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

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