Version: 8.0.0
Date: Tue Jan 28 2025
155 results for st3gal5
Allele/Variant Molecular Consequence: intron 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)2:85839800G>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)2:85839884C>T

(Homo sapiens)
Allele/Variant
Source: rs112475538
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)2:85839884C>T

(GRCh38)2:85840004T>A

(Homo sapiens)
Allele/Variant
Source: rs531229046
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)2:85840004T>A

(GRCh38)2:85839200G>A

(Homo sapiens)
Allele/Variant
Source: rs761892496
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)2:85839200G>A

(GRCh38)2:85839495G>A

(Homo sapiens)
Allele/Variant
Source: rs1681754258
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)2:85839495G>A

(GRCh38)2:85839689C>T

(Homo sapiens)
Allele/Variant
Source: rs886056388
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)2:85839689C>T

(GRCh38)2:85840291T>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85840291T>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)2:85840291T>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)2:85839781T>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)2:85840322C>T

(Homo sapiens)
Allele/Variant
Source: rs1313087028
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)2:85840322C>T

(GRCh38)2:85840324C>T

(Homo sapiens)
Allele/Variant
Source: rs370536081
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)2:85840324C>T

(GRCh38)2:85840172A>G

(Homo sapiens)
Allele/Variant
Source: rs1287781304
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)2:85840172A>G

(GRCh38)2:85839535C>G

(Homo sapiens)
Allele/Variant
Source: rs886056387
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)2:85839535C>G

(GRCh38)2:85839662C>T

(Homo sapiens)
Allele/Variant
Source: rs115544178
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)2:85839662C>T

(GRCh38)2:85839550C>T

(Homo sapiens)
Allele/Variant
Source: rs116456890
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)2:85839550C>T

(GRCh38)2:85839712C>T

(Homo sapiens)
Allele/Variant
Source: rs753191965
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)2:85839712C>T

(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)2:85840296T>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)2:85840197C>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85840197C>G
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)2:85840197C>G

(GRCh38)2:85840198C>T

(Homo sapiens)
Allele/Variant
Source: rs765309675
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)2:85840198C>T

(GRCh38)2:85840237C>T

(Homo sapiens)
Allele/Variant
Source: rs950472318
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)2:85840237C>T

(GRCh38)2:85840238A>G

(Homo sapiens)
Allele/Variant
Source: rs755800174
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)2:85840238A>G

(GRCh38)2:85840272T>C

(Homo sapiens)
Allele/Variant
Source: rs748173859
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)2:85840272T>C

(GRCh38)2:85840275C>G

(Homo sapiens)
Allele/Variant
Source: rs147305893
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)2:85840275C>G

(GRCh38)2:85839194C>T

(Homo sapiens)
Allele/Variant
Source: rs886056386
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)2:85839194C>T

(GRCh38)2:85840206A>G

(Homo sapiens)
Allele/Variant
Source: rs950495632
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)2:85840206A>G

(GRCh38)2:85840207G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.85840207G>A
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)2:85840207G>A

(GRCh38)2:85839466G>A

(Homo sapiens)
Allele/Variant
Source: rs188807604
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)2:85839466G>A

(GRCh38)2:85840157T>A

(Homo sapiens)
Allele/Variant
Source: rs1681837789
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)2:85840157T>A

(GRCh38)2:85840189C>T

(Homo sapiens)
Allele/Variant
Source: rs148195895
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)2:85840189C>T

(GRCh38)2:85840308G>A

(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>A

(GRCh38)2:85840075T>C

(Homo sapiens)
Allele/Variant
Source: rs886056391
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)2:85840075T>C

(GRCh38)2:85840154C>T

(Homo sapiens)
Allele/Variant
Source: rs200683924
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)2:85840154C>T

(GRCh38)2:85839729A>G

(Homo sapiens)
Allele/Variant
Source: rs112372963
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)2:85839729A>G

(GRCh38)2:85839997G>A

(Homo sapiens)
Allele/Variant
Source: rs1017206945
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)2:85839997G>A