ZMP
zgc:153119
Ensembl ID:
ZFIN ID:
Description:
UPF0692 protein C19orf54 homolog [Source:UniProtKB/Swiss-Prot;Acc:B0V3H4]
Human Orthologue:
C19orf54
Human Description:
chromosome 19 open reading frame 54 [Source:HGNC Symbol;Acc:24758]
Mouse Orthologue:
BC024978
Mouse Description:
cDNA sequence BC024978 Gene [Source:MGI Symbol;Acc:MGI:3041247]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14663 | Nonsense | Available for shipment | Available now |
sa29064 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14663
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 |
---|---|---|---|---|---|
ENSDART00000057733 | Nonsense | 51 | 307 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 33752846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35433688 |
GRCz11 | 18 | 35408534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTTTACCAGGCTTTAGCAGAGGGAAGGACYGCTGTAGAGGGAGACTA[T/A]GAAGAGGCCAGTATTATTATARGACAGAGAGAAAGCAGGTGGACTACAAA
Long Flanking Sequence:
ATTTTTACATTTTTTTCGTGACTTACGACCATGGGAATATATGACCTTATTTGGTATTCTCTAAGTTGGGAACACTCACTGCAGCTGGAGTTCACAGTCAGTTAACGTTACCAGCAGATAGCGAAATAACTTACTGGACGCTGATGTGGGTTCGTGTGATTTTAATTAAGTGCATGTAACTAACACTCCGTTTTAATGTCGCTTTCTTGTCACTTTATCGTTAAGTAGTTATTAGTTGCACGCGCATGACATCCTATCTTGTATATCACAATATACCCTTAAATGTTGCTTATGTATTTTATCCTCATTCCCTCCCCAGTGTACAAGTGTCTGTACAAGTACTGTAGTATGTCATTGGAAAACGATGCAGCAGCACCTCCACCTCCTCCTCTACCTCCCCCACCTCCTCCTCAACCTCCTTCACTGGCGCGCTCAGAGTCCAGCAAGAAGAAGCTTTACCAGGCTTTAGCAGAGGGAAGGACTGCTGTAGAGGGAGACTA[T/A]GAAGAGGCCAGTATTATTATAGGACAGAGAGAAAGCAGGTGGACTACAAATCACAATTACATACTTATAAAAGACATGTTCTGTACAGTCATGATTTCATCACAGTATTTCTCCTTTAAGTTTTAGCAAGGATCTGCAGTGGCTGCTGTTTAATAACTATGTGCCCTCACTCATTCAAGATGGTCCCCAGTAAGTAAAAAAAAAACATTACTTATTGATGTATTTATTTATTTATTTTTGGGTGGACAAGACCAATATGGCTGATATAAACCACCAGGGGTCTAACAATGTATCGTGGTACAATTATTTGCAATACAAAAATGTCACAATATGCATCGTGGCATTATGACTATTTTATTGCGTTATGACATCTGTTTTCTCTTATTGGTTGAGCTCATAGGTTGAGCTACAATACACATGCTGTCACATGCATTCAGATTGCTTGATCTAGCAGCAGTAGCAGGCCAATATGAGTGCAGCTGAAATAGAGGATGCCCCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29064
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057733 | Essential Splice Site | 172 | 307 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 33756257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35437099 |
GRCz11 | 18 | 35411945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCTGTCATTCTTAAACACCTCATTAACAGGCAGCCCATTCTTATACC[G/T]TATCTTTACTGCTTACATTTGTAATCTCTTATGTAGGTTCACATGTTTTT
Long Flanking Sequence:
GGCTGTGCACTTCAGGAGGATGTTTGATTGCTCTTGTATAAATCTCTTCAGATGTGGTCTTGTGGCCTTATGGATGGCGGCTCATTTACTCCAGCCTCCTAAAACGCTGCTCCTGGAAACTCTAGTGCAGACGGCAAAAGACAATGGCTACACTGAACAAGGAGAAATGTTTTCTGGTAAACAGTTATTTTTAAATGTCATCTTTGAACTAAATGTAACCAGCACACATTTAATAGTCAAAGCGATGTTTGAATTAAATGATAGGTCGTTATCTCTGAAATTTAAAGATTTCTACTGAATGTCTTTAAATATTTCTTGAATTAGCTGAAAAGTTTATATTTAATTTTTTTTCTTTTCTGTTTTGAAATAGCCAGTGACATGGCCAAGCTGGCGGAGGACGTGTGCGGGTGCAGAGTTCAGAGGTTGTCAGGAGGCATGCTGGGAGAAAACACTGCTGTCATTCTTAAACACCTCATTAACAGGCAGCCCATTCTTATACC[G/T]TATCTTTACTGCTTACATTTGTAATCTCTTATGTAGGTTCACATGTTTTTACATAGTTTTTTTATTATTATTATGTTTTATTTTTTATATTTGTGTATTTTATTCATTTATTTGTTTAATATATTTTAGTTAATTGCTATAAAAAAAGAATCAGAAAGATTATTATTATTATATTATTTAATATAAAAGTGTTAATGGCGACGCCGTGGTGCAGTAGGTAGTGCTGTCGGCTTACAGCAAGAAGGTCGCTGGTTCGAGCCTCGGCTGGGGGTTGGCTTTTTTGTGTGGAGTTTGTTGCATGTTCTCCCTGAATTCGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATTATATATTATAATCTTTTATATTTAATTTTTAATACACACACACACACACACACACACACACACACATATATATATGATGTAGATATAGATTGATAGATAGATAGATAGATTTAAATTAAAT
Associated Phenotype:
Not determined