ZMP
pdia2
Ensembl ID:
ZFIN ID:
Description:
protein disulfide isomerase family A, member 2 [Source:RefSeq peptide;Acc:NP_957342]
Human Orthologue:
PDIA2
Human Description:
protein disulfide isomerase family A, member 2 [Source:HGNC Symbol;Acc:14180]
Mouse Orthologue:
Pdia2
Mouse Description:
protein disulfide isomerase associated 2 Gene [Source:MGI Symbol;Acc:MGI:1916441]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19434 | Nonsense | Available for shipment | Available now |
sa31193 | Essential Splice Site | Available for shipment | Available now |
sa32599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10302 | Nonsense | Available for shipment | Available now |
sa12819 | Nonsense | Available for shipment | Available now |
sa13027 | Nonsense | Available for shipment | Available now |
sa15452 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19434
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 138 | 555 | 2 | 11 |
ENSDART00000130181 | Nonsense | 119 | 518 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9034576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9274381 |
GRCz11 | 1 | 9958492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTGCCTCAGAGTTCAGTGTGGACAGTTTTCCCACTCTCAAATTCTTC[A/T]AAGAAGGAAACAGACAAAATGCCACTACTTTCTTTGGTAAAGTGTCTATT
Long Flanking Sequence:
CCTAAAGCACAATATTTCATTGGTTTATCAATTTTTATTGCATTAGTGACACACTAACATATCTGGCCCAGTTCAGGCTCAGTAATGGCTAATCAACTTGGCTGAGACTTGACCCAGATATGGTCCATGTTTGTGTCTTGTCTGGAAGCCAGACTTGGTTGAGTTTTGATTCATGTACTGTGATTCACTACAGCATGTGGGCCAAAAAGCTAATTGTGTGGGCCAGAGATTTTTTGCTATGAGGGATATATCCTAGATCTTTGTCTGTTAGCCTTTAATACACATGAAATGTTTTTCTGAACATTGCACTTTTCTTTTAACCCTAAAAAGATGCTCCATGGTGTGGACACTGTCGCAGTCTGGAGCCCATTTATGCTGAAGTGGCTGGACAGCTGAAAAATGCATCATCTGAAGTACGACTGGCCAAAGTAGACGCGATAGAAGAGAAAGAGCTTGCCTCAGAGTTCAGTGTGGACAGTTTTCCCACTCTCAAATTCTTC[A/T]AAGAAGGAAACAGACAAAATGCCACTACTTTCTTTGGTAAAGTGTCTATTTGTGTGATGCTGTCGAATGTGTGGTGTCCCTTTAATAAAGTGATACAATCTATAGGCTTAATTCTTTGATTTGAACAGGAAAGCGAACTCTGAAAGGGATCAAAAGGTGGCTGGAGAAGCACACAGCGCCCAGCGCTACTGTCCTCAATGATGTGAAGAGCGCAGAGGCTCTGCTGGAGGCCAATGAAGTGCTTGTGGTCGGATTCTTCAAGGTAAATCATATGTATTTGCATGAAGTAACTAACGTTAAAGAGTCAACACTGCCTTGTTCTAATATATAGCATGCAATAAAAAAAATAAAATAATGACAAACTATTTCAGATTCACTAATTGTTGCAAAATAATTTTTTCCATCCACTCAGAATTAGTCATTGAAAAACTAATGGTTTATAGTCTGAATAGCACATAAGTCTATGCTACAGTCACAGAAACAAATAAGTATACAGAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31193
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Essential Splice Site | 195 | 555 | 4 | 11 |
ENSDART00000130181 | Essential Splice Site | 176 | 518 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9035729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9275534 |
GRCz11 | 1 | 9959645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGAATCATGCAGTAGTTGAGTTCAATTTAATTATCTCCCTCTGCCCC[A/G]GGATTTGGAAGGAGAAAAGGCGAAGACATTCTATGATGTAACTTTAATTG
Long Flanking Sequence:
GTTGGTTTTTGGTAATGTTCAATCAAAATCTAACCGTTTGTTTCCACTGTTTAATGGCAGTCAGTCTATGATGATGTCACTTTGATGTCTTGGGCAAAATATGCTTAGCCACGCCCCTTCAATCGTTAGTTTGATGCAAGTAAAACCCACCTATTAATATTCATAATATTTCAGTTGAAAATACTTTATCATATTGAATTAAAAGTGTGCAATGTCCAATTCAAGCAATCTGGATCTTTTTGTACAAATATGTACCTCTGAATCTGAGAGTGATCAAAATACAGTAGCTTAAATCACCTTTTGAAAGTAACTTCACAAGTCAAATGAAAATTGTATCAGTTGCATCATTAAGCCAGTAGGTGGCGACAAGTAGCTACATTAAAAATGCATAATGAATCTTACCCGATCGATTCAAGAATCAATTTAGAATTTCTCTCAAATCTCAACTGATCCAGAATCATGCAGTAGTTGAGTTCAATTTAATTATCTCCCTCTGCCCC[A/G]GGATTTGGAAGGAGAAAAGGCGAAGACATTCTATGATGTAACTTTAATTGCAGTGGACGTTAACTTTGGCATCACAAGCGACCCAGAGCTCTTCAAGAAGTATGAAGTGAAGACTGATTCGCTGGTGCTCTTCAAAAAGGTAACTCAAAGCTTCATTTTAACTGTATTAATCATATTTCATTTTTAACCTTAAAGGAATAATACACCAAAATATGAAATTCACTTGTCACAAACAGTGCCTTGTGAAGTGCCTTTTCTCTATTCAACACAAAAGAAGATATTTTGAGGAATGCTGAAAACCAGCAACTAATGGCATCCATAGTGAAAAGTTTGAGGAAACATAACTATTTTGATTTTAGTAACTAGTTTAGAGGCTAGTTCATATGTATTCAGTCGTGTGAAAATGTATGATTTAAAAAAAAAATGTGTGGCACCAAACCCGACCCCTAACCCCAACCGTCATTAGGGGATGAGCAAATCATACTAAATTGTATGAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32599
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 473 | 555 | 9 | 11 |
ENSDART00000130181 | Nonsense | 454 | 518 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9038544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9278349 |
GRCz11 | 1 | 9962460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTGCCAAAATGGACGCCACAGAAAATGATGTGGAAGATCTGACAATA[C/T]AGGGATTTCCCACAATTAAATACTTTCCTGCTGGGACCGAAAAAAAGGTT
Long Flanking Sequence:
AATGAATGCTACTTTTCTAATTACCACAATTAATATTTTATAGTTACAAATTATCACAATCACAATTATTTGGATTAATCTCTATCATTTGGTTGCTTGAGTAATTATGCATTCTCTCACATCATATTACACGCATAAGAGTGATGGGCCGATGATAAAGAAATTTTTCTTTCACAGAGGTAATCTGTCATCAAACTATGATGTCAAACTGAGACAAAATGTAAAACAAACCAGTTTTGCAGCTCACCTTCCATAAATAGCAGATGTTTTGAGTGACTTGCAGACATTTTAATTAGTGAACTCCTTACAGCAATAGATGAAAACAAATTTGTCTTCACACACTTTTAACATTTATGTTTCTCACAGATGCTCCATGGTGTGGTCACTGTCAACAACTTGCTCCTGTGTGGGATGAGCTAGGCGAGAAGTACAAAGACCAAGAGAATATAATCATTGCCAAAATGGACGCCACAGAAAATGATGTGGAAGATCTGACAATA[C/T]AGGGATTTCCCACAATTAAATACTTTCCTGCTGGGACCGAAAAAAAGGTTTGCAATAACACACTTAGCCTAACCTAAACTTAATCCAAACCCACATACAAATACAAAGACACAGGTATCTTTAAGGTGACTTCTCATAGACGTATTGATTTTTATACTGTTCAAACTGTATCTACCCCCCTACCCCAACCCTAGCCCTAAACCTTATCCTCAGAAAAACAATCTCTATTTTTTTCATTTTCAAAATTCATTCTGTGTGATTTATGATTCATTTTCCTCATGGGGACCAAAATAATAAATATATTCCACACAAGGCAAAAATATGCTGGTATTGCTATACTTGTAGGGACATTTATTTAGAATACAACATACAAACACACACACAAGGTACACAAAAACACATACACAATATTAAATTTATAAATGTATGTTGCAACCCAGGCTCATTATGAGTACGTACCCCTGTATACATTTCTAGAGAGCGCAAAATACATCCCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10302
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 496 | 555 | 10 | 11 |
ENSDART00000130181 | Nonsense | 477 | 518 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9040403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9280208 |
GRCz11 | 1 | 9964319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTSGAAATAATGNAWTTTTTTTTAAAACAGATTGTTGACTRTGATGGAAAT[A/T]GAGATTTGGAGAYTTTCTCAAAGTTCCTGGAWAATGGAGGAGTTTTACCR
Long Flanking Sequence:
TTAAACATTAGGTGTGCAGGTTACATTGTAACTCTGTGTCCTAACAATACGCTACATGATGAGATTTGCAGTAATAAGCAGTTTGGCTTTTTGCACCAGAAATTTAAATACAGCCATTCAGAAGCACAGAATAGTGCACTTACTGCACTTCAACAGAAGGGTAAGACTTATAATCTAATTAATACATATTAAACCCCTTTAGCTTTATGAAATGTACATGCTGAATCAATGATATGTAATGTCATCAATCTGGCAACCTGCACTCGCGTGTGTTTTAACCAGGCGTGCAATACTTAGTTCAACCACTGGGTGTCAAACTTACATAATGCAACTTTAAAGACGAAATGCAGCCCTATGAGCCTCTGACTACATAATTCACAATCGGCAGAAATGTATATAGGGGTACACATTCACAATGAGCCAGTGTTGGTATTTTAGGTAGGTTTAGGTTTCGAAATAATGATTTTTTTTTAAAACAGATTGTTGACTATGATGGAAAT[A/T]GAGATTTGGAGACTTTCTCAAAGTTCCTGGATAATGGAGGAGTTTTACCAAAAGAAGAGAGTAAAGAAGATGAAGATGATGATGATGACGACAATGATGATGATGATGAAGATAAGGTCAGTCAAAAGCCAACCGGTCAAAAGCCAGTTATTCACTTGATTATTTAGCCTCTTATTAGTAATTAACTACTTATTAATATTTATTGAGTTGATTAAATCAGCTTTTGTGTTTCTTTCTAATTTTTTAGCCAACAGACGAATCAAAAGAAGAGTCACCAAAAGCCACCAATGAAACCGACAAGGATGAGCTGTAAAAACAAGGCTTAAATCAAGCGATCAATGTGATGTTTTTATGCAACATGAGCAAGATTGATGTCATTTTCTCTGCACTAGACAATTTGTATAAACTACAAACCTGACAAAATATAATAAAAAAACACAAGTTTATTTATATCTCTGGTGCATTGCTTTAATGACATGTTAAACATTAGTGATGACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12819
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9040681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9280486 |
GRCz11 | 1 | 9964597 |
KASP Assay ID:
2259-0224.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTTTCTAATTTTTTAGYCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAKCCACCAATGAAACCGACAAGGATGAGCTGTDAAAACAAGGCTTAAAT
Long Flanking Sequence:
CCAGGCGTGCAATACTTAGTTCAACCACTGGGTGTCAAACTTACATAATGCAACTTTAAAGACGAAATGCAGCCCTATGAGCCTCTGACTACATAATTCACAATCGGCAGAAATGTATATAGGGGTACACATTCACAATGAGCCAGTGTTGGTATTTTAGGTAGGTTTAGGTTTCGAAATAATGATTTTTTTTTAAAACAGATTGTTGACTATGATGGAAATAGAGATTTGGAGACTTTCTCAAAGTTCCTGGATAATGGAGGAGTTTTACCAAAAGAAGAGAGTAAAGAAGATGAAGATGATGATGATGACGACAATGATGATGATGATGAAGATAAGGTCAGTCAAAAGCCAACCGGTCAAAAGCCAGTTATTCACTTGATTATTTAGCCTCTTATTAGTAATTAACTACTTATTAATATTTATTGAGTTGATTAAATCAGCTTTTGTGTTTCTTTCTAATTTTTTAGCCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAGCCACCAATGAAACCGACAAGGATGAGCTGTAAAAACAAGGCTTAAATCAAGCGATCAATGTGATGTTTTTATGCAACATGAGCAAGATTGATGTCATTTTCTCTGCACTAGACAATTTGTATAAACTACAAACCTGACAAAATATAATAAAAAAACACAAGTTTATTTATATCTCTGGTGCATTGCTTTAATGACATGTTAAACATTAGTGATGACTAATTTGATTGATAAAGTATAAACAGCTCAATCATTTTGAGCTATTTTGCAAATAATATTTTCAATTATGCACACATTCGCTCTTATTTGTATGTCTAACAGGAAGATTTTTAAATGTCCTCATATTCAGTTGGGAATTGCATTTATCACATAGCTTATGCCATATTTTAGTTGTTTTTGATTACTGGATATTATTATTGTTATCTTTGTAATTTATAAAATGTTTTCTGTTTCACTGAAGTCATGATTAAGTCAAAACTGACACTATTTTGTTAGACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13027
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9040681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9280486 |
GRCz11 | 1 | 9964597 |
KASP Assay ID:
2259-0224.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTTTCTAATTTTTTAGYCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAKCCACCAATGAAACCGACAAGGATGAGCTGTDAAAACAAGGCTTAAAT
Long Flanking Sequence:
CCAGGCGTGCAATACTTAGTTCAACCACTGGGTGTCAAACTTACATAATGCAACTTTAAAGACGAAATGCAGCCCTATGAGCCTCTGACTACATAATTCACAATCGGCAGAAATGTATATAGGGGTACACATTCACAATGAGCCAGTGTTGGTATTTTAGGTAGGTTTAGGTTTCGAAATAATGATTTTTTTTTAAAACAGATTGTTGACTATGATGGAAATAGAGATTTGGAGACTTTCTCAAAGTTCCTGGATAATGGAGGAGTTTTACCAAAAGAAGAGAGTAAAGAAGATGAAGATGATGATGATGACGACAATGATGATGATGATGAAGATAAGGTCAGTCAAAAGCCAACCGGTCAAAAGCCAGTTATTCACTTGATTATTTAGCCTCTTATTAGTAATTAACTACTTATTAATATTTATTGAGTTGATTAAATCAGCTTTTGTGTTTCTTTCTAATTTTTTAGCCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAGCCACCAATGAAACCGACAAGGATGAGCTGTAAAAACAAGGCTTAAATCAAGCGATCAATGTGATGTTTTTATGCAACATGAGCAAGATTGATGTCATTTTCTCTGCACTAGACAATTTGTATAAACTACAAACCTGACAAAATATAATAAAAAAACACAAGTTTATTTATATCTCTGGTGCATTGCTTTAATGACATGTTAAACATTAGTGATGACTAATTTGATTGATAAAGTATAAACAGCTCAATCATTTTGAGCTATTTTGCAAATAATATTTTCAATTATGCACACATTCGCTCTTATTTGTATGTCTAACAGGAAGATTTTTAAATGTCCTCATATTCAGTTGGGAATTGCATTTATCACATAGCTTATGCCATATTTTAGTTGTTTTTGATTACTGGATATTATTATTGTTATCTTTGTAATTTATAAAATGTTTTCTGTTTCACTGAAGTCATGATTAAGTCAAAACTGACACTATTTTGTTAGACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15452
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
ENSDART00000005895 | Nonsense | 545 | 555 | 11 | 11 |
ENSDART00000130181 | Nonsense | 508 | 518 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 9040681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9280486 |
GRCz11 | 1 | 9964597 |
KASP Assay ID:
2259-0224.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTTTCTAATTTTTTAGYCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAKCCACCAATGAAACCGACAAGGATGAGCTGTRAAAACAAGGCTTAAAT
Long Flanking Sequence:
CCAGGCGTGCAATACTTAGTTCAACCACTGGGTGTCAAACTTACATAATGCAACTTTAAAGACGAAATGCAGCCCTATGAGCCTCTGACTACATAATTCACAATCGGCAGAAATGTATATAGGGGTACACATTCACAATGAGCCAGTGTTGGTATTTTAGGTAGGTTTAGGTTTCGAAATAATGATTTTTTTTTAAAACAGATTGTTGACTATGATGGAAATAGAGATTTGGAGACTTTCTCAAAGTTCCTGGATAATGGAGGAGTTTTACCAAAAGAAGAGAGTAAAGAAGATGAAGATGATGATGATGACGACAATGATGATGATGATGAAGATAAGGTCAGTCAAAAGCCAACCGGTCAAAAGCCAGTTATTCACTTGATTATTTAGCCTCTTATTAGTAATTAACTACTTATTAATATTTATTGAGTTGATTAAATCAGCTTTTGTGTTTCTTTCTAATTTTTTAGCCAACAGACGAATCAAAAGAAGAGTCACCA[A/T]AAGCCACCAATGAAACCGACAAGGATGAGCTGTAAAAACAAGGCTTAAATCAAGCGATCAATGTGATGTTTTTATGCAACATGAGCAAGATTGATGTCATTTTCTCTGCACTAGACAATTTGTATAAACTACAAACCTGACAAAATATAATAAAAAAACACAAGTTTATTTATATCTCTGGTGCATTGCTTTAATGACATGTTAAACATTAGTGATGACTAATTTGATTGATAAAGTATAAACAGCTCAATCATTTTGAGCTATTTTGCAAATAATATTTTCAATTATGCACACATTCGCTCTTATTTGTATGTCTAACAGGAAGATTTTTAAATGTCCTCATATTCAGTTGGGAATTGCATTTATCACATAGCTTATGCCATATTTTAGTTGTTTTTGATTACTGGATATTATTATTGTTATCTTTGTAATTTATAAAATGTTTTCTGTTTCACTGAAGTCATGATTAAGTCAAAACTGACACTATTTTGTTAGACCAC
Associated Phenotype:
Not determined