ZMP
ENSDARG00000089821
Ensembl ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18868 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9072 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18868
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 |
---|---|---|---|---|---|
ENSDART00000130347 | Nonsense | 148 | 648 | 5 | 19 |
ENSDART00000130347 | Nonsense | 148 | 648 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 20929159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19519595 |
GRCz11 | 7 | 19771563 |
KASP Assay ID:
2259-8646.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAAAGTGCAGTGCCGTCCTTTCCTCTGCAAGCAGCCCAGTCACAAAC[C/T]AATCAACAACAGTGAGTTAAACCAATCAGCCTGTTTATCTTATATGTGAG
Long Flanking Sequence:
AGCAGAGAGCATTTATGCAGATGACTTCAATATAAGCTGTTTTTACACTAACCAAAGACTTTTAGTCATGAAACTAGCAGGATGTTTTTCTAGCACAGTGATCTCTTATATATCAAAAAAGCAGGGGAATTTAGTTTTTCAGTTCATGACCCCTTTAATTTATTTGCTTTATTGAGCTGAAAAACACAAAATATGTTCTCTTAATGAGCACAAAATCTGTTCTCTCTATTACTGTGCATCTCTGTCTCTCAGACCTGGAGAGTAATGAAGAGACTCGGCTTAAAGCTAACATCAATGTGGTGTCACTGAAAGTGGGAAGTCTGGTGGACATTAATAAAGGTCTGTTGCACTGCTAAATATAATTTTAAAGCATTAACTTACCCATGCAAATCAGCTCAACTTCTCTATCTGTAGCATCTGCAATACAGAGCACCCAGAAACCAGTGCATTGTGCAAAGTGCAGTGCCGTCCTTTCCTCTGCAAGCAGCCCAGTCACAAAC[C/T]AATCAACAACAGTGAGTTAAACCAATCAGCCTGTTTATCTTATATGTGAGTGTTACTTGTGTTTAAAATGTAGGTTTTTGTCTCTCCAGCTGTGGTGCTGTGAGTTTTGTGGAAAGGAGAATGTTTTCCCCCAGTCTTCACTGAAAAGGGGCCGGTTTACCTCTCGCAGTCCTCCAGGCAGAGATGTGCTTTACATGGACGAGAAGGAAACAGACTACGAGAATCTGGATGATATGCTTATTGTCCTGTGTGTGGACATTTCCGGAAGCATGAGCGTCACTTCTGAGGTTCTGTTCTATTTACTTTATTGTCATTGTACGTCATGCAATACAGTTTTGTTTGGTGAATCTTAGGTTAATATAAACTAAAATGGAGTCAATCAACACAGAATAAATAACGAACAACAGTTGCCAAATACGACGCGGTGGCACAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGACCCTTGGCTGGGTCAGTTGGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9072
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 |
---|---|---|---|---|---|
ENSDART00000130347 | Nonsense | 148 | 648 | 5 | 19 |
ENSDART00000130347 | Nonsense | 148 | 648 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 20929159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19519595 |
GRCz11 | 7 | 19771563 |
KASP Assay ID:
2259-8646.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCAAAGTGCAGTGCCRTCCTTTCCTCTGCAAGCAGCCCAGTCACAAAC[C/T]AATCAACAACAGTGAGTTAAACCAATCAGCCTGTTTATCTKATATGTGAG
Long Flanking Sequence:
AGCAGAGAGCATTTATGCAGATGACTTCAATATAAGCTGTTTTTACACTAACCAAAGACTTTTAGTCATGAAACTAGCAGGATGTTTTTCTAGCACAGTGATCTCTTATATATCAAAAAAGCAGGGGAATTTAGTTTTTCAGTTCATGACCCCTTTAATTTATTTGCTTTATTGAGCTGAAAAACACAAAATATGTTCTCTTAATGAGCACAAAATCTGTTCTCTCTATTACTGTGCATCTCTGTCTCTCAGACCTGGAGAGTAATGAAGAGACTCGGCTTAAAGCTAACATCAATGTGGTGTCACTGAAAGTGGGAAGTCTGGTGGACATTAATAAAGGTCTGTTGCACTGCTAAATATAATTTTAAAGCATTAACTTACCCATGCAAATCAGCTCAACTTCTCTATCTGTAGCATCTGCAATACAGAGCACCCAGAAACCAGTGCATTGTGCAAAGTGCAGTGCCGTCCTTTCCTCTGCAAGCAGCCCAGTCACAAAC[C/T]AATCAACAACAGTGAGTTAAACCAATCAGCCTGTTTATCTTATATGTGAGTGTTACTTGTGTTTAAAATGTAGGTTTTTGTCTCTCCAGCTGTGGTGCTGTGAGTTTTGTGGAAAGGAGAATGTTTTCCCCCAGTCTTCACTGAAAAGGGGCCGGTTTACCTCTCGCAGTCCTCCAGGCAGAGATGTGCTTTACATGGACGAGAAGGAAACAGACTACGAGAATCTGGATGATATGCTTATTGTCCTGTGTGTGGACATTTCCGGAAGCATGAGCGTCACTTCTGAGGTTCTGTTCTATTTACTTTATTGTCATTGTACGTCATGCAATACAGTTTTGTTTGGTGAATCTTAGGTTAATATAAACTAAAATGGAGTCAATCAACACAGAATAAATAACGAACAACAGTTGCCAAATACGACGCGGTGGCACAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGACCCTTGGCTGGGTCAGTTGGCATT
Associated Phenotype:
Not determined