ZMP
zgc:77051
Ensembl ID:
ZFIN IDs:
Description:
phospholipid scramblase 1 [Source:RefSeq peptide;Acc:NP_998031]
Human Orthologue:
PLSCR3
Human Description:
phospholipid scramblase 3 [Source:HGNC Symbol;Acc:16495]
Mouse Orthologue:
Plscr3
Mouse Description:
phospholipid scramblase 3 Gene [Source:MGI Symbol;Acc:MGI:1917560]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34074 | Nonsense | Available for shipment | Available now |
| sa34073 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34074
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099003 | Nonsense | 101 | 314 | 4 | 8 |
| ENSDART00000101057 | Nonsense | 101 | 314 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 27717193)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 26320132 |
| GRCz11 | 7 | 26591325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGTCCTCAATGTTGTTACTAGTATTTTCTTTACATTTCAGATTGAC[C/T]AGATCCTTATTCATCAGAAAGTGGAGTTGTTGGAGGGTGAGTTATTTCTC
Long Flanking Sequence:
AGCTTTGCTTGACTAAAAGAGTTTTAAAACATAACATTACCTGTCTAAATGAAACACTTCAGCCATGGTGTCGTCCTTCCTTCAGCGTGCAAAAGTCACTCCAATATTGATTCAGCATTTGTTTTTACTGCTGTAAAACAGACAGACAGTTTGGGCTACTTTTCAGAATTATGGGAATTATCAGCCTGACAAATTTCAATTGGATGAACATTTTTTAGTCTCATGCCTTACCCAGAATATAAAAACACATATAAACACATTTAGATCATTTACTTTAATCATTACTATTAGACTGTCTTCAGAAACATTTTAGTTGTGCTGGTTGAAAGTCTCTACACAATCACCTACTGCACTTTTAGATAAAGTATTCTTTCCAAATAGAGCTAGTCATCTGGTTACATTGTTTTCTTCGAATTGTGCAATGTCATTATCTATTTTTGACCAAATATCATGCAGTCCTCAATGTTGTTACTAGTATTTTCTTTACATTTCAGATTGAC[C/T]AGATCCTTATTCATCAGAAAGTGGAGTTGTTGGAGGGTGAGTTATTTCTCTATTATGAGTATGTCGTTTGAATCAGTTCGGTGTTGAACTTAAAGTTAGGTGCAGTTAGACAAAATCTATTTAGTTTTTTTTTCTAAGTTTTTATAATTATATGAACCCTGCAACATTTATTTTATTCACAACAACTTCATGAGTGTGTTTACACTTGTGGTTATGCTCACATCGTTCTCTTGGTTTCAGCTGGGAAAAATAAAACAAAATGATACATTTTGTGCTAGTTCACATAGAATTCACACTTTCAGGACCAACCTAAAGATGGTAAACAAAAATGTTTTTTTATGAGGCTTTTTATGAGTTTTTTTTAAACAAAATTAAAGGATGGCAATTGAAACAATGTTGCGTGTTGAGCTAAAAGGGGTTGTGCATGCATGCATCGAATAATTTAGCATATGTGAACCTGTGAAGTGCTTTTAAATGTGTCAATACTGTGGTTGGAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34073
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 |
|---|---|---|---|---|---|
| ENSDART00000099003 | Essential Splice Site | 295 | 314 | 7 | 8 |
| ENSDART00000101057 | Essential Splice Site | 295 | 314 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 27710678)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 26313617 |
| GRCz11 | 7 | 26584810 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGGATGTTAAGATGAAGGCTGTACTTATGGGAACTTGCTTTCTTATC[G/T]TGAGTATTGAGCTAATGGTACAATTAATTATCCATACCATAGATCAGTGC
Long Flanking Sequence:
GAGGGGCCCTGCATGGCCTGCAACTGCTGTGGAGACGTACACTTTGAGGTAAAGTTATTAAATTAGAATAAAAGTGAAATGTTGTTTCTCTTGTCATATACAAAATTCAAAGGCAAATATTATAATAACATTTTCAGAACTGGCAGACCTATGCTCTCTTTGTGAATTTGTATTATTATTATTATTAATAATATTGGTATTACTATTATTACTACTACTAGTGCTGTCCAATGATTAATTACATCCAAAACATAATAAATGTGTGGATACTGTGCAAATGTTTATTATGTACAAACGTACACAAATAATACATTAATGAATTGTTTTATTTTAAGCTCAAAGGCAAGGATGGCACTGGGAAGCCTATTGGTCGGATCAGTAAGCAGTGGACTGGTCTGTTGAAGGAAGTCTTTACCGACGCCGACAACTTCGGTATTCAGTTCCCTCTGGATATGGATGTTAAGATGAAGGCTGTACTTATGGGAACTTGCTTTCTTATC[G/T]TGAGTATTGAGCTAATGGTACAATTAATTATCCATACCATAGATCAGTGCTTTTCAATCCAGCTCTGAAGTTTTTTTTTAAAGCCTCCCAAATAAAACACAACTGATTCAACTCATCAGCTTTTTATTCAGATTTACCGATCTGCTCACATGCTGTTTTTCACATCCTACCTAGGAGGGAAGTCATTTTAGATAAGGTCCGTTTCGGATTCTACTCTGTACTGTTGAGGTACTACAGGACCTGGTTTCGGATGCACTAGATCATAAGATAATACTTGATAATAGCTTTACGTTACACATGAGACTACATCTCATTGACCATTTTGCAGTCAATAAATCAAATTACTCCCTTTCCCGTATTGATAGCTGGATCAATAACCAAATGGGGATTTAAAAGCCTTAAAACAATAAATGTGTAGAACAGGTTTAGAACGCACACTGTTACATTACAAAATATTAATCAATTTATTAATTTATCTTTGTTCATTCATTTGTTTGTTC
Associated Phenotype:
Not determined