ZMP
ENSDARG00000074102
Ensembl ID:
Human Orthologues:
ERCC6, PGBD1, PGBD2, PGBD3, PGBD4
Human Descriptions:
excision repair cross-complementing rodent repair deficiency, complementation group 6 [Source:HGNC S
piggyBac transposable element derived 1 [Source:HGNC Symbol;Acc:19398]
piggyBac transposable element derived 2 [Source:HGNC Symbol;Acc:19399]
piggyBac transposable element derived 3 [Source:HGNC Symbol;Acc:19400]
piggyBac transposable element derived 4 [Source:HGNC Symbol;Acc:19401]
piggyBac transposable element derived 1 [Source:HGNC Symbol;Acc:19398]
piggyBac transposable element derived 2 [Source:HGNC Symbol;Acc:19399]
piggyBac transposable element derived 3 [Source:HGNC Symbol;Acc:19400]
piggyBac transposable element derived 4 [Source:HGNC Symbol;Acc:19401]
Mouse Orthologue:
Pgbd1
Mouse Description:
piggyBac transposable element derived 1 Gene [Source:MGI Symbol;Acc:MGI:2441675]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10426 | Nonsense | Available for shipment | Available now |
sa10493 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10426
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108759 | Nonsense | 301 | 495 | 6 | 7 |
ENSDART00000108759 | Nonsense | 301 | 495 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 28752511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 29506689 |
GRCz11 | 4 | 29461332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAAAGCGCAAGTCATCTCTGAATGGGCTGAGCWATGRGTCTGTCATG[G/T]SACTCAWAGATGAAAAKTATCTGGGCACTGGTYATAAGCTGTAYGTGGAC
Long Flanking Sequence:
ACATCTCAGTGGAAGACCTGAAGTCTTACCTGGCGCTTGTGATTTTCATGGGTCTCTTGAAGGTTTGTGCTTTGACAGACTATTGGAGGAGGTCTGACGTGTATAGTGTTCCCCTTTCTGCAAGGACCATGTCCTGTAGGAAGTTTCTGAACATCGCTAATGCTCTCCATCTTAGCGATCCTGAGGATGATGAAGCAAATGAAGGTAAGAAGGCAACCGCAGCCTATGACGGCTTGGGGGAGATCAAGCCTTTGTATGACAACATTAGGGATGCCTGCAGAGCGTTTTATCATCCTGGTCAAAACATCTAGATAAATGAAAGGATGGTGGCATCCAAGCTGAGGTCTGGACTCAAGCAGTACATGAAGAACAAACCCACTAAAAGGGGCTACAAGCTTTTTGTTTTGGCAGATTCCCAGTGTGGTTACACATCAGAGTTCTTTGTGTACGAAGGAAAGCGCAAGTCATCTCTGAATGGGCTGAGCTATGAGTCTGTCATG[G/T]GACTCATAGATGAAAAGTATCTGGGCACTGGTTATAAGCTGTATGTGGACAACTTTTACACCAGTCCCAAGCTTTTCAGAGACCTCCTCTCTAAAAGGATTTGGGTATGTGGCACCATTCGTCCAAACAGGATTGGTTTCTCAAAGATTGCCACCAATAAGCTGCCACAGGATGCTCCACGAGGGTCAATGCGATGTATCAGAGAGGACGACCTGCTGTTTGTGGAATGGAAAGACACCCGGGAAGTGCTTATATGCTCCACTTTCTACAAAGCATATGGAGGTGACATAGTGGAAAGGAAGATCAAGAACAAAGATGGGCAGTGATCTATTGTGCATGTGCCAATCCCTGGTGTTGTGCTGGACTTCAACAGGTTCATGGGGGGAGTGGACCTGTCAGATGCCCTCATTTGTTACTACAAAGTGCTTCACAAGACACGGAAGTGGTACCGAACCTTCTTTTACCACTTTGTAGACATTGCTGTTGTCAATGCCTTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10493
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108759 | Nonsense | 301 | 495 | 6 | 7 |
ENSDART00000108759 | Nonsense | 301 | 495 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 28752511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 29506689 |
GRCz11 | 4 | 29461332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAAAGCGCAAGTCATCTCTGAATGGGCTGAGCWATGRGTCTGTCATG[G/T]SACTCAWAGATGAAAAKTATCTGGGCACTGGTYATAAGCTGTAYGTGGAC
Long Flanking Sequence:
ACATCTCAGTGGAAGACCTGAAGTCTTACCTGGCGCTTGTGATTTTCATGGGTCTCTTGAAGGTTTGTGCTTTGACAGACTATTGGAGGAGGTCTGACGTGTATAGTGTTCCCCTTTCTGCAAGGACCATGTCCTGTAGGAAGTTTCTGAACATCGCTAATGCTCTCCATCTTAGCGATCCTGAGGATGATGAAGCAAATGAAGGTAAGAAGGCAACCGCAGCCTATGACGGCTTGGGGGAGATCAAGCCTTTGTATGACAACATTAGGGATGCCTGCAGAGCGTTTTATCATCCTGGTCAAAACATCTAGATAAATGAAAGGATGGTGGCATCCAAGCTGAGGTCTGGACTCAAGCAGTACATGAAGAACAAACCCACTAAAAGGGGCTACAAGCTTTTTGTTTTGGCAGATTCCCAGTGTGGTTACACATCAGAGTTCTTTGTGTACGAAGGAAAGCGCAAGTCATCTCTGAATGGGCTGAGCTATGAGTCTGTCATG[G/T]GACTCATAGATGAAAAGTATCTGGGCACTGGTTATAAGCTGTATGTGGACAACTTTTACACCAGTCCCAAGCTTTTCAGAGACCTCCTCTCTAAAAGGATTTGGGTATGTGGCACCATTCGTCCAAACAGGATTGGTTTCTCAAAGATTGCCACCAATAAGCTGCCACAGGATGCTCCACGAGGGTCAATGCGATGTATCAGAGAGGACGACCTGCTGTTTGTGGAATGGAAAGACACCCGGGAAGTGCTTATATGCTCCACTTTCTACAAAGCATATGGAGGTGACATAGTGGAAAGGAAGATCAAGAACAAAGATGGGCAGTGATCTATTGTGCATGTGCCAATCCCTGGTGTTGTGCTGGACTTCAACAGGTTCATGGGGGGAGTGGACCTGTCAGATGCCCTCATTTGTTACTACAAAGTGCTTCACAAGACACGGAAGTGGTACCGAACCTTCTTTTACCACTTTGTAGACATTGCTGTTGTCAATGCCTTCATT
Associated Phenotype:
Not determined