HOXD13
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 2[11]
- Cytogenetic location
- 2q31.1[17]
- Encodes
- Homeobox D13[9]
- Expressed in
- urethra, vagina, muscle layer of sigmoid colon, ectocervix, Achilles tendon, seminal vesicula, prostate, canal of the cervix, vulva, rectum[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- brachydactyly-syndactyly syndrome, brachydactyly type E1, VACTERL association, syndactyly[12][13][14][15]
- HomoloGene ID
- 20147[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en SPD1
en BDE
en BDSD
en homeobox D13
en HOX4I
en HOXD13
en SPD
ar HOXD١٣
fa HOXD13 هموباکس d13
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000128714
- Ensembl transcript ID
- ENST00000392539
- Entrez Gene ID
- 3239
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxffn
- HGNC ID
- 5136
- HGNC gene symbol
- HOXD13
- Microsoft Academic ID (discontinued)
- 2780103563
- OMIM ID
- 142989
- RefSeq RNA ID
- NM_000523, XM_011511068, XM_011511069
- UMLS CUI
- C1415687
🔗 Connections
Expressed in 8
← Genetic association 3
Genetic association 2
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
HOXD13 is a gene[1].