ZMP

wdr41

Ensembl ID:

ENSDARG00000009851

ZFIN ID:

ZDB-GENE-050706-152

Description:

WD repeat-containing protein 41 [Source:RefSeq peptide;Acc:NP_001025432]

Human Orthologue:

WDR41

Human Description:

WD repeat domain 41 [Source:HGNC Symbol;Acc:25601]

Mouse Orthologue:

Wdr41

Mouse Description:

WD repeat domain 41 Gene [Source:MGI Symbol;Acc:MGI:2445123]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45727	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa17407	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa45727

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
ENSDART00000021272	Essential Splice Site	55	282	2	14
ENSDART00000121813	Essential Splice Site	55	449	2	13

Genomic Location (Zv9):

Chromosome 21 (position 7549211)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	7871678
GRCz11	21	7609346

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGGACACTTTGACATTGTTCGATTTCTGGTGCAGATTGATGACTTAAGG[T/C]AAGCAATCCTCTTCTCCTCTGACCAGTGATTGACAGCTCCGACCGAGCCA

Long Flanking Sequence:

GTAAAACATATGCCACAATAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTAAAAAATAAGGGACTAATCTGAAGGAAAATGAAGGAACCTATTATTCTACAGAAAAGCTGCTATCAGCCATACGTTTGAGCCATGCATTCTCCAACTTCCCGAAACTCCAGAGTTTTGTAGCATGACCCGCATCCATTTTACTGCCATTATTTACCAATAAGCAGCAGACGAGAAACGAGTTTGAGTGTCCAGTTGTCTTAAAGACGAATCTTGGAGTACATGTATCAGAGAGACAGGCCGACGCAGTCCAGCAAACAGCAGTCATTTCAGCACATTCGGAGCTAGATTGAAGCAATGATTCGTTTGTCTATTATATTCCCTCCGTGGGCAGAAGAGCGCGGCGCTGTTCATTGGGGAGGAACAGCCCAAAAACTGCTTCACGGAGATGCAGGTGCTGAAAGGACACTTTGACATTGTTCGATTTCTGGTGCAGATTGATGACTTAAGG[T/C]AAGCAATCCTCTTCTCCTCTGACCAGTGATTGACAGCTCCGACCGAGCCAGATCCTCTCCAAAAGCAGACTTACAGAGCGTGACAAGAGCTTAATCATCACAGCTGGAGGGTGTGTGTGTGTGAGTGTGTGTGTGTGCTCTCTTGATAGTGTCCATCTGATCTGGACTCGTCCGCATATTGAGGTAAAGTTGGTTTTATATTCGCACATTGGTCACATGTGACACACTCTCTATATTTTTACCCATGCTACTTTGAATATTTGGTCTGAAATCGCATGCAAGTGTGACTTCAAAACAACATTAGCACTATTTAACTGACTGTGAAAAGTGTTTTACTTTGACAGTCATTGGCTACCAATATGTTTTAACTATTTAGAATTTGCAAAGAGAAGGTCGCTGGTTCGAGTCCCGGCTGAGCCAGTTGGATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGCGTGGGTTTCCTCTGGATGCTCCGGTTTCCCCCACAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17407

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000021272	Nonsense	77	282	4	14
ENSDART00000121813	Nonsense	77	449	4	13

Genomic Location (Zv9):

Chromosome 21 (position 7554173)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	7876640
GRCz11	21	7614308

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGCCNTTTTTTAGCCTTKTATTTTGTGTGTTTCAGACTGGTGATTGTTTGT[T/A]GGAGTTGCGCGGCCACACACAGCAGATCACAGCRATGACATCATACACCT

Long Flanking Sequence:

TTTGCAGATATTTAAGAAACATGCTAGGTGAACATTCTTGTTTATCTGAAAAACAGTGCTGAAAATGTGTTTTCTGTGTCGGAACGGCTGTCTTTGTTTTGGTTCTTTTAACCTGCCCACGCACCCCAAGTTGCCTTGATAGAAAACCGCATATTTCATTCATTCAGTCAGAAAGGCTGTCTGATAAAGGGGTCGAGTGAAAATGTGTTTTCATTCAGGAGTGCAATACCTAGTTCAACCACTGGGTGTCAAACTTGCATACATCTTTAAATATAAACACTTTAATTTGTTTTTGATAAGAATATGTTAGAGTTTAGATTCTCTGCCTGAGCCTAGACTTGACCCAACCTGACCTGACCGGGCTGGGCTGGGCTGATATTTCCTGCCACTATCTTTTGGGCCAGGGCCGGGTCGTGATTAAGAATATGTTTTAGCTGTTGTTGTTTTCTCAGCCTTTTTTAGCCTTTTATTTTGTGTGTTTCAGACTGGTGATTGTTTGT[T/A]GGAGTTGCGCGGCCACACACAGCAGATCACAGCGATGACATCATACACCTTCATCAGAGGAGGAAACACACACACAGCTCTCATCACGGCCTCTTCAGATCGAACACTCAGTGTATCCTGAACAAACATCTGATCAAAGGTGTTTGTGTTTTGTGTTACTGTTTACCTCCTTAACTCAGCAGCAGTTGTGGGATCCAGATTCAGGAAACCGAGTGCAGAATATATCAGATCTGCAGTCCTCTGTAAAGGTGTGTGTTGTGTTCCTGTTTCATTGTGCCGATGGTTTGGGGTGTGTGTCTGTTCCTCTTTTAGAGTGTGTTTAGACTGATGTGTGTGTGTGTGTTTCAGTGTTTGCTGGTGTTGAATCTACTGGACATGTGGCTCTCAGGAGGAAATGAACTGTGTGTTTGGAACCAAGACTTTGAGCTGCAGTGTAAAACAGTTCATCACAGTGACACAGGTACACAATCCAAAACACACAGAAACAAATACACACATCA

Associated Phenotype:

Not determined