RASGRF1 - Ras protein specific guanine nucleotide releasing factor 1 Gene

Also Known as GNRP; GRF1; CDC25; GRF55; CDC25L; H-GRF55; PP13187; ras-GRF1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5923

About RASGRF1

Cytogenetic location: 15q25.1 Genomic coordinates (GRCh38): 15:78,959,906-79,090,780 (from NCBI)

This gene has 9 transcripts (splice variants), 249 orthologues and 24 paralogues. Biased expression in brain (RPKM 10.4) and lung (RPKM 4.4).

Summary

The protein encoded by this gene is a guanine nucleotide exchange factor (GEF) similar to the Saccharomyces cerevisiae CDC25 gene product. Functional analysis has demonstrated that this protein stimulates the dissociation of GDP from Ras protein. The studies of the similar gene in mouse suggested that the Ras-GEF activity of this protein in brain can be activated by Ca2+ influx, muscarinic receptors, and G protein beta-gamma subunit. Mouse studies also indicated that the Ras-GEF signaling pathway mediated by this protein may be important for long-term memory. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Mar 2009]

RASGRF1 Products (3)

mRNA Protein Name
NM_001145648.3 NP_001139120.1 ras-specific guanine nucleotide-releasing factor 1 isoform 3
NM_002891.6 NP_002882.3 ras-specific guanine nucleotide-releasing factor 1 isoform 1
NM_153815.3 NP_722522.1 ras-specific guanine nucleotide-releasing factor 1 isoform 2
Molecular Function GO Annotation Evidence References Source
enables guanyl-nucleotide exchange factor activity IMP
IMP: Inferred from mutant phenotype
27856453 GOA
Biological Process GO Annotation Evidence References Source
involved in response to endoplasmic reticulum stress IMP
IMP: Inferred from mutant phenotype
27856453 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RASGRF1 Protein Structure

PH

PH: PH domain (25 - 127)

RhoGEF

RhoGEF: RhoGEF domain (245 - 423)

RasGEF_N

RasGEF_N: RasGEF N-terminal motif (647 - 758)

RasGEF

RasGEF: RasGEF domain (1038 - 1220)

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  • 1273 a.a.
Protein Preferred Names Protein Names

ras-specific guanine nucleotide-releasing factor 1

  • CDC25 like

RASGRF1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82705 CDC25 Antibody (YA2450) WB Rat
HY-P82705A CDC25 Antibody (YA2450)(PBS only) WB Rat

Related Diseases

Diseases Alias
Bleeding Disorder, Platelet-Type, 18
  • Platelet-Type Bleeding Disorder 18

  • BDPLT18

  • Bleeding Disorder Due To Calcium- And Dag-Regulated Guanine Exchange Factor-1 Deficiency

  • Bleeding Disorder Due To Caldag-Gefi Deficiency

  • Bleeding Disorder, Platelet Type 18

Myopia
  • Near-Sightedness

  • Short-Sightedness

  • Nearsightedness

  • Nearsighted

  • Near Vision

  • Close Sighted

  • Myopic

  • Short-Sighted

  • Near Sighted

Degenerative Myopia
  • Pathological Myopia

  • Myopia, Degenerative

  • Degenerative Progressive High Myopia

  • Progressive High Myopia

  • Progressive High Myopia

Phaeohyphomycosis
  • Infection By Dematiacious Fungi

  • Phaehyphomycosis

  • Phaeomycosis

  • Pheohyphomycosis

  • Infection By Dematiacious Fungi [Phaehyphomycosis]

  • Dematiaceous Fungal Infection

Transient Neonatal Diabetes Mellitus
  • Diabetes Mellitus, Transient Neonatal

  • Tndm

  • Chromosome 6-Associated Transient Diabetes Mellitus

  • Dmtn

  • Diabetes Mellitus, 6q24-Related Transient Neonatal

  • Tndm1

  • Neonatal Diabetes Mellitus, Transient

  • Tndm -[Transient Neonatal Diabetes Mellitus]

Refractive Error
  • Refractive Errors

Inflammatory Bowel Disease
  • Inflammatory Bowel Diseases

  • Bowel Disease, Inflammatory

Beckwith-Wiedemann Syndrome
  • Wiedemann-Beckwith Syndrome

  • BWS

  • Exomphalos-Macroglossia-Gigantism Syndrome

  • Emg Syndrome

  • Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

  • Emg Abnormality

  • Wbs

  • Exomphalos Macroglossia Gigantism Syndrome

  • Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

  • Macroglossia Exomphalos Gigantism

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris RASGRF1 VGNC VGNC:45370
Bos taurus RASGRF1 VGNC VGNC:33745
Mus musculus RASGRF1 MGD MGI:99694
Felis catus RASGRF1 VGNC VGNC:69249
Rattus norvegicus RASGRF1 RGD RGD:620395
Others RASGRF1 NCBI