ZMP
si:ch211-282c13.6
Ensembl ID:
ZFIN IDs:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A6H4]
Human Orthologue:
NIN
Human Description:
ninein (GSK3B interacting protein) [Source:HGNC Symbol;Acc:14906]
Mouse Orthologue:
Nin
Mouse Description:
ninein Gene [Source:MGI Symbol;Acc:MGI:105108]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11160 | Essential Splice Site | Available for shipment | Available now |
| sa11058 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11160
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084815 | Essential Splice Site | 323 | 741 | 9 | 16 |
| ENSDART00000112007 | Essential Splice Site | 323 | 1272 | 8 | 24 |
| ENSDART00000129562 | None | None | 340 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 37231553)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 36703855 |
| GRCz11 | 13 | 36829687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATTACAGGAWGTTTTTAATKAGCTTTTATGCATGCTTTTTATTTTGT[A/G]GGCTCTGGATTTTAATCTGGAAGGTAAAGTGAATCTGTCGGAGCTCACCG
Long Flanking Sequence:
AACAGAAGGTCCTTGTGTGTTCAAATCCTCCAAGGTGGGTGAGGATCTATTACAGTGTGCTGATGAAAGCCTAATGGATGTGCAGGAGTTTATCTCATGTGTAATAAACCACAGCAAACCACCCACACCATCAGCATCCACACCCTACAGACAATTAAAGAGAATCCACTCCACTCAGGTACTGTGCTAAAATAGGCTTTGTGTATTGTAGCTGCCCAAATATAAAAGTTTAACATCTTTTTCTTCTTCAAGTTTGATGAGTCAGGCCGTAGGATCTCATGCGCTTTAAGCAGTACAATCGCTCTACGGGTGTTTTCTGATTTGGATGATGGATCGGGACACGCTCCTGTGGAAACTCTGCTGAACAGGTGGATGGAGGAGGGAGTGGACAACAGCTCGGAGATCCTGCAGGTAAAACACATTAGTAGTTTAGACCTCTATATGTCTGTGTTTATTACAGGATGTTTTTAATGAGCTTTTATGCATGCTTTTTATTTTGT[A/G]GGCTCTGGATTTTAATCTGGAAGGTAAAGTGAATCTGTCGGAGCTCACCGTTGCTCTAGAGAACGAGCTGCTGAGCACTAAGAACTCAATCCACCAGGCGGCGCTACTGAGCTTCAAGGCAGAAATCAGACATCTGCTGTAAGTCCATGTGTCTTTCTTGCTCAATCCAGATGCGTGATTCAGAATAATAACTTTATAATCATCTGAAGAATGAATTTAATCAAACTCTACCCGGAGCTCTGCATAAATCATATTAAATTACTTCAGTTTGTTGTTCACATTTACTCTGCCTCATCAGTGGTTCTCAGTTTCAGCAAAGCGACAAGATGAGCTTAAAATTAATTAAGATAAAACTTTTTTTTTTTGTTAGTTTTTTTTTTACAAGGTAAATTTTCTAGAAATCTACATGTAAATTACGAGGCAGCCACCTCCATCAAATGTTGCATCAACTACACCTTTTGACAAAAATCAGGCTGGCAGTCACAGCTACCAACAGACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11058
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 |
|---|---|---|---|---|---|
| ENSDART00000084815 | Nonsense | 465 | 741 | 11 | 16 |
| ENSDART00000112007 | Nonsense | 465 | 1272 | 10 | 24 |
| ENSDART00000129562 | None | None | 340 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 37228133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 36700435 |
| GRCz11 | 13 | 36826267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGCTTGAACAAGAAATTAGCAAGATGAGAGATGATGAAACCTTCCTA[C/T]GAGAACACCTAACGCTTACCATTAAAGTAATCATCACTGATTTCATGTTT
Long Flanking Sequence:
ATATAATAATAATAATAATAATATTACAGAAATTAATATAAAAAGATGCAAGTTGCTGATGTAAATAAAAATCTGATTTCTTTTTGCACAGATTCCATGTGGGCCTAGTGATCACTTATTATTTTACGCTTAACATAAAAGAACCACCCATAAGATCTCATCTCCATGCATCTCATTTGTGACATGACCTTTTTTTCTAGCAATATCTGTGTTTACATGCAGATTTCTGTTGCATAAGCACAGAAGGCTTGTTCTGTCCTAATTTATGGTCTGTACACGTGGGTGTGAGCATGTGTAATCATGTCATGCATGTGTGTTTTTTTTTTATGTTCAATCATACAAATATGCACAGGAGGGTGGAGCAGGAGTATAAAGAGAGTATGACTGCTCTGAGGACAGAGCTCAGTAAAGAGATGGAGCTTGTGCAACAGCAGGCCAATCAGCAACGAGAAGAGCTTGAACAAGAAATTAGCAAGATGAGAGATGATGAAACCTTCCTA[C/T]GAGAACACCTAACGCTTACCATTAAAGTAATCATCACTGATTTCATGTTTTAATTTAAACCACTAATTGCCTGTTGTGTTTACACATCACATTCCTGTCAGCATGGATGTGATTAATTATTTGGTTGTTGGAACTGGAGAATGTGTTATATATTTGTTTGTCTTCGATGAATGCGTTGTGTAGGAAAATGGTCGTCTGGAGTCAGAGCTTATTGAGACCACAGAGAAACTGGTGGAGGCTGAAAACCAGTTGAACAAAGTACAGAAAAACCTGGATGGTGTTTTGAAAGAGAAGGTACTGAAACCAGCAAATCAGTTCTGACATACAATAAATAGAAACAAGCATACGTCATATGACAAATAGACATTTCTTTTATGACATCATTAAACAAAGCTTTGAAATTATTTAGATCAGGGATCTCACCTGAAAATCTTAAACCTGAATTTATGAGGTAGGTTTTTTAGATAGGATTTCTAGACCTGAAAATGTCATGTGAATTA
Associated Phenotype:
Not determined