NM_025114.4(CEP290):c.4909_4910del (p.Leu1637fs) AND multiple conditions
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Apr 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003790581.2
Allele description [Variation Report for NM_025114.4(CEP290):c.4909_4910del (p.Leu1637fs)]
NM_025114.4(CEP290):c.4909_4910del (p.Leu1637fs)
Condition(s)
- Name:
- Familial aplasia of the vermis
- Synonyms:
- CEREBELLOPARENCHYMAL DISORDER IV; Joubert syndrome; Cerebelloparenchymal disorder 4; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0018772; MedGen: C0431399; Orphanet: 475; OMIM: PS213300
- Name:
- Meckel-Gruber syndrome
- Synonyms:
- DYSENCEPHALIA SPLANCHNOCYSTICA; Gruber syndrome; Dysencephalia splachnocystica
- Identifiers:
- MONDO: MONDO:0018921; MedGen: C0265215; OMIM: PS249000
- Name:
- Nephronophthisis
- Synonyms:
- juvenile nephronophthisis
- Identifiers:
- MONDO: MONDO:0019005; MedGen: C0687120; OMIM: PS256100; Human Phenotype Ontology: HP:0000090
-
Homo sapiens microtubule-associated protein 4 (MAP4), transcript variant 3, mRNA
Homo sapiens microtubule-associated protein 4 (MAP4), transcript variant 3, mRNAgi|14195627|ref|NM_030885.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024