ZMP

ENSDARG00000095744

Ensembl ID:

ENSDARG00000095744

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 is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa31870	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa31870

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
ENSDART00000142362	Nonsense	174	336	4	7

Genomic Location (Zv9):

Chromosome 12 (position 17942697)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	16753871
GRCz11	12	16875745

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAAAGCTGATTTCTATGAGTGAGCAAAACTTGGTGGACTGTTCCAGACCA[C/T]AGGGCAATCAAGGGTGTAACGGAGGCCTCATGGACCAGGCCTTTCAGTAT

Long Flanking Sequence:

AGACTGTTTTTTTTTTTTTTTCTTACTATCTATTTTTTAGACAAATGAGGAGTTCAGACAGGCAATGAATGGTTATAAGCATGACCCCAACCGGACGTCACAGGGCCCGTTGTTCATGGAACCCAGCTTTTTTGCAGCCCCACAACAGGTTGACTGGAGACAGAGGGGCTATGTTACTCCTGTCAAAGACCAGGTGAGTTTAAAGTAACTGAAAACTGCAAATGTTTTATGCTAAATTAGGACCTATAGTTGCATCTATTACAATTGATCTATTTACAGTTGATCTGGTAAACCCAGTTAAATGTATAAATGGCTATTAAATGTCAGTATGTGTATCTGTAGCTTTACTGTTTTGTGACTCTTCTGTTTTGTGGTTTTAGAAACAATGTGGATCTTGCTGGTCTTTCAGTTCAACGGGTGCCTTGGAAGGTCAGCTCTTCCGTAAAACTGGAAAGCTGATTTCTATGAGTGAGCAAAACTTGGTGGACTGTTCCAGACCA[C/T]AGGGCAATCAAGGGTGTAACGGAGGCCTCATGGACCAGGCCTTTCAGTATGTTAAAGAAAACAAGGGGCTGGATTCTGAGCAGTCATACCCTTATCTTGCAAGGGTAAGAATCATATTGTGACAGTTTCTGAGCAAGGAAAACTCTTTTGAAGACATGGGATTAAACTGCTGTATTTGCAGATTGTGGAAAAATGTCATTTTAGTTTTTTAATCTCTTTGAATGAAGGTCATTAAGTATTTTAAGACTTCAATGTACCACTTTTTTCTTATTTTAACTTTGTGCTTGCAGGATGATCTGCCATGCCGGTATGACCCCCGTTTTAATGTCGCTAAAATCACCGGATTCGTGGACATCCCCAGAGGTAATGAGCTTGCCCTAATGAATGCTGTTGCTGCTGTGGGTCCTGTATCTGTTGCTATTGACGCATCACATCAATCCCTACAGTTCTATCAGTCTGGTAGGTGCCTGATATCCCTCAACTCTAGTTTTAATTCAATA

Associated Phenotype:

Not determined