ZMP

WDR25

Ensembl ID:

ENSDARG00000091201

Description:

WD repeat domain 25 [Source:HGNC Symbol;Acc:21064]

Human Orthologue:

WDR25

Human Description:

WD repeat domain 25 [Source:HGNC Symbol;Acc:21064]

Mouse Orthologue:

Wdr25

Mouse Description:

WD repeat domain 25 Gene [Source:MGI Symbol;Acc:MGI:3045255]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32114	Nonsense	Available for shipment	Available now
sa17036	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa32114

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128782	Nonsense	81	215	2	4

Genomic Location (Zv9):

Chromosome 17 (position 143362)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	1452433
GRCz11	17	812451

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCACTGATGCCGTCAGTCGAGACTCAGCCGACCGAACACTCATCGTCT[G/A]GGACTTCCAGACCAACGCCAAACTCTCCAACCAGATCTTCCATGTAAGAA

Long Flanking Sequence:

NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGAGAGTTGGCGATCACAGAGTTGATAGTAAGAGAGTTGGCGGTAGAAGGGAAATAATATATAAGTAAGAAAAAAATATAAACGTTAAAAAAAAGAGAAAAATCAGGAGAATGGTTGGACTTACTGTAAATATGTAAACGTGTAATACATAAAGCAGCTATTGTCTGATTATGAGTATTTAAAAAAGTGTTTTCTTTTTACAAAACTATCAAGTACCTGATTTCTACAATCTGACCATGTGTGTGTGATGTGTGTGTGATGTGTGTGTGTGTTCAGGTGCTGCATGTGTACAGATCTGCAGTTCAGCAGACTCTGGATCTGCTGTTTGTAAATGCAGGACGAGAGTTCGTGAGCAGCACTGATGCCGTCAGTCGAGACTCAGCCGACCGAACACTCATCGTCT[G/A]GGACTTCCAGACCAACGCCAAACTCTCCAACCAGATCTTCCATGTAAGAATCACTGCTGACGGAGAGGTTCTGAATAATCATCCGTATGCTTCCATTCAAAGATGTGAAGTAGATTTATGCGCCACACTGTCATATCACATTAAACATGATGTGATCGCGTCTTCATCAATGATGCACAGTAGAGCATCACCTCCTCAGCTCCTGCTGCTCCTGCACTGATATCACTAAGAGAAGTGGAGTCTGCTGCACTGTTGGGATTCTCCACTGTGGTGTTGTTTCTCTAATAAATGAGCCTCAGTAGACCAAGACCAAACACAATGAACGCGGTGAATACGGTGGCTTCTGAAGGTGTGAGACGGGAGCGCAGACAGATGCTCAAGACAGTTCTGGAGGGAATAATAATAGAAGAAGAAGAATACTGAAGCACTGAATCATCAGTACTGACAGTGAAGTACAGCAGCTGTTCTCCTGTGTTATAGTTTGTTTGTGTGTGTTTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17036

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
ENSDART00000128782	Nonsense	173	215	4	4

Genomic Location (Zv9):

Chromosome 17 (position 142222)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	1451293
GRCz11	17	811311

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGTGTCGTGGCCTCTGGGAGCTCCACCGGTTCTGTCCACTTCTATGACTA[T/A]CAGAGCTCGAGGACACKGAAGACACTACAGGCTCATGAGSATGCGTGTGT

Long Flanking Sequence:

CAAGGTCACCACACACACACAACACATATGCAGATACACACACATAGGTACATACACACACACACACACACACACACTCACTCACTCAGACAGACACAACCAGTTTCACACATAATCTGCTATCTGTTGTGGTGATTCTACAGTTGCTTTGGTAACATGACAGCTATTATAGTAATTAATCTGTTGTGGTGATTCTACAGTTGCTATGGTAACACGACAACTATTAGAGTAATTAATCTATTATGCTGATTCTCAGTTGCTATGGTAACACAACAACTATACTAGTTGATCAGCAGCAGTGTGCTTCAGAATATACAGAGTGATGTGCAAGTCTCCTGTCTTTATGTGCACCATCATATTCAGTCAGGAGTGTGTGTCAGCTGTCTCTGCATGTGTGTGTGTGTGCAGGTGGAGGGGTTTGCAGTGCATTGTGGGTTCTCTGCAGACGGCAGTGTCGTGGCCTCTGGGAGCTCCACCGGTTCTGTCCACTTCTATGACTA[T/A]CAGAGCTCGAGGACACTGAAGACACTACAGGCTCATGAGGATGCGTGTGTGTGTGTGGAGATGCATCCCATAATCCCTGGCGTCGCCGCCACCGCAGACTGGACTGGTCAGATCAATCTGTGGACGTGAGGATAGTGAAGAACACTGATCCAGGTTCAGCACTGCAGTATATGATGTAGAACTACACACTGCACAGTAATCACCCACTGAAGATGTGCAATGTTACACTCCACGACTACATTACAGCGATCACATTTACACACCATGATCAATCACTGTGCATGTGGACAGACGTGAAGCCTTCAACTAATAAGAAGCACAGGTTTATTCAGGAAAGACAGCACACATATAGACGCATGCGTGTGGAAGCGGCCGAGCAGACTGAGGTAGAACAGAAACACACAGTAAAGAGCAGCTGATACAGTCATGCATTTACAGTCTTAAACACTGCTCCAGCTCACCTCCATCTTAATAAAGCAGAAGGAGACGGTGTTCATCAC

Associated Phenotype:

Not determined