NM_025114.4(CEP290):c.441+18T>C AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002079472.6
Allele description [Variation Report for NM_025114.4(CEP290):c.441+18T>C]
NM_025114.4(CEP290):c.441+18T>C
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
-
C-terminal-binding protein-like isoform X1 [Penaeus japonicus]
C-terminal-binding protein-like isoform X1 [Penaeus japonicus]gi|2080963466|ref|XP_042875383.1|Protein
-
CtBP [Penaeus japonicus]
CtBP [Penaeus japonicus]Gene ID:122255395Gene
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Last Updated: Sep 29, 2024