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Gene Gene information from NCBI Gene database.
Entrez ID 162073
Gene name ITPRIP like 2
Gene symbol ITPRIPL2
Synonyms (NCBI Gene)
D1C
Chromosome 16
Chromosome location 16p12.3
miRNA miRNA information provided by mirtarbase database.
1520 Show/Hide all (1520)
miRTarBase ID miRNA Experiments Reference
MIRT049933 hsa-miR-30a-5p CLASH 23622248
MIRT040116 hsa-miR-615-3p CLASH 23622248
MIRT040116 hsa-miR-615-3p CLASH 23622248
MIRT522930 hsa-miR-3156-5p HITS-CLIP 21572407
MIRT511362 hsa-miR-1277-5p HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3MIP1
Protein name Inositol 1,4,5-trisphosphate receptor-interacting protein-like 2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03281 Mab-21 162 → 454 Mab-21 protein Family
Sequence
MSVHYTLNLRVFWPLVTGLCTALVCLYHVLRGSGGARAEPADGVDGGFPLLKVAVLLLLS
YVLLRCRHAVRQRFLPGSPRLEGHAAFSSRHFREPGLSILLESYYEHEVRLSPHVLGHSK
AHVSRIVGELVRAGRARGSPGLIPGGALALAFRGDFIQVGSAYEQHKIRRPDSFDVLVPL
RLPPLVALEPRSLGEEPALAPAFRGCFLCALKAPPSPSGASGGHWLRDCKPFADAFCVDV
RGRRHLSATLVLRWFQSHLQRSLATVRYSLEGRCRVTLTPGGLEQPPTLHILPCRTDYGC
CRLSMAVRLIPAVHLGDGVFLVAPPPPPLPSAPLLELPEGLRAEALWGVNTARQEQKLLS
WLQERAAPGACYLKCLQLLKALRDLGARGLDSAAATQWGRILSSYVLKTVLLAVLLRKGA
PGQGWDEEHLGRCLEELVQFLRDCLLRRHTLFHC
VLGPGGAAAEVGPLPKALREAAPVDL
LAAFDGHARELAAARLLSTWQRLPQLLRAYGGPRYLARCPPPRSQRTQGFLEGEP
Sequence length 535
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 Reference Evidence Score
COLOR VISION DISORDER — GWAS catalog 37359372
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations