MRX42
MCID: MNT205
MIFTS: 13

Mental Retardation, X-Linked 42 (MRX42)

Categories: Fetal diseases, Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Mental Retardation, X-Linked 42

MalaCards integrated aliases for Mental Retardation, X-Linked 42:

Name: Mental Retardation, X-Linked 42 56 13 71
Mrx42 56

Classifications:



External Ids:

OMIM 56 300372
OMIM Phenotypic Series 56 PS309530
UMLS 71 C1845810

Summaries for Mental Retardation, X-Linked 42

MalaCards based summary : Mental Retardation, X-Linked 42, also known as mrx42, is related to autism x-linked 2. An important gene associated with Mental Retardation, X-Linked 42 is MRX42 (Mental Retardation, X-Linked 42). Affiliated tissues include testes.

More information from OMIM: 300372 PS309530

Related Diseases for Mental Retardation, X-Linked 42

Symptoms & Phenotypes for Mental Retardation, X-Linked 42

Clinical features from OMIM:

300372

Drugs & Therapeutics for Mental Retardation, X-Linked 42

Search Clinical Trials , NIH Clinical Center for Mental Retardation, X-Linked 42

Genetic Tests for Mental Retardation, X-Linked 42

Anatomical Context for Mental Retardation, X-Linked 42

MalaCards organs/tissues related to Mental Retardation, X-Linked 42:

40
Testes

Publications for Mental Retardation, X-Linked 42

Articles related to Mental Retardation, X-Linked 42:

# Title Authors PMID Year
1
MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation. 61 56
11807862 2002
2
Fragile X and X-linked intellectual disability: four decades of discovery. 6
22482801 2012
3
Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. 6
21956720 2011
4
Familial deletion within NLGN4 associated with autism and Tourette syndrome. 6
18231125 2008
5
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. 6
14963808 2004

Variations for Mental Retardation, X-Linked 42

Expression for Mental Retardation, X-Linked 42

Search GEO for disease gene expression data for Mental Retardation, X-Linked 42.

Pathways for Mental Retardation, X-Linked 42

GO Terms for Mental Retardation, X-Linked 42

Sources for Mental Retardation, X-Linked 42

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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