Version: 8.1.0Date: Fri Apr 18 2025
Category
ST8SIA5
(Homo sapiens)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: sialyltransferase 8E (alpha-2, 8-polysialytransferase), SIAT8E, MGC119671, SIAT8-E, alpha-2,8-sialyltransferase 8E, sialyltransferase St8Sia V, ST8 alpha-N-acetylneuraminate alpha-2,8-sialyltransferase 5, ST8SiaV, MGC119670, sialytransferase St8Sia V
Source: HGNC:17827
Biotype: protein coding gene
Symbol: ST8SIA5 (Hsa)
Symbol: ST8SIA5
Strict Orthology Symbols: st8sia5
St8sia5
(Rattus norvegicus)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: SIAT8E, sialyltransferase 8E, SATV, SIAT8-E, alpha-2,8-sialyltransferase 8E, sialyltransferase St8Sia V, ST8 alpha-N-acetylneuraminate alpha-2,8-sialyltransferase 5, ST8SiaV, alpha-2,8-sialyltransferase
Source: RGD:1302934
Biotype: protein coding gene
Symbol: St8sia5 (Rno)
Symbol: St8sia5
Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5); PARTICIPATES
Automated Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5).
Strict Orthology Symbols: st8sia5
St8sia5
(Mus musculus)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: Siat8e, SIAT8E, sialyltransferase 8 (alpha-2, 8-sialyltransferase) E, SIAT8-E, SATV, ST8SiaV
Source: MGI:109243
Biotype: protein coding gene
Symbol: St8sia5 (Mmu)
Symbol: St8sia5
Automated Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5).
Strict Orthology Symbols: st8sia5
Alleles: St8sia5
st8sia5
(Danio rerio)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-060322-8
Biotype: protein coding gene
Symbol: st8sia5 (Dre)
Symbol: st8sia5
Automated Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5).
Strict Orthology Symbols: st8sia5
st8sia5
(Xenopus tropicalis)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: LOC108707349, st8sia5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Source: Xenbase:XB-GENE-988459
Biotype: gene
Symbol: st8sia5
Symbol: st8sia5 (Xtr)
Automated Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5).
Synonyms: st8sia5...st8sia5...st8sia5
Strict Orthology Symbols: st8sia5
ST8SIA5-DT
(Homo sapiens)Gene
Name: ST8SIA5 divergent transcript
Synonyms: LOC105372097, uncharacterized LOC105372097
Source: HGNC:55267
Biotype: ncRNA gene
Symbol: ST8SIA5-DT (Hsa)
Symbol: ST8SIA5-DT
st8sia5.L
(Xenopus laevis)Gene
Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Synonyms: LOC108707349, st8sia5.L, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5
Source: Xenbase:XB-GENE-17332752
Biotype: gene
Symbol: st8sia5.L (Xla)
Automated Gene Synopsis: Orthologous to human ST8SIA5 (ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5).
Strict Orthology Symbols: st8sia5
Symbol: st8sia5.L
St8sia5em1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7306872
Genes: St8sia5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St8sia5
Genes: St8sia5 (Mmu)
Symbol: St8sia5em1Gpt
Source: GO:0003828
Synonyms:
- alpha-2,8-sialyltransferase activity
- alpha-N-acetylneuraminide alpha-2,8-sialyltransferase activity
Branch: molecular function
Genes: st8sia5 (Dre)...ST8SIA5 (Hsa)...St8sia5 (Rno)...St8sia5 (Mmu)
Gene Ontology
Source: GO:0008373
Synonyms: Not Available
Branch: molecular function
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)...St8sia5 (Rno)...St8sia5 (Mmu)
Gene Ontology
Source: GO:0009311
Synonyms:
- multicellular organismal oligosaccharide metabolic process
- oligosaccharide metabolism
Branch: biological process
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)...St8sia5 (Rno)...St8sia5 (Mmu)
Gene Ontology
Source: GO:0006688
Synonyms:
- glycosphingolipid anabolism
- glycosphingolipid biosynthesis
Branch: biological process
Genes: ST8SIA5 (Hsa)...St8sia5 (Rno)...St8sia5 (Mmu)
Gene Ontology
Source: GO:0006491
Synonyms:
- N-linked glycoprotein maturation
- glycoprotein trimming involved in glycoprotein maturation
Branch: biological process
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)...St8sia5 (Rno)...St8sia5 (Mmu)
Tg(St8sia5-EGFP)MC10Gsat
(Mus musculus)Allele/Variant
Source: MGI:4847460
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(St8sia5-EGFP)MC10Gsat
Gene Ontology
Source: GO:0006486
Synonyms:
- protein amino acid glycosylation
- protein-carbohydrate complex assembly
Branch: biological process
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)...St8sia5 (Rno)...St8sia5 (Mmu)
Gene Ontology
Source: GO:0016757
Synonyms:
- transferase activity, transferring glycosyl groups
- transferase activity, transferring other glycosyl groups
Branch: molecular function
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)
Gene Ontology
Source: GO:0000139
Synonyms:
- Golgi apparatus membrane
Branch: cellular component
Genes: St8sia5 (Mmu)...ST8SIA5 (Hsa)...St8sia5 (Rno)...st8sia5 (Dre)
Gene Ontology
Source: GO:0005975
Synonyms:
- carbohydrate metabolism
Branch: biological process
Genes: ST8SIA5 (Hsa)
Gene Ontology
Source: GO:0006629
Synonyms:
- lipid metabolism
Branch: biological process
Genes: ST8SIA5 (Hsa)
sa11310
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-130411-1155
Genes: st8sia5 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: st8sia5 (Dre)
sa6662
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18436
Genes: st8sia5 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: st8sia5 (Dre)
Gene Ontology
Source: GO:0005794
Synonyms:
- Golgi
- Golgi complex
Branch: cellular component
Genes: ST8SIA5 (Hsa)...st8sia5 (Dre)
Gene Ontology
Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: st8sia5 (Dre)
Gene Ontology
Source: GO:0016020
Synonyms:
- integral component of membrane
- integral to membrane
Branch: cellular component
Genes: st8sia5 (Dre)...ST8SIA5 (Hsa)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: ST8SIA5 (Hsa)
(GRCh38)18:46681365C>T
(Homo sapiens)Allele/Variant
Source: rs207476809
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46681365C>T
(GRCh38)18:46726890A>G
(Homo sapiens)Allele/Variant
Source: rs207476810
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46726890A>G
(GRCh38)18:46686187C>T
(Homo sapiens)Allele/Variant
Source: rs757247613
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46686187C>T
(GRCh38)18:46680320C>A
(Homo sapiens)Allele/Variant
Source: rs201140949
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680320C>A
(GRCh38)18:46686213C>T
(Homo sapiens)Allele/Variant
Source: rs115206837
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46686213C>T
(GRCh38)18:46686271G>A
(Homo sapiens)Allele/Variant
Source: rs781238196
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46686271G>A
(GRCh38)18:46688895G>A
(Homo sapiens)Allele/Variant
Source: rs34504902
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46688895G>A
(GRCh38)18:46680329G>C
(Homo sapiens)Allele/Variant
Source: rs200781006
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680329G>C
(GRCh38)18:46686209G>T
(Homo sapiens)Allele/Variant
Source: rs143784819
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46686209G>T
(GRCh38)18:46680196A>G
(Homo sapiens)Allele/Variant
Source: rs143043666
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680196A>G
(GRCh38)18:46680493T>C
(Homo sapiens)Allele/Variant
Source: rs776557263
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680493T>C
(GRCh38)18:46688859A>C
(Homo sapiens)Allele/Variant
Source: rs76732091
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46688859A>C
(GRCh38)18:46688894C>T
(Homo sapiens)Allele/Variant
Source: rs758551027
Genes: ST8SIA5 (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)18:46688894C>T
(GRCh38)18:46680424T>C
(Homo sapiens)Allele/Variant
Source: rs780537448
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680424T>C
(GRCh38)18:46680337G>A
(Homo sapiens)Allele/Variant
Source: rs765111904
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680337G>A
(GRCh38)18:46680389T>G
(Homo sapiens)Allele/Variant
Source: rs201640419
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680389T>G
(GRCh38)18:46680404C>T
(Homo sapiens)Allele/Variant
Source: rs200156474
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680404C>T
(GRCh38)18:46680100A>T
(Homo sapiens)Allele/Variant
Source: rs1568246567
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680100A>T
(GRCh38)18:46680364G>A
(Homo sapiens)Allele/Variant
Source: rs1274598306
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680364G>A
(GRCh38)18:46680461C>A
(Homo sapiens)Allele/Variant
Source: rs1295767347
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680461C>A
(GRCh38)18:46680305G>T
(Homo sapiens)Allele/Variant
Source: rs1177786941
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680305G>T
(GRCh38)18:46680341G>A
(Homo sapiens)Allele/Variant
Source: rs2039378596
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680341G>A
(GRCh38)18:46680260G>C
(Homo sapiens)Allele/Variant
Source: NC_000018.10:g.46680260G>C
Genes: ST8SIA5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46680260G>C
(GRCh38)18:46756385T>C
(Homo sapiens)Allele/Variant
Source: rs2040246689
Genes: ST8SIA5 (Hsa), ST8SIA5-DT (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)18:46756385T>C
(mRatBN7.2)18:70784106T>C
(Rattus norvegicus)Allele/Variant
Source: rs106561135
Genes: St8sia5 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:70784106T>C