ZMP
zgc:193613
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC322327 [Source:RefSeq peptide;Acc:NP_001124058]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22838 | Essential Splice Site | Available for shipment | Available now |
sa42718 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22838
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058964 | Essential Splice Site | 89 | 141 | None | 4 |
ENSDART00000135084 | Essential Splice Site | 89 | 141 | None | 4 |
The following transcripts of ENSDARG00000015866 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 26219135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 24064810 |
GRCz11 | 16 | 23979842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAACTGAAGAAAAGCCCAAGAGTGGAGAGCTTCATCAAAATCGCTGGG[T/C]AAGGGATACCGTACAGTGAATATTCCATTAAAAAATCATTCAAGTTTTTT
Long Flanking Sequence:
CTGTTCATCTTTATTAGCTACTCAGGAAAAAAAATGTTCAGTTTTAAGTGGATTAAATTGATCTAAAGTGATCAAATCAGCTGTACATGTCACCATTTAGTTGTGTTTTACTACTAAGAGTTTACTAACCACACAAATACTTTATTCCTGCAGTCTGTTTCTCATGTCTCCACAAAAAAAACAAGACTTTAGATGCTAGGAAGTCTTCCTTAAATATGGACAAAACAGGCTGTTTAATCCCATTCTTAAGAATTTCTTCTTCTCTTGCAGTGTCAGTGTGTGTCTGGGCACAGGAATGGCCCGTTCCTGACAAGGAGTTAGTGGATAAATATGACGGACTGAGGACAGTTTTCATCAAGAGGCTTGTCAATGCTTGGGAAAAGATCAAAACTGCAGTTGAGCCAGCACTAGAGGGCTCACCAACAGCAGGCAGTCTGAAGGATGTTGTTGAGGAACTGAAGAAAAGCCCAAGAGTGGAGAGCTTCATCAAAATCGCTGGG[T/C]AAGGGATACCGTACAGTGAATATTCCATTAAAAAATCATTCAAGTTTTTTGTTCGTGTGAGTGTAAACTTGCTTATTTTGTGAACTTCTTCCAGTGGTTTGGCCTCTGAACTCGAACCAGTTGTGGACAAAGCTCGCCTGAATGCTCTCGGTGTTTACGGCCATTACTTCAGACCCTATGTTGGTGCGTACCTGGACAGTGCCATCAACAACGTCAAGCCCGTGCTGGACACCGTACTGCCCCAGGGAAATTAAGAGTCTTGTTGACTCCCTCAACCATGTATTTTCATTACTTTAATTATGGATACCAATCTGACAGCTGTGTGTCCATTCGTTATGTCAGTACAGTTAGTTTTTGCATGTATATACTGTATCTGTGTCTTTGATACTGTCCTGTTCAGAGCAGGAAAATAACATCCCGTCCAGCATTAATAGAGTTTGAATTATGTGATTTTGTGTTCCTCATGAAGAAAAAGCAAGACTCATACAAAATAAAAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42718
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 |
---|---|---|---|---|---|
ENSDART00000058964 | Nonsense | 130 | 141 | 4 | 4 |
ENSDART00000135084 | Nonsense | 130 | 141 | 4 | 4 |
The following transcripts of ENSDARG00000015866 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 26219351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 24065026 |
GRCz11 | 16 | 23980058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCAGACCCTATGTTGGTGCGTACCTGGACAGTGCCATCAACAACGTC[A/T]AGCCCGTGCTGGACACCGTACTGCCCCAGGGAAATTAAGAGTCTTGTTGA
Long Flanking Sequence:
TGGACAAAACAGGCTGTTTAATCCCATTCTTAAGAATTTCTTCTTCTCTTGCAGTGTCAGTGTGTGTCTGGGCACAGGAATGGCCCGTTCCTGACAAGGAGTTAGTGGATAAATATGACGGACTGAGGACAGTTTTCATCAAGAGGCTTGTCAATGCTTGGGAAAAGATCAAAACTGCAGTTGAGCCAGCACTAGAGGGCTCACCAACAGCAGGCAGTCTGAAGGATGTTGTTGAGGAACTGAAGAAAAGCCCAAGAGTGGAGAGCTTCATCAAAATCGCTGGGTAAGGGATACCGTACAGTGAATATTCCATTAAAAAATCATTCAAGTTTTTTGTTCGTGTGAGTGTAAACTTGCTTATTTTGTGAACTTCTTCCAGTGGTTTGGCCTCTGAACTCGAACCAGTTGTGGACAAAGCTCGCCTGAATGCTCTCGGTGTTTACGGCCATTACTTCAGACCCTATGTTGGTGCGTACCTGGACAGTGCCATCAACAACGTC[A/T]AGCCCGTGCTGGACACCGTACTGCCCCAGGGAAATTAAGAGTCTTGTTGACTCCCTCAACCATGTATTTTCATTACTTTAATTATGGATACCAATCTGACAGCTGTGTGTCCATTCGTTATGTCAGTACAGTTAGTTTTTGCATGTATATACTGTATCTGTGTCTTTGATACTGTCCTGTTCAGAGCAGGAAAATAACATCCCGTCCAGCATTAATAGAGTTTGAATTATGTGATTTTGTGTTCCTCATGAAGAAAAAGCAAGACTCATACAAAATAAAAAAGCCTCTTGATATTGCAAAGCCTGCTTTTGAGTGTGATTATGACAAATGCATAGGCTCAAACGTGTATCAATGAAAAAGTACAGTAAAACATGGGTCCTTAAAAAACAGCATCATTTAGAGGTTTAACACAGAAAGGTCAGCATTCTCAAGCGCATTAAACTCTTACAATGCTGAGCTCCAAAGTTTCTCTCTAGCCTGACATGAACTTAATTTGTAAT
Associated Phenotype:
Not determined