Version: 8.0.0Date: Tue Jan 28 2025
Category
Gene Ontology
Source: GO:0001568
Synonyms: Not Available
Branch: biological process
Genes: gmds (Dre)
Gene Ontology
Source: GO:0016829
Synonyms: Not Available
Branch: molecular function
Genes: GMDS (Hsa)
sa43452
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-9000
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gmds (Dre)
sa6635
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18412
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gmds (Dre)
sa37043
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-5074
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gmds (Dre)
sa6636
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18413
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gmds (Dre)
rw685
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-090610-8
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
Genes: gmds (Dre)
p31erb
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-051012-8
Genes: gmds (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, missense_variant
Diseases: congenital disorder of glycosylation type IIc
Variant Name: Not Available
Genes: gmds (Dre)
Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: GMDS (Hsa)
(GRCh38)6:1960923A>G
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.1960923A>G
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1960923A>G
(GRCh38)6:1742554C>T
(Homo sapiens)Allele/Variant
Source: rs143104834
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1742554C>T
(GRCh38)6:2117477A>G
(Homo sapiens)Allele/Variant
Source: rs369492511
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:2117477A>G
(GRCh38)6:1959956T>C
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.1959956T>C
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1959956T>C
(GRCh38)6:1960950G>A
(Homo sapiens)Allele/Variant
Source: rs1462367301
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1960950G>A
(GRCh38)6:2117538G>A
(Homo sapiens)Allele/Variant
Source: rs771650335
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:2117538G>A
(GRCh38)6:1624190C>T
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.1624190C>T
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1624190C>T
(GRCh38)6:2117541G>A
(Homo sapiens)Allele/Variant
Source: rs1391141392
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:2117541G>A
(GRCh38)6:1641136G>C
(Homo sapiens)Allele/Variant
Source: rs207466655
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1641136G>C
(GRCh38)6:1742555G>A
(Homo sapiens)Allele/Variant
Source: rs749276776
Genes: GMDS (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)6:1742555G>A
(GRCh38)6:1742484T>C
(Homo sapiens)Allele/Variant
Source: rs888240313
Genes: GMDS (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)6:1742484T>C
(GRCh38)6:1624201C>T
(Homo sapiens)Allele/Variant
Source: rs149819971
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1624201C>T
(GRCh38)6:1960938G>A
(Homo sapiens)Allele/Variant
Source: rs774625510
Genes: GMDS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:1960938G>A
(GRCh38)6:2245397G>A
(Homo sapiens)Allele/Variant
Source: rs761030409
Genes: GMDS (Hsa), GMDS-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:2245397G>A
Gene Ontology
Source: GO:0042802
Synonyms:
- isoform-specific homophilic binding
- protein homopolymerization
Branch: molecular function
Genes: Gmds (Mmu)...Gmds (Rno)...GMDS (Hsa)
Gene Ontology
Source: GO:0070062
Synonyms:
- exosome
- extracellular vesicular exosome
Branch: cellular component
Genes: GMDS (Hsa)
(mRatBN7.2)17:32095776C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323167637
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32095776C>T
(mRatBN7.2)17:32096703C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322994178
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32096703C>T
(mRatBN7.2)17:32097715G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323156712
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32097715G>A
(mRatBN7.2)17:32101070C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322994251
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32101070C>T
(mRatBN7.2)17:32129580T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322917201
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32129580T>C
(mRatBN7.2)17:32119932T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322716068
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32119932T>C
(mRatBN7.2)17:32101734A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322994167
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32101734A>G
(mRatBN7.2)17:32109855T>G
(Rattus norvegicus)Allele/Variant
Source: rs3323058885
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32109855T>G
(mRatBN7.2)17:32130542T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323179701
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32130542T>C
(mRatBN7.2)17:32130667G>C
(Rattus norvegicus)Allele/Variant
Source: rs3323105176
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32130667G>C
(mRatBN7.2)17:32228029C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323058923
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32228029C>T
(mRatBN7.2)17:32229594T>A
(Rattus norvegicus)Allele/Variant
Source: rs3323108501
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32229594T>A
(mRatBN7.2)17:32144055C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322965594
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32144055C>T
(mRatBN7.2)17:32287412G>T
(Rattus norvegicus)Allele/Variant
Source: rs3323108610
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32287412G>T
(mRatBN7.2)17:32290461A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322994206
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32290461A>G
(mRatBN7.2)17:32293115C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323105300
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32293115C>T
(mRatBN7.2)17:32294028A>C
(Rattus norvegicus)Allele/Variant
Source: rs3323602406
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32294028A>C
(mRatBN7.2)17:32372803G>T
(Rattus norvegicus)Allele/Variant
Source: rs3323108548
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32372803G>T
(mRatBN7.2)17:32336187T>G
(Rattus norvegicus)Allele/Variant
Source: rs198836547
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32336187T>G
(mRatBN7.2)17:32345373C>A
(Rattus norvegicus)Allele/Variant
Source: rs3322994253
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32345373C>A
(mRatBN7.2)17:32100192T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322994129
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32100192T>C
(mRatBN7.2)17:32102956C>A
(Rattus norvegicus)Allele/Variant
Source: rs3323156561
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32102956C>A
(mRatBN7.2)17:32103949T>G
(Rattus norvegicus)Allele/Variant
Source: rs3323156622
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32103949T>G
(mRatBN7.2)17:32106488C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322994038
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32106488C>G
(mRatBN7.2)17:32107608T>G
(Rattus norvegicus)Allele/Variant
Source: rs3323156510
Genes: Gmds (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:32107608T>G