Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
145447
Gene name Gene Name - the full gene name approved by the HGNC.
Abhydrolase domain containing 12B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ABHD12B
Synonyms (NCBI Gene) Gene synonyms aliases
BEM46L3, C14orf29, c14_5314
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018993 hsa-miR-335-5p Microarray 18185580
MIRT759540 hsa-miR-2053 CLIP-seq
MIRT759541 hsa-miR-31 CLIP-seq
MIRT759542 hsa-miR-3662 CLIP-seq
MIRT759543 hsa-miR-3674 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004622 Function Phosphatidylcholine lysophospholipase activity IBA
GO:0005515 Function Protein binding IPI 32814053
GO:0005789 Component Endoplasmic reticulum membrane IBA
GO:0006660 Process Phosphatidylserine catabolic process IBA
GO:0016787 Function Hydrolase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q7Z5M8
Protein name Protein ABHD12B (EC 3.-.-.-) (Abhydrolase domain-containing protein 12B) (Alpha/beta hydrolase domain-containing protein 12B)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12146 Hydrolase_4 137 280 Serine aminopeptidase, S33 Family
Sequence
MDAQDCQAAASPEPPGPPARSCVAAWWDMVDRNLRYFPHSCSMLGRKIAALYDSFTSKSL
KEHVFLPLIDMLIYFNFFKAPFLVDLKKPELKIPHTVNFYLRVEPGVMLGIWHTVPSCRG
EDAKGKDCCWYEAALRDGNPIIVYLHGSAEHRAASHRLKLVKVLSDGGFHVLSVDYRGFG
DSTGKPTEEGLTTDAICVYEWTKARSGITPVCLWGHSLGTGVATNAAKVLEEKGCPVDAI
VLEAPFTNMWVASINYPLLKIYRNIPGFLRTLMDALRKDK
IIFPNDENVKFLSSPLLILH
GEDDRTVPLEYGKKLYEIARNAYRNKERVKMVIFPPGFQHNLLCKSPTLLITVRDFLSKQ
WS
Sequence length 362
Interactions View interactions
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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
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Embryonal Associate 26659575
Chronic Periodontitis Associate 25056994, 36360171
Periodontitis Associate 35179257
Testicular Germ Cell Tumor Associate 26659575