ZMP
LOC563543
Ensembl ID:
Human Orthologue:
INPP5B
Human Description:
inositol polyphosphate-5-phosphatase, 75kDa [Source:HGNC Symbol;Acc:6077]
Mouse Orthologue:
Inpp5b
Mouse Description:
inositol polyphosphate-5-phosphatase B Gene [Source:MGI Symbol;Acc:MGI:103257]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12274 | Essential Splice Site | Available for shipment | Available now |
sa36025 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22739 | Nonsense | Available for shipment | Available now |
sa22740 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12274
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061706 | Essential Splice Site | 78 | 907 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 5066348)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 4284150 |
GRCz11 | 16 | 4083203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTCTGGGCCAAATCATTCCCATTTCTTATGACTTTTCGGTTGTTGAAG[G/A]TAAGACATATTGAGTTAATMGRTCACACTTTACWATAAGGTTCATTAGTT
Long Flanking Sequence:
CAAACGAGTGATAATCTTCCGGAAATCGTGCATTCTCAAATACGTTGCGCATCCGTCCCCACCGCATTCCTCATCGCTCTTCAGACACGTCGCGCGCACCCTGTCAAACACCACCAAACCACCACCCCGCTGACAGCTGAGCAGGACTCTTTTAGTCCGTTTAGAAGTTTTGCCGTGTGAAAGCGAACCGCACCAAGAACAAAGAGCAACAATGTAACCATTTAAATCTCTGTTTCAGAACAACTGAATCGATTCACAGGTGTGAAAGCACCCTAAGTCAAAGAAAAATGAATGAATGAACTTTATAAATCCTAATAGCAAAACCAGCTGATAAAGATAATCCGATGCTACGTTTGCAAAGACTGAACTTGTCTGATTTATTTTATTCTTTTATTTGATCAGGTTGTTTATATATTCCCATCGAAGGATGGCCATCACTGGTGAGGATGTCACTCTGGGCCAAATCATTCCCATTTCTTATGACTTTTCGGTTGTTGAAG[G/A]TAAGACATATTGAGTTAATCGGTCACACTTTACAATAAGGTTCATTAGTTTATGTTAATTAATTTATTTACTAAAATGAACAAACAATGAACAATATATTTACTACTGTATTTGTTCATGTTAGTTGACGTTAGTTAATGAAAATACAGTAGTTCATTGTTAGTTCATGTTAACTCATGGTGCATTAACTAATGTTAACTAGCATGGACTTGAATGTTAAAGGGTCACGAAACACCAAAACACATGTTTTGAGCTGTTGACAGTCGTATGTGTGTCCCACACTGCTAAAAACACTATTAGGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTCGTACTTCCTGTTTGAAACGAATTTTTGAAGCTGCGTCTTGGTCATGAGATAATAGCGTGTATTCCAGCGTGCAGACTGGACATCTGTGCCAGAGTGAGTCTTATTACATCTTACAGTGTGCTGTATTAATGCATGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36025
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000061706 | Essential Splice Site | 287 | 907 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 5091283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 4308285 |
GRCz11 | 16 | 4107338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAATGAGTTAGCACAGTTATGTGATTGGGATGTGTTTTCCTCCGGTA[G/A]TTTCCAGGAGCTGGATCTCAGCAAGGAGGCGTTTCTCTTCAATGACACTC
Long Flanking Sequence:
GTCTACATGCCTAAATGCATTGAGTTGCTGTTATGTGATTGGCTAATTAGAAATTTGCATTAACAAGCAGTTTGACAGGTGTAGCTAATAAAGTGGTTGGTGAGTGTATGGTTTGTATGAACTATCATGTCATTGCTTTAAAATGTTTTGCGTTTTGAAGCATATAATGTTTATTATTTTTAAATGTTACATTTTATAATGAAGCTAAATATTTGGCTCAGTTTAAAGAGTTTAATTTCTATTTAAATGTAGTGCATTTATACATTTTATAGTGTCTAGTCAAGTAATTAAATAACTTATTGAGTAACTGGCTTACTTTGTCAAACATTGTAATTAAAATGTAATTTAAATACAAAATTTAATGATGTGATTTAGTAGTTAATTACTTTTCTGAAGTAGCTTACCCAGCACTGGTATTACTCTACAATATGACATTAATATTCATCTAAGCAGTAATGAGTTAGCACAGTTATGTGATTGGGATGTGTTTTCCTCCGGTA[G/A]TTTCCAGGAGCTGGATCTCAGCAAGGAGGCGTTTCTCTTCAATGACACTCCTAAGGAGCCCGAGTGGATGTTAGCCGTCTATAAGGGTCTCCATCCAGATGCCAAGTATGCTTTAGTAAGGACTTCCTTTGCCCCTCTCATCCATCATTTTAAATGCAGCAATGTAGTTAATTCCTAATTCCACCAACATTGTATTTAGTGTGGTAATCTTTAATCAAAGTCTGACCATTTGCTTCTGAGGGTGTACATACCACTATTTACAGTTGCCTTAAACTGGGTCGAAGCACGCTTGTCCCCCCTTCCGTCTCCCCCGACGGCCAGCACTCACATTAAATTTGGGCCTGGGCATGCTTACGTCATCGATAATGCGTTGTTCAGTAATGGTGCTTTCACACCTGGCTTATTTAGTTCGGTTGAATCGCACTAGAGTTCGTTTTTTCTTTTGGTGCGGTTCGTTTGGGCAGGTGAGAATGCAGCAATCGTACTCGAGTGCGCACCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22739
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061706 | Nonsense | 413 | 907 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 5099200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 4316197 |
GRCz11 | 16 | 4115250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGTCGCAATCAAGACTTTAAAGACATCTGTCGCAGAATTCAGTTCAGA[C/T]AGGAGGATCCCACATTACCACCCCTCACCATCCTCAAACACAAGTATGGA
Long Flanking Sequence:
TCATATTTTCATTTTAGTTTCAGAAGTATTTTCATAAGTTTTGTTTTTTCCTGTAAATGATTCAATAAATACCGTACCAAGACATTCATACCGAGGTATTACCGTACCGTGAAATTCTGATACCGTTACATCCCTAGTCTTAACACACCTCCTTTTCAGACGGCACACCCATAATTCCACAAAGTGGTGCAAATGGATTAGCTATTTAAACAATGTGGTGCAAAACGTGAAAATTAAAGTTGCGCTGGTCTGAAAAAAGCAACAAATCGTGCAATACACATCTTATGTATGATAAGGCCCTAGCTGTGCATACACCCAGTTCATAATCTAAGCATGATGTTTTATTCTCCATTCAGGGTAATAAAGGCGCAGTTTCCATCCGCTTCCAGTTCCACAACTCGGACATCTGTGTGGTGAACTCGCATCTCGCCGCACACACCGAAGAGTTCGAGCGTCGCAATCAAGACTTTAAAGACATCTGTCGCAGAATTCAGTTCAGA[C/T]AGGAGGATCCCACATTACCACCCCTCACCATCCTCAAACACAAGTATGGACGGCCGAGATGCACCACATCTGTTTTAAAGGGTTAAATCAAGTTCTGATTGGTTATTCATCAACGAATCACAGCGCGAGAACAAAACTGAAGTGATGTAAATTAAGCCTTGCTTAAGCTAATTAGGTCAGAATACACTAAATAGCATATCCCTCAAAACACTAAAAACCTAGATAAATTGTATGAATAAATTAGATGTAATTTAAATAAACACATACATTTAATTACTGAAGCATGTATCATACAAACTAATATTACCAAAAAAGTTGACCTCCCTGATCGTCAATAGCCTCTTTCACACAGTGATACCAGTAAATATCTGGAAAATTTCCAGAACGACTTAACCGGTGAATTCAAAAAAGCGCCGTTCACACAGGCAAGAACGTTACGGATTTCTTCCAGAAAAGACCGTTCATTGCAAAATACCATCATTATCCAGAAATGAGCTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22740
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061706 | Essential Splice Site | 583 | 907 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 16 (position 5105838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 4322829 |
GRCz11 | 16 | 4121882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGACTGGAGAACGACTGCATCCCTTCAGTATCTCTGTCTGAGAGAGAGG[T/C]CAGCACATCTCAGCTTCTTACGTCATACCAAGTTTGTGGATGACCGGATT
Long Flanking Sequence:
AGGTACTGCAAAGAGGAACAGGCAAAAATTCCTAAAGACAGGTGTGCCAAGCTTGTGGCATCATACTCAAAAAGACTTGAGGCTTTAATTGCAGCCAAAGGTGCATCAACAAATTAGGCTGTGAAAACTGATGTACATGTGATTTTTCAGCTTTTTTACTTAGAATAAATTTGCAACAATTTCAAAAACTCTTTTATCACATTGTCATTATGGGGGATTGTGTGTAGAATGTTGAGGAAATAAATTAACTTAATCCATTTTGCAATGCGGATGGAACATTAAAAAATATGGAAAAAGTGAAGCGCTATGAATACTTTCCAGATGCACTGTAATGTTCAAACAGAATTCTTGCAGCCTTTTCTAACATCTGCTCTCTCTCTCTCGGCAGATCAAGGTGGTGAACGAGGAGTCTTACAAGCGCACGTTTGAGGAGATCGTGAGGCAAATCGATAGACTGGAGAACGACTGCATCCCTTCAGTATCTCTGTCTGAGAGAGAGG[T/C]CAGCACATCTCAGCTTCTTACGTCATACCAAGTTTGTGGATGACCGGATTCGACATTTTCATGTGTTTTACCACATATTAATTAGCCAACCAAATGTCAAAATAAGTGATATGATTTTAATTTAAGACAGGAATAATATTATTGCAGTTTAGTAAAATAATTGTTTTAAATACTCAATATTAGATTGTTTTATTAACTGTTTTGAGTATTACTTTTATTAATTCTATTATCATTGACATGTAGTTTTTATTAATAGTTTTAAGTAAACAAAATAAAATACAATAAAAATATAATTTGATTTGCACAAATGTTGTCAACATTTTCAATTAACACTTGCAAATTAATAATAAGTGTACAGTAATACTAATAAATATTCTAATTAGCATATTATGATGATTTGTGGAGGTGACCGGTCATGTGACCGAAGAGTTTAAATAATTAATTTTGATTTGTAATGATGTTTCAAAATATTAGTTTTAATGCTATATAGCAGGGGTCAC
Associated Phenotype:
Not determined