ZMP
ENSDARG00000086485
Ensembl ID:
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12552 | Nonsense | Available for shipment | Available now |
sa13087 | Nonsense | Available for shipment | Available now |
sa12541 | Nonsense | Available for shipment | Available now |
sa19074 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44800 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12552
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 2651176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2356021 |
GRCz11 | 14 | 2274372 |
KASP Assay ID:
2260-7161.1 (used for ordering genotyping assays)
KASP Sequence:
TTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTWTGATT[T/A]GCAATTGATTGCAGWAGATGGCGGAAAACCTGCCAAATCAGGCACAATGA
Long Flanking Sequence:
TGCTGTGGGAAATATTGGGAAGGATTTGGGTATTGATCCCAGAACCCTTAAAGAGCGAGGATTTCGCATCGTCTCAACCTCAGGCGAGTCAATGTTCATTGTGAACCAGAATGACGGAGTACTGTATGTGAACGGTAAGATAGACCGAGAGGAGGTCTGCGAGAGAAGCACGCCGTGTTTAATAAATGTGAAAATAGCATTAGAAAATCCTCTTGAAATACATTATGTGACTGTTGAGATTCTGGATGTGAACGATCACGCTCCGAGTTTTCCTGAAAGCGAGATGCATTTAGAAATAGGGGAATCTGCCCTGCCCGGTGCGAGATTTCAGCTTCAGGCTGCACGCGATTCTGATAGCGGCAGTAATTCAGTGCATCATTACAAACTCAGTCATAATGATAATTTCCGACTTGAAGTCAAAGATCGAGGAGAAGATGGTAAAATTCCTATTTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTTTGATT[T/A]GCAATTGATTGCAGTAGATGGCGGAAAACCTGCCAAATCAGGCACAATGACCATAACGATTAGTGTTTTGGATATAAATGATAATTTCCCAGTGTTTACAAAAGACGCATACTCGGTCATGCTGAGTGAAAATGCGCCTATCGGTACTACTGTGATTCGGGTCAACGCGACAGACTCAGATGAGGGCCCGAACGGCGAGATAGTTTATTCATTTGGAAAAAGTGTTAGTAGTAAAGTGCAAAAGTTGTTTAATATTGACACCATCACTGGGGAAATAACTGTAAAAGGACTATTAGATTATGAGGACAAAGACAGATATGAAATTGATATACAAGCATCAGACAAGGGATTAATCCCCCTGATTACAGATAAAACTGTGACCATAAAGATAGTTGATGTAAATGATAATGCACCTGAAATTGAGGTGACATCCTTATCCAACTCCATTCCAGAGGACTCCAGACCTGGCACTACAGTGGCTTTAATTAGTGTCTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13087
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 2651176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2356021 |
GRCz11 | 14 | 2274372 |
KASP Assay ID:
2260-7161.1 (used for ordering genotyping assays)
KASP Sequence:
TTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTWTGATT[T/A]GCAATTGATTGCAGWAGATGGCGGAAAACCTGCCAAATCAGGCACAATGA
Long Flanking Sequence:
TGCTGTGGGAAATATTGGGAAGGATTTGGGTATTGATCCCAGAACCCTTAAAGAGCGAGGATTTCGCATCGTCTCAACCTCAGGCGAGTCAATGTTCATTGTGAACCAGAATGACGGAGTACTGTATGTGAACGGTAAGATAGACCGAGAGGAGGTCTGCGAGAGAAGCACGCCGTGTTTAATAAATGTGAAAATAGCATTAGAAAATCCTCTTGAAATACATTATGTGACTGTTGAGATTCTGGATGTGAACGATCACGCTCCGAGTTTTCCTGAAAGCGAGATGCATTTAGAAATAGGGGAATCTGCCCTGCCCGGTGCGAGATTTCAGCTTCAGGCTGCACGCGATTCTGATAGCGGCAGTAATTCAGTGCATCATTACAAACTCAGTCATAATGATAATTTCCGACTTGAAGTCAAAGATCGAGGAGAAGATGGTAAAATTCCTATTTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTTTGATT[T/A]GCAATTGATTGCAGTAGATGGCGGAAAACCTGCCAAATCAGGCACAATGACCATAACGATTAGTGTTTTGGATATAAATGATAATTTCCCAGTGTTTACAAAAGACGCATACTCGGTCATGCTGAGTGAAAATGCGCCTATCGGTACTACTGTGATTCGGGTCAACGCGACAGACTCAGATGAGGGCCCGAACGGCGAGATAGTTTATTCATTTGGAAAAAGTGTTAGTAGTAAAGTGCAAAAGTTGTTTAATATTGACACCATCACTGGGGAAATAACTGTAAAAGGACTATTAGATTATGAGGACAAAGACAGATATGAAATTGATATACAAGCATCAGACAAGGGATTAATCCCCCTGATTACAGATAAAACTGTGACCATAAAGATAGTTGATGTAAATGATAATGCACCTGAAATTGAGGTGACATCCTTATCCAACTCCATTCCAGAGGACTCCAGACCTGGCACTACAGTGGCTTTAATTAGTGTCTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12541
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 2651176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2356021 |
GRCz11 | 14 | 2274372 |
KASP Assay ID:
2260-7161.1 (used for ordering genotyping assays)
KASP Sequence:
TTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTWTGATT[T/A]GCAATTGATTGCAGWAGATGGCGGAAAACCTGCCAAATCAGGCACAATGA
Long Flanking Sequence:
TGCTGTGGGAAATATTGGGAAGGATTTGGGTATTGATCCCAGAACCCTTAAAGAGCGAGGATTTCGCATCGTCTCAACCTCAGGCGAGTCAATGTTCATTGTGAACCAGAATGACGGAGTACTGTATGTGAACGGTAAGATAGACCGAGAGGAGGTCTGCGAGAGAAGCACGCCGTGTTTAATAAATGTGAAAATAGCATTAGAAAATCCTCTTGAAATACATTATGTGACTGTTGAGATTCTGGATGTGAACGATCACGCTCCGAGTTTTCCTGAAAGCGAGATGCATTTAGAAATAGGGGAATCTGCCCTGCCCGGTGCGAGATTTCAGCTTCAGGCTGCACGCGATTCTGATAGCGGCAGTAATTCAGTGCATCATTACAAACTCAGTCATAATGATAATTTCCGACTTGAAGTCAAAGATCGAGGAGAAGATGGTAAAATTCCTATTTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTTTGATT[T/A]GCAATTGATTGCAGTAGATGGCGGAAAACCTGCCAAATCAGGCACAATGACCATAACGATTAGTGTTTTGGATATAAATGATAATTTCCCAGTGTTTACAAAAGACGCATACTCGGTCATGCTGAGTGAAAATGCGCCTATCGGTACTACTGTGATTCGGGTCAACGCGACAGACTCAGATGAGGGCCCGAACGGCGAGATAGTTTATTCATTTGGAAAAAGTGTTAGTAGTAAAGTGCAAAAGTTGTTTAATATTGACACCATCACTGGGGAAATAACTGTAAAAGGACTATTAGATTATGAGGACAAAGACAGATATGAAATTGATATACAAGCATCAGACAAGGGATTAATCCCCCTGATTACAGATAAAACTGTGACCATAAAGATAGTTGATGTAAATGATAATGCACCTGAAATTGAGGTGACATCCTTATCCAACTCCATTCCAGAGGACTCCAGACCTGGCACTACAGTGGCTTTAATTAGTGTCTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19074
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 |
---|---|---|---|---|---|
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
ENSDART00000127511 | Nonsense | 182 | 758 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 2651176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2356021 |
GRCz11 | 14 | 2274372 |
KASP Assay ID:
2260-7161.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTTTGATT[T/A]GCAATTGATTGCAGTAGATGGCGGAAAACCTGCCAAATCAGGCACAATGA
Long Flanking Sequence:
TGCTGTGGGAAATATTGGGAAGGATTTGGGTATTGATCCCAGAACCCTTAAAGAGCGAGGATTTCGCATCGTCTCAACCTCAGGCGAGTCAATGTTCATTGTGAACCAGAATGACGGAGTACTGTATGTGAACGGTAAGATAGACCGAGAGGAGGTCTGCGAGAGAAGCACGCCGTGTTTAATAAATGTGAAAATAGCATTAGAAAATCCTCTTGAAATACATTATGTGACTGTTGAGATTCTGGATGTGAACGATCACGCTCCGAGTTTTCCTGAAAGCGAGATGCATTTAGAAATAGGGGAATCTGCCCTGCCCGGTGCGAGATTTCAGCTTCAGGCTGCACGCGATTCTGATAGCGGCAGTAATTCAGTGCATCATTACAAACTCAGTCATAATGATAATTTCCGACTTGAAGTCAAAGATCGAGGAGAAGATGGTAAAATTCCTATTTTAATTTTACAAAAGGCTTTAGACCGAGAGGTTATTCGAAACTTTGATT[T/A]GCAATTGATTGCAGTAGATGGCGGAAAACCTGCCAAATCAGGCACAATGACCATAACGATTAGTGTTTTGGATATAAATGATAATTTCCCAGTGTTTACAAAAGACGCATACTCGGTCATGCTGAGTGAAAATGCGCCTATCGGTACTACTGTGATTCGGGTCAACGCGACAGACTCAGATGAGGGCCCGAACGGCGAGATAGTTTATTCATTTGGAAAAAGTGTTAGTAGTAAAGTGCAAAAGTTGTTTAATATTGACACCATCACTGGGGAAATAACTGTAAAAGGACTATTAGATTATGAGGACAAAGACAGATATGAAATTGATATACAAGCATCAGACAAGGGATTAATCCCCCTGATTACAGATAAAACTGTGACCATAAAGATAGTTGATGTAAATGATAATGCACCTGAAATTGAGGTGACATCCTTATCCAACTCCATTCCAGAGGACTCCAGACCTGGCACTACAGTGGCTTTAATTAGTGTCTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44800
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 |
---|---|---|---|---|---|
ENSDART00000127511 | Nonsense | 730 | 758 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 2652819)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCATCCAGTACAGATCTGGAGACAAACGCTACATGTTAGTTGGACCC[A/T]GAATGAGTATCGGCTCTACTATAGCACCAGGCAGTAATAGGAATACTCTA
Long Flanking Sequence:
TGGTGACTAAAGTAAGAGCCTATGACGCAGATATAGGATACAACGGCTGGTTATTATTCTCACTGCAGGAAGTTAGTGAGCACAGTCTCTTTGCTTTGGACCGCTATACAGGACAGATAAGGACCCTTCGCTCATTCACAGAAACAGACGAGGCCCAGCATAAACTGGTCATACTGGTCAAGGACAATGGGAACGTTTCCCTCTCAGCAACAGCGACTGTGATTGTGAAAGTTGTGGAGCCCAAAGAGGCTTTTGCAGCTTCTGATGTTAAAAACGCAGAGAAAGACGAGGAGGAAAACAACGTGACATTTTATTTGATCATCACTTTGGGCTCGGTTTCGGTGCTTTTCGTCATCAGCATCATCGTGTTGATTGTAATGCAGTGCTCCAAATCTACAGACTATTCGTCCAAGTATTTACAGGACACAAATTATGACGGGACACTGTGTCACAGCATCCAGTACAGATCTGGAGACAAACGCTACATGTTAGTTGGACCC[A/T]GAATGAGTATCGGCTCTACTATAGCACCAGGCAGTAATAGGAATACTCTAGTCATACCAGATCGCAGGAGGAGAGACTCTGGAGAGGTAAGAGATGTGATTACTCAATAAAACAATACTTTATCTCGCTTAGCGTCAAATAGTATTTTTTTTTCAAGTAGGCTATTATTAAAATATTTGTTACATTATATTTTCTAACTGATGAAAACACTCTTTACGCATTGCTCTTTGGCATTTACAAAGCTTTGAGTGGGTCATATTTGCTGTCCATGGTGCTGAAATGTTTCACTTCTAAACTCTCAGAAATAAAGGTGTGTGAGCTGTCACTGTGGTGGTACCTTTTTAAAAGGTACACATTTGTACTTGAAGGGTCCATATTTGTACATCAAAAGTATAAATTAATACCTACAAATTTTAACAGGAAGACTTTTGTACTTTTTAGGTACTAATATGTACCCTTGAGGGGTGTTAATATGGACCTTTTAGGTACAAATGTGTACC
Associated Phenotype:
Not determined