Version: 8.0.0
Date: Tue Jan 28 2025
1,148 results for txndc9

Txndc9

(Mus musculus)
Gene
Name: thioredoxin domain containing 9
Synonyms: expressed sequence AI098020, ATP binding protein associated with cell differentiation, Apacd, AI098020
Source: MGI:2138153
Biotype: protein coding gene
Symbol: Txndc9 (Mmu)
Symbol: Txndc9
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

txndc9

(Danio rerio)
Gene
Name: thioredoxin domain containing 9
Synonyms: wu:fb15e07, zgc:55522, fb15e07
Source: ZFIN:ZDB-GENE-030131-8569
Biotype: protein coding gene
Symbol: txndc9 (Dre)
Symbol: txndc9
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

TXNDC9

(Homo sapiens)
Gene
Name: thioredoxin domain containing 9
Synonyms: ATP binding protein associated with cell differentiation, ATP-binding protein associated with cell differentiation, thioredoxin domain-containing protein 9, APACD, protein 1-4, PHLP3
Source: HGNC:24110
Biotype: protein coding gene
Symbol: TXNDC9 (Hsa)
Symbol: TXNDC9
Strict Orthology Symbols: txndc9

Txndc9

(Rattus norvegicus)
Gene
Name: thioredoxin domain containing 9
Synonyms: MGC108568, ENSRNOG00000063081, ES cell-related protein, thioredoxin domain-containing protein 9, LOC280671, ATP binding protein
Source: RGD:708355
Biotype: protein coding gene
Symbol: Txndc9 (Rno)
Symbol: Txndc9
Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9); INTERACTS WITH 2,4-dinitrotoluene; 2,6
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

txndc9

(Xenopus tropicalis)
Gene
Name: thioredoxin domain containing 9
Synonyms: txndc9, thioredoxin domain containing 9
Source: Xenbase:XB-GENE-990778
Biotype: gene
Symbol: txndc9
Symbol: txndc9 (Xtr)
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Synonyms: txndc9...txndc9...txndc9
Strict Orthology Symbols: txndc9

txndc9.L

(Xenopus laevis)
Gene
Name: thioredoxin domain containing 9
Synonyms: thioredoxin domain containing 9, txndc9.L
Source: Xenbase:XB-GENE-990785
Biotype: gene
Symbol: txndc9.L (Xla)
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9
Symbol: txndc9.L

PLP1

(Saccharomyces cerevisiae)
Gene
Name: Phosducin-Like Protein
Synonyms: YDR183W
Source: SGD:S000002591
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

txdc-9

(Caenorhabditis elegans)
Gene
Name: ThioredoXin Domain Containing protein homolog 9
Synonyms: CELE_C05D11.3, tag-170, C05D11.3
Source: WB:WBGene00006515
Biotype: protein coding gene
Gene Synopsis: txdc-9 encodes a thioredoxin domain-containing protein orthologous to human TXNDC9 and ENSG00000145268
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

PhLP3

(Drosophila melanogaster)
Gene
Name: Phosducin-like protein 3
Synonyms: CG4511
Source: FB:FBgn0037843
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human TXNDC9 (thioredoxin domain containing 9).
Strict Orthology Symbols: txndc9

Hsap\TXNDC9UAS.Tag:HA

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0366463
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\TXNDC9
Construct Expressed Component: TXNDC9 (Hsa)

microtubule cytoskeleton organization

Gene Ontology
Source: GO:0000226
Synonyms:
  • microtubule cytoskeleton organisation
  • microtubule cytoskeleton organization and biogenesis
Branch: biological process
Genes: txndc9 (Dre)...Txndc9 (Mmu)...Txndc9 (Rno)...TXNDC9 (Hsa)

midbody

Gene Ontology
Source: GO:0030496
Synonyms: Not Available
Branch: cellular component
Genes: Txndc9 (Mmu)...Txndc9 (Rno)...TXNDC9 (Hsa)

cadherin binding

Gene Ontology
Source: GO:0045296
Synonyms: Not Available
Branch: molecular function
Genes: TXNDC9 (Hsa)

centrosome

Gene Ontology
Source: GO:0005813
Synonyms: Not Available
Branch: cellular component
Genes: Txndc9 (Rno)...Txndc9 (Mmu)...TXNDC9 (Hsa)

sa13931

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-12342
Genes: txndc9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: txndc9 (Dre)

sa17131

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-13275
Genes: txndc9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: txndc9 (Dre)

cytoskeleton

Gene Ontology
Source: GO:0005856
Synonyms: Not Available
Branch: cellular component
Genes: TXNDC9 (Hsa)

cytosol

Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: Txndc9 (Mmu)...Txndc9 (Rno)...TXNDC9 (Hsa)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: Txndc9 (Rno)...TXNDC9 (Hsa)...Txndc9 (Mmu)...txndc9 (Dre)

nucleus

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: Txndc9 (Rno)...TXNDC9 (Hsa)...Txndc9 (Mmu)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Txndc9 (Rno)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: TXNDC9 (Hsa)

(GRCh38)2:99333044C>T

(Homo sapiens)
Allele/Variant
Source: rs1403241808
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333044C>T

(GRCh38)2:99327537G>C

(Homo sapiens)
Allele/Variant
Source: rs1217226709
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99327537G>C

(GRCh38)2:99322164G>T

(Homo sapiens)
Allele/Variant
Source: rs908232770
Genes: TXNDC9 (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)2:99322164G>T

(GRCh38)2:99319726T>G

(Homo sapiens)
Allele/Variant
Source: rs1213875510
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99319726T>G

(GRCh38)2:99321973G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.99321973G>A
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99321973G>A

(GRCh38)2:99333074C>T

(Homo sapiens)
Allele/Variant
Source: rs767681836
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333074C>T

(GRCh38)2:99322130T>C

(Homo sapiens)
Allele/Variant
Source: rs750758972
Genes: TXNDC9 (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)2:99322130T>C

(GRCh38)2:99333075G>A

(Homo sapiens)
Allele/Variant
Source: rs866880642
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333075G>A

(GRCh38)2:99322028G>C

(Homo sapiens)
Allele/Variant
Source: rs761714942
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99322028G>C

(GRCh38)2:99337578G>C

(Homo sapiens)
Allele/Variant
Source: rs752474657
Genes: TXNDC9 (Hsa), EIF5B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99337578G>C

(mRatBN7.2)9:40214027G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197370953
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40214027G>A

(mRatBN7.2)9:40277881T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321579101
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40277881T>C

(mRatBN7.2)9:40277997G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.40277997G>A
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40277997G>A

(mRatBN7.2)9:40220170G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321343644
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40220170G>A

(mRatBN7.2)9:40359105C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321601620
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40359105C>T

(mRatBN7.2)9:40359685G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321581837
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40359685G>A

(mRatBN7.2)9:40359888G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321624776
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40359888G>T

(mRatBN7.2)9:40362968A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321597791
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40362968A>G

(mRatBN7.2)9:40367417C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321637712
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40367417C>T

(mRatBN7.2)9:40372088C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321601587
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40372088C>T

(mRatBN7.2)9:40217300G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321507381
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40217300G>A

(mRatBN7.2)9:40220163G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321580689
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40220163G>C

(mRatBN7.2)9:40371643T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321462206
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40371643T>C

(mRatBN7.2)9:40372287C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321462165
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40372287C>T

(mRatBN7.2)9:40373867G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321507397
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40373867G>A

(mRatBN7.2)9:40369602T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.40369602T>C
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40369602T>C

(mRatBN7.2)9:40370650G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321507329
Genes: Txndc9 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:40370650G>A

(GRCz11)9:21821203T>A

(Danio rerio)
Allele/Variant
Source: ss5201425050
Genes: txndc9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)9:21821203T>A