ZMP

cpa2

Ensembl ID:

ENSDARG00000010146

ZFIN ID:

ZDB-GENE-040801-182

Description:

carboxypeptidase A2 (pancreatic) [Source:RefSeq peptide;Acc:NP_001003446]

Human Orthologues:

CPA2, CPA4

Human Descriptions:

carboxypeptidase A2 (pancreatic) [Source:HGNC Symbol;Acc:2297]
carboxypeptidase A4 [Source:HGNC Symbol;Acc:15740]

Mouse Orthologues:

Cpa2, Cpa4

Mouse Descriptions:

carboxypeptidase A2, pancreatic Gene [Source:MGI Symbol;Acc:MGI:3617840]
carboxypeptidase A4 Gene [Source:MGI Symbol;Acc:MGI:1919041]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24634	Essential Splice Site	Available for shipment	Available now
sa30224	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44261	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24634

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011397	Essential Splice Site	234	422	8	11

Genomic Location (Zv9):

Chromosome 25 (position 16952423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16498967
GRCz11	25	16595367

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATAAAAGTTTCACAGTATTTCTAATGACATTACAAACTAATGACCCCTT[A/T]GCCGTTTCACCGTTTGTGGCGTAAGAGCCGGTCTGTGACCTCTAACCCAA

Long Flanking Sequence:

ATCTGCTTGATTTTATTTAATATTTTCCCCTAACATATAAATTTGGACTAATTATTGAACCATTATTGTAAGTTATTTTGTTAGATTAGCTCCAGATTTGGCTTCAGCACTGACTAAACTAATGTATATGTATATGCACCCATATATTATTGTAAGATTTGTGAGGTGTGTACTTATATATCCTGAGCACTCTATTGCTGTGATTGGATGATTGTTCTGAGATTATTGGATAAAATCTACATAGCATGTACAACAGAGACTTTTTAAAATTCTGAACTGCTCTTCTTGTCCCTCCAGATTGCCACAGACTTTAAGGAAAACCGTGCTCTTGCTCGCAATGTCCTTAGTAAAATGGACATTTACTTGATGATTGTGGCCAATCCTGATGGATACGTCTTCTCCCACCTCACCGTCCGGGTAAGCTATCATTCACTTGTCGCATAGCACAGAAATAAAAGTTTCACAGTATTTCTAATGACATTACAAACTAATGACCCCTT[A/T]GCCGTTTCACCGTTTGTGGCGTAAGAGCCGGTCTGTGACCTCTAACCCAAACTGCCCTGGTGTCGACCTCAACAGAAACTTTGATGCTGAATTTAGTGGTACGTTCAACTTCATACTGATATTTTTGACACATTAGAAGGTATTTACAATACAATACAATTATGTAATTGGCAAAATCTTTTATGAAACACAGCTTGCATTGTGTTGAAGGTACACATTGTATCAGTTCTTTCATTCTCTGGGAACCAAACCCATAACATTTAAGGTGCTAGTGCCAAACTCTACTGTTTAAGCCAGGGATGGGCAAACTTGATCCTCAAGGGCCGGTGTCCCTGCAGAGTTTTGTTCCAACACTAGTCAAACACACCTGAACATGCTAATCAGTGTCTTTAAGATCACAAGAACTCTATAAGCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTGTGCAGGACACCGGCCCTCCAGGACCGAGTTTGCCCACCCCTGGTTTAAGCTAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30224

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:

G > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011397	Essential Splice Site	265	422	8	11

Genomic Location (Zv9):

Chromosome 25 (position 16952324)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16498868
GRCz11	25	16595268

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACTGCCCTGGTGTCGACCTCAACAGAAACTTTGATGCTGAATTTAGTG[G/C]TACGTTCAACTTCATACTGATATTTTTGACACATTAGAAGGTATTTACAA

Long Flanking Sequence:

GGCTTCAGCACTGACTAAACTAATGTATATGTATATGCACCCATATATTATTGTAAGATTTGTGAGGTGTGTACTTATATATCCTGAGCACTCTATTGCTGTGATTGGATGATTGTTCTGAGATTATTGGATAAAATCTACATAGCATGTACAACAGAGACTTTTTAAAATTCTGAACTGCTCTTCTTGTCCCTCCAGATTGCCACAGACTTTAAGGAAAACCGTGCTCTTGCTCGCAATGTCCTTAGTAAAATGGACATTTACTTGATGATTGTGGCCAATCCTGATGGATACGTCTTCTCCCACCTCACCGTCCGGGTAAGCTATCATTCACTTGTCGCATAGCACAGAAATAAAAGTTTCACAGTATTTCTAATGACATTACAAACTAATGACCCCTTAGCCGTTTCACCGTTTGTGGCGTAAGAGCCGGTCTGTGACCTCTAACCCAAACTGCCCTGGTGTCGACCTCAACAGAAACTTTGATGCTGAATTTAGTG[G/C]TACGTTCAACTTCATACTGATATTTTTGACACATTAGAAGGTATTTACAATACAATACAATTATGTAATTGGCAAAATCTTTTATGAAACACAGCTTGCATTGTGTTGAAGGTACACATTGTATCAGTTCTTTCATTCTCTGGGAACCAAACCCATAACATTTAAGGTGCTAGTGCCAAACTCTACTGTTTAAGCCAGGGATGGGCAAACTTGATCCTCAAGGGCCGGTGTCCCTGCAGAGTTTTGTTCCAACACTAGTCAAACACACCTGAACATGCTAATCAGTGTCTTTAAGATCACAAGAACTCTATAAGCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTGTGCAGGACACCGGCCCTCCAGGACCGAGTTTGCCCACCCCTGGTTTAAGCTAAAGGAGAGATTAAATTTGTTATTTAATTAATTATGACTGGCCTGCCGGTGTGCTTATTTGCCACAATTACAATCTATACTTAACCTGAACTAATTCTGACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44261

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011397	Essential Splice Site	361	422	10	11

Genomic Location (Zv9):

Chromosome 25 (position 16950070)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16496614
GRCz11	25	16593014

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTGGCATGGCACCATTTATAAAGTTGGAAGCATCTTCCACACTATTGG[T/A]AAGTGGACTGTGGAAGTGGACTGGTTTTTGACACATTTTAAGCATTTTCC

Long Flanking Sequence:

AACTTCTCTCCGTTTAACAGAAATTGGGGGGGGGGGATAAACAGGGGGGCTAATAATCCAGGGGGCTAATAATTCTGACTTCAATTGTACACTCAAAAATGGATGTGAAGGTTAACAGATGAACAATATCTCTCTTCAGGTCCTGGAGCCAGTGATGACCCATGTGCTGAAGACTATCGCGGCCCTTCTGCTCATTCAGAGATTGAAGTGACGAACATTGCGGATTTCATTTTGAGCCACGGCAACTTCAAATCCTTCATGACCCTCCATGCTTATTCTCAGCTTCTAATGTATCCCTACGGCTACACCGGCTCAAATGCTCCTGACCAGCCTGACCTTGTAAGCAAAATTTTAACCACAAACCTCTGGTTTTCCTCTCATTCTGCTGAATATCTCTTTGTATGTCTTTTCAAGCATGATGTGGCCACTCAGGCGAACAAAGCCCTCAATTCTTGGCATGGCACCATTTATAAAGTTGGAAGCATCTTCCACACTATTGG[T/A]AAGTGGACTGTGGAAGTGGACTGGTTTTTGACACATTTTAAGCATTTTCCATTAAACTGAAATGACCTGTAAATAGCTGTAATACAAAAGCACCTGTAAATCAAACATAAATAATGAACTGAAGCCATTATTAATGTTCAATAATTCTAAATGCTTAAATGTAAAAGAGAACATCTGATTCTGTGGTTTGTTAAACTTTTTAAACAGTGTTGATGATAACAGAGTTGACATACCCCACCATTTTGTGCACAAAATAAATTTTTTGAACACTGAAAATACAAATAATAGAAAATGTTTCATTTAAATCTTTTTTCAACTTGCTAGACACACAAAAAAGATGAAAATGAGACATAATGTTTCATAATTGAAGCTAAATGTATGATTCAGGAGGTGAAGACACAAAAAAAAGTTTAAGTGTTTAAGGTAACATTTTTTTCCATTACATTTATTAGCCTGAAATACACATACAAACATTTTTTTTTTGGAGATAACCTGATATA

Associated Phenotype:

Not determined