ZMP

waslb

Ensembl ID:

ENSDARG00000006283

ZFIN ID:

ZDB-GENE-040426-718

Description:

Wiskott-Aldrich syndrome-like [Source:RefSeq peptide;Acc:NP_957353]

Human Orthologue:

WASL

Human Description:

Wiskott-Aldrich syndrome-like [Source:HGNC Symbol;Acc:12735]

Mouse Orthologue:

Wasl

Mouse Description:

Wiskott-Aldrich syndrome-like (human) Gene [Source:MGI Symbol;Acc:MGI:1920428]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9782	Nonsense	Available for shipment	Available now
sa7555	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9782

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000028016	Nonsense	357	518	9	11

Genomic Location (Zv9):

Chromosome 4 (position 3978943)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4097556
GRCz11	4	4106469

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CACCCTCCAGACCAGGYATGGGTGCCCCACCACCTCCTCCTCCACCCAGC[A/T]GAGGCCCCACACAGGCTCCWCCGCCACCCCCACCACCCCATTCGGCCTCC

Long Flanking Sequence:

AATCCACCCTGCTGCTGATAAAAGCATGAACAAGTTTCTCTAAGTCTTCACTGGAAACAAAGCATCTAATTCTTGTAATGTTTTTGAGATGATAGTATGCTGATTTGCTAACTGCTTTGACATGACTATTAAAGCTCAAATCTGACTCCAGTCACCAAGATTCTTGACAATTAGTTAACAATTAATCACCCACCCCTACAGTAGTAATTAAAAGGTCTGTCTTGACACATTCCTTACTTTGTAGACTATTCATATGTTTTTAAATTCACATCTCATTGTTCTCCAATCTATCTCCAGCTCCTCCTCCGCCTCCACCATCCAGAGGAGGCGCTCCACCACCTCCTCCTCCCCACAACTCCGCTCCTCCGCCCCCACCTCCTTCCAGAGGCAGAGGGGCACCTCCTCCACCTCCCCCATCCAGAGCGCCCACATCTGCCCCCCCTCCACCTCCACCCTCCAGACCAGGCATGGGTGCCCCACCACCTCCTCCTCCACCCAGC[A/T]GAGGCCCCACACAGGCTCCTCCGCCACCCCCACCACCCCATTCGGCCTCCATATCTCCACCAGCGCCTCCTTCTATTGGTGGAGCTCCACCGCCACCACCACCACCTCCTCCTCCTCCAGGACCCCCTCCACCAGGACCTCCTCCACCACAAGATGTTGATTCTGGAGACTCTCCGGGAGGCAGATCTGCATTTCTGGACCAAATTCGAGAGGGAGCGCAGCTCAAGAAAGTGGACCAAAACAACAAGCCACCCGTGTCAACTGGAGGCCGTGGTGCACTTTTAGACCAAATACGGCAGGGGATTCAACTTAAAACTGTGAGTACACTGGCAAAGTTAAAGTCCAGCAGTTTAAAGTTAGTAGTGGACATTTTTTTCTTAAGGCAGGGGTGTCCAAACTCTGTCTTGGAGCGCCGGTGTCCTGCAGAGTTCAGCTCCAACTTGCTTCAACACACCTGCCAGGAAGTTTCTAGTATATCTAGTAAGAGATTGATTAGCTGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7555

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000028016	Missense	491	518	10	11

Genomic Location (Zv9):

Chromosome 4 (position 3982604)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4101217
GRCz11	4	4110130

KASP Assay ID:

554-4060.1 (used for ordering genotyping assays)

KASP Sequence:

TGCTCCTTCAGATGGGATTGTGGGAGCRCTRATGGAGGCMATGAAGAACC[G/A]TAGCAAAGTGATCCACTGTTCAGGTGAGCCAAGCTGCTTTTAAAGGGGAC

Long Flanking Sequence:

AAAATCTTGACTGATATTAATGATGTGACGTACTTCCGGAAACTTTCTACTTCTCTCTTTATCCATCTGATTTTAAGGTCAGCTTCTTTTGACCGCCCCCTGTCGTTTTAAAGAATATCACAACGGCGAACGCAGCGAGTACTCGGCCGTTCCGTGAGGTGTGTGCGCACTCAGCAGGGGGTACGCGATGTGGCGCCAGGCGATAGTATTAATCTTACATAAATAAACAAATAAATTGAATGAAAGGCTCGAAAATACGTGGATTTCTTCGTGCACAGATTTTGTTTGCCTACCCATAGCATTATTAAAACCCCAGACTCCTCATTACATTTATTTTCAGAACACACAGCTGTTGTTGTTGTTGTTGTTGTTGTTGTACCAGTCCATCAAAAACGTCCTGAATGTTCATTTTCAGGTAACTGATGCTCCAGAGTCTCCTCCGCCCTCTCTTGCTCCTTCAGATGGGATTGTGGGAGCGCTGATGGAGGCCATGAAGAACC[G/A]TAGCAAAGTGATCCACTGTTCAGGTGAGCCAAGCTGCTTTTAAAGGGGACCTATCAGGCCTCTTTTTACAAGATGCAAAATAAGTCTCCGATATCCCTAGAAGTTGTGAAGTTTCAGCTCAAAATAGCCACACAAATAACGTGTTTTCACTTGTTGAATCTGACCCTTTTAGGCTTCGATTAAAATTGTGCCCTTTTGGTAACTGTCGCTTTAAATTCAAATGAGATTGTGCTCTTTTCTAAAGGGGGCGGAGCTAGAATTGCCTGTATGTCAGCATAGTGGCAGATATAAAAACAAGACTTGCGTCCTATGCTAATGAGGGAGAGATGGTCACTAGTGGGCGGGGTTTTCCCCCTCTGATGACACGTACAAATGGAGAATGTTAATCAAAGTGTTTCTGCAGACTGATTTTATCAAGTCTTATCATAACAAATAAAATTAATACGTTTACCATTAGAAGCTGCTTAAATGCACACACAACCGTGTTTAAACCCCTTATA

Associated Phenotype:

Not determined