Mitral and aortic valve stenosis in alkaptonuria. ( 26823449 )
2016
13
A Founder Effect for the HGD G360R Mutation in Italy: Implications for a Regional Screening of Alkaptonuria. ( 26960557 )
2016
14
Minocycline-induced Cartilage Hyperpigmentation Mimicking Alkaptonuria in a Patient with Knee Pain. ( 27037242 )
2016
15
Mending a Darkened Heart: Alkaptonuria Discovered During Aortic Valve Replacement. ( 27002086 )
2016
16
Comparative proteomics in alkaptonuria provides insights into inflammation and oxidative stress. ( 27590860 )
2016
17
Quick Diagnosis of Alkaptonuria by Homogentisic Acid Determination in Urine Paper Spots. ( 27074788 )
2016
18
Difficult epidural in a patient with undiagnosed alkaptonuria. ( 27512176 )
2016
19
Alkaptonuria. ( 27158826 )
2016
20
Analysis of Melanin-like Pigment Synthesized from Homogentisic Acid, with or without Tyrosine, and Its Implications in Alkaptonuria. ( 27943071 )
2016
21
Neurological Assessment and Nerve Conduction Study Findings in 22 Patients with Alkaptonuria from Jordan. ( 28217270 )
2016
22
Acute fatal metabolic complications in alkaptonuria. ( 26596578 )
2016
23
A Case of Alkaptonuria with Degenerative Collagenous Plaques and Foot Drop. ( 27904192 )
2016
24
Bronchoscopic Findings in a Patient With Alkaptonuria: Black Bronchoscopy. ( 27623417 )
2016
25
Tyrosinase, could it be a missing link in ochronosis in alkaptonuria? ( 27142149 )
2016
26
Angiogenesis in alkaptonuria. ( 27671890 )
2016
27
Oxidative stress and mechanisms of ochronosis in alkaptonuria. ( 25733348 )
2015
28
Old treatments for new insights and strategies: proposed management in adults and children with alkaptonuria. ( 25860819 )
2015
29
Alkaptonuria in a 6 Year Old Patient: Case Report. ( 26793547 )
2015
30
Spontaneous Achilles tendon rupture in alkaptonuria. ( 26620992 )
2015
31
Fatal oxidative haemolysis and methaemoglobinaemia in a patient with alkaptonuria and acute kidney injury. ( 25713720 )
2015
32
Homogentisate 1,2 dioxygenase is expressed in brain: implications in alkaptonuria. ( 25762405 )
2015
33
Analysis of HGD Gene Mutations in Patients with Alkaptonuria from the United Kingdom: Identification of Novel Mutations. ( 25681086 )
2015
34
Osteoarticular cells tolerate short-term exposure to nitisinone-implications in alkaptonuria. ( 26024586 )
2015
35
Alkaptonuria and ochronotic spondyloarthropathy: a delayed imaging diagnosis. ( 26454244 )
2015
36
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy. ( 25804398 )
2015
37
The Pigment in Alkaptonuria Relationship to Melanin and Other Coloured Substances: A Review of Metabolism, Composition and Chemical Analysis. ( 26093627 )
2015
38
Serum markers in alkaptonuria: simultaneous analysis of homogentisic acid, tyrosine and nitisinone by liquid chromatography tandem mass spectrometry. ( 25628464 )
2015
39
Investigating the Robustness and Diagnostic Potential of Extracellular Matrix Remodelling Biomarkers in Alkaptonuria. ( 25786641 )
2015
40
Relationship Between Serum Concentrations of Nitisinone and Its Effect on Homogentisic Acid and Tyrosine in Patients with Alkaptonuria. ( 25772318 )
2015
41
Renal and prostate stones composition in alkaptonuria: a case report. ( 26396096 )
2015
42
Progress in Alkaptonuria--are we near to an effective therapy? ( 26280757 )
2015
43
A role for interleukins in ochronosis in a chondrocyte in vitro model of alkaptonuria. ( 26474772 )
2015
44
Alkaptonuria, more than just a mere disease. ( 25883496 )
2015
45
Age-Related Deviation of Gait from Normality in Alkaptonuria. ( 25786642 )
2015
46
Back pain in a middle-aged man: alkaptonuria. ( 25768073 )
2015
47
What does the arthropathy of alkaptonuria teach us about disease mechanisms in osteoarthritis and ageing of joints? Lessons from a rare disease. ( 26712212 )
2015
48
Metabolic Effects of Increasing Doses of Nitisinone in the Treatment of Alkaptonuria. ( 25665838 )
2015
49
Amyloidosis in alkaptonuria. ( 25868666 )
2015
50
Detection of alkaptonuria in a 1-week-old infant. ( 25956497 )
2015

Variations for Alkaptonuria

UniProtKB/Swiss-Prot genetic disease variations for Alkaptonuria:

66 (show top 50) (show all 68)
id Symbol AA change Variation ID SNP ID
1 HGD p.Glu42Ala VAR_005272 rs373921680
2 HGD p.Trp60Gly VAR_005273
3 HGD p.Tyr62Cys VAR_005274
4 HGD p.Trp97Gly VAR_005275
5 HGD p.Ala122Asp VAR_005276
6 HGD p.Asp153Gly VAR_005277 rs775274569
7 HGD p.Gly161Arg VAR_005278 rs28941783
8 HGD p.Ser189Ile VAR_005279
9 HGD p.Ile216Thr VAR_005280 rs767201131
10 HGD p.Arg225His VAR_005281 rs562853291
11 HGD p.Phe227Ser VAR_005282
12 HGD p.Pro230Ser VAR_005283 rs28942100
13 HGD p.Pro230Thr VAR_005284
14 HGD p.Asp291Glu VAR_005285 rs754428438
15 HGD p.Val300Gly VAR_005286 rs120074170
16 HGD p.Met368Val VAR_005287 rs120074173
17 HGD p.Arg330Ser VAR_008744 rs120074171
18 HGD p.His371Arg VAR_008745 rs120074172
19 HGD p.Leu25Pro VAR_009618
20 HGD p.Glu168Lys VAR_009619 rs375283568
21 HGD p.Gly270Arg VAR_009620 rs120074174
22 HGD p.Glu3Ala VAR_073076 rs200412910
23 HGD p.Glu13Lys VAR_073077
24 HGD p.Asp18Asn VAR_073078
25 HGD p.Gln33Arg VAR_073079
26 HGD p.Leu44Phe VAR_073080
27 HGD p.Arg53Gln VAR_073081 rs200808744
28 HGD p.Leu61Pro VAR_073082
29 HGD p.Phe73Leu VAR_073083
30 HGD p.Pro92Thr VAR_073084
31 HGD p.Trp97Arg VAR_073085
32 HGD p.Gly115Arg VAR_073086 rs755734596
33 HGD p.Leu116Pro VAR_073087 rs569846003
34 HGD p.Cys120Phe VAR_073088 rs752153829
35 HGD p.Cys120Trp VAR_073089 rs149165166
36 HGD p.Ala122Val VAR_073090 rs544956641
37 HGD p.Gly123Ala VAR_073091 rs374473331
38 HGD p.Gly123Arg VAR_073092 rs564979861
39 HGD p.Leu137Pro VAR_073093
40 HGD p.Gly152Ala VAR_073094
41 HGD p.Pro158Leu VAR_073095 rs375396766
42 HGD p.Glu168Asp VAR_073096 rs780173554
43 HGD p.Phe169Leu VAR_073097 rs756134838
44 HGD p.Lys171Asn VAR_073098
45 HGD p.Glu178Gly VAR_073100
46 HGD p.Gln183Arg VAR_073101
47 HGD p.Arg187Gly VAR_073102
48 HGD p.Arg197Gly VAR_073103
49 HGD p.Gly217Trp VAR_073104
50 HGD p.Asn219Ser VAR_073105

ClinVar genetic disease variations for Alkaptonuria:

6 (show all 41)
id Gene Variation Type Significance SNP ID Assembly Location
1 HGD NM_000187.3(HGD): c.688C> T (p.Pro230Ser) single nucleotide variant Pathogenic rs28942100 GRCh37 Chromosome 3, 120363252: 120363252
2 HGD NM_000187.3(HGD): c.899T> G (p.Val300Gly) single nucleotide variant Pathogenic/Likely pathogenic rs120074170 GRCh37 Chromosome 3, 120357409: 120357409
3 HGD NM_000187.3(HGD): c.990G> T (p.Arg330Ser) single nucleotide variant Pathogenic rs120074171 GRCh37 Chromosome 3, 120357318: 120357318
4 HGD NM_000187.3(HGD): c.481G> A (p.Gly161Arg) single nucleotide variant Pathogenic rs28941783 GRCh37 Chromosome 3, 120365888: 120365888
5 HGD NM_000187.3(HGD): c.457dupG (p.Asp153Glyfs) duplication Pathogenic rs397515346 GRCh37 Chromosome 3, 120366736: 120366736
6 HGD NM_000187.3(HGD): c.16-1G> A single nucleotide variant Pathogenic rs397515347 GRCh37 Chromosome 3, 120394711: 120394711
7 HGD NM_000187.3(HGD): c.175delA (p.Ser59Alafs) deletion Pathogenic rs397515517 GRCh37 Chromosome 3, 120393749: 120393749
8 HGD NM_000187.3(HGD): c.1112A> G (p.His371Arg) single nucleotide variant Pathogenic rs120074172 GRCh37 Chromosome 3, 120352070: 120352070
9 HGD NM_000187.3(HGD): c.1102A> G (p.Met368Val) single nucleotide variant Pathogenic rs120074173 GRCh37 Chromosome 3, 120352080: 120352080
10 HGD NM_000187.3(HGD): c.808G> A (p.Gly270Arg) single nucleotide variant Pathogenic rs120074174 GRCh37 Chromosome 3, 120360507: 120360507
11 HGD NM_000187.3(HGD): c.1111dupC (p.His371Profs) duplication Pathogenic rs397515516 GRCh37 Chromosome 3, 120352071: 120352071
12 HGD NM_000187.3(HGD): c.140C> T (p.Ser47Leu) single nucleotide variant Pathogenic rs369517993 GRCh37 Chromosome 3, 120393784: 120393784
13 HGD NM_000187.3(HGD): c.342+1G> A single nucleotide variant Pathogenic/Likely pathogenic rs397515518 GRCh37 Chromosome 3, 120371438: 120371438
14 HGD NM_000187.3(HGD): c.360T> G (p.Cys120Trp) single nucleotide variant Pathogenic rs149165166 GRCh37 Chromosome 3, 120369695: 120369695
15 HGD NM_000187.3(HGD): c.16-272_87+305del deletion Pathogenic GRCh38 Chromosome 3, 120675487: 120676135
16 HGD NM_000187.3(HGD): c.1336T> C (p.Ter446Arg) single nucleotide variant Likely pathogenic rs143370662 GRCh37 Chromosome 3, 120347229: 120347229
17 HGD NM_000187.3(HGD): c.674G> A (p.Arg225His) single nucleotide variant Likely pathogenic rs562853291 GRCh37 Chromosome 3, 120363266: 120363266
18 HGD NM_000187.3(HGD): c.652delG (p.Ala218Profs) deletion Likely pathogenic rs786204662 GRCh38 Chromosome 3, 120644441: 120644441
19 HGD NM_000187.3(HGD): c.365C> T (p.Ala122Val) single nucleotide variant Likely pathogenic rs544956641 GRCh38 Chromosome 3, 120650843: 120650843
20 HGD NM_000187.3(HGD): c.342+1G> T single nucleotide variant Likely pathogenic rs397515518 GRCh37 Chromosome 3, 120371438: 120371438
21 HGD NM_000187.3(HGD): c.11T> A (p.Leu4Ter) single nucleotide variant Likely pathogenic rs786204422 GRCh38 Chromosome 3, 120682101: 120682101
22 HGD NM_000187.3(HGD): c.1201G> C (p.Glu401Gln) single nucleotide variant Likely pathogenic rs767159114 GRCh38 Chromosome 3, 120628517: 120628517
23 HGD NM_000187.3(HGD): c.1188+1G> T single nucleotide variant Likely pathogenic rs760206323 GRCh38 Chromosome 3, 120633146: 120633146
24 HGD NM_000187.3(HGD): c.1064dupG (p.Gly356Trpfs) duplication Likely pathogenic rs1057516847 GRCh38 Chromosome 3, 120633271: 120633271
25 HGD NM_000187.3(HGD): c.1017_1019delGAGinsTA (p.Met339Ilefs) indel Pathogenic rs1057517081 GRCh38 Chromosome 3, 120633316: 120633318
26 HGD NM_000187.3(HGD): c.970dupG (p.Val324Glyfs) duplication Likely pathogenic rs1057517371 GRCh38 Chromosome 3, 120638491: 120638491
27 HGD NM_000187.3(HGD): c.956delC (p.Pro319Hisfs) deletion Likely pathogenic rs1057517089 GRCh38 Chromosome 3, 120638505: 120638505
28 HGD NM_000187.3(HGD): c.781dupT (p.Ser261Phefs) duplication Likely pathogenic rs1057517418 GRCh38 Chromosome 3, 120641687: 120641687
29 HGD NM_000187.3(HGD): c.649+2T> C single nucleotide variant Likely pathogenic rs1057516307 GRCh38 Chromosome 3, 120646265: 120646265
30 HGD NM_000187.3(HGD): c.409delC (p.Leu137Serfs) deletion Likely pathogenic rs1057516921 GRCh38 Chromosome 3, 120650799: 120650799
31 HGD NM_000187.3(HGD): c.390delG (p.Ala132Leufs) deletion Likely pathogenic rs1057516352 GRCh38 Chromosome 3, 120650818: 120650818
32 HGD NM_000187.3(HGD): c.376_377delAA (p.Lys126Valfs) deletion Likely pathogenic rs1057516976 GRCh38 Chromosome 3, 120650831: 120650832
33 HGD NM_000187.3(HGD): c.346delC (p.Leu116Cysfs) deletion Likely pathogenic rs1057516911 GRCh38 Chromosome 3, 120650862: 120650862
34 HGD NM_000187.3(HGD): c.339_342+2del6 deletion Likely pathogenic rs1057516662 GRCh38 Chromosome 3, 120652590: 120652595
35 HGD NM_000187.3(HGD): c.179G> A (p.Trp60Ter) single nucleotide variant Likely pathogenic rs1057516467 GRCh38 Chromosome 3, 120670530: 120670530
36 HGD NM_000187.3(HGD): c.177-1G> A single nucleotide variant Likely pathogenic rs1057517370 GRCh38 Chromosome 3, 120670533: 120670533
37 HGD NM_000187.3(HGD): c.158G> A (p.Arg53Gln) single nucleotide variant Likely pathogenic rs200808744 GRCh38 Chromosome 3, 120674919: 120674919
38 HGD NM_000187.3(HGD): c.58delC (p.Arg20Alafs) deletion Likely pathogenic rs1057516849 GRCh38 Chromosome 3, 120675821: 120675821
39 HGD NM_000187.3(HGD): c.31_32delGGinsATT (p.Gly11Ilefs) indel Likely pathogenic rs1057516362 GRCh38 Chromosome 3, 120675847: 120675848
40 HGD NM_000187.3(HGD): c.15+1G> A single nucleotide variant Likely pathogenic rs552207335 GRCh37 Chromosome 3, 120400943: 120400943
41 HGD NM_000187.3(HGD): c.3G> C (p.Met1Ile) single nucleotide variant Likely pathogenic rs1057516355 GRCh37 Chromosome 3, 120400956: 120400956

Expression for Alkaptonuria

Search GEO for disease gene expression data for Alkaptonuria.

Pathways for Alkaptonuria

GO Terms for Alkaptonuria

Biological processes related to Alkaptonuria according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 oxidation-reduction process GO:0055114 9.43 DCXR HGD HPD
2 aromatic amino acid family metabolic process GO:0009072 9.33 FAH GSTZ1 HPD
3 L-phenylalanine catabolic process GO:0006559 9.26 FAH GSTZ1 HGD HPD
4 tyrosine catabolic process GO:0006572 8.92 FAH GSTZ1 HGD HPD

Molecular functions related to Alkaptonuria according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 oxidoreductase activity GO:0016491 9.13 DCXR HGD HPD
2 dioxygenase activity GO:0051213 8.62 HGD HPD

Sources for Alkaptonuria

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
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