Busch Lab

ZMP

wnt8a

Ensembl ID:
ENSDARG00000078507
ZFIN ID:
ZDB-GENE-980526-332
Description:
wnt8-like protein 2 [Source:RefSeq peptide;Acc:NP_001018637]
Human Orthologue:
WNT8A
Human Description:
wingless-type MMTV integration site family, member 8A [Source:HGNC Symbol;Acc:12788]
Mouse Orthologue:
Wnt8a
Mouse Description:
wingless-related MMTV integration site 8A Gene [Source:MGI Symbol;Acc:MGI:107924]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa31997 Nonsense Available for shipment Available now
sa11601 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa31997
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105649 Nonsense 14 354 1 6
ENSDART00000147756 Nonsense 14 353 1 6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 35625712)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 34154989
GRCz11 14 34495303
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAAAATAATGGCTTACTTCTTCCGTTGGGCCTTTCTATTCCCTATTT[G/A]GGACAAAGCTATCCTTGGACACACTTGGTAAGTGGATCATCAACTGCGAT
Long Flanking Sequence:
TTTATATTGTTATTTTTTAAACTCACATTGTTTATATGTAAATATTAAATTGACTTATTTTGTAGTGGGAAGCACATTAGATATTTAAAACGAAAAATCACTGTCTCCTAGTTGTCAATTTAATTGCGCGGTTTGGATGCCATTGGTTAAAAAGTTTATTGGTAAATTAAAGGTGTAAAATCACACTCAACCACACTTGAATAATGCATCTGCCCCAGCAACTTTGGGATCATGCCCGCAGAGGGAGAATCATCTGTCGTGTATTGGCATCCTTTGAAGTTCTGGAGGCGTTTCCTTGACTTGGCTGTGAAGTATGGACCAATAGCTTGGTAGGAATTCTGCAACAATAGGTATTCTTCCTTCTGACCCCCTTTGGAGGAATATAAAGTACACGACGGAGCGCGCATCACTTCCTCGAATCAGTACATTGCCTTTGTCTTATCACTTTGGATTTAAAATAATGGCTTACTTCTTCCGTTGGGCCTTTCTATTCCCTATTT[G/A]GGACAAAGCTATCCTTGGACACACTTGGTAAGTGGATCATCAACTGCGATAATGTAAACAGTTTTGCTTTTGTTAACGCGTTTTTTTAACCTTTTCTATTCATAGGACAATGAACAATTTGCTGATAACTGGGCCAAAGGTAAATTTTCTGTAACTTAAAAAATACGACCACCTTAAAAATCATGAAACAAAACTTGACCACCTAATCATTTGGCTTGTGGCGAAGCGTGAGTGTCAAAACACCCATATCTTTTCCTATCTTTCCAGGCTTATCTTACCTATGCAAATAGTGTGCGGGTTGGGGCACAGAGTGGGATACATGAGTGCAAACACCAGTTTGCATGGGACAGGTGGAACTGCCCGGACACCGCTCTGCAACTCTCTACTCACAAAGGCTTGAGAAGTGGTAAGATATATGCTGTATAACTTTAAAAATAAAAAACAACGCCTGGAAAATAACTGCATGCCCATATTGCATCTCTAGCAACAAGAGAGTCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11601
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105649 Essential Splice Site 35 354 None 6
ENSDART00000147756 Essential Splice Site 35 353 None 6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 35625978)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 34155255
GRCz11 14 34495569
KASP Assay ID:
2260-7758.1 (used for ordering genotyping assays)
KASP Sequence:
TTGWGGCGAAGCGTGAGTGTCAAAACACCCATATCTYTTCCTATCTTTCC[A/T]GGCTTATYTTACCTATGCAAATAGTGTGCGGGTTGGGGCACAGAGTGGGA
Long Flanking Sequence:
GCATCCTTTGAAGTTCTGGAGGCGTTTCCTTGACTTGGCTGTGAAGTATGGACCAATAGCTTGGTAGGAATTCTGCAACAATAGGTATTCTTCCTTCTGACCCCCTTTGGAGGAATATAAAGTACACGACGGAGCGCGCATCACTTCCTCGAATCAGTACATTGCCTTTGTCTTATCACTTTGGATTTAAAATAATGGCTTACTTCTTCCGTTGGGCCTTTCTATTCCCTATTTGGGACAAAGCTATCCTTGGACACACTTGGTAAGTGGATCATCAACTGCGATAATGTAAACAGTTTTGCTTTTGTTAACGCGTTTTTTTAACCTTTTCTATTCATAGGACAATGAACAATTTGCTGATAACTGGGCCAAAGGTAAATTTTCTGTAACTTAAAAAATACGACCACCTTAAAAATCATGAAACAAAACTTGACCACCTAATCATTTGGCTTGTGGCGAAGCGTGAGTGTCAAAACACCCATATCTTTTCCTATCTTTCC[A/T]GGCTTATCTTACCTATGCAAATAGTGTGCGGGTTGGGGCACAGAGTGGGATACATGAGTGCAAACACCAGTTTGCATGGGACAGGTGGAACTGCCCGGACACCGCTCTGCAACTCTCTACTCACAAAGGCTTGAGAAGTGGTAAGATATATGCTGTATAACTTTAAAAATAAAAAACAACGCCTGGAAAATAACTGCATGCCCATATTGCATCTCTAGCAACAAGAGAGTCATCATTTGTCCATGCAATAAGCGCAGCCGGCGTAATGTACACTTTAACCAGAAACTGCAGTCTTGGAGATCTAAACGAATGCGGGTGTGACAGCTCGAGGAACGGCAGACTTGGTAAGAACAGTTTTGGCCAATTCGCATACTAAAACATCCTAATATAGACAGAGCTGTTAAATTTATAAACCACAAAGACGACTAACTAATTTAATCATGGAATTAAAGTTGGCTATTTACTGTATTTACATCAGTCACGATGCATTTTACTTTTAG
Associated Phenotype:
Not determined