ZMP

wnt7ba

Ensembl ID:

ENSDARG00000022858

ZFIN ID:

ZDB-GENE-041210-178

Description:

Protein Wnt [Source:UniProtKB/TrEMBL;Acc:Q5RGZ3]

Human Orthologue:

WNT7B

Human Description:

wingless-type MMTV integration site family, member 7B [Source:HGNC Symbol;Acc:12787]

Mouse Orthologue:

Wnt7b

Mouse Description:

wingless-related MMTV integration site 7B Gene [Source:MGI Symbol;Acc:MGI:98962]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31394	Nonsense	Available for shipment	Available now
sa26281	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31394

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003156	Nonsense	52	353	2	4
ENSDART00000142343	Nonsense	37	338	1	3

Genomic Location (Zv9):

Chromosome 4 (position 17775465)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	18718305
GRCz11	4	18707281

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTTGGGCGCAAACATCATCTGCAACAAGATCCCCGGCCTGGCCCCCCGA[C/T]AGCGTGCCATCTGCCAGAGCCGCCCAGATGCCATCATCATCATTGGGGAA

Long Flanking Sequence:

AATGAATATGTTTTTTTTGGCCAATAGCTTTAGTCGTAGTGTTTTTGTTTACTAAAATAGCCTTGCAAGGAACCATTTGAGCAAAAAATTCTTCATCAACCTTCTAACAAGAACATAGTCACATGGGGACTTGTGGAGCTGTGCATCGATGGATTTGCTCTTCAGTGTTTTGACTTTCAGCAGTGAACTTTAAACCACACTGAACTAAAGTGATCTTCAACTCTGAAAACCAAACTGACAATTTCAATTTACTAGAACTTCTATGTTAAGCTGCTTTGACACAATCAACAGTGTAAAATCGCTATAGAAATAAACATGACATGTCGATTAGAATAAATTAATCCTAAATTTTCATTTTTGGTTGAACCATCTTTTTAAATACCTCATCTATATCAGCTGCTTACATCAGTGTGTCTGGTCTCCTCCAAAGGGCTTTGTCTTCAGTCGTGGCTTTGGGCGCAAACATCATCTGCAACAAGATCCCCGGCCTGGCCCCCCGA[C/T]AGCGTGCCATCTGCCAGAGCCGCCCAGATGCCATCATCATCATTGGGGAAGGCGCTCAGCTGGGCATCAACGAGTGCCAGTATCAGTTTCGCTACGGCCGGTGGAACTGCTCTGCCCTTGGCGAGAGGACCGTCTTTGGGCAAGAGCTGAGAGTAGGTCAGTAGGTGCAGCCCCGTGAGCTGTGCTTTCATGTCACATTCATAGTATGTGAGTGTGGGTGTGTGTGTGTGTGTATGTATGTTGTTTTGGCTGGATCTGTTTCCATTAGAGCCCTGCAAAACAAATGAGACAAAAAAGAGGTTAAAGCAGATACAATCAGTCCGCAATTACTTTAGAAAAAATCTCTTTCAAAAAACATTTGAACACACACACACACACACACACACACACACACAAACACACACACACACACGGACAAAAATGGCATCAGTGACTTTCTGAGAACCAAGGAAACACACAGTAATATGCTTTTCTTTAATATTGCACTCTCATATAAATTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa26281

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003156	Nonsense	262	353	4	4
ENSDART00000142343	Nonsense	247	338	3	3

Genomic Location (Zv9):

Chromosome 4 (position 17781885)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	18724725
GRCz11	4	18713701

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAGAGCCACCCGTTTTCGACAGCCCTCCTTCCTACGTCTCAAGCAGTCT[C/T]GAGGGTACATCAAGCCCACAGACACAGACTTGGTGTTCTTAGAGCGCTCC

Long Flanking Sequence:

AAAGGGTAAAAAATGAACCAACAACATTGTCAAAACATTCGATTTGAATCCAGTGTTCAACTGTAATCATACAGAGCTCCAAAAACAATTTTATGCACCTGATCCAAAAACAATCCTTTCACGTAAGGTCAGGGTGCATCTTTACTATAAAAATATCTTAATTTGTGTTCTGAAGATGAATGAAGGTCATAGCAGATTAGAACAACATACAGGTGAGTAATTAATAACAGAATTAACATTTTTGGATGAATTAACCCTTTAAAATACCTTAAGTGACATTTTGTTTCCTACTGTCGCAGGTTCTAGAAGAAAGGATGAAGCTGGAATGTAAATGTCATGGTGTCTCTGGCTCATGCACCACCAAAACCTGCTGGACAACTTTGCCAAAATTCCGAGAGATCGGCTACGTGCTGAAGGAGCGTTACACCACCGCGCTTGAGGTGGAGGCTGTGAGAGCCACCCGTTTTCGACAGCCCTCCTTCCTACGTCTCAAGCAGTCT[C/T]GAGGGTACATCAAGCCCACAGACACAGACTTGGTGTTCTTAGAGCGCTCCCCCAATTACTGCGAAGAGGACACTGTGACGGGGAGCGCAGGAACGAGAGGACGCCTATGTAACCACACGTCTCCTCTCACAGATGGTTGCAACCTGATGTGCTGCGGCCGAGGACACAACACTCATCAGTACACACGCGTGTGGCAGTGCAACTGCAAGTTCCAGTGGTGCTGCTTTGTGAAGTGTAACACCTGCAGCGAAAAGACAGAGGTGTTCACTTGTAAATGAAGATGCGGAAAAGGTTATGGACAAGAAAGAAAGGCCAAAAGCCAATGGAGAGAAGCAGAAAGTGCCACGGCTTCTTCATTTTGCACATCAGGCAGTCTTTAGACAAGAAAGGCCCTTTGTTGAGGAAGAATAAAGAAGATGTCTGAACTTTAAGAGGAAAATGCACTGACCTCAGACTGATTTTCTTGCAAATGTGGACACTTCATTTGAGTGCAAGGCTTT

Associated Phenotype:

Not determined