Busch Lab

ZMP

pex13

Ensembl ID:
ENSDARG00000071037
ZFIN ID:
ZDB-GENE-040426-1544
Description:
peroxisome biogenesis factor 13 [Source:RefSeq peptide;Acc:NP_956939]
Human Orthologue:
PEX13
Human Description:
peroxisomal biogenesis factor 13 [Source:HGNC Symbol;Acc:8855]
Mouse Orthologue:
Pex13
Mouse Description:
peroxisomal biogenesis factor 13 Gene [Source:MGI Symbol;Acc:MGI:1919379]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa42928 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16520 Nonsense Available for shipment Available now
sa42929 Nonsense Mutation detected in F1 DNA Not yet available
sa15170 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa42928
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000021177 Essential Splice Site 24 416 1 4
Genomic Location (Zv9):
Chromosome 17 (position 23755160)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 23908602
GRCz11 17 23927003
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGGGAAAGGCGAATCCCAGGAACCATAACAGCACCGTTAAACTATCG[G/A]TTTGTAAAAACTCGTTGTATTTTGCCCAGTATTTACAAATGTAGCAACGC
Long Flanking Sequence:
TTTTAAATTAAACGTCTATGACAAGAATTACAGAAATCGCTACTTACCAGTGTTGAATCTACAGCAGTTACATTGTCACGAATTTACTGTGAAATATACAGCACATACATTCGTAAGTTACTTGGTGAGAACAATAAGCAGCATTTTTTGTTTTAGCCAATTTTGGTGGCATATCTTCTGACATGCATTGTACTGAATTTATAACCGCACATCACACAGGCTATGCTTGGTAAATAGTTTACGATTATATAGCCAAGCCAGCCTTCAAGTACTTCACAATCGATTCAGTGGTTGATTGTTTTAGTCTCGTGTAGCCAGCCAGTAAGAGCGATGTGAATGATCGATTGCTCTAGTCTGGCGAATGGGATACTGTACGTGTTAACGGTTGTTGCTCAGTGCAGCTCGACTTTGGCCTGAAATATAAAAATAATGGCTCAGCCTCCTCCAAAACCATGGGAAAGGCGAATCCCAGGAACCATAACAGCACCGTTAAACTATCG[G/A]TTTGTAAAAACTCGTTGTATTTTGCCCAGTATTTACAAATGTAGCAACGCTAGCAAACACTTAGCCACCTAACACACAACATACAAATCTTACTAACGATATTTTTGTAAGTTTTACTTACTTTGGTTTTACTACAGTGCTGATAAATATACCGCTAGGTTATCATGACATTTGTACCCGAGCGTTAGTGTGTTTCATAAACTTGATATTTGGCTCGTGTACGAGCACGTCAGTGTTTGCATGTGAGTGTCAAAGTTCACTCCAACATACCCATGCTGTGTTCTGTCATATACTTTTAAACAGGGGTGGGCGAAATTGGGGTAAATTTGACTTTCTCATCAATAATATAAATTCAGAAAAACATTCCTTTAAATTCTAAATAGTGATATTATATTAGCAGCCAATGACTATCAAAGAACATTGTTCACAGTCAAATAAATAGTGCTTGAGTTGTTTCAAAGTCATACCTGCATGAAATTGCAGACCGAATATTCAAAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16520
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000021177 Nonsense 58 416 2 4
Genomic Location (Zv9):
Chromosome 17 (position 23757835)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 23911277
GRCz11 17 23929678
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCAGTTCTAACACGAGTGGTGCCACCGATTCCTCCACGAYCTGTTCGA[C/T]AGTCATACCGCCCRACATACAGCTCGTTTCCCTCCTCGTACAGCCCTTAT
Long Flanking Sequence:
AAGAGGCCTTAGTCATATCTCCACAGTCTGCCACCAATGGCTGATCTCGCTTCTCCGTAGTTGTGACACAAAAATACATGTCCAAATCTAGAGGGGAGCCGAGCTTTTTGACACGGGGGCACTGGCTCCAGTTCAAAATATCTTTTTACTACATTTATGAAATGTAATGGTAAAAGTAAAAAGTACTATGGTTTGGAATGTAGCAAAGTAAAAGTTGCCTAAATACAAATACTCTGATAATGATAAAATGTACTTAAATGTGGAGAACTTAAATAAAATATTGTCACCGTCCATGATTGCTTTTAAATAAAGAACATTTGTCAACTTTTTTCTTATTTTTGTTTAGTTTTTTACCATTTACACTTTTCATTTGACTGACTTTTTGTTTTCTTTTATCAAGCTCTACGGACTTTGGATCAGTATCCCAAAGTGGGCCATCAGGTTCTGGTCCTCCAGTTCTAACACGAGTGGTGCCACCGATTCCTCCACGACCTGTTCGA[C/T]AGTCATACCGCCCAACATACAGCTCGTTTCCCTCCTCGTACAGCCCTTATGGGAACTCCATGTATGGTGGCTACAGCCCCTACAGCTACAGTGGTTATGGAGTCGGAGGCGGCCTGGGATATAACCGATTCAACACAATGGACGAAATCCCACCCAGTCGTTTTGTCCAACAGGCCGAGGAGAGCAGCCGCGGAGCATTTCAGTCTATTGAGAGCATCGTCCATGCATTTTCATCAGTCAGCATGATGATGGATGCTACTTTCTCTGCCGTCTACAACAGCTTCCGAGCTGTTCTGGATGTGGCCAATCACTTCTCCCGCTTACGCATACATTTCACAAAAGTGCTGTCAGCTTTTGCCCTGGTTAGGACTCTTCGATATCTGTATCGCAGGCTGCAGAGGCTGATGGGATTGCGTCAGGGTTCAGAGGTGGATGATTTGTGGGCAGACAGCGCAGCCTCTTCTTCAGTGGTGTCTGCTTCAGGAGCCAGAGGTGCAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42929
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
ENSDART00000021177 Nonsense 184 416 2 4
Genomic Location (Zv9):
Chromosome 17 (position 23758215)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 23911657
GRCz11 17 23930058
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTCACAAAAGTGCTGTCAGCTTTTGCCCTGGTTAGGACTCTTCGATA[T/A]CTGTATCGCAGGCTGCAGAGGCTGATGGGATTGCGTCAGGGTTCAGAGGT
Long Flanking Sequence:
TTTTGTTTTCTTTTATCAAGCTCTACGGACTTTGGATCAGTATCCCAAAGTGGGCCATCAGGTTCTGGTCCTCCAGTTCTAACACGAGTGGTGCCACCGATTCCTCCACGACCTGTTCGACAGTCATACCGCCCAACATACAGCTCGTTTCCCTCCTCGTACAGCCCTTATGGGAACTCCATGTATGGTGGCTACAGCCCCTACAGCTACAGTGGTTATGGAGTCGGAGGCGGCCTGGGATATAACCGATTCAACACAATGGACGAAATCCCACCCAGTCGTTTTGTCCAACAGGCCGAGGAGAGCAGCCGCGGAGCATTTCAGTCTATTGAGAGCATCGTCCATGCATTTTCATCAGTCAGCATGATGATGGATGCTACTTTCTCTGCCGTCTACAACAGCTTCCGAGCTGTTCTGGATGTGGCCAATCACTTCTCCCGCTTACGCATACATTTCACAAAAGTGCTGTCAGCTTTTGCCCTGGTTAGGACTCTTCGATA[T/A]CTGTATCGCAGGCTGCAGAGGCTGATGGGATTGCGTCAGGGTTCAGAGGTGGATGATTTGTGGGCAGACAGCGCAGCCTCTTCTTCAGTGGTGTCTGCTTCAGGAGCCAGAGGTGCAGGGGTTGAAGAACCCGGAGTGAATTCTGTCAAATCATGGCCTATTTTCTTGTTTTTTGCTGTTGTTCTCGGAGGGCCGTATTTAATCTGGAGGCTTTTAAGTTCTGCTGAGGGTGCTGAGGAAAATGGTGAGACTTTTATCCACTTGCTGTAGTTTGTTCTCATTCTAGTCTTACACCTTGACTGTCCTTCTTGTGATAAACTGGTCTGACATGAGAGCTAAAGATGCGTTTAAACTTTGACTCAATAACAAAACTTCCAGACAATTTTTATAACTGCTGTTTTTGTTTTAACATGGGGCCATTAATGAGAAGGATTTTACTCTAACATTCAGATTCAGAAGAGTTGGGTATTCTTTTAAATAAAAGTATACATTTATTTACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15170
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000021177 Essential Splice Site 307 416 4 4
Genomic Location (Zv9):
Chromosome 17 (position 23761768)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 23915210
GRCz11 17 23933611
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTAAGCGCTGACCTACACCRKGTACTCACTGTTGTTCACTCTCRTTTTC[A/T]GAACAACAGCCMCGGGTGCGTGGCTGGCTGTTAGCCAGTGTGGATGGRCA
Long Flanking Sequence:
TGCGAGAGCGTGAATGTGTGTTTCCCAGTGCTTGGTTGTTGCTGGATAGGCATTCGCTGTGTAAAACCTATTCCTGAATAGTGGTGGTTCATTCCGCTTTGGCCACCCTTGATAAATATAAGACTATCAATGAATGAGTGAATGAATTATATATTTTAATGCTGCAAAGTACTTTCTTTTACATTGTAATAATTAAAAATGTTTTTGATATGTTATTTCCTTATAGTTATTAATAACTTTAATGTCATGTGTTTTGTAAATAATAGAAAGAATAAATACAGTAGTTTTTGCAGTGTTAAAGAGAACCCTGACATTTTACTCTGGTATTTTTCCAACTACAAAAATGTTGGTACCTTGTCAACACTAATAGCGAGTTAATAAAAGAATAGAAATGGAAAACAAAACAACTAAATAAAAATAGCTCTGTGTCACTAATGTCAAGTATTATGTCCTAAGCGCTGACCTACACCATGTACTCACTGTTGTTCACTCTCATTTTC[A/T]GAACAACAGCCACGGGTGCGTGGCTGGCTGTTAGCCAGTGTGGATGGGCAAACTACCGGCCTCGTCCCTGCCAACTACGTCAAAGTGTTGGGCCGAAGGAGAGGCAGAAAGCATGCTGAATTAGAGAGGATGGCACAGGCCCAGGAGCCTGCACAGAACCTTCCAGCACCTCAAACGGCCCTCATTACAGCTTCTGTCCCAACGACAACACATTCAGAGGATCTGCTGGAGTCCGTTTATGGGGAAACACAAGGCCTTGGACTGGAGGTGCAAGCATCCACACACAACAGCCGTGATACTTTAGTGATGCATTCAGAAAAGATGGACTTATGAGTAATCGATATGTGCAGGTGGTGGGTGTTTCTGTAGGGAAAATGTCTTCTTTGTTTTTTGAATGTATCACCCTTGATATAATTCAGTTCAACCACAAAAAGTGAAGAGGAGCTAATGAAAATACTGAGGTGTTGAAGAGAAGGTGAATAATGCTTTAATGGGTTAGT
Associated Phenotype:
Not determined