ZMP

wdr18

Ensembl ID:

ENSDARG00000041113

ZFIN ID:

ZDB-GENE-040905-4

Description:

WD repeat-containing protein 18 [Source:RefSeq peptide;Acc:NP_001005206]

Human Orthologue:

WDR18

Human Description:

WD repeat domain 18 [Source:HGNC Symbol;Acc:17956]

Mouse Orthologue:

Wdr18

Mouse Description:

WD repeat domain 18 Gene [Source:MGI Symbol;Acc:MGI:2158400]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa17072	Nonsense	Available for shipment	Available now
sa35048	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa17072

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000060251	Nonsense	74	431	2	10

Genomic Location (Zv9):

Chromosome 11 (position 13830404)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	13587227
GRCz11	11	13644886

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATTTTGCTCTGTGTAACATTCTGCCCCAAACTTCTTTTCAGGRCCAGCTA[C/T]AGCAGAAGATTGTGTGTCCTGGGATCGTTACAWGTCTTTGCGCGTCTCCT

Long Flanking Sequence:

CAACACACGCAGAGATCTCAGATCAGTTTATCCAGACATTCTAATCTGATTCCCGAACTCGTTTGAAGAACCAAATTAGCGAGAGATCAGTTATCAAGATTAAAAGATCCGGGATCTGCCAAATAATCTTAGATCATTTAAGCGAGGTACGAAGAACGGACCCCTGATGTCCTAAAACAACAACAACAACAACAACAACAACAAAACAAAAAGTTGAACACATACCTTAGGAATGGTATAGCAAAAAATGTTGATGGTTTTAAAACCTTGAATTTTCCAAACCACGGTATACCTTGAAAACGGTTATCGTCCCATGCCTAAAAGCAACACTTCTATGTGTCTGGAACAGATGTTCAAATCAGTTAAAGTTGAAATGTATTTAATCTGCAATATAGAGTTTATAGTGTTCTTCCAAAAATGTGAGGTTTTTGTGAATAATACATGTTCAATATTTTGCTCTGTGTAACATTCTGCCCCAAACTTCTTTTCAGGACCAGCTA[C/T]AGCAGAAGATTGTGTGTCCTGGGATCGTTACATGTCTTTGCGCGTCTCCTGATGGTCTTTATGTGCTAGCAGGCATTGCTGAAGCTATATACCTGTGGGAGGTGAGAAGATGCATTTTGCTCTTCAATACATATTTTAAAGCTTTGTTTTATGTTGACAAGATTCTCATCGTTCGACCTGTCACAATATTCACTGTATAGATTTATCACACAATACATGGATATGAGCTCAGAATGTTTTGATGATGCAGTATATATAACACTGTTGATGTTTACATAAAAATGAATGTCACAACATTTTAGCTGATTGCGAATCCTCTGTTACTTCATCCAATCTCTGTTGGAGGCGGCAATGAGCTCAAGTCACTTCTTACTGAAAAGGCTTACTGACAGCTGAAGAAAAGCTACATTGAAAACTAATGGTTTTTGTAGAAGTTGTCTAAATGAGCACTTTCAAAGCTGCAGTCCACTTTAAAAAAAGTGAAAGTGTAAAATGCACAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35048

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000060251	Essential Splice Site	199	431	4	10

Genomic Location (Zv9):

Chromosome 11 (position 13854044)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	13610867
GRCz11	11	13668526

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGACCACAAGCTCGTGTTGCCACTGCTTCCCTGGACCAAACCGTTAAGG[T/A]GAGTTTTGGCCAGGCCCTACTAATTATGAAATGTAAAAACTGTTATTTTT

Long Flanking Sequence:

CATACATATATATATACATATATATATATATATATATACATATGTGCACAGGATCTGAAGTGTAAAATCAACAATGGTCTTCCTAGAAACCGTTTCTTTCAAGGTCACTGCACAAGCCTCTGAGGTCAATGATGTTTGTTTGGAGAGAATTTCAATATCAATCTTATTAGTACACTTACGCCCAGTATATCATATTTTAATATTTCACATTCATCAAATTTTAATTAACTCATCATCGCACAAATAGTATGTGATAGGATTTGTGACACATAATTAATTGTTATTGTCCTGAGAGTGTCATTTATAATAAAGAATTCATAACGGTTGGTTAATGGAAGATGGTTTATTGTGTTTCAGTGTTGTTCAGCTGGATTCATCCCGTACACCAGAACCCCGACACATTCTGTCCCGACACTCTCTCCCAATCACTGACATCCACTGTGGCCTGATGGGACCACAAGCTCGTGTTGCCACTGCTTCCCTGGACCAAACCGTTAAGG[T/A]GAGTTTTGGCCAGGCCCTACTAATTATGAAATGTAAAAACTGTTATTTTTTCTTTTTATAAAAGTGTTCCTGTATAAACAGGGATGGTTCACCCAAAAATAAAAAATATGTGTCGATCGTTTAATCACATATACTTCTTTTAAACATGGTTTTTCTTCTGTTGAACATTAAAAAATATTTTGAGCAGTGTTTTGTAAATTGTAAGCCATTAACTTTCAATGTACATGTTTCTATTATTGATGTTTGCGGCAACTGGCTTCCAACATTCTTCAAAATTCAATTTATAAATGGTTTATAAATGTCCTAAATGTTATAACACTCAATTTAATTTACATATAAACTTTTGAGGGTGTGAAAATAGGTATTATAAGGTCTAAAAAAGCTGGTTTTACCAGACAACATTATTTCTAACAGTAACTTCCTGAAAGATGGCTATACAGCCAGAACACACAACAAAACAGACCATCCACAGTGAAAGGTGTTAAAGCAGTCCTGCTTTT

Associated Phenotype:

Not determined