Version: 8.1.0
Date: Fri Apr 18 2025
629 results for Tbc1d10c

Tbc1d10c

(Mus musculus)
Gene
Name: TBC1 domain family, member 10c
Synonyms: Carabin, AI428527, RGD1311490, 1810062O14Rik, RIKEN cDNA 1810062O14 gene, expressed sequence AI428527
Source: MGI:1922072
Biotype: protein coding gene
Symbol: Tbc1d10c (Mmu)
Symbol: Tbc1d10c
Automated Gene Synopsis: Orthologous to human TBC1D10C (TBC1 domain family member 10C).
Strict Orthology Symbols: Tbc1d10c
Alleles: Tbc1d10c (Mmu)...Tbc1d10c (Mmu)...Tbc1d10c (Mmu)

Tbc1d10c

(Rattus norvegicus)
Gene
Name: TBC1 domain family, member 10C
Synonyms: LOC361697, similar to DKFZP434P1750 protein, RGD1311490, carabin
Source: RGD:1311490
Biotype: protein coding gene
Symbol: Tbc1d10c (Rno)
Symbol: Tbc1d10c
Gene Synopsis: Orthologous to human TBC1D10C (TBC1 domain family member 10C); INTERACTS WITH (+)-schisandrin B; 2,3,7,8
Automated Gene Synopsis: Orthologous to human TBC1D10C (TBC1 domain family member 10C).
Strict Orthology Symbols: Tbc1d10c

TBC1D10C

(Homo sapiens)
Gene
Name: TBC1 domain family member 10C
Synonyms: EPI64C, FLJ00332, TBC1 domain family, member 10C, MGC46488, carabin
Source: HGNC:24702
Biotype: protein coding gene
Symbol: TBC1D10C (Hsa)
Symbol: TBC1D10C
Strict Orthology Symbols: Tbc1d10c

tbc1d10c

(Danio rerio)
Gene
Name: TBC1 domain family, member 10C
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-130125-1
Biotype: protein coding gene
Symbol: tbc1d10c (Dre)
Symbol: tbc1d10c
Automated Gene Synopsis: Orthologous to human TBC1D10C (TBC1 domain family member 10C).
Strict Orthology Symbols: Tbc1d10c

Tbc1d10ctm1.1Psou

(Mus musculus)
Allele/Variant
Source: MGI:5578033
Genes: Tbc1d10c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tbc1d10c (Mmu)
Genes: Tbc1d10c (Mmu)
Symbol: Tbc1d10ctm1.1Psou

Tbc1d10ctm1Nju

(Mus musculus)
Allele/Variant
Source: MGI:7256539
Genes: Tbc1d10c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tbc1d10c (Mmu)
Genes: Tbc1d10c (Mmu)
Symbol: Tbc1d10ctm1Nju

Tbc1d10ctm1.2Psou

(Mus musculus)
Allele/Variant
Source: MGI:5578034
Genes: Tbc1d10c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tbc1d10c (Mmu)
Genes: Tbc1d10c (Mmu)
Symbol: Tbc1d10ctm1.2Psou

Tbc1d10ctm1.2Psou/Tbc1d10ctm1.2Psou [background:] involves: 129S2/SvPas * C57BL/6J

(Mus musculus)
Model
Id: MGI:5578120
Synonyms: Not Available
Symbol: Tbc1d10c/Tbc1d10c [background:] involves: 129S2/SvPas * C57BL/6J (Mmu)
Genes: Tbc1d10c (Mmu)
Alleles: Tbc1d10c (Mmu)
Name: Tbc1d10c/Tbc1d10c [background:] involves: 129S2/SvPas * C57BL/6J

Tbc1d10ctm1.1Psou/Tbc1d10ctm1.2Psou Cd79atm1(cre)Reth/Cd79a+ [background:] involves: 129S2/SvPas * BALB/c * C57BL/6J

(Mus musculus)
Model
Id: MGI:5578118
Synonyms: Not Available
Symbol: Tbc1d10c/Tbc1d10c Cd79a/Cd79a<+> [background:] involves: 129S2/SvPas
Genes: Tbc1d10c (Mmu)
Alleles: Tbc1d10c (Mmu)
Name: Tbc1d10c/Tbc1d10c Cd79a/Cd79a<+> [background:] involves: 129S2/SvPas

Tbc1d10ctm1.1Psou/Tbc1d10ctm1.2Psou Tg(Lck-cre)#Nik/0 [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * DBA/2

(Mus musculus)
Model
Id: MGI:5578119
Synonyms: Not Available
Symbol: Tbc1d10c/Tbc1d10c Tg(Lck-cre)#Nik/0 [background:] involves: 129S2/SvPas * C57BL
Genes: Tbc1d10c (Mmu)
Alleles: Tbc1d10c (Mmu)
Name: Tbc1d10c/Tbc1d10c Tg(Lck-cre)#Nik/0 [background:] involves: 129S2/SvPas * C57BL

tbc-10

(Caenorhabditis elegans)
Gene
Name: TBC (Tre-2/Bub2/Cdc16) domain family 10
Synonyms: CELE_R06B10.5, R06B10.5
Source: WB:WBGene00019915
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human TBC1D10A (TBC1 domain family member 10A) and TBC1D10C (TBC1 domain family member
Automated Gene Synopsis: Orthologous to several human genes including TBC1D10C (TBC1 domain family member 10C).
Strict Orthology Symbols: Tbc1d10c

wkd

(Drosophila melanogaster)
Gene
Name: whacked
Synonyms: Wkd, CG5344, cg5344, Whacked
Source: FB:FBgn0037917
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to several human genes including TBC1D10C (TBC1 domain family member 10C).
Strict Orthology Symbols: Tbc1d10c

MSB3

(Saccharomyces cerevisiae)
Gene
Name: Multicopy Suppressor of Bud Emergence
Synonyms: GYP3, YNL293W
Source: SGD:S000005237
Biotype: protein coding gene
Strict Orthology Symbols: Tbc1d10c

negative regulation of B cell activation

Gene Ontology
Source: GO:0050869
Synonyms:
  • down regulation of B cell activation
  • down-regulation of B cell activation
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

negative regulation of calcineurin-NFAT signaling cascade

Gene Ontology
Source: GO:0070885
Synonyms:
  • down regulation of calcineurin-NFAT signaling cascade
  • down-regulation of calcineurin-NFAT signaling cascade
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

calcineurin-NFAT signaling cascade

Gene Ontology
Source: GO:0033173
Synonyms:
  • calcineurin-NFAT signaling pathway
  • calcineurin-NFAT signalling pathway
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

filopodium membrane

Gene Ontology
Source: GO:0031527
Synonyms: Not Available
Branch: cellular component
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

Ewing sarcoma

Disease
Source: DOID:3369
Definition: A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm.
Genes: Tbc1d10c (Mmu)

B cell activation

Gene Ontology
Source: GO:0042113
Synonyms:
  • B lymphocyte activation
  • B-cell activation
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

ERK1 and ERK2 cascade

Gene Ontology
Source: GO:0070371
Synonyms:
  • ERK cascade
  • ERK1 and ERK2 signaling pathway
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

negative regulation of ERK1 and ERK2 cascade

Gene Ontology
Source: GO:0070373
Synonyms:
  • down regulation of ERK1 and ERK2 cascade
  • down-regulation of ERK1 and ERK2 cascade
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...Tbc1d10c (Mmu)

ficolin-1-rich granule membrane

Gene Ontology
Source: GO:0101003
Synonyms: Not Available
Branch: cellular component
Genes: TBC1D10C (Hsa)

regulation of cilium assembly

Gene Ontology
Source: GO:1902017
Synonyms:
  • regulation of ciliogenesis
  • regulation of cilium biogenesis
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)

retrograde transport, endosome to Golgi

Gene Ontology
Source: GO:0042147
Synonyms:
  • retrograde (endosome to Golgi) transport
Branch: biological process
Genes: TBC1D10C (Hsa)...Tbc1d10c (Rno)...tbc1d10c (Dre)...Tbc1d10c (Mmu)

GTPase activator activity

Gene Ontology
Source: GO:0005096
Synonyms:
  • ARF GAP activity
  • ARF GTPase activator activity
Branch: molecular function
Genes: Tbc1d10c (Mmu)...TBC1D10C (Hsa)...tbc1d10c (Dre)

sa12491

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2215
Genes: tbc1d10c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tbc1d10c (Dre)

cytosol

Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: Tbc1d10c (Rno)...Tbc1d10c (Mmu)...TBC1D10C (Hsa)

plasma membrane

Gene Ontology
Source: GO:0005886
Synonyms:
  • bacterial inner membrane
  • cell membrane
Branch: cellular component
Genes: Tbc1d10c (Rno)...Tbc1d10c (Mmu)...TBC1D10C (Hsa)

membrane

Gene Ontology
Source: GO:0016020
Synonyms:
  • integral component of membrane
  • integral to membrane
Branch: cellular component
Genes: TBC1D10C (Hsa)

(GRCh38)11:67406914G>A

(Homo sapiens)
Allele/Variant
Source: rs373696431
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67406914G>A

(GRCh38)11:67408997G>A

(Homo sapiens)
Allele/Variant
Source: rs775695502
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67408997G>A

(GRCh38)11:67409564G>A

(Homo sapiens)
Allele/Variant
Source: rs764659138
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67409564G>A

(GRCh38)11:67405119C>T

(Homo sapiens)
Allele/Variant
Source: rs147100387
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405119C>T

(GRCh38)11:67405173C>T

(Homo sapiens)
Allele/Variant
Source: rs565585080
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405173C>T

(GRCh38)11:67406895G>T

(Homo sapiens)
Allele/Variant
Source: rs150801783
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67406895G>T

(GRCh38)11:67409483C>T

(Homo sapiens)
Allele/Variant
Source: rs1186992446
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67409483C>T

(GRCh38)11:67409444G>A

(Homo sapiens)
Allele/Variant
Source: rs202004214
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67409444G>A

(GRCh38)11:67405170C>T

(Homo sapiens)
Allele/Variant
Source: rs758893581
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405170C>T

(GRCh38)11:67409521G>A

(Homo sapiens)
Allele/Variant
Source: rs1344791009
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67409521G>A

(GRCh38)11:67409683C>T

(Homo sapiens)
Allele/Variant
Source: rs199697725
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67409683C>T

(GRCh38)11:67405147C>T

(Homo sapiens)
Allele/Variant
Source: rs151087425
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405147C>T

(GRCh38)11:67409018G>A

(Homo sapiens)
Allele/Variant
Source: rs367546852
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67409018G>A

(GRCh38)11:67409576A>G

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.67409576A>G
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67409576A>G

(GRCh38)11:67406886C>T

(Homo sapiens)
Allele/Variant
Source: rs142410416
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67406886C>T

(GRCh38)11:67409443C>T

(Homo sapiens)
Allele/Variant
Source: rs1389163921
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67409443C>T

(GRCh38)11:67405414C>T

(Homo sapiens)
Allele/Variant
Source: rs141022722
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405414C>T

(GRCh38)11:67404237C>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.67404237C>T
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67404237C>T

(GRCh38)11:67406903A>G

(Homo sapiens)
Allele/Variant
Source: rs757865363
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67406903A>G

(GRCh38)11:67409098C>T

(Homo sapiens)
Allele/Variant
Source: rs772830757
Genes: PPP1CA (Hsa), TBC1D10C (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)11:67409098C>T

(GRCh38)11:67405100T>C

(Homo sapiens)
Allele/Variant
Source: rs142040344
Genes: PPP1CA (Hsa), TBC1D10C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:67405100T>C