ZMP

plrdgb

Ensembl ID:

ENSDARG00000089101

ZFIN ID:

ZDB-GENE-000406-3

Description:

PITP-less RdgB-like protein [Source:RefSeq peptide;Acc:NP_571650]

Human Orthologue:

PITPNM1

Human Description:

phosphatidylinositol transfer protein, membrane-associated 1 [Source:HGNC Symbol;Acc:9003]

Mouse Orthologue:

Pitpnm1

Mouse Description:

phosphatidylinositol transfer protein, membrane-associated 1 Gene [Source:MGI Symbol;Acc:MGI:1197524

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43707	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39344	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43707

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126531	Nonsense	410	543	12	14
ENSDART00000147718	None	None	68	None	2

Genomic Location (Zv9):

Chromosome 21 (position 38686423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	39826654
GRCz11	21	39850207

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTAATCTGTTTTACCCATCGGACCCCTCTGCCTCACGCCTGGAGCCAT[T/A]ATTGCACTCAGTTCTCACCCAGTTGCCTCCTTTTCCTGTTCCCCGGTACC

Long Flanking Sequence:

TCATGGGGGCACAAAGGACCTCTTGGATGACATCAGCATGATATAAAAAGCATTAATTGTGATGAATCATTAATTAGGAGTTAATAATTAATGAAGATAACTGGCTTTCCATGCATGCTGTCTCACAGTCTGTCTCAGGACGATCAGTGTGGCTCCAGGCAGGCTCTCAGTCCAGGCTGCTTTGAGTTTGAAGTATCAGACTGCTTTCTGCTGGGATGCCCACTGGGACTAGTGCTGGCGATGAGGAGAACGGTGGTCCCTGGCGTGGATGGTACAAATCGGCTTCTTTCTCACACACATACACAGATAAATTGTTAATTTTAAAATTAATATTCAAGTTGACCATATGATTTATAGTGTTTTTATTAGAGTAATTTCCTGATAGATGATTACTCTGTTCTGTCCTCCCTCTCTATTAGTGGCTCAGCTCAGGCCAGCTTGTTCGCAGATTTTTAATCTGTTTTACCCATCGGACCCCTCTGCCTCACGCCTGGAGCCAT[T/A]ATTGCACTCAGTTCTCACCCAGTTGCCTCCTTTTCCTGTTCCCCGGTACCAGCGCTGCCCTCTGGGTGATGGACGCTCCACTCTCATTGGTAAGAGCTTGCATCATACAGTAATACGGCTGTAAAATGTTGTTGGAGAGTTATTAGTTACCATTTGAATGTTTTGTTTTTTCAAACCAACCAAGCCTGCTTAATTTGTATGACTGCCTTACAGAAATCATAAAATGGGGCAAATATAACAGTGTATATAAAACATCTCATACACTACTGGTCAAAAGTTGGAGTCATTAGGATTGTTAAATGTTTTTAAAAATATATTATCCTGCTTAACATGGCTGAATTTATTTAATCAAAAATACAGTACAAACTGTAAAATTGTGAAATGTTATTACACTATATAATAAGTGTTCAAAAGTAGTTTATAAATTAATTTTATAATTTATTAGAGTGATTTTATTGATGAATTTTCAGCTTCATTACTCCAGTCTTCAGTCACAGGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39344

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126531	Essential Splice Site	493	543	13	14
ENSDART00000147718	None	None	68	None	2

Genomic Location (Zv9):

Chromosome 21 (position 38708833)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	39849064
GRCz11	21	39872617

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCGGCTCTGAGGGCACTGCCCCGAGCGAGCCTGTTAGCATCTCACAAGG[T/C]GAGTCTCCAGAGCACCAAATGTCCTTGAATCGGCTGCTTTCAGGCTCTTC

Long Flanking Sequence:

TGTTATGAATGATGAGTGATAAGTGCAGTATATTGTGAATCCATTTAATTTGCAATTCAACAAGTTGAAATTGTAATAGAAATTGATCTACTAGTTTGTTTCCTCTATGTAGGTCTTTAGCTTCTTCAGTTTTGTGTTGTTTGTGAATCTGTAAATCACTGCACGTTTAGTATGGCTTTTTTGTTTTGTTAATAAAGTTTTTGAAGCAACAAGATCTCCTAGTCATATGCAGTTTTTCATTTTCTTCTTATTGTCTATTGATATTTGAACTGTTTATTTATAGTTTTGCTTTCTCACATTTGTATAAATAAGTTTTCTTTTTTTTTCTTTCTCCTCAAAGTGGACACGGTGCTCAGACATGTGACAGAGGGTGGTGTTTCTGCAGATGGAGCAGCGGATCAGTGCTATGGAGGAAGTGTGTCTCGCAGAGGCAGTGATCGAGCTGTTCCACTCGGCTCTGAGGGCACTGCCCCGAGCGAGCCTGTTAGCATCTCACAAGG[T/C]GAGTCTCCAGAGCACCAAATGTCCTTGAATCGGCTGCTTTCAGGCTCTTCCTATGTTTTATTTATTTCCACACGGAAGTCAGAGTCTTTGATTGATACGGAGATGTTTGTGTGTGTTTCAGTGATGTGTAACATAAATCTTCTCTTTCTCTCTCAGTATGCAGTAGGTGGTGGGGTTCGAAGAGGTTAGATTATGTGCTGTATTGTCCAGATGTGCTCACTACATTTCCTACAATAGCTCTGCCTCACCTGTTTCACGCTTCATACTGGGAGTCCACAGATGCTGTGGCTTTTATTCTTAGACAGGTAAGAACAGATGCTCTTATGCTCTGCTTATACTTTACAACTTGGGCCATGATTAGTTTGTCTGAGACTAATTTTGGAAATCCTAAATTTCTTATAATACCAGGCTAAAATCTGTGTGATGATTAGTTTATAATGTTTACAGACAGATGATTTAATGGCTACTGTGATCTAATTTCCTTCCAATGAAATGTTGTT

Associated Phenotype:

Not determined