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Category

1,003 results for TXNDC12

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Txndc12

(Rattus norvegicus)

Gene

Name: thioredoxin domain containing 12

Synonyms: LOC298370, similar to RIKEN cDNA 0610040B21, thioredoxin domain containing 12 (endoplasmic reticulum), RGD1305960, thioredoxin domain-containing protein 12

Source: RGD:1305960

Biotype: protein coding gene

Symbol: Txndc12 (Rno)

Symbol: Txndc12

Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12); PARTICIPATES IN glutathione metabolic

Automated Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Allele/Variant (155)

Txndc12

(Mus musculus)

Gene

Name: thioredoxin domain containing 12 (endoplasmic reticulum)

Synonyms: 0610040B21Rik, RIKEN cDNA 0610040B21 gene, ERp16, RGD1305960

Source: MGI:1913323

Biotype: protein coding gene

Symbol: Txndc12 (Mmu)

Symbol: Txndc12

Automated Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Alleles: Txndc12 (Mmu)...Txndc12 (Mmu)...Txndc12 (Mmu)...Txndc12 (Mmu)...Txndc12 (Mmu)

txndc12

(Danio rerio)

Gene

Name: thioredoxin domain containing 12 (endoplasmic reticulum)

Synonyms: zgc:110680, wu:fc47c08

Source: ZFIN:ZDB-GENE-050522-497

Biotype: protein coding gene

Symbol: txndc12 (Dre)

Symbol: txndc12

Automated Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Allele/Variant (1)

TXNDC12

(Homo sapiens)

Gene

Name: thioredoxin domain containing 12

Synonyms: hTLP19, TLP19, endoplasmic reticulum resident protein 18, endoplasmic reticulum resident protein 19, ER protein 18, endoplasmic reticulum thioredoxin superfamily member, 18 kDa, ER protein 19, thioredoxin-like protein p19, hAG-1, AG1, thioredoxin domain-containing protein 12, PDIA16, ERP18, ERP19, ERP16, anterior gradient homolog 1, protein disulfide isomerase family A, member 16, thioredoxin domain containing 12 (endoplasmic reticulum), endoplasmic reticulum protein ERp19, AGR1

Source: HGNC:24626

Biotype: protein coding gene

Symbol: TXNDC12 (Hsa)

Symbol: TXNDC12

Strict Orthology Symbols: txndc12.L...txndc12.S...Txndc12...txndc12

Allele/Variant (25)

TXNDC12-AS1

(Homo sapiens)

Gene

Name: TXNDC12 antisense RNA 1

Synonyms: Not Available

Source: HGNC:30008

Biotype: ncRNA gene

Symbol: TXNDC12-AS1 (Hsa)

Symbol: TXNDC12-AS1

txndc12

(Xenopus tropicalis)

Gene

Name: thioredoxin domain containing 12 (endoplasmic reticulum)

Synonyms: pdia16, ag-1, agr1, ag1, thioredoxin domain containing 12 (endoplasmic reticulum), erp18, txndc12, erp19

Source: Xenbase:XB-GENE-997973

Biotype: gene

Symbol: txndc12 (Xtr)

Symbol: txndc12

Synonyms: txndc12...txndc12

Strict Orthology Symbols: txndc12.L...txndc12.S

txndc12.S

(Xenopus laevis)

Gene

Name: thioredoxin domain containing 12 (endoplasmic reticulum)

Synonyms: pdia16, txndc12.S, ag-1, agr1, ag1, thioredoxin domain containing 12 (endoplasmic reticulum), erp18, erp19

Source: Xenbase:XB-GENE-17338579

Biotype: gene

Symbol: txndc12.S (Xla)

Automated Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Symbol: txndc12.S

txndc12.L

(Xenopus laevis)

Gene

Name: thioredoxin domain containing 12 (endoplasmic reticulum)

Synonyms: pdia16, txndc12.L, ag-1, agr1, ag1, thioredoxin domain containing 12 (endoplasmic reticulum), erp18, erp19

Source: Xenbase:XB-GENE-6253846

Biotype: gene

Symbol: txndc12.L (Xla)

Automated Gene Synopsis: Orthologous to human TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Symbol: txndc12.L

Txndc12^em1(IMPC)Bay

(Mus musculus)

Allele/Variant

Source: MGI:6361230

Genes: Txndc12 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Txndc12 (Mmu)

Genes: Txndc12 (Mmu)

Symbol: Txndc12^em1(IMPC)Bay

Gene (1)

Txndc12^em2Cya

(Mus musculus)

Allele/Variant

Source: MGI:7587371

Genes: Txndc12 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Txndc12 (Mmu)

Genes: Txndc12 (Mmu)

Symbol: Txndc12^em2Cya

Gene (1)

Txndc12^{Gt(OST69558)Lex}

(Mus musculus)

Allele/Variant

Source: MGI:4173257

Genes: Txndc12 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Txndc12 (Mmu)

Genes: Txndc12 (Mmu)

Symbol: Txndc12^{Gt(OST69558)Lex}

Txndc12^em1Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7308127

Genes: Txndc12 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Txndc12 (Mmu)

Genes: Txndc12 (Mmu)

Symbol: Txndc12^em1Gpt

Gene (1)

Txndc12^em18Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7308126

Genes: Txndc12 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Txndc12 (Mmu)

Genes: Txndc12 (Mmu)

Symbol: Txndc12^em18Gpt

Gene (1)

Txndc12^{Gt(OST69558)Lex}/Txndc12^{Gt(OST69558)Lex} [background:] involves: 129S5/SvEvBrd * C57BL/6J

(Mus musculus)

Model

Id: MGI:5429582

Synonyms: Not Available

Symbol: Txndc12/Txndc12 [background:] involves: 129S5/SvEvBrd * C57BL/6J (

Genes: Txndc12 (Mmu)

Alleles: Txndc12 (Mmu)

Name: Txndc12/Txndc12 [background:] involves: 129S5/SvEvBrd * C57BL/6J

Gene (1)

txdc-12.2

(Caenorhabditis elegans)

Gene

Name: ThioredoXin Domain Containing protein homolog 12.2

Synonyms: CELE_F49H12.5, F49H12.5

Source: WB:WBGene00018656

Biotype: protein coding gene

Gene Synopsis: Is an ortholog of human TXNDC12 (thioredoxin domain containing 12).

Automated Gene Synopsis: Orthologous to several human genes including TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

txdc-12.1

(Caenorhabditis elegans)

Gene

Name: ThioredoXin Domain Containing protein homolog 12.1

Synonyms: CELE_Y57A10A.23, Y57A10A.23

Source: WB:WBGene00013263

Biotype: protein coding gene

Gene Synopsis: Is an ortholog of human TXNDC12 (thioredoxin domain containing 12).

Automated Gene Synopsis: Orthologous to several human genes including TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

aifm1

(Xenopus tropicalis)

Gene

Name: apoptosis inducing factor, mitochondria associated 1

Synonyms: apoptosis inducing factor, mitochondria associated 1, pdcd8, aifm1, programmed cell death 8

Source: Xenbase:XB-GENE-1016872

Biotype: gene

Automated Gene Synopsis: Orthologous to several human genes including TXNDC12 (thioredoxin domain containing 12).

Strict Orthology Symbols: TXNDC12

Disease (10)

protein-disulfide reductase (glutathione) activity

Gene Ontology

Source: GO:0019153

Synonyms:

glutaredoxin reductase
glutathione-insulin transhydrogenase activity

Branch: molecular function

Genes: TXNDC12 (Hsa)...Txndc12 (Mmu)...txndc12 (Dre)...Txndc12 (Rno)

Genes Annotated with this GO Term (13)

detoxification of hydrogen peroxide

Gene Ontology

Source: GO:0061691

Synonyms: Not Available

Branch: biological process

Genes: txndc12 (Dre)

Genes Annotated with this GO Term (11)

negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway

Gene Ontology

Source: GO:1902236

Synonyms:

down regulation of ER stress-induced apoptosis
down regulation of apoptosis in response to ER stress

Branch: biological process

Genes: Txndc12 (Rno)...TXNDC12 (Hsa)...Txndc12 (Mmu)

Genes Annotated with this GO Term (69)

protein-disulfide reductase (NAD(P)H) activity

Gene Ontology

Source: GO:0047134

Synonyms:

NAD(P)H:protein-disulfide oxidoreductase activity
disulfide reductase activity

Branch: molecular function

Genes: txndc12 (Dre)

Genes Annotated with this GO Term (50)

protein-disulfide reductase activity

Gene Ontology

Source: GO:0015035

Synonyms:

haem lyase disulphide oxidoreductase activity
heme lyase disulfide oxidoreductase activity

Branch: molecular function

Genes: Txndc12 (Rno)...TXNDC12 (Hsa)...Txndc12 (Mmu)

Genes Annotated with this GO Term (192)

endoplasmic reticulum lumen

Gene Ontology

Source: GO:0005788

Synonyms:

ER cisterna
ER lumen

Branch: cellular component

Genes: TXNDC12 (Hsa)...Txndc12 (Rno)...txndc12 (Dre)...Txndc12 (Mmu)

Genes Annotated with this GO Term (638)

oxidoreductase activity

Gene Ontology

Source: GO:0016491

Synonyms:

oxidoreductase activity, acting on other substrates
redox activity

Branch: molecular function

Genes: txndc12 (Dre)...Txndc12 (Rno)...TXNDC12 (Hsa)

Genes Annotated with this GO Term (4673)

DNA damage response

Gene Ontology

Source: GO:0006974

Synonyms:

cellular DNA damage response
cellular response to DNA damage stimulus

Branch: biological process

Genes: txndc12 (Dre)

Genes Annotated with this GO Term (3657)

endoplasmic reticulum

Gene Ontology

Source: GO:0005783

Synonyms:

Branch: cellular component

Genes: TXNDC12 (Hsa)...Txndc12 (Rno)...Txndc12 (Mmu)...txndc12 (Dre)

Genes Annotated with this GO Term (8935)

sa1870

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-120411-300

Genes: txndc12 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: txndc12 (Dre)

protein binding

Gene Ontology

Source: GO:0005515

Synonyms:

glycoprotein binding
protein amino acid binding

Branch: molecular function

Genes: TXNDC12 (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)1:52028595C>G

(Homo sapiens)

Allele/Variant

Source: rs752379909

Genes: TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52028595C>G

(GRCh38)1:52055084G>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.52055084G>A

Genes: TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52055084G>A

(GRCh38)1:52055075C>T

(Homo sapiens)

Allele/Variant

Source: rs190576327

Genes: TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52055075C>T

(GRCh38)1:52024519G>C

(Homo sapiens)

Allele/Variant

Source: rs199849902

Genes: TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52024519G>C

(GRCh38)1:52032948G>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.52032948G>A

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52032948G>A

(GRCh38)1:52033082C>T

(Homo sapiens)

Allele/Variant

Source: rs374491748

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033082C>T

(GRCh38)1:52033265G>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.52033265G>A

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033265G>A

(GRCh38)1:52033476G>A

(Homo sapiens)

Allele/Variant

Source: rs201065316

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033476G>A

(GRCh38)1:52032943C>A

(Homo sapiens)

Allele/Variant

Source: rs774872195

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52032943C>A

(GRCh38)1:52033049G>A

(Homo sapiens)

Allele/Variant

Source: rs79423354

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033049G>A

(GRCh38)1:52033008G>C

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.52033008G>C

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033008G>C

(GRCh38)1:52033308G>A

(Homo sapiens)

Allele/Variant

Source: rs746833246

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033308G>A

(GRCh38)1:52033455A>C

(Homo sapiens)

Allele/Variant

Source: rs755857517

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033455A>C

(GRCh38)1:52033712C>T

(Homo sapiens)

Allele/Variant

Source: rs1685826456

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033712C>T

(GRCh38)1:52033196G>C

(Homo sapiens)

Allele/Variant

Source: rs138486051

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033196G>C

(GRCh38)1:52033508T>C

(Homo sapiens)

Allele/Variant

Source: rs200200454

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033508T>C

(GRCh38)1:52033164A>C

(Homo sapiens)

Allele/Variant

Source: rs139909329

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033164A>C

(GRCh38)1:52033659C>T

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.52033659C>T

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033659C>T

(GRCh38)1:52033725C>A

(Homo sapiens)

Allele/Variant

Source: rs781405918

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033725C>A

(GRCh38)1:52033339G>C

(Homo sapiens)

Allele/Variant

Source: rs750795944

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52033339G>C

(GRCh38)1:52032761T>C

(Homo sapiens)

Allele/Variant

Source: rs759988298

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52032761T>C

(GRCh38)1:52032918G>C

(Homo sapiens)

Allele/Variant

Source: rs145860172

Genes: KTI12 (Hsa), TXNDC12 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:52032918G>C

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