ZMP

si:ch211-206k20.4

Ensembl ID:

ENSDARG00000069269

ZFIN ID:

ZDB-GENE-060810-148

Description:

WD repeat-containing protein 35 [Source:RefSeq peptide;Acc:NP_001139061]

Human Orthologue:

WDR35

Human Description:

WD repeat domain 35 [Source:HGNC Symbol;Acc:29250]

Mouse Orthologue:

Wdr35

Mouse Description:

WD repeat domain 35 Gene [Source:MGI Symbol;Acc:MGI:1921932]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22338	Essential Splice Site	Available for shipment	Available now
sa14117	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa22338

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
ENSDART00000100663	Essential Splice Site	146	1203	5	29
ENSDART00000140099	None	None	213	None	7

The following transcripts of ENSDARG00000069269 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 32847569)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	32493517
GRCz11	13	32623967

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCTGCATTGTGTATGAGGACGGTGCTGTGATTGTGGGCTCAGTGGATGG[T/C]AAACATTAATATAATCTTACTAATAGCAATACTATATATTTTTTTCCCAA

Long Flanking Sequence:

CTTATTCTCTTATGTAAGGAGAGATATCCAAGGAGAGATAAGTATTATACTTGGAGGGGAAATATGCTTTGTGCATTATACAGCTTGACGCATCAGAATCGGTACTCCGTATCAGCCGATTGTCATGACAAGGAATCGGTTCTTGGTATCGGCTGCAAAAATCCTGATCGGAGCATCCCTACTCTACTTTAAAAGCTTAATGTTGGTTGCTATTAACTGCTAATACATTGAATAAAATCTTCTGTTTTCTGAAAAAAGAACATATGACATTAGAATGAAATCAGGGTGATGATAAAACAGTAATTTTTGGCTTATCTGCCTCTTTATTAATGTGCAGCTCTGTGTTTACTTTACAAATATTGACAAACAGGTTCATGGTATGAGGAAATGATCAATAACAGGAATAAGTCTGTGGTGAGGAGCATGAGCTGGAATGCTGATGGTCTGAAGATCTGCATTGTGTATGAGGACGGTGCTGTGATTGTGGGCTCAGTGGATGG[T/C]AAACATTAATATAATCTTACTAATAGCAATACTATATATTTTTTTCCCAATTTGATTTATGTCAATTGATTGTATTATTGTATTTTAATGGAAGCAAAGCCATTCAGATGTAAATATGTAAATTTTTGTGTGATTTATTTATTTTATTTTTTTTAAGAAATATATATGTAATTATAACTTTGTTTTCTCACAGGCAACAGGATCTGGGGTAAAGAACTGAAGGGGACTCAGTTGGCACACGTGGCCTGGTCTCCAGACAGTAAGATCCTGCTGTTTGGCATGGCCAATGGAGAGATCCACATCTATGACAACCAGGGGAACTTCATAGTGAGTGCTGAGATGCTAGAAACACTACTTGTTTTTGTTGTCGTCATCATTGTCATTATTATATATCTTGATGTCATTCTTGATGAGTCATTGAAACTAGACAAACATATTAGTTTGGTTATTGGCTCCAATTTTTATCAACTCTGTTTGCTGTCTAAAGTCAAACATTTCTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa14117

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
Order Allele From EZRC

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100663	Essential Splice Site	539	1203	None	29
ENSDART00000140099	None	None	213	None	7

The following transcripts of ENSDARG00000069269 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 32825953)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	32471901
GRCz11	13	32602351

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGAGATCCGATCTGCTGCATCACAGCATCAGACAAGATGCTCCTWGTGG[T/C]ATGTCYGATTTACGCAAGCACAYACTTTTACATCCCAAAGCTTCTGTGAG

Long Flanking Sequence:

ACTGAGCTATTGGGATTTGAAGAACCCCCTTGACAGGAAAGGACCTGATTCCCTCTATACATAAACACACTTCATACATGTGCACACCATGCGCTCTATACATATAGACACTCATGATACACTACATACATATGCCCTCATGATACACTCTATACATATAAACTCTAAAAATACATTCCATACACATACACACATGTCAGGGTCACATGACACATGATATACTCCATGATACATTCCATACATTGTACATTTTATCATGTCAGGGTCTGGGATAGAACCAAATGTTCCTTTCAATACTTAAGCATTTTGCATTATTTTACATTAACATTTTATTCAGTTTACTATAAATGATACTTTTGTTTTTTGTATGTTTTTCCTGTTTGGAAAATGCTTGAAACGCTAAGACTCTAAAATGAGTCTTATGTTTTTGTTTTATGGGTTTCAGGCTACCAGAGATCCGATCTGCTGCATCACAGCATCAGACAAGATGCTCCTAGTGG[T/C]ATGTCTGATTTACGCAAGCACACACTTTTACATCCCAAAGCTTCTGTGAGAGTGATGTGTCTGTGGTTTTTTATATCTGCAGGGACGTGAGTCTGGTATCTTACAGAGATACAGCCTGCCCAACATCAGCCTCCTGCAGAAATATTCTCTCACATCTAGACCGTATCAGCTCTCCCTTAATTGTAACTCCAGGTCTGATTACTTTCTTACCTTTTCTCCTTTTTCTTTTTGTCTCATTAGAACTCTTAGATATATATGATTTATGAAATTTTATGCTAATAATGCTTCCATGTTGATATTTAGTTTGTACTTGCTTGTATTGTTTGTTTTTTCAGTCGTCTGGCTATAATAGACATCACAGGAGTGTTGACCTTTTTGGATGTAGAGACGCGAGGTTCAATGGGAGATGCAGAGGGCGGGTCTACAGCTGGAGACCCATCTAAATTTGAGCGCAAGGATGTCTGGGATATGAAATGGGCCAATGACAACCCAGATCTGTT

Associated Phenotype:

Not determined