Busch Lab

ZMP

chsy1

Ensembl ID:
ENSDARG00000079027
ZFIN ID:
ZDB-GENE-030131-3127
Description:
chondroitin sulfate synthase 1 [Source:RefSeq peptide;Acc:NP_997843]
Human Orthologue:
CHSY1
Human Description:
chondroitin sulfate synthase 1 [Source:HGNC Symbol;Acc:17198]
Mouse Orthologue:
Chsy1
Mouse Description:
chondroitin sulfate synthase 1 Gene [Source:MGI Symbol;Acc:MGI:2681120]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa9893 Nonsense Available for shipment Available now
sa40837 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9893
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104536 Nonsense 381 801 3 3
Genomic Location (Zv9):
Chromosome 7 (position 10289537)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 9263318
GRCz11 7 9508805
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCACCAACGTGAGGAGGTGCTGGAATGGGAATTCCTCACGGGAAAGTA[C/A]ATTTTCTCATCCTCAGATGGACAGCCTCCCCGTCGAGGCATTGACTCCTC
Long Flanking Sequence:
AATTGCTTGTTTGCATTACAGTTTGGCCCTTTAATTGGAAAATAAGACGCGAGAGGTCTTGCTAAAGACGTATTATTTTCACTTTCAATTATATCAACCCAGTTGTGACGTCAATCTATTATTTACAAGTCTAAACCAATCACTAACATCTAGTTTTCTCTTTTACAGATGCAGCAGCTGTTCTATGAGAATTACGAGCCAAACAAGAAGGGCTACATCCGTGATCTCCACAACAGTAAGATCCACAGAGCCATAACCCTTCACCCCAACAAGAACCCACCTTACCAGTATCGGTTGCACAGCTACATGTTGAGCCGGAAGATTGCAGAGCTGCGCCACCGCACCATTCAGCTCCATCGTGAGATTGTGCAAATGAGCCGCTACAGCAACACCGAGGTGCACAGGGAAGACCTTCAACTGGGCATGCCTCCATCCTTCATGCGCTTTCATCCCCACCAACGTGAGGAGGTGCTGGAATGGGAATTCCTCACGGGAAAGTA[C/A]ATTTTCTCATCCTCAGATGGACAGCCTCCCCGTCGAGGCATTGACTCCTCGCAGAAGATGGCGCTGGACGACATCATCATGCAAGTTATGGAGATGATTAACGCCAATGCCAAGACACGCGGAAGAGTCATTGACTTCAAAGAGATCCAATATGGCTACCGAAGGGTCAACCCTATGTATGGTGCAGAGTACGTACTGGATCTGCTGCTGCTCTACAAGAAGCACAAGGGGAAGACTATGACAGTGCCCGTAAGGAGGCATGCGTATCTTCAGCAGACCTTCAGCAAGATCCAGTTCTTGGAAGAAGAAGAGATGGACGCTCGAGTCCTGGCTGCCAGGATCAACCAAGACTCCGACTCGCTGTCTTTCTTGTCCAACTCCCTCAAGATGCTCGTCCCGTTCAAGTTGAGCAGCCCAGGCATCGAACAACACGAACCCAAAGAGAAGAAGATCAACATCCTTGTGCCGCTGGCCGGACGCTACGAGATTTTTCTGCGCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40837
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
ENSDART00000104536 Nonsense 389 801 3 3
Genomic Location (Zv9):
Chromosome 7 (position 10289559)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 9263340
GRCz11 7 9508827
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAATGGGAATTCCTCACGGGAAAGTACATTTTCTCATCCTCAGATGGA[C/T]AGCCTCCCCGTCGAGGCATTGACTCCTCGCAGAAGATGGCGCTGGACGAC
Long Flanking Sequence:
TTGGCCCTTTAATTGGAAAATAAGACGCGAGAGGTCTTGCTAAAGACGTATTATTTTCACTTTCAATTATATCAACCCAGTTGTGACGTCAATCTATTATTTACAAGTCTAAACCAATCACTAACATCTAGTTTTCTCTTTTACAGATGCAGCAGCTGTTCTATGAGAATTACGAGCCAAACAAGAAGGGCTACATCCGTGATCTCCACAACAGTAAGATCCACAGAGCCATAACCCTTCACCCCAACAAGAACCCACCTTACCAGTATCGGTTGCACAGCTACATGTTGAGCCGGAAGATTGCAGAGCTGCGCCACCGCACCATTCAGCTCCATCGTGAGATTGTGCAAATGAGCCGCTACAGCAACACCGAGGTGCACAGGGAAGACCTTCAACTGGGCATGCCTCCATCCTTCATGCGCTTTCATCCCCACCAACGTGAGGAGGTGCTGGAATGGGAATTCCTCACGGGAAAGTACATTTTCTCATCCTCAGATGGA[C/T]AGCCTCCCCGTCGAGGCATTGACTCCTCGCAGAAGATGGCGCTGGACGACATCATCATGCAAGTTATGGAGATGATTAACGCCAATGCCAAGACACGCGGAAGAGTCATTGACTTCAAAGAGATCCAATATGGCTACCGAAGGGTCAACCCTATGTATGGTGCAGAGTACGTACTGGATCTGCTGCTGCTCTACAAGAAGCACAAGGGGAAGACTATGACAGTGCCCGTAAGGAGGCATGCGTATCTTCAGCAGACCTTCAGCAAGATCCAGTTCTTGGAAGAAGAAGAGATGGACGCTCGAGTCCTGGCTGCCAGGATCAACCAAGACTCCGACTCGCTGTCTTTCTTGTCCAACTCCCTCAAGATGCTCGTCCCGTTCAAGTTGAGCAGCCCAGGCATCGAACAACACGAACCCAAAGAGAAGAAGATCAACATCCTTGTGCCGCTGGCCGGACGCTACGAGATTTTTCTGCGCTTCATGGCCAACTTCGAGAAGATC
Associated Phenotype:
Not determined