ZMP
zgc:163021
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC795573 [Source:RefSeq peptide;Acc:NP_001082976]
Human Orthologue:
PRF1
Human Description:
perforin 1 (pore forming protein) [Source:HGNC Symbol;Acc:9360]
Mouse Orthologue:
Prf1
Mouse Description:
perforin 1 (pore forming protein) Gene [Source:MGI Symbol;Acc:MGI:97551]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30641 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45327 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30641
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032407 | Nonsense | 203 | 516 | 3 | 3 |
ENSDART00000143623 | Nonsense | 203 | 225 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 30521025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29663751 |
GRCz11 | 8 | 29672983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACTGAATTCTCAAAACATCTCCAAACACTTCCAACACAGTATGATGAC[C/T]AATCTAAACACCTGTACCAGAAAATGATCGAAACCTACGGCACTCACTAC
Long Flanking Sequence:
CACCTGGAGATTTACAAGATATAAAAACTTATTTATTTTTTAATTTTTTGGACATTTTTTATAAATTATTATGCACTAAGATTTTAGCTAAAAACCTTGAATGTTCTATCGAGGAAGAAAAGTTCCCAATCTTGGATGGCCTGAGAATAAGTAAATTTACAGAAAGAAAATACAATATAGAGTAAACGATCCCATTAAAGACACTTTGAATTATAAAGAAAATTATATTAGGTTAAAAATAATCTATGAGTACTGTGAACTTACTACATTTAAGATGAAGTAATCAGGTATTTAATTAACTCATTACCTTCAACACTGAGTTCAAAACTTTTTTCAAATGAGTAGAATTAACTTTCAGCACATTTTGAGTTGAAAAGCACGCTCGCATGATAATGACAATAAGTATTTCTTCATTTTGTAGTTACAGATTAAGAGACCACCCAGAGCTCAGCACTGAATTCTCAAAACATCTCCAAACACTTCCAACACAGTATGATGAC[C/T]AATCTAAACACCTGTACCAGAAAATGATCGAAACCTACGGCACTCACTACATACGCCAAGTCCATCTGGGAGGGCGTGTGAGGTGGGTCACAGCTTTTCGGACATGTCTTGCAACCCTGAAGGGCTTCTCTGAAATTGACATTAAACACTGTCTGAACATGGATTTCATGATAAAGTTGGGGTTCCAGCAAGCTACAGCCTCGTTTTCGAACAAATGTTCTAAAATCCTTGTGGAGGAAATGGGCATGGGCTTCTACCAGACCTTCATGACACACAAGACAGAGGTTCTGGGAGGAGAGAAATACTTCCCAGAGCTTGTTTTAAACCAAAGCCCGGCTGAAGCTTACTCACAATGGAGAAAGAGCCTGCATGACAACCCTGACGTTATTTCATATGCTATTTTCCCTCTCCATCATCTGGTGGCGGATCCTGAGGTTAGTGCTAATCTGAAAAGAGCAGTAACACAATATATTGAAGAGAACGCGATTTCTATAGACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45327
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 |
---|---|---|---|---|---|
ENSDART00000032407 | Nonsense | 416 | 516 | 3 | 3 |
ENSDART00000143623 | None | None | 225 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 30520384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29663110 |
GRCz11 | 8 | 29672342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGAGCCACAGGCATGAATGAAGATTATTTTTCATCTTCTGATGGTTA[T/A]GTGAAAGCTTGGTACAATGGTATATACAAGGAGACTGAGGTAATTCTGGA
Long Flanking Sequence:
ATTAAACACTGTCTGAACATGGATTTCATGATAAAGTTGGGGTTCCAGCAAGCTACAGCCTCGTTTTCGAACAAATGTTCTAAAATCCTTGTGGAGGAAATGGGCATGGGCTTCTACCAGACCTTCATGACACACAAGACAGAGGTTCTGGGAGGAGAGAAATACTTCCCAGAGCTTGTTTTAAACCAAAGCCCGGCTGAAGCTTACTCACAATGGAGAAAGAGCCTGCATGACAACCCTGACGTTATTTCATATGCTATTTTCCCTCTCCATCATCTGGTGGCGGATCCTGAGGTTAGTGCTAATCTGAAAAGAGCAGTAACACAATATATTGAAGAGAACGCGATTTCTATAGACCACAAGGAATATGAAGCATGTTCTAAAATGTCAAATCTGGATCAAAACTGCTGTCCTTTGAGAGCCGGTCGTGGCACATTAGTAGTGTTTATGATGGGAGCCACAGGCATGAATGAAGATTATTTTTCATCTTCTGATGGTTA[T/A]GTGAAAGCTTGGTACAATGGTATATACAAGGAGACTGAGGTAATTCTGGACAATAATGACCCTGATTGGAACACCAACTTTAATTTTGGGTCAGTTGAGTTTGGCCATCAACTAAAATTTGAAGTTTGGGACAGTGATGTGAATTTTGATGATTTTGTGGGCGAATGTGTGATCAGTCCTGAAAGTGGGATGCACATACACAGATGTAAATTACAGAGAGGGTTCTTTTATTTCATCTACAGGGCTTTATGTGATGATCACTTGACAGGACCTAGGTGTAGCAGATATTCACCAGAATTATAAGACCTACAGTGTTTAGGTGCAGATTACTTTTACATAGATAAAAGGTGTGGTGTGTAGCATTGATTTGCATCTAATTTTCCAACCAGTTTGAAATAATTTACAAATGTGTTTAATTAATAGCTTTTAACTTGGAACATGCACGTGAACAAAAGGACAATGACGATGAACATCACGTTGTTCAAATCTGCCTAACACTG
Associated Phenotype:
Not determined