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