Version: 8.1.0Date: Fri Apr 18 2025
Category
Ssr3
(Rattus norvegicus)Gene
Name: signal sequence receptor subunit 3
Synonyms: TRAP-gamma, TRAP-complex gamma subunit, translocon-associated protein subunit gamma, signal sequence receptor subunit gamma, signal sequence receptor, gamma, SSR-gamma
Source: RGD:621630
Biotype: protein coding gene
Symbol: Ssr3 (Rno)
Symbol: Ssr3
Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3); PARTICIPATES IN Endoplasmic Reticulum-associated
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
ssr3
(Danio rerio)Gene
Name: signal sequence receptor, gamma
Synonyms: zgc:56300, wu:fb01d07, fb01d07
Source: ZFIN:ZDB-GENE-030131-9134
Biotype: protein coding gene
Symbol: ssr3 (Dre)
Symbol: ssr3
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
SSR3
(Homo sapiens)Gene
Name: signal sequence receptor subunit 3
Synonyms: TRAP-gamma, signal sequence receptor, gamma (translocon-associated protein gamma), TRAP-complex gamma subunit, translocon-associated protein gamma subunit, translocon-associated protein subunit gamma, signal sequence receptor subunit gamma, SSR gamma, SSR-gamma, TRAPG
Source: HGNC:11325
Biotype: protein coding gene
Symbol: SSR3 (Hsa)
Symbol: SSR3
Strict Orthology Symbols: ssr3
Ssr3
(Mus musculus)Gene
Name: signal sequence receptor, gamma
Synonyms: AL022999, expressed sequence AU022074, translocon-associated protein gamma, AW553833, expressed sequence AW553833, Trap-gamma, expressed sequence AL022999, RIKEN cDNA 0610038P07 gene, 0610038P07Rik, AU022074
Source: MGI:1914687
Biotype: protein coding gene
Symbol: Ssr3 (Mmu)
Symbol: Ssr3
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
Alleles: Ssr3
ssr3
(Xenopus tropicalis)Gene
Name: signal sequence receptor, gamma (translocon-associated protein gamma)
Synonyms: ssr3-b, signal sequence receptor, gamma (translocon-associated protein gamma), XTRAP-g, ssr3-a, ssr3, XTRAP-gamma, trapg
Source: Xenbase:XB-GENE-964603
Biotype: gene
Symbol: ssr3
Symbol: ssr3 (Xtr)
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Synonyms: ssr3...ssr3...ssr3
Strict Orthology Symbols: ssr3
ssr3.S
(Xenopus laevis)Gene
Name: signal sequence receptor, gamma (translocon-associated protein gamma)
Synonyms: ssr3-b, ssr3.S, signal sequence receptor, gamma (translocon-associated protein gamma), XTRAP-g, ssr3-a, XTRAP-gamma, trapg
Source: Xenbase:XB-GENE-6255821
Biotype: gene
Symbol: ssr3.S (Xla)
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
Symbol: ssr3.S
ssr3.L
(Xenopus laevis)Gene
Name: signal sequence receptor, gamma (translocon-associated protein gamma)
Synonyms: ssr3-b, signal sequence receptor, gamma (translocon-associated protein gamma), XTRAP-g, ssr3-a, ssr3.L, XTRAP-gamma, trapg
Source: Xenbase:XB-GENE-964608
Biotype: gene
Symbol: ssr3.L (Xla)
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
Symbol: ssr3.L
Ssr3em1(IMPC)Bay
(Mus musculus)Allele/Variant
Source: MGI:7709811
Genes: Ssr3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ssr3
Genes: Ssr3 (Mmu)
Symbol: Ssr3em1(IMPC)Bay
Ssr3tm1Ryn
(Mus musculus)Allele/Variant
Source: MGI:4881708
Genes: Ssr3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ssr3
Genes: Ssr3 (Mmu)
Symbol: Ssr3tm1Ryn
Ssr3em1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7306839
Genes: Ssr3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ssr3
Genes: Ssr3 (Mmu)
Symbol: Ssr3em1Gpt
Model
Id: MGI:4881709
Synonyms: Not Available
Symbol: Ssr3/Ssr3 [background:] involves: C57BL/6 * CBA (Mmu)
Genes: Ssr3 (Mmu)
Alleles: Ssr3
Name: Ssr3/Ssr3 [background:] involves: C57BL/6 * CBA
CG5885
(Drosophila melanogaster)Gene
Name: Not Available
Synonyms: BEST:CK01296, AI945207, CK01296
Source: FB:FBgn0025700
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
trap-3
(Caenorhabditis elegans)Gene
Name: TRanslocon-Associated Protein 3
Synonyms: Y38F2AR.2, Y38F2A_6126.e, CELE_Y38F2AR.2
Source: WB:WBGene00021420
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human SSR3 (signal sequence receptor subunit 3).
Automated Gene Synopsis: Orthologous to human SSR3 (signal sequence receptor subunit 3).
Strict Orthology Symbols: ssr3
Source: GO:0006614
Synonyms:
- ER translocation
- SRP-dependent cotranslational membrane targeting
Branch: biological process
Genes: Ssr3 (Rno)...SSR3 (Hsa)...ssr3 (Dre)...Ssr3 (Mmu)
Gene Ontology
Source: GO:0005784
Synonyms:
- Sec61p-Sbh1p-Sss1p complex
Branch: cellular component
Genes: Ssr3 (Rno)
Gene Ontology
Source: GO:0005789
Synonyms:
- ER membrane
Branch: cellular component
Genes: SSR3 (Hsa)...ssr3 (Dre)...Ssr3 (Mmu)...Ssr3 (Rno)
Gene Ontology
Source: GO:0005783
Synonyms:
- ER
Branch: cellular component
Genes: SSR3 (Hsa)...ssr3 (Dre)...Ssr3 (Rno)...Ssr3 (Mmu)
Gene Ontology
Source: GO:0016020
Synonyms:
- integral component of membrane
- integral to membrane
Branch: cellular component
Genes: SSR3 (Hsa)...ssr3 (Dre)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: SSR3 (Hsa)
(GRCh38)3:156544358G>A
(Homo sapiens)Allele/Variant
Source: rs939255657
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544358G>A
(GRCh38)3:156543286G>A
(Homo sapiens)Allele/Variant
Source: rs200289824
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156543286G>A
(GRCh38)3:156543253T>C
(Homo sapiens)Allele/Variant
Source: rs757676113
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156543253T>C
(GRCh38)3:156544390A>C
(Homo sapiens)Allele/Variant
Source: rs149167845
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544390A>C
(GRCh38)3:156555013G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.156555013G>A
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156555013G>A
(GRCh38)3:156548976A>G
(Homo sapiens)Allele/Variant
Source: rs16826514
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156548976A>G
(GRCh38)3:156553761G>A
(Homo sapiens)Allele/Variant
Source: rs958249594
Genes: SSR3 (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)3:156553761G>A
(GRCh38)3:156548853C>T
(Homo sapiens)Allele/Variant
Source: rs6809188
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156548853C>T
(GRCh38)3:156553699C>T
(Homo sapiens)Allele/Variant
Source: rs765382943
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156553699C>T
(GRCh38)3:156548935C>T
(Homo sapiens)Allele/Variant
Source: rs554757087
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156548935C>T
(GRCh38)3:156544421A>G
(Homo sapiens)Allele/Variant
Source: rs6768440
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544421A>G
(GRCh38)3:156548985C>T
(Homo sapiens)Allele/Variant
Source: rs9296
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156548985C>T
(GRCh38)3:156553675C>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.156553675C>T
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156553675C>T
(GRCh38)3:156548896G>A
(Homo sapiens)Allele/Variant
Source: rs970465326
Genes: SSR3 (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)3:156548896G>A
(GRCh38)3:156544443C>G
(Homo sapiens)Allele/Variant
Source: rs6792998
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544443C>G
(GRCh38)3:156544412A>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.156544412A>T
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544412A>T
(GRCh38)3:156544453A>G
(Homo sapiens)Allele/Variant
Source: rs2108445906
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544453A>G
(GRCh38)3:156553646C>T
(Homo sapiens)Allele/Variant
Source: rs761135018
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156553646C>T
(GRCh38)3:156553758T>C
(Homo sapiens)Allele/Variant
Source: rs1486771803
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)3:156553758T>C
(GRCh38)3:156553769C>T
(Homo sapiens)Allele/Variant
Source: rs772542660
Genes: SSR3 (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)3:156553769C>T
(GRCh38)3:156555022T>C
(Homo sapiens)Allele/Variant
Source: rs1225837452
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156555022T>C
(GRCh38)3:156544357C>T
(Homo sapiens)Allele/Variant
Source: rs781493375
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544357C>T
(GRCh38)3:156548916C>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.156548916C>G
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156548916C>G
(GRCh38)3:156544339A>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.156544339A>G
Genes: SSR3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:156544339A>G
(mRatBN7.2)2:149610498A>G
(Rattus norvegicus)Allele/Variant
Source: rs105692113
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149610498A>G
(mRatBN7.2)2:149613397C>G
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.149613397C>G
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149613397C>G
(mRatBN7.2)2:149613401C>G
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.149613401C>G
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149613401C>G
(mRatBN7.2)2:149616490C>G
(Rattus norvegicus)Allele/Variant
Source: rs106289924
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149616490C>G
(mRatBN7.2)2:149616574T>A
(Rattus norvegicus)Allele/Variant
Source: rs64455550
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149616574T>A
(mRatBN7.2)2:149616574T>C
(Rattus norvegicus)Allele/Variant
Source: rs64455550
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149616574T>C
(mRatBN7.2)2:149616657T>C
(Rattus norvegicus)Allele/Variant
Source: rs105438461
Genes: Ssr3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:149616657T>C