ZMP
LOC100151335
Ensembl ID:
Human Orthologue:
PLCXD1
Human Description:
phosphatidylinositol-specific phospholipase C, X domain containing 1 [Source:HGNC Symbol;Acc:23148]
Mouse Orthologue:
Plcxd1
Mouse Description:
phosphatidylinositol-specific phospholipase C, X domain containing 1 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7026 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20633 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7026
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104965 | Essential Splice Site | 114 | 302 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 6 (position 8649446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8910841 |
GRCz11 | 6 | 9146380 |
KASP Assay ID:
554-5108.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGCGATTTCTTCTTCTATCATGGATTGTACACAACGATGACTGTGAAG[G/A]TTGTTGACCTGATTCAGTTTTTTGTTATTTAAATKAATTGAATTCAACAG
Long Flanking Sequence:
AATTACAGTTAATGTGTCGAACCAGGCCAGACTTGTAAACAAGACGCACAGGTTCGGGTAGGGTCAGGTTTCATTGTATGGACCTAATCTAAGCTCTACACTCTGTGACTCTAGAAATTAGACAAAAATTGATACAAAACACATTTCTTTTAGGCAGCCACGATGCTATGGCCTACAGCTTAGACATGGACTCTCCAGTCCTGGAACCTGACAGTCTCAAACCTATGGACAACATGTTCAGTGCATTCTTAAGGCCCATTGTCAAGAAATGGGGCACCGCTCAGGTAAAATATCTATCAAAATACAATAATCGCACAGTCAATGATGATGAATCCATGATCCAGTCTTTGTGTTTATGTTTTCAATTAATCATCCAGGATAAAACCATCTCTGAGCAGCTTGATGCTGGTACGCGCTATTTTGATCTGCGGGTTGCTGGAAAGCCTGAATCCAGCGATTTCTTCTTCTATCATGGATTGTACACAACGATGACTGTGAAG[G/A]TTGTTGACCTGATTCAGTTTTTTGTTATTTAAATTAATTGAATTCAACAGGCTTACAAAAGGCTGCAATAATCATATATTAAAGTTATAGTTCACCCAAAAATATTTATTCTGTCATCGTTTACTCACTCTTTACTTGTTTCTATCTTGAACACAAGAAGATATTATGAAGACCTGGAGGGTCTTGGAGGGTTGGGAGAAAGCTAGGACAATTTTAAATGGTCACGAAACACCAAAACACTTTTTTTGAGATGTTGACAGTCATATATGTGTCCCACGCTGCTAAAACACTATTAGGACACATATTTCACAAAGTCAAGTTTATGTATAAACAAATTTTGAGAGGAAAAAAAGGTGTTTACAGCCTGGTCCAAATAACGATTTTGGTTCATACAGCTAATATTACTCTTAATGACAACTGTGAGGGGGGTGAATATTTTTCATAACTCATCAGTTTCCTTTATATTAGTTTATATTAAGTTTGCATAATTAAGGGCGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20633
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104965 | Essential Splice Site | 114 | 302 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 6 (position 8649445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8910842 |
GRCz11 | 6 | 9146381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGATTTCTTCTTCTATCATGGATTGTACACAACGATGACTGTGAAGG[T/C]TGTTGACCTGATTCAGTTTTTTGTTATTTAAATTAATTGAATTCAACAGG
Long Flanking Sequence:
ATTACAGTTAATGTGTCGAACCAGGCCAGACTTGTAAACAAGACGCACAGGTTCGGGTAGGGTCAGGTTTCATTGTATGGACCTAATCTAAGCTCTACACTCTGTGACTCTAGAAATTAGACAAAAATTGATACAAAACACATTTCTTTTAGGCAGCCACGATGCTATGGCCTACAGCTTAGACATGGACTCTCCAGTCCTGGAACCTGACAGTCTCAAACCTATGGACAACATGTTCAGTGCATTCTTAAGGCCCATTGTCAAGAAATGGGGCACCGCTCAGGTAAAATATCTATCAAAATACAATAATCGCACAGTCAATGATGATGAATCCATGATCCAGTCTTTGTGTTTATGTTTTCAATTAATCATCCAGGATAAAACCATCTCTGAGCAGCTTGATGCTGGTACGCGCTATTTTGATCTGCGGGTTGCTGGAAAGCCTGAATCCAGCGATTTCTTCTTCTATCATGGATTGTACACAACGATGACTGTGAAGG[T/C]TGTTGACCTGATTCAGTTTTTTGTTATTTAAATTAATTGAATTCAACAGGCTTACAAAAGGCTGCAATAATCATATATTAAAGTTATAGTTCACCCAAAAATATTTATTCTGTCATCGTTTACTCACTCTTTACTTGTTTCTATCTTGAACACAAGAAGATATTATGAAGACCTGGAGGGTCTTGGAGGGTTGGGAGAAAGCTAGGACAATTTTAAATGGTCACGAAACACCAAAACACTTTTTTTGAGATGTTGACAGTCATATATGTGTCCCACGCTGCTAAAACACTATTAGGACACATATTTCACAAAGTCAAGTTTATGTATAAACAAATTTTGAGAGGAAAAAAAGGTGTTTACAGCCTGGTCCAAATAACGATTTTGGTTCATACAGCTAATATTACTCTTAATGACAACTGTGAGGGGGGTGAATATTTTTCATAACTCATCAGTTTCCTTTATATTAGTTTATATTAAGTTTGCATAATTAAGGGCGTGGC
Associated Phenotype:
Not determined