ZMP
ENSDARG00000076178
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 |
---|---|---|---|
sa44402 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44402
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108620 | Nonsense | 357 | 554 | 3 | 4 |
Genomic Location (Zv9):
Chromosome Zv9_NA260 (position 3208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149950.1 | 3208 |
GRCz11 | KN149950.1 | 3208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTCCAAACAGGATTGGTTTTCCAAAAATGGCCACCAATAAGCTGCCA[C/T]AGGATGCTCCACGAGGGTCAATGCGATGGATCAGAGAGGACGACCTGCTG
Long Flanking Sequence:
ATCTTAGCGATCCTGTGGATGACGAAGCAAATGAAGGCAGGAAGGGAACCGCAGCCTATGACCGCTTGGGGAAGATCAAGCCTTTGTATGACAACATCAGGGATGCCTGCAGAGCGTTTTATCATCCTGGTCAAAACATCTCCATAGATGAAAGGATGGTGGCATCCAAGGCGAGGTCTGGACTCAAGCAGTACATGAAGAACAAACCCACTAAATGGGGCTACAAGCTTTTTGTTTTGGCAGATTCCCAGTGTGGTTACACATCAGAGTTCTTTGTGTACGAAGGTAAGCGCATGTCATCGCCGAATGGGCTGAGCTATGAGTCTGTCATGGCACTCATAGATGAAAAGTATCTGGGCACTGGTTATAAGCTGTACGTGGACAACTTTTACACCAGTCCCAAGCTTTTCAGAGACCTCCTCTCTAAGAGGATTTATGCATGTGGCACCATCCGTCCAAACAGGATTGGTTTTCCAAAAATGGCCACCAATAAGCTGCCA[C/T]AGGATGCTCCACGAGGGTCAATGCGATGGATCAGAGAGGACGACCTGCTGTTTGTGGAATGGAAAGACACCAGGGAAGTGCTGATGTGCTCCACTTTCCACAAAGCATATGGAGGTGACATAGTGGAAAGGAAGAGCAAGGACAATGATGGGCAGTGGTCTACTGTGCATGTGCCAATCCCTGGTGCTGTGCTGGACTACAACAGGTTCATGGGGGGAGTGGACCTGTCAGATGCCCTCATTTGTTACTACAAAGTGCTTCACAAGACACGGAAGTGGTACCGAACCTTCTTTTATCACTTTGTCGACATCGCTGTTGTCAATGCCTTCATTTTGCATCAAAAACTGGCCAGAGCAAAGAAGGAAAGACCCCTGACCCAGAAAGCATTCAGGGAAACGCTTGTTATGGAACTTGCAGGTTTAGAATCAGGTGCTTCTCCAATCCCAACTCCATCTACCATCTGCCACAATCCCAAGTACATCTCGGGTGACAGCACTTCT
Associated Phenotype:
Not determined