ZMP
wu:fd14g04
Ensembl ID:
ZFIN ID:
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43721 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29663 | Splice Site | Mutation detected in F1 DNA | Not yet available |
sa29662 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9299 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10348 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43721
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 |
---|---|---|---|---|---|
ENSDART00000125534 | Nonsense | 16 | 1236 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 42042294)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43641340 |
GRCz11 | 21 | 43636516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTATGAATCATTTAGATTATTTTGCAAAGCTCTTTATTTTCTTGCTGT[T/A]GCGTCATTACTGGGTGTGTTATGGTGAGTTACTCTTGTAAGAAAAATCCT
Long Flanking Sequence:
ACCGTGTCATTTAGGGAAACTCCTGAGGTAAATAAGTGATATCTCTGAACTTTAATAATAAATCTAAATAAAATGCAGCGCTTCCCATCTCCAGTCGCAATGACTTCTGGGACTTCCAGAGCGAGTTCGGTGCTCAAGTCTGCATCGTTGCGTCCTCGATATCACGATCACATCCGGGAAGTTTCACGCGTCCTCCGTACTTGCGGTCTTGAGTATTGGAACTGAACTTAGGCAGCTGATGATGACGTTGCACGAGAACACGAGGACGCAAGATCGCTGAAGAACACATATTTAGAAACAGCCAATGATTTGGATCGTAGTCTGAGTGTGTGCACCTGCTGCCAATTACCAATGAAGCCACAAACAAGTGCTGCCAATCAGGCCAAGCTATAAATGTTGCTGTGAAACTCAAGGTTCTATAGGAATAGAGAGTGTTGCTGTTTTTGATGCAGTTATGAATCATTTAGATTATTTTGCAAAGCTCTTTATTTTCTTGCTGT[T/A]GCGTCATTACTGGGTGTGTTATGGTGAGTTACTCTTGTAAGAAAAATCCTGTTTTAACAAGCGTAGTACTTTGTTAGTGGGTGCTGATTATGTGCATGTCCGTTTTTTTTACATGCGACAACAAAGTGATGAAGTGGTGTAAAATTTAGCTTCAAGCAGAGATTTGAGTGTTGCTTCGTGTTTAGTAATTGCCCTATGTAAGTGTTTAGCTTTAGTTGACCTTAATGTGTCTATGCAAAAAAAAAATTGAACCACTTTAACTTTTCAATCTTTCTAGTTAAGGAAGATGAATAGGTTAGCTTATTTTTAAATTTTTTTTTTTTTTATTTGCCTAATTTAAGGTGATCCATTTTATTTACAGTGTCAGTTTATCTAGAGCCTTTAATCTTCTGTTTTGTGACTGCTGAAATGAAAATGCGGTCACCAACAAACCAAATTCAAGATTTCTTGTTTCACAAATTCAAGATTTCTCTCCACAGCTGATACCCCTGCAAGAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29663
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 > G
Consequence:
Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125534 | Splice Site | None | 1236 | None | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 42040975)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43640021 |
GRCz11 | 21 | 43635197 |
KASP Assay ID:
2261-6089.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGAGCCTAGATGCTGATGCAGAATCTAATTCAACTCTGCATGGTAACT[T/G]AAGTCTGGATACTGCTGCAGAATCCAACTCCACCCTAAATGCTAACTTTA
Long Flanking Sequence:
AACTGGCTATAGTTTGCTGCATCTAAAGAGATTTGTAGGTTATGTATTTTGCTAGAGCATCCTAAATTTCCTACCCATCTTGACCTTTCTTTGATTAATTCGGTATAAATGTCGGGGGTTGGCAACTTGATGTAAAACGTGCTATTGCTTTAAGGTATGGTGTCACCTGTGCTAGTTTACCATACAAAAAGACACTGAGTTGTAATTTGCAAGTCAAACAAGTTTATAATTTTTTTTGCAAATCTGTATGTACTTGTATAATGGGAATTCTTTTTTTTTTTTTTTTTTTTTTTTTAAACTGCGTCTTTCTGTAGATTTGCTTGGTGATCTTCAGATTGATGTCCTCAAAGAGAATGTGCATGGAAATTTCAGCCTGGAGTTTACGGATGCAAATGGTAACTTCAGCCTGTATGCAGATGCTGTGGAGACTGGTTCCAATGTGCATGGCAACTTGAGCCTAGATGCTGATGCAGAATCTAATTCAACTCTGCATGGTAACT[T/G]AAGTCTGGATACTGCTGCAGAATCCAACTCCACCCTAAATGCTAACTTTACCCTAAACAATGCTGCAGAATCAAACTCCACCCTTCATGGTAACTTGAGCCTAGATGATGCTACAGATCGTAACAATAACTTCAGCCTGGATGCTGCTGTGGAATCCAACTCCACCCTTAATGGTACCTTTACCCTAGACAATGCTGCAGAATCAAACTCAACCCTTCATGGTAACTTGAGCCTAGATGATGCTACAGATGGTCACCTAAACTTCAGCCTGGATGCTTCTGCGGTATCCAACTCAAGCCTACAAGGTAACTTAAGCCAAGGTGGCACTAAAGATGTTAACCCTAAGGTCAGCCTAAACATCCCATTAATATACAACCCGTTGTTCTGGCATAATTTTGATTAACTCTTCGAATGACCTCAAAAGTGTGCAAAGAAACAGACCTGGAGTTTATGAATGTGAATGGTAACTTGTGCCTGATTGCAGATGCTGTTGATTCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29662
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125534 | Essential Splice Site | 207 | 1236 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 42040331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43639377 |
GRCz11 | 21 | 43634553 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCAACTTCAGTCTAGATGCTGCTGCAGAATCCAACTCAACCCTACAAG[G/T]TAACTCTGGCTGGTTGACACTTAAGATTGGAACCATAACTGAAGCCTAAA
Long Flanking Sequence:
CTGCTGTGGAATCCAACTCCACCCTTAATGGTACCTTTACCCTAGACAATGCTGCAGAATCAAACTCAACCCTTCATGGTAACTTGAGCCTAGATGATGCTACAGATGGTCACCTAAACTTCAGCCTGGATGCTTCTGCGGTATCCAACTCAAGCCTACAAGGTAACTTAAGCCAAGGTGGCACTAAAGATGTTAACCCTAAGGTCAGCCTAAACATCCCATTAATATACAACCCGTTGTTCTGGCATAATTTTGATTAACTCTTCGAATGACCTCAAAAGTGTGCAAAGAAACAGACCTGGAGTTTATGAATGTGAATGGTAACTTGTGCCTGATTGCAGATGCTGTTGATTCTGGTTCCAATGTGCATGGCAACTTGAGCCTAGATGCTGACACAGAATCCAACTCAACCCTACATGGTAACTTCAGCTTTGACACCGCAGATGGTAACCGCAACTTCAGTCTAGATGCTGCTGCAGAATCCAACTCAACCCTACAAG[G/T]TAACTCTGGCTGGTTGACACTTAAGATTGGAACCATAACTGAAGCCTAAATATTCAATTAATTGGGGATATTTGGCAGAGCTCTTTACTTGCAGTTCCATAGTCTCTAGCTGTTAAAATTGTAAGTCTTCATGCAAAAGTACGTTTTCCTGTCTTAATCTTTCAATGAGGATAATTGCCATGCATTTTAAAGGGTCCATCTACAATTGGCCGTGTTACAAATCCAGTCTAAATAAAACCCCTTATTTTGGTTTAAGTTGTACAAATGTACTGCAAGTTCTTGGTTCATGTGATGTTGTTGTGACAGAATTTATCAAATGTAAATGCTGCCCTTGGTTGCCAGCAAAACATGAATTAAATTCAAGGTTTCACTTTAAATTCTCTCCAGCTGTTAAAAGTCCGGGATCAGCTAAAGTGGCTGTGCGCTCATTGGAGGATGTGCCTGACTCTGTTTTTGCAGGTGAGGAAGCCCACCCCCCCCCCCCCTCTTTTTTTATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9299
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125534 | Nonsense | 369 | 1236 | 8 | 11 |
ENSDART00000125534 | Nonsense | 369 | 1236 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 42039081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43638127 |
GRCz11 | 21 | 43633303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGACCCTGTATGATAACTTTAGCCTGGATGATGCTGCGGAATCCAATT[C/A]AACCCTGTATARAAACTTCAGCCTAAATGCTGCAGAATCAAACTCCACCC
Long Flanking Sequence:
TTTCAAAGAGCATTACCTTTCCAATCCTGTGAATGTTTGTCGACTGAATTATGCAATGTTGTAAATGACACCCTTTTTGTTTAATATAGATTTTTTCCGAGATCTTCAGAATGGCCTCTCAAGGGAAATATTGCAAGGAAACTTCAGCCTTGAGTTTACAGATGCCAATGGAAACTTTACCCTGTATGCAGATGCTGTGGAACCTGGTTCCAACATTCATGGCAATATCACCCTAGATAAATCTGCAGAATCCAACTCGACCCTGCATGGAAACATCAGCCTAAATGATGCTGCAGAATCAAATTTAACCCTATATGGTAACGTCAGCCTAGATGATGCTGCAGAATCCAACTTAACCCTGCATGGTAACGTCAGCCTAGATGATACTGCAGAATCCAACTCTACCCTGTATGGTAACTTCATTCTAGATGATGCTGCTGAAGAATTCAACTCGACCCTGTATGATAACTTTAGCCTGGATGATGCTGCGGAATCCAATT[C/A]AACCCTGTATAAAAACTTCAGCCTAAATGCTGCAGAATCAAACTCCACCCTGCATGGTAACATCAGTCTGGATGCTGCTGAAGAATTCAACTCAACCCTGCATGGTAACTTCAGCCTAGATGATGCAGAATCCAACTCTACACTGTACAGCAACTTCAGCCTAGATGACGCAGAATCCAACTCTACCCTATATGGTAACGTCAGCCTAGATGCTGCTGCAGAATCAAGCTCCACCCTGTATGGTAACTTCACCCTAGATGTTGCAGATTTCAACTCAACCCTGCATGGGAACATCAGCCTAGATGCTGCAGAAACCAACTCAACCCTGTACGGCAACTTCAGCCTAGATGATGACGCAGAATCCAACTCAACCCTATATGGTAACGTCAGTCTAGATGCTACAGAATCCAACTCTACCCTGTATGGTAATGTCAGTCTAGATGCTGCTGCAGAATCCAACTCAACCCTGCATGGTAACTTCAGCCTAGATGATACTGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10348
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 |
---|---|---|---|---|---|
ENSDART00000125534 | Nonsense | 369 | 1236 | 8 | 11 |
ENSDART00000125534 | Nonsense | 369 | 1236 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 42039081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43638127 |
GRCz11 | 21 | 43633303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGACCCTGTATGATAACTTTAGCCTGGATGATGCTGCGGAATCCAATT[C/A]AACCCTGTATARAAACTTCAGCCTAAATGCTGCAGAATCAAACTCCACCC
Long Flanking Sequence:
TTTCAAAGAGCATTACCTTTCCAATCCTGTGAATGTTTGTCGACTGAATTATGCAATGTTGTAAATGACACCCTTTTTGTTTAATATAGATTTTTTCCGAGATCTTCAGAATGGCCTCTCAAGGGAAATATTGCAAGGAAACTTCAGCCTTGAGTTTACAGATGCCAATGGAAACTTTACCCTGTATGCAGATGCTGTGGAACCTGGTTCCAACATTCATGGCAATATCACCCTAGATAAATCTGCAGAATCCAACTCGACCCTGCATGGAAACATCAGCCTAAATGATGCTGCAGAATCAAATTTAACCCTATATGGTAACGTCAGCCTAGATGATGCTGCAGAATCCAACTTAACCCTGCATGGTAACGTCAGCCTAGATGATACTGCAGAATCCAACTCTACCCTGTATGGTAACTTCATTCTAGATGATGCTGCTGAAGAATTCAACTCGACCCTGTATGATAACTTTAGCCTGGATGATGCTGCGGAATCCAATT[C/A]AACCCTGTATAAAAACTTCAGCCTAAATGCTGCAGAATCAAACTCCACCCTGCATGGTAACATCAGTCTGGATGCTGCTGAAGAATTCAACTCAACCCTGCATGGTAACTTCAGCCTAGATGATGCAGAATCCAACTCTACACTGTACAGCAACTTCAGCCTAGATGACGCAGAATCCAACTCTACCCTATATGGTAACGTCAGCCTAGATGCTGCTGCAGAATCAAGCTCCACCCTGTATGGTAACTTCACCCTAGATGTTGCAGATTTCAACTCAACCCTGCATGGGAACATCAGCCTAGATGCTGCAGAAACCAACTCAACCCTGTACGGCAACTTCAGCCTAGATGATGACGCAGAATCCAACTCAACCCTATATGGTAACGTCAGTCTAGATGCTACAGAATCCAACTCTACCCTGTATGGTAATGTCAGTCTAGATGCTGCTGCAGAATCCAACTCAACCCTGCATGGTAACTTCAGCCTAGATGATACTGCCG
Associated Phenotype:
Not determined