Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
744
Gene name Gene Name - the full gene name approved by the HGNC.
Metallophosphoesterase domain containing 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MPPED2
Synonyms (NCBI Gene) Gene synonyms aliases
239FB, C11orf8
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p14.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene likely encodes a metallophosphoesterase. The encoded protein may play a role a brain development. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017152 hsa-miR-335-5p Microarray 18185580
MIRT732399 hsa-miR-448 Luciferase reporter assay, qRT-PCR, Western blot 27698780
MIRT732399 hsa-miR-448 Luciferase reporter assay, qRT-PCR, Western blot 27698780
MIRT732399 hsa-miR-448 Luciferase reporter assay, qRT-PCR, Western blot 27698780
MIRT732399 hsa-miR-448 Luciferase reporter assay, qRT-PCR, Western blot 27698780
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0005515 Function Protein binding IPI 19060904, 25416956, 32296183
GO:0008081 Function Phosphoric diester hydrolase activity IEA
GO:0008081 Function Phosphoric diester hydrolase activity ISS
GO:0016208 Function AMP binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600911 1180 ENSG00000066382
Protein
UniProt ID Q15777
Protein name Metallophosphoesterase MPPED2 (EC 3.1.-.-) (Fetal brain protein 239) (239FB) (Metallophosphoesterase domain-containing protein 2)
Protein function Displays low metallophosphoesterase activity (in vitro). May play a role in the development of the nervous system.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00149 Metallophos 58 256 Calcineurin-like phosphoesterase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in fetal brain.
Sequence
Sequence length 294
Interactions View interactions
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Asthma N/A N/A GWAS
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Dental caries Dental caries N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 30846004
Colorectal Neoplasms Associate 30846004
Dental Caries Associate 21940522, 24556642, 24810274
Glioblastoma Inhibit 33734003
Neoplasms Inhibit 33734003
Polyps Associate 30846004
Salivary Gland Diseases Associate 25985088
Thyroid Cancer Papillary Associate 17914110
Uterine Cervical Neoplasms Associate 26417997