ABCD3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[15]
- Cytogenetic location
- 1p21.3[18]
- Expressed in
- secondary oocyte, jejunal mucosa, epithelium of nasopharynx, Epithelium of choroid plexus, mucosa of paranasal sinus, bronchial epithelial cell, kidney tubule, retinal pigment epithelium, palpebral conjunctiva, skin of thigh[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[14]
- Genetic association
- congenital bile acid synthesis defect 5[16]
- HomoloGene ID
- 2140[3]
- Strand orientation
- forward strand[17]
🏷️ Also known as
en ABC43
en ABCD3
en ATP binding cassette subfamily D member 3
en CBAS5
en PMP70
en PXMP1
en ZWS2
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000117528
- Ensembl transcript ID
- ENST00000493416, ENST00000315713, ENST00000370214, ENST00000464165, ENST00000468860, ENST00000484213, ENST00000647998
- Entrez Gene ID
- 5825
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxpl4
- HGNC ID
- 67
- HGNC gene symbol
- ABCD3
- Microsoft Academic ID (discontinued)
- 2775832604
- OMIM ID
- 170995
- RefSeq RNA ID
- XM_011541877, NM_001122674, NM_002858, XM_006710802
- UMLS CUI
- C1412090
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