Busch Lab

ZMP

LOC100332293

Ensembl ID:
ENSDARG00000037357
Human Orthologue:
WIPI1
Human Description:
WD repeat domain, phosphoinositide interacting 1 [Source:HGNC Symbol;Acc:25471]
Mouse Orthologue:
Wipi1
Mouse Description:
WD repeat domain, phosphoinositide interacting 1 Gene [Source:MGI Symbol;Acc:MGI:1261864]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa31850 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41929 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31850
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054353 Essential Splice Site 244 413 9 13
Genomic Location (Zv9):
Chromosome 12 (position 1241986)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 1009254
GRCz11 12 1044831
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAACACCGAGACGGTTCACGTCTTCAAACTGGAGCATCACAGTCCCAA[G/T]TAATCAAACACATCATGAAAATGATCAACATGTGTTACATGCACAACAAT
Long Flanking Sequence:
CCAACTTTCGGATGAGATGTACACTGAGGTCCTGACTCTCTGTAGTCATTACAAATCCCATAGCACTTCTGGTGAAGAGTAAGGGTGTAACCCTGATGTCCTGGCCAAATTCCCATCATGACCTCCCAATCATCCCCATCCACTGAATTAGCTCTATCACTGTCTCTCCACTCCACCTATAGCTGGTGTGTGGTAAAGCACTGCACCATTGTCCTGTGGCTGCTGTCGCATCACCCAAGTGGAGCCGCACACTGGTGGAGGTGTGGGGAGATGATCATGATGGTGAAGCTTTTCGGGCGTACAGTAAACGCGCTATATAAATACACATTACATTACATTATTGCAATATATTGAATTTCCCACTGGGGGATTTGCTCTGTGTTTGTGTTCAGGTACGTGAGCATCAGTTCTCTGTCGTTCAGCGCAGATGAACAGCTTCTGTGTGTTTCCAGCAACACCGAGACGGTTCACGTCTTCAAACTGGAGCATCACAGTCCCAA[G/T]TAATCAAACACATCATGAAAATGATCAACATGTGTTACATGCACAACAATACATTGAGCTTTGTGTCAGGCTTTAGCAAAGTAGCTATTTTCCCTCTGCAGTCCCTTTAAACAATTAAAATATATATTAATATTAATAGTATCATCCGTATCACAGAGAGGTGATGAATTCATTGTATTTTATGTGTCAAGAATTTGTCTCTTGCATGCATAGGCTGCTTGACCAATCAGATTAGCCCTCACTATCTTAAACTCCGCCTCCCCAGCAGGTGCTGTTCTGCTATTGGCTAGAAGGTGAACCCAGAGCTAAATAATAATCACTAATGGCTAAAAATTGAAAATTACAACAGCAAACAATGAGGCTTTCAGTCATCTATAGTGTTTTAAAGTCTAAATGCTGGCACTTTGTTCTGTTTTAGTCTGAATTAGATTTATCTATTAAAATATTGATTAATAAACCTATTAAAAATCTGTTATCTGTTCATTTTAGTATAAAGCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41929
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
ENSDART00000054353 Essential Splice Site 333 413 11 13
Genomic Location (Zv9):
Chromosome 12 (position 1238122)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 1005390
GRCz11 12 1040967
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTGAATCTGCAGGATGGTGGAGACTGTCGTTTAGTCCAGAAGCACAG[G/A]TCACAATACACATTATTACTGAACACAATTAGCTTTAGCTTTTTTGAAGC
Long Flanking Sequence:
TCCAATAGAGCAGCTTTGGGATGTGGTGGAACGGCAAATTGGCATCATGGATGTGCAGCCGACAAATCTGCAGCAACTGTGTGATGCTATCATGTCTATATGGAGCAAAATCTCTGAGGATTATTTCCAGTATCTTGTTGAATCTCTGCCACAAAGGATTAAGGCAGTTCTGAACGCAAAAGGGGTCCAATCTGGTATTAGTAAGGTGTACCTAATAAAGTGGCCGGTTAGTGTATATCGCAGTAAAACAAAATATTGCAATGTCAGACTTTTTCCAATATCATTTAGTCCTAATCCAAATGTCATCGATTTGACGTTGCAGTGCGGTTTTCCCCGCCCACTGATATTGATTGACAGGTGGGTATTAACATCAGATTCATCACTGTGTGCAGGATCCAGAAGGTTCCTCGACTGCTGGTGGCTTCATCAGACGGTCATCTCTACATCTATAATGTGAATCTGCAGGATGGTGGAGACTGTCGTTTAGTCCAGAAGCACAG[G/A]TCACAATACACATTATTACTGAACACAATTAGCTTTAGCTTTTTTGAAGCACAAATATAAAAATCGAAGATAAATTTGTGTTTCGTTCATTAACAGACTGTTTGAAAGGGCAGATGAAGCTCTGGTGGCGTCAGATTTACATGTGGAAACTCCATCATATGCTGAAACTGTTGCCACAAACACAAACCAGGACTCTACACCTTCCAGTTCACTCACAGGTGCATCACGTCTGCTTTATGTTACTTTATAAAAGTGACCAGTCAGACCAGTGAAGGGTCATCTGACCAATCAGAGCAGAGTAGAGCTATCTTACCTATGAGAACAAAGAAGGGTTATTTGACCAATCAGATCAGAGTGGAGTTATCTGCCCAAGCAATCAGATCAAAGCGGTGTCATCTGACCAATCAAAACAGAGTACAGCCATTTGACCAATTAGATCAGAGTGAGCCACCTGGCCAATCACAGTAGTGCCATCTGACCAATCATAAAAGAGCTATCTG
Associated Phenotype:
Not determined