ZMP
si:ch211-251b21.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PLCH2, phospholipase C, eta 2 (PLCH2) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
PLCH2
Human Description:
phospholipase C, eta 2 [Source:HGNC Symbol;Acc:29037]
Mouse Orthologue:
Plch2
Mouse Description:
phospholipase C, eta 2 Gene [Source:MGI Symbol;Acc:MGI:2443078]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34490 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25407 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34490
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 |
|---|---|---|---|---|---|
| ENSDART00000007624 | Nonsense | 489 | 1020 | 10 | 22 |
| ENSDART00000131460 | Nonsense | 6 | 537 | 1 | 14 |
The following transcripts of ENSDARG00000059960 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 49730258)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 47582235 |
| GRCz11 | 8 | 47571227 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCTACTGTATGTGTTTGTTTGTGTTTACAGGGCAAGAAACTACCCT[C/A]AAATATAGATGAGAACGCAGAGGAGGGGGACGTGTCTGATGAAGACAGTG
Long Flanking Sequence:
GCAGACGTTTTTGACTCTTTATTGATTAACCCATTTCTGTCACTGACATTTTTTCCTGTTAATGTCCATGTCAATGTCGGCGCTGAGTTTCTGGAGTCAATGCATACAGTAAGAGTGCTGTTCTCTACCGCTCAGTTATATTACAAATCAACTCAAGTGCCCTATTGCTGTGCAATACATTCTCACTCCCGACTCGTCACATATTGACGCTCAACACAATTTAAAACTACTATAGATTTGACTATAAATTACTATAGTATTTTTTTAGGTGTGAAGAACTGTGATTTGTATCAGGAATGTATTAAATTTATTGCCTTAAGCTTGTGTAATTGCATATAGCATTGAATTTAAATAATAAAGAAAGTGTGAGGTTTTTAAACTCTTCCACTTTTTACACTGGACCGTAGTGTTTAGTGTGTGCAACTCATTTCACAAATGTTTTATTTACATGTCTTCTACTGTATGTGTTTGTTTGTGTTTACAGGGCAAGAAACTACCCT[C/A]AAATATAGATGAGAACGCAGAGGAGGGGGACGTGTCTGATGAAGACAGTGCAGATGAGATGGAGGACGATTGTAAGCTGTTGAATGGAGATGTAAGTAATTCTAGATGGTTCTGGTGCAGATGTGTATAAACACAGTTTCCATGGCAGCATTAAATGTTGAAAACGTAACTTGGCATTTCAATAAAGTGACTTTTAAAATGTAGTTTGAAATTATATGTTAGTGTCATGTTTACCAGTGAACAAACCACCAGATGTCGCTGGTAAACACTCACTCATGAAACTACAAGTCTGCCAGTAAATGGACTACGTATTCAGTCATGCCACACACACACGCACCTGCTTCAAGTCTCCACTGATTAGACTCCCACAGCTGATCCTGCTTCAAGACTGATTACACACAGTATTTAAGCAGCACACACACTCATTCACATTGCCGAGTCTTCTTATCTGTCACAGTGACATTACAACGGTTTCCTTTGTCTGTCTTTGCCGTGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25407
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 |
|---|---|---|---|---|---|
| ENSDART00000007624 | Nonsense | 632 | 1020 | 13 | 22 |
| ENSDART00000131460 | Nonsense | 149 | 537 | 4 | 14 |
The following transcripts of ENSDARG00000059960 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 49750292)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 47602269 |
| GRCz11 | 8 | 47591261 |
KASP Assay ID:
554-7584.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGGACACCGACACCGATCAGGAGAGCTCAAGCGGGGCATCTAAAGCA[C/T]AAGCACATCACAGCAGGTACCATTTAGAATTACTCTTGATGATTAGATTT
Long Flanking Sequence:
GCCTAGCCAATCCCCTGACTTGAATCCAATAGAGAACACAAAATAAAGATGAGATTTGATAGACTCACAGAAACATCAAGATTTTTACACTCGGTTGAAGTCTGTGATAAACTCACACCTAAGCAGTGCATGTGACTTCATTCTCCATATGAGAGGCGTCTTTAAGCTGCCATCATTAAAAAAGCCTTTATTTAAAGTATTAAATAGATTTCAGTAGTTGTGTCAATATCGTGTTCTTACAAAAAAATTTAAAAAATTGTTATTTGTATCTAAATTTGGTTTAATTTCATGTCAACAGCTTCTTTTAGAAATATTTTTCCCAGGAAAACCCGTGATGTGTTCAGTACTTCTTCCCCCACTGTACATGACTCTCTGGAGTACTTGACATTAACCTCTACTCCATCTGTTTACTGTAGAAAAAGACTAGCAAAGTGAAGAAATCCTCTAGTTTTGAGGACACCGACACCGATCAGGAGAGCTCAAGCGGGGCATCTAAAGCA[C/T]AAGCACATCACAGCAGGTACCATTTAGAATTACTCTTGATGATTAGATTTATTTTAAATACATGATTTATTTTTCATTAGGCATAGTTCACCAATCTATCTTATCTTCAAATCTGCCTTAAATGAACAGCTGACCTGAAAAATTCAAGTTACTTCATCATTTACTTTCTCTCACATGGCTTTATACCATTATAACTTTCTTTCTTCTGTTGAAAACTAAAGAAGATACTTTGAAGAATGCTAATTCCTGGCGCACATTGACTTCCATTTATTCATTCTTCTTCAGCTTTGTTCCTTTATTCACCAGGGGTCGCCACAGCGGAATGAACTAAAACACATTGGGTGGCCTACCAGCTGCAACCCAGTACTGGGAAACATCCATACACACTCATACACTATAAACCAGGGGTCTCAAACTCAATTTACCTGGGGGCCACAGGAGGCAAAGTCTGGGTGAGGCTGGGCCGCATAAGGGATTTCACAAAAAAAAGTCCTCAAATG
Associated Phenotype:
Not determined