2,624 results for st3gal5

ST3GAL5

(Homo sapiens)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: SIAT9, SATI, ST3 beta-galactoside alpha-23-sialyltransferase 5, sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase), sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase, GM3 synthase), CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase, lactosylceramide alpha-2,3-sialyltransferase, GM3 synthase, ST3GalV, ganglioside GM3 synthase, SIATGM3S, ST3Gal V, alpha 2,3-sialyltransferase V, SPDRS
Source: HGNC:10872
Biotype: protein coding gene
Symbol: ST3GAL5 (Hsa)
Symbol: ST3GAL5
Strict Orthology Symbols: st3gal5

St3gal5

(Mus musculus)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: [a]2, GM3-specific sialytransferase, Siat9, GM3 synthase, sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase), ST3Gal V, mST3Gal V, 3S-T
Source: MGI:1339963
Biotype: protein coding gene
Symbol: St3gal5 (Mmu)
Symbol: St3gal5
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Strict Orthology Symbols: st3gal5
Alleles: St3gal5 (Mmu)...St3gal5 (Mmu)...St3gal5 (Mmu)...St3gal5 (Mmu)...St3gal5 (Mmu)

St3gal5

(Rattus norvegicus)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: Siat9, GM3 synthase, sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase), sialyltransferase 9 (CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase, GM3 synthase), ST3GalV, ganglioside GM3 synthase, ST3Gal V, CMP-NeuAc:lactosylceramide alpha-2,3-sialyltransferase, lactosylceramide alpha-2,3-sialyltransferase
Source: RGD:620875
Biotype: protein coding gene
Symbol: St3gal5 (Rno)
Symbol: St3gal5
Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5); PARTICIPATES IN ganglioside
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Strict Orthology Symbols: st3gal5

st3gal5

(Danio rerio)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: zST3GalV-1, GM3 synthase, wu:fc08a12, ST3Gal5, st3gal5-r1
Source: ZFIN:ZDB-GENE-060322-1
Biotype: protein coding gene
Symbol: st3gal5 (Dre)
Symbol: st3gal5
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Synonyms: ST3Gal5...ST3Gal5
Strict Orthology Symbols: st3gal5

st3gal5

(Xenopus tropicalis)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: ST3 beta-galactoside alpha-2,3-sialyltransferase 5, st3gal5
Source: Xenbase:XB-GENE-955106
Biotype: gene
Symbol: st3gal5
Symbol: st3gal5 (Xtr)
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Synonyms: st3gal5...st3gal5...st3gal5
Strict Orthology Symbols: st3gal5

ST3GAL5-AS1

(Homo sapiens)
Gene
Name: ST3GAL5 antisense RNA 1 (head to head)
Synonyms: Not Available
Source: HGNC:51129
Biotype: ncRNA gene
Symbol: ST3GAL5-AS1 (Hsa)
Symbol: ST3GAL5-AS1

st3gal5.S

(Xenopus laevis)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: ST3 beta-galactoside alpha-2,3-sialyltransferase 5, st3gal5.S
Source: Xenbase:XB-GENE-17345695
Biotype: gene
Symbol: st3gal5.S (Xla)
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Strict Orthology Symbols: st3gal5
Symbol: st3gal5.S

st3gal5.L

(Xenopus laevis)
Gene
Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 5
Synonyms: ST3 beta-galactoside alpha-2,3-sialyltransferase 5, st3gal5.L
Source: Xenbase:XB-GENE-17345694
Biotype: gene
Symbol: st3gal5.L (Xla)
Automated Gene Synopsis: Orthologous to human ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5).
Strict Orthology Symbols: st3gal5
Symbol: st3gal5.L

St3gal5tm1Kfk

(Mus musculus)
Allele/Variant
Source: MGI:7525156
Genes: St3gal5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St3gal5 (Mmu)
Genes: St3gal5 (Mmu)
Symbol: St3gal5tm1Kfk

St3gal5tm1Rlp

(Mus musculus)
Allele/Variant
Source: MGI:2655771
Genes: St3gal5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St3gal5 (Mmu)
Genes: St3gal5 (Mmu)
Symbol: St3gal5tm1Rlp

St3gal5em2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586846
Genes: St3gal5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St3gal5 (Mmu)
Genes: St3gal5 (Mmu)
Symbol: St3gal5em2Cya

St3gal5tm1Skoz

(Mus musculus)
Allele/Variant
Source: MGI:5751066
Genes: St3gal5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St3gal5 (Mmu)
Genes: St3gal5 (Mmu)
Symbol: St3gal5tm1Skoz

St3gal5em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306856
Genes: St3gal5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: St3gal5 (Mmu)
Genes: St3gal5 (Mmu)
Symbol: St3gal5em1Gpt

ST3GAL5P1

(Homo sapiens)
Gene
Name: ST3GAL5 pseudogene 1
Synonyms: ST3 beta-galactoside alpha-2,3-sialyltransferase 5 pseudogene 1
Source: HGNC:45175
Biotype: pseudogene
Symbol: ST3GAL5P1 (Hsa)
Symbol: ST3GAL5P1

Id: MGI:5766793
Synonyms: Not Available
Symbol: St3gal5/St3gal5 [background:] Not Specified (Mmu)
Genes: St3gal5 (Mmu)
Alleles: St3gal5 (Mmu)
Name: St3gal5/St3gal5 [background:] Not Specified

Id: MGI:2655772
Synonyms: Not Available
Symbol: St3gal5/St3gal5 [background:] involves: 129S/SvEv * C57BL/6 (Mmu)
Genes: St3gal5 (Mmu)
Alleles: St3gal5 (Mmu)
Name: St3gal5/St3gal5 [background:] involves: 129S/SvEv * C57BL/6

Id: MGI:6360937
Synonyms: Not Available
Symbol: St3gal5/St3gal5 [background:] involves: C57BL/6JJmsSlc (Mmu)
Genes: St3gal5 (Mmu)
Alleles: St3gal5 (Mmu)
Name: St3gal5/St3gal5 [background:] involves: C57BL/6JJmsSlc

Source: GO:0047291
Synonyms:
  • CMP-acetylneuraminate-lactosylceramide-sialyltransferase
  • GM3 synthase activity
Branch: molecular function
Genes: St3gal5 (Rno)...St3gal5 (Mmu)...st3gal5 (Dre)...ST3GAL5 (Hsa)

Source: DOID:0060470
Definition: A syndrome characterized by severe intellectual disability, epilepsy, scoliosis, choreoathetosis, dysmorphic facial features and altered dermal pigmentation that has_material_basis_in homozygous or compound heterozygous mutation in the SIAT9 gene on chromosome 2p11.2.
Genes: St3gal5 (Rno)...St3gal5 (Mmu)...st3gal5 (Dre)...st3gal5 (Xtr)...ST3GAL5 (Hsa)

WT + MO1-st3gal5

(Danio rerio)
Model
Id: ZFIN:ZDB-FISH-150901-5601
Synonyms: Not Available
Genes: st3gal5 (Dre)
Name: WT + MO1-st3gal5

Id: MGI:6360944
Synonyms: Not Available
Genes: St3gal5 (Mmu)
Alleles: St3gal5 (Mmu)
Name: B4galnt1/B4galnt1 St3gal5/St3gal5 [background:] involves: 129S6/SvEvTac
Symbol: B4galnt1/B4galnt1 St3gal5/St3gal5 [background:] involves: 129S6/SvEvTac

Source: GO:0006688
Synonyms:
  • glycosphingolipid anabolism
  • glycosphingolipid biosynthesis
Branch: biological process
Genes: st3gal5 (Dre)...ST3GAL5 (Hsa)

Source: GO:0003836
Synonyms: Not Available
Branch: molecular function
Genes: ST3GAL5 (Hsa)

Source: GO:0008373
Synonyms: Not Available
Branch: molecular function
Genes: St3gal5 (Rno)...st3gal5 (Dre)...ST3GAL5 (Hsa)

Source: GO:0001574
Synonyms:
  • ganglioside anabolism
  • ganglioside biosynthesis
Branch: biological process
Genes: ST3GAL5 (Hsa)

Hsap\ST3GAL5UAS.cYa

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0344964
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\ST3GAL5
Construct Expressed Component: ST3GAL5 (Hsa)

Source: GO:0006486
Synonyms:
  • protein amino acid glycosylation
  • protein-carbohydrate complex assembly
Branch: biological process
Genes: St3gal5 (Rno)...St3gal5 (Mmu)...ST3GAL5 (Hsa)...st3gal5 (Dre)

Gene Ontology
Source: GO:0000139
Synonyms:
  • Golgi apparatus membrane
Branch: cellular component
Genes: St3gal5 (Mmu)...ST3GAL5 (Hsa)...St3gal5 (Rno)...st3gal5 (Dre)

Source: GO:0016757
Synonyms:
  • transferase activity, transferring glycosyl groups
  • transferase activity, transferring other glycosyl groups
Branch: molecular function
Genes: ST3GAL5 (Hsa)...st3gal5 (Dre)

Source: GO:0006629
Synonyms:
  • lipid metabolism
Branch: biological process
Genes: St3gal5 (Mmu)...ST3GAL5 (Hsa)...St3gal5 (Rno)

sa22430

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-16519
Genes: st3gal5 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ST3Gal5
Genes: st3gal5 (Dre)

sa38981

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-16378
Genes: st3gal5 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ST3Gal5
Genes: st3gal5 (Dre)

sa9293

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-19956
Genes: st3gal5 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ST3Gal5
Genes: st3gal5 (Dre)

Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: st3gal5 (Dre)

Gene Ontology
Source: GO:0016020
Synonyms:
  • integral component of membrane
  • integral to membrane
Branch: cellular component
Genes: st3gal5 (Dre)...ST3GAL5 (Hsa)

(GRCh38)2:85840146A>G

(Homo sapiens)
Allele/Variant
Source: rs1681835024
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85840146A>G

(GRCh38)2:85844420C>T

(Homo sapiens)
Allele/Variant
Source: rs1573580842
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844420C>T

(GRCh38)2:85839800G>A

(Homo sapiens)
Allele/Variant
Source: rs1681790908
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85839800G>A

(GRCh38)2:85840300T>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85840300T>C
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85840300T>C

(GRCh38)2:85840308G>C

(Homo sapiens)
Allele/Variant
Source: rs775647232
Genes: ST3GAL5 (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)2:85840308G>C

(GRCh38)2:85846364T>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85846364T>C
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85846364T>C

(GRCh38)2:85846425C>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85846425C>T
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85846425C>T

(GRCh38)2:85861171G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85861171G>A
Genes: ST3GAL5 (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)2:85861171G>A

(GRCh38)2:85861203T>A

(Homo sapiens)
Allele/Variant
Source: rs568003096
Genes: ST3GAL5 (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)2:85861203T>A

(GRCh38)2:85848014T>C

(Homo sapiens)
Allele/Variant
Source: rs2103959368
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85848014T>C

(GRCh38)2:85840029G>A

(Homo sapiens)
Allele/Variant
Source: rs193077813
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85840029G>A

(GRCh38)2:85844270G>C

(Homo sapiens)
Allele/Variant
Source: rs2280316
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844270G>C

(GRCh38)2:85844387C>T

(Homo sapiens)
Allele/Variant
Source: rs762640650
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844387C>T

(GRCh38)2:85844405G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85844405G>A
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844405G>A

(GRCh38)2:85839781T>G

(Homo sapiens)
Allele/Variant
Source: rs886056389
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85839781T>G