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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
formin BNI1
Summary
- Gene Symbol
-
- BNI1
- Organism
- Saccharomyces cerevisiae S288C
Annotation
- Keyword
-
- 3D-structure
- Actin-binding
- Cell membrane
- Cell projection
- Coiled coil
- Cytoskeleton
- Phosphoprotein
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P41832 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| actin cytoskeleton organization | ||
| formin-nucleated actin cable assembly | ||
| establishment or maintenance of actin cytoskeleton polarity |
|
|
| regulation of protein localization | ||
| vesicle targeting |
|
GO Hierarchy
biological process
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of cellular process [inference]
regulation of actin filament-based process [inference]
negative regulation of cellular process [inference]
regulation of cellular component organization [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitotic actomyosin contractile ring | ||
| mating projection tip | ||
| cell cortex | ||
| incipient cellular bud site | ||
| cell division site |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| actin binding | ||
| actin filament binding | ||
| small GTPase binding | ||
| identical protein binding |
|
|
| profilin binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- formin
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| actin binding |
| actin cytoskeleton organization |
Alliance of Genome Resources
- Expression
| Location | References |
|---|---|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060690 | autosomal dominant auditory neuropathy 1 | |
| DOID:0080858 | primary ovarian insufficiency 2A | |
| DOID:0110541 | autosomal dominant nonsyndromic deafness 1 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:5426 | primary ovarian insufficiency |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 1729 | HGNC:2876 | |||
| 1730 | HGNC:2877 | |||
| 22379 | MGI:109569 | |||
| 23002 | HGNC:18142 | |||
| 31075 | FB:FBgn0025641 | |||
| 81624 | HGNC:15480 | |||
| 186392 | WB:WBGene00018976 | |||
| 300225 | RGD:1583854 | |||
| 493573 | Xenbase:XB-GENE-1003193 | |||
| 798465 | ZFIN:ZDB-GENE-070709-1 |
