ZMP

LOC100151335

Ensembl ID:

ENSDARG00000071139

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.

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.

Availability:

Order Allele From ZIRC

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