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Category

932 results for tmem39b

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tmem39b

(Danio rerio)

Gene

Name: transmembrane protein 39B

Synonyms: wu:fi31h12, zgc:55419, fi31h12

Source: ZFIN:ZDB-GENE-030131-6042

Biotype: protein coding gene

Symbol: tmem39b (Dre)

Symbol: tmem39b

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Tmem39b

(Mus musculus)

Gene

Name: transmembrane protein 39b

Synonyms: 6330509E05Rik, RIKEN cDNA 6330509E05 gene, cDNA sequence BC037095, BC037095, MGC:59407

Source: MGI:2682939

Biotype: protein coding gene

Symbol: Tmem39b (Mmu)

Symbol: Tmem39b

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Alleles: Tmem39b (Mmu)

Allele/Variant (762)

Tmem39b

(Rattus norvegicus)

Gene

Name: transmembrane protein 39b

Synonyms: similar to hypothetical protein FLJ10315, LOC362608

Source: RGD:1359450

Biotype: protein coding gene

Symbol: Tmem39b (Rno)

Symbol: Tmem39b

Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Allele/Variant (125)

TMEM39B

(Homo sapiens)

Gene

Name: transmembrane protein 39B

Synonyms: RP11-277A4.3, FLJ10315

Source: HGNC:25510

Biotype: protein coding gene

Symbol: TMEM39B (Hsa)

Symbol: TMEM39B

Strict Orthology Symbols: tmem39b

Allele/Variant (22)

tmem39b

(Xenopus tropicalis)

Gene

Name: transmembrane protein 39B

Synonyms: MGC89136, transmembrane protein 39B, tmem39b

Source: Xenbase:XB-GENE-5904816

Biotype: gene

Symbol: tmem39b

Symbol: tmem39b (Xtr)

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Synonyms: tmem39b...tmem39b...tmem39b

Strict Orthology Symbols: tmem39b

tmem39b.L

(Xenopus laevis)

Gene

Name: transmembrane protein 39B

Synonyms: MGC89136, transmembrane protein 39B, tmem39b.L

Source: Xenbase:XB-GENE-17342901

Biotype: gene

Symbol: tmem39b.L (Xla)

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Symbol: tmem39b.L

tmem39b.S

(Xenopus laevis)

Gene

Name: transmembrane protein 39B

Synonyms: tmem39b.S, MGC89136, transmembrane protein 39B

Source: Xenbase:XB-GENE-5904855

Biotype: gene

Symbol: tmem39b.S (Xla)

Automated Gene Synopsis: Orthologous to human TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Symbol: tmem39b.S

Tmem39b^{em1(IMPC)Kmpc}

(Mus musculus)

Allele/Variant

Source: MGI:7377647

Genes: Tmem39b (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Tmem39b (Mmu)

Genes: Tmem39b (Mmu)

Symbol: Tmem39b^{em1(IMPC)Kmpc}

Gene (1)

tmem39b^{zko3151b/zko3151b} (AB)

(Danio rerio)

Model

Id: ZFIN:ZDB-FISH-231220-1

Synonyms: Not Available

Symbol: tmem39b (AB) (Dre)

Genes: tmem39b (Dre)

Name: tmem39b (AB)

Gene (1)

tmem39b^{zko3151a/zko3151a} (AB)

(Danio rerio)

Model

Id: ZFIN:ZDB-FISH-231221-1

Synonyms: Not Available

Symbol: tmem39b (AB) (Dre)

Genes: tmem39b (Dre)

Name: tmem39b (AB)

Gene (1)

tmem39b^zko3151a/+ (AB)

(Danio rerio)

Model

Id: ZFIN:ZDB-FISH-231221-2

Synonyms: Not Available

Symbol: tmem39b (AB) (Dre)

Genes: tmem39b (Dre)

Name: tmem39b (AB)

Gene (1)

CG13016

(Drosophila melanogaster)

Gene

Name: Not Available

Synonyms: tmem39

Source: FB:FBgn0033899

Biotype: protein coding gene

Automated Gene Synopsis: Orthologous to human TMEM39A (transmembrane protein 39A) and TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Allele/Variant (43)

tmem-39

(Caenorhabditis elegans)

Gene

Name: TMEM (human TransMEMbrane protein) homolog 39

Synonyms: D1007.5, CELE_D1007.5

Source: WB:WBGene00017003

Biotype: protein coding gene

Gene Synopsis: Is an ortholog of human TMEM39A (transmembrane protein 39A) and TMEM39B (transmembrane protein 39B).

Automated Gene Synopsis: Orthologous to human TMEM39A (transmembrane protein 39A) and TMEM39B (transmembrane protein 39B).

Strict Orthology Symbols: tmem39b

Allele/Variant (32)

zko3151a

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-231218-4

Genes: tmem39b (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: tmem39b (Dre)

zko3151b

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-231218-5

Genes: tmem39b (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: tmem39b (Dre)

Hsap\TMEM39B^UAS.cBa

(Drosophila melanogaster)

Allele/Variant

Source: FB:FBal0403108

Genes: Not Available

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hsap\TMEM39B

Construct Expressed Component: TMEM39B (Hsa)

endoplasmic reticulum membrane

Gene Ontology

Source: GO:0005789

Synonyms:

ER membrane

Branch: cellular component

Genes: Tmem39b (Mmu)...tmem39b (Dre)...Tmem39b (Rno)...TMEM39B (Hsa)

Genes Annotated with this GO Term (5234)

sa6317

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-161003-18158

Genes: tmem39b (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: Not Available

Genes: tmem39b (Dre)

sa38955

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-161003-16356

Genes: tmem39b (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: Not Available

Genes: tmem39b (Dre)

endoplasmic reticulum

Gene Ontology

Source: GO:0005783

Synonyms:

Branch: cellular component

Genes: tmem39b (Dre)...TMEM39B (Hsa)

Genes Annotated with this GO Term (8935)

membrane

Gene Ontology

Source: GO:0016020

Synonyms:

integral component of membrane
integral to membrane

Branch: cellular component

Genes: Tmem39b (Mmu)...tmem39b (Dre)...TMEM39B (Hsa)...Tmem39b (Rno)

Genes Annotated with this GO Term (10000)

biological_process

Gene Ontology

Source: GO:0008150

Synonyms:

biological process
physiological process

Branch: biological process

Genes: tmem39b (Dre)...TMEM39B (Hsa)

Genes Annotated with this GO Term (10000)

molecular_function

Gene Ontology

Source: GO:0003674

Synonyms:

molecular function

Branch: molecular function

Genes: Tmem39b (Mmu)...tmem39b (Dre)

Genes Annotated with this GO Term (10000)

protein binding

Gene Ontology

Source: GO:0005515

Synonyms:

glycoprotein binding
protein amino acid binding

Branch: molecular function

Genes: TMEM39B (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)1:32074957G>A

(Homo sapiens)

Allele/Variant

Source: rs1557908819

Genes: TMEM39B (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)1:32074957G>A

(GRCh38)1:32094854T>G

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.32094854T>G

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32094854T>G

(GRCh38)1:32076805A>G

(Homo sapiens)

Allele/Variant

Source: rs912694006

Genes: TMEM39B (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)1:32076805A>G

(GRCh38)1:32094958G>A

(Homo sapiens)

Allele/Variant

Source: rs143966385

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32094958G>A

(GRCh38)1:32077234C>T

(Homo sapiens)

Allele/Variant

Source: rs372163088

Genes: TMEM39B (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)1:32077234C>T

(GRCh38)1:32076808G>A

(Homo sapiens)

Allele/Variant

Source: rs1285327600

Genes: TMEM39B (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)1:32076808G>A

(GRCh38)1:32094907G>A

(Homo sapiens)

Allele/Variant

Source: rs753416444

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32094907G>A

(GRCh38)1:32102635G>C

(Homo sapiens)

Allele/Variant

Source: rs1337060207

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32102635G>C

(GRCh38)1:32075014C>T

(Homo sapiens)

Allele/Variant

Source: rs1468009880

Genes: TMEM39B (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)1:32075014C>T

(GRCh38)1:32094910G>A

(Homo sapiens)

Allele/Variant

Source: rs778742208

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32094910G>A

(GRCh38)1:32091944A>G

(Homo sapiens)

Allele/Variant

Source: rs200048180

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32091944A>G

(GRCh38)1:32076838G>A

(Homo sapiens)

Allele/Variant

Source: rs149666383

Genes: TMEM39B (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)1:32076838G>A

(GRCh38)1:32077275T>C

(Homo sapiens)

Allele/Variant

Source: rs1419668726

Genes: TMEM39B (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)1:32077275T>C

(GRCh38)1:32091818C>T

(Homo sapiens)

Allele/Variant

Source: rs202228399

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32091818C>T

(GRCh38)1:32102669C>T

(Homo sapiens)

Allele/Variant

Source: rs200464245

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32102669C>T

(GRCh38)1:32077194C>T

(Homo sapiens)

Allele/Variant

Source: rs754727698

Genes: TMEM39B (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)1:32077194C>T

(GRCh38)1:32094826C>G

(Homo sapiens)

Allele/Variant

Source: rs200998933

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32094826C>G

(GRCh38)1:32091751A>G

(Homo sapiens)

Allele/Variant

Source: rs200803971

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32091751A>G

(GRCh38)1:32092006G>A

(Homo sapiens)

Allele/Variant

Source: rs202154275

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32092006G>A

(GRCh38)1:32102596C>T

(Homo sapiens)

Allele/Variant

Source: rs1213310168

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32102596C>T

(GRCh38)1:32075035A>T

(Homo sapiens)

Allele/Variant

Source: rs1051594832

Genes: TMEM39B (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)1:32075035A>T

(GRCh38)1:32102645A>C

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.32102645A>C

Genes: TMEM39B (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:32102645A>C

(mRatBN7.2)5:142028193A>C

(Rattus norvegicus)

Allele/Variant

Source: rs198119290

Genes: Tmem39b (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)5:142028193A>C

(mRatBN7.2)5:142042874C>A

(Rattus norvegicus)

Allele/Variant

Source: rs3320706894

Genes: Tmem39b (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 5_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)5:142042874C>A

(mRatBN7.2)5:142031047C>T

(Rattus norvegicus)

Allele/Variant

Source: NC_051340.1:g.142031047C>T

Genes: Tmem39b (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)5:142031047C>T

(mRatBN7.2)5:142033671T>C

(Rattus norvegicus)

Allele/Variant

Source: rs3320538021

Genes: Tmem39b (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)5:142033671T>C

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