ZMP
itpr2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8HAL5]
Human Orthologue:
ITPR2
Human Description:
inositol 1,4,5-triphosphate receptor, type 2 [Source:HGNC Symbol;Acc:6181]
Mouse Orthologue:
Itpr2
Mouse Description:
inositol 1,4,5-triphosphate receptor 2 Gene [Source:MGI Symbol;Acc:MGI:99418]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa794 | Essential Splice Site | Available for shipment | Available now |
sa13636 | Essential Splice Site | Available for shipment | Available now |
sa14152 | Essential Splice Site | Available for shipment | Available now |
sa10652 | Nonsense | Available for shipment | Available now |
sa23267 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa794
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061134 | Essential Splice Site | 31 | 1947 | 1 | 42 |
Genomic Location (Zv9):
Chromosome 18 (position 15616779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15969191 |
GRCz11 | 18 | 15937703 |
KASP Assay ID:
554-0699.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCTCTGTATGCGGAGGGAACTGTCAATGGATTTATCAGCACTTTAGGG[T/G]GAGTTACTGTACCTTCCAGTGTTTAGTGCATTGCTCTTAAAGATTTGTAA
Long Flanking Sequence:
AAAACACACCGAAAACCTGCGCGCGTCTGTGCACGCAAGACTGCACAAATGAGCAAAGTTGCATTCTCAATTTCTGAGTTGCATACCACAGCATAAAGACTAGACAGCATCACTTCCTTGATTTCACGGGACAGAGAGCGAGTCTCCTCCCACTCGAGTGGCATATTGGTGAGAAAAAGCCTCGTTTGTCTCACAGGAAGAAGTTGAAAACATGAAGAAACGCTTCAGTTAGAGGATTCACAACTCAAAAGTCACTAACGCGGCGCGTCTCTTCTCTGGACGCCTGGATTAAAATGCGTTACTGTCAGGGCGAATAAACAAGTGGATTGATACACTGAATCGCCTGAACACATTGCGCTGGGTCACAGTGCTCAAATATCAGATAAACTACTCAAAAACCTGCAGAAATGTCGGAACACAGGTCTAGTTTCCTTCACATTGGGGATATCGTGTCTCTGTATGCGGAGGGAACTGTCAATGGATTTATCAGCACTTTAGGG[T/G]GAGTTACTGTACCTTCCAGTGTTTAGTGCATTGCTCTTAAAGATTTGTAAACATGGCATTTGTAAATTTCCCTCAGATAAACTGGTGTGATTTTTATTGCAAGGCAAGGTGCCTAAAATGAGTGAGTAAGGCAAACTGAAGATGCATTAGAGTGTGAAAGGTGTTTAATCCCCCTCGTGTCAGATGTAGTTTGCTGAGTGGAAGTAGGAAGTGATTTGAGTACATACTGCAGGCCAGGAGTTCAGTGTGACAGCGTTGCTTCAAAAGTCATGCAAATCACTGAACAGGAATGCAAAGTTTGCCGTTACCTTATGCACTAACAGTGATGCAACTAATGTAATATGGCGAATATGGTGTTGGCTAAATAAAAAGGGTTTAAAACACATTAACTTAACAGTATCAAACTACACTAGTTTCGCAAACTACACAAGTTACGCAATTCACCTGACTTGAAAAATCCAAGCATTTTTTTTGTCAACATTTTGTGTCAATTGGCAAGG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13636
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 |
---|---|---|---|---|---|
ENSDART00000061134 | Essential Splice Site | 236 | 1947 | 7 | 42 |
ENSDART00000061134 | Essential Splice Site | 236 | 1947 | 7 | 42 |
Genomic Location (Zv9):
Chromosome 18 (position 15641937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15994349 |
GRCz11 | 18 | 15962861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGCTCTTCAWGAAGTTCAGTGAATACAGAGATGATAYTTTAAAAGGGG[T/C]GAGTCTTYTGCATGTGTGMACTGATGCGTTRTTGGTTTGGGTTTGTTTTA
Long Flanking Sequence:
TATATAGGATAATATAGGCAATTTCGAGGGATGTAAACAAAAACAATGGCCCAGCATATTTCCTGTTTTACAATTTAAAATTTTATAGCTTCCAAGAATCCAAAAAGAACCACAAATTGATAAATAATGTTATGATAGCTGCTTTAACATTAAGCTATGATAGAATTGTCTCTGGTTACAGTTATATAATGGTTTGATAACAAGCAGGAAATGTTTATGGGCCAATGACATGACCACATTGAAATGGTCTATAACCATAATAATAAATAAATACAATCACAGGTGTATCTCAATAATACTAAAATCAATGTGAGGAAAAAATAAGAAAATGAATAAATTAAATAAAGAAACTACATATAACTGGAAAAGAGATTAAATTTACTGGAAATTTAATTCAGATGTGTGTCTCATTCAGGTAAATGCTTTGAACTGCAATACTAGCTGGAAGGTGACGCTCTTCATGAAGTTCAGTGAATACAGAGATGATATTTTAAAAGGGG[T/C]GAGTCTTCTGCATGTGTGCACTGATGCGTTGTTGGTTTGGGTTTGTTTTATATTTGACCGTGTTTTGTCATTTCTGTTTGACTGACTCAGGGGGATGTGGTGAGATTGTTTCACGCCGAGCAAGAAAAGTTTCTCACTTGTGATGAGTACAAGAAGCAGCAGTATGTGTTCTTGCGCACCACGCTCCGCCAGTCTGCAACCTCTGCCACCAGTTCAAAAGCACTCTGGGAAGTAGAGGTACAGCTCTGTGTGATGATAACAGTTGAAGAATATTGCTCATTATTATCTGATCTGAATTCATCCATTTATGTGGTTTATACATGTATACGTTACGATTTTAAGATAAATAAATAAATGTAAATTAGAATAAAGATTTTAACTTTATTTTTAAGGTATTTAATTCGTATTTTTCCATTTTATTTTATTAAGATTTACATTTTCTCATTAAAAGTTTCCTCTTTTTAAAATTTTAATTTATTAAGTGGGATTTTTTTGTAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14152
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 |
---|---|---|---|---|---|
ENSDART00000061134 | Essential Splice Site | 236 | 1947 | 7 | 42 |
ENSDART00000061134 | Essential Splice Site | 236 | 1947 | 7 | 42 |
Genomic Location (Zv9):
Chromosome 18 (position 15641937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15994349 |
GRCz11 | 18 | 15962861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGCTCTTCAWGAAGTTCAGTGAATACAGAGATGATAYTTTAAAAGGGG[T/C]GAGTCTTYTGCATGTGTGMACTGATGCGTTRTTGGTTTGGGTTTGTTTTA
Long Flanking Sequence:
TATATAGGATAATATAGGCAATTTCGAGGGATGTAAACAAAAACAATGGCCCAGCATATTTCCTGTTTTACAATTTAAAATTTTATAGCTTCCAAGAATCCAAAAAGAACCACAAATTGATAAATAATGTTATGATAGCTGCTTTAACATTAAGCTATGATAGAATTGTCTCTGGTTACAGTTATATAATGGTTTGATAACAAGCAGGAAATGTTTATGGGCCAATGACATGACCACATTGAAATGGTCTATAACCATAATAATAAATAAATACAATCACAGGTGTATCTCAATAATACTAAAATCAATGTGAGGAAAAAATAAGAAAATGAATAAATTAAATAAAGAAACTACATATAACTGGAAAAGAGATTAAATTTACTGGAAATTTAATTCAGATGTGTGTCTCATTCAGGTAAATGCTTTGAACTGCAATACTAGCTGGAAGGTGACGCTCTTCATGAAGTTCAGTGAATACAGAGATGATATTTTAAAAGGGG[T/C]GAGTCTTCTGCATGTGTGCACTGATGCGTTGTTGGTTTGGGTTTGTTTTATATTTGACCGTGTTTTGTCATTTCTGTTTGACTGACTCAGGGGGATGTGGTGAGATTGTTTCACGCCGAGCAAGAAAAGTTTCTCACTTGTGATGAGTACAAGAAGCAGCAGTATGTGTTCTTGCGCACCACGCTCCGCCAGTCTGCAACCTCTGCCACCAGTTCAAAAGCACTCTGGGAAGTAGAGGTACAGCTCTGTGTGATGATAACAGTTGAAGAATATTGCTCATTATTATCTGATCTGAATTCATCCATTTATGTGGTTTATACATGTATACGTTACGATTTTAAGATAAATAAATAAATGTAAATTAGAATAAAGATTTTAACTTTATTTTTAAGGTATTTAATTCGTATTTTTCCATTTTATTTTATTAAGATTTACATTTTCTCATTAAAAGTTTCCTCTTTTTAAAATTTTAATTTATTAAGTGGGATTTTTTTGTAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10652
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061134 | Nonsense | 1332 | 1947 | 31 | 42 |
Genomic Location (Zv9):
Chromosome 18 (position 15676255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16028667 |
GRCz11 | 18 | 15997179 |
KASP Assay ID:
2261-2007.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCAAAGCATGATGTGTTCAGGGCTGGATGAGACGGGGGCTCTGATGTA[T/G]CACATCACCYTGGTGGAGCTGCTGGCCGCCTGCACTGAGGGCAAGAACGT
Long Flanking Sequence:
AAGAAAAGTTGAATTATTATTAATAATTGAATAATAAATAATTTAAATAATAATAATTACAACAATTGAACAATGAAGACACTTATAATAATAAAATAATAATTTATAAATAAATTATTTAAAAGAGATTTCACTAAATTTGACCTTAATGCATTAATGGATGGAAAGATAGATTTTTATTTTTATATATTATTTAGTTATTTTCTATTTTATGATTTAAAAATACTTTAAATTTTTTTTATTTTTGTTTTAAGTTCTTTTAAAACATATATTTTCTCCTATAATACATTTTTAGAATATCTTAATTTTTATTATTTCCCCAGTCCACTAACTGACCTCAGACATTATCTAAAGAAGTAAATGAGCCTGTCTGTTGTTTTTGTGCTGTAGCTGGTGAATGGTGGAGAAGACGTGCTGGTGTTTTATAATGACCGAGCCTCGTTCCCTGCTCTGCAAAGCATGATGTGTTCAGGGCTGGATGAGACGGGGGCTCTGATGTA[T/G]CACATCACCCTGGTGGAGCTGCTGGCCGCCTGCACTGAGGGCAAGAACGTGGACACTGAGCTCAAGTGCAATTCGCTCCTGCCGCTCGATGACATCGTCAATGTGGTCACGTATGACGGCTGCACTCCTGAGGTGACTCAACAATTTGAGAATATGTGAATAAATAAATAGTTGTTGTTTACTAAAGACAAATTTAGGTTCTTAAAAAAAGAAATCAATTTATTTCAATAAAATTATAGAAAAATCATCATATTCACAAAATGTGAGATGGTTTTATATTTACAAGTCACCACTAATGTTATGTAATGTAATGTGTATTCATATAGCCCATTTATTGTGTATGGCCATACACCCAAATCGCTTCACAATCATGAGGGGGGGTCCCTCCACACGATCACCACCGTTCAGCATCCACTTGGATGATGCAACGGCAGCCGCAGGACAACGGTGCCAGTGCGCTCACCACACACCAGCTATAGGTAGAGTGGAGAGACAGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23267
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061134 | Nonsense | 1892 | 1947 | 42 | 42 |
Genomic Location (Zv9):
Chromosome 18 (position 15721325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16073737 |
GRCz11 | 18 | 16042249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTTGTATACAGAACTTTCTGCGAGATCAGAACAACAAAACCAATTA[T/A]AACCTGGTGTGTGAGACGCTGCAGTTTCTCGACTGTATCTGCGGCAGTAC
Long Flanking Sequence:
TGGGAACAACAGGAGATGCGACAGAGGAAGTGGTCGAGGAAATCCAAATGAGCCAGGCCATCACCATCATGAAGCCCATCTTACGCTTCCTTCAGCTGCTCTGTGAAAATCACAACAGAGACCTTCAGGTGATCTAAAACTTTTATTGCTCATCTTTTTGACTCTGAGCCATTTTATTAGTACTCATGTTAGCTGTACCCTACAAGTTGAGATACACCATGTTCTTACAAGTAAAATCCTGGTTTTGTGTCAGAAATTAAATCCCTAAATTAATGATTTTTACCAATGTGACGCCAATAAGCACCTTGTTGTTAGAAAAGATTTTTTTTTTGTCGTACAGATTCAGTATCTCAAGGGACCCCCGACCTAGTATGGACGAATCTGTCTAAATTGAGATGCCAATTACTGCCACTCAAAACTTGACTTGTGTTGTAAGTCCAAATTTTCCTGTTCTCTTGTATACAGAACTTTCTGCGAGATCAGAACAACAAAACCAATTA[T/A]AACCTGGTGTGTGAGACGCTGCAGTTTCTCGACTGTATCTGCGGCAGTACAACGGGTGGCCTGGGTCTGCTGGGGCTCTACATTAATGAGAGGAACGTGTACCTGGTCATACAGACACTAGAGACCATCACAGAGTACTGCCAGGGTCCTTGCCATGAAAATCAGGTATTGATGCACCATATTTGTTGGAAAACAGGATCAAATGTCCTTTTGTATGGAAAAGTAAGTGCAAATGTTGGGTGCTTTCACTCCTAGACTTTTGTTTTGGAACCTGTCTCGTTTGCCCAGTTAGCGCGGTTCGTTTGGCATATGTGAATCCAGCAATCGTGCTCTGATTCGCGTCATAGCAATTGGTCCGAGATTGCGTGAATGAGGTGTTCTTGGCTTGATTGAAACGAACTCTGGAGCGGATCAATTGTATTGAGAAAACAATACGATTCGGACCCAGCTATATCACAGTGTTTTATGGATATGTAATAGGCATACGGCTATATGAAGAG
Associated Phenotype:
Not determined