ZMP
zgc:114045
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC569643 [Source:RefSeq peptide;Acc:NP_001025409]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14791 | Essential Splice Site | Available for shipment | Available now |
sa5406 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38602 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14791
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100804 | Essential Splice Site | 56 | 246 | None | 8 |
ENSDART00000113793 | Essential Splice Site | 56 | 246 | None | 8 |
ENSDART00000145832 | Essential Splice Site | 56 | 207 | None | 5 |
ENSDART00000146335 | None | None | 253 | None | 9 |
The following transcripts of ENSDARG00000069334 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21268100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19858536 |
GRCz11 | 7 | 20110504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGACATCACCGTGGGGTGCTTCGTGTGCACGTCATGCTCCGGAATGTTG[T/A]GARTTATAATACCCAAGTGCATGYGATTATTAGTGATTACAAACAGATTT
Long Flanking Sequence:
TTTTTTGCGCCCACAGGAGAAAAACCGCAGCAATGAATAAATAAACGGGGCGGTTGTAAAACTCCAGGCGGATCGGCCAGTCGTGACCACGGAGGCTACGCACGCATGTGAGATTCGTTTCTTGTCAATTCAAGTGTATGGCCGGTCGATCGGACGCTTGATTTTGGCACCATACAAGAAGAAGAGCTGCAGCCGCATAGCCGTGCTCAGAATGCGGGCGTGAGAGACGGACTACGGCGGGGGAATTAAAGTGCAACGGTGGGCGAGTGAACGGCTCCCCCACAACAGTCTCGAGGGCCAGGGGGTGTGTGCGACTGCAGGGCACCAGCAGCATGTCGAACCGAAAACACCGGGACAACCAGGAGATCTGCGCCCGCAAGGTCCGCGAGCTCGCCCAGACGGGAGTGAACAAGCACTGCTTCGAGTGCAACCAACCCGGGGTGACTTACATCGACATCACCGTGGGGTGCTTCGTGTGCACGTCATGCTCCGGAATGTTG[T/A]GAGTTATAATACCCAAGTGCATGTGATTATTAGTGATTACAAACAGATTTGTATTAATGTTGTTATTCCTCAAACTCTGAACTGAACCTTCAGGAAATATGCAGATGCAGCGCAGTTACAGATCTCTGGTTGTGTTTACATTCATGAACACAGTCCGTAATTACTACTTTGTCGTTTTCAGGCGTGCCCCGGTCTCGCCTGCGTTACGTATCATTTCGTCATGATTTCAGGTTTGCCATCAATATAAACGTGTTTTCTGCATGTGGGCAAAGGAATGGTGTGATTCCACCTCAGTTTCAGTCTGCAACTGCACTTACTGTATACGAACAAACACATCTTGCTAGTTCTTCACTGTGCACTGAAGAAAAAAACAAACGCAGCCCGCTTCCTTTACGGTTTTGTCATTTGTTACTGCAAGAGGTTCTTGCAGGCTCTCATTTTCACAGCCCTGTCACATCCCACCCTATCGATGTTAAAAATGAAGGCAAGCCCTCATCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5406
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100804 | Nonsense | 100 | 246 | 3 | 8 |
ENSDART00000113793 | Nonsense | 100 | 246 | 3 | 8 |
ENSDART00000145832 | Nonsense | 100 | 207 | 3 | 5 |
ENSDART00000146335 | None | None | 253 | None | 9 |
The following transcripts of ENSDARG00000069334 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21275565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19866001 |
GRCz11 | 7 | 20117969 |
KASP Assay ID:
554-3546.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGGGGTTGTTAGGTTGGAAGGAGGACCTGGCTCTGCACATTTGACCCC[A/T]AAACCGACGGCTGTTTTGATGCACGTGACACGCAGAAGCTGAAGGAGTTC
Long Flanking Sequence:
ACAAATTCTGCACCTTTGTCAGTGAGCCGTGGGTCTTCTGAACTCTTCGAACCCCCCTGGCTACGGGCTTGTATTATATTATCCTATTATAGGTGCAAATAATTTAACTTGCATTTAGAAACACCCTTAAAAGAAAATTGCACTGACGTAGGCTGTATATTTATTTTGTGGGGTATAAAGTGAAACAATTTCACAGCATAATACTCACTACTTTCTATTCTTGAGTTCTTTTAAAATGACTACCTTTTACTTTAAGTATTAAAGAGAACAGATACTTTTATTTTACTTGCACTTCATTTTTTGGCAAGTAATGGTCCTTGAGTATGATTTCTCAGTACTATTTCCAGCACTGCTGTAGGGTCACCCTAAGCAAACATGTTTGAGGAAGTACTCTGTGTAAACTTTGTTAACGAGGCTTTAAAAGTAGCTTAACTGTGTGTATTCTTGGGCTGTGGGGTTGTTAGGTTGGAAGGAGGACCTGGCTCTGCACATTTGACCCC[A/T]AAACCGACGGCTGTTTTGATGCACGTGACACGCAGAAGCTGAAGGAGTTCTTGCAGGACAAATATGAGAGGAAGAAATGGTGAGCGAGAAGTAGTGTGGTCATAAAGGGTGTTTCAGAGCGGATCAGAATGAATTATTAATGCATGCTGAACCATGCTGCTGTTCTCACTGGATTATCTGTAGATGAAAGTCAAAGAATGCTTGACTTAAGAGGGGTCTGTTTTTTCTCCCCAGGCATTTCTCTAAAAGCAAGATGCGCCGGGATACAGACACACCGTGGGGTCCAGGGGTTCAGGCTATTCCAGCTCCACATGGGCCTGCTCAGAATCAGCCTCCGCCTGGACATCCACTGAACCCCACTAACCGGCCCACTCGCACACTGGTGAGGAAGAAACAGAGTGGTCCAGGGATTTCATATATCTTTGAATTCAAATGAAAAATGAGCGAGGCAAATAAAAGAAAATCAATAGTGCCTTTTTGAATGTGTATTCATGTCTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38602
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100804 | Essential Splice Site | 238 | 246 | 7 | 8 |
ENSDART00000113793 | None | None | 246 | None | 8 |
ENSDART00000145832 | None | None | 207 | None | 5 |
ENSDART00000146335 | Essential Splice Site | 41 | 253 | 2 | 9 |
The following transcripts of ENSDARG00000069334 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 21282932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19873368 |
GRCz11 | 7 | 20125336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTTATTTCACAGCCAGTAGCACTTTCAAAAACAGCTTTACTTTAGG[T/G]AAGTCCCATAATCGCACACTGCAGACACTTCAGCTGTACCTCAGACCATC
Long Flanking Sequence:
TGTGGAGAGACAGAGACCAGGAGTTATGTCTTCAGGAATTGGACCCCAGAATCATCCCTCCTCTTTCCCAGCCCTGCCACGTCCTTCAGGTACACCCAGACACAAACATTAAGTACGAGTTTGAACTCTGTTTAAAGTATGATTTTTAGTTGTTATGAATTACACAGGACACAAAGACATGTCCACATAAACCACTTCAACATTTTAACACCAAGCTCATAACCATTTCATTACACACATTTCCTCATAAACCACCAAGACACACACACACACACATCCAGTAATGTACAGACATCTTCAGCTAAAGCACAAAATACTGTCACCTCCATTATTGTCAACTCTGTTACTGTTTAAAATGTGGGATTTCACTATATATTGATATTTCTGTAATGTTTAATGCATTGTCCATTAAGCCATACCAGGTTCCTTTTAACTCATCTTCCCTCTTTTGTTCCTTATTTCACAGCCAGTAGCACTTTCAAAAACAGCTTTACTTTAGG[T/G]AAGTCCCATAATCGCACACTGCAGACACTTCAGCTGTACCTCAGACCATCTGGCTGCAATGCTGAGTGAGCCAGCCATGACAGGCAATGAGAAAACGCATTCATTACTGTGCAGATATAATGTTGCCGTATATATGTGAGTGTGTCAGGGAGAAAGAAACAGAAAAGAAAAGCTTGACGCTATGCAGAATGAAACCCCTGTGGAATGATGCTGTTAGCAATAAACCAGCGGTTTACATCAAGATCAAATTGCCAAGCAAGTTTTAATGCACAATAAACACAAACTGTTTTGGATGTCTGCAGTATTAGAGTTGAAGATCAAATTATTAGCCCTTCAGTGAAATGAATTCTTTTTAACAGAAAACAGAGATTTAAAATACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGCAAATTTCTAATCAGCCAATCACATGGGAGCAACTCAATGCATTTAGGCATGTAGACATGGTCAAGACAATCT
Associated Phenotype:
Not determined