ZMP

si:ch211-271b14.7

Ensembl ID:

ENSDARG00000059466

ZFIN ID:

ZDB-GENE-060531-55

Description:

Novel protein similar to vertebrate WAS protein family, member 3 (WASF3) [Source:UniProtKB/TrEMBL;Ac

Human Orthologue:

WASF3

Human Description:

WAS protein family, member 3 [Source:HGNC Symbol;Acc:12734]

Mouse Orthologue:

Wasf3

Mouse Description:

WAS protein family, member 3 Gene [Source:MGI Symbol;Acc:MGI:2658986]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7015	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa40600	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa14326	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa7015

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082688	Essential Splice Site	89	484	2	13
ENSDART00000143199	Essential Splice Site	89	481	2	8

Genomic Location (Zv9):

Chromosome 5 (position 70952733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	67338418
GRCz11	5	68016129

KASP Assay ID:

554-5279.1 (used for ordering genotyping assays)

KASP Sequence:

TGACCGTCTCGCAGTCAAGGTCACTCAGCTGGACTCWAGCGTGGAAGAAG[G/A]TCAGTCAAAAACCAAAATGCACAGTGCATTYAAAAAAGCAGTCACTTTTT

Long Flanking Sequence:

GCTAGTAAGTGCTGTGCAGGTAAACCTCACTCCTCCAAACTCTAAAGGTGCTCTAGCGACATATGCTAGAGGCCATGGTCTTTAGCCTCCTTGGTAGAGCAACCAACTCCCATGCGAAAGGTCGCCGGTTCGATACCAGCTCGGAGCGAGTTGGGTGGCGTATTATCGGCATTTATATAAACAATAAAAATATTTCTGTAAACAAGGTATTTTGCAACACCTCGACATAAGTAATAGAGCATAACATGAAACTATAGACTTTTTGTTTTGTCCAAACGACATATATTGTCATACTGCACACAATGCACAGCCCTAGTTTCAGTTCATCTCTGATCTGCAGTCTTTTCCCCACTCATCTATTAAAGGTAAACATGCAGAAGACGTGTTTGGTGAGCTCTTCAATGAAGCCAACACATTCTACCTGCGTGCAAACTCTCTGCAGGACCGTATTGACCGTCTCGCAGTCAAGGTCACTCAGCTGGACTCTAGCGTGGAAGAAG[G/A]TCAGTCAAAAACCAAAATGCACAGTGCATTTAAAAAAGCAGTCACTTTTTCACAGCCTTCATCCAAAATCGATCAGTTTCATTATTTTCCTCGAAATTCAACAAATACCACCCCATCATGATAGAAGTTTCAAATTTATAAAAATTTGAAATTAAGAAAAAAAATGACATGTACATAAATATTCACAGCCTTTGCCATGACATTCAAAATTGAGTGTTTTGTTTCCACTAACCTTATTGTACATCTTCCCGACAGGAAAAACCACCAACACTCAAGAATGCATGATTATATGCTGTTATGGCATTGCAATAAAAATGCGATTATAATGGGTCAATGGGGCAAAAACAGCCCCCAACATAACCAAAGGGTAGTCAATTAGTCCACAGTGTATTGTTGAGTTTTTGAAAACATTTCAAGGCATTTTCCCAAAATGTGTTCAAATAAGATTTGTCACCAAAACTCATTCCATTTGCTGAACACACGGAGAACATTGTGGCCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40600

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
ENSDART00000082688	Essential Splice Site	138	484	5	13
ENSDART00000143199	None	None	481	None	8

Genomic Location (Zv9):

Chromosome 5 (position 70954300)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	67336851
GRCz11	5	68014562

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCAGCAACTTTCAGTTTACGCAGACTTTAAGATGTTTATGTGTTTTGTT[T/A]GTTTTGTCTAGGGATGATCACATTGACGGAATTAAGTTCTACACAGACCC

Long Flanking Sequence:

AGCATTTAAGAGCTCCACTGTTCAAGACCAGCAGGTGGTGACAAAGAGCAGCGTTCCAAACCCCATCACAGAGATGTACAACACCAGCGACAAACCACCACCACTCAACATACTGTCAGCTTACAGGTGTGTGTGTGTGTGTATGTGCGTGTGCGTGTGCGTGTGCGCGCTGCTTTTTGATTCTTTTTCAATATTAAAGGTACTGTACTTGACTTTTTGACTCTTTTAAAGCTATTTAAAACTAATCTAATCAGTCGGAACTTAGCAGACGTTTAGAAAACATGCCAAGTCACACAGTTAGTTTGCTGTGAATAAAAGATGAGGTGGAAAAAATAAAAACCCACCCCCTACTCAAAAGAAATGTTGTTGGAAAAACTAAAGTTGCATAGGAAAATGCATTAGGAAAAAAAAAGCAATAAAAAAAATCATCATCATACTGAAATAAAGGTCTGCAGCAACTTTCAGTTTACGCAGACTTTAAGATGTTTATGTGTTTTGTT[T/A]GTTTTGTCTAGGGATGATCACATTGACGGAATTAAGTTCTACACAGACCCCTCCTATTTCTTTGACTTGTGGAAGGAGAAAATGCTTCAAGACACTGAAGACAAGAGAAAAGAGAAGAGGAAGCATAGGGTAAAGTAATCTGGCTTTTGAATATTGGCAGACTATGAAATGAAGAAATGCATTTGTTTTTTTTAATTTGGCTGCAAAACAAAACCCCTGTTGTCAATGCTTAAATGTGGCATACCTTATTAACTGAGTTATTAAGACTTTAAATTACACTATTACCTGTAATTCAATTTTGGGCTTGGGGCAAACATTCCATGGAATATGTTATTTTGATCACTGCAACACTACATTACACCACACAACACTGTACTGTACTATACTATACTTTACTATACTATACTACACTATACTACACTTCACTATAGTATATACTATACAACACTACACTTTACTGTGCTGTATGATATACTATATACTATATAGTATACTATATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa14326

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082688	Nonsense	476	484	13	13
ENSDART00000143199	Nonsense	473	481	8	8

Genomic Location (Zv9):

Chromosome 5 (position 70961661)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	67329490
GRCz11	5	68007201

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCTCTCCCGCCGCATCGCCGTCGAGTAYAGCGACKCAGAAGACGACTCA[G/T]AGCTGGATGACAACGAATGGTCAGACTGAAGACTGTCAGCNNNNCACACACA

Long Flanking Sequence:

TGTCCTGCACAGCTACCAAACCCAAACATTATTGTGTAACTTTAGGGTGTTTTGGAGGAGCGAGTCAGAAATGTTTTTTTTTTTCCTGACTTTTTTCCTGGCCACTATTCTGCAAGAAGAATGGCTCGAAATTCCTCTGGCCACTGTGCAGGACTTGTATCTGTCATTTTCATTTTTGGCGAACTATCCCATTAAGACTGTAAGGGTGTGTGTCCACCAAAGCGTTTTTGTTGCACTGCAGAAACAGAAGAACAGAAAAGAAAAAGAAAATGAGCTGCAGCGCAACATGTACCCTAAGACTGTCAAACTGCCAATCACAAAACAACTACATTTTTATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGCATTCAACTAAAGAAAGTACAGGAGCAACAAGAGCAGCAGGCTAAAAGAGAGCCCGTGGGCAACGATGTGGCCACTATTCTCTCCCGCCGCATCGCCGTCGAGTACAGCGACTCAGAAGACGACTCA[G/T]AGCTGGATGACAACGAATGGTCAGACTGAAGACTGTCAGCCACACACACACACACAATGGTAGATAGAGACCTTTGTCATAAATATGCAACTACTTCACGTGCTGAATTTTACATACAGTTAATTATTAAAAATGATATCTGATTTTATAAAGGAATTATGTGTGTTGAGGAAAGTGAGGAAAGACATATTTAAAGTGGCTTGAAAATACCAGTTATAGTTTACAATAAGGTTGGATTAGTTCAGGGGTTCCCAAACTTTTCCCCCAAAATAACAATGATGGTGACTCAATACCAGTGGTGTAGTCCTTGCTGTACGCACGTATACTCAGTATGCTTACTTTTTTCCATGAGCTGTTTGGGTATTACCACTTCTGAGGATCAATAATTGAGTTTACCCTCAGTATACTCACTTGTTTTTCTGATTAAACTTCCCTAATTTACATGTATTTGCGTCCCCTTTAACTGTATACCAAACTTTTTGTTTTTTTTAACTCACAAC

Associated Phenotype:

Not determined