Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3233
Gene name Gene Name - the full gene name approved by the HGNC.
Homeobox D4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HOXD4
Synonyms (NCBI Gene) Gene synonyms aliases
HHO.C13, HOX-5.1, HOX4, HOX4B, Hox-4.2
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q31.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene cluster
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT623680 hsa-miR-6835-3p HITS-CLIP 23824327
MIRT623679 hsa-miR-451b HITS-CLIP 23824327
MIRT648193 hsa-miR-6734-3p HITS-CLIP 23824327
MIRT623678 hsa-miR-302a-5p HITS-CLIP 23824327
MIRT623677 hsa-miR-4326 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IMP 1756725
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
142981 5138 ENSG00000170166
Protein
UniProt ID P09016
Protein name Homeobox protein Hox-D4 (Homeobox protein HHO.C13) (Homeobox protein Hox-4B) (Homeobox protein Hox-5.1)
Protein function Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00046 Homeodomain 155 211 Homeodomain Domain
Sequence
MVMSSYMVNSKYVDPKFPPCEEYLQGGYLGEQGADYYGGGAQGADFQPPGLYPRPDFGEQ
PFGGSGPGPGSALPARGHGQEPGGPGGHYAAPGEPCPAPPAPPPAPLPGARAYSQSDPKQ
PPSGTALKQPAVVYPWMKKVHVNSVNPNYTGGEPKRSRTAYTRQQVLELEKEFHFNRYLT
RRRRIEIAHTLCLSERQIKIWFQNRRMKWKK
DHKLPNTKGRSSSSSSSSSCSSSVAPSQH
LQPMAKDHHTDLTTL
Sequence length 255
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Lymphoblastic Leukemia Leukemia, acute lymphoblastic, susceptibility to N/A N/A ClinVar
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arachnoid Cysts Associate 26545093
Breast Neoplasms Associate 19232136
Carcinoma Hepatocellular Associate 22976466
Carcinoma Renal Cell Associate 37827698
Lymphatic Metastasis Stimulate 30588951
Neoplasms Associate 30588951, 36213580, 37827698
Neuroblastoma Associate 7501971
Neurofibroma Associate 32366326
Ovarian Neoplasms Associate 36213580
Plaque Atherosclerotic Associate 25856389