FKBP14
protein-coding gene in the species Homo sapiens
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Summary
FKBP14 is a gene[1]. FKBP14 is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 23059[4]
- Genomic start: 30010587[5], 30050203[6]
- Genomic end: 30066300[7], 30026702[8]
- Ortholog: Fkbp14[9]
- Encodes: FKBP prolyl isomerase 14[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 7[12]
- Genetic association: Ehlers-Danlos syndrome, kyphoscoliotic and deafness type[13]
- Strand orientation: reverse strand[14]
- Exact match: http://identifiers.org/ncbigene/55033[15]
- Cytogenetic location: 7p14.3[16]
- Expressed in: tibia[17], corpus epididymis[18], cartilage tissue[19], stromal cell of endometrium[20], smooth muscle tissue[21], tail of epididymis[22], right ventricle[23], skin of hip[24], skin of thigh[25], islet of Langerhans[26]