ZMP
pex14
Ensembl ID:
ZFIN ID:
Human Orthologue:
PEX14
Human Description:
peroxisomal biogenesis factor 14 [Source:HGNC Symbol;Acc:8856]
Mouse Orthologue:
Pex14
Mouse Description:
peroxisomal biogenesis factor 14 Gene [Source:MGI Symbol;Acc:MGI:1927868]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13868 | Essential Splice Site | Available for shipment | Available now |
sa14078 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13868
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078171 | Essential Splice Site | 191 | 377 | 7 | 9 |
ENSDART00000134121 | Essential Splice Site | 237 | 423 | 8 | 10 |
ENSDART00000078171 | Essential Splice Site | 191 | 377 | 7 | 9 |
ENSDART00000134121 | Essential Splice Site | 237 | 423 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 29148417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28978984 |
GRCz11 | 23 | 28905525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACAGAAGAAAATACAGGAGCTGACACAAGAGCTGGCTAACTCACAGG[T/C]ACGCACACACACATTYGMCACAATGGACACATTGAYGAAAATTCTGTCAT
Long Flanking Sequence:
GAAAATGAGCTGTATTTAGTAAGATTAGTGAGGACAGAAGCGTCTAGCCCTCCTGCCTCCCAAATGAGCGGCTTTTTTTCCATCTTGTTGATTGTTTGGAGAGTTTGATAGAGCCGGCGTTTCAAAGCCATGCTAATGGAGGTTAAGAGACCCTGATTTGATATAAGAGCAGACGTAGGTGATTAATCTTCTACAAATAGAGGTGTCTTATATTACTGATTGAGCTAAAGGCTAAATCAAAGAGAAAACCGCTGCATGTTGATCGTCGGTAATGCTCTCAGACAAACAGATGTGTCCGTTCGCACTGCGTATGGACTCGAGCTGCTGCTTTTCTTGCTTGTGAACTTCTGGTAACTGTTTTGGGTGTAGTCTTACCTTCATTTGTGTGTTTTTGGATGCAGTCACCCAGCTGCAGATGACCCTGGCTTCGGTGCAGGAGCTGCTGGTCCAACAACAGAAGAAAATACAGGAGCTGACACAAGAGCTGGCTAACTCACAGG[T/C]ACGCACACACACATTTGCCACAATGGACACATTGATGAAAATTCTGTCATTAAATACTCGTTCCATGTCGTTTCAAACCAATATTTTTTTTTTTGGAACATTATATTTTTTTGGGTTTTTAGATTTTTCATACACACACATACTGTCCTATACATGCCCCAAACCTTTATAGTGCCACAAATAAATTTAAACAAGTAAACATAAATAAGTCAGGTTCTATCTACAGTAAGCATTCTGTCCTGTTACACTCAAGTTAGAAATAAAGCTGCCCCAGCATTTGACAAACAAATCTTGACACTTTTTTTTTTTTTCAAACGAAATGATATTTTTCCAAAGGCATATAAGATGACACTTCTTTAATCCACATGGAAGTAAAAGGTGGTTTTGAATCCTTCCATCTCAAAGATGAATGTATTTTATGGCTGTTAGGAGGGCTAGTCTGACAAATCTCAGATTAATTCTTTGTTGATCAAGTAGTGCAGTATCTCCTAGGAGGGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14078
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078171 | Essential Splice Site | 191 | 377 | 7 | 9 |
ENSDART00000134121 | Essential Splice Site | 237 | 423 | 8 | 10 |
ENSDART00000078171 | Essential Splice Site | 191 | 377 | 7 | 9 |
ENSDART00000134121 | Essential Splice Site | 237 | 423 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 29148417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28978984 |
GRCz11 | 23 | 28905525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACAGAAGAAAATACAGGAGCTGACACAAGAGCTGGCTAACTCACAGG[T/C]ACGCACACACACATTYGMCACAATGGACACATTGAYGAAAATTCTGTCAT
Long Flanking Sequence:
GAAAATGAGCTGTATTTAGTAAGATTAGTGAGGACAGAAGCGTCTAGCCCTCCTGCCTCCCAAATGAGCGGCTTTTTTTCCATCTTGTTGATTGTTTGGAGAGTTTGATAGAGCCGGCGTTTCAAAGCCATGCTAATGGAGGTTAAGAGACCCTGATTTGATATAAGAGCAGACGTAGGTGATTAATCTTCTACAAATAGAGGTGTCTTATATTACTGATTGAGCTAAAGGCTAAATCAAAGAGAAAACCGCTGCATGTTGATCGTCGGTAATGCTCTCAGACAAACAGATGTGTCCGTTCGCACTGCGTATGGACTCGAGCTGCTGCTTTTCTTGCTTGTGAACTTCTGGTAACTGTTTTGGGTGTAGTCTTACCTTCATTTGTGTGTTTTTGGATGCAGTCACCCAGCTGCAGATGACCCTGGCTTCGGTGCAGGAGCTGCTGGTCCAACAACAGAAGAAAATACAGGAGCTGACACAAGAGCTGGCTAACTCACAGG[T/C]ACGCACACACACATTTGCCACAATGGACACATTGATGAAAATTCTGTCATTAAATACTCGTTCCATGTCGTTTCAAACCAATATTTTTTTTTTTGGAACATTATATTTTTTTGGGTTTTTAGATTTTTCATACACACACATACTGTCCTATACATGCCCCAAACCTTTATAGTGCCACAAATAAATTTAAACAAGTAAACATAAATAAGTCAGGTTCTATCTACAGTAAGCATTCTGTCCTGTTACACTCAAGTTAGAAATAAAGCTGCCCCAGCATTTGACAAACAAATCTTGACACTTTTTTTTTTTTTCAAACGAAATGATATTTTTCCAAAGGCATATAAGATGACACTTCTTTAATCCACATGGAAGTAAAAGGTGGTTTTGAATCCTTCCATCTCAAAGATGAATGTATTTTATGGCTGTTAGGAGGGCTAGTCTGACAAATCTCAGATTAATTCTTTGTTGATCAAGTAGTGCAGTATCTCCTAGGAGGGTAC
Associated Phenotype:
Not determined