ZMP

NP_001096588.1

Ensembl ID:

ENSDARG00000095072

Description:

hypothetical protein LOC564906 [Source:RefSeq peptide;Acc:NP_001096588]

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
sa9764	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa9764

Status:

Available for shipment
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Availability:

Order Allele From ZIRC
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Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113478	Essential Splice Site	None	335	1	8

The following genes are also affected by this mutation:

Genomic Location (Zv9):

Chromosome 12 (position 18008245)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	16819419
GRCz11	12	16941293

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACACACTCAATTGTAAGCAATTACAGTCAACAAGGTTTGCTTGTGAAAGG[T/A]AAGTGTAAATCTTNNNNCCCCCCCCCTCCTTTCCTTTATAGGAGACATTG

Long Flanking Sequence:

TTTCTAAATGGACTCTGTGTTTCCTCTTGCATTATTCTCTTGGATTAGTTTCTGTCTAAGCATGTGGAATTTGTCAAACACACCCTTATGTGACAAACACAAACAATGATTAAAACAAACGAAACAAACAGAATGTAACAAACCTAAAAAAAATCTCCACATCCCCCAATCAAGTGAAGCATATTCTAGTATGCTTTCCACTTGTGTATTGTAAATGTTGATTTTTATAAACTGTGGAAATAACAAAACATTTCTGATTGCCTTAATCTTGTTGCAGTCTACTAATAATATAAAGAATCACCATAGTCCATTGATGAATACTTCATCTTGTGATGCTGGATCACATGACAAGATGAAGCTCTTGCTGCACCTGATTGGCTGTAAATTGACTAGTTTCATCATCAACGTCAGCCAATGAGAGACCGTCTCTATGTTCAGACAGGCTATAAAACACACTCAATTGTAAGCAATTACAGTCAACAAGGTTTGCTTGTGAAAGG[T/A]AAGTGTAAATCTTTCTCCCCCCCCCCTCCTTTCCTTTATAGGAGACATTGCTTGTATTATATTAATGTGACATTTAGCTCAACTCACAGTAAAGTGAACTGCTTGTGCTGTTGCCTGTTTAAAGTGTTTTGTTAATGTTTGTAAATTTTCTTTACATTTGCTTTAAATAGAGATTTTTACTATTATTGTGTTTTTTTTTTCTGTTAGTCTTCCTGGCAGGATGATGTTTGCTTTGCTCATCACGCTGTGCATAAGTGCAGTGTTCACTGCTCCATCTATAGACATCCAGTTAGACGACCACTGGAACTCCTGGAAGAGCCAGCATGGAAAAAGCTATCATGAGGTGGGAAGACTGTAGTCTGTAGCCATGTATCAGCTTAACATGAATGAATGATGCAGTGCATGTGTTTATGTTGAACTGTTGCTTTGCAATAGCTGATACTGTATCTACTTTCTACTCCAGGACGTAGAGGTCGGGAGGAGAATGATTTGGGAGGAGA

Associated Phenotype:

Not determined