ZMP

wdr45l

Ensembl ID:

ENSDARG00000021557

ZFIN ID:

ZDB-GENE-040426-863

Description:

WD repeat domain phosphoinositide-interacting protein 3 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUW6]

Human Orthologue:

WDR45L

Human Description:

WDR45-like [Source:HGNC Symbol;Acc:25072]

Mouse Orthologue:

Wdr45l

Mouse Description:

Wdr45 like Gene [Source:MGI Symbol;Acc:MGI:1914090]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa27847	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa41925	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa27847

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
ENSDART00000033237	Essential Splice Site	81	344	3	11

Genomic Location (Zv9):

Chromosome 12 (position 289874)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	272231
GRCz11	12	45532

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGGCTCTGGTCGGAGGAGGAAAAAAGCCCAAATATCCCCCCAATAAAG[G/A]TGTGTGTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGTGTGTCCT

Long Flanking Sequence:

TGCTGCTGCTTAGGTGAATCTGTTTATAATATTAATAAAGAGTCATCCTGCTGCTGTTCACTGAATTATTCTGTTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCTCCTCCTCAGGGTGTTTTGCGTGTGGGATGGAGAATGGATTCAGGGTTTATAACACAGACCCCCTTAAAGAGAAGGAGAAACAAGGTGAGTGTCCACACTGCAGATGTGCACTAGTTAGGGGACTAGTTTTGTAGAAAACAGTGTGCTAGTGACTCTGGGTTCTGCAGCTCGTCTGATTTTGTGTGTGAGTGTGAGAGTGTGTGTGTTGAGTGTTTGCGCGGCTGACCCCAGGTCAGTGTCTTCAGGCTGGTCTTCTGATCTCCTTCATAACTCTCATGTTCTCCTCAGAGTTCCTGGAAGGAGGAGTGGGACATGTGGAGATGCTCTTCAGATGTAACTATCTGGCTCTGGTCGGAGGAGGAAAAAAGCCCAAATATCCCCCCAATAAAG[G/A]TGTGTGTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGTGTGTCCTCAGATGGGTCATGGAGCAGGTTCAGTACTGAAGCTCATGCGGGTCTGCTGGTCATCCCGCTGAACGCTCCTGCTGTTTCTGAAGTGTTGGAACAGCAGCGAGGAGGGCCTCTGACGTGTGTGTGTGTGTTTCTCTGTTCTGTGCATCAGTGATGATCTGGGACGACCTGAAGAAGAAGACTGTGATTGAGATCGAGTTCTCCACCGAGGTCAAAGCGGTGAAGCTGCGGCGTGACAGGTACCACACTCTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAATCAGTGGTTGTACCTGCTGCTTGTACTGTGAAACATCATGGGCTCCTTGTGATTATTTGGATGCTGTGTTGCTTTAATTAGTGTTAGTTATTCCAAATAAAATTAATCAACTGTGTGTGAGAGGATGTAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41925

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
ENSDART00000033237	Essential Splice Site	235	344	7	11

Genomic Location (Zv9):

Chromosome 12 (position 288153)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	270510
GRCz11	12	43811

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTGATCCAGGAGCTCAGAAGAGGATCCCAGACTGCCAACATCTACTGG[T/C]ACACACACACACACACACACACACACACTCTCTCTCTCTCTCTCTCTCTC

Long Flanking Sequence:

ATCATCAACATCATCATCAACATCATCATCATCATCAACATCATCATCATCATCATCAACATCATCAACATTATTATTATTATTATTATGTTTGGGTTTTCTGTGTTACTCAAATGGTCAGGTGTGGAGTGTGCTGGTCAGGTGTGGAGTGTGCTGGTCAGGTGTGGAGTGTGCTGGTCAGGTGTGGATCTACACTGACGCCAGTCGCGCCGCCCTCACGGTGTTCATGCCGCCATATTGACCACAGTGAAGAGTGGGCGGAGTCTCCCTACCACCGCTAGCCAGAATCCACCCATGCCTACCTGCCCCACTGTACATCACCTGCAGCACCAGTGTCAGAGAAGGTGTGTGTGTGCTGCAAGTACTCAGCGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGGGAACGCTCATCAGGATATTTGACACGTCTGCGGGTCAGCTGATCCAGGAGCTCAGAAGAGGATCCCAGACTGCCAACATCTACTGG[T/C]ACACACACACACACACACACACACACACTCTCTCTCTCTCTCTCTCTCTCCATCCTCGTCTGTTCACCTGAGGACTAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGCATCAACTTTAACCAGGACGCGTCTCTGATCTGCGTGTCCAGTGATCACGGCACCGTCCACATATTCGCTGCAGAGGATCCCAAACGGAACAAGCAGTCCAGGTCAGTGTCAGCGGAGTGTGTGTGTGTGTGTGTGTACACCTGCTCTGCGTCAGGCTGCTCTCACTCAGGTCCTCTTCTCCACAGCCTTGCCTCCGCCAGCTTCCTGCCCAAGTATTTCAGCTCCAAGTGGAGTTTCTCCAAGTTCCAGGTGCCGTCGGGCTCTCCGTGTGTGTGTGCCTTCGGGACAGAGCCCAACGCTGTCATAGGTGAGCCGGATGTACACACACACACACACACAGACTCACACTGGTGTCACTGAGAGTAACGTGTGTGTGTGTGTGTGT

Associated Phenotype:

Not determined