OTX2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 14[13]
- Cytogenetic location
- 14q22.3[17]
- Encodes
- Orthodenticle homeobox 2[11]
- Expressed in
- secondary oocyte, retinal pigment epithelium, cerebellar hemisphere, right hemisphere of cerebellum, lateral nuclear group of thalamus, nasal epithelium, gonad, tibialis anterior muscle, substantia nigra, olfactory zone of nasal mucosa[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- fundus dystrophy, hypopituitarism[14][15]
- HomoloGene ID
- 11026[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en CPHD6
en MCOPS5
en Orthodenticle homeobox 2
en OTX2
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- Protein OTX2 PDB 2dms.png ↗
- Ensembl gene ID
- ENSG00000165588
- Ensembl transcript ID
- ENST00000555804, ENST00000339475, ENST00000408990, ENST00000554559, ENST00000554788, ENST00000554845, ENST00000555006, ENST00000672125, ENST00000673035, ENST00000672264, ENST00000673481, ENST00000685244
- Entrez Gene ID
- 5015
- Exact match
- identifiers.org
- Freebase ID
- /m/03gycz_
- HGNC ID
- 8522
- HGNC gene symbol
- OTX2
- Microsoft Academic ID (discontinued)
- 2781056311
- OMIM ID
- 600037
- RefSeq RNA ID
- NR_073036, NM_001270523, NM_001270524, NM_001270525, NM_021728, NM_172337, NR_073034
- UMLS CUI
- C1418202
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