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ADTRP (androgen dependent TFPI regulating protein)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84830
Gene nameGene Name - the full gene name approved by the HGNC.
Androgen dependent TFPI regulating protein
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
ADTRP
SynonymsGene synonyms aliases
AIG1L, C6orf105, dJ413H6.1
ChromosomeChromosome number
6
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p24.1
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001934 Process Positive regulation of protein phosphorylation IMP 28341552
GO:0002042 Process Cell migration involved in sprouting angiogenesis IMP 28341552
GO:0002686 Process Negative regulation of leukocyte migration IMP 28341552
GO:0003332 Process Negative regulation of extracellular matrix constituent secretion IMP 28341552
GO:0005515 Function Protein binding IPI 32296183
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q96IZ2
Protein name Androgen-dependent TFPI-regulating protein (Fatty acid esters of hydroxy fatty acids hydrolase ADTRP) (FAHFA hydrolase ADTRP) (EC 3.1.-.-)
Protein function Hydrolyzes bioactive fatty-acid esters of hydroxy-fatty acids (FAHFAs), but not other major classes of lipids (PubMed:27018888). Show a preference for FAHFAs with branching distal from the carboxylate head group of the lipids (PubMed:27018888). Regulates the expression and the cell-associated anticoagulant activity of the inhibitor TFPI in endothelial cells (in vitro) (PubMed:21868574).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04750 Far-17a_AIG1
5 216
FAR-17a/AIG1-like protein
Family
Sequence
Sequence length 230
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Coronary artery disease Coronary Artery Disease rs137852988, rs121918313, rs-1, rs121918529, rs121918531, rs137852340, rs405509, rs1555800701, rs1215189537 21378986
Coronary heart disease Coronary heart disease rs-1 21378986
Unknown
Disease name Disease term dbSNP ID References
Coronary arteriosclerosis Coronary Arteriosclerosis 21378986
Development disorder Child Development Disorders, Pervasive 30804558

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