ZMP
si:ch73-194h10.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
INPP5D
Human Description:
inositol polyphosphate-5-phosphatase, 145kDa [Source:HGNC Symbol;Acc:6079]
Mouse Orthologue:
Inpp5d
Mouse Description:
inositol polyphosphate-5-phosphatase D Gene [Source:MGI Symbol;Acc:MGI:107357]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18179 | Nonsense | Available for shipment | Available now |
sa40704 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18179
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113405 | Nonsense | 362 | 1108 | 10 | 27 |
ENSDART00000137907 | Nonsense | 372 | 835 | 10 | 23 |
The following transcripts of ENSDARG00000074283 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 27870551)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28171762 |
GRCz11 | 6 | 28162323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGTCACAGAAGATGCACAACAGACTTGTATTGGTGGTAGAGACAGAG[A/T]AAGGAAAAACTCAGAGCAAAGACTTTGTCTTTGAWGACACAAAGGTAAAA
Long Flanking Sequence:
CAAAGGACCTATAGACAGGAATTGAACTCTGGTCACCCTAAGCACCTCAGTACTATACTCAGTAGCCTACTGTCGGCACACTTAACCAGTAGACTTCAAACAGCTGGTTTTCATTAACTTTTCCATCAACCTTTTTCCCTTACCAGCACTTTCTATTTCAGATGAAAATAAAATAAAAAGCTTTCTATGTGTTTCTTTTGTCCTCATTTTGATAAAGTGTTTGTGAAATGAATACATTCACATATCACATTTTTTTGCAATGCAATTATGCATTTGCAATAATGGACAGCTAAGCAGGTGAACCTAATAAAGTGGCCAGTTGGTGTATTTTTAAGTAAGTCGGAATCTAGTGTTCTAGAGAATTTATAGTCATGTAAACAATGTGTGAAACCCATTAAATAATTTAATAACTGGAACATGCAAAATTCTTATTTGCAGTCTTACAGTTGGTGAAGTCACAGAAGATGCACAACAGACTTGTATTGGTGGTAGAGACAGAG[A/T]AAGGAAAAACTCAGAGCAAAGACTTTGTCTTTGATGACACAAAGGTAAAAACCTTACAGCTAATGTTTTTTTATGTTACATTCACTCACTCATTCACTCACTCACTCCCTTTTTTTTTTGACTTGTCCCTGCTTTATCAGGGATCGCAGACAGGAATTAAAGACTGTAACAATGAAATGCTTTCAGATGGCATTTTTTTTAGGCAGAAACATAAATGAACGAAAATAATATACTGTTTCCATGTTTTTTTTTTTGCATATTTCAATGTATCACTGTGTAAAAGTGTGTCTTTAAAACACATATTTAGAAGAGAGAAGGCTTTTGCCAGCTTCTTCAGCAGATGAAGAATAAGCACTCAGGAAAACCTGAGCCGGATATGATCACCATCTTTGTTGGCACTTGGAACATGGGTGAGATGTCTTAAGTCATATAACATTTAACCTTTTAAAGTGCTTAACCCTTTATAGGAATTATTGAAATAGTTATCTAAAAAACTCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40704
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113405 | Nonsense | 449 | 1108 | 12 | 27 |
ENSDART00000137907 | Nonsense | 459 | 835 | 12 | 23 |
The following transcripts of ENSDARG00000074283 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 27871552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28172763 |
GRCz11 | 6 | 28163324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGATGACACAGCCAATCAAATCCCACATGACATCTACGTAATCGGGACA[C/T]AGGAGGACCCACTGGGAGAGAAAGAGTGGATTGAGACAATTAGAGGAGCC
Long Flanking Sequence:
AGTATAACTGGGGTTATTACAACTTTTATGACCTACTTGTTGGAGCTGAAACATAAAATCTTGTGATAAAATTGCAGTCACACTGATCATCTAACTAGCCTAGTAAAAAAGTACATTTAAGCAATGAAAATGTGCTCATAAATGCACATAATATATCTTTAAAGAACCCACTTAAATGTGAACTGAATGTACGTCTTATATTTACAATTGCATGTTATTGGCTTTAGAATTAATAAAATCTACAGTAGTTTAATTTGCATTAATTGTAACTAGTTTTTCTGACCCATGTTCACATGTAATGGCATAATAACACCTATTGCATATGACATGTGGCTGTTTGCTAAAAGAGAAACTATAGATTAAAGAAAACCTTTTCTGTCCATCCAGGAAATGCTAATCCACCACAAAACATCACTTCTTGGTTCCAGTCAAAGGGTCAGGGGAAAACTCACGATGACACAGCCAATCAAATCCCACATGACATCTACGTAATCGGGACA[C/T]AGGAGGACCCACTGGGAGAGAAAGAGTGGATTGAGACAATTAGAGGAGCCCTTAGAGATATAACCAACATTAGCTTCAAACAAGTAAGTGACAAAAAAAAAAAAAAAAAAACTAGAAAGGATGTGGGTGCTTTGTAATATGCATATTATGTTGGATCGTTATTGCTATGACTACAGATGCTATGATAATGTATATACAACCCCAAATCAGACAAAAAGTACAGTATGGAAAAAACAAATAAAAAAGAAGTGATTTCTACATTTTCTTTGACTTGTATTTCATTGCAGACATTACAACAGCACATTATTTAATGTATTCCTCATGATTTTTGTTTTTAAATAAACATGTATTACAGTTTTAGTTTTAGTTACATTTCAAAAAGGTTGTACCAGTAAAGCATTTATCACTTTGTGATGTTACCATTTCTTTTCACAACACTTAAATGATATTTAGGGACTCAAGACACCAAGTGATGAAATGTTTTAGGTGTAATTTTGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40705
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113405 | Nonsense | 952 | 1108 | 26 | 27 |
ENSDART00000137907 | None | None | 835 | None | 23 |
The following transcripts of ENSDARG00000074283 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 27898648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28199859 |
GRCz11 | 6 | 28190420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAATATGCTAAACTCAATCTTATTCTTGCTTTTAGACCTGTGGACGGT[C/T]AACCACCAGAGATGTTTGACAATCCTCTTTATGGCTCAATGAGTGGATCC
Long Flanking Sequence:
TAATTTTATACAAGAAACCGTACAATTGTAGGTAAGAAATATGTACATTCATTCATTCATTTTCCTTCAGCATACTTTCTGAATGAACCGCCAACTTATCCAACATATGTTTTACACGGCAGATGCCCTTCCAACTGCAACCCAGTACTGAGAAACATCCATACACAATAATCCCCCACATAGACTAAGGCCTATTCAGTTTATTCATTTCACCTGTACCACATGTCTTTGGGCTGTAGGGAAAACCGGAGCACCCTGAGAAAACCCACACAAACACAGGGAGAGCATGCAAATTCCACACAAAAATGCCAAATTTGGACTCAAACCAGTGACCTTTATGCTGTGAGGTGACAGTGCTAACTGAGCCACTGTGTCGCCCTGAAATTAGTACAAATAAACAGATTTATTATTAGAACAACTGACAGCATGCGTTCAATAAAGTAATTCAGCATTAATATGCTAAACTCAATCTTATTCTTGCTTTTAGACCTGTGGACGGT[C/T]AACCACCAGAGATGTTTGACAATCCTCTTTATGGCTCAATGAGTGGATCCAGAGGAGCAAAGGAACATCACCCTCCTCCAGATGCTCTCTTTGCCTTTCCCAAACCCACAGACTTTGATTCAGATCGTCAGCCTCCAGTCCCGACCCCTCGCTTACGCTCATATACCTGTTCTGAAACCAAACCCCAGTCATCTTCATCCACAAACCTGAACATGAGCAGCCTGCTGCCCCAGAGCATTACCAAGAAGCCTGTGGTGCCTTCACGATCCGAAGGAGGAATGATTGGCCCCAACAGACCTCCAGTGCCGATGAAATCCCGATCTGGTCAGACACAAGAACCGCAGACAAAGCCAAGAGACTACAGGGACAGTTCAGAGCTCCCGTCTAAGATACGACCACCGACCAGAGCAGGGCAGACCAAAGATGGTACAATCACAACACTATATTTTAGTAGTCTCATACAGTGTCACAGAAAATCTGCTGAATTGGCCCATAGGTGG
Associated Phenotype:
Not determined