Gene Gene information from NCBI Gene database.
Entrez ID 85450
Gene name Inositol 1,4,5-trisphosphate receptor interacting protein
Gene symbol ITPRIP
Synonyms (NCBI Gene)
D1ADANGERKIAA1754bA127L20bA127L20.2
Chromosome 10
Chromosome location 10q25.1
Summary This gene encodes a membrane-associated protein that binds the inositol 1,4,5-trisphosphate receptor (ITPR). The encoded protein enhances the sensitivity of ITPR to intracellular calcium signaling. Alternative splicing results in multiple transcript varia
miRNA miRNA information provided by mirtarbase database.
215
miRTarBase ID miRNA Experiments Reference
MIRT019219 hsa-miR-335-5p Microarray 18185580
MIRT022688 hsa-miR-124-3p Microarray 18668037
MIRT028624 hsa-miR-30a-5p Proteomics 18668040
MIRT038902 hsa-miR-93-3p CLASH 23622248
MIRT687824 hsa-miR-5011-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0004860 Function Protein kinase inhibitor activity IBA
GO:0004860 Function Protein kinase inhibitor activity IEA
GO:0005515 Function Protein binding IPI 25464930, 32296183, 35271311
GO:0005634 Component Nucleus IEA
GO:0005640 Component Nuclear outer membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620205 29370 ENSG00000148841
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IWB1
Protein name Inositol 1,4,5-trisphosphate receptor-interacting protein (Protein DANGER)
Protein function Enhances Ca(2+)-mediated inhibition of inositol 1,4,5-triphosphate receptor (ITPR) Ca(2+) release.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03281 Mab-21 280 483 Mab-21 protein Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain where it is concentrated in cerebellar Purkinje cells (at protein level). {ECO:0000269|PubMed:16990268}.
Sequence
MAMGLFRVCLVVVTAIINHPLLFPRENATVPENEEEIIRKMQAHQEKLQLEQLRLEEEVA
RLAAEKEALEQVAEEGRQQNETRVAWDLWSTLCMILFLMIEVWRQDHQEGPSPECLGGEE
DELPGLGGAPLQGLTLPNKATLGHFYERCIRGATADAARTREFLEGFVDDLLEALRSLCN
RDTDMEVEDFIGVDSMYENWQVDRPLLCHLFVPFTPPEPYRFHPELWCSGRSVPLDRQGY
GQIKVVRADGDTLSCICGKTKLGEDMLCLLHGRNSMAPPCGDMENLLCATDSLYLDTMQV
MKWFQTALTRAWKGIAHKYEFDLAFGQLDSPGSLKIKFRSGKFMPFNLIPVIQCDDSDLY
FVSHLPREPSEGTPASSTDWLLSFAVYERHFLRTTLKALPEGACHLSCLQIASFLLSKQS
RLTGPSGLSSYHLKTALLHLLLLRQAADWKAGQLDARLHELLCFLEKSLLQKKLHHFFIG
NRK
VPEAMGLPEAVLRAEPLNLFRPFVLQRSLYRKTLDSFYEMLKNAPALISEYSLHVPS
DQPTPKS
Sequence length 547
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
UTERINE FIBROID GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Lupus Nephritis Lupus Nephritis BEFREE 26223295
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 28504304
★☆☆☆☆
Found in Text Mining only
Multiple Myeloma Multiple myeloma BEFREE 26537080
★☆☆☆☆
Found in Text Mining only
Multiple Myeloma Multiple myeloma Pubtator 26537080 Associate
★☆☆☆☆
Found in Text Mining only