ZMP
si:ch211-59c24.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1MTA3]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16748 | Nonsense | Available for shipment | Available now |
sa36584 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44883 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16748
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 |
---|---|---|---|---|---|
ENSDART00000133555 | None | None | 129 | None | 5 |
ENSDART00000147613 | Nonsense | 328 | 1017 | 5 | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 10337209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 10920455 |
GRCz11 | 18 | 10889173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTGAAGAGTGCAGAGATTAGAAAAAGTTTAGGGCTYACTCCCCTGGAA[C/T]GAAGCAAAACTGYGGTGGAGAAGAGCATTGTGAAAACKCCAACACCCGAA
Long Flanking Sequence:
ATGAAGTTTCTCCTGTAGTACTAGTTAAATCTCCTGGTGCACGTTTCTTCCCTGAGCCCTATCTGCCTGATAAAGTCAAGCAGAACATTCCCCCGCCTCAGAGTCCTGATGTTAAAACCCCTCATTCTCCTGTAGCTCAAATCATTGCGCTGTCGCCCATCTGTTCCCAGCCTGTTCCACAACCAGGCACAGCATCTCCCAAATCTCCAGTCCAACCACAGCCTTGTGCCTGTTCTCCAACAGGCAATCCTTTGTCTCCGATTTGTACCCAATCGCAACCCTGCAATGAGCCACCTTCACCCCTATCCACAAGCTCCCCCGTCAGGACTCAACCAGTCCCAGCAGTAACTTCTACTCCTTTAGCTAAACCTGCTTCCGAGAATAGGACTAATGAACATTTGAAAGATTCAACTCCTGAGCTTAAGAAAACAGACCTCATTGAGGAGTTCTGGTTGAAGAGTGCAGAGATTAGAAAAAGTTTAGGGCTCACTCCCCTGGAA[C/T]GAAGCAAAACTGCGGTGGAGAAGAGCATTGTGAAAACTCCAACACCCGAATCATCATCTCCTAAGTCTTATACCCCAGAGGACTTGTCTGAGGAACAGAAGCCTACATTTACGGGCCGTTCTATCATACGCAGGATCAATATTACCTTGGAGGGTCAGGTTATATCTCCGGTGGAACCTAAAAGTAATGGTTCAGAAAAGAAGGACTTAAGCAGCAGTTCAGGGTTGGGTCTAAACGGAAGTGTGACCACCAGTCAGACAGCTGCTAGCGACAGCTACAACAACTCTGATTCTACAATGCTTACCCCTCCTTCCAGTCCACCACCTCCTCCACCCAGGGAGGAACCTGCTTGTCTCCAAAACAAGAAGTCTCAGGTTTCCTGGGACAACCTCCTTGAAGGCACAGAAGAACCCAAATCTGAGACCATGCCCATTAAGCCCAGGACTCCAGTTAGTCCCCCTCAACCAAAACAAAAACCAGTTACAGCTCCAGTGCCAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36584
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 |
---|---|---|---|---|---|
ENSDART00000133555 | None | None | 129 | None | 5 |
ENSDART00000147613 | Essential Splice Site | 783 | 1017 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 10338576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 10921822 |
GRCz11 | 18 | 10890540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGAGACTCGGGGAAGAAGAAAGATTCACCCCTGGACAGGTCCTCAGG[T/C]CAGCTGGAAGTTTTTCATTTGAATGGCTCATCTTTTTTTCTAGCAGTCTT
Long Flanking Sequence:
GATGCAATGGCCAAGCAGCTTACAAAGATGAAAGATTCTGAGGTTGCCAAGGGGGCTGTAGCAAAAGTAGCCTGGGATATTCCTGAAACAAAAGGAAAAAGCAAAAAGCAATCTAAAGCCCAGAAGGACTCTGCAGTGAAGGCCTTGGAGTCCAAAAAGCAAGCAGACACACTTCCAGACCGTTTCTTCTCTACACCATCTAGTAAGGCCTTAGACAGCTCTGTCACATCTTCAGAGAGCTCCACAGGGGGCAAAAGCAAGAAACGCAGCTCACTGTTTTCTCCACGCAAAAACAAAAAAGAAAAGAAAGCCAAAAATGAAAGACTGTCCAGCACTGAAGAAACGCCGCCCAAGCACAAGTCCCTTTGGAAAGCAGTGTTCTCCGGCTACAAGAAGGACAAAAAGAAGAAAGATGACAAGTCATGCCCAAGTACACCCTCAAGCTCTACAACTGGAGACTCGGGGAAGAAGAAAGATTCACCCCTGGACAGGTCCTCAGG[T/C]CAGCTGGAAGTTTTTCATTTGAATGGCTCATCTTTTTTTCTAGCAGTCTTACAGAATTTATATAGTCCTACTCTGACACCATCCTAAGCATCATTAAACCTCTTAAATGACTGATTTAGATCAATTTGTGCAGTACATTTAATTTAGTTCGCTGTCAGTATACGATAATTTCCTCAAAAAGCAGCTCACTTCAGACCCTCATGGGTTTTGTTCTTGCAGAATTTTGCTGAAATTTAGTTTGACTTGCATTTTTTCTCAGTCTTTTTCCACTTACGCAAAGATCTGTTTAATTTACCGCTGTAGATTTACGTCTGAGGAGAAATCTAAGCTTTTCTGAGGACTCTGATCTCTCCTGTGACGATGTTCTGGAAAGATCCTCTCAGAAGTCCAAGGGTGATGTAAGTGTATATAATATTTAAAGAGTTTCTTCTTTCTGATTTCAGTCAAATGTTTTTTTTTTCTCTCTGCAGCTTAAACTTTAATGAAATCTTTTGCTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44883
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 |
---|---|---|---|---|---|
ENSDART00000133555 | Nonsense | 88 | 129 | 5 | 5 |
ENSDART00000147613 | Nonsense | 976 | 1017 | 12 | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 10369292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 10952538 |
GRCz11 | 18 | 10921256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGACAGAGGAGGAGCTGGCAGAGGAGAAGCAGATTCTGAATGAGATGT[T/A]GGAGGTGGTGGAGCAGCGAGACTCTCTGGTGGCCCTGCTGGAGGAACAGA
Long Flanking Sequence:
CCAAGCTCATGGGAGTCATACACAATATTCAATCTTTTTCCACTGCAGCATGACTTTATATTTTATACTGTACAGTATTTCTGTTAAGTGACAAGACTTTTGTTTAAGAAAATTCAGAGCTTACTGTCCTAATTAAATTATTAAAAATCAAGGCATGATCATATTTTATTTTGGTAAAATAAGCCTAATCTAGAGGCCTTTGTTTTTTATATAAGACACTTCTGATACCAAATGATCAACTAGAAGTCAAGTTATTATTTGTTGTTTCTAAAACTTGCATAGGTGACAAGACTTTTGTCAGGCAGTGTACATAGCGGCTATAGCAAAACACACATTTTTTTTTTACAACAAACAATCCAACAGGAAAAAGAAACGACTGTTGTATTTCATGATGTATGGCCGTTTTGTCTTTTAAAAGAAGCTAAAATCCCCCCTGTCTGCAGATCATCTGAAGACAGAGGAGGAGCTGGCAGAGGAGAAGCAGATTCTGAATGAGATGT[T/A]GGAGGTGGTGGAGCAGCGAGACTCTCTGGTGGCCCTGCTGGAGGAACAGAGACTCAGGGAGAAGGAAGAAGATAAAGACCTGGAGGCGGTGATGCTCTCCAAAGGATTCAACCTCAACTGGGCTTAACATAACAATGTCCAAAAACCATCTAACCCGCCAGCGCTTCACTACAGGGAGTACAAAAAAAAATCTAAATCTCAGAAAGAGTCGCTCTTGGTTTTATTGGGCATGTCAACAACGTTTACAAACCTATTCATGAGCTCGATGGTGATGTTTTTATGAGGTTTCCTGGCACGACTCAGGGCGTTTTGTCCAATCGGCAGCCAAGGCAAGGCGTTCTCCATTTCGGAAATAAGGAGAACATAAATTTTTATTTAGTAATTTCTGGGACATATCAATCAATCCTGCTGATGTTGAGGAAGTCTGAGACTAAATGACTCTACATATAAAGCCAGTCTTGTTTATCAGAGAATGTCTGGTCAATCAACTGTTACGTTTT
Associated Phenotype:
Not determined