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HUMAN:INF2

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Species (Taxon ID) Homo sapiens (Human). (9606)
Gene Name(s) INF2 (synonyms: C14orf151, C14orf173)
Protein Name(s) Inverted formin-2

HBEBP2-binding protein C

External Links
UniProt Q27J81
EMBL AK025709
AK290083
AL583722
CH471061
BC006173
BC008756
BC064828
BX248757
DQ395338
DQ395339
DQ395340
AL832905
CCDS CCDS41999.1
CCDS45173.1
CCDS9989.2
RefSeq NP_001026884.3
NP_071934.3
NP_116103.1
UniGene Hs.24956
ProteinModelPortal Q27J81
SMR Q27J81
BioGrid 122172
IntAct Q27J81
MINT MINT-7034523
STRING 9606.ENSP00000376410
iPTMnet Q27J81
PhosphoSite Q27J81
SwissPalm Q27J81
BioMuta INF2
DMDM 166215588
EPD Q27J81
MaxQB Q27J81
PaxDb Q27J81
PRIDE Q27J81
DNASU 64423
Ensembl ENST00000330634
ENST00000392634
ENST00000398337
GeneID 64423
KEGG hsa:64423
UCSC uc001yoy.5
CTD 64423
GeneCards INF2
HGNC HGNC:23791
HPA HPA000724
MalaCards INF2
MIM 610982
613237
614455
neXtProt NX_Q27J81
Orphanet 93114
93213
PharmGKB PA162392025
eggNOG KOG1922
ENOG410XQR0
GeneTree ENSGT00760000118986
HOVERGEN HBG081794
InParanoid Q27J81
OMA QPVDHAQ
OrthoDB EOG7T4MN4
PhylomeDB Q27J81
TreeFam TF326300
ChiTaRS INF2
GeneWiki INF2
GenomeRNAi 64423
PMAP-CutDB Q27J81
PRO PR:Q27J81
Proteomes UP000005640
Bgee Q27J81
CleanEx HS_INF2
ExpressionAtlas Q27J81
Genevisible Q27J81
GO GO:0048471
GO:0030036
GO:0090140
InterPro IPR016024
IPR015425
IPR010472
IPR014768
IPR010473
IPR027649
IPR003124
PANTHER PTHR23213:SF5
Pfam PF06367
PF06371
PF02181
PF02205
SMART SM01139
SM01140
SM00498
SUPFAM SSF48371
PROSITE PS51444
PS51232
PS51082

Annotations

Qualifier GO ID GO term name Reference ECO ID ECO term name with/from Aspect Extension Notes Status
GO:0090141

positive regulation of mitochondrial fission

PMID:26305500[1]

ECO:0000316

UniProtKB:D3Z495


P

Figure 6C: Cells overexpressing active INF2 and Spire1C show shortened mitochondria as compared to control, while cells overexpressing INF2 and Spire1C that lacks the KIND domain show elongated, tubular mitochondria. Figure 6D: Cells overexpressing Spire1C treated with INF2 siRNA show elongated mitochondria as compared to cells treated with scrambled siRNA.

complete
CACAO 12179

part_of

GO:0048471

perinuclear region of cytoplasm

PMID:20023659[2]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

involved_in

GO:0090140

regulation of mitochondrial fission

PMID:23349293[3]

ECO:0000315

mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

enables

GO:0003779

actin binding

GO_REF:0000002

ECO:0000256

match to sequence model evidence used in automatic assertion

InterPro:IPR003124
InterPro:IPR010472
InterPro:IPR010473

F

Seeded From UniProt

complete

involved_in

GO:0016043

cellular component organization

GO_REF:0000002

ECO:0000256

match to sequence model evidence used in automatic assertion

InterPro:IPR010472

P

Seeded From UniProt

complete

enables

GO:0017048

Rho GTPase binding

GO_REF:0000002

ECO:0000256

match to sequence model evidence used in automatic assertion

InterPro:IPR010473

F

Seeded From UniProt

complete

involved_in

GO:0030036

actin cytoskeleton organization

GO_REF:0000002

ECO:0000256

match to sequence model evidence used in automatic assertion

InterPro:IPR010473
InterPro:IPR027649

P

Seeded From UniProt

complete

part_of

GO:0005737

cytoplasm

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0963

C

Seeded From UniProt

complete

enables

GO:0003779

actin binding

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0009

F

Seeded From UniProt

complete

part_of

GO:0048471

perinuclear region of cytoplasm

GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-SubCell:SL-0198

C

Seeded From UniProt

complete

Notes

References

See Help:References for how to manage references in GONUTS.

  1. Manor, U et al. (2015) A mitochondria-anchored isoform of the actin-nucleating spire protein regulates mitochondrial division. Elife 4 PubMed GONUTS page
  2. Brown, EJ et al. (2010) Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat. Genet. 42 72-6 PubMed GONUTS page
  3. Korobova, F et al. (2013) An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2. Science 339 464-7 PubMed GONUTS page