ZMP
ENSDARG00000077221
Ensembl ID:
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10424 | Essential Splice Site | Available for shipment | Available now |
sa10492 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10424
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113791 | Essential Splice Site | 322 | 409 | 2 | 4 |
ENSDART00000113791 | Essential Splice Site | 322 | 409 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 47414013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 47348084 |
GRCz11 | 20 | 47251805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTRCAAAGTCTAGATACAGTGAGAGATGACAACGCTRTGAAATCTGATAA[G/C]TCAGAGAAAAWWTTTTTTGTCTGTCATAATGCCAAATCACYATCTGACAG
Long Flanking Sequence:
GTCACAAGATGGAACTCACAGTTCAGGGCTGTCACAAAACTTGCAGGGCTTCCAGAAGAAAAGCTGAAGGAGATCTGTGATAAACTTGGTGTGCCAAGTCTTCATCCACAAAAGTATGTATTCCTGAATGAGTACAATGAGATTCTGAAGCCTCTAGCTGTTGCCATTGACATTCTCCAGGGTGAAAGCAAATGTTACCTAGGATTTTTAATCCCTACTTTGCTTAGCCTCAAGACAAAGCTATTTGAAAAGATGCCCCATTTGCTTTATAATTCATACATTGTTACCACTATCTGTGAGGCCATAGAAGAACGCTTTGGAACAGTGTTAACCAGCTATGAAGCAAAGATGGCAACGGCAACCCTGCCCAAGTTCCGCTTAAACTAGCTTAGCCCTGAGAAGAGAGACGACATGAGAACCTTAATGCAGGAAGCCATTGCTCAGGAACCACTGCAAAGTCTAGATACAGTGAGAGATGACAACGCTGTGAAATCTGATAA[G/C]TCAGAGAAAAAATTTTTTGTCTGTCATAATGCCAAATCACTATCTGACAGCACAACTCATGATGAAGTCAGAAAGTACTTAAAAGATTCAAATAACAACCTGACGTCTCTTAAGACATTTCCCACAGTTAAGAGTTTTTTTTATCAAGTACAACACTACATTGCCTTCCAGTGCTCCAGTGGAGCGTCTTTTTAGTCATGGAGGTAATCTTTTGACCTCATCTCGAAACAGAATGAGGGATGAGCACATGGAACAGGTCTTACTGCTCTGTTACAACAAACAGCACTATCCAAGTGACCTAACCTATGATGACTGATGTGTGGTGTGGACACTTTATCTGTCACTCTATTCCCATTATGTTTTTTGGGAATAAAGAGCTTTGTTCCCGTTCACACACACACACACACACACACACACACACACACACACACATACATGTAAATACATGTGTATGCATGTATATATGTATGTGTATGTATATATGTATGCACTCATACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10492
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113791 | Essential Splice Site | 322 | 409 | 2 | 4 |
ENSDART00000113791 | Essential Splice Site | 322 | 409 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 47414013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 47348084 |
GRCz11 | 20 | 47251805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTRCAAAGTCTAGATACAGTGAGAGATGACAACGCTRTGAAATCTGATAA[G/C]TCAGAGAAAAWWTTTTTTGTCTGTCATAATGCCAAATCACYATCTGACAG
Long Flanking Sequence:
GTCACAAGATGGAACTCACAGTTCAGGGCTGTCACAAAACTTGCAGGGCTTCCAGAAGAAAAGCTGAAGGAGATCTGTGATAAACTTGGTGTGCCAAGTCTTCATCCACAAAAGTATGTATTCCTGAATGAGTACAATGAGATTCTGAAGCCTCTAGCTGTTGCCATTGACATTCTCCAGGGTGAAAGCAAATGTTACCTAGGATTTTTAATCCCTACTTTGCTTAGCCTCAAGACAAAGCTATTTGAAAAGATGCCCCATTTGCTTTATAATTCATACATTGTTACCACTATCTGTGAGGCCATAGAAGAACGCTTTGGAACAGTGTTAACCAGCTATGAAGCAAAGATGGCAACGGCAACCCTGCCCAAGTTCCGCTTAAACTAGCTTAGCCCTGAGAAGAGAGACGACATGAGAACCTTAATGCAGGAAGCCATTGCTCAGGAACCACTGCAAAGTCTAGATACAGTGAGAGATGACAACGCTGTGAAATCTGATAA[G/C]TCAGAGAAAAAATTTTTTGTCTGTCATAATGCCAAATCACTATCTGACAGCACAACTCATGATGAAGTCAGAAAGTACTTAAAAGATTCAAATAACAACCTGACGTCTCTTAAGACATTTCCCACAGTTAAGAGTTTTTTTTATCAAGTACAACACTACATTGCCTTCCAGTGCTCCAGTGGAGCGTCTTTTTAGTCATGGAGGTAATCTTTTGACCTCATCTCGAAACAGAATGAGGGATGAGCACATGGAACAGGTCTTACTGCTCTGTTACAACAAACAGCACTATCCAAGTGACCTAACCTATGATGACTGATGTGTGGTGTGGACACTTTATCTGTCACTCTATTCCCATTATGTTTTTTGGGAATAAAGAGCTTTGTTCCCGTTCACACACACACACACACACACACACACACACACACACACACATACATGTAAATACATGTGTATGCATGTATATATGTATGTGTATGTATATATGTATGCACTCATACATA
Associated Phenotype:
Not determined