ZMP
zgc:152968
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC564848 [Source:RefSeq peptide;Acc:NP_001071033]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30801 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa897 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30801
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053780 | None | None | 506 | None | 12 |
ENSDART00000075160 | Nonsense | 1045 | 1213 | 13 | 17 |
ENSDART00000130013 | Nonsense | 1052 | 1220 | 15 | 19 |
ENSDART00000139636 | Nonsense | 1083 | 1251 | 13 | 17 |
The following transcripts of ENSDARG00000037002 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 35701878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35261736 |
GRCz11 | 1 | 35993763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGTTAGCCTTCAGGGCTTTGTGAGCAGTCTTCATCAGTCTGCGGTG[G/T]GAAAAACATGTCCAGGAATCTATGCCATTGACACACAAACAGTAAGGTTT
Long Flanking Sequence:
CTCCGTCGACAGGAGTGGAAAACACACACGCAGAGAAGAGTGTAACTATCATTATGGAAAAGTCATAGAGAATAGAGGTAAGAATGTTTTCAAAATTGATTTGAGTTTTTATTTCCATCAATATCTATTATTTACTCTTTCTTCTGCCATAGTGCCAGGCGGTGTTGAGACGCGCTACAGTTGTTGTGAGAATGCAGTTGGGTCACCTGGATGTCAAGTCTTCAATGTATTATAATCTCTGTTCCAATTATACTCATGCTTTATTAGAGGGACTGAAAACATTTCACCTGATTTGTCTTCACTCTATTATGCTATGATTTTTGTCCTTGAACTTTGATTCAATTGTGATATTGTAGCATTTCACCAAAGCCATTAACCTGATGTTTTCAATGACCAAAGTTGACTTTCAGTGTATTTTCTTGTGTACTTATTTACAGCTTCACGTGCATGATGCAGTTAGCCTTCAGGGCTTTGTGAGCAGTCTTCATCAGTCTGCGGTG[G/T]GAAAAACATGTCCAGGAATCTATGCCATTGACACACAAACAGTAAGGTTTAAGTACTGATCATAGTTGAGAGTTAAAAAATAATAATAACCAAGGAAAAAAAGCAGGTAATTTGATATTTAATTTTGTTTTTCACCAGTGTTACACGACTCAAGGTCTGGAACTAGCAAGAGTGACTGTAGTGAGCAGCAGTTTGCAAGTTGTCTTTGACTCCTTTGTCAAGCCTGATAATGATGTCATTGACTATAATACCAGGTAGGGATTGCTTTCAAGGCATAACACTAAATTTGGCAACATTTGAATTGGATCATCACCTTTCATCAAAGTTTTCCACTGTTTCCTGTTTTAAGACAATTTTGACAAACTTTTTTGACATACTTTAAATGTTGATTGGTTTATTTTGCTTTTCACAATGTTGTTTTAGATGAGTGGGGGCATGGTGACATTGACATGGTAATGGTGACATTCAAAAGAACTATAGGTGTTTATTGTACTTGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa897
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 |
---|---|---|---|---|---|
ENSDART00000053780 | None | None | 506 | None | 12 |
ENSDART00000075160 | Essential Splice Site | 1184 | 1213 | 16 | 17 |
ENSDART00000130013 | Essential Splice Site | 1191 | 1220 | 18 | 19 |
ENSDART00000139636 | Essential Splice Site | 1222 | 1251 | 16 | 17 |
The following transcripts of ENSDARG00000037002 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 35704191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35264049 |
GRCz11 | 1 | 35996076 |
KASP Assay ID:
554-0804.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAACAGTCTGACTGCAGACTACCTCCGGAGAATTATACAAGAGAGTGG[T/C]ATGTTGGCCTACTRCACACATTTGTAAACAATGACCATGAGAAAGCCTCC
Long Flanking Sequence:
TACATCTGTAAAAACCTTAAATTCAAAATGTCAAAACTAAACATGAAATTCGAACCTGGCTTGCTCCGGTGTTCTCAAACTGTGCTAAATTATGTCAATTATAACTCTTTATCCTGCACAGATTCTCAGGCATCAGTGAAGCTGATGTGAAGAGCAGCAGCTCGTCTTTGCGTGATGTACAAGCAGTGCTTTTGAGTTTTATTAATGCGGACACAATTCTGATTGGCCATGGCTTGGAGAATGACTTGGCTGCCCTCAAAGTGAGTTCCAACAGTATGCCGAAATAACAGTATAAACTGTCAACATTATCAACCTGGCATTGGCTTTTTTGATTAGAGGCTCACAAGAATCACCTGTTGGTTGTTCTGCCATCTTCAGATTATTCACAGCACTGTGGTTGATACCTCTGTGGTGTTTCCCCATCGTCTGGGTTTGCCACACAAAAGAGAGCTAAACAGTCTGACTGCAGACTACCTCCGGAGAATTATACAAGAGAGTGG[T/C]ATGTTGGCCTACTGCACACATTTGTAAACAATGACCATGAGAAAGCCTCCCTCAATCACAGCCTGTAGCTTTGGATACCAGGGGCCTGTTTCAGTAAGGAGGTTCAAACAACTCTGAGTTTAAACTTGAACTCTGAGTTGATTTACCGAGAGATTAAAAACTCAGAGTTTTCGGTTTCAGAATAGCTGATTTGAGTTAGGTCAATCAACTTTGAGTAGACCAACTCAAAGTTAAGCGTGCATACCGTGACTATAAAAAGGCATCATCAATGGACCGCAGATATTATGAGTGACAATGGCAACATCTTAAAAAAAAGAGATCAGCATTTCTTTCTCCGGCTGAATTTGATCTGCTCATGCAAAGTTATAGCAAATATGAGCGTATATATTTAAAAAGAAGCAACCATCAGTGAAACAGAAACAGTTAGCCTGGGAAAACAGCTGCTCAAGTAAATGCGCAATTTTTAATTTAAAGTATTTAAATATTTAAGTATAATAAAA
Associated Phenotype:
Not determined