Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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114793 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Formin like 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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FMNL2 |
SynonymsGene synonyms aliases
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FHOD2 |
ChromosomeChromosome number
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2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q23.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. Alternatively spliced transcript variants encoding different isoforms have been described but their full-length natu |
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 |
Q96PY5 |
Protein name |
Formin-like protein 2 (Formin homology 2 domain-containing protein 2) |
Protein function |
Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the cortical actin filament dynamics. |
PDB |
4YC7
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF06371 |
Drf_GBD |
23 → 159 |
Diaphanous GTPase-binding Domain |
Family |
PF06371 |
Drf_GBD |
202 → 275 |
Diaphanous GTPase-binding Domain |
Family |
PF06367 |
Drf_FH3 |
278 → 475 |
Diaphanous FH3 Domain |
Family |
PF02181 |
FH2 |
616 → 982 |
Formin Homology 2 Domain |
Family |
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Sequence |
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Sequence length |
1086 |
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
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Glaucoma |
Glaucoma, Glaucoma, Open-Angle |
rs121918355, rs1566660365, rs1566635134, rs121918356, rs1566634475, rs28936700, rs55771538, rs28936701, rs104893622, rs55989760, rs72549387, rs104893628, rs2125316417, rs104893629, rs74315328, rs121909193, rs74315330, rs74315329, rs74315332, rs74315334, rs74315336, rs74315338, rs74315341, rs121909194, rs74315331, rs1558603396, rs387907175, rs587778873, rs587778875, rs104894979, rs137854895, rs766425037, rs72549380, rs148542782, rs541217363, rs753021890, rs771076928, rs56010818, rs777678299, rs1446110883, rs1573274915, rs1587545234, rs751768343, rs944452644 |
30054594, 29891935 |
Leukemia |
Leukemia, Myelocytic, Acute |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 |
27903959 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Corneal astigmatism |
Regular astigmatism - corneal |
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30306274 |
Stroke |
Cerebrovascular accident |
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22384361 |
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