Busch Lab

ZMP

inpp4a

Ensembl ID:
ENSDARG00000063352
ZFIN ID:
ZDB-GENE-060312-5
Description:
type I inositol-3,4-bisphosphate 4-phosphatase [Source:RefSeq peptide;Acc:NP_001035062]
Human Orthologue:
INPP4A
Human Description:
inositol polyphosphate-4-phosphatase, type I, 107kDa [Source:HGNC Symbol;Acc:6074]
Mouse Orthologue:
Inpp4a
Mouse Description:
inositol polyphosphate-4-phosphatase, type I Gene [Source:MGI Symbol;Acc:MGI:1931123]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa25416 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41352 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31700 Nonsense Available for shipment Available now
sa38723 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25416
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
ENSDART00000092480 Essential Splice Site 349 931 11 22
ENSDART00000114731 Essential Splice Site 349 385 12 12
ENSDART00000127959 Essential Splice Site 349 936 11 23
ENSDART00000135576 Essential Splice Site 76 145 5 7
ENSDART00000148047 Essential Splice Site 349 385 11 11
ENSDART00000148181 Essential Splice Site 349 937 11 23
Genomic Location (Zv9):
Chromosome 9 (position 7087882)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 7067975
GRCz11 9 7046366
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTTTACATAATTTTTTTATTTTTATTTTTTACAAAATTTCTGAACA[G/A]ATCGCACATATGACGTAGTGACCACAGGGGCTCCTGCTGCACACCATCAG
Long Flanking Sequence:
TAAAATAGCAACGCGCCAGCGGTCCGCCTCAGAACGCCTTCCTTTTTAGACCAGAACGCCTATGGGCGCACAAATGAGCGCTAATGCATTTGGTATTTAAACAGCGTAGCGCAACGCCTCAAAACGACTCTTGCGCCAAGCTGAAACTACCAAAAGACTACTGCGCCGCGTCTCGCGCCACACTGCGCCGTGTGTATGATAGGGCCCAAAGAAGACAGTCAGGGTTGAGGTCTTCAATTGTCATAAGAATTTAATTTTAGATTATAGTTTTAATCTTAGTTTTAGTTTTCATTTACTAAAATAACCTTGGTTAAAATGGAAAAATAGGTTAATAAATTATATGTATTTTGAGTCCAATCAACATCTCTAACTTTTGTTGTTTAAATGATGTCAGGTCTAGCTAGATCAATTTCCTATTGACTCTTCTTACTATTGTACACCAGAGTGGGGTGATTTTTACATAATTTTTTTATTTTTATTTTTTACAAAATTTCTGAACA[G/A]ATCGCACATATGACGTAGTGACCACAGGGGCTCCTGCTGCACACCATCAGGGCTTTAAAGGCAGTGGACTGAGGAAGCTCATTCAAAAATTTGAGGAGGCCAAAAAACAGTAAGTATAAGAGCAACCCAGTAGAAGATCCCAGTATAAGAGCAACAAATAATAACTTGATTTCTAGTTGATCGTTTGAAAAAGTGGCAAAAGTTTGGTGAAAGAAAAATAATGGATTGGAGTTATATTCAGTTTGAGGCCGTGAGTCTACGTGTGAAAGCACCCTTAAAAGATTTGTGTTTGGAAAACATGCATGAATTGTGTGGAGCCCAGCATTTTTTACAGTGTAGGTCATGTGTTTGGTCTTGTTTTGTTCTTGTATCCAGCTTTTTTTTCCAATTCAAGGTAAAAAAAAACATAATTGTGGCATAAACGTACCAAAAAAAAAAAAAAAAACTAGAACAATTCTTGCAGTGATCACCTTTTCCCTCAGAGATGCAGCTTAATATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41352
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
ENSDART00000092480 Essential Splice Site 567 931 14 22
ENSDART00000114731 None None 385 None 12
ENSDART00000127959 Essential Splice Site 572 936 15 23
ENSDART00000135576 None None 145 None 7
ENSDART00000148047 None None 385 None 11
ENSDART00000148181 Essential Splice Site 573 937 15 23
Genomic Location (Zv9):
Chromosome 9 (position 7098588)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 7078681
GRCz11 9 7057072
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGAAGACGTGTTTCTGTCGGACCAGCAGGCCGACACCAGCAAGAGAG[G/A]TAGCAAGGGCAATGCATTCTGGATCAACCCTGGTGACGGGCTCTCGTCTC
Long Flanking Sequence:
GAGTGCTGCCCGGCCAGAGTTCATCGCTTCCAGAGGCTCTCCGTCCGCCCATGACACTGAGCGTGTGGTGCTGAGGAACGACCAGGGCTCTCCACAGGCCAAATGGAGTGGAAAGGGGAACAGAGCGTCTGTCAACTTAACATGGCAGGAGGAGGAATGGGTGAGTTGCACATCCTCCAAGCAGCAGGATTATATATGACAATATATATATATAACAACTTATTATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATATACATACATACATACATACATACATACATGCATACATACATGCATACATATATATGTATAATATTTCTGCTTCAGGAGAAGATCTGGCTGAACGTGGACAAGAGTCTGGAGTGCGTGATCCGCTGTGTGGACCGTCTGCTGACCCGAGAGCGCATGCACAGCGACAGCAGCGAAGACGTGTTTCTGTCGGACCAGCAGGCCGACACCAGCAAGAGAG[G/A]TAGCAAGGGCAATGCATTCTGGATCAACCCTGGTGACGGGCTCTCGTCTCCTTCCTCGTCACACCCCTTATCAGCTCCGTCATTATCACCATCCTCCTCACCCTTTCTGAACCCTGCATGCCCATCCACTCCTAACACTCACTCCTGTAGGTTCTCCTTTGGTTTCTCTTTCAAAACCTGCTCACATGTAATACAGATGCTTTCAGTTTTACGTCCTCTTTTGAAAATGCTGCACTCCATTCAAAGCGGATGTGCGATTTACCTGATCAGCGAGTGTATTGTGAAAAATCAGTGGTGTGAAAAAGTGTTTGCCCCCTTACAGATTTCATTTTTGGTCAATATTTGTCACACTTTAATGCTTCAGATAGTTAAGATAGACAGTTTAAATATTGGTCAAAGGTAATACGCATCAGTTTTGAAATTAGGATTTTTATTATTAACCCTCATGTACTGTTGGGGATATTTTCATCCACTCTGGGATGAGTTTGAGTCTTCAATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31700
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092480 Nonsense 800 931 20 22
ENSDART00000114731 None None 385 None 12
ENSDART00000127959 Nonsense 805 936 21 23
ENSDART00000135576 None None 145 None 7
ENSDART00000148047 None None 385 None 11
ENSDART00000148181 Nonsense 806 937 21 23
Genomic Location (Zv9):
Chromosome 9 (position 7105649)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 7085742
GRCz11 9 7064133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGGTTATTTTTTAGTCCTCACCTCTTGAATGCCTCCTCCATAGGTT[T/A]GCCACGCTCTCGCAGTCAAAACTGTGTGCCTGAGCTTCTCCGGTTCCTCA
Long Flanking Sequence:
TCTCCATATAAAGGCTTTCCACACAGCATTTCCTTTCCAGCCTTTCATCACTCTCGGCCGCCCTTGCCAGATCCGGCAGCAATGAAAGTGTGCCATCATCAAAAACAGTTCAAACACAATAAACACCTTTTATAGACCCAGATTACAGATCTCTCATTAGCCAGCTGCACACAAGCACTTCTACTCTGTGATGCTGCGAAAAATTACACCTGAAGCTACAATAGGTTATATATCAAACACAGTGGTAATTGAAATACAGATAATTAAGTGTAATGTTAAACTTAACCACGTTTGTTTAGGTTTGGAGACACGTCACTGCAGGAAGTCGTGAATATGGAGAGTCTCGCTCGTCTTACCTCTTATTATGACCAGTTTAAAGAAGTGCTGCCTGAAGACTGTGAGTTCTGAAAGCTCTACTGTATCCCTCTTGTTCCTTTATGAAACATTAGTAGGTGGGTTATTTTTTAGTCCTCACCTCTTGAATGCCTCCTCCATAGGTT[T/A]GCCACGCTCTCGCAGTCAAAACTGTGTGCCTGAGCTTCTCCGGTTCCTCAGTCAAAATATCAATGCCAGGAAGAGCAAGAACGTGGACATCCTGTTGCAGGCAGCAGAGGTACAGTGATACATCTGATGTTTCATTTTCATCATATTTAATAAAATGACTAGGAAGAAATGAAATTTAATTTAATTTAATTTAATTTTAGTTTATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTGATTCATTTTATTTTATTTTATTTTATTTTAAAGAGCCCCTATTATGGGTTTTTTAAAAGACCTTTTTTTAAATTTAATTTAATTTTATTTTATTTTATTTAATTTTATTTTATTTTGATTCATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa8329
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092480 Nonsense 864 931 21 22
ENSDART00000114731 None None 385 None 12
ENSDART00000127959 Nonsense 869 936 22 23
ENSDART00000135576 None None 145 None 7
ENSDART00000148047 None None 385 None 11
ENSDART00000148181 Nonsense 870 937 22 23
Genomic Location (Zv9):
Chromosome 9 (position 7107878)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 7087971
GRCz11 9 7066362
KASP Assay ID:
2260-1464.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGCTGCAAGAGTGCAAAGGATCGGACGGCCATGTCGGTGACAYTGGAG[C/T]AGTGTCAGATCCTCCAGAGTGAGCACTGCATGGCCYCGCAGGTCTTCACG
Long Flanking Sequence:
AATTATTTTATTTATTTATTTTTTATTAATGGATTTATTTTTTATTGTATTTATGTATTTAATATGGTTTTATTTATTTATTTACTCATTTTTATTTATTAATATTTATTGTATATATTTAATTTTATTTATGGATTTATTTTTATTGTAATTATTTAATTTATTTAATTTTTATAAATGGATTTCTTTTTATTGTATTTATGTATTTAATATGTATTTATTTATTTATTTACTCATTTTTGCAAATAATTCAGGGGGGCTAAAAATTCTGACTTCAACTGTATATGTTATAACATAATAATTCCTCCAACTGGGGAAACCCCTGTAGCTTTTGTCCCTTCATAATAAATGCGTTAAACCTCAGGGCGGCAGATATTCATCTGAATTCAAATGATTATTTTTTCCTTACTCGTTTCAAGATTTGTCGGCGTCTGAATGGTGTGCGGGTGACCAGCTGCAAGAGTGCAAAGGATCGGACGGCCATGTCGGTGACACTGGAG[C/T]AGTGTCAGATCCTCCAGAGTGAGCACTGCATGGCCCCGCAGGTCTTCACGCAGGCCCTCGACTGTATGCGCAGGTGAGACTGGATTTACAGCAGTGTTCAGCCTAAAAGTTTTCATTAGCATTTTTCTCAAATATTTTCTACAGATGAAAACAAGATTTTAACAAAATCAAAAAAGCATTTAGTTGTTTAAAAAAGCTTTGTATGAGTCAATAAAAATGCCATTATTTTATAAAAGCCTTTTATTATACAGTGTATCAATCTTAATTGCCTCTCCGGTCCCACAGTGAGGGCTGTCGACGAGAAAACACCATGAAAAACGTGGGCAGCCGCAAATACGCCTTCAACTCGCTCCAGCTAAAGACCTTCCCTAAGCAGTACAGACCACCAGAGGGAACCTTCGGGAAAGTGGAGACCTGATCTGCGACGAGAGCTGCATGTTCCCCCCTCGTCCTCCTTACTTTATCACCACATATCTGAAGGAAAGTTTTATTATGCACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38723
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092480 Nonsense 865 931 21 22
ENSDART00000114731 None None 385 None 12
ENSDART00000127959 Nonsense 870 936 22 23
ENSDART00000135576 None None 145 None 7
ENSDART00000148047 None None 385 None 11
ENSDART00000148181 Nonsense 871 937 22 23
Genomic Location (Zv9):
Chromosome 9 (position 7107883)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 7087976
GRCz11 9 7066367
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAGAGTGCAAAGGATCGGACGGCCATGTCGGTGACACTGGAGCAGTG[T/A]CAGATCCTCCAGAGTGAGCACTGCATGGCCCCGCAGGTCTTCACGCAGGC
Long Flanking Sequence:
TTTTATTTATTTATTTTTTATTAATGGATTTATTTTTTATTGTATTTATGTATTTAATATGGTTTTATTTATTTATTTACTCATTTTTATTTATTAATATTTATTGTATATATTTAATTTTATTTATGGATTTATTTTTATTGTAATTATTTAATTTATTTAATTTTTATAAATGGATTTCTTTTTATTGTATTTATGTATTTAATATGTATTTATTTATTTATTTACTCATTTTTGCAAATAATTCAGGGGGGCTAAAAATTCTGACTTCAACTGTATATGTTATAACATAATAATTCCTCCAACTGGGGAAACCCCTGTAGCTTTTGTCCCTTCATAATAAATGCGTTAAACCTCAGGGCGGCAGATATTCATCTGAATTCAAATGATTATTTTTTCCTTACTCGTTTCAAGATTTGTCGGCGTCTGAATGGTGTGCGGGTGACCAGCTGCAAGAGTGCAAAGGATCGGACGGCCATGTCGGTGACACTGGAGCAGTG[T/A]CAGATCCTCCAGAGTGAGCACTGCATGGCCCCGCAGGTCTTCACGCAGGCCCTCGACTGTATGCGCAGGTGAGACTGGATTTACAGCAGTGTTCAGCCTAAAAGTTTTCATTAGCATTTTTCTCAAATATTTTCTACAGATGAAAACAAGATTTTAACAAAATCAAAAAAGCATTTAGTTGTTTAAAAAAGCTTTGTATGAGTCAATAAAAATGCCATTATTTTATAAAAGCCTTTTATTATACAGTGTATCAATCTTAATTGCCTCTCCGGTCCCACAGTGAGGGCTGTCGACGAGAAAACACCATGAAAAACGTGGGCAGCCGCAAATACGCCTTCAACTCGCTCCAGCTAAAGACCTTCCCTAAGCAGTACAGACCACCAGAGGGAACCTTCGGGAAAGTGGAGACCTGATCTGCGACGAGAGCTGCATGTTCCCCCCTCGTCCTCCTTACTTTATCACCACATATCTGAAGGAAAGTTTTATTATGCACAGTCATG
Associated Phenotype:
Not determined