ZMP

xpnpep2

Ensembl ID:

ENSDARG00000026017

ZFIN ID:

ZDB-GENE-040426-1151

Description:

xaa-Pro aminopeptidase 2 [Source:RefSeq peptide;Acc:NP_957326]

Human Orthologue:

XPNPEP2

Human Description:

X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound [Source:HGNC Symbol;Acc:12823]

Mouse Orthologue:

Xpnpep2

Mouse Description:

X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound Gene [Source:MGI Symbol;Acc:MGI:2180001

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35721	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa22514	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa35721

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010022	Essential Splice Site	45	703	1	21

Genomic Location (Zv9):

Chromosome 14 (position 34588618)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	33273318
GRCz11	14	33613632

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAGCTCCTCAGGCTGGATACTGGCTGTGTGTCTTGTGGTTCTTGGAGG[T/C]AAATAAATAAATAAGTGTGTATGCGATGCCGATTTCATCTCGATGATGTG

Long Flanking Sequence:

CCTTTCTTGCACAATTTCCTGGCATTGACCAGCAGTGGGATGTTGTTATTTCAAAATGTGGAAGAAAAACGAATCAGAAAATTGTGGCTCAGAAACATGCAACATATGTAACAGGAGACAACAGTAAGCTATCATTTACTATGGACCTACAGTTGCTTCGCCATGCATGGGTAAATGCACTGCACATTAAAGACGGACTAGAGAGAGAGAGTGACCATGCTTTTATTACAGTAGTAAAGATTAGAGTCACAGCCAAAGTTCCTCCCACTCCGCTATTTCACATGGCTCTGGTTGGGAAGTCTCTGAGTCAAGATAATTCATGTAGTTTCGGATAGGACATACACACCCTTGTGCACAGACACTCACATGCGCACACACTCACAAGACAGAGACACTTGTGTCCCGCTGTCACACTCTGTGTGTGGACTTGCTTGGAGCAGATGGTCTAAAATGAGCTCCTCAGGCTGGATACTGGCTGTGTGTCTTGTGGTTCTTGGAGG[T/C]AAATAAATAAATAAGTGTGTATGCGATGCCGATTTCATCTCGATGATGTGGTGTTAACTATGCATTAATGCAACTGTAATACACTGTGTGAGTAAGGCTTTCATTAAGGCAACATTTCTGTTCACCATCTGTCTTTGTGTCATGTGTGTTGGTTTATTGCTGGATATATTTGCATGTCATTAGCCTGGAAATTAATTCTGCAGTAAAATGTTGCTTGTTTGCTCAGTTATCCATAAAATGAAACTGAATGCGTATAATTATGTGAAAGACTTTGCTTAAAGCATTTTTCATTCGTTATAGAATGTCATAATTGGTGTGTTTAGTATATATGTGGATAGTTTACACATTGTTTTTTGAGATTTTTGTGCATTATATAATGTTGGTTCTGCAATACGGTCATGTAAAAAATGTCTTGCTGGCTTATAAAGGCATATATTTAACAGTGATTGCTGACCTTTGATCAGCACATGAGCTGACTGAGTTTAAAACATTTACTCTTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22514

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010022	Nonsense	330	703	10	21

Genomic Location (Zv9):

Chromosome 14 (position 34577761)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	33262461
GRCz11	14	33602775

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATTTGAATGCTTCGTGCTACCAGTCGCTCTGTGTTCATCTGCTCGAGTA[C/A]AGCTCTGTGCGCACGTATCTGCAGTCATATCTGCAGAGACCCAACGTCAG

Long Flanking Sequence:

TGAACTCTTTCTTTGAAATGTGAAGTAAATGCTATTGTGACTGTGTGTGTGTTTGTTCTGTTGTTCAGAAAGGACCTGGCCAATGAAAGTGGAGCAAATACGAGCCCAAATAATTGACAATCCATACAAGCCCACTGCTGTGCTACTTTCTGCTCTGGACGAGACCGCATGTAAGCACATCACAAACCCACAAACTCATGCTGGAGATCTTCTCTAAATCCTTGGTTAAATCGCTCTCTATTTTCAGGGCTATTTAATCTACGAGGCAACGATGTCCCTTATAATCCATTCTTCTATTCTTACACTCTGCTGTCGATGGATGACATATGGCAAGTTTCTCCATTTCACATGAACAGCACTATACTTAGCTGGTGTAGAGTTTCTGACTAACTAACCTCCTTCATCAGGCTCTTTGTGCACACAGAACGAATAACAGAAGAGCTGAAGGTGTATTTGAATGCTTCGTGCTACCAGTCGCTCTGTGTTCATCTGCTCGAGTA[C/A]AGCTCTGTGCGCACGTATCTGCAGTCATATCTGCAGAGACCCAACGTCAGGGTTTGGGTTGGTACAGAGTACACCAACCAGGCCCTATATGAGCTCATTACTCCTGAGGTAAGACCTGGATCCAAAATACTTGTATGCACATATAAGCTTTGTAGTTATCTGTGGGTTGAATATATTTTAGATATGGTTACACAGAGGTTCTCTGGTGTTAATAATACTCAATGTTTAGAAATAATGAACTGTATTAACTGTAATAAACTGATATGTTCCCCATATGGCTTTCTAAAGACACACAAGCCTGTGCACTCACATCTGTGGAGAAAGTTTAGTTATGCTATATACATCAGACACACATCACAGTGGGATAAAATTAGATATAAGTGAAGCTGTATCTATTTTTGACACACTGCACAGCTGATCAGCCACTTTATTTTGCCCTTTCAAGTTTGAAATGCAGTGAATGGATGGTAGGATAAACAGATAAACTGAAGAATGGATGA

Associated Phenotype:

Not determined