Gene Gene information from NCBI Gene database.
Entrez ID 122622
Gene name Adenylosuccinate synthase 1
Gene symbol ADSS1
Synonyms (NCBI Gene)
ADSSL1MPD5
Chromosome 14
Chromosome location 14q32.33
Summary This gene encodes a member of the adenylosuccinate synthase family of proteins. The encoded muscle-specific enzyme plays a role in the purine nucleotide cycle by catalyzing the first step in the conversion of inosine monophosphate (IMP) to adenosine monop
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000287 Function Magnesium ion binding IEA
GO:0002376 Process Immune system process NAS 15786719
GO:0003924 Function GTPase activity IEA
GO:0004019 Function Adenylosuccinate synthase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612498 20093 ENSG00000185100
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N142
Protein name Adenylosuccinate synthetase isozyme 1 (AMPSase 1) (AdSS 1) (EC 6.3.4.4) (Adenylosuccinate synthetase, basic isozyme) (Adenylosuccinate synthetase, muscle isozyme) (M-type adenylosuccinate synthetase) (Adenylosuccinate synthetase-like 1) (AdSSL1) (IMP--asp
Protein function Component of the purine nucleotide cycle (PNC), which interconverts IMP and AMP to regulate the nucleotide levels in various tissues, and which contributes to glycolysis and ammoniagenesis. Catalyzes the first committed step in the biosynthesis
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00709 Adenylsucc_synt 34 454 Adenylosuccinate synthetase Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in skeletal muscle and heart, as well as in several hematopoietic cell lines and solid tumors. {ECO:0000269|PubMed:15786719}.
Sequence
Sequence length 457
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
78
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely pathogenic rs376223981 RCV005929999
ADSS1-related disorder Likely pathogenic; Pathogenic rs140614802 RCV003401191
Arthrogryposis multiplex congenita Likely pathogenic; Pathogenic rs769542442 RCV000855488
Colon adenocarcinoma Likely pathogenic rs761489014 RCV005930001
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Likely benign; Uncertain significance rs376218660, rs375602969 RCV005929994
RCV005929998
Familial cancer of breast Uncertain significance rs375602969 RCV005929997
Lung cancer Benign rs370851579 RCV005929996
Uterine carcinosarcoma Uncertain significance rs761597174 RCV005930002
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Fetal akinesia syndrome X linked Associate 31680123
Neoplasms Associate 17624250
Polycythemia Vera Associate 17624250
Tuberculosis Pulmonary Associate 37493735