ZMP
wu:fc49f05
Ensembl ID:
ZFIN IDs:
Description:
DNA cross-link repair 1A [Source:RefSeq peptide;Acc:NP_001018385]
Human Orthologue:
DCLRE1A
Human Description:
DNA cross-link repair 1A [Source:HGNC Symbol;Acc:17660]
Mouse Orthologue:
Dclre1a
Mouse Description:
DNA cross-link repair 1A, PSO2 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1930042]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11323 | Nonsense | Available for shipment | Available now |
sa8485 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12063 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11323
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075876 | Nonsense | 461 | 904 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32108910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30390015 |
GRCz11 | 12 | 30504917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATGGCTCCTAGGAGGACTCAGATAAAGGCAGGTCCCTCTGGATTKAAA[C/T]AAACAGACATTGGGGTGTTTTTTGGCCTGAAGCCGCTRCATGAAAAAAAG
Long Flanking Sequence:
TTCCAGAAGTGGATGAGGAGCACAGGGTGGAAAAATCCAATAATGACAGACATTTTTATAGTACTGCATTGCAGGAGGATGATGATTCTCTTAATCTTTTCAGTGATGAAGATGATGATCTGTTCTTTGATGTGATAGACCAGTATGAGGAACATGGGCCAGACAAAAGCTCATTAGACACCTGTGAGAAACAGCAAACATCATTAGCACCAGAAAGTCACCTGACTGCTTCCAGTTCCACAGGTGTTTCATTTCATCACTGCTCAACAAACAACAACAGTTCAAACTCCCAGCTACAGTCACCCCAAAGCTTGGTATTAGAGCATCTTCGGGACCGCATATCTACTCCTACACATGTCAAGAGCTTGACTTCATCTTTTGAGGAAGTTAACTTCACTCAAACAAACCAAGAGTCGTTTTCCAACCAAGCAGATCTATCCGCAACACAGTCTATGGCTCCTAGGAGGACTCAGATAAAGGCAGGTCCCTCTGGATTGAAA[C/T]AAACAGACATTGGGGTGTTTTTTGGCCTGAAGCCGCTGCATGAAAAAAAGGCTGGGAAGGAAGTAAAGCCATTGGTCAGAGAGGCCGATCTGCAAAAGTCTAGAAGAGTGAGGGTTTCAGAAGCTCAAGGGGAAGACGGTAAGCGTCAGGGTAGATGGCGTGGGAAGAGCAAAGCACCATCTGAAGGGTCCGGTGTCTCGCCTGCTGTAGAAGATAGTGTGGCTCTGCCCACGCAAACAGAAGGAAAGAGAGGAGGGAGGGCAGAGGGGCGGAAAAGATGGAACAGAGGAAAAGCGACAGATGGAGATCCCAAGGAGCCCAAACGCTGTCCATTCTACAAGAAAATTCCTGGTTTGTGAATGCTTTTTTTGACCTACTTAGAAACAATTGTTATGATTGCATAAGCGGGTATACTAGTAGCTGTACCCGAACTTAAATGTACTTTTAATCTTCTTTTATTATAATAATTCCTCTATTATTATTTAGTTTGTGGGACAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8485
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075876 | Nonsense | 757 | 904 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32102205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30396720 |
GRCz11 | 12 | 30511622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RTTTTATTTTTTNACTCTCTCACCTGTTTTTYTAGCTGTATCAGAAGTGT[T/A]GAGCTCTAAAGTATGTTTGTCCAAGGATAAGTATAACACCATGTGCTGCC
Long Flanking Sequence:
GTACTCCGTTGGGAAAGAGAAGGTCTTTCTAGGTGAGAAAGCAACGTTGTCCTGCTTTGTCCAGGCCTTGTGCTACTTTATTCGCTCTTGAAAGGACAGATTGTTCGCTTTTCTATTAACCGTGACCATCATGAATGAGCCTCCTATAAAACAAGTGTTTACAGAAGAGGTTTGCAGATGATGTCCTAGCTTGACTTTGAGATGACGTTCCTCTTTAATAGTTTGTCTTACAGGCTTATTGTTCTTTTTATAAATTACATCTATGATTAATGTCCTACGCCCATTTATTTCTACAAGCTCTGATCACATAATATCCTGCTCTGGGCCATTTCCTCAGTTTACAACTAATGTGTGATTTCTGTTGGCTGTCTTACTGAGTTGCAACTTCTTTCCAAATCCCAGTTACCAATTTTCATTCATTTTTTGTGACTATAGAGATGTACTCATTTTATTTTATTTTTTTACTCTCTCACCTGTTTTTCTAGCTGTATCAGAAGTGT[T/A]GAGCTCTAAAGTATGTTTGTCCAAGGATAAGTATAACACCATGTGCTGCCTGGAGTCTGAGGATATTGGCCAGCGCATCACTACGAATTGGCAGTCTGCCCAAGTGCATGTGCTTCCTATGATGCAGATCAATTTCAAAGTGAGTTAAACCGCACATAAAACTTCTGTGACTATAATTCTGCTCTAAATTACGAAATGCAGTTTTCCCCCGTTTGAGTTCATAGGTGTATAAAAATAGCCGATTATGCTAAACACAATCAATGAAGCTGTGTTTACTTATTCAATTTGGACTTTAAAATTCATACAGCGTTCAGTGTTATCTTTAATTTTCCTTGACAGCGCGTTTATGCTAATGCCAGAGGAAAAAAATACGATTCTAATTACAGAGACCAAGTGCCAACGCAGCAATTCTGGCACCGGTAGCACTGATTGAGTCAGCGTGACTGAAAGTACATTCTAATGAGACAGTCGCAGATAATAAAGATCAGCCATTTGATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12063
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 |
---|---|---|---|---|---|
ENSDART00000075876 | Essential Splice Site | 803 | 904 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32102064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30396861 |
GRCz11 | 12 | 30511763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTCTGCCCAAGTGCAWGTGCTTCCTATGATGCAGATCAATTTCAAAG[T/C]GAGTTAAACCGCACATAAAACTTCTGTGACTATAATTCTGCTCTAAATTA
Long Flanking Sequence:
TCCTATAAAACAAGTGTTTACAGAAGAGGTTTGCAGATGATGTCCTAGCTTGACTTTGAGATGACGTTCCTCTTTAATAGTTTGTCTTACAGGCTTATTGTTCTTTTTATAAATTACATCTATGATTAATGTCCTACGCCCATTTATTTCTACAAGCTCTGATCACATAATATCCTGCTCTGGGCCATTTCCTCAGTTTACAACTAATGTGTGATTTCTGTTGGCTGTCTTACTGAGTTGCAACTTCTTTCCAAATCCCAGTTACCAATTTTCATTCATTTTTTGTGACTATAGAGATGTACTCATTTTATTTTATTTTTTTACTCTCTCACCTGTTTTTCTAGCTGTATCAGAAGTGTTGAGCTCTAAAGTATGTTTGTCCAAGGATAAGTATAACACCATGTGCTGCCTGGAGTCTGAGGATATTGGCCAGCGCATCACTACGAATTGGCAGTCTGCCCAAGTGCATGTGCTTCCTATGATGCAGATCAATTTCAAAG[T/C]GAGTTAAACCGCACATAAAACTTCTGTGACTATAATTCTGCTCTAAATTACGAAATGCAGTTTTCCCCCGTTTGAGTTCATAGGTGTATAAAAATAGCCGATTATGCTAAACACAATCAATGAAGCTGTGTTTACTTATTCAATTTGGACTTTAAAATTCATACAGCGTTCAGTGTTATCTTTAATTTTCCTTGACAGCGCGTTTATGCTAATGCCAGAGGAAAAAAATACGATTCTAATTACAGAGACCAAGTGCCAACGCAGCAATTCTGGCACCGGTAGCACTGATTGAGTCAGCGTGACTGAAAGTACATTCTAATGAGACAGTCGCAGATAATAAAGATCAGCCATTTGATGTGGCCTAAACCATTATAAGCAACTTTTCTCACCCATGACAATGTGGATGTTGATTCAAAAGCAATTTCAAAGCTGTTCCCAATGAGAGAAGTGTTTAAATGGTTATGACAGGAAGAGGAGAAAATATAAAAAGGTTAATTGTA
Associated Phenotype:
Not determined