Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
339896
Gene name Gene Name - the full gene name approved by the HGNC.
Glutamate decarboxylase like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GADL1
Synonyms (NCBI Gene) Gene synonyms aliases
ADC, CSADC, HuADC, HuCSADC
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p24.1-p23
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT613531 hsa-miR-4311 HITS-CLIP 23824327
MIRT607370 hsa-miR-8485 HITS-CLIP 23824327
MIRT613531 hsa-miR-4311 HITS-CLIP 23824327
MIRT607370 hsa-miR-8485 HITS-CLIP 23824327
MIRT613531 hsa-miR-4311 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000098 Process Sulfur amino acid catabolic process TAS
GO:0004068 Function Aspartate 1-decarboxylase activity IEA
GO:0004782 Function Sulfinoalanine decarboxylase activity IEA
GO:0005829 Component Cytosol TAS
GO:0008652 Process Cellular amino acid biosynthetic process TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615601 27949 ENSG00000144644
Protein
UniProt ID Q6ZQY3
Protein name Acidic amino acid decarboxylase GADL1 (Aspartate 1-decarboxylase) (ADC) (HuADC) (EC 4.1.1.11) (Cysteine sulfinic acid decarboxylase) (CSADC) (HuCSADC) (EC 4.1.1.29) (Glutamate decarboxylase-like protein 1)
Protein function May catalyze the decarboxylation of L-aspartate, 3-sulfino-L-alanine (cysteine sulfinic acid), and L-cysteate to beta-alanine, hypotaurine and taurine, respectively. Does not exhibit any decarboxylation activity toward glutamate. {ECO:0000269|Pu
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00282 Pyridoxal_deC 77 445 Pyridoxal-dependent decarboxylase conserved domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed very weakly in neurons and not detected in astrocytes, brain or liver. {ECO:0000269|PubMed:26327310}.
Sequence
Sequence length 521
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  beta-Alanine metabolism
Taurine and hypotaurine metabolism
Pantothenate and CoA biosynthesis
Metabolic pathways
  Degradation of cysteine and homocysteine
Aspartate and asparagine metabolism
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Takayasu Arteritis Takayasu Arteritis GWAS
Frontal Fibrosing Alopecia Frontal Fibrosing Alopecia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bipolar Disorder Associate 24369049, 30923325, 31767892
Idiopathic Hypogonadotropic Hypogonadism Associate 33208564
Immune System Diseases Associate 31767892
Inflammation Associate 28355295
Neuroblastoma Associate 30923325
Osteoarthritis Associate 27974301
Tuberculosis Pulmonary Associate 28355295