ZMP
ENSDARG00000042698
Ensembl ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11109 | Nonsense | Available for shipment | Available now |
sa39277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11109
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 |
---|---|---|---|---|---|
ENSDART00000122414 | Nonsense | 168 | 370 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 23831888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23950689 |
GRCz11 | 20 | 23849789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACTTACCAAGACAAGACGCTAGACCAGTTTTTCCTCAATACACACAA[C/T]GTAAGTCTTAAGATGTGTTTTGGTTTTCACTACAGTKCAGTTGGAGGTTT
Long Flanking Sequence:
AATGGCTTTTTAATTGGTCGTTTTAGCTGGTCAACAGTGACCTTGCCCTTTTCATATTCTTGAAGCTAAAGTGTTGTTACTGTTTTGAGCAAGAAACTCTTTTTGCAAAAATACAATTTTAATTAAAGTGGATCAATGTTTTGTGACCAGATCAGATTTATGTTGTAATTTTGCTGATTTCTAATGGTGACTATTTTGACCAAGAATACAACTTAATTTAATCAACATAATAGGAGACGATGGTTTTTGTGTCAGGAAGGTCTAAGTAAAATGCATGTATTCAAATTGCAAGAATAAACGAACATACTAATTTGGCCCTCAAGCCAATGTCATTCCTCCTGGAAATCACTTGCTTGGGAAAGGTTTTAAAACCTGGTTAAGGTATGCTTTTCATTTCTAATGTGAAACCACCACTGACGATTTGTTATTTCTCAGCAGAAACACCAATGATCAACTTACCAAGACAAGACGCTAGACCAGTTTTTCCTCAATACACACAA[C/T]GTAAGTCTTAAGATGTGTTTTGGTTTTCACTACAGTGCAGTTGGAGGTTTTATTTTGTTATTTTCAGGCAACATGTTCCAGACAGGTCTTGACACCATTGCTAAGACGAATGATTACAATTATTTCAACAGCAAAGATAAATAAATAAAATACACAAAGACACTGACCAAGCAAATTAATATTCTATATTTAATATTCTAATTAATATTCTAAATATATATAAGCTGTCGCCTCATAGCAAGAAGGTCGCTGGTTCGAACCTCAGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCGCATGGGTTTCCTCGAGGTGCTCCAGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTAAATTGGGTAGTCCGTAGTGTATGAGAGAGTGTGTGTGTGGATGTTTCCCAGAGAAGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCACTGTGGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39277
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 |
---|---|---|---|---|---|
ENSDART00000122414 | Nonsense | 233 | 370 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 23830733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23949534 |
GRCz11 | 20 | 23848634 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTACCCAAATGAAGAGGTTGAGAGTCACAAGAACAGAGTGAAACTGT[T/A]AAATCAAAACACTCCAGGAAATCTGTCTCTGCTCATATCAGCACTGACCA
Long Flanking Sequence:
GTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATGGACTTGTATAAAAATTGGATAAAGAAGACAAAAAAATTTTTTCAAAACGTTTTGTCAACTTTTTGCCTTTTTTGTGGTCCAAATGTTTTCACATTTGACTTAGATTAGTAGCATAAATGATTTTTCACTATGGGTACTACAATGTTGATGTTGCAATAGGTTGAAATCTTTTTAACGCAGTTTAAACTGGTGTTATTTGTGTAAATTTGTCTTTAGAGTGTGATCTGGTCAATAAAGAAAGTAAAACTGGTGTGACTGGATATTCAGGAGAGTCTGTTGTTCTACCCTGCTGGTGCACTAACCTACTGTCCAGACCTGAACACATACAATGGATGTACTGGACAGAGAATGGCTATAAAGAAATTTACCCAAATGAAGAGGTTGAGAGTCACAAGAACAGAGTGAAACTGT[T/A]AAATCAAAACACTCCAGGAAATCTGTCTCTGCTCATATCAGCACTGACCATAAAACACCAAGGAACCTACTACTGTACTGTTCTGCCTCAACAACATGTCTACTTCACACTTAATGTTAAAGGTAATTTTCTTTGTGTTTTTATTTAATTTGACTATTTATTACATATTATAAAATATGTTTTGATAATACAAACATGTTTTACAGTGGTATTTATAGCTGAATATAACAGATTATTCTCCTCTCAACAGAGAAACCACAAGTTTATCCAACCAGTTCTTCAACACATAGATCTTCACACCAAACACAAGAACTTCCACCACCCCAACAAACACATCACACACCTCTGTGTAAGTCACAGGCTTGATTATCAACTGTGATGATTATGATTGTGTATTTTTCTCATGAACGTGTTACAGCATGTGTATTTCTCCACAGATGTTTTTATTCTAGTGGCAGTGTTTACTTCAGTTGTGTTACTGGCATTTCTGGCGTTGTCTA
Associated Phenotype:
Not determined