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Category

1,275 results for ccnf

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CCNF

(Homo sapiens)

Gene

Name: cyclin F

Synonyms: F-box only protein 1, cyclin-F, FBX1, FBXO1, FTDALS5, G2/mitotic-specific cyclin-F

Source: HGNC:1591

Biotype: protein coding gene

Symbol: CCNF (Hsa)

Symbol: CCNF

Strict Orthology Symbols: ccnf

Allele/Variant (109)

ccnf

(Danio rerio)

Gene

Name: cyclin F

Synonyms: cb443

Source: ZFIN:ZDB-GENE-021030-2

Biotype: protein coding gene

Symbol: ccnf (Dre)

Symbol: ccnf

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Strict Orthology Symbols: ccnf

Allele/Variant (3)

Ccnf

(Rattus norvegicus)

Gene

Name: cyclin F

Synonyms: cyclin-F

Source: RGD:67401

Biotype: protein coding gene

Symbol: Ccnf (Rno)

Symbol: Ccnf

Gene Synopsis: Orthologous to human CCNF (cyclin F); INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Strict Orthology Symbols: ccnf

Allele/Variant (117)

Ccnf

(Mus musculus)

Gene

Name: cyclin F

Synonyms: Fbxo1, CycF

Source: MGI:102551

Biotype: protein coding gene

Symbol: Ccnf (Mmu)

Symbol: Ccnf

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Strict Orthology Symbols: ccnf

Alleles: Ccnf (Mmu)...Ccnf (Mmu)...Ccnf (Mmu)...Ccnf (Mmu)

ccnf

(Xenopus tropicalis)

Gene

Name: cyclin F

Synonyms: cyclin F, Fbxo1, ccnf

Source: Xenbase:XB-GENE-963729

Biotype: gene

Symbol: ccnf

Symbol: ccnf (Xtr)

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Synonyms: ccnf...ccnf...ccnf

Strict Orthology Symbols: ccnf

ccnf.L

(Xenopus laevis)

Gene

Name: cyclin F

Synonyms: ccnf.L, cyclin F, Fbxo1

Source: Xenbase:XB-GENE-963734

Biotype: gene

Symbol: ccnf.L (Xla)

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Strict Orthology Symbols: ccnf

Symbol: ccnf.L

ccnf.S

(Xenopus laevis)

Gene

Name: cyclin F

Synonyms: cyclin F, Fbxo1, ccnf.S

Source: Xenbase:XB-GENE-17344699

Biotype: gene

Symbol: ccnf.S (Xla)

Automated Gene Synopsis: Orthologous to human CCNF (cyclin F).

Strict Orthology Symbols: ccnf

Symbol: ccnf.S

Ccnf^em1Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7296468

Genes: Ccnf (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Ccnf (Mmu)

Genes: Ccnf (Mmu)

Symbol: Ccnf^em1Gpt

Gene (1)

Ccnf^tm1Sje

(Mus musculus)

Allele/Variant

Source: MGI:3040862

Genes: Ccnf (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Ccnf (Mmu)

Genes: Ccnf (Mmu)

Symbol: Ccnf^tm1Sje

Ccnf^em3Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7296469

Genes: Ccnf (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Ccnf (Mmu)

Genes: Ccnf (Mmu)

Symbol: Ccnf^em3Gpt

Gene (1)

Ccnf^tm1.1Sje

(Mus musculus)

Allele/Variant

Source: MGI:3040863

Genes: Ccnf (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Ccnf (Mmu)

Genes: Ccnf (Mmu)

Symbol: Ccnf^tm1.1Sje

Ccnf^tm1Sje/Ccnf^tm1.1Sje Tg(Fabp1-cre)1Jig/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N

(Mus musculus)

Model

Id: MGI:3041859

Synonyms: Not Available

Symbol: Ccnf/Ccnf Tg(Fabp1-cre)1Jig/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB

Genes: Ccnf (Mmu)

Alleles: Ccnf (Mmu)

Name: Ccnf/Ccnf Tg(Fabp1-cre)1Jig/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB

Gene (1)

Ccnf^tm1Sje/Ccnf^tm1.1Sje Tg(Col1a1-cre)1Kry/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB

(Mus musculus)

Model

Id: MGI:3041866

Synonyms: Not Available

Symbol: Ccnf/Ccnf Tg(Col1a1-cre)1Kry/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB

Genes: Ccnf (Mmu)

Alleles: Ccnf (Mmu)

Name: Ccnf/Ccnf Tg(Col1a1-cre)1Kry/0 [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB

Gene (1)

Ccnf-ps2

(Rattus norvegicus)

Gene

Name: cyclin F, pseudogene 2

Synonyms: LOC100910118, cyclin-F-like

Source: RGD:6500147

Biotype: pseudogene

Symbol: Ccnf-ps2 (Rno)

Symbol: Ccnf-ps2

Ccnf^tm1.1Sje/Ccnf^tm1.1Sje [background:] involves: 129S7/SvEvBrd * C57BL/6

(Mus musculus)

Model

Id: MGI:3041854

Synonyms: Not Available

Symbol: Ccnf/Ccnf [background:] involves: 129S7/SvEvBrd * C57BL/6 (Mmu)

Genes: Ccnf (Mmu)

Alleles: Ccnf (Mmu)

Name: Ccnf/Ccnf [background:] involves: 129S7/SvEvBrd * C57BL/6

Gene (1)

negative regulation of centrosome duplication

Gene Ontology

Source: GO:0010826

Synonyms: Not Available

Branch: biological process

Genes: Ccnf (Mmu)...CCNF (Hsa)...Ccnf (Rno)...ccnf (Dre)

Genes Annotated with this GO Term (48)

re-entry into mitotic cell cycle

Gene Ontology

Source: GO:0000320

Synonyms: Not Available

Branch: biological process

Genes: Ccnf (Mmu)...CCNF (Hsa)...Ccnf (Rno)

Genes Annotated with this GO Term (28)

anaphase-promoting complex binding

Gene Ontology

Source: GO:0010997

Synonyms:

APC binding

Branch: molecular function

Genes: Ccnf (Mmu)...CCNF (Hsa)...Ccnf (Rno)

Genes Annotated with this GO Term (42)

gi6

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-241106-7

Genes: ccnf (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: ccnf (Dre)

Gene (1)

mde49

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-250424-9

Genes: ccnf (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: ccnf (Dre)

Gene (1)

cyclin-dependent protein serine/threonine kinase regulator activity

Gene Ontology

Source: GO:0016538

Synonyms:

G1/S-specific cyclin
G2/M-specific cyclin

Branch: molecular function

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (271)

cyclin-dependent protein kinase holoenzyme complex

Gene Ontology

Source: GO:0000307

Synonyms:

CDK holoenzyme

Branch: cellular component

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (350)

placenta development

Gene Ontology

Source: GO:0001890

Synonyms:

placental development
placentation

Branch: biological process

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)

Genes Annotated with this GO Term (604)

SCF-dependent proteasomal ubiquitin-dependent protein catabolic process

Gene Ontology

Source: GO:0031146

Synonyms:

SCF-dependent proteasomal ubiquitin-dependent protein breakdown
SCF-dependent proteasomal ubiquitin-dependent protein catabolism

Branch: biological process

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (322)

SCF ubiquitin ligase complex

Gene Ontology

Source: GO:0019005

Synonyms:

CDL1 complex
CRL1 complex

Branch: cellular component

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (372)

G1/S transition of mitotic cell cycle

Gene Ontology

Source: GO:0000082

Synonyms: Not Available

Branch: biological process

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (386)

microtubule organizing center

Gene Ontology

Source: GO:0005815

Synonyms:

MTOC
microtubule organising centre

Branch: cellular component

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (3628)

centriole

Gene Ontology

Source: GO:0005814

Synonyms:

daughter centriole
mother centriole

Branch: cellular component

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (641)

regulation of cell cycle

Gene Ontology

Source: GO:0051726

Synonyms:

arrest of mitotic cell cycle progression
cell cycle arrest

Branch: biological process

Genes: Ccnf (Rno)...Ccnf (Mmu)...CCNF (Hsa)

Genes Annotated with this GO Term (4643)

cell division

Gene Ontology

Source: GO:0051301

Synonyms: Not Available

Branch: biological process

Genes: Ccnf (Mmu)...Ccnf (Rno)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (2665)

perinuclear region of cytoplasm

Gene Ontology

Source: GO:0048471

Synonyms: Not Available

Branch: cellular component

Genes: Ccnf (Mmu)...Ccnf (Rno)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (2879)

protein ubiquitination

Gene Ontology

Source: GO:0016567

Synonyms:

protein ubiquitinylation
protein ubiquitylation

Branch: biological process

Genes: Ccnf (Mmu)...Ccnf (Rno)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (2757)

protein kinase binding

Gene Ontology

Source: GO:0019901

Synonyms: Not Available

Branch: molecular function

Genes: Ccnf (Rno)

Genes Annotated with this GO Term (2783)

centrosome

Gene Ontology

Source: GO:0005813

Synonyms: Not Available

Branch: cellular component

Genes: Ccnf (Mmu)...CCNF (Hsa)

Genes Annotated with this GO Term (2679)

sa30435

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-161003-14080

Genes: ccnf (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: ccnf (Dre)

cytoskeleton

Gene Ontology

Source: GO:0005856

Synonyms: Not Available

Branch: cellular component

Genes: Ccnf (Mmu)...Ccnf (Rno)...CCNF (Hsa)...ccnf (Dre)

Genes Annotated with this GO Term (10000)

(GRCh38)16:2449866T>A

(Homo sapiens)

Allele/Variant

Source: NC_000016.10:g.2449866T>A

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2449866T>A

(GRCh38)16:2453546C>T

(Homo sapiens)

Allele/Variant

Source: rs201692958

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2453546C>T

(GRCh38)16:2433009G>A

(Homo sapiens)

Allele/Variant

Source: rs4589553

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2433009G>A

(GRCh38)16:2448935G>C

(Homo sapiens)

Allele/Variant

Source: rs954539468

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2448935G>C

(GRCh38)16:2449010T>C

(Homo sapiens)

Allele/Variant

Source: rs8060813

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2449010T>C

(GRCh38)16:2455530C>T

(Homo sapiens)

Allele/Variant

Source: rs117232772

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2455530C>T

(GRCh38)16:2433179T>C

(Homo sapiens)

Allele/Variant

Source: rs9934102

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2433179T>C

(GRCh38)16:2435806G>A

(Homo sapiens)

Allele/Variant

Source: rs770482472

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2435806G>A

(GRCh38)16:2437125G>A

(Homo sapiens)

Allele/Variant

Source: rs374319260

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2437125G>A

(GRCh38)16:2437155G>A

(Homo sapiens)

Allele/Variant

Source: rs376056912

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2437155G>A

(GRCh38)16:2433051C>G

(Homo sapiens)

Allele/Variant

Source: rs756107653

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2433051C>G

(GRCh38)16:2443760C>G

(Homo sapiens)

Allele/Variant

Source: rs771852887

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2443760C>G

(GRCh38)16:2445535A>G

(Homo sapiens)

Allele/Variant

Source: rs777646899

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2445535A>G

(GRCh38)16:2449456G>A

(Homo sapiens)

Allele/Variant

Source: rs201271212

Genes: CCNF (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)16:2449456G>A

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