Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
221002
Gene name Gene Name - the full gene name approved by the HGNC.
RasGEF domain family member 1A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RASGEF1A
Synonyms (NCBI Gene) Gene synonyms aliases
CG4853
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q11.21
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017006 hsa-miR-335-5p Microarray 18185580
MIRT534778 hsa-miR-520a-3p PAR-CLIP 22012620
MIRT534777 hsa-miR-302c-3p PAR-CLIP 22012620
MIRT534776 hsa-miR-302a-3p PAR-CLIP 22012620
MIRT534775 hsa-miR-302b-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade TAS
GO:0005085 Function Guanyl-nucleotide exchange factor activity IDA 17121879, 19645719
GO:0005829 Component Cytosol TAS
GO:0007264 Process Small GTPase mediated signal transduction IEA
GO:0016477 Process Cell migration IDA 17121879
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614531 24246 ENSG00000198915
Protein
UniProt ID Q8N9B8
Protein name Ras-GEF domain-containing family member 1A
Protein function Guanine nucleotide exchange factor (GEF) with specificity for RAP2A, KRAS, HRAS, and NRAS (in vitro). Plays a role in cell migration.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00618 RasGEF_N 44 149 RasGEF N-terminal motif Domain
PF00617 RasGEF 217 411 RasGEF domain Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain and spinal cord. Highly expressed in a number of intrahepatic cholangiocarcinoma tissue biopsies. {ECO:0000269|PubMed:17121879}.
Sequence
Sequence length 481
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RAF/MAP kinase cascade
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hirschsprung disease Hirschsprung Disease rs76262710, rs75996173, rs77316810, rs75076352, rs76534745, rs76764689, rs76449634, rs377767412, rs193922699, rs75030001, rs606231342, rs1553540620, rs759944122, rs1057519322, rs1057519323
View all (4 more)
19196962
Unknown
Disease term Disease name Evidence References Source
Multiple Sclerosis Multiple Sclerosis GWAS
Asthma Asthma GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 36404533
Carcinoma Renal Cell Associate 36404533
Cholangiocarcinoma Associate 36404533
Hirschsprung Disease Associate 23270508, 25310821, 32948616, 36404533
Leukemia Myeloid Acute Associate 36404533
Lymphoma Large B Cell Diffuse Associate 36404533
Pain Postoperative Stimulate 36895017