ZMP
zgc:195037
Ensembl ID:
ZFIN ID:
Description:
vacuolar protein sorting-associated protein 54 [Source:RefSeq peptide;Acc:NP_001124248]
Human Orthologue:
VPS54
Human Description:
vacuolar protein sorting 54 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:18652]
Mouse Orthologue:
Vps54
Mouse Description:
vacuolar protein sorting 54 (yeast) Gene [Source:MGI Symbol;Acc:MGI:2178798]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32785 | Nonsense | Available for shipment | Available now |
sa2004 | Essential Splice Site | F2 line generated | Not yet available |
sa32784 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32785
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074034 | Nonsense | 128 | 997 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 55576823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 54359844 |
GRCz11 | 1 | 55037495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCTTCATTCTACCTGCCCAACATCACCCGAGAACACTTCAGCTCATA[C/A]CTGCAGGACACGGCTCAGGTGAACACACACACACACACACACACACACAC
Long Flanking Sequence:
CATTATTTTTTATTATTACCATAATATGTATTATAATTTTATCTTTATTTATTCGTTATTTTTATTTAATGTTGTTATAATTATCATCATAATAATGCTAATTATTATTATTATTTTATTATGTAAAATGAAAGTGAATGTGGGATGTAAACTGTTTGCTGTGTTTACATGATTGTAATGTACAAACTGAAACTCTAATAAATATATTTTAATTAAAATAATAATAATAATAACCTTAATGTCAGGCATAATAAACCCATAGTGTTCTTCTGCACAGGTGATGGCGGTGGTCTGTGCGAGGGTCCGTCTGTTGTGGCCGATCAGCACCGCTGGACTGTGTATAACTCTAAAGTGAATCTCCCCGCGGCACTCAATGACCCCCGGCTGGCCAAAAGAGAGTCTGACTTCTTCACTAAAACCTGGGGTTTGGATTTCAGCGAGACCGAAGTCATGCCTTCATTCTACCTGCCCAACATCACCCGAGAACACTTCAGCTCATA[C/A]CTGCAGGACACGGCTCAGGTGAACACACACACACACACACACACACACACACATCAATAATTCACACACACAGAGAGTCCTGAAACTGCCTCACAGACAGCACTACATACAGTTCAAGGCAAAATTATTCACCCTCCTGTGAAATATATTTGTTCTTTTTTTAAATATCTCTCAAGTGATATTTAGCAGATGGAGGAAAATTTCACAGTAATTTTGATAATATTTTTTCTTTTGGAGAAAGTCTTATTTTATTTTGGCTAGAATAAAAGCAGTTTTTAATTTTTTAAACCCATTTTAAGGTCAATATTATTAGCCCTCTTTATCAATATTTGTTTTTTTAATTGTCTACAAAATAAACCACTGTTATACAGTGACTTGCCTAATTGCACTAACTTGCCTAATTAACCTAGTTAAGCCTTTAGATATCACTTTAAGCTGAAGACTAGTCTCTTGAATACTAATATCTTAAAAAAGATTATTTACTATCATCATGGCAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2004
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074034 | Essential Splice Site | 442 | 997 | 9 | 22 |
ENSDART00000074034 | Essential Splice Site | 442 | 997 | 9 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 55564019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 54347586 |
GRCz11 | 1 | 55025237 |
KASP Assay ID:
554-3242.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTGAAGTCCCTGTCTCAGGTCAATGAGGTCGACGCAGACACTGTCAGG[T/C]GAGTTCACTTCTCTATAAATCCCACATTTCWATAATAATYACTAGCCGAG
Long Flanking Sequence:
GAAACAGAGCCTTTAGCTGAACAACAACATGCTTATATGTGCATCAAATAATTTAAAAAGAAATCCCGCAGTAAATGTTTTCACTATAATTTATTCTCATCTTACTGTATAAAAAGAAATCATCCAATACAATCAAGAACTTATGATACTTAAGCACAATTTAATATTTTACATGCATATTTATCTATTGTTTTTATGTAATATCCAAAAAAGTGCATAAAAGGCTTTTGTGTGTGTTTTTCTTGCATTCCAGGATCGCTTGCAGTCTCTAGTCTTTGGGCTGTTGCGGCAGAGGAAGCTGGATTTCCTGGACATCTACAGTGAAGAGATGATCCGCGCAGCTAAAAACGTGGTCCGGCAGGTAAAGCAATTAGTACATGAGTTAAAAAGAGTGTATGGTGAAGCCAGGAGTGAATGTTTCAGTGTAATCCCGTTTCTCCCTGCAGTGTGTTGTGAAGTCCCTGTCTCAGGTCAATGAGGTCGACGCAGACACTGTCAGG[T/C]GAGTTCACTTCTCTATAAATCCCACATTTCTATAATAATCACTAGCCGAGTTTACATCTTAAAGGTGCTGTATGTAAGTTTTGGACTCTTCTAATGCATGAAAATGCCATTATATGTTTGCAGATATTTCAGAAACATGCTAAGTGAAATATGTTTATCTGAAAAACAACACTGAAGTCAGATATTCTGCTTTGAAAGTGTGTTTTCTGTACCGGAACGGCTGTCGTTGTTTTGTTCCCTTTAACCTAGCCAATGCTACTTTAGCCAATTATATTGACCAAATTTTATTAAAGAAATTACCATTAGATCCTAAGATTTTGATCCTGGGTATATTTCCTGTCAGCCCTCTCTTACAAAGCAAAGAGGTCAGATTCATAAACGTGTATTTTACAATTATTATTGCTCTTAATTGGAAAAATATAAATGAACCTAGAATAGGAAAGTGGGTTAAAGAAATGGAATCGCATATGTCAATGGAAAAGATCACGTACATTATCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32784
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 |
---|---|---|---|---|---|
ENSDART00000074034 | Nonsense | 931 | 997 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 55553165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 54336104 |
GRCz11 | 1 | 55013755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGAAGATGCACGAGGCCATTCATGAGCTGCTGCCGGAGGAACAAACG[C/T]AGGTCAGACACACTCACACACATGTTTGTTTTTGTGAATTGTGGGGACAT
Long Flanking Sequence:
GACATACAGATACACTCAAACACACACACTCCCAAACATACACAAACTCAAATATATACACACACACACACCCAAACACATCACCAAGGTTAAAACACACACATACATGCATGTGCACAATAAAATACAGACTATCAAACACACACACACACACACACACACATGTCATGCATGCTAGTGTTGTGATGCTAACAGCGATGTGTGTTTCTCTGCAGGACTATAATGACCACATCGCAGAGGTCTCGGCTAAGCTGGTGGCCATCATGGACAGTATGTTCGAGAAGGCTCTGTCTAAGGTCAGTCTCTGCGCTGGTATATTAATATTATTATCATCATTATCATCATCACTATCACTGCAGCTGTGTGTGTGTGTCTGTGTGCGTGTGTGTGTGCAGTATGAGGTGAAGGCGCCGATGCCGTCTGCGTGTTTGCGTAACGTGTGTAAGCAGATGCTGAAGATGCACGAGGCCATTCATGAGCTGCTGCCGGAGGAACAAACG[C/T]AGGTCAGACACACTCACACACATGTTTGTTTTTGTGAATTGTGGGGACATTTTCCACTGTACAATCTGTATTTTCTATCGCCCCCACCCCTAAACCCAGCCCTCACAGGAGACTGTGGACAGTTTCACCTCCTGTAAAACTCATTGTGTGTGATCTATAAGCTGTATGAGAAGTGAAGATATGTTGTCCTCATATTTGACCATTTTCTTGTAATACCTTTGTCATAATGCAGATGTGTGTCCTCATATGTCACAAAACATGTCCACATACACACACACGCACACACTGATACTGGAGCCAGCTGTGCAGAGAGAGAGGTTTACTCTGTGTTCGTGTGTGTGTGTGTGTTTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCAGATGCTGTTCCTCAGGATAAACGCCAGCTTTAAGCTCCACCTGAAGAGACAGTTGTCACGGCTGGGGGTCAGCAATGATGGAGGACCACAGAATGGGTGAGAGAT
Associated Phenotype:
Not determined