ZMP
zgc:113276
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553748 [Source:RefSeq peptide;Acc:NP_001018555]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12326 | Nonsense | Available for shipment | Available now |
sa41864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45431 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12326
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 |
---|---|---|---|---|---|
ENSDART00000079175 | Nonsense | 151 | 513 | 3 | 9 |
The following transcripts of ENSDARG00000056650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 30821899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29697885 |
GRCz11 | 11 | 29945059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATTTCAGTCTTCCAGGAACACAGCTCAGTATTGACTWCTTCCRGGAG[C/T]AGGTCTGAGCCTCACTCRGCATGAGGAATTGAAAGGAATGCCYGACTAAC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTCGTTTAACTACTGTAAATCTCATGAGGCCAATAACTGATTTTAGAACACATAAATGTGTTAAACTATTGAAATAGTATCTTCAAATAGTATCATATCAATGGTACTTTGTTGTGACTTTTTTAACTGGTTAGAGAAGAACAATGTGCAAACATTATAGTGATATTGCCCATTAAAGGTCTAATAGTTTCTTCATCTCAATGTGCAATAGAAAGCCTTGCAGGACTTTGTGTTGGAGCAAAATCGGGAGGCGGAACTGCACAGTCTACCTGAGCAAATGTACATTCAGGACGAGCATGCCTTTTTTAATGACAATCGCCTGGGAAAGAAAGACAAAAAGCTGCTTAGCACAACAAAAGGCCTGCAGAAAAACCTGTATTTCAGTCTTCCAGGAACACAGCTCAGTATTGACTTCTTCCAGGAG[C/T]AGGTCTGAGCCTCACTCAGCATGAGGAATTGAAAGGAATGCCTGACTAACAATAATTAATAATACACTGATTGTGAAAGATTGGCTTTAACAGCAACTCTGGTGGCAAGAAAAAGCTGCATGATACAAATATGATCAATTATCTCATTTGGAATGCTATGTGTGTTAATATTTTTTAAAAATTCACTGAAGACTCTCTTTTTTATACTTGCCTATCTGTATGTTATGTGTTCGATCAGTTTGATACGTTATAAGGCCTCTTCTTAAGTGTAAAGTGCTTTAAGAATTAAGTTATGTAAGGCACTGAACAAAAATACATTTTAATTTTACTTGCATTATGGAACGTGCATTATGGAAAAACTAAATTATGGATTACATTGCCAAGGACTTCCTCTCAGGTTCGCAAATATGACCTGGAGAGTGTCTTAATCAAAGCCACGGTGGACAGAATCATCCCAGTCTTAACTGAGGACGAGAGCAATGTGAAGTTTTTCAAGGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41864
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 |
---|---|---|---|---|---|
ENSDART00000079175 | Nonsense | 355 | 513 | 6 | 9 |
The following transcripts of ENSDARG00000056650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 30819060)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29695046 |
GRCz11 | 11 | 29942220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATGATAAAACAAGCCAGGAAAGGAGGAGCAGTGACCCCTGAGGCCTA[T/A]GCACAACTTCAGCCTTTTATTCAGAGCGGAAAGCTGCTCATCAGAGCTCA
Long Flanking Sequence:
TGGAAACCAGACTTGTTCCAGTTATGTCCTGTAATTCACTGCGGCATGTGGGCCAAGCAAAACCTGATTGATTGGGCCGGAGCTGGGCCAGAGAAATTTGTCTCTGTGGGATGGTTACAAAACTTTTATCAATAAGCTAATTGAGAAGAGATTACAGAGCCATGAATATACAATTATAACATGGCTTTAAACAAACATATATTATAAATATTATTTCATTACAATAAGCATTGCAAAATTAATAAAGATATAGTTAACTAATTAATGGAGTATATAAATCCTCTCTGTTGAATATGACTCTGTTTCGCTCTTTGGCAGCTGAAGCAGTTTGACGTTGGGGATGTTGAGAGTCTTATTGGACGCTATTCACATGTTGAGCATGGGATCAAATTAGATGGCCTGGCCTACTTAAAGCAGTTCTATAATGAAAGAAGTCTTTATAAAAGACTAGTAATGATAAAACAAGCCAGGAAAGGAGGAGCAGTGACCCCTGAGGCCTA[T/A]GCACAACTTCAGCCTTTTATTCAGAGCGGAAAGCTGCTCATCAGAGCTCACTGTCAGGTTGGTCACTTTTTGCTGTACTGCAAGGCTGCTGTGCTCGCGTTATTAACCACTCATCAGTATTCTGTGTTTTATCCTAAGGTGACCAAAGCTAAATGGTGTTATGAGTCTCAGCAATGGAGGGTCTCCTTGTGCAGTGGCGAACAATGGAGAGGAGAACAGATTTGGCTGGCAACTGGCTGCAAACTGGATGTCACTCAGGACCCTTTACTCTCTGATGTCAAGAGACAATTCCCCATTCATGTGAGAAAGTGATAATGTATAAAGTTTGCATCATTCAATTTCATATAACAATTCATTGTTATATATAAAAAAGTTGTGTAACAAACAAAGTTAAAACGTTCAAACAAAGTAAAAAAGCTACAAGTTACTAAAAGTTTGGGAGATAAATTATATATCATTTATACATACTTACTCCCAGGGCCATTTATATCGAAGTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45431
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 |
---|---|---|---|---|---|
ENSDART00000079175 | Essential Splice Site | 428 | 513 | 7 | 9 |
The following transcripts of ENSDARG00000056650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 30818759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29694745 |
GRCz11 | 11 | 29941919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTCAGGACCCTTTACTCTCTGATGTCAAGAGACAATTCCCCATTCAT[G/A]TGAGAAAGTGATAATGTATAAAGTTTGCATCATTCAATTTCATATAACAA
Long Flanking Sequence:
GTTTCGCTCTTTGGCAGCTGAAGCAGTTTGACGTTGGGGATGTTGAGAGTCTTATTGGACGCTATTCACATGTTGAGCATGGGATCAAATTAGATGGCCTGGCCTACTTAAAGCAGTTCTATAATGAAAGAAGTCTTTATAAAAGACTAGTAATGATAAAACAAGCCAGGAAAGGAGGAGCAGTGACCCCTGAGGCCTATGCACAACTTCAGCCTTTTATTCAGAGCGGAAAGCTGCTCATCAGAGCTCACTGTCAGGTTGGTCACTTTTTGCTGTACTGCAAGGCTGCTGTGCTCGCGTTATTAACCACTCATCAGTATTCTGTGTTTTATCCTAAGGTGACCAAAGCTAAATGGTGTTATGAGTCTCAGCAATGGAGGGTCTCCTTGTGCAGTGGCGAACAATGGAGAGGAGAACAGATTTGGCTGGCAACTGGCTGCAAACTGGATGTCACTCAGGACCCTTTACTCTCTGATGTCAAGAGACAATTCCCCATTCAT[G/A]TGAGAAAGTGATAATGTATAAAGTTTGCATCATTCAATTTCATATAACAATTCATTGTTATATATAAAAAAGTTGTGTAACAAACAAAGTTAAAACGTTCAAACAAAGTAAAAAAGCTACAAGTTACTAAAAGTTTGGGAGATAAATTATATATCATTTATACATACTTACTCCCAGGGCCATTTATATCGAAGTTGATATTTAGTTGCACCACATTCGTGTTTCATAACATCCAGTTTTTATAAGGCGAGTTGTTAGCCCAACACTCAACCCCCACTACACAATACACTACAAACAATTTAGCTTACTTAAATTCACCTACAGTACATGTCTTTGGACTGTGGGGGAAATCAGAGCACCCAGAGGTAACCCATGAGAACACTGCGAGAACATGCAAACTCCACACAGAAATGCCTACTGACCCAGCTCGGGCTCATTGTATACATTACCGTAAATATTTTCTTTAAAAAAATTATGTACAGTTGAAATCAGATTTATTG
Associated Phenotype:
Not determined