ZMP
pdia4
Ensembl ID:
ZFIN ID:
Description:
protein disulfide-isomerase A4 [Source:RefSeq peptide;Acc:NP_956073]
Human Orthologue:
PDIA4
Human Description:
protein disulfide isomerase family A, member 4 [Source:HGNC Symbol;Acc:30167]
Mouse Orthologue:
Pdia4
Mouse Description:
protein disulfide isomerase associated 4 Gene [Source:MGI Symbol;Acc:MGI:104864]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13170 | Nonsense | Available for shipment | Available now |
sa44116 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37857 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13170
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018868 | Nonsense | 98 | 642 | 3 | 10 |
ENSDART00000081851 | None | None | 228 | None | 4 |
ENSDART00000018868 | Nonsense | 98 | 642 | 3 | 10 |
ENSDART00000081851 | None | None | 228 | None | 4 |
The following transcripts of ENSDARG00000018491 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17884682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17191158 |
GRCz11 | 24 | 17335577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTACACTTTTTCAGGTGTGGCCACTGCAAACAGTTTGCTCCCGAGTA[T/G]GAAAAGATCGCTCAGACGCWGAAGGAAAATGACCYACCTATTCCAGTGGC
Long Flanking Sequence:
CACTTTTAGCTAGCTTGGTGCATTGTTGCTGTTTAGGGCTACACTGGAGGTTAAACAGCGTTCTGTGGTGATCATACATGCAACGTGCACACAATAATGATTCATTTTGTTATGATACCTAAGAAAACTATCAAGGAACAACAGGAAATTCAAATTTATTAGCTTGATGCATTTCCTATTTGTTCATGAATAAATTTGTTGTTTAGATTCAGCAGAAGATCTGGGAGAAGAGGAAGATGATGATGATGACGACGATGATGAGGATGCAGATGACACTGAAGTAAAGGAAGAGAATGGGGTGCTAGTCCTGACAGATGCAAACTTTGACACCTTCATCGAGGGCAAAGACACCGTATTGGTGGAGTTTTATGCACCATGGTAGGTTTTCTTTATTTGGCATGAGTTGGACACATACAGTATCATTGCCTGACAAAGATCTTGTCCATGCAAATATTACACTTTTTCAGGTGTGGCCACTGCAAACAGTTTGCTCCCGAGTA[T/G]GAAAAGATCGCTCAGACGCTGAAGGAAAATGACCCACCTATTCCAGTGGCAAAGGTTGATGCCACTAAAGCCAGTGGTTTGGGCAGCAGGTTCGAAGTTTCTGGATATCCCACCATCAAAATACTTAAAAAGGGAGAGCCCCTGGACTATGATGGGGATCGGAGTGAGCATGGTGAGTTAGAGAACTTCCTTTAGCTTGCTCTGAATTTAAACTGATTATGTTTCCTGGTCTATTGTTTAGCGATCATGATTTTAACTTTCATTTTTTACAGCCATCGTGGAACGGGTTAAAGAAGTTGCCCAACCAGACTGGAAACCTCCTCCAGAGGCTACTCTAGTCTTGACTAAAGACAATTTTGATGATGTGGTGAACAATGCTGACATCATTCTGGTGGAGTTTTATGCACCCTGGTTTGTATATTTACTTATACCTGCTTATATTCATATATAAACGTGTTTATTCTCACAGCGACTAGGGCTGGGCGATATTGCAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44116
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018868 | Nonsense | 98 | 642 | 3 | 10 |
ENSDART00000081851 | None | None | 228 | None | 4 |
ENSDART00000018868 | Nonsense | 98 | 642 | 3 | 10 |
ENSDART00000081851 | None | None | 228 | None | 4 |
The following transcripts of ENSDARG00000018491 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17884682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17191158 |
GRCz11 | 24 | 17335577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTACACTTTTTCAGGTGTGGCCACTGCAAACAGTTTGCTCCCGAGTA[T/A]GAAAAGATCGCTCAGACGCTGAAGGAAAATGACCCACCTATTCCAGTGGC
Long Flanking Sequence:
CACTTTTAGCTAGCTTGGTGCATTGTTGCTGTTTAGGGCTACACTGGAGGTTAAACAGCGTTCTGTGGTGATCATACATGCAACGTGCACACAATAATGATTCATTTTGTTATGATACCTAAGAAAACTATCAAGGAACAACAGGAAATTCAAATTTATTAGCTTGATGCATTTCCTATTTGTTCATGAATAAATTTGTTGTTTAGATTCAGCAGAAGATCTGGGAGAAGAGGAAGATGATGATGATGACGACGATGATGAGGATGCAGATGACACTGAAGTAAAGGAAGAGAATGGGGTGCTAGTCCTGACAGATGCAAACTTTGACACCTTCATCGAGGGCAAAGACACCGTATTGGTGGAGTTTTATGCACCATGGTAGGTTTTCTTTATTTGGCATGAGTTGGACACATACAGTATCATTGCCTGACAAAGATCTTGTCCATGCAAATATTACACTTTTTCAGGTGTGGCCACTGCAAACAGTTTGCTCCCGAGTA[T/A]GAAAAGATCGCTCAGACGCTGAAGGAAAATGACCCACCTATTCCAGTGGCAAAGGTTGATGCCACTAAAGCCAGTGGTTTGGGCAGCAGGTTCGAAGTTTCTGGATATCCCACCATCAAAATACTTAAAAAGGGAGAGCCCCTGGACTATGATGGGGATCGGAGTGAGCATGGTGAGTTAGAGAACTTCCTTTAGCTTGCTCTGAATTTAAACTGATTATGTTTCCTGGTCTATTGTTTAGCGATCATGATTTTAACTTTCATTTTTTACAGCCATCGTGGAACGGGTTAAAGAAGTTGCCCAACCAGACTGGAAACCTCCTCCAGAGGCTACTCTAGTCTTGACTAAAGACAATTTTGATGATGTGGTGAACAATGCTGACATCATTCTGGTGGAGTTTTATGCACCCTGGTTTGTATATTTACTTATACCTGCTTATATTCATATATAAACGTGTTTATTCTCACAGCGACTAGGGCTGGGCGATATTGCAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37857
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018868 | Nonsense | 206 | 642 | 5 | 10 |
ENSDART00000081851 | None | None | 228 | None | 4 |
The following transcripts of ENSDARG00000018491 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17886504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17192980 |
GRCz11 | 24 | 17337399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACTTTTTTGAAAGTACTGCGTTTACATTTAAACAGGTGTGGACACTG[T/A]AAGAGACTTGCACCTGAATATGAAAAGGCTGCTAAAGAGCTCAGCAACCG
Long Flanking Sequence:
GAAGCAGATTGAGATTCATGCAAGTAGAACAAACCAGTGCACTTGCGGCATTTGAAAAAGTTCAGGTGGTTTTCAAATTGGGTGTACCTGGAAAATGCGCACCAATTTATTGGCATTGCTTCTAAGGCACATGTTCAGCAGCCCCATTTAAATTAAACTATATAGCCTTCATACCGAAACTTCATACCAATTTCTTTTTTTATCGATATTGACAATGGTGTTCGGTCAATAAATACTGATATTTTATCGCCCAGCCCAACTGTGACATTTGCTTACGAGTTAAAAAAAAAAAAGTTGAGTGTGCTGCATTTGCTGGAAATGTTTTCTTTGGCAAACTGTTTCGAACTGCTAAAACTCCAAACAGATTTATTTTGCCATTACTAAAAAAAAAAAAAAAAGTCTTTATTTTGCTTTATTCAGTATCTTTGCTTTTCTCTCTGAAGCATCAGTTTAACTTTTTTGAAAGTACTGCGTTTACATTTAAACAGGTGTGGACACTG[T/A]AAGAGACTTGCACCTGAATATGAAAAGGCTGCTAAAGAGCTCAGCAACCGCACTCCTCCTATTCCACTGGCTAAAGTGGATGCCACTGCAGAAAGTGATTTAGCAACACGGTTTGGTGTTTCTGGCTACCCAACTCTCAAAATCTTCAGAAAGGGAAAGGCTTTTGACTACAATGGACCCCGGGAGAAGTTTGGTAGGTTACTGTCAAATTGTCTTCGTGACCAATTAGTGTATTTTCAGAAATGTCCAACTTTTCCCTCTTTTTCCTTTAGGTATTGTTGATTACATGTCAGACCAGGCTGGTCCTCCATCAAAGCAGGTCCAGACCCTGAAACAGGTTCAGGAGCTGCTCAGGGATGGAGATGATGCTGTTATTGTTGGCGTTTTCTCCAGCGATGAAGATGCAGCGTATGAGATCTATCAAGAAGCATGTGTGTATTATGCTGCCTGGACGTAATTCTTTTTTAATGATTTATTTATTTACTTTTTTTTCAAACCCT
Associated Phenotype:
Not determined