Version: 8.0.0
Date: Tue Jan 28 2025
2,597 results for st3gal5
Allele/Variant

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

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)

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)

(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

(GRCh38)2:85840361A>G

(Homo sapiens)
Allele/Variant
Source: rs1681871908
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)2:85840361A>G

(GRCh38)2:85847931T>A

(Homo sapiens)
Allele/Variant
Source: rs2103958837
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)2:85847931T>A

(GRCh38)2:85848157G>A

(Homo sapiens)
Allele/Variant
Source: rs1558654601
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85848157G>A

(GRCh38)2:85863439C>T

(Homo sapiens)
Allele/Variant
Source: rs776016166
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, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85863439C>T

(GRCh38)2:85848190A>G

(Homo sapiens)
Allele/Variant
Source: rs368298013
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, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85848190A>G

(GRCh38)2:85840195G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85840195G>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)2:85840195G>C

(GRCh38)2:85844420C>A

(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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844420C>A

(GRCh38)2:85840296T>C

(Homo sapiens)
Allele/Variant
Source: rs745878094
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)2:85840296T>C

(GRCh38)2:85840377C>A

(Homo sapiens)
Allele/Variant
Source: rs367638648
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)2:85840377C>A

(GRCh38)2:85840389C>T

(Homo sapiens)
Allele/Variant
Source: rs758368552
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)2:85840389C>T

(GRCh38)2:85844544A>G

(Homo sapiens)
Allele/Variant
Source: rs989255908
Genes: ST3GAL5 (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)2:85844544A>G

(GRCh38)2:85844741G>A

(Homo sapiens)
Allele/Variant
Source: rs2280314
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)2:85844741G>A

(GRCh38)2:85846360G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85846360G>A
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85846360G>A

(GRCh38)2:85847845A>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85847845A>G
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85847845A>G

(GRCh38)2:85846392T>C

(Homo sapiens)
Allele/Variant
Source: rs1336205358
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85846392T>C

(GRCh38)2:85844404G>A

(Homo sapiens)
Allele/Variant
Source: rs200541102
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844404G>A

(GRCh38)2:85844561A>G

(Homo sapiens)
Allele/Variant
Source: rs1573581572
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85844561A>G

(GRCh38)2:85847874C>G

(Homo sapiens)
Allele/Variant
Source: rs767789131
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)2:85847874C>G

(GRCh38)2:85846455G>C

(Homo sapiens)
Allele/Variant
Source: rs1682805181
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)2:85846455G>C

(GRCh38)2:85846464T>G

(Homo sapiens)
Allele/Variant
Source: rs1191405507
Genes: ST3GAL5 (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)2:85846464T>G

(GRCh38)2:85846509A>C

(Homo sapiens)
Allele/Variant
Source: rs756594825
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, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85846509A>C

(GRCh38)2:85848441C>G

(Homo sapiens)
Allele/Variant
Source: rs115173488
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)2:85848441C>G

(GRCh38)2:85848459C>T

(Homo sapiens)
Allele/Variant
Source: rs11694145
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)2:85848459C>T

(GRCh38)2:85848001G>C

(Homo sapiens)
Allele/Variant
Source: rs766829186
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, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85848001G>C

(GRCh38)2:85861188T>A

(Homo sapiens)
Allele/Variant
Source: rs1138484
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, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85861188T>A

(GRCh38)2:85888817C>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85888817C>G
Genes: ST3GAL5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:85888817C>G