Busch Lab

ZMP

wu:fb37b09

Ensembl ID:
ENSDARG00000095254
ZFIN ID:
ZDB-GENE-030131-572
Human Orthologues:
CTSL1, CTSL2
Human Descriptions:
cathepsin L1 [Source:HGNC Symbol;Acc:2537]
cathepsin L2 [Source:HGNC Symbol;Acc:2538]
Mouse Orthologues:
4930486L24Rik, BC051665, Cts3, Cts6, Cts7, Cts8, Ctsj, Ctsl, Ctsll3, Ctsm, Ctsq, Ctsr
Mouse Descriptions:
RIKEN cDNA 4930486L24 gene Gene [Source:MGI Symbol;Acc:MGI:1922258]
cDNA sequence BC051665 Gene [Source:MGI Symbol;Acc:MGI:2682300]
cathepsin 3 Gene [Source:MGI Symbol;Acc:MGI:2151929]
cathepsin 6 Gene [Source:MGI Symbol;Acc:MGI:1889619]
cathepsin 7 Gene [Source:MGI Symbol;Acc:MGI:1860262]
cathepsin 8 Gene [Source:MGI Symbol;Acc:MGI:1860275]
cathepsin J Gene [Source:MGI Symbol;Acc:MGI:1349426]
cathepsin L Gene [Source:MGI Symbol;Acc:MGI:88564]
cathepsin L-like 3 Gene [Source:MGI Symbol;Acc:MGI:1917452]
cathepsin M Gene [Source:MGI Symbol;Acc:MGI:1927229]
cathepsin Q Gene [Source:MGI Symbol;Acc:MGI:2137385]
cathepsin R Gene [Source:MGI Symbol;Acc:MGI:1861723]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa31868 Nonsense Available for shipment Available now
sa27925 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31868
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
ENSDART00000133962 Nonsense 190 335 4 7
Genomic Location (Zv9):
Chromosome 12 (position 17660585)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16471759
GRCz11 12 16593633
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGGCAATCAAGGGTGTAATGGAGGCCTCATGGACCAGGCCTTCCAGTA[T/A]GTTAAAGAAAACAAGGGGCTGGATTCTGAGCAGTCATACCCTTATCTTGC
Long Flanking Sequence:
AGTTCAGACAGGCAATGAATGGTTATAAGCATGACCCCAACCGGACGTCACAGGGCCCGTTGTTCATGGAACCCAAATTTTTTGCAGCCCCACAACAGGTTGACTGGAGACAGAGGGGCTATGTTACTCCTGTCAAAGACCAGGTGAGTTTAAAGTAACTGAAAACTGCAAATGTTTTATGCTAAATTAGGACCTATAGTTGCATCTATGACAATTGATCTATTTACAGTTGATCTGGTAAACCCAGTTTAATGTATAAATGGCTATTACATGTCAGTATGTGTATCTGTAGCTTTACTGTTTGGTGACTCTTCTGTTTTGTGGTTTTAGAAACAATGTGGATCTTGCTGGTCTTTCAGTTCAACGGGTGCATTGGAAGGTCAGCTCTTCCGTAAAACTGGAAAGCTGATTTCTATGAGTGAGCAAAACTTGGTGGACTGTTCCAGACCACATGGCAATCAAGGGTGTAATGGAGGCCTCATGGACCAGGCCTTCCAGTA[T/A]GTTAAAGAAAACAAGGGGCTGGATTCTGAGCAGTCATACCCTTATCTTGCAAGGGTAAGAATCATATTGTGACTGAGCAATGAAAAAATTTTCTTTTGAGGCATGGGATTAAACTGCTGTATTTGCAGATTGTGGAAAAATGTCATTTTAGTTTTTTAATCTCTTTGAATGAAGGTCATTAAGTATTTTAAGACTTCAATGTACCATGTTTTTCTTATTTTAACTTTGTGCTTGCAGGATGATCTGCCATGCCGCTATGACCCCCGTTTTAATGTCGCTAAAATCACCGGATTCGTGGACATTCCCAAAGGTAATGAGCTTGCCCTAATGAATGCTGTTGCTGCTGTGGGTCCTGTATCTGTTGCTATTGACGCATCACATCAATCTCTACAGTTCTATCAGTCTGGTAGGTGTCTGATATCCCTCAACTCTAGTTTTAATTCAATATATATCCAAAATTATTACAAACTTATTACTGAACTTACTCTGCCTTAACTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27925
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000133962 Nonsense 205 335 4 7
Genomic Location (Zv9):
Chromosome 12 (position 17660540)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16471714
GRCz11 12 16593588
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTATGTTAAAGAAAACAAGGGGCTGGATTCTGAGCAGTCATACCCTTA[T/A]CTTGCAAGGGTAAGAATCATATTGTGACTGAGCAATGAAAAAATTTTCTT
Long Flanking Sequence:
CGTCACAGGGCCCGTTGTTCATGGAACCCAAATTTTTTGCAGCCCCACAACAGGTTGACTGGAGACAGAGGGGCTATGTTACTCCTGTCAAAGACCAGGTGAGTTTAAAGTAACTGAAAACTGCAAATGTTTTATGCTAAATTAGGACCTATAGTTGCATCTATGACAATTGATCTATTTACAGTTGATCTGGTAAACCCAGTTTAATGTATAAATGGCTATTACATGTCAGTATGTGTATCTGTAGCTTTACTGTTTGGTGACTCTTCTGTTTTGTGGTTTTAGAAACAATGTGGATCTTGCTGGTCTTTCAGTTCAACGGGTGCATTGGAAGGTCAGCTCTTCCGTAAAACTGGAAAGCTGATTTCTATGAGTGAGCAAAACTTGGTGGACTGTTCCAGACCACATGGCAATCAAGGGTGTAATGGAGGCCTCATGGACCAGGCCTTCCAGTATGTTAAAGAAAACAAGGGGCTGGATTCTGAGCAGTCATACCCTTA[T/A]CTTGCAAGGGTAAGAATCATATTGTGACTGAGCAATGAAAAAATTTTCTTTTGAGGCATGGGATTAAACTGCTGTATTTGCAGATTGTGGAAAAATGTCATTTTAGTTTTTTAATCTCTTTGAATGAAGGTCATTAAGTATTTTAAGACTTCAATGTACCATGTTTTTCTTATTTTAACTTTGTGCTTGCAGGATGATCTGCCATGCCGCTATGACCCCCGTTTTAATGTCGCTAAAATCACCGGATTCGTGGACATTCCCAAAGGTAATGAGCTTGCCCTAATGAATGCTGTTGCTGCTGTGGGTCCTGTATCTGTTGCTATTGACGCATCACATCAATCTCTACAGTTCTATCAGTCTGGTAGGTGTCTGATATCCCTCAACTCTAGTTTTAATTCAATATATATCCAAAATTATTACAAACTTATTACTGAACTTACTCTGCCTTAACTCCTTTGTAATATTCTGATCTTTAGGCATCTATTATGAGAGAGCATGTA
Associated Phenotype:
Not determined