MINPP1
Multiple inositol polyphosphate phosphatase 1
Also known as: MINP1_HUMAN, MIPP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UNW1
- Gene
- MINPP1
- Ensembl
- ENSG00000107789
- Chromosome
- 10
- Canonical length
- 487 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009]
Canonical amino-acid sequenceUniProt
487 residues, UniProt reviewed canonical sequence.
>Q9UNW1|MINPP1
1 MLRAPGCLLR TSVAPAAALA AALLSSLARC SLLEPRDPVA SSLSPYFGTK TRYEDVNPVL
61 LSGPEAPWRD PELLEGTCTP VQLVALIRHG TRYPTVKQIR KLRQLHGLLQ ARGSRDGGAS
121 STGSRDLGAA LADWPLWYAD WMDGQLVEKG RQDMRQLALR LASLFPALFS RENYGRLRLI
181 TSSKHRCMDS SAAFLQGLWQ HYHPGLPPPD VADMEFGPPT VNDKLMRFFD HCEKFLTEVE
241 KNATALYHVE AFKTGPEMQN ILKKVAATLQ VPVNDLNADL IQVAFFTCSF DLAIKGVKSP
301 WCDVFDIDDA KVLEYLNDLK QYWKRGYGYT INSRSSCTLF QDIFQHLDKA VEQKQRSQPI
361 SSPVILQFGH AETLLPLLSL MGYFKDKEPL TAYNYKKQMH RKFRSGLIVP YASNLIFVLY
421 HCENAKTPKE QFRVQMLLNE KVLPLAYSQE TVSFYEDLKN HYKDILQSCQ TSEECELARA
481 NSTSDELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MINPP1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 29 nTPM
- liver: 27 nTPM
- adrenal gland: 20 nTPM
- placenta: 18 nTPM
- duodenum: 17 nTPM
- kidney: 16 nTPM
Single-cell type
- erythrocyte progenitors: 225 nCPM
- megakaryocyte-erythroid progenitors: 121 nCPM
- megakaryocyte progenitors: 80 nCPM
- hepatocytes: 69 nCPM
- goblet cells: 34 nCPM
- prostatic glandular cells: 33 nCPM
Immune cell
- T-reg: 17 nTPM
- myeloid DC: 14 nTPM
- intermediate monocyte: 14 nTPM
- memory CD8 T-cell: 13 nTPM
- non-classical monocyte: 13 nTPM
- NK-cell: 12 nTPM
Brain region
- choroid plexus: 15 nTPM
- hypothalamus: 12 nTPM
- white matter: 10 nTPM
- spinal cord: 9.4 nTPM
- cerebellum: 9.3 nTPM
- midbrain: 9.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MINPP1.
Disease | AllUniProt
Conditions MINPP1 is implicated in, by any mechanism.
- Thyroid cancer, non-medullary, 2 (NMTC2) MIM:188470
- Pontocerebellar hypoplasia 16 (PCH16) MIM:619527
Disease | GeneticClinVar
16 pathogenic / likely-pathogenic of 110 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Pontocerebellar hypoplasia, type 16
- Thyroid cancer, nonmedullary, 2
- Pontoneocerebellar hypoplasia
- MINPP1-related disorder
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.76
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.58
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- bone mineralization
- inositol phosphate metabolic process
- intracellular monoatomic cation homeostasis
- ossification
Molecular functions
- acid phosphatase activity
- inositol bisphosphate phosphatase activity
- inositol phosphate phosphatase activity
- inositol trisphosphate phosphatase activity
- inositol-1,3,4,5,6-pentakisphosphate 3-phosphatase activity
- inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity
- bisphosphoglycerate 3-phosphatase activity
- inositol hexakisphosphate 3-phosphatase activity
- inositol hexakisphosphate 4-phosphatase activity
- inositol hexakisphosphate phosphatase activity
- inositol pentakisphosphate phosphatase activity
- inositol-1,4,5,6-tetrakisphosphate 6-phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Histidine phosphatase superfamily, clade-2
- Histidine phosphatase superfamily
- Histidine phosphatase superfamily (branch 2)
- Histidine acid phosphatase, eukaryotic
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MINPP1 as an antibody target. Whether an autoantibody or antibody against MINPP1 could matter depends on whether native MINPP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MINPP1 is annotated at the cell surface, where native MINPP1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label MINPP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...