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9,487 results for tbc1d22a

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Tbc1d22a

(Mus musculus)

Gene

Name: TBC1 domain family, member 22a

Synonyms: cDNA sequence BC023106, DNA segment, Chr 15, ERATO Doi 781, expressed, D15Ertd781e, BC023106, RGD1306588, MGC:28337

Source: MGI:1289265

Biotype: protein coding gene

Symbol: Tbc1d22a (Mmu)

Symbol: Tbc1d22a

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A).

Strict Orthology Symbols: tbc1d22a

Alleles: Tbc1d22a (Mmu)...Tbc1d22a (Mmu)...Tbc1d22a (Mmu)

tbc1d22a

(Danio rerio)

Gene

Name: TBC1 domain family, member 22a

Synonyms: zgc:101677

Source: ZFIN:ZDB-GENE-041114-144

Biotype: protein coding gene

Symbol: tbc1d22a (Dre)

Symbol: tbc1d22a

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A).

Strict Orthology Symbols: tbc1d22a

Allele/Variant (1131)

TBC1D22A

(Homo sapiens)

Gene

Name: TBC1 domain family member 22A

Synonyms: TBC1 domain family, member 22A, putative GTPase activator, HSC79E021, C22orf4

Source: HGNC:1309

Biotype: protein coding gene

Symbol: TBC1D22A (Hsa)

Symbol: TBC1D22A

Strict Orthology Symbols: tbc1d22a

Allele/Variant (33)

Tbc1d22a

(Rattus norvegicus)

Gene

Name: TBC1 domain family, member 22a

Synonyms: similar to cDNA sequence BC023106, LOC366968, TBC1 domain family member 22A, RGD1306588, LOC678774, TBC1 domain family member 22A-like, similar to TBC1 domain family member 22A

Source: RGD:1306588

Biotype: protein coding gene

Symbol: Tbc1d22a (Rno)

Symbol: Tbc1d22a

Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A); INTERACTS WITH 2,3,7,8-Tetrachlorodibenzofuran

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A).

Strict Orthology Symbols: tbc1d22a

Allele/Variant (827)

tbc1d22a

(Xenopus tropicalis)

Gene

Name: TBC1 domain family member 22A

Synonyms: tbc1d22a, TBC1 domain family member 22A, LOC108711168

Source: Xenbase:XB-GENE-5866746

Biotype: gene

Symbol: tbc1d22a

Symbol: tbc1d22a (Xtr)

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A).

Synonyms: tbc1d22a...tbc1d22a...tbc1d22a

Strict Orthology Symbols: tbc1d22a

TBC1D22A-AS1

(Homo sapiens)

Gene

Name: TBC1D22A antisense RNA 1

Synonyms: Not Available

Source: HGNC:51221

Biotype: ncRNA gene

Symbol: TBC1D22A-AS1 (Hsa)

Symbol: TBC1D22A-AS1

TBC1D22A-DT

(Homo sapiens)

Gene

Name: TBC1D22A divergent transcript

Synonyms: Not Available

Source: HGNC:55388

Biotype: ncRNA gene

Symbol: TBC1D22A-DT (Hsa)

Symbol: TBC1D22A-DT

Tbc1d22al

(Rattus norvegicus)

Gene

Name: TBC1 domain family, member 22a like

Synonyms: uncharacterized protein LOC108351584, uncharacterized LOC108351584, LOC108351584

Source: RGD:11406985

Biotype: ncRNA gene

Symbol: Tbc1d22al (Rno)

Symbol: Tbc1d22al

Allele/Variant (3)

Tbc1d22a^{tm1a(KOMP)Wtsi}

(Mus musculus)

Allele/Variant

Source: MGI:5014583

Genes: Tbc1d22a (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Tbc1d22a (Mmu)

Genes: Tbc1d22a (Mmu)

Symbol: Tbc1d22a^{tm1a(KOMP)Wtsi}

Gene (1)

Tbc1d22a^{tm1b(KOMP)Wtsi}

(Mus musculus)

Allele/Variant

Source: MGI:5636942

Genes: Tbc1d22a (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Tbc1d22a (Mmu)

Genes: Tbc1d22a (Mmu)

Symbol: Tbc1d22a^{tm1b(KOMP)Wtsi}

Tbc1d22a^em1Cya

(Mus musculus)

Allele/Variant

Source: MGI:7586969

Genes: Tbc1d22a (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Tbc1d22a (Mmu)

Genes: Tbc1d22a (Mmu)

Symbol: Tbc1d22a^em1Cya

Gene (1)

Tbc1d22a^{tm1b(KOMP)Wtsi}/Tbc1d22a^{tm1b(KOMP)Wtsi} [background:] C57BL/6N-Tbc1d22a^{tm1b(KOMP)Wtsi}/Wtsi

(Mus musculus)

Model

Id: MGI:5797854

Synonyms: Not Available

Symbol: Tbc1d22a/Tbc1d22a [background:] C57BL/6N-Tbc1d22a/Wtsi

Genes: Tbc1d22a (Mmu)

Alleles: Tbc1d22a (Mmu)

Name: Tbc1d22a/Tbc1d22a [background:] C57BL/6N-Tbc1d22a/Wtsi

Gene (1)

tbc-3

(Caenorhabditis elegans)

Gene

Name: TBC (Tre-2/Bub2/Cdc16) domain family 3

Synonyms: CELE_F32B6.8, F32B6.8

Source: WB:WBGene00009322

Biotype: protein coding gene

Gene Synopsis: Is an ortholog of human TBC1D22A (TBC1 domain family member 22A) and TBC1D22B (TBC1 domain family member

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A) and TBC1D22B (TBC1 domain family member

Strict Orthology Symbols: tbc1d22a

Allele/Variant (28)

Tbc1d22

(Drosophila melanogaster)

Gene

Name: TBC1 domain family member 22

Synonyms: CG5745, dTBC1D22

Source: FB:FBgn0038855

Biotype: protein coding gene

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A) and TBC1D22B (TBC1 domain family member

Strict Orthology Symbols: tbc1d22a

Allele/Variant (89)

GYP1

(Saccharomyces cerevisiae)

Gene

Name: Gtpase-activating protein for YPt1p

Synonyms: YOR29-21, YOR070C

Source: SGD:S000005596

Biotype: protein coding gene

Automated Gene Synopsis: Orthologous to human TBC1D22A (TBC1 domain family member 22A) and TBC1D22B (TBC1 domain family member

Strict Orthology Symbols: tbc1d22a

Allele/Variant (13)

la024547Tg

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-120806-10853

Genes: tbc1d22a (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: tbc1d22a (Dre)

Gene (1)

la024546Tg

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-120806-9407

Genes: tbc1d22a (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: tbc1d22a (Dre)

Gene (1)

la011387Tg

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130129-2008

Genes: tbc1d22a (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: tbc1d22a (Dre)

Gene (1)

14-3-3 protein binding

Gene Ontology

Source: GO:0071889

Synonyms: Not Available

Branch: molecular function

Genes: TBC1D22A (Hsa)...Tbc1d22a (Rno)...Tbc1d22a (Mmu)

Genes Annotated with this GO Term (129)

Hsap\TBC1D22A^UAS.Tag:HA

(Drosophila melanogaster)

Allele/Variant

Source: FB:FBal0356385

Genes: Not Available

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hsap\TBC1D22A

Construct Expressed Component: TBC1D22A (Hsa)

regulation of cilium assembly

Gene Ontology

Source: GO:1902017

Synonyms:

regulation of ciliogenesis
regulation of cilium biogenesis

Branch: biological process

Genes: TBC1D22A (Hsa)...Tbc1d22a (Rno)

Genes Annotated with this GO Term (341)

GTPase activator activity

Gene Ontology

Source: GO:0005096

Synonyms:

ARF GAP activity
ARF GTPase activator activity

Branch: molecular function

Genes: Tbc1d22a (Mmu)...Tbc1d22a (Rno)...tbc1d22a (Dre)...TBC1D22A (Hsa)

Genes Annotated with this GO Term (1201)

protein homodimerization activity

Gene Ontology

Source: GO:0042803

Synonyms:

dimerization activity

Branch: molecular function

Genes: Tbc1d22a (Rno)...Tbc1d22a (Mmu)...TBC1D22A (Hsa)

Genes Annotated with this GO Term (2588)

Golgi apparatus

Gene Ontology

Source: GO:0005794

Synonyms:

Golgi
Golgi complex

Branch: cellular component

Genes: Tbc1d22a (Rno)...tbc1d22a (Dre)...Tbc1d22a (Mmu)...TBC1D22A (Hsa)

Genes Annotated with this GO Term (6596)

sa856

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-161003-19308

Genes: tbc1d22a (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: tbc1d22a (Dre)

protein binding

Gene Ontology

Source: GO:0005515

Synonyms:

glycoprotein binding
protein amino acid binding

Branch: molecular function

Genes: TBC1D22A (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)22:46797455G>A

(Homo sapiens)

Allele/Variant

Source: rs1267287718

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797455G>A

(GRCh38)22:46894809G>A

(Homo sapiens)

Allele/Variant

Source: rs139839482

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46894809G>A

(GRCh38)22:47111572G>A

(Homo sapiens)

Allele/Variant

Source: rs1198950585

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCh38)22:47111572G>A

(GRCh38)22:46793784A>G

(Homo sapiens)

Allele/Variant

Source: rs749281882

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793784A>G

(GRCh38)22:46793671C>T

(Homo sapiens)

Allele/Variant

Source: rs141580250

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793671C>T

(GRCh38)22:46793850G>C

(Homo sapiens)

Allele/Variant

Source: rs141713070

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793850G>C

(GRCh38)22:46797495C>T

(Homo sapiens)

Allele/Variant

Source: rs187687977

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797495C>T

(GRCh38)22:46793719C>T

(Homo sapiens)

Allele/Variant

Source: rs146025212

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793719C>T

(GRCh38)22:46793781C>A

(Homo sapiens)

Allele/Variant

Source: rs112995262

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793781C>A

(GRCh38)22:46793782C>G

(Homo sapiens)

Allele/Variant

Source: rs201151937

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793782C>G

(GRCh38)22:47111515C>T

(Homo sapiens)

Allele/Variant

Source: rs768020083

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCh38)22:47111515C>T

(GRCh38)22:46797518A>G

(Homo sapiens)

Allele/Variant

Source: rs146205023

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797518A>G

(GRCh38)22:46894788A>G

(Homo sapiens)

Allele/Variant

Source: rs775351336

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46894788A>G

(GRCh38)22:46974322G>A

(Homo sapiens)

Allele/Variant

Source: rs199657694

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46974322G>A

(GRCh38)22:47111544G>A

(Homo sapiens)

Allele/Variant

Source: rs367838104

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)22:47111544G>A

(GRCh38)22:46797447G>T

(Homo sapiens)

Allele/Variant

Source: rs762974977

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797447G>T

(GRCh38)22:47037179G>A

(Homo sapiens)

Allele/Variant

Source: rs753037531

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:47037179G>A

(GRCh38)22:46797461G>A

(Homo sapiens)

Allele/Variant

Source: rs759900287

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797461G>A

(GRCh38)22:46797549C>T

(Homo sapiens)

Allele/Variant

Source: rs761726540

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797549C>T

(GRCh38)22:46797588A>G

(Homo sapiens)

Allele/Variant

Source: rs569400492

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46797588A>G

(GRCh38)22:47037127C>T

(Homo sapiens)

Allele/Variant

Source: rs1438074649

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:47037127C>T

(GRCh38)22:46793809C>T

(Homo sapiens)

Allele/Variant

Source: rs563554988

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46793809C>T

(GRCh38)22:46891317C>G

(Homo sapiens)

Allele/Variant

Source: rs764993895

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46891317C>G

(GRCh38)22:46838568A>G

(Homo sapiens)

Allele/Variant

Source: rs207478021

Genes: TBC1D22A (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)22:46838568A>G

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