ZMP
LOC100332784
Ensembl ID:
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32595 | Nonsense | Available for shipment | Available now |
sa32594 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12177 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32595
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110790 | Nonsense | 213 | 956 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 8596908)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8836713 |
GRCz11 | 1 | 9520824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATATTCCTGTTTCTCATACAGATAACAGACCCGACTGAAAAGAGGTA[C/A]GAGGTGCCTATAGATGTCCCTGTGGTTCATAAAAGAGCCTCAAACCCCTC
Long Flanking Sequence:
TTTCTAATATGCTGATTTGCCATTTTATTATTATTATTATTATTATTATTAATATTATTATTGTTGTTGATGTTGTTGTTGTTATTATTACCTTTATTATTATTATTATTAAAGCTGAAAATATATATTTTTTTCACAAATCTTGATTTATAGAATGATTGAATGATGTAGAATGATTTATATGATTTTTAAGTCTTTTTTATTTGTTTGGCTTAAATGTGACATTTCAAAACGAATATCCATTTTATCTGTGCATTGTAATTTATAAAGACCAACTTCACTTGTAGAATTTAAATCAGGTGATTTCTTGTGAAAATCTTTTGTAAGGTGAAATCTTTTTTTTAAGTGTTTTGTTTTAATTTATGTAGACAACAAAGTATTGACTTTTAACATGACAAACGCCAGCTTTAATCTTAATTTTGAAAACATTTTCAGACTTTTTATGTTCTCATAATATTCCTGTTTCTCATACAGATAACAGACCCGACTGAAAAGAGGTA[C/A]GAGGTGCCTATAGATGTCCCTGTGGTTCATAAAAGAGCCTCAAACCCCTCGTACACTGTAGACTTCATCAAAGAGCCGTTTGGACTGATAGTCAAGAGAACGCAGACTGGAGCTGTACTGTAAGTCCACAACACAAACACAAATACACAGACCTGCCTTTCAAATTCACAGAGTAGTTTCAAGCCATCACCAGAAAACTGGCCAACAAGGAGATCTATAATGAATGCCAGAAGTAACATGTATGTTTCTGTGCTGCCAGGCTGAACACATCCATCGCTCCTCTCTTCTACGCGGATCAGTTCCTCCAGATGTCCTCATCTCTACCCACACGTTTCATCTACGGACTGGGTGAACATCGCTCCAACTTTCTGCATGATGTCCAGTGGAACACTCTCACCATGTGGGCTCGAGATGTTCCTCCAATGGTAACTTGACCTTTGTTCGTTCAAACGGCATTTCCCATTAGGAGAACTATTGGTGACCGTAGTGGACTTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32594
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110790 | Essential Splice Site | 501 | 956 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 8590120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8829925 |
GRCz11 | 1 | 9514036 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGGCATCTTCATCAATGACTCAAATGGAGACATCCTTATTGGAAAGG[T/C]ACACAAATCTAAGCTTTTTCTGATCAAAAATAGAGTAAAAACGGTAATAC
Long Flanking Sequence:
TTCAATTATAGAGGCTGTCTAAATATCAGAGTCATTAAAATGGATTATAATAGAGTAAATAAGGCTTAATCAGGGCTCAACAATAAGGACTGCTCGATGGTCCGGGGCCAGTGCGAGAGACGCTTGGGACAGTAGACATTTACTGAAAGCAAATAAACTATAAAAGTGAAAGGAGAGAGGCCAATGCATTCTGCAGGATTATTAGTATGTTTCTCCTGCAAAACATCCACATGACACGCTTCCTCATTTAGGTCTCGTCTCTTTTTTGAAGCATTAGATCAGACTGACAGTCATGAGGCCCATTTGGCAATTGAATGTTTCACATGACTGTAGTTGAAACCCTCACTGAAGCATTAGGATGTGTTACTGAAGTGTGTTTCCTCATCAGGATCCTGGAATTAGTAACTCTCAGCCACCTGGCTCTTACTGGCCGTTTGATGAGGGTAAGAAGAAGGGCATCTTCATCAATGACTCAAATGGAGACATCCTTATTGGAAAGG[T/C]ACACAAATCTAAGCTTTTTCTGATCAAAAATAGAGTAAAAACGGTAATACTGTGAAATCGTATGTATTAGGGGTGTGACGAGACGAGACGCGAGATTGGGTTCATGAGAACGAGACAAGATTTTTACACTATTTTAAAGAAATCCCTAAAGATGAAACGTATGAATAGAATAGTCTTAGAATTCAAATATTTTGCTAATTTATGAATGAAAAATATTTTTTTTTAATTTAAAAAAATCACAAAATGCAAAACAATTTTGGTGTTTCTTTTAATCAACCTGTAATAAATTTACGTCCATTTTAATGAACATGCATATAATTTTATGTATGCAATAGTTTTATATTAATTTACATTGAATTCTATGCAACGAACATGCAAACACTGCAAAATATTTGTTTAGATATTAATAGAAAATAGCAAACTACTGACTGGCTTTTTCCCTATAGAATTTCAGAGTATTTACATTGCAGATCTTGATTTTCAATTCGGATTTTGTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12177
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 |
---|---|---|---|---|---|
ENSDART00000110790 | Nonsense | 877 | 956 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 8581539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8821344 |
GRCz11 | 1 | 9505455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGATCTGTACTGGGATGATGGAGAGACCATTGASTCGTATGARAGCAAT[C/T]AATACGCTTACATCTATTTCACAGTAGAACAGGTACTGAAAACAGCCCCA
Long Flanking Sequence:
CCGGATGCCCTGTATATTCCTCATTATTCATGGGAGTTCTGTTCTAAAAATAACCTCCAATAGGCAAAATCCGCAAAGTTGTCAACTTTAATTTTATAATCATTATAGATGTTTTAAGGCAGTAAAACCCCTCACTGCACACTTTATACACTTTTCTCAGACAGGCATTAACATTTTCACACTTATCTAAATAAGTCCAGCATTATAGAATGAACCCAAAGATCTAAATCATTTGATCTTCATATATTTATTCTGTAATGCATGTGTGTGCATCTTTTTTCAAGTTATTATATGTTATAGTATTATATGTTATATATTATTATAAGTTAAAGTTATTATATATAAATAATGTTGTGTTTGTGTTTCAGAGACCGAACACCACATTATGGGTGAGCAGCGGTCAGCCTCTTCATCTGATTGTGAGTCTGAGCGAGGACGGCCGGGCCAAGGGTGATCTGTACTGGGATGATGGAGAGACCATTGACTCGTATGAGAGCAAT[C/T]AATACGCTTACATCTATTTCACAGTAGAACAGGTACTGAAAACAGCCCCAGCGGGCTCTACTTTCAGCTTTCATCAGATCCTCACACTATGGACACATTAGAATACATTTACTTATTTAACTGTTTAAATGCTACTCTTGTTTTCATATCATTGTTTTTTTATTAAAGTACAAATGACATCAAAAGTAACCATGTGATTTTGTAAGCTCACATTGCTAGTTTTGGAGTGAACATTTCATCCGTGCATGTCATTAAGAAAAAATTGTTTGCCCTTGAAATCATTCATTGAAATCTGATATGTTATTTTTTAGTTAAATACTCAAATTATGGGCCCTATCATACACCCGGCGCAGTGTGGCGCAAGGCGTGGCGCAGTAGTCTTTTGGTAGTTTAAGCTTGGCGCAGGAGTCGTTTTGAGGCGATGCGCTACGCTGTTTAAATAGCAAATGCATTAGCGCTCATTTTTGCGCCCATAGGCGTTCTGGTCTAAAAAGGAAGGC
Associated Phenotype:
Not determined