Busch Lab

ZMP

ST3GAL1 (2 of 5)

Ensembl ID:
ENSDARG00000057593
Description:
ST3 beta-galactoside alpha-2,3-sialyltransferase 1 [Source:HGNC Symbol;Acc:10862]
Human Orthologue:
ST3GAL1
Human Description:
ST3 beta-galactoside alpha-2,3-sialyltransferase 1 [Source:HGNC Symbol;Acc:10862]
Mouse Orthologue:
St3gal1
Mouse Description:
ST3 beta-galactoside alpha-2,3-sialyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:98304]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa39223 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36761 Nonsense Mutation detected in F1 DNA Not yet available
sa23416 Nonsense Mutation detected in F1 DNA Not yet available
sa29131 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39223
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080290 Essential Splice Site 84 204 3 5
Genomic Location (Zv9):
Chromosome 19 (position 4502758)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4851054
GRCz11 19 4742657
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTATCTTCTTGGATTACCTGCACATTTGTTGTCATATGACTTTTTCTA[A/C]TCTTATTTTACTGAACAGAACACGAATGAAGGTTATCAACAAGTTACAAG
Long Flanking Sequence:
AACACTGGACCTCCAGTGGCTCACCAGCACTTTAACTAATGGGACCATCAAGCGGTGAGGGAAAGGTTAAATATCACACAGATATAAGATCACATTCATTCATTTTATTTTTGGCTTAGTCCCTTTAATAATCTGGGGTCACCACAGCAGAATGTACTGCCAACTTATCCAGGATATATTTTAAGCAGCGGATGCCCTTCCAGCTGCAACCCATCATTGGGAAATTCCCAAACACACTCATTCACACACATACACTACAGACAATTTAGCTTACCCAATTCACCTATATAATATGTTTTTGGACTGTGGGGGAAACCCACACCAACACTGGGAGAACATGCAAACTCCACACAGAAATGCTAACTGAACTAGCCTAGGCTTGAACCTGCAACCTTCTTGCTGTGAGGCAATCGTACTACCCACTGTGCTACCATTATGCCCCATTGGTTTTATTATCTTCTTGGATTACCTGCACATTTGTTGTCATATGACTTTTTCTA[A/C]TCTTATTTTACTGAACAGAACACGAATGAAGGTTATCAACAAGTTACAAGCCGACAAGAACAAGGTAAAACCACACAGTACCTTGATTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTGTCAAAAATAATCCTTTGACCAGAACAGTTAATTTAAAGATTTTTTTTGGTTAACAGTTAGGAGTAGTAAAGTTTATCTAATGGGACTGGACAGCTATGGAGACTAATTTTAGGGTACGCAGAGAACTGAGATACTGTCACAACAATACCATGACCGTTAGAAAAGATACTAATTATTTTACCATTCCTGAAATTGTACGTGCATCATTCATTCATAATCAATATGGAAAACTCAAATTTCAGATAATAAAAATAATAATTATTATTATTTATTGGATTTTTTTATATTAATCAAAAGACAAATGTGTCTATAAAAAATAATATATTATTATGGTTTTTACATTTCTATATTTTTAATTATACAGTTAGTCAGATTTATTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36761
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080290 Nonsense 85 204 3 5
Genomic Location (Zv9):
Chromosome 19 (position 4502752)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4851048
GRCz11 19 4742651
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTTGGATTACCTGCACATTTGTTGTCATATGACTTTTTCTAATCTTA[T/G]TTTACTGAACAGAACACGAATGAAGGTTATCAACAAGTTACAAGCCGACA
Long Flanking Sequence:
GGACCTCCAGTGGCTCACCAGCACTTTAACTAATGGGACCATCAAGCGGTGAGGGAAAGGTTAAATATCACACAGATATAAGATCACATTCATTCATTTTATTTTTGGCTTAGTCCCTTTAATAATCTGGGGTCACCACAGCAGAATGTACTGCCAACTTATCCAGGATATATTTTAAGCAGCGGATGCCCTTCCAGCTGCAACCCATCATTGGGAAATTCCCAAACACACTCATTCACACACATACACTACAGACAATTTAGCTTACCCAATTCACCTATATAATATGTTTTTGGACTGTGGGGGAAACCCACACCAACACTGGGAGAACATGCAAACTCCACACAGAAATGCTAACTGAACTAGCCTAGGCTTGAACCTGCAACCTTCTTGCTGTGAGGCAATCGTACTACCCACTGTGCTACCATTATGCCCCATTGGTTTTATTATCTTCTTGGATTACCTGCACATTTGTTGTCATATGACTTTTTCTAATCTTA[T/G]TTTACTGAACAGAACACGAATGAAGGTTATCAACAAGTTACAAGCCGACAAGAACAAGGTAAAACCACACAGTACCTTGATTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTGTCAAAAATAATCCTTTGACCAGAACAGTTAATTTAAAGATTTTTTTTGGTTAACAGTTAGGAGTAGTAAAGTTTATCTAATGGGACTGGACAGCTATGGAGACTAATTTTAGGGTACGCAGAGAACTGAGATACTGTCACAACAATACCATGACCGTTAGAAAAGATACTAATTATTTTACCATTCCTGAAATTGTACGTGCATCATTCATTCATAATCAATATGGAAAACTCAAATTTCAGATAATAAAAATAATAATTATTATTATTTATTGGATTTTTTTATATTAATCAAAAGACAAATGTGTCTATAAAAAATAATATATTATTATGGTTTTTACATTTCTATATTTTTAATTATACAGTTAGTCAGATTTATTAGCCCCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23416
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080290 Nonsense 132 204 4 5
Genomic Location (Zv9):
Chromosome 19 (position 4501571)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4849867
GRCz11 19 4741470
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTGCATTCATGCATTACGTGCACAATACATGGCTGCATATTAAAGCT[C/T]GAAGATCTTATCCATCCACCGGTATCCTCGTGTTAATCTTCGCCCTCCAC
Long Flanking Sequence:
ATAACGATGGTTTGTTCTGTAGACAAAATTATTTATCGGGAAAATAAATAGCTTAAAGGGGTTAATAATATTGACATTAAAATTGTGTTTAAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAGACCTTTTTCCAGAAGAAAAAATATTATTGGAAATACTGTGAAAATGATCTTGCTGTTAAACATAATTTGGGAAATATTTGAAAAATAAAAATGCACAGGAGCAAATAATTTTGATCTAAACTTTATTCCAATACAAACAATGCCGTCAAAACATGTTCAACCATTTAAAACCCTGTTTATATCTGTATTTATTGTCATCCACGTATAATCACACCAAAAAAAGCAGCATCTTAATAAATGCAAAATGGTCTTTAGATTGTTTCTTCGGTTCTGAAGGGGTTTATAATCCTCCTGTTGTTCCAGGTGATGGTAATGCACCCTGCATTCATGCATTACGTGCACAATACATGGCTGCATATTAAAGCT[C/T]GAAGATCTTATCCATCCACCGGTATCCTCGTGTTAATCTTCGCCCTCCACATCTGCGACCAGGTAAATCTTTACACATTTTTTAAACCCCAATATCAGCTACTGTCTCTCACCTGTTTTTCGGTGTTTAGGTCAGCGTGTTTGGCTTTGGCGCAAACAGCAAAGGATATTGGTATCACTATTTCGAAAAGATGCCCAAGTTCTTCTGGCGCACCGGCTTACACAGTGGAGGAATTGAGCATGACGTCATTAAAGAGCTTCAGAAAAGAAAACTGATCGATCTTTACAAAGGATGGTGAGGAGGACCATGAGCTTGAGATGTTATTAAATGAAAATTGATTGGTACTTTATGATAAGTGTATTGTGATATAAAAGTCGAAGTCTGAATTATGAGCCCCCCTGTATATTTTATACTCCATTTCTGTTTAATGGAGAGATTATTTATTCAACACGTTTCTAAACATAAGTTTTAATAACTCATTTCTAATAACTGATTTATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29131
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080290 Essential Splice Site 152 204 4 5
Genomic Location (Zv9):
Chromosome 19 (position 4501508)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 4849804
GRCz11 19 4741407
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCCACCGGTATCCTCGTGTTAATCTTCGCCCTCCACATCTGCGACCAG[G/A]TAAATCTTTACACATTTTTTAAACCCCAATATCAGCTACTGTCTCTCACC
Long Flanking Sequence:
AATAATATTGACATTAAAATTGTGTTTAAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAGACCTTTTTCCAGAAGAAAAAATATTATTGGAAATACTGTGAAAATGATCTTGCTGTTAAACATAATTTGGGAAATATTTGAAAAATAAAAATGCACAGGAGCAAATAATTTTGATCTAAACTTTATTCCAATACAAACAATGCCGTCAAAACATGTTCAACCATTTAAAACCCTGTTTATATCTGTATTTATTGTCATCCACGTATAATCACACCAAAAAAAGCAGCATCTTAATAAATGCAAAATGGTCTTTAGATTGTTTCTTCGGTTCTGAAGGGGTTTATAATCCTCCTGTTGTTCCAGGTGATGGTAATGCACCCTGCATTCATGCATTACGTGCACAATACATGGCTGCATATTAAAGCTCGAAGATCTTATCCATCCACCGGTATCCTCGTGTTAATCTTCGCCCTCCACATCTGCGACCAG[G/A]TAAATCTTTACACATTTTTTAAACCCCAATATCAGCTACTGTCTCTCACCTGTTTTTCGGTGTTTAGGTCAGCGTGTTTGGCTTTGGCGCAAACAGCAAAGGATATTGGTATCACTATTTCGAAAAGATGCCCAAGTTCTTCTGGCGCACCGGCTTACACAGTGGAGGAATTGAGCATGACGTCATTAAAGAGCTTCAGAAAAGAAAACTGATCGATCTTTACAAAGGATGGTGAGGAGGACCATGAGCTTGAGATGTTATTAAATGAAAATTGATTGGTACTTTATGATAAGTGTATTGTGATATAAAAGTCGAAGTCTGAATTATGAGCCCCCCTGTATATTTTATACTCCATTTCTGTTTAATGGAGAGATTATTTATTCAACACGTTTCTAAACATAAGTTTTAATAACTCATTTCTAATAACTGATTTATCATCTTTGCCATGATGACATGCAACTAAATATCATTAGAATATTAGCAGACTGTTTATTTCTGCT
Associated Phenotype:
Not determined