ZMP
ENSDARG00000095708
Ensembl ID:
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11718 | Nonsense | Available for shipment | Available now |
sa39019 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6361 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11718
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000137870 | Nonsense | 323 | 771 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 891521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 931824 |
GRCz11 | 15 | 892627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGAGAAAAGCGTTATACCTGCCTACAGTGTGGAAAGAGTTTCTCYTG[G/A]AATCGTCACCTTGCCATCCATATGAGGATTCACACTGGAGAAAAGCCTTA
Long Flanking Sequence:
ACAAAACACATGAGGATTCACACTGGAGAAAAACCTTACAATTGCCAACAGTGTGGAAAAAGTTTTTCTTGGAAACAATACCTTACAGACCATATGAGGACTCACACTGCTCACACTGCAGAAAAGCAACATACCTGCCACCAGTGTGGAAAAGGTTTCACTTGCAAACGAAACCTTTTAAATCATATGATTATTCACACAGGAGAAAAGCCTTACACTTGCCAACAATGTGGAAAGAGTTTCAATCGGAGGCAAAACTTAAAAGAACATGAGAAGATTCACAATGGAGAAAAACTTTACATTTGCCAACAGTGTGGAAAGAGTTTCGCTCGCAAACAATACCTTATAATCCATATGAGGATTCATACAGGAGAAAAGCCTTACAATTGCCAACAGTGTGGAAGGAGTTTTACCTATCAACAACACCTTACAGACCATATGAGGATGCTCCATGGAGAAAAGCGTTATACCTGCCTACAGTGTGGAAAGAGTTTCTCTTG[G/A]AATCGTCACCTTGCCATCCATATGAGGATTCACACTGGAGAAAAGCCTTACACTTGCCAGCAATGTGGAAAGAGTTTTAATCGGAGGCAAAACTTAAAAGAGCATATGAAGATTCATAATAGAGAAAAGCTTTACACTTGCCTACAGTGTGGAAAGAGTTTCACTTGGAAACAAAACCTTACAATCCATATGAGGATTCACACTGGAGTAAAGCCGTTCAATTGCCAACAGTGTGAAAAGAGTTTCACTTGTAAACAACACCTTACAGACCATGTGAGGATTCACACTGGAGAAAAGCCTTACACTTGCCAACAATGTGGAAAGACTTTCTCACGGAAACAATACCTTACACACCATATGAGGATTCACACTGGAGAAAAACGACACAACTGCCTACATTGTGGAAAGAGTTTCACTTGGAAACATCACCTTGTAACCCATATGAGGATTCACACTGAAAAAAAGCCTTACAATTGCAAACACTGTGGAAAGGGTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39019
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000137870 | Nonsense | 408 | 771 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 891774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 932077 |
GRCz11 | 15 | 892880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGTAAAGCCGTTCAATTGCCAACAGTGTGAAAAGAGTTTCACTTGT[A/T]AACAACACCTTACAGACCATGTGAGGATTCACACTGGAGAAAAGCCTTAC
Long Flanking Sequence:
AAAACTTAAAAGAACATGAGAAGATTCACAATGGAGAAAAACTTTACATTTGCCAACAGTGTGGAAAGAGTTTCGCTCGCAAACAATACCTTATAATCCATATGAGGATTCATACAGGAGAAAAGCCTTACAATTGCCAACAGTGTGGAAGGAGTTTTACCTATCAACAACACCTTACAGACCATATGAGGATGCTCCATGGAGAAAAGCGTTATACCTGCCTACAGTGTGGAAAGAGTTTCTCTTGGAATCGTCACCTTGCCATCCATATGAGGATTCACACTGGAGAAAAGCCTTACACTTGCCAGCAATGTGGAAAGAGTTTTAATCGGAGGCAAAACTTAAAAGAGCATATGAAGATTCATAATAGAGAAAAGCTTTACACTTGCCTACAGTGTGGAAAGAGTTTCACTTGGAAACAAAACCTTACAATCCATATGAGGATTCACACTGGAGTAAAGCCGTTCAATTGCCAACAGTGTGAAAAGAGTTTCACTTGT[A/T]AACAACACCTTACAGACCATGTGAGGATTCACACTGGAGAAAAGCCTTACACTTGCCAACAATGTGGAAAGACTTTCTCACGGAAACAATACCTTACACACCATATGAGGATTCACACTGGAGAAAAACGACACAACTGCCTACATTGTGGAAAGAGTTTCACTTGGAAACATCACCTTGTAACCCATATGAGGATTCACACTGAAAAAAAGCCTTACAATTGCAAACACTGTGGAAAGGGTTTTTCTTGTAAAGAATACCTTACAGACCATATGAAGATTCACACTGGAGAAAAACGATATAGCTGCCTACAGTGTGGAAAGGGTTTCACACGGAAACTAAACCTTACAAAACACATGAGGATTCACACTGGAGAAAAGCCTTCACTTGCCAACAGTGTGGAATAAGCTTTGCATGTACAAAATCCCTTAATACCCATGTGATGCGTCATACTGGATAGAAGCCTGACACCTGTGTTTTTGACAAAAAGTAAATCTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6361
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000137870 | Nonsense | 584 | 771 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 898519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 938822 |
GRCz11 | 15 | 899625 |
KASP Assay ID:
554-5352.1 (used for ordering genotyping assays)
KASP Sequence:
GCCAACAGYRTGGAAAGAGTTTCAATCRGAGACAAAACTTAAAAGAACAT[G/T]AGAAGATTCACAATGGAGAAAAGCCTTACACTTGCCAACAGTGTGGAAAG
Long Flanking Sequence:
ATCAGAACAAAGTAGAAGAGAAGGATCAGCATGAGGAATGTCTGGATTTCAGATCTAGAGAAAAATCAGAACAGACAAAGACCTCATCACAAACAACAGCCGAATCTTATACCTGCCACCAGTGTGGAAAGAGTTTCACACGGAAACAAAACCTTTCAGCCCATTTGAGGATTCACACTGGAGAAAAGCCTTACACTTGCCAACATTGTGGAAAGAGTTTTACACGGAAACAAAACCTTTCAGCCCATATGAAGATGCACAATGAAGAAAAACATAATATCTGCCTACATTGTGGAAAAAGTTTCACTTGGAAAAAAGACCTTACGATACATATGAGGATTCACACTGGAGAAAAGCCATTCAATTGCCAACAATGTGGAAAGAGTTTCAATCGGAGACAAAACTTGAAAGAACATGAGAAGATTCACAATGGAGAAAAGCCTTACACTTGCCAACAGCATGGAAAGAGTTTCAATCGGAGACAAAACTTAAAAGAACAT[G/T]AGAAGATTCACAATGGAGAAAAGCCTTACACTTGCCAACAGTGTGGAAAGAGTTTCGCTCGCAAACAATACCTTACAACCCATATGAGGATTCACACTGGAGAAAAGCCATTCAATTGCCAACATTGTGGAAAGAGTTTCACTTATAAACAACACCTTACAGACCATGTGAGGATTCACACTGGAGAAAAACCTTACACTTGTCAACAATGTGGAAAGAGTTTTAATCGGAGAGAAAACTTAAAAGAGCATATGAAGATTCATAACGGAGAAAAGCTTTACACTTGCCAACAGTGTGGAAAGAGTTTTACTTGGAAACAAAACTTTACAATCCATATGAGGATTCACACTGAAGAAACACCATTCAATTGCCAACATTGTGGAAAGAGTTTCACTTATAAACAACATCTTACAGACCATGTGAGGATTCACACTGGAGAAAAGCCTTACAATTGCCAACATTGTGAAAAGAGTTTCTCACGGAAACGATCCCTTAAAGAT
Associated Phenotype:
Not determined