NM_013382.7(POMT2):c.1997A>G (p.Tyr666Cys) AND Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
- Germline classification:
- Pathogenic (2 submissions)
- Last evaluated:
- Oct 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000003377.12
Allele description [Variation Report for NM_013382.7(POMT2):c.1997A>G (p.Tyr666Cys)]
NM_013382.7(POMT2):c.1997A>G (p.Tyr666Cys)
Condition(s)
- Name:
- Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
- Synonyms:
- MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2; WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED; Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2
- Identifiers:
- MONDO: MONDO:0013154; MedGen: C3150411; Orphanet: 588; Orphanet: 899; OMIM: 613150
-
heterogeneous nuclear ribonucleoprotein M isoform X5 [Ailuropoda melanoleuca]
heterogeneous nuclear ribonucleoprotein M isoform X5 [Ailuropoda melanoleuca]gi|1845660089|ref|XP_011234518.2|Protein
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Last Updated: May 7, 2024