ZMP
si:dkey-149i17.9
Ensembl ID:
ZFIN ID:
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30819 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39832 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16089 | Nonsense | Available for shipment | Available now |
sa18395 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30819
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088795 | Essential Splice Site | 44 | 258 | 2 | 5 |
ENSDART00000134936 | None | None | 212 | None | 3 |
ENSDART00000088795 | Essential Splice Site | 44 | 258 | 2 | 5 |
ENSDART00000134936 | None | None | 212 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 24667949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25242726 |
GRCz11 | 2 | 24898360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGCAATTAAGTTTGCCAACACCAAGAACGTCAAGTTCATCGACATT[G/A]TAAGTATGCTGTGCTCTTCTACTCTCATTCACTGTTTCATTTCACCTATC
Long Flanking Sequence:
TCAGGTATCATCAATTTTCATCAATTAATATCTAGATCACCGCTTTAAATCAGAATATCAGATAAAAATAATGGATAGATATGGGATTCTTATTTTTGAGCTAACTTAAACTGTTTCTTTGTTAAACTGTTTAGTGTTAATGACTGAAATTCAGCCTGATCTCAAGAGAAAACTGAACTATTTTACCTTTGGTCACTTAGTGGCTAATTGTGGCTTATCGTATGAAAATGTATGATTTTTAAAAGGATGTGTGGCATCAAACCCCAGCCCTAAACCCAACTGTCAATATGGATAAGCAAATTACAAGAATGAGATTGTACAAATTCATACAAATCAGCCACTAAATCAAAAAGTGACAAATTTCCACGAGATGGCATTGGACAAATGTGAACTCTGAACACAATAACTGTATATAATTCTATAACACATGCTTTCTTTGTTCTGTTGAGCAGGTGGCAATTAAGTTTGCCAACACCAAGAACGTCAAGTTCATCGACATT[G/A]TAAGTATGCTGTGCTCTTCTACTCTCATTCACTGTTTCATTTCACCTATCTATAACTCACAAGACAAACTGTTATCGTCGTCATGTTTTACACAATATCCATCCAATCATCATAACAAATATATTTCTTCCAGGACGGCTATCCGGAATCACTTCCAATGGAGGTTGCTCTTTCAATTCTTGCAAACCAAGAACCCGCAATACCGGAAATAATTAAGCTTTTGGACTGGCGTGTGGACGAGGAAGAGTACATCATGGTCCTAGAGCGGCCCATGCCCGCTGAAGAGCTGAGCACCTTTCTCATGTGCCAAGAGTCGTTCATTGATGAGGATCTGGCACGGGTGATCATGCGGCAGGCAACACTGGCAGCTCAAACGTGCTGCCGGCGCAAAGTGTTTCATCGCGACATCAAGATGGAGAACTTCCTGATCAACCCAGACACCCTCGAAGTCAAATTGATCGACTTTGGATGCGGGGAAATCCTCACCGATGCTCCTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39832
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088795 | Essential Splice Site | 44 | 258 | 2 | 5 |
ENSDART00000134936 | None | None | 212 | None | 3 |
ENSDART00000088795 | Essential Splice Site | 44 | 258 | 2 | 5 |
ENSDART00000134936 | None | None | 212 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 24667949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25242726 |
GRCz11 | 2 | 24898360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGCAATTAAGTTTGCCAACACCAAGAACGTCAAGTTCATCGACATT[G/A]TAAGTATGCTGTGCTCTTCTACTCTCATTCACTGTTTCATTTCACCTATC
Long Flanking Sequence:
TCAGGTATCATCAATTTTCATCAATTAATATCTAGATCACCGCTTTAAATCAGAATATCAGATAAAAATAATGGATAGATATGGGATTCTTATTTTTGAGCTAACTTAAACTGTTTCTTTGTTAAACTGTTTAGTGTTAATGACTGAAATTCAGCCTGATCTCAAGAGAAAACTGAACTATTTTACCTTTGGTCACTTAGTGGCTAATTGTGGCTTATCGTATGAAAATGTATGATTTTTAAAAGGATGTGTGGCATCAAACCCCAGCCCTAAACCCAACTGTCAATATGGATAAGCAAATTACAAGAATGAGATTGTACAAATTCATACAAATCAGCCACTAAATCAAAAAGTGACAAATTTCCACGAGATGGCATTGGACAAATGTGAACTCTGAACACAATAACTGTATATAATTCTATAACACATGCTTTCTTTGTTCTGTTGAGCAGGTGGCAATTAAGTTTGCCAACACCAAGAACGTCAAGTTCATCGACATT[G/A]TAAGTATGCTGTGCTCTTCTACTCTCATTCACTGTTTCATTTCACCTATCTATAACTCACAAGACAAACTGTTATCGTCGTCATGTTTTACACAATATCCATCCAATCATCATAACAAATATATTTCTTCCAGGACGGCTATCCGGAATCACTTCCAATGGAGGTTGCTCTTTCAATTCTTGCAAACCAAGAACCCGCAATACCGGAAATAATTAAGCTTTTGGACTGGCGTGTGGACGAGGAAGAGTACATCATGGTCCTAGAGCGGCCCATGCCCGCTGAAGAGCTGAGCACCTTTCTCATGTGCCAAGAGTCGTTCATTGATGAGGATCTGGCACGGGTGATCATGCGGCAGGCAACACTGGCAGCTCAAACGTGCTGCCGGCGCAAAGTGTTTCATCGCGACATCAAGATGGAGAACTTCCTGATCAACCCAGACACCCTCGAAGTCAAATTGATCGACTTTGGATGCGGGGAAATCCTCACCGATGCTCCTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16089
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 |
---|---|---|---|---|---|
ENSDART00000088795 | Nonsense | 157 | 258 | 3 | 5 |
ENSDART00000134936 | Nonsense | 113 | 212 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 24667477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25242254 |
GRCz11 | 2 | 24897888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTGATCAAYCCAGACACCCTYGAAGTCAAATTGATCGACTTTGGATG[C/A]GGGGAAATCCTCACCGATGCTCCTTACAGAGRTTTTGCTGGTATGTATGA
Long Flanking Sequence:
CACCAAGAACGTCAAGTTCATCGACATTGTAAGTATGCTGTGCTCTTCTACTCTCATTCACTGTTTCATTTCACCTATCTATAACTCACAAGACAAACTGTTATCGTCGTCATGTTTTACACAATATCCATCCAATCATCATAACAAATATATTTCTTCCAGGACGGCTATCCGGAATCACTTCCAATGGAGGTTGCTCTTTCAATTCTTGCAAACCAAGAACCCGCAATACCGGAAATAATTAAGCTTTTGGACTGGCGTGTGGACGAGGAAGAGTACATCATGGTCCTAGAGCGGCCCATGCCCGCTGAAGAGCTGAGCACCTTTCTCATGTGCCAAGAGTCGTTCATTGATGAGGATCTGGCACGGGTGATCATGCGGCAGGCAACACTGGCAGCTCAAACGTGCTGCCGGCGCAAAGTGTTTCATCGCGACATCAAGATGGAGAACTTCCTGATCAACCCAGACACCCTCGAAGTCAAATTGATCGACTTTGGATG[C/A]GGGGAAATCCTCACCGATGCTCCTTACAGAGGTTTTGCTGGTATGTATGATCCCTTAAACTGTGAAGTGTCTCAAACTGTAGTGATGAGTTCAGACTCTGAGTGGGTCAAGCTCTCACATACAGTAGCATCATAGAATGGAGTCCACTGATCTATTAAGACTGAAGATCTGGTGTATTAAAGGGATTGAAGATTTGTCCACTATTTACTCTTCCTCGAGTGATTTTAAACTTTTATGAGTTTCTTTTGTTGATATTTTGAAGAAAACTGAAAACCTGTAACCACTATGAAAGTCAATGGTTAGAGGTTTCCTACTTTCTTCAAAACATCTTCTTTTGTGCTCAGCATAAGAAACTCAAAAGGTTTGAAACTGGTCAAGAGTGAGTAAATGATGACAGAGTTTTACTTTTTGGCTGAACTGTCTTTTTAATGAATGAACTGAAAAACATTGCTTAATCCCTGTTGTAAATCGAATACTTTATTGCTGAGTGATGACTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18395
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 |
---|---|---|---|---|---|
ENSDART00000088795 | Nonsense | 211 | 258 | 4 | 5 |
ENSDART00000134936 | Nonsense | 167 | 212 | 2 | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24666816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25241593 |
GRCz11 | 2 | 24897227 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCTCTCGGAGTACTCCTTTATGCGATGATGTGTGGGGAGTTTCCAAAT[C/T]GACACGACCTGCAAATGATCAGATATAACATCTGGACCAAAGATCACTTG
Long Flanking Sequence:
CTGAAGATCTGGTGTATTAAAGGGATTGAAGATTTGTCCACTATTTACTCTTCCTCGAGTGATTTTAAACTTTTATGAGTTTCTTTTGTTGATATTTTGAAGAAAACTGAAAACCTGTAACCACTATGAAAGTCAATGGTTAGAGGTTTCCTACTTTCTTCAAAACATCTTCTTTTGTGCTCAGCATAAGAAACTCAAAAGGTTTGAAACTGGTCAAGAGTGAGTAAATGATGACAGAGTTTTACTTTTTGGCTGAACTGTCTTTTTAATGAATGAACTGAAAAACATTGCTTAATCCCTGTTGTAAATCGAATACTTTATTGCTGAGTGATGACTATTTGATTAACAAAATGACTAACGGTTAAAATCTCTCTCATTCAGGCACAAATGAATATATACCACCTGAGTATCTTATGACTGGCGAGTACCACGGTGAACCAACGACAGTGTGGTCTCTCGGAGTACTCCTTTATGCGATGATGTGTGGGGAGTTTCCAAAT[C/T]GACACGACCTGCAAATGATCAGATATAACATCTGGACCAAAGATCACTTGACAAAAGGTAAAATCTCTATTTGGGTCAAGGAAAGTGGTCAATCTGAATAACACAAACTAGAGTTGTGAAGTAAATTTATGCTCTCTCTCTACTTTCTGCACAGAATGCTGTGATTTGATCCGCTGCTGTCTCCAGATCGACCCAGCGCAGCGAATTGAACTTGAGAAACTGAGTCTCCATGACTGGTTTATGGTATTGTTCACATTCTGAACATGTTTGATATTTCTTATGCACTCTTTTTACTAAATTTTCATAATCGTTTCGTTTACATACAGTTGAAGTCAGAACTATTTGCCCTCCTGAATTATCAGACCGCTTGTTTATTTTTCCTCCTATTTCTGTTTAACGGAGAGATTTTTTTAACACATTTCTAAACATAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGATATTTGTCAAGACACT
Associated Phenotype:
Not determined