USH2A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[11]
- Cytogenetic location
- 1q41[15]
- Expressed in
- testicle, right lobe of liver, gonad, sperm, islet of Langerhans, right testis, left testis, apex of heart, muscle of thigh, right auricle of heart[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Usher syndrome type 2A, retinitis pigmentosa 39[12][13]
- HomoloGene ID
- 66151[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en Usher syndrome 2A (autosomal recessive, mild)
en dJ1111A8.1
en RP39
en US2
en USH2
en USH2A
en usherin
ar USH٢A
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000042781
- Ensembl transcript ID
- ENST00000481786, ENST00000307340, ENST00000366942, ENST00000463147, ENST00000674083
- Entrez Gene ID
- 7399
- Exact match
- identifiers.org
- Freebase ID
- /m/03cwr85
- HGNC ID
- 12601
- HGNC gene symbol
- USH2A
- OMIM ID
- 608400
- UMLS CUI
- C1421381
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
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