Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3636
Gene name Gene Name - the full gene name approved by the HGNC.
Inositol polyphosphate phosphatase like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
INPPL1
Synonyms (NCBI Gene) Gene synonyms aliases
OPSMD, SHIP2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
OPSMD
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.4
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is an SH2-containing 5`-inositol phosphatase that is involved in the regulation of insulin function. The encoded protein also plays a role in the regulation of epidermal growth factor receptor turnover and actin remodellin
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs655423 G>A,C Pathogenic Splice donor variant
rs368970014 C>G,T Pathogenic Synonymous variant, stop gained, coding sequence variant
rs397514508 C>T Pathogenic Missense variant, coding sequence variant
rs397514509 C>A,G,T Pathogenic Missense variant, stop gained, coding sequence variant
rs397514510 C>T Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003238 hsa-miR-205-5p Western blot, Luciferase reporter assay, Northern blot 19033458
MIRT003238 hsa-miR-205-5p Western blot, Luciferase reporter assay, Northern blot 19033458
MIRT003238 hsa-miR-205-5p Western blot, Luciferase reporter assay, Northern blot 19033458
MIRT003238 hsa-miR-205-5p Western blot, Luciferase reporter assay, Northern blot 19033458
MIRT004354 hsa-miR-184 Western blot, Luciferase reporter assay, Northern blot 19033458
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001958 Process Endochondral ossification IMP 23273569
GO:0002376 Process Immune system process IEA
GO:0003779 Function Actin binding IEA
GO:0005515 Function Protein binding IPI 9485206, 11158326, 12504111, 16302969, 18692052, 20368287, 20933011, 21712384, 24728074
GO:0005634 Component Nucleus ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600829 6080 ENSG00000165458
Protein
UniProt ID O15357
Protein name Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 (EC 3.1.3.86) (Inositol polyphosphate phosphatase-like protein 1) (INPPL-1) (Protein 51C) (SH2 domain-containing inositol 5'-phosphatase 2) (SH2 domain-containing inositol phosphatase 2) (SHIP-2)
Protein function Phosphatidylinositol (PtdIns) phosphatase that specifically hydrolyzes the 5-phosphate of phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P3) to produce PtdIns(3,4)P2, thereby negatively regulating the PI3K (phosphoinositide 3-kinase) pat
PDB 2K4P , 2KSO , 2MK2 , 3NR8 , 4A9C , 5OKM , 5OKN , 5OKO , 5OKP , 6SQU , 6SRR
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00017 SH2 21 102 SH2 domain Domain
PF03372 Exo_endo_phos 429 718 Endonuclease/Exonuclease/phosphatase family Domain
PF00536 SAM_1 1200 1258 SAM domain (Sterile alpha motif) Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, most prominently in skeletal muscle, heart and brain. Present in platelets. Expressed in transformed myeloid cells and in primary macrophages, but not in peripheral blood monocytes. {ECO:0000269|PubMed:12676785, ECO:0
Sequence
MASACGAPGPGGALGSQAPSWYHRDLSRAAAEELLARAGRDGSFLVRDSESVAGAFALCV
LYQKHVHTYRILPDGEDFLAVQTSQGVPVRRFQTLGELIGLY
AQPNQGLVCALLLPVEGE
REPDPPDDRDASDGEDEKPPLPPRSGSTSISAPTGPSSPLPAPETPTAPAAESAPNGLST
VSHDYLKGSYGLDLEAVRGGASHLPHLTRTLATSCRRLHSEVDKVLSGLEILSKVFDQQS
SPMVTRLLQQQNLPQTGEQELESLVLKLSVLKDFLSGIQKKALKALQDMSSTAPPAPQPS
TRKAKTIPVQAFEVKLDVTLGDLTKIGKSQKFTLSVDVEGGRLVLLRRQRDSQEDWTTFT
HDRIRQLIKSQRVQNKLGVVFEKEKDRTQRKDFIFVSARKREAFCQLLQLMKNKHSKQDE
PDMISVFIGTWNMGSVPPPKNVTSWFTSKGLGKTLDEVTVTIPHDIYVFGTQENSVGDRE
WLDLLRGGLKELTDLDYRPIAMQSLWNIKVAVLVKPEHENRISHVSTSSVKTGIANTLGN
KGAVGVSFMFNGTSFGFVNCHLTSGNEKTARRNQNYLDILRLLSLGDRQLNAFDISLRFT
HLFWFGDLNYRLDMDIQEILNYISRKEFEPLLRVDQLNLEREKHKVFLRFSEEEISFPPT
YRYERGSRDTYAWHKQKPTGVRTNVPSWCDRILWKSYPETHIICNSYGCTDDIVTSDH
SP
VFGTFEVGVTSQFISKKGLSKTSDQAYIEFESIEAIVKTASRTKFFIEFYSTCLEEYKKS
FENDAQSSDNINFLKVQWSSRQLPTLKPILADIEYLQDQHLLLTVKSMDGYESYGECVVA
LKSMIGSTAQQFLTFLSHRGEETGNIRGSMKVRVPTERLGTRERLYEWISIDKDEAGAKS
KAPSVSRGSQEPRSGSRKPAFTEASCPLSRLFEEPEKPPPTGRPPAPPRAAPREEPLTPR
LKPEGAPEPEGVAAPPPKNSFNNPAYYVLEGVPHQLLPPEPPSPARAPVPSATKNKVAIT
VPAPQLGHHRHPRVGEGSSSDEESGGTLPPPDFPPPPLPDSAIFLPPSLDPLPGPVVRGR
GGAEARGPPPPKAHPRPPLPPGPSPASTFLGEVASGDDRSCSVLQMAKTLSEVDYAPAGP
ARSALLPGPLELQPPRGLPSDYGRPLSFPPPRIRESIQEDLAEEAPCLQGGRASGLGEAG
MSAWLRAIGLERYEEGLVHNGWDDLEFLSDITEEDLEEAGVQDPAHKRLLLDTLQLSK
Sequence length 1258
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Inositol phosphate metabolism
Metabolic pathways
Phosphatidylinositol signaling system
B cell receptor signaling pathway
Fc gamma R-mediated phagocytosis
Insulin signaling pathway
  Synthesis of PIPs at the plasma membrane
Synthesis of IP3 and IP4 in the cytosol
Interleukin receptor SHC signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Brachydactyly Brachydactyly rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
25635986, 12086927
Hypertension Hypertensive disease rs13306026 15220217
Unknown
Disease term Disease name Evidence References Source
Schneckenbecken Dysplasia schneckenbecken dysplasia GenCC
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 22533436
Breast Neoplasms Associate 19065064, 34990021
Carcinogenesis Stimulate 27716613
Carcinogenesis Inhibit 28117748
Carcinoma Hepatocellular Associate 24228114
Carcinoma Non Small Cell Lung Associate 24133597
Carcinoma Squamous Cell Associate 19033458
Chronic Urticaria Associate 19477690
Colonic Neoplasms Associate 24943349
Colorectal Neoplasms Associate 19433066, 24943349, 25525286