ZMP

impa1

Ensembl ID:

ENSDARG00000003517

ZFIN ID:

ZDB-GENE-040718-245

Description:

inositol monophosphatase 1 [Source:RefSeq peptide;Acc:NP_001002745]

Human Orthologue:

IMPA1

Human Description:

inositol(myo)-1(or 4)-monophosphatase 1 [Source:HGNC Symbol;Acc:6050]

Mouse Orthologue:

Impa1

Mouse Description:

inositol (myo)-1(or 4)-monophosphatase 1 Gene [Source:MGI Symbol;Acc:MGI:1933158]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31280	Essential Splice Site, Splice Site	Available for shipment	Available now
sa7262	Essential Splice Site, Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31280

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:

T > C

Consequence:

Essential Splice Site, Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010683	Essential Splice Site	None	282	None	9
ENSDART00000131411	Splice Site	None	239	None	8
ENSDART00000137933	Essential Splice Site	None	20	None	2

Genomic Location (Zv9):

Chromosome 2 (position 26831341)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27027537
GRCz11	2	26683171

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAACCCGGAAACACAACAATCTGACAGCCTGTCTACATTTCGCCGGTTGG[T/C]AAGCATTTTCTCTCCGTATTATTATTATTATTGGTTGTGTTTCAACGAGT

Long Flanking Sequence:

CAGCTAAGACCAGGCTGTAAATGGCCAAAAAACCCTCTAAAACCAGCCAGCTTAGGCTGATTTAAGCAGTTTTCTTCCCACAGGGAATAAAGTACAAAAACCACGGAGAGAAAAATGTTTGTAGCTGTGAACACTTGACACGTGCTCGTCAAAAAAAAAGAGAAAACCTCTTTGCTTCAGTTTAAATAATGAATAGTAAGTATTAAAGAATAAAATAACTAACCTAGTTGTGTCAGGCGATCGTGATGCTTACACAATGCGCATGCGCATTAACATTAATACGAGTTATACGATAGCTACTGTATTTCAACACACTGATGGTAAACAGGACATTGAAACGTATAGTATAAGCTACACATATACAGAGAGGATATTTCTCTATACTAAATGCTTAGGTGGTTTTCTAAAAATACCCAGATAACGTAGGGTTAATCTTCTCTGCTCCTCCAAGAACCCGGAAACACAACAATCTGACAGCCTGTCTACATTTCGCCGGTTGG[T/C]AAGCATTTTCTCTCCGTATTATTATTATTATTGGTTGTGTTTCAACGAGTTAGTTATGTCACTGTATTTGCGCTTCCATCATAAAGCAAGTTTAGCATCGATGTTTATATTTGGCTTAATTATAAAGGTATAGCAATGAACCGAAGCAGATTTGTACAGGAGGATCTTTACTATCATTAGCCAAAGCTCATCTGTGTTTTGAATGAGAGTATGCTTGTGCAGTTCAGACATGCACTTCAGGAGCTATAAAATATTATACATTTTGTGGATTTTCAGGGTGTTTAGCTTCTAACAGCTTAATGTTGTAGGTATTTATTTTTATTAAAGGTAACATTACAACATTTTTATTTTATGTGTATAAAAATGATTTTCCTTGATAATTATTTATTAATATAAGCCCTTTATATGCATCCCTAATGTTTATATATAAATGAAAAATGTGCCAAAGAAAATTTTTTTTTTCTTGTAGTACATGAAATGTTTTTTTTTATGGTTGTAGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7262

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, Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010683	Essential Splice Site	None	282	2	9
ENSDART00000131411	Essential Splice Site	None	239	2	8
ENSDART00000137933	Splice Site	None	20	None	2

Genomic Location (Zv9):

Chromosome 2 (position 26832847)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27029043
GRCz11	2	26684677

KASP Assay ID:

554-4605.1 (used for ordering genotyping assays)

KASP Sequence:

WGACTGCAATTTRAAACTGAAGAGAATAATTTTTATTTATTTTTTTTTTA[G/A]AAAGGCATCCTAGAATATAAAGGCACAATGCCTGACCTTTGGCAGGATGC

Long Flanking Sequence:

TAAAGAAAACAAACTGTTGTGGAATATAGTCAAATGAGGATTTCTGTTAAACATTTGCTGTTATTACATTGCATCTAATGGAGGGCATCCAGCATTAGACATCATTCAATTCATTCAAAATTCATTATTGGGTGAATTATCTCTTTTACATAAATGAGAAATAGATAAAATAATACTAATAATAGTATCATGATTTTACAGCTGATGGCAGCTATTATAATGTAAATCAAAGCTGCCATAGTACTTTTTTTTTTGCTTGGTTCTTCAGTCAAAGAACCAATTAGGGGCCCAGTTATTTATAGGAATAACTCTATATAAGGAGTGTGTGCAGGGATTCAGGAACTCAGGGAAAATATGGGATTAATCAGAAACATAAACTGCCTTCTCAAACAAAATAGGGTTTTAAAAATGAACTGTGATCTGAATTGATTTACATCATTATGGTGTTTGTGACTGCAATTTAAAACTGAAGAGAATAATTTTTATTTATTTTTTTTTTA[G/A]AAAGGCATCCTAGAATATAAAGGCACAATGCCTGACCTTTGGCAGGATGCCATGGACCATGCTGTAACTTTGGCCAGAAAAGCAGGAGAGGTGAGATGTCATTGCACTTTTAAAACATTTTTTTGTTGTGTTTTTTTGTGCACTGAAGTCTTACTCTTTCTTTCTCTCTCTACCAGATTGTGAGGGAGGCTTTGCAGAACGACCTGAAGATCATGTGCAAGAGCTCATCTGTTGACCTGGTCACCAAAACAGACCAGAATGTGGAGCAGCTTATTATTACGTCAGTGAAGGAGAAGTTTCCTGAACACAGGTATTGACTTGAGTCCTTTATGCTAATATTAGATCACATTGAATCAACAGTAAAGAGAACGCACAGCATCTGCTTCTGTTTATTGTAGTTTCATTGGTGAGGAGTCTGTGGCTGCTGGAGAACCTTGTGTTTTGACTGAAAACCCAACATGGATTGTTGACCCTGTGGATGGGACCACTAACTTTGTGCA

Associated Phenotype:

Not determined