ZMP

pdia5

Ensembl ID:

ENSDARG00000069242

ZFIN ID:

ZDB-GENE-030521-5

Description:

protein disulfide-isomerase A5 [Source:RefSeq peptide;Acc:NP_001107048]

Human Orthologue:

PDIA5

Human Description:

protein disulfide isomerase family A, member 5 [Source:HGNC Symbol;Acc:24811]

Mouse Orthologue:

Pdia5

Mouse Description:

protein disulfide isomerase associated 5 Gene [Source:MGI Symbol;Acc:MGI:1919849]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7634	Missense	Mutation detected in F1 DNA	Not yet available
sa41480	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7634

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100592	Missense	193	528	8	17
ENSDART00000122797	Missense	206	541	8	17

Genomic Location (Zv9):

Chromosome 9 (position 38846906)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	37984802
GRCz11	9	37794597

KASP Assay ID:

554-4309.1 (used for ordering genotyping assays)

KASP Sequence:

GAATTACTAATGTTACTTTTACATCTCTTCTACTTGTAGGGTGTGGAGTA[T/A]GTAAAAGGATGCAGCCCATTTTCCAACAAGCAGCCACAGAGACTAAAGGA

Long Flanking Sequence:

TAATGTCAAGCCCTGCTTAAGTCTATTCAACTGAATACATTGAAATTACATTACAACATCGATGCTGTAAAAGCAGCCTTGTTTATTTGAAAGTACATTATAATTTACTGAAAAACACTAACTGTGTATACAGCCGATTAAATTTTGTGTTTATTTAGCAATTGCTATGGGGATTTCTGGGTTTCTTCTTCTGCATATTTGTAGTTTCTGTTTGACAGTGCTCTCTGGGCTTCGGAAAGAGATTCAATCCCAAAACCAAGATTATCTGACAAGATATATATGAGTCACAACTTTTGCCTACATAAAGATTTTGATTTCATTTCGATTTGTAGTGAAGCCTTAGTTCAGGGTGGACACACATTGATTCACTTTCTGTTGCTGATTGGTCTGGAAGTGAAATCTGTGTGATTTATACATTACACTTCACTTTTTTCTCACCAAGTTTAGACAGAATTACTAATGTTACTTTTACATCTCTTCTACTTGTAGGGTGTGGAGTA[T/A]GTAAAAGGATGCAGCCCATTTTCCAACAAGCAGCCACAGAGACTAAAGGAAAATATGTAAGTACAGTAGCATGTTAGACCCTCTCTTTTCTACTTTTCAATTATATCTGGTACAGTTGTTGAATTACTTAACAGGTGGGATGTTTTGCAAAACCATTGATGTCCCTTTTTCGACAAAATGTTTAGTTCCCCCTCATTAGAGCGAGAGCCAATTTTGCTTAAAAGCCCTTTTGCTGATTTCATAGTACAGTTATAGGATGCAGTTCCTGCTGTTGAGGTCTGTGGTGAAGTATGGATTAAATGCCAGCTCAGCTCAATATCTCTATGTGCACTGCTGGGAGACCCACAGTACACTTGACCACACATTTTCTCTCCCTCAGTACTTCACTTTTTTTGATCTCCCACTCTCTCTTTCTCCACTGCCCATCTCAGAATGTTCACAGAAGCACAAATATAGACGCTTTCATTCAAACTCATCTAAATCTAAACTGAATGTATTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41480

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
ENSDART00000100592	Nonsense	431	528	14	17
ENSDART00000122797	Nonsense	444	541	14	17

Genomic Location (Zv9):

Chromosome 9 (position 38872618)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	38010514
GRCz11	9	37820309

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GATTTCAGGGAATCGCTGAAAAAGAAGAAACACGCCTTGGTCATGTTTTA[T/A]GCTCCATGTAAGCCTTCTGTTTTTTCTAAAATACTGCAGCTGTAGTTTAT

Long Flanking Sequence:

GCCTAAGCATAGTTTAAAACTTGCGTCTGAGCTGAGATTTTTTTTAATATAGAGTGAAGATGACCATTTAACTGAAACTGTTAATTAAAGGTAATGATCTAGGTAATGGTGTCTGGATAGTTACTTATTGTTGTTTTATTTTTATCTTTATTTTAATAATTATTTTAAGTAATGTAAATTCTGTGGCTTAAATATTTTTTAAACCATCCAGTTTTGATGAATTTATACGCAACAGCTTTTAATCACTATATTAACCTGATAATTTGAATGTATTATTATCTAGAAACCAAACATGATGTAATTGTTGCAGTTCCAGATATCTCCTTCCCAGCGGCTCACCTATTATCTCACAGGCTCTCTTTCTCTCTTGCTCTCAGTCCCCAGGCTCCACCTCCTCCAGAAAAGTCATGGGATGAGATGCCGTCCAGCGTGAGCCACCTGGGAGCCGAAGATTTCAGGGAATCGCTGAAAAAGAAGAAACACGCCTTGGTCATGTTTTA[T/A]GCTCCATGTAAGCCTTCTGTTTTTTCTAAAATACTGCAGCTGTAGTTTATGTCTCAAAGCACGTATCCAGGCTCCTATCAATCCTTTAGTCAGAGTTATAGGCAAATGAGTCCAAATTTTAGTGCATTCTCCTAAAGCAACATGTGCGACAGCAATTATTTGAAGCTCTGAAATGTGCAGGTGGCGTAACATCTGCTTAATGGCACCGTAGCTTCCTGCATATAATGTTTTATTTCAATGGTTTAAGTAGGCATCAACAGTTAAATATGATGTATGCATATCTTTACAATTCTGAACCATTACAAATGTTTACCATAAAGAAACAAAAGGAGATTAATTATTGGTGTCTTTTAATAGTCAGTTGCTATTTGTGAAATGCAATTCTTTTCAATTCACCTTAGTTATATAGTGCTTTTTGTATTACATATTGTTCCAGACTAGCTTTACAAAGAATAGGGCCCTAACAAAGACTCTTAATGAACAAGACAAAGGTAGCTGCT

Associated Phenotype:

Not determined