Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
30851
Gene name Gene Name - the full gene name approved by the HGNC.
Tax1 binding protein 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TAX1BP3
Synonyms (NCBI Gene) Gene synonyms aliases
TIP-1, TIP1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a small, highly conserved protein with a single PDZ domain. PDZ (PSD-95/Discs large/ZO-1 homologous) domains promote protein-protein interactions that affect cell signaling, adhesion, protein scaffolding, and receptor and ion transporter
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022204 hsa-miR-124-3p Microarray 18668037
MIRT028783 hsa-miR-26b-5p Microarray 19088304
MIRT049449 hsa-miR-92a-3p CLASH 23622248
MIRT043024 hsa-miR-324-5p CLASH 23622248
MIRT696718 hsa-miR-4494 HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001650 Component Fibrillar center IDA
GO:0005515 Function Protein binding IPI 10940294, 11163757, 15492812, 21139582, 25416956
GO:0005737 Component Cytoplasm NAS 10940294
GO:0005829 Component Cytosol TAS
GO:0005886 Component Plasma membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616484 30684 ENSG00000213977
Protein
UniProt ID O14907
Protein name Tax1-binding protein 3 (Glutaminase-interacting protein 3) (Tax interaction protein 1) (TIP-1) (Tax-interacting protein 1)
Protein function May regulate a number of protein-protein interactions by competing for PDZ domain binding sites. Binds CTNNB1 and may thereby act as an inhibitor of the Wnt signaling pathway. Competes with LIN7A for KCNJ4 binding, and thereby promotes KCNJ4 int
PDB 2KG2 , 2L4S , 2L4T , 2VZ5 , 3GJ9 , 3SFJ , 4E3B , 4NNL , 4NNM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00595 PDZ 17 110 PDZ domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Detected in brain, heart, kidney, lung, small intestine and skeletal muscle. Detected in various cell lines including HeLa. Weakly expressed in peripheral blood leukocytes. {ECO:0000269|PubMed:10940294, ECO:0000269|PubMed:1
Sequence
Sequence length 124
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RHO GTPases Activate Rhotekin and Rhophilins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Apraxia Apraxia of Phonation rs121908377, rs121908378, rs1135401820, rs1178491246, rs1584969672
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
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