ZMP
LOC100150489
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 is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23578 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23578
Status:
Available for shipment
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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 |
---|---|---|---|---|---|
ENSDART00000110925 | Nonsense | 285 | 374 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 41101009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 40553547 |
GRCz11 | 19 | 40140667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGGCTCCTCTATCGCCGTCATCTCACCCAGAAGCAGGAGAAGAAGTA[T/A]ATGCCACTTCTTGACTTCCGTGTTCAAGTTGCAGATGCCCTCATCAAGGT
Long Flanking Sequence:
TGCTTTTTCAACAACTGGTTCCCTTCCCCTGAACTCATTGTAGTACTGAAGAAAATGGTAATTTTAACAGTTGCTACCATCAATCGTAACCGTCTCCGTGGATGTACCCTCAAGAGTGATAAGGAACTCTCAAAGGCCGGGTGTGGTGCGTATGAAGTGAAATACGAAAAGACAAGTGGGATGTCCATCATGAAGTGGTATGATAACAAGGCAGTGTTGCTGGCATCATCCTTCATCGGCCCTGAACCTGTTGAGAGATGCAGAAGGTGGTCGAAAGAGAAGAAGGAATATGTGGAAGTGGACAGACCCCACATTGTCAAGGTGTACAACCACAACATGGGAGGAGTAGACTTAGCAGACAAGTTTGCAGCTCTCTATCGCACTGACTTCCGCCCACGTCGTTGGTATCTGCGCATCTTGTACTACTTGATTGACCTATCACTGGTCAATGGTTGGCTCCTCTATCGCCGTCATCTCACCCAGAAGCAGGAGAAGAAGTA[T/A]ATGCCACTTCTTGACTTCCGTGTTCAAGTTGCAGATGCCCTCATCAAGGTTGGCAAACAGGTTGACTTGAACAGTAGGAAAAGAGTACGACCTTCATTGGAAGATGATCCAACGTCCCATCAAGCTGCCTCACCTCCACTTCAGAGGATCTCTGCACCATCGGTTGATGTCAGATTAGACCGATGCGATCATTTCCCCATCCATGCTGAGAAACGTGGACGATGCAGACTGTGCAAGAATGGCTACACGCAAATGGCCTGCCTGAAGTGCAAAGTACTTCTGTGCTTTACAAAAGACAAAAACTGTTTCTTGGAGTACCACATGACAAAGTGACTTGTAAACATGGCCTACTCAATGAGGATTTAAGATATTGGATTTGGATCCCATATTGTTTTTGTTGTTGTTCTGCCACTGAAAAGCAATTTGTTACATTGTTTGAAAAGTTGTATGTAAAAAGTTATTGTTCATATCATATTCAGTAGTCAGTGTCTAATTACCAC
Associated Phenotype:
Not determined