LCA5
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 6[11]
- Cytogenetic location
- 6q14.1[15]
- Encodes
- Lebercilin LCA5[9]
- Expressed in
- mucosa of paranasal sinus, bronchial epithelial cell, caput epididymis, testicle, Achilles tendon, secondary oocyte, right uterine tube, ventricular zone, ganglionic eminence, gonad[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Leber congenital amaurosis 5, fundus dystrophy[12][13]
- HomoloGene ID
- 32718[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en Leber congenital amaurosis 5
en C6orf152
en LCA5
en LCA5, lebercilin
en lebercilin LCA5
ar LCA٥
pt Lebercilina
pt Lebercilina LCA5
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000135338
- Ensembl transcript ID
- ENST00000467898, ENST00000369846, ENST00000392959
- Entrez Gene ID
- 167691
- Exact match
- identifiers.org
- Freebase ID
- /m/043nsg1
- HGNC ID
- 31923
- HGNC gene symbol
- LCA5
- OMIM ID
- 611408
- RefSeq RNA ID
- XM_011535504, NM_001122769, NM_181714, XM_005248665, XM_047418251
- UMLS CUI
- C1537529
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
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