Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
9855 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
FERM, ARH/RhoGEF and pleckstrin domain protein 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
FARP2 |
SynonymsGene synonyms aliases
|
FIR, FRG, PLEKHC3 |
ChromosomeChromosome number
|
2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
2q37.3 |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
O94887 |
Protein name |
FERM, ARHGEF and pleckstrin domain-containing protein 2 (FERM domain-including RhoGEF) (FIR) (FERM, RhoGEF and pleckstrin domain-containing protein 2) (Pleckstrin homology domain-containing family C member 3) (PH domain-containing family C member 3) |
Protein function |
Functions as a guanine nucleotide exchange factor that activates RAC1. May have relatively low activity. Plays a role in the response to class 3 semaphorins and remodeling of the actin cytoskeleton. Plays a role in TNFSF11-mediated osteoclast di |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF09379 |
FERM_N |
48 → 111 |
FERM N-terminal domain |
Domain |
PF00373 |
FERM_M |
127 → 234 |
FERM central domain |
Domain |
PF09380 |
FERM_C |
238 → 328 |
FERM C-terminal PH-like domain |
Domain |
PF08736 |
FA |
333 → 376 |
FERM adjacent (FA) |
Family |
PF00621 |
RhoGEF |
539 → 724 |
RhoGEF domain |
Domain |
PF00169 |
PH |
756 → 852 |
PH domain |
Domain |
PF00169 |
PH |
930 → 1026 |
PH domain |
Domain |
|
Sequence |
|
Sequence length |
1054 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
2q37 deletion syndrome |
Chromosome 2q37 deletion syndrome |
rs748900140, rs1064797002 |
19365831 |
Autism |
Autistic Disorder |
rs121964908, rs121912597, rs2710102, rs7794745, rs142990298, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699, rs1553510219, rs1684182454, rs1559060428, rs1553510677, rs1576352885, rs1574152522, rs1574152672, rs1696658542, rs1751123722, rs1750373491, rs1751075634 |
19365831 |
Nasopharyngeal carcinoma |
Nasopharyngeal carcinoma |
rs200046052 |
20512145 |
Prostate cancer |
Malignant neoplasm of prostate, Prostate carcinoma |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
23535732, 29892016, 23535732 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Lymphocytic leukemia |
Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma |
|
20062064, 23770605, 23770605 |
Vitiligo |
Vitiligo |
|
27723757 |
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