Gene Gene information from NCBI Gene database.
Entrez ID 285016
Gene name ALK and LTK ligand 2
Gene symbol ALKAL2
Synonyms (NCBI Gene)
AUGAFAM150BPRO1097RGPG542
Chromosome 2
Chromosome location 2p25.3
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0005125 Function Cytokine activity IDA 30061385, 34646012, 34819673
GO:0005125 Function Cytokine activity IEA
GO:0005515 Function Protein binding IPI 26418745
GO:0005576 Component Extracellular region IDA 30061385
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619671 27683 ENSG00000189292
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UX46
Protein name ALK and LTK ligand 2 (Augmentor alpha) (AUG-alpha)
Protein function Cytokine that acts as a physiological ligand for receptor tyrosine kinases LTK and ALK, leading to their activation (PubMed:26418745, PubMed:26630010, PubMed:30061385, PubMed:33411331, PubMed:34646012, PubMed:34819673). Cytokine-binding is suffi
PDB 7LS0 , 7MZX , 7N00 , 7NWZ , 9G5I
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15129 FAM150 33 150 FAM150 family Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with highest levels in adrenal gland and modest levels in pancreas, testis and uterus. {ECO:0000269|PubMed:25331893}.
Sequence
Sequence length 152
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
RESTLESS LEGS SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations