ZMP

wnt5b

Ensembl ID:

ENSDARG00000034894

ZFIN ID:

ZDB-GENE-980526-87

Description:

Protein Wnt-5b [Source:UniProtKB/Swiss-Prot;Acc:Q92050]

Human Orthologues:

WNT5A, WNT5B

Human Descriptions:

wingless-type MMTV integration site family, member 5A [Source:HGNC Symbol;Acc:12784]
wingless-type MMTV integration site family, member 5B [Source:HGNC Symbol;Acc:16265]

Mouse Orthologues:

Wnt5a, Wnt5b

Mouse Descriptions:

wingless-related MMTV integration site 5A Gene [Source:MGI Symbol;Acc:MGI:98958]
wingless-related MMTV integration site 5B Gene [Source:MGI Symbol;Acc:MGI:98959]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33385	Nonsense	Mutation detected in F1 DNA	Not yet available
sa45164	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa33385

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041852	Nonsense	78	363	4	6
ENSDART00000074651	Nonsense	78	363	5	7
ENSDART00000122986	Nonsense	95	380	2	4

Genomic Location (Zv9):

Chromosome 4 (position 7518811)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	8639725
GRCz11	4	8640641

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCAGAGGAAGCTCTGCCAGCTCTATCAGGACCACATGGTTTATATTGGA[G/T]AGGGGGCGAAGACGGGCATCAAAGAGTGCCAGTATCAGTTCAGACAGAGG

Long Flanking Sequence:

AGCAAAAGTTGTATGTCTAAACTGCACAGCACAGTCTCCCCTGGTAATAGATCGTGTTGATTGACCATTATTGTTCTTGTGTGCCACAAACTCACATAATGGAGGTGGAGCATATCCATTTAAAATTTTAAAAATCATACAAGCATCAGCCAAATATTTCATATTATCAAAGCTCAATAAATAATGTTTTTTTGTTATTTTACAATGATGATACCTAATAGATTTCCCATTATATACATCATTAGGGTAGCCTGATGAAGTTTTACATTATAAATAACAATTTAGAGTCACAAATAGTCATGCATATTTAATCCTGTGCTATATTTAGCTGATGGTAAAAGCTTTGGTCTTGCTTTCTCAGGTCATTAGCCATGAACCCCATCCAGAGACCGGAGATGTACATCATTGGAGCACAGCCTCTGTGCAGCCAGCTGACGGGCCTATCTCAGGGTCAGAGGAAGCTCTGCCAGCTCTATCAGGACCACATGGTTTATATTGGA[G/T]AGGGGGCGAAGACGGGCATCAAAGAGTGCCAGTATCAGTTCAGACAGAGGCGATGGAACTGCAGTACAGTGGACAACACGTCAGTGTTCGGCCGCGTCATGCATATAGGTGAGTTGACCTGGTGATCTCTAAAAGTACATGGCTAAAAGACTAAAAGTGGAGTATATGCCAAATTATCTTGTTAGGTGTATTTAGAATAAAAATCATTTGATGCCATCTTTGGATAACACTGCAGCACCAAATACTAATTACTTGACATTTTCATTATTTATTCTTAAATCTGTCCTTCAAATGACCCATTTGCCAGCCTAACATTTTAATTATTTCAAAATATAATAATTTAGTTTGATCACTTGTTATTTTTATTAGTCAAGAGAAGTATGTTGTTTATTATTTACATAAATGTGTCTGTCACACTGAATGACAACAGAACTTTTTTCACCAATATTTTGACATTGTGTTTTTTACAAAAGTTGTTTGCAACATTTAATCAGGCTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45164

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
ENSDART00000041852	Essential Splice Site	211	363	5	6
ENSDART00000074651	Essential Splice Site	211	363	6	7
ENSDART00000122986	Essential Splice Site	228	380	3	4

Genomic Location (Zv9):

Chromosome 4 (position 7513473)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	8645165
GRCz11	4	8646081

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACACGCACGCACGCTTATGAATCTGCAGAACAATGAAGCCGGAAGAATG[G/A]TGAGGAAATAAACACACACATCAGTGATCTGCTTTCTTATTTTTGGCTGT

Long Flanking Sequence:

TTCACATTTGTCCGTGCTTTTATTTTCTTTATTTAATTTAAATGCATGATTTACTCCTCTACAGAATCATCCAAATCCAGAGCTGTTCAAGCTCTCTGTTAAAATTGTCCATAGAAAAACAAAATATTGCAATGTCATATTTTTTCTAATATCACACAGCCCTAGTGGAATGTTTCCTAATTATGTGTTCATGTGTGTTTTGTGCAGGCAGCCGAGAAACAGCTTTTACATACGCCGTCAGCGCAGCGGGTGTTGTGAATGCTGTGAGTCGAGCGTGCCGTGAGGGTGAGCTTTCCACCTGCGGCTGCAGTCGAGCGGCTCGTCCCAGAGACCTGCCCAGAGACTGGCTGTGGGGCGGCTGCGGGGACAACGTCAACTATGGCTACCGCTTCGCCCGGGAGTTTGTGGACGCTCGTGAACGTGAGAAGAACTACCCACGCGGATCGGTGGAACACGCACGCACGCTTATGAATCTGCAGAACAATGAAGCCGGAAGAATG[G/A]TGAGGAAATAAACACACACATCAGTGATCTGCTTTCTTATTTTTGGCTGTGGATGCCATACTGGGCGTTAATAAGACCAGTTTGGGTTCATACAAGTGTTTATACTGTAAGAAAAATTCATGAAAAACAGATATTATACTGGCAGGTACCGTGCATTCGGAAAGTATTGATAGCACTTCACTTTTTCCAAATTATTTATGTTACAGCCTTATTCCAAAATGGATTAAATTAAGTTATTTCCACAAAATTCTACACTCAATCCCCCATAATGACAATGAAAAAAAAGAGTTTTTGAAATTGGTGCAAATTTTATTGAAAAATAAAAAAACCTGAAAAATGACATGTACATCAGTATTCACAACCTCACTACTTTGCTCTGTAAGTTTGCTCTTTGTCTCTGTGCAATGCTGCATTCATCTTTCCCTCTATCCTGACTAGTCCTCCAGTTCCTGCTGCTGAAATACATCTTTACAGCATGAGACTGCCACCACCATGCTTCA

Associated Phenotype:

Not determined