PAX1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 20[13]
- Cytogenetic location
- 20p11.22[16]
- Encodes
- Paired box 1[11]
- Expressed in
- thymus, testicle, tibia, oral cavity, buccal mucosa cell, tonsil, amniotic fluid, olfactory zone of nasal mucosa, superior surface of tongue, bronchial epithelial cell[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- otofaciocervical syndrome[14]
- HomoloGene ID
- 4514[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en HUP48
en OFC2
en paired box 1
en PAX1
ar PAX١
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000125813
- Ensembl transcript ID
- ENST00000613128, ENST00000398485, ENST00000444366, ENST00000460221, ENST00000485038
- Entrez Gene ID
- 5075
- Exact match
- identifiers.org
- Freebase ID
- /m/03g__p3
- HGNC ID
- 8615
- HGNC gene symbol
- PAX1
- OMIM ID
- 167411
- RefSeq RNA ID
- NM_006192, NM_001257096
- UMLS CUI
- C1418273
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Instance of 1
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