Busch Lab

ZMP

EXT1A_DANRE

Ensembl ID:
ENSDARG00000020373
Description:
Exostosin-1a [Source:UniProtKB/Swiss-Prot;Acc:Q5IGR8]
Human Orthologue:
EXT1
Human Description:
exostosin 1 [Source:HGNC Symbol;Acc:3512]
Mouse Orthologue:
Ext1
Mouse Description:
exostoses (multiple) 1 Gene [Source:MGI Symbol;Acc:MGI:894663]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa22952 Nonsense Available for shipment Available now
sa9715 Splice Site, Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa22952
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006439 Nonsense 324 730 2 11
Genomic Location (Zv9):
Chromosome 16 (position 51878640)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 48602953
GRCz11 16 48544971
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATAAAGAAATGCTGCACAACTCCACATTCTGTCTGGTGCCGAGAGGA[C/T]GACGCCTGGGCTCTTTCCGCTTCCTGGAGGCTCTGCAGGTACACTTTTAC
Long Flanking Sequence:
TAATATTTGTTAAACTGCTTGTTGCTTGCTGTATGTGGGCGGAGTAATACACAGAGGTGAAGGGTGAAGAGGCCTTTTTTTGATGTTACTGGCAAAATATTGCACGACTATCAGCCAATCAGATTCAAGAACCAGACAGAGCTGTTTTTTTTTTTTTACAGTGCATCAATTCAGCATCGATATCGCCATGTGTCCACTAGGATGCGCAATATAGAGTAGGCATTATACATGAGCGAAACCACAGTTTGAAACCCATGTAATCTGTAGCTTAACTGTAAAGTTTACCCATTTGGAATTAAAGTTCATAACGTGTGTGTGTTTTTCCAGAGCTTGCTCTTTCTCCAAGCTGCAGCATTTGTAATCTCTGCTAGATGTTTTGAGCTTTAACTGTTTTCCTGCTCCAGGATGTTTTGTGACCTCAGTGTTTCCTTCTTGTCCTCCACAGGTACGACTATAAAGAAATGCTGCACAACTCCACATTCTGTCTGGTGCCGAGAGGA[C/T]GACGCCTGGGCTCTTTCCGCTTCCTGGAGGCTCTGCAGGTACACTTTTACAGTCCAATTTTGTTGCTAATTACAGGCTGTTACTGTTAAGCAACATGACAGATGACAAATGTAATGATTTGCCACAATATTTCTGTCTTTACTGTATTTTTATTAGGCAAGACAGGTTGATTTGTATAGCCCATTTCATACACAATGCCAATTCAAAGTGCTTTACATAATCAGATTAAGAGAATCAATAAATAATCGCACGACAAGTAAAAGGAATAAAAACAACGAATAATTAATATGATTAAAAACAGATTTAACATATTAATATTGAATAACTGCAGCCTTGATTAGAGTTAGAGAATATTCAACATATTTTCTACATAAAGTATTTGAACAAAAATAAAATATATATTGTGAAATATTATTTTAATTCTTATTAATTAGTATTCACTGTGTTAGTGGATTTTTATTCAAATAAATACAGCTTTGGGGGAAGCTCGGTGACGCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9715
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006439 Splice Site, Nonsense 528 730 7 11
Genomic Location (Zv9):
Chromosome 16 (position 51901087)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 48625400
GRCz11 16 48567418
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCGCTGGCCTGCTACTTCAGTTCCTGTCATCGTAATCGARGGCGAGAGC[A/T]AGGWRAATCTGCGCCGTCTTTATATTCTCTTATCAAATCAARTGTCTGGT
Long Flanking Sequence:
TTCAAATGATCTATTCAGATAGAGTCTGCAGTTAATGACTCACGGATTCAAATGATCCATTCCTAGAGAGTCTGCATTTAACTTCTCACTGATTCAAATGATCTATTCAGATAGAGTCTGCAGTTAATGACTCACTAATTCAAATGATCTATTCATATAGAGTCTGTAGTTAGGACTCACTGATTCAAATCATCTATTCAGATAGAGTCTGCAGTTAATGACTCACTGATTCAAATGATCCATTCAGAGTGCGTCTAGAGTTTTACTTTAAAATTAAATTGAAGACTATATTTTTTTTACTGGAGTAATATTTCCTTTAGAGTACCCGTACTTTTGCTCAAGTGCTTGTTTTGTGTACTGTTATTTACACACTGTTGAATTAAAGTTTTTATTGTCTGTATTTTCAGATCATGGTCTTGTGGAACTGTGATAAACCTCTTCCCTCGAAGCATCGCTGGCCTGCTACTTCAGTTCCTGTCATCGTAATCGAGGGCGAGAGC[A/T]AGGTGAATCTGCGCCGTCTTTATATTCTCTTATCAAATCAAGTGTCTGGTGCTGTGCGGCGGATGATGGATGGCCTATGGATTTGTAGCTGCTCTCCTTCTTGAATGTTTTTATCTTGCTAAAGTCTGGATTTGATGTGTAGGTGATGAGTAGCCGATTCCTGCCGTATGAAAACATCATAACTGATGCAGTCCTGAGTCTGGATGAAGACACTGTGCTCTCCACCACTGAGGTTCTTTCTTTTATCCTCACTTGTAAACTACTTTAGATAAAAGTCTCTGGTAAAAGAGTAAACTGAAACATAAAGTGAATTAGCAAATCTCAGGGTTTATGTTTTCATGGCTGTCTACACACAGTATTTACCTTAGTGCCCTTATTCCTGCAGGTGGATTTTGCCTTCACCGTCTGGCAGAGTTTCCCAGAGAGGATTGTGGGGTATCCTGCACGGAGCCATTTCTGGGACTCCAATAAGGAGCGATGGGGCTACACCTCTAAATGGA
Associated Phenotype:
Not determined