Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
85458
Gene name Gene Name - the full gene name approved by the HGNC.
DIX domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DIXDC1
Synonyms (NCBI Gene) Gene synonyms aliases
CCD1
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q23.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a positive regulator of the Wnt signaling pathway. The encoded protein is found associated with gamma tubulin at the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms.
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1419374563 C>G,T Likely-pathogenic Genic downstream transcript variant, coding sequence variant, missense variant, stop gained, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016151 hsa-miR-615-3p Sequencing 20371350
MIRT051092 hsa-miR-16-5p CLASH 23622248
MIRT438828 hsa-miR-582-5p qRT-PCR 23295946
MIRT438826 hsa-miR-582-3p qRT-PCR 23295946
MIRT438828 hsa-miR-582-5p qRT-PCR 23295946
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001725 Component Stress fiber IEA
GO:0003779 Function Actin binding IEA
GO:0005515 Function Protein binding IPI 17043677, 20823832, 21189423, 31413325, 33961781
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610493 23695 ENSG00000150764
Protein
UniProt ID Q155Q3
Protein name Dixin (Coiled-coil protein DIX1) (Coiled-coil-DIX1) (DIX domain-containing protein 1)
Protein function Positive effector of the Wnt signaling pathway; activates WNT3A signaling via DVL2. Regulates JNK activation by AXIN1 and DVL2.
PDB 3PZ7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00307 CH 20 128 Calponin homology (CH) domain Domain
PF00778 DIX 599 678 DIX domain Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed with higher expression in cardiac and skeletal muscles. {ECO:0000269|PubMed:16814745}.
Sequence
MLACLTRGNLLDVLQEGFNEQQLQAYVAWVNAQLKKRPAVKPVQDLRQDLRDGVILAYLI
EIVAGEKLSGVQLSPGNQQEMKNNVEKVLQFVASKKIRMHQTSAKDIVDGNLKSIMRLVL
ALAAHFKP
GSSRTVNQGRDSRAPLQSHRPHCATAVAQGAAAALADVCHDMSRSGRDVFRY
RQRNSSMDEEIENPYWSVRALVQQYEGQQRSPSESSCSSLTSPSPIHSAKSESIITQSEE
KADFVIIPAEGIENRTEGTDSPLSRDWRPGSPGTYLETSWEEQLLEQQEYLEKEMEEAKK
MISGLQALLLNGSLPEDEQERPLALCEPGVNPEEQLIIIQSRLDQSMEENQDLKKELLKC
KQEARNLQGIKDALQQRLTQQDTSVLQLKQELLRANMDKDELHNQNVDLQRKLDERNRLL
GEYKKELGQKDRLLQQHQAKLEEALRKLSDVSYHQVDLERELEHKDVLLAHCMKREADEA
TNYNSHNSQSNGFLLPTAGKGATSVSNRGTSDLQLVRDALRSLRNSFSGHDPQHHTIDSL
EQGISSLMERLHVMETQKKQERKVRVKSPRTQVGSEYRESWPPNSKLPHSQSSPTVSSTC
TKVLYFTDRSLTPFMVNIPKRLEEVTLKDFKAAIDREGNHRYHFKALDPEFGTVKEEIFH
DDDAIPGWEGKIVAWVEE
DHGEN
Sequence length 683
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)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Obesity obesity rs1419374563 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Brain Neoplasms Associate 22688887
Carcinoma Hepatocellular Inhibit 27468723
Colorectal Neoplasms Associate 27817168
Glioma Associate 22688887, 27817168
Neoplasms Inhibit 27468723
Squamous Cell Carcinoma of Head and Neck Associate 32495922
Stomach Neoplasms Associate 27817168, 28800791, 34898351