Protein-coding gene in the species Homo sapiens
HOXD9 Identifiers Aliases HOXD9 , HOX4, HOX4C, Hox-4.3, Hox-5.2, homeobox D9External IDs OMIM: 142982; MGI: 96210; HomoloGene: 8409; GeneCards: HOXD9; OMA:HOXD9 - orthologs Gene location (Human) Chr. Chromosome 2 (human)[1] Band 2q31.1 Start 176,122,719 bp[1] End 176,124,937 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2 C3|2 44.13 cM Start 74,528,071 bp[2] End 74,530,552 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in body of uterus tendon of biceps brachii canal of the cervix vagina ectocervix myometrium muscle layer of sigmoid colon buccal mucosa cell testicle stromal cell of endometrium
Top expressed in Gonadal ridge gastrula decidua medullary collecting duct endothelial cell of lymphatic vessel seminal vesicula medial head of gastrocnemius muscle cumulus cell tail of embryo urothelium
More reference expression data
BioGPS More reference expression data
Gene ontology Molecular function
DNA binding
sequence-specific DNA binding
RNA polymerase II transcription regulatory region sequence-specific DNA binding
DNA-binding transcription factor activity
DNA-binding transcription repressor activity, RNA polymerase II-specific
DNA-binding transcription factor activity, RNA polymerase II-specific
Cellular component Biological process
embryonic skeletal system morphogenesis
forelimb morphogenesis
peripheral nervous system neuron development
proximal/distal pattern formation
regulation of transcription, DNA-templated
adult locomotory behavior
negative regulation of transcription by RNA polymerase II
hindlimb morphogenesis
transcription, DNA-templated
single fertilization
embryonic skeletal system development
mammary gland development
multicellular organism development
regulation of gene expression
skeletal muscle tissue development
embryonic forelimb morphogenesis
anterior/posterior pattern specification
positive regulation of transcription by RNA polymerase II
Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez Ensembl UniProt RefSeq (mRNA) RefSeq (protein) Location (UCSC) Chr 2: 176.12 – 176.12 Mb Chr 2: 74.53 – 74.53 Mb PubMed search [3] [4]
Wikidata View/Edit Human View/Edit Mouse
Homeobox protein Hox-D9 is a protein that in humans is encoded by the HOXD9 gene.[5] [6] [7]
^ a b c GRCh38: Ensembl release 89: ENSG00000128709 – Ensembl, May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000043342 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine .
^ McAlpine PJ, Shows TB (Aug 1990). "Nomenclature for human homeobox genes". Genomics . 7 (3): 460. doi:10.1016/0888-7543(90)90186-X. PMID 1973146.
^ Scott MP (Dec 1992). "Vertebrate homeobox gene nomenclature". Cell . 71 (4): 551–3. doi:10.1016/0092-8674(92)90588-4. PMID 1358459. S2CID 13370372.
^ "Entrez Gene: HOXD9 homeobox D9".
Last Update: 2023-09-06T12:57:11Z
Homeobox protein Hox-D9 is a protein that in humans is encoded by the HOXD9 gene. This gene belongs to the homeobox family of genes. The homeobox genes...
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Last Update: 2024-04-01T17:54:09Z
HOXC4, HOXC5, HOXC6, HOXC8, HOXC9, HOXC10, HOXC11, HOXC12, HOXC13 HOXD@ chromosome 2 HOXD1, HOXD3, HOXD4, HOXD8, HOXD9 , HOXD10, HOXD11, HOXD12, HOXD13...
Word Count : 6046
Last Update: 2023-09-23T02:10:54Z
ENSG00000175879 Homeodomain Known motif – High-throughput in vitro [409] HWMATTWDB HOXD9 ENSG00000128709 Homeodomain Known motif – High-throughput in vitro [410]...
Word Count : 81
Last Update: 2024-04-01T17:00:44Z
HOXC5, HOXC6, HOXC8, HOXC9, HOXC10, HOXC11, HOXC12, HOXC13 HOXD - HOXD@ chromosome 2 HOXD1, HOXD3, HOXD4, HOXD8, HOXD9 , HOXD10, HOXD11, HOXD12, HOXD13...
Word Count : 4469
Last Update: 2024-04-11T04:08:24Z
posterior ZPA (where HOXD9 , 10, 11, 12, and 13 are all expressed), while less expression occurs around the AER, where only HOXD9 and HOXD10 are expressed...
Word Count : 3322
Last Update: 2024-04-04T22:42:44Z
Collins AL, Scambler PJ (February 2002). "A 117-kb microdeletion removing HOXD9 -HOXD13 and EVX2 causes synpolydactyly". American Journal of Human Genetics...
Word Count : 1247
Last Update: 2022-09-14T23:16:36Z
Majewski F, Collins AL, Scambler PJ (2002). "A 117-kb Microdeletion Removing HOXD9 –HOXD13 and EVX2 Causes Synpolydactyly". Am. J. Hum. Genet. 70 (2): 547–55...
Word Count : 825
Last Update: 2024-04-16T20:57:14Z
F, Collins AL, Scambler PJ (Feb 2002). "A 117-kb microdeletion removing HOXD9 -HOXD13 and EVX2 causes synpolydactyly". American Journal of Human Genetics...
Word Count : 1110
Last Update: 2023-12-12T11:33:52Z
Majewski F, Collins AL, Scambler PJ (2002). "A 117-kb Microdeletion Removing HOXD9 –HOXD13 and EVX2 Causes Synpolydactyly". Am. J. Hum. Genet. 70 (2): 547–55...
Word Count : 761
Last Update: 2022-12-19T23:27:11Z
Majewski F, Collins AL, Scambler PJ (2002). "A 117-kb Microdeletion Removing HOXD9 –HOXD13 and EVX2 Causes Synpolydactyly". Am. J. Hum. Genet. 70 (2): 547–55...
Word Count : 881