ZMP
wu:fc28f08
Ensembl ID:
ZFIN ID:
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35051 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14951 | Nonsense | Available for shipment | Available now |
sa8736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35051
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 |
---|---|---|---|---|---|
ENSDART00000102518 | Nonsense | 15 | 485 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 14553433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14254729 |
GRCz11 | 11 | 14312388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTTATGAATTCAATAAGTTTTAAATACCTGCGTCGTGAATGTGTATA[T/A]TCTCGGTATTGCTGTGTCCCGTTTTGTAAAATTTCATCAAGGTTTAATTC
Long Flanking Sequence:
TCATCTTAGATCATTTAAGCGAGGTACGAAGAACGGACCCCTGAACAAGTTAATGTTTGATCTGTAATGCCCAATAAATGCCACATGGTGTCACCTAATCGTCTAGTATTCACTGCCTCCTATGGCAGGGGGGGAAGTCAGTAAACCTTAAATTGACAACCTATTCCATTATTTTAGATAGTATTGTATTTTGACAAATCATGATTGTTATTTCGATGATTTTTTTAAGGAAATATTATTTACTGCATTTTTGACGAGTTTTTAATCACGACGAGCGTTACCACTAGAGTGAGGGGCATTTAATGCTACAACGTCTTGCCATATGGATACGGCTCGTACGGCTAACATCGACGTATTTCCGCTAGAATCTCAGTGTTCATGTGAGTTTCCGTTGTGCGTCTGATGGTTAGTCAAAGTTTTTTTTTTTTTAATAAATAGGCCATATATTAAATAGTTATGAATTCAATAAGTTTTAAATACCTGCGTCGTGAATGTGTATA[T/A]TCTCGGTATTGCTGTGTCCCGTTTTGTAAAATTTCATCAAGGTTTAATTCTGTGATCAGTTTCCATAAATTACCTTTGGACAGAGCAACACGAAAGATGTGGCTTCACAATATCCGGCGAAAGACTTTTGAAGTCAGCCCTCATGTAAGAGTTTGTAGCCGACACTTCACAAATGATGATTTTATTGAGCCGTCGTATCCTACAGCACGCAGACTGCTGAAGAAGGGTGCTGTACCCACATTGTTCAGGTGGAACAACGATTCCACTTCAGGCCAAAAGCGCTTTAGACTATGGGAGAAAAAAGCTTCCTCCTCCTCTGATCAGGAAGAAGAACTTGTGCCTATGGACTTCCAGCATGAGGACCATAATTACTATTGCACATCTCGAGTCCAAAATGATGAGGTTGTGGATCCGACTGATGATCTCCGAAATGAAGTGGAGGTCCTGAAGAGAAAGGTTGCAGAGTTTTCTGTCAATCAGAGATTTTGTTTGGGGCGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14951
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 |
---|---|---|---|---|---|
ENSDART00000102518 | Nonsense | 179 | 485 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 14553924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14255220 |
GRCz11 | 11 | 14312879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCCTGAAGAGAAAGGTTGCAGAGTTTTCTGTCAATCAGAGATTTTGTT[T/A]GGGRCGATTTGCAGCATCTGAYGATGACATAAGGTTTTAYACTAGGTAAG
Long Flanking Sequence:
ATGTGTATATTCTCGGTATTGCTGTGTCCCGTTTTGTAAAATTTCATCAAGGTTTAATTCTGTGATCAGTTTCCATAAATTACCTTTGGACAGAGCAACACGAAAGATGTGGCTTCACAATATCCGGCGAAAGACTTTTGAAGTCAGCCCTCATGTAAGAGTTTGTAGCCGACACTTCACAAATGATGATTTTATTGAGCCGTCGTATCCTACAGCACGCAGACTGCTGAAGAAGGGTGCTGTACCCACATTGTTCAGGTGGAACAACGATTCCACTTCAGGCCAAAAGCGCTTTAGACTATGGGAGAAAAAAGCTTCCTCCTCCTCTGATCAGGAAGAAGAACTTGTGCCTATGGACTTCCAGCATGAGGACCATAATTACTATTGCACATCTCGAGTCCAAAATGATGAGGTTGTGGATCCGACTGATGATCTCCGAAATGAAGTGGAGGTCCTGAAGAGAAAGGTTGCAGAGTTTTCTGTCAATCAGAGATTTTGTT[T/A]GGGGCGATTTGCAGCATCTGACGATGACATAAGGTTTTACACTAGGTAAGAGCTTAAATTTAAATGCATATGTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTACTTGTAGTGTACATACAACTGTAATTATATATGCTTTTTATAAAAGTTAATATTTTACTTTATATTTTAAGTCTAATTAATTGTACTTAATTCTTAACAAAATTTTTTGATGTTCCAAGACTTTTGCCCAGTAATTAATATATTTCCATATTTAAAACTTATTTAGGTCTTATTTGTTTTGGGGTTTAAATGTAGGCCTATACAAAATTAGTAACAACACATTTTTTTAAATTGCTTGCTTATTTATTTATTTATTTATTTAAAGATTTAAAGAAAGGCAATAGATGTAAATAGGGCCAATGTTTTTATTCAAAGGATGTACATTTGAATAAAATATTGGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8736
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102518 | Nonsense | 329 | 485 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 14559472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14260768 |
GRCz11 | 11 | 14318427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCAGACACACAAGTGATAATTGACTGTATAGAGCTTTGTTGYCGAATA[C/T]AATCATCTGACCTGTTCCCAGATGAAGGGTACGATTGCACCTTCAAGGGG
Long Flanking Sequence:
ATTCAGCCTGCTTCCCACAACATGTTTCGCGTAACCAGAGCCAGGGCAGATACAACAAAGTGTGATGTTCAAGCAACAGACAAGGCATCTGTAAATACATTTTTTTATATAAATTAATATTACATTATATGTTCCCTATTAAATGCAACATTATTTGCATTTTGTAGGCAAGAAAATGTCATGTACCTAAATTATTATTATTTTTATTTTTTATTTTATTTTAACAGGTTCAGTTCTTGCTGCCTATAGATGAGTTTTTCCTCTTCATGGTCCATCTCTCTGTTGGACTGACAAAGAGGGATCTAGCCCACAGATTCAATGTCCATCAGTCCACCGTGAGTCAAATCATTTCAACCTGGGCCAATTTTCTGTACACAATTCTTGGATCAGTGCACATTTGGATGTCCAAGGAGGCGGTCAAGGCTCAAATGCCAAAGGAATTCCAAGACTACCCAGACACACAAGTGATAATTGACTGTATAGAGCTTTGTTGCCGAATA[C/T]AATCATCTGACCTGTTCCCAGATGAAGGGTACGATTGCACCTTCAAGGGGTTAATTGGCATGGCACCACATGGTGCAGTCACTTTTGTGTCATCTTTGTATGCAGGGTCGGTCAGTGACAATGAGGTTCTTAAGAAGTCTGGGATTGTGTTGTACCTGAAACCTGAAATGGCCATCATGGTTAACAAAGATTTTCTTGTAGATGACTCTATACTATGCACAGTTTACAGACCAGCTTATCCAGTCAAGAGAGAACTGATGGAGGCTGATGAGGATGTGGGAAAGATGGGTGACACTCAGTCCATTGCTCAACTGAGGGTCCACATTGAGCATCTCATCTGCAGGGTGAAGCAGCACAAGCTTCTTGATTCAGTCATGCCTTTTACCAGCACAAGGACCATCAACCGGCTATACATAGTAGCTTGCCTTTTTATAAACTACCAGGATGGTCCTTTGTTAAAAAGATGGACATGATTAAAGGCTAGATGGAACAATCACTGT
Associated Phenotype:
Not determined