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GOT1 (glutamic-oxaloacetic transaminase 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2805
Gene nameGene Name - the full gene name approved by the HGNC.
Glutamic-oxaloacetic transaminase 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
GOT1
SynonymsGene synonyms aliases
AST1, ASTQTL1, GIG18, cAspAT, cCAT
ChromosomeChromosome number
10
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.2
SummarySummary of gene provided in NCBI Entrez Gene.
Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. [provided by RefSeq, Jul 2008]
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs749913156 TTG>- Pathogenic Coding sequence variant, inframe deletion
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT039193 hsa-miR-769-5p CLASH 23622248
MIRT497413 hsa-miR-7641 PAR-CLIP 22291592
MIRT497414 hsa-miR-4448 PAR-CLIP 22291592
MIRT497415 hsa-miR-549a PAR-CLIP 22291592
MIRT497416 hsa-miR-205-5p PAR-CLIP 22291592
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004069 Function L-aspartate:2-oxoglutarate aminotransferase activity IBA 21873635
GO:0004069 Function L-aspartate:2-oxoglutarate aminotransferase activity IDA 2182221, 2241899, 2731362, 6391741
GO:0004069 Function L-aspartate:2-oxoglutarate aminotransferase activity ISS
GO:0004609 Function Phosphatidylserine decarboxylase activity IEA
GO:0005634 Component Nucleus HDA 21630459
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P17174
Protein name Aspartate aminotransferase, cytoplasmic (cAspAT) (EC 2.6.1.1) (EC 2.6.1.3) (Cysteine aminotransferase, cytoplasmic) (Cysteine transaminase, cytoplasmic) (cCAT) (Glutamate oxaloacetate transaminase 1) (Transaminase A)
Protein function Biosynthesis of L-glutamate from L-aspartate or L-cysteine. Important regulator of levels of glutamate, the major excitatory neurotransmitter of the vertebrate central nervous system. Acts as a scavenger of glutamate in brain neuroprotection. The aspartate aminotransferase activity is involved in hepatic glucose synthesis during development and in adipocyte glyceroneogenesis. Using L-cysteine as substrate, regulates levels of mercaptopyruvate, an important source of hydrogen sulfide. Mercaptopyruvate is converted into H(2)S via the action of 3-mercaptopyruvate sulfurtransferase (3MST). Hydrogen sulfide is an important synaptic modulator and neuroprotectant in the brain.
PDB 3II0 , 3WZF , 6DNA , 6DNB , 6DND , 6LIG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00155 Aminotran_1_2
31 405
Aminotransferase class I and II
Domain
Sequence
Sequence length 413
Interactions View interactions

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