Gene Gene information from NCBI Gene database.
Entrez ID 132160
Gene name Protein phosphatase, Mg2+/Mn2+ dependent 1M
Gene symbol PPM1M
Synonyms (NCBI Gene)
PP2C-etaPP2CEPP2Ceta
Chromosome 3
Chromosome location 3p21.2
miRNA miRNA information provided by mirtarbase database.
16
miRTarBase ID miRNA Experiments Reference
MIRT037613 hsa-miR-744-5p CLASH 23622248
MIRT738978 hsa-miR-3174 CLIP-seq
MIRT738976 hsa-miR-4486 CLIP-seq
MIRT738977 hsa-miR-921 CLIP-seq
MIRT1254713 hsa-miR-154 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0004721 Function Phosphoprotein phosphatase activity IEA
GO:0004722 Function Protein serine/threonine phosphatase activity IEA
GO:0004741 Function [pyruvate dehydrogenase (acetyl-transferring)]-phosphatase activity IBA
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608979 26506 ENSG00000164088
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96MI6
Protein name Protein phosphatase 1M (EC 3.1.3.16) (Protein phosphatase 2C isoform eta) (PP2C-eta) (PP2CE)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00481 PP2C 8 119 Protein phosphatase 2C Family
PF00481 PP2C 132 254 Protein phosphatase 2C Family
Sequence
Sequence length 270
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
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations