Busch Lab

ZMP

wnt9b

Ensembl ID:
ENSDARG00000037889
ZFIN ID:
ZDB-GENE-080201-1
Description:
protein Wnt-9b [Source:RefSeq peptide;Acc:NP_001131132]
Human Orthologue:
WNT9B
Human Description:
wingless-type MMTV integration site family, member 9B [Source:HGNC Symbol;Acc:12779]
Mouse Orthologue:
Wnt9b
Mouse Description:
wingless-type MMTV integration site 9B Gene [Source:MGI Symbol;Acc:MGI:1197020]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa20083 Nonsense Available for shipment Available now
sa16500 Nonsense Available for shipment Available now
sa26124 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20083
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
ENSDART00000055225 Nonsense 66 358 2 4
Genomic Location (Zv9):
Chromosome 3 (position 37570946)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 37434306
GRCz11 3 37576164
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGTAAAGCGCACCTGAAGCAATGCGAGCAGATGACTCTGACGCGCCGG[C/T]AAAAGCGCCTGTGCCGTCGGGAACCAGGGCTGGCAGAGACTCTGCGAGAA
Long Flanking Sequence:
TTTATTTAAGAGCGCTAATTGAAGTTTGTTGCGCGCCACAGTAAAGCCAGAGCGCTTCGTGAAAGACTGGGGAAAAGAACAAGTGCAGTTTTGTGCATGCTTTATTCAAACACGACTATTCAAATTATTTAAACATTATTCAAAGCACGTGTGGCAACAAAGTGCATTCTGAAAAGGTTATATATTTTAAAATACCTACAGCAAAACTGGTGTCAAAGTTTAACCTATGAAAATTAAATAAATATTACCAAGTTACTTAAAGTAATTTGATAACATAATATTAACACCATTTTAAAGAAATTTGTGGAAACTAAACGCGTGGTTTGTGTATATAAACTAAACAAAATGAAGCAGCTGAAAAATATATCTGTAATTATTGTGTTTTCGTTAGGCTTACAGGTCGCGAGCCTCTGGTTTTTCTGCCGGGTCCATTTGCCAACGAGCCTACAAACGGTAAAGCGCACCTGAAGCAATGCGAGCAGATGACTCTGACGCGCCGG[C/T]AAAAGCGCCTGTGCCGTCGGGAACCAGGGCTGGCAGAGACTCTGCGAGAATCTGTCCGCCTCAGCCTCCTCGAGTGCCGCTACCAGTTCCGCAACGAGCGCTGGAATTGTAGTATGGATGGCCGTGGAAGTCTTTTAAAGCGAGGTAAGAAAAGACCCTCTAGGTGTTTTTTTTACATTTATTCGCACATACGAAAATTGTGATTCTTTTGTAGCTAAAATATAGACAGACTATTTACGTGTTCTATTTACGTGCTAAACATTTTAATTTAGGATGAGATATGGTTCATTCATTATTAGGCTAGACTATTAATCAACTATCAGCCTTGCAGCTCAAGGTCAAGAAACTAAAAGCTGATTATACAGCATTTCTTAAATTTAATCATAAACGTTTTAAATTAAATTATATGACCACTAAAATTATATATAGGTAATAATATCTCTATATAACCTACCCTACTAGTTTTTATAGAACTAAAGGGCTCAGGGCATGAAAAAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16500
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
ENSDART00000055225 Nonsense 221 358 4 4
Genomic Location (Zv9):
Chromosome 3 (position 37575181)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 37438541
GRCz11 3 37580399
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGTGGACTTAAGACTACTTGTAAGTGTCATGGTGTTTCCGGTTCATG[T/A]GCTGTAAGGACGTRCTGGAAGCAGCTCTCCCCGTTTCAAGACACAGGTCA
Long Flanking Sequence:
GCGAATTGATGGAAACTAACTAACTGACTGACTAACTAAATACATTAAAAAAAAAAAAAAAAAGCTTCATAGGCTTTATTTTTCTCTATACACTCACTTTAATTTGATGACCTCCTTTAGGCATCTTTGTGACTATAAGCAATTTTTCAAGCACCTGATCATTGGTACGGATAGGGTCAGTAGAACAAGTTGACATGTGCTTGCAAAAAAAATTATAGTCAGTCTGACTGAGGATCAAAATAAATTTATAGCAGACTTTAACTTAGATAACAAATATTATAATAACTGTTCACATGTAGACGCAAAGTGACTTATATAGTCAACTGAATGCTAGATGTTTAGGTCTAAATAAATAGACCACATATAGACTTGTTTTTCACAAGAGCATTGTGTTGTATTCGGTAATGTTCATGCTTACAATTTTGTTATTGTGCTTACTTTCAGGCCGTGAAAAGTGGACTTAAGACTACTTGTAAGTGTCATGGTGTTTCCGGTTCATG[T/A]GCTGTAAGGACGTGCTGGAAGCAGCTCTCCCCGTTTCAAGACACAGGTCATCTGTTGAAGTACCGCTATGACACAGCTGTCAGAGTGCACAGCGTTACCAACTCTGCCACGGGGGAAACAGAACTGGCGGGCCCTCGCCGCCACAGCATCACGCTTCCCCGACCCCGTCCCACTGAACTGGTGTTTCTGGAGGAGTCGCCCAGCTTCTGCAGGCCATCCCGCTACTCGCCTGGGACTGCAGGCAGACCGTGCTCCAAGGACACCAGCTGCAGCAGCCTGTGCTGTGGACGGGGCTACAACACTGCCCTTCGCCTCACCACCCTCTCCTGCCACTGTCAGGTCCGCTGGTGCTGTCACGTTGAATGTCAAACCTGTCTCAGAGAGGAGGAGGTCTATACGTGCAAGAAACACTGATTAACCTTGCAAGACACAGAGTGAGAGGGGAAGTAAACAGAGGCAAATGAGTGGGACATGGGGAGTGCTGAGAATTGTGTATGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26124
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
ENSDART00000055225 Nonsense 275 358 4 4
Genomic Location (Zv9):
Chromosome 3 (position 37575341)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 37438701
GRCz11 3 37580559
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGGGAAACAGAACTGGCGGGCCCTCGCCGCCACAGCATCACGCTTCCC[C/T]GACCCCGTCCCACTGAACTGGTGTTTCTGGAGGAGTCGCCCAGCTTCTGC
Long Flanking Sequence:
ATTGGTACGGATAGGGTCAGTAGAACAAGTTGACATGTGCTTGCAAAAAAAATTATAGTCAGTCTGACTGAGGATCAAAATAAATTTATAGCAGACTTTAACTTAGATAACAAATATTATAATAACTGTTCACATGTAGACGCAAAGTGACTTATATAGTCAACTGAATGCTAGATGTTTAGGTCTAAATAAATAGACCACATATAGACTTGTTTTTCACAAGAGCATTGTGTTGTATTCGGTAATGTTCATGCTTACAATTTTGTTATTGTGCTTACTTTCAGGCCGTGAAAAGTGGACTTAAGACTACTTGTAAGTGTCATGGTGTTTCCGGTTCATGTGCTGTAAGGACGTGCTGGAAGCAGCTCTCCCCGTTTCAAGACACAGGTCATCTGTTGAAGTACCGCTATGACACAGCTGTCAGAGTGCACAGCGTTACCAACTCTGCCACGGGGGAAACAGAACTGGCGGGCCCTCGCCGCCACAGCATCACGCTTCCC[C/T]GACCCCGTCCCACTGAACTGGTGTTTCTGGAGGAGTCGCCCAGCTTCTGCAGGCCATCCCGCTACTCGCCTGGGACTGCAGGCAGACCGTGCTCCAAGGACACCAGCTGCAGCAGCCTGTGCTGTGGACGGGGCTACAACACTGCCCTTCGCCTCACCACCCTCTCCTGCCACTGTCAGGTCCGCTGGTGCTGTCACGTTGAATGTCAAACCTGTCTCAGAGAGGAGGAGGTCTATACGTGCAAGAAACACTGATTAACCTTGCAAGACACAGAGTGAGAGGGGAAGTAAACAGAGGCAAATGAGTGGGACATGGGGAGTGCTGAGAATTGTGTATGCATCTACTAGTCAGCTAGAAGAATTTGGAAGGGTTTGGAGGTTGTTGAGGATGATTTGCCAGCCTAACCTGATTTAGATGAGATGGCTTAATGGTCGAGTGTCACTTTCTGAAACTCTAGGCTCCTACATGGAGCAGATGCTTGACGGGAGACCATGTTCATT
Associated Phenotype:
Not determined