ZMP
ENSDARG00000091100
Ensembl ID:
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17702 | Nonsense | Available for shipment | Available now |
sa21865 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17702
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 |
---|---|---|---|---|---|
ENSDART00000127595 | Nonsense | 120 | 404 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 12979696)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 12864105 |
GRCz11 | 11 | 12921764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGATTTGKACWATCTCATGGCCGARAGTCRAGAAAGGCTRAGWGTTT[T/A]GAGGCTACAGAYGGAGTCRGAGCGGGAAAGACTAGATGAACTGGAGAGAC
Long Flanking Sequence:
GCCTTATGTTCAGGGTAACATTGAATGAACTTCTACATCCAGCATTTTGCATTCTCACTAGCTGTGAACACTCTTTATCAGATGGTACTAGAAATTATAGGCTAAGGTCTTTTATAAGAGATTCTGCATGTACAAAGAAGACTCTTCTGAAGCATTATGCATTTTGGATTCATAGAAAGTGTTACAATTTATTTTTTAGTTTGATTATTGTTTTTGACATTTTACATAAGCATTTCTTTTTCTACACCATCAGGAACTGGAATTTTTCGACTGCTCTAAATTAACCAATCAGACAATTCAAAAGTTGGGTCACATCATACAGACACCTTGTTTTCAGCCAGACTCTGTACGAGATATGAGTCGGGCTTGTGAGTCTTTGTGTCGCTGGGTGAGAGCAGTATACCAGTATGCTTGCATACAGCGCCACATTGCACCCCAAAAGGCTAAAAAGCAAGATTTGGACTATCTCATGGCCGAAAGTCGAGAAAGGCTGAGTGTTT[T/A]GAGGCTACAGATGGAGTCAGAGCGGGAAAGACTAGATGAACTGGAGAGACAGCAGGAGCTCAACAAACAAGACATGGAGTTGCTGAAGGCCCAACTCAGTACCGCTGAGGCTCAAGAGAGGGAGTCATGTGCTATTCTTAAACTGGCTGAACATCACATTAAAGACTGGATATCAGAAGGAAAGGTGGGTGAAGTTTTTGCTGTAAATATTACTATACAAGCAATTACTTACTTTACACCACTGCTTGTAGTTCATTCATTCATTTTCTTGTCGGCTTAGTCCTTTTTTAATCCGGGGTCGCCACAGCAGAATGAACCGCCAACTTATCCAGCATGTTTTTACGTAGCGAATGCTCTTCCAGCCGCAACCCTGGGAAACATCCACACACACACACACCTGTACCGCATGTCTTTGGACTGTGGGGAAAACCAGAGCACCTGGATCCACGCAAACGCTGATGAAGATGAAGTCAGAATTATTAGCCCCCCACAGATTCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21865
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 |
---|---|---|---|---|---|
ENSDART00000127595 | Nonsense | 137 | 404 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 12979746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 12864155 |
GRCz11 | 11 | 12921814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGCTACAGATGGAGTCAGAGCGGGAAAGACTAGATGAACTGGAGAGA[C/T]AGCAGGAGCTCAACAAACAAGACATGGAGTTGCTGAAGGCCCAACTCAGT
Long Flanking Sequence:
ATTCTCACTAGCTGTGAACACTCTTTATCAGATGGTACTAGAAATTATAGGCTAAGGTCTTTTATAAGAGATTCTGCATGTACAAAGAAGACTCTTCTGAAGCATTATGCATTTTGGATTCATAGAAAGTGTTACAATTTATTTTTTAGTTTGATTATTGTTTTTGACATTTTACATAAGCATTTCTTTTTCTACACCATCAGGAACTGGAATTTTTCGACTGCTCTAAATTAACCAATCAGACAATTCAAAAGTTGGGTCACATCATACAGACACCTTGTTTTCAGCCAGACTCTGTACGAGATATGAGTCGGGCTTGTGAGTCTTTGTGTCGCTGGGTGAGAGCAGTATACCAGTATGCTTGCATACAGCGCCACATTGCACCCCAAAAGGCTAAAAAGCAAGATTTGGACTATCTCATGGCCGAAAGTCGAGAAAGGCTGAGTGTTTTGAGGCTACAGATGGAGTCAGAGCGGGAAAGACTAGATGAACTGGAGAGA[C/T]AGCAGGAGCTCAACAAACAAGACATGGAGTTGCTGAAGGCCCAACTCAGTACCGCTGAGGCTCAAGAGAGGGAGTCATGTGCTATTCTTAAACTGGCTGAACATCACATTAAAGACTGGATATCAGAAGGAAAGGTGGGTGAAGTTTTTGCTGTAAATATTACTATACAAGCAATTACTTACTTTACACCACTGCTTGTAGTTCATTCATTCATTTTCTTGTCGGCTTAGTCCTTTTTTAATCCGGGGTCGCCACAGCAGAATGAACCGCCAACTTATCCAGCATGTTTTTACGTAGCGAATGCTCTTCCAGCCGCAACCCTGGGAAACATCCACACACACACACACCTGTACCGCATGTCTTTGGACTGTGGGGAAAACCAGAGCACCTGGATCCACGCAAACGCTGATGAAGATGAAGTCAGAATTATTAGCCCCCCACAGATTCAGGAATTTTTCACAGTATTTCCTATAATATTTTTTTGTTCTGGGGAAAGCCTT
Associated Phenotype:
Not determined