ZMP
zgc:153292
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100003014 [Source:RefSeq peptide;Acc:NP_001070137]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7545 | Missense | Mutation detected in F1 DNA | Not yet available |
sa33202 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16741 | Nonsense | Available for shipment | Available now |
sa15015 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7545
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103421 | Missense | 157 | 415 | 5 | 13 |
ENSDART00000123055 | Missense | 173 | 431 | 5 | 13 |
The following transcripts of ENSDARG00000070458 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 31235656)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30953695 |
GRCz11 | 3 | 31084537 |
KASP Assay ID:
554-4204.1 (used for ordering genotyping assays)
KASP Sequence:
CAAATGGTTCCAGCCGTGGACTCTTTCAYGCTGGCAGCYTCCAYGAKGAC[T/C]ACTGCAAACCTCAGGTTATTGATTGTTGTTTTATGTTTAGCGGCTTTAGG
Long Flanking Sequence:
AAATGTTTGCTTGTTTGTTTTAAACGTAGCTGCTAGACTGCAAAACATCCAAATGTTGTAAAGTTGGTTTTACCACAATTGTTATTTTACTTTTGGATTAGCGTTCTTATTAAATCTGGAGGGAATCAGTGGGGAAATGGTCTTAAGTTTTGACATCACAGCTGCAGTGCTCTTATGTGACACTACTAATCTTTTCAATATTCATACTTTATTTTTTATTCTTATTTCAAGTGATTATTTGTTTACTTTGCATGTTTAAGAATCGTACGCCGGTTGCAGTGCCTATTAAACCAAAACCAACCCTAGTGTCAGCACCAGTAACACCACGGTAAAGTACAGTATCTGGTATCAAATAAGTCAGAATCTGCAGTTGTTTTCCTTCTATCTGATCATCACTTGTTTATGGGTTTGCTAGGCTTGAAGGGACATTTGTTCGTGTGAATGTGGATTCAAATGGTTCCAGCCGTGGACTCTTTCACGCTGGCAGCTTCCACGATGAC[T/C]ACTGCAAACCTCAGGTTATTGATTGTTGTTTTATGTTTAGCGGCTTTAGGCTGCAAGTTTATTATACACTTAAACATTAATACATCAAACCATATGTTTTCACAGAGCTTTCACTGGATGAAGCTGTCGGAGGGTGATGGCGAATCTGATGATGACTCTAGTGTATGTAGTCCTTTATATTCTTTCAGTGTCTAAATCTCAAAACAAGTAGTGTGACTAGAAGACATATAATATAACTATTCAATCAATGTATACCTCAGTTTTTCCTTACTATTTTACTTACTCTTCAGTTTTTCATACTGTTGTTCTTACTAAATTCTTATGGTTATTTATATTATATTATACTATATATTATATAAAGATATGGCTAACATCCCCAAAAAAATTTATACAAACATGTAAATTGCTAAGACTCTAAGATTTAGCATTAATGTCTACGTTAATGTCGTTTGTTGCTAATATATATTAATTTACACAGTGACATAACCTGTTTACAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33202
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103421 | Nonsense | 228 | 415 | 8 | 13 |
ENSDART00000123055 | Nonsense | 244 | 431 | 8 | 13 |
The following transcripts of ENSDARG00000070458 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 31233900)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30951939 |
GRCz11 | 3 | 31082781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGAGTATAGATGTAACCGGGCCATTTCAAGAAAGCAAAGGCCCCTA[C/A]AGTCACATCGTGGTCATCTGTGACTATTACACCAAGTGGATTGAAATTTT
Long Flanking Sequence:
ACATTGTTATTAAATTTAAAAAAAATTATTGACATGTCTATTTTGTGTCTGACACATTTAATTTTGCATTTTAAAATTACTGATTTATTTTTACATGTAAGCAACAGCATACAGAACATATATCGGTTCATCTAAAAAGTTATCGGTATCGGCCCAAAAATGTAATAATTAAATTATATATTATATAATTATATATTGTCATATATATGAATATACATTTTTTCGCTATACTTCTACAGGACCCTGAAAGTGATGTCACCAGTGATGATGCACCTCTTGAAACCCCACAAAATCCAAACTCCAAGTTTATCAAGGTCTGTCTCTTACAGATTTATATGCAAATCTATTTCTCTGTGAAGACTAGGAAAAAAATAGCCTAAATAGATAATATAGATATATAGTTAACTTTCAAACTTTTTTTACACTTTCCAGGTGACAGAGAGATGGCAGTGGCTGAGTATAGATGTAACCGGGCCATTTCAAGAAAGCAAAGGCCCCTA[C/A]AGTCACATCGTGGTCATCTGTGACTATTACACCAAGTGGATTGAAATTTTCCCGACAGAAAAGCCTAATTCTGATTCTGTTGCCCTGCTTATGTGTGATGCCATTTCCCGATATGGTTTTCCTCTAGGGTTTCTCACTCCTTGGGGAGCAAGAGGGATTCAGGTCAGAACGGTAAGTCCTGCATTATGACTCCCTGGATAATACCAGAACAGTTCATGCATGCTTTTATTTTGGTCTCTTAAAATGTGAAGAGACGTTTCTTAATGCAGTTTAATGAATGACCTTCTCCAAATTTGCTTCTTATTATTTTCAAGGTTAACAGAGCACTGAATAACATTTTGATGATAAAGGATATTTCCCTTGTCTCTCGACATCACCAGGCGTCACAGCTGGAGCCACACACTCAGTATCACATTATCAAGTATGTTTGTTTATCTTCTGGACATATGCCACAGTGTAAGTTTGGAGTCATTTTGAAATGATTGTCCTGTTTCTCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16741
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103421 | Nonsense | 266 | 415 | 8 | 13 |
ENSDART00000123055 | Nonsense | 282 | 431 | 8 | 13 |
The following transcripts of ENSDARG00000070458 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 31233786)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30951825 |
GRCz11 | 3 | 31082667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCKAATTCTGATTCTGTYGCCCTGCTTATGTGTGATGCCATTTCCCGATA[T/A]GGTTTTCCTCTRGGGTTTCTCACTCCTTGGGGAGCAAGAGGGATTCAGGT
Long Flanking Sequence:
AACATATATCGGTTCATCTAAAAAGTTATCGGTATCGGCCCAAAAATGTAATAATTAAATTATATATTATATAATTATATATTGTCATATATATGAATATACATTTTTTCGCTATACTTCTACAGGACCCTGAAAGTGATGTCACCAGTGATGATGCACCTCTTGAAACCCCACAAAATCCAAACTCCAAGTTTATCAAGGTCTGTCTCTTACAGATTTATATGCAAATCTATTTCTCTGTGAAGACTAGGAAAAAAATAGCCTAAATAGATAATATAGATATATAGTTAACTTTCAAACTTTTTTTACACTTTCCAGGTGACAGAGAGATGGCAGTGGCTGAGTATAGATGTAACCGGGCCATTTCAAGAAAGCAAAGGCCCCTACAGTCACATCGTGGTCATCTGTGACTATTACACCAAGTGGATTGAAATTTTCCCGACAGAAAAGCCTAATTCTGATTCTGTTGCCCTGCTTATGTGTGATGCCATTTCCCGATA[T/A]GGTTTTCCTCTAGGGTTTCTCACTCCTTGGGGAGCAAGAGGGATTCAGGTCAGAACGGTAAGTCCTGCATTATGACTCCCTGGATAATACCAGAACAGTTCATGCATGCTTTTATTTTGGTCTCTTAAAATGTGAAGAGACGTTTCTTAATGCAGTTTAATGAATGACCTTCTCCAAATTTGCTTCTTATTATTTTCAAGGTTAACAGAGCACTGAATAACATTTTGATGATAAAGGATATTTCCCTTGTCTCTCGACATCACCAGGCGTCACAGCTGGAGCCACACACTCAGTATCACATTATCAAGTATGTTTGTTTATCTTCTGGACATATGCCACAGTGTAAGTTTGGAGTCATTTTGAAATGATTGTCCTGTTTCTCTTCAGCATGGTAGAAAATCTGGTGAAGAAGCATCCAGACAGTTGGCATGTTCATTTGCCTGTTAGCGTGCTGCGATTTAACTGCAGTGTCCATCCAGAAACCAAACACAGACCCTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15015
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 |
---|---|---|---|---|---|
ENSDART00000103421 | Essential Splice Site | 406 | 415 | None | 13 |
ENSDART00000123055 | Essential Splice Site | 422 | 431 | None | 13 |
The following transcripts of ENSDARG00000070458 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 31232227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30950266 |
GRCz11 | 3 | 31081108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAACCAAATCCTTTAAAAGAAATTGAGGCACTTAAACGAATATTCCG[T/C]GAGTATAACCCTATGCTGTCTGAAGCATTATCAGTGTCTGCTTTTCCTTT
Long Flanking Sequence:
CACTTTATTTAAAAAAAATGTACCCTTTAGTAAATTTTGATTTTGCTTGATTCTACATGTTTACAATAAACAAAATAGGGGTCAAAGTATTCTGGTGTATATTAGGCTCATAAAGGCTGTATTTATTTTGTCATTTCAAAGCGAACAGTTATATTGTGAAAAATTGTTACTAAGTATTTAAAAATTATTTTAAATGTAATGTTAGCCATTACTGCCATTTAATGTCACATGACTGAAGTTCAAAAGCAATTAATTGATCCTTTGAAACAAACAAAAAAAAACTGAAGGTTTGAAACCTTTATTGTAACATGTTCTTGCTGTGTAGATGTTTCTTTTCAAAAATATCTTTATCTTCTGAATGGTTGTTTTTAGATTGTAAATAATGAAATGTATATTTTTTGTCCAATCAAGCTCAGTGAAGATGATCTTGCAAAGTACTCATTCAAAATCCAGAAACCAAATCCTTTAAAAGAAATTGAGGCACTTAAACGAATATTCCG[T/C]GAGTATAACCCTATGCTGTCTGAAGCATTATCAGTGTCTGCTTTTCCTTTACATCTGTGGTCATTAACTTTTCAAATTTAACACAGGAGAATCAGCGGATTGCATTGTTATTTCATGAAGCAAGCTCTGGGTAAGTGTGAGTTAACAGTACCAAGTTGTTGTTGTTACTTATGGTTGTTGCTTATTTGTTAATCTCCAGAATGTTCAGTAGTTTTCTTTTTTTTTCTGTTGCTAGTGTGCCTGAATATCATTACTGGAGTGTGAGGAAGAAGCTCTGTACAGAACGTATCAATGAAGGGATGGAGGATAATGAACCCTGGAGTCCAGAGAGACTGTTATTATGATTGTGACTTTCATATTGAAATATAATGCAACATTGTGAATAAATACCTTTTTAATGGTATACAATAGAGTAGTATTAATATAAACTGCTGGAAAAAGAGGGTAAGAAAAGAGAAAAGTTTTATTTGGTCGGTAAATAACTGATTTAATGAGATAAA
Associated Phenotype:
Not determined