Gene Gene information from NCBI Gene database.
Entrez ID 148823
Gene name Germinal center associated signaling and motility like
Gene symbol GCSAML
Synonyms (NCBI Gene)
C1orf150
Chromosome 1
Chromosome location 1q44
Summary This gene encodes a protein thought to be a signaling molecule associated with germinal centers, the sites of proliferation and differentiation of mature B lymphocytes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT022808 hsa-miR-124-3p Microarray 18668037
MIRT045165 hsa-miR-186-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0050855 Process Regulation of B cell receptor signaling pathway IEA
GO:2000401 Process Regulation of lymphocyte migration IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5JQS6
Protein name Germinal center-associated signaling and motility-like protein
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15666 HGAL 48 134 Germinal center-associated lymphoma Family
Sequence
Sequence length 135
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEMORRHAGIC DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
THROMBOCYTOPENIA 4 GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
URTICARIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations