Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1746
Gene name Gene Name - the full gene name approved by the HGNC.
Distal-less homeobox 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DLX2
Synonyms (NCBI Gene) Gene synonyms aliases
TES-1, TES1
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.
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT043264 hsa-miR-331-3p CLASH 23622248
MIRT042820 hsa-miR-324-3p CLASH 23622248
MIRT036105 hsa-miR-1296-5p CLASH 23622248
MIRT567747 hsa-miR-551b-5p PAR-CLIP 20371350
MIRT567746 hsa-miR-300 PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0000785 Component Chromatin ISA
GO:0000976 Function Transcription cis-regulatory region binding IEA
GO:0000976 Function Transcription cis-regulatory region binding ISS
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
126255 2915 ENSG00000115844
Protein
UniProt ID Q07687
Protein name Homeobox protein DLX-2
Protein function Acts as a transcriptional activator (By similarity). Activates transcription of CGA/alpha-GSU, via binding to the downstream activin regulatory element (DARE) in the gene promoter (By similarity). Plays a role in terminal differentiation of inte
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12413 DLL_N 51 132 Homeobox protein distal-less-like N terminal Family
PF00046 Homeodomain 153 209 Homeodomain Domain
Sequence
MTGVFDSLVADMHSTQIAASSTYHQHQQPPSGGGAGPGGNSSSSSSLHKPQESPTLPVST
ATDSSYYTNQQHPAGGGGGGGSPYAHMGSYQYQASGLNNVPYSAKSSYDLGYTAAYTSYA
PYGTSSSPANNE
PEKEDLEPEIRIVNGKPKKVRKPRTIYSSFQLAALQRRFQKTQYLALP
ERAELAASLGLTQTQVKIWFQNRRSKFKK
MWKSGEIPSEQHPGASASPPCASPPVSAPAS
WDFGVPQRMAGGGGPGSGGSGAGSSGSSPSSAASAFLGNYPWYHQTSGSASHLQATAPLL
HPTQTPQPHHHHHHHGGGGAPVSAGTIF
Sequence length 328
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
Breast cancer Breast cancer N/A N/A GWAS
Carcinoma Basal cell carcinoma N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Astrocytoma Associate 20233874
Autism Spectrum Disorder Associate 18728693
Autistic Disorder Associate 18728693
Autoimmune Diseases Associate 36317140
Carcinoma Hepatocellular Associate 31059056
Carcinoma Renal Cell Associate 36344906
Carcinoma Squamous Cell Associate 36317140
Colorectal Neoplasms Associate 34789836
Hematologic Neoplasms Associate 26799321
Immune System Diseases Stimulate 36317140