Gene Gene information from NCBI Gene database.
Entrez ID 2621
Gene name Growth arrest specific 6
Gene symbol GAS6
Synonyms (NCBI Gene)
AXLLGAXSF
Chromosome 13
Chromosome location 13q34
Summary This gene encodes a gamma-carboxyglutamic acid (Gla)-containing protein thought to be involved in the stimulation of cell proliferation. This gene is frequently overexpressed in many cancers and has been implicated as an adverse prognostic marker. Elevate
miRNA miRNA information provided by mirtarbase database.
14
miRTarBase ID miRNA Experiments Reference
MIRT022472 hsa-miR-124-3p Microarray 18668037
MIRT1012277 hsa-miR-1193 CLIP-seq
MIRT1012278 hsa-miR-3125 CLIP-seq
MIRT1012279 hsa-miR-3916 CLIP-seq
MIRT1012277 hsa-miR-1193 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
99
GO ID Ontology Definition Evidence Reference
GO:0001764 Process Neuron migration IEA
GO:0001786 Function Phosphatidylserine binding IDA 21501828
GO:0001934 Process Positive regulation of protein phosphorylation IDA 7854420
GO:0001934 Process Positive regulation of protein phosphorylation ISS
GO:0001961 Process Positive regulation of cytokine-mediated signaling pathway IMP 18840707
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600441 4168 ENSG00000183087
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q14393
Protein name Growth arrest-specific protein 6 (GAS-6) (AXL receptor tyrosine kinase ligand)
Protein function Ligand for tyrosine-protein kinase receptors AXL, TYRO3 and MER whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival d
PDB 1H30 , 2C5D , 4RA0 , 5VXZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00594 Gla 53 93 Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain Domain
PF12661 hEGF 129 148 Human growth factor-like EGF Domain
PF12662 cEGF 177 200 Complement Clr-like EGF-like Domain
PF12661 hEGF 207 227 Human growth factor-like EGF Domain
PF07645 EGF_CA 238 277 Calcium-binding EGF domain Domain
PF00054 Laminin_G_1 325 454 Laminin G domain Domain
PF02210 Laminin_G_2 513 651 Laminin G domain Domain
Tissue specificity TISSUE SPECIFICITY: Plasma. Isoform 1 and isoform 2 are widely expressed, isoform 1 being expressed at higher levels than isoform 2 in most tissues. Isoform 2 is the predominant form in spleen. {ECO:0000269|PubMed:8336730, ECO:0000269|PubMed:9326368}.
Sequence
Sequence length 678
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  EGFR tyrosine kinase inhibitor resistance
Efferocytosis
  Platelet degranulation
Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus
Removal of aminoterminal propeptides from gamma-carboxylated proteins
Cell surface interactions at the vascular wall
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Post-translational protein phosphorylation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
18
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
ANORECTAL MALFORMATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARCINOMA, ADENOID CYSTIC CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMEGALY CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute Coronary Syndrome Coronary Syndrome BEFREE 19369636
★☆☆☆☆
Found in Text Mining only
Acute Kidney Insufficiency Acute Kidney Insufficiency CTD_human_DG 19564549
★☆☆☆☆
Found in Text Mining only
Acute lymphocytic leukemia Lymphocytic Leukemia BEFREE 19922767
★☆☆☆☆
Found in Text Mining only
Acute monocytic leukemia Monocytic Leukemia BEFREE 23982172
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 23242819, 28440492
★☆☆☆☆
Found in Text Mining only
Adenoid Cystic Carcinoma Adenocarcinoma CTD_human_DG 16762588
★☆☆☆☆
Found in Text Mining only
Adult Acute Lymphocytic Leukemia Lymphocytic Leukemia BEFREE 19922767
★☆☆☆☆
Found in Text Mining only
Adult Acute Myeloblastic Leukemia Myeloblastic Leukemia BEFREE 24326683
★☆☆☆☆
Found in Text Mining only
Age related macular degeneration Age-related macular degeneration BEFREE 23209669, 25450174
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis BEFREE 30852796
★☆☆☆☆
Found in Text Mining only