Busch Lab

ZMP

st3gal5

Ensembl ID:
ENSDARG00000037556
ZFIN ID:
ZDB-GENE-060322-1
Description:
lactosylceramide alpha-2,3-sialyltransferase [Source:RefSeq peptide;Acc:NP_955810]
Human Orthologue:
ST3GAL5
Human Description:
ST3 beta-galactoside alpha-2,3-sialyltransferase 5 [Source:HGNC Symbol;Acc:10872]
Mouse Orthologue:
St3gal5
Mouse Description:
ST3 beta-galactoside alpha-2,3-sialyltransferase 5 Gene [Source:MGI Symbol;Acc:MGI:1339963]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa22430 Nonsense Available for shipment Available now
sa9293 Nonsense Mutation detected in F1 DNA Not yet available
sa38981 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22430
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054690 Nonsense 137 364 4 7
ENSDART00000135449 None None 41 None 3
ENSDART00000137274 Nonsense 83 183 4 6

The following transcripts of ENSDARG00000037556 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 9664946)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 9186786
GRCz11 14 9492800
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAACCTCTTACCAGTTTCTTCTGAACAGAGGCTTGGGGAGCGAGATTG[T/A]CGACGCTGTGTAGTGGTTGGGAATGGAGGGATACTGAAAGGATTAGGACT
Long Flanking Sequence:
TGGTACCCTTTCGAAAGGGTGCCGAAAAAGTGGTACAGTACGTTTAGGTTTGGTACACCTTTTGATAGTGGAAACGACCATAAAAAGCGTACCAAACCAAACCGTACCATACCACTCAGTGGAAACGGAACATAATACAATAAACCATTTTAAAAGTTGTAACAGTCTTTCAGGTAGAATCTAAAAAAAAAGTAGTGCCTGTTGAAATTTTATTTATTTATTTTTAATCACTGCATGTTTCACTTGCAGCGTGTCCATTCTCATGTCCGAGAGATACTAGACAAAGAATGCAGACCTTCCTTTGCCCGGCAGAGAATGGTGACTGAACATCATGGCTCCACACCAACAATAGATCCTTTTTTGAACAAGAACATGAAGTTAGATGAACAAATATTCCAGTATCCTCCACCCTTTGGGTTCCTGGACATGAAGAACAAGCTTGAGGAAATCCTAAACCTCTTACCAGTTTCTTCTGAACAGAGGCTTGGGGAGCGAGATTG[T/A]CGACGCTGTGTAGTGGTTGGGAATGGAGGGATACTGAAAGGATTAGGACTCGGACATCTACTTAATCGTTTCGATATTATCATCAGGTAAGAATGTGCTCCTCCTAATCTGTGATTTATATATTGCTCTGAAATGGCAAAGAGGAAAATCATTTCTACCGTTAACAATAACTAAGTGAATTCTGAATATGAATGCAAACAGAGTTTAAAGTGCAAGCTTTTAAAATATGTTTAAAATATATGTAATTATTACCAGAACACAGGGCTTTGTGAGAAGTCATGCTCTTGTATTACATTACTTTTTACTTTTGCTAATTAGTTGACAACAAAACGAACAATGGCAAACTGCAGTATAGTACAACAATAGCTATGTTTCCATCCAAAAATGTGAATTTAATGTATGCACAAAACTGGAAAATTGCATAAAAAATGTGCAGATGAAGCAGCGTTTCCATCCAATTTGCTGTGGTAGGAGAAGCTCCGTAAATCTTCTCTTCTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9293
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
ENSDART00000054690 Nonsense 250 364 6 7
ENSDART00000135449 None None 41 None 3
ENSDART00000137274 None None 183 None 6

The following transcripts of ENSDARG00000037556 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 9667271)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 9189111
GRCz11 14 9495125
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTGTTTTTCTGGCAGAACGTGCCAATGAGCRTTCCAGTCAAGACCTCC[C/T]AGTTTCATCTCCTGAATCCCCAGATTATYCGTGARATGGCDTTGGATCTG
Long Flanking Sequence:
GCATTAACCTTTAATATGTAATGAAAATGCTCATTGAAGAGCCTATGACTGGGTACATGCTTTAGTCTCTATTAGGGTCGGAGTTTCTCAAATGTTTTATTGCATATGTTTGAGAGCGCAGAGGAAACTTCTTGGCTATTTCTGTGCAGACTGAACAGTGGTCCTCTTCAAGACTTCAGTGCAGATGTTGGGAACCGCACCACTATCAGAATGAGCTACCCTGAAAGCTGCCCGAAGGTCTGGGAAGATACGGATCCAGACCTCAAATATGTGGCTGTGATATTCAAGTCTGTAGACTTCCACTGGCTTCGTGCAATGATCAGCAGGACACCAGTTGTGAGTGCTCATTAAAATTGATTGATTTATACCAAAAGAGATGATTCTGAGACTTGTTTAGTGCTGTGTGCATCAATATCAAATGCAACATCGTCTTTCAGTCGCTGTGGGACAGGCTGTTTTTCTGGCAGAACGTGCCAATGAGCGTTCCAGTCAAGACCTCC[C/T]AGTTTCATCTCCTGAATCCCCAGATTATCCGTGAGATGGCGTTGGATCTGCTTAATTATCCCGAGCCTAAAAAGCGGCTCTGGAGCTGGGACCAGGTCAGTTCCTTTTTGCTCTGTTTTATTGGCTAAAGCCCCGGTCAGATCTCACGATTTTTATTGTCTGTTACGAAAGTCACTGTCAGATTATGCAATTTATTTATTTATTTATTTATTTATTCTCCTTGATAAAATCTTGACTTGTCATGAGTAACACATGTGCCGGACTACACATTCCTTCACGATTAGTCATCCCGTGACATCTACATTGATAATAACTACAATATGTAAGGGCATTAGTTACCATGGATGGGATCAAGCTTATGATTCCTTTTTAATATTAAGATACTTTCTTTGAAATCTAAAGAAAATTTTTCTGCCATGGGTTTCTTATTAAACACTACGTCTGAACTTCCCGCAAATGAGCTGAGAAAATGAGAGCATATAAGCAGCAGCAAGGGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38981
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
ENSDART00000054690 Nonsense 257 364 6 7
ENSDART00000135449 None None 41 None 3
ENSDART00000137274 None None 183 None 6

The following transcripts of ENSDARG00000037556 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 9667292)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 9189132
GRCz11 14 9495146
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAATGAGCGTTCCAGTCAAGACCTCCCAGTTTCATCTCCTGAATCCC[C/T]AGATTATCCGTGAGATGGCGTTGGATCTGCTTAATTATCCCGAGCCTAAA
Long Flanking Sequence:
TGAAAATGCTCATTGAAGAGCCTATGACTGGGTACATGCTTTAGTCTCTATTAGGGTCGGAGTTTCTCAAATGTTTTATTGCATATGTTTGAGAGCGCAGAGGAAACTTCTTGGCTATTTCTGTGCAGACTGAACAGTGGTCCTCTTCAAGACTTCAGTGCAGATGTTGGGAACCGCACCACTATCAGAATGAGCTACCCTGAAAGCTGCCCGAAGGTCTGGGAAGATACGGATCCAGACCTCAAATATGTGGCTGTGATATTCAAGTCTGTAGACTTCCACTGGCTTCGTGCAATGATCAGCAGGACACCAGTTGTGAGTGCTCATTAAAATTGATTGATTTATACCAAAAGAGATGATTCTGAGACTTGTTTAGTGCTGTGTGCATCAATATCAAATGCAACATCGTCTTTCAGTCGCTGTGGGACAGGCTGTTTTTCTGGCAGAACGTGCCAATGAGCGTTCCAGTCAAGACCTCCCAGTTTCATCTCCTGAATCCC[C/T]AGATTATCCGTGAGATGGCGTTGGATCTGCTTAATTATCCCGAGCCTAAAAAGCGGCTCTGGAGCTGGGACCAGGTCAGTTCCTTTTTGCTCTGTTTTATTGGCTAAAGCCCCGGTCAGATCTCACGATTTTTATTGTCTGTTACGAAAGTCACTGTCAGATTATGCAATTTATTTATTTATTTATTTATTTATTCTCCTTGATAAAATCTTGACTTGTCATGAGTAACACATGTGCCGGACTACACATTCCTTCACGATTAGTCATCCCGTGACATCTACATTGATAATAACTACAATATGTAAGGGCATTAGTTACCATGGATGGGATCAAGCTTATGATTCCTTTTTAATATTAAGATACTTTCTTTGAAATCTAAAGAAAATTTTTCTGCCATGGGTTTCTTATTAAACACTACGTCTGAACTTCCCGCAAATGAGCTGAGAAAATGAGAGCATATAAGCAGCAGCAAGGGAAAATCAGATGCTTAAGACATAAAA
Associated Phenotype:
Not determined