ZMP
caprin1b
Ensembl ID:
ZFIN ID:
Description:
cell cycle associated protein 1b [Source:RefSeq peptide;Acc:NP_998233]
Human Orthologue:
CAPRIN1
Human Description:
cell cycle associated protein 1 [Source:HGNC Symbol;Acc:6743]
Mouse Orthologue:
Caprin1
Mouse Description:
cell cycle associated protein 1 Gene [Source:MGI Symbol;Acc:MGI:1858234]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23351 | Nonsense | Available for shipment | Available now |
| sa29071 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23351
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 |
|---|---|---|---|---|---|
| ENSDART00000098889 | Nonsense | 301 | 695 | 9 | 18 |
| ENSDART00000139519 | None | None | 87 | None | 3 |
| ENSDART00000143016 | None | None | 127 | None | 5 |
The following transcripts of ENSDARG00000054272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 36696640)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 38278343 |
| GRCz11 | 18 | 38259351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTGTTCTCTCCAGTTTGTAAATAGGCAGTTTGTTTCGGAGAGCACGTA[T/G]AGTACTGGTGAAAAGGAGCAAAGAGAAGACTGGAGCGTGGAACCTGAGGT
Long Flanking Sequence:
TTATGTAAAAAACATTGTTACTCGACATTTGACCCAATATAAAAATCTACTTTACTGACTATCCTTTTTTTCTTTGGTCTGTGCAATGTTAATGTAAGTTTGTATCTTGTTTGTTGTTTGAATCAATTATCATTAGCTGAAATCAAAAATCTAACAAATGTATTTCAGATAGTAGTAAAAAGACTAAACTAGTAAAAAATACTTTACAAATTAAGAGATGACCTAACACAAAATATTAATAAAAATGGTTATGATCTTGTTTCTAAAGCATTACTTGTTTGTTTGTGAATGTGTTCAGTGTAACTGTGAAAACTGAACTATAGACCTTTCACAACAGTTGACCTTGGAGTGAAAATGACTGTGAATGAACCTTATGTCTAACCCTATTATCTGGAGGGTACAGTTTAAGTTCCATCTCTTCCTAATTACCTATAATGTTCTTTACCTTGCTCTTGTTCTCTCCAGTTTGTAAATAGGCAGTTTGTTTCGGAGAGCACGTA[T/G]AGTACTGGTGAAAAGGAGCAAAGAGAAGACTGGAGCGTGGAACCTGAGGTAACTTGAGGACCCCACCCCCACATCTCATAGTAAAGAAAAGGTGATATTATGCAGCTTCTGTTTCTAATCCGCTAGATTAAAACGTGGTTTTCTTTGGTGCATATGCAGGTGGTGAACTCAATACTGCAGCCGGTTCAGGCTGCCCCCATTCCTGTCGTCCCAGAACCTCATCCACTGCCCACAGTAACTCCAACACCCCCCTCAGACCCTGTGTGCAGACAGCAGGTGGTTCAGGACCTCATGGCACAGATGCAGGGACCATACAACTTTATGCAGGTAGGCATAAACAACACTGATGTTGGTGATGCTAAGTTATATTAAGCACCAGACTTGGAATAGTTTTGTCCGTGATGATTTACTCGCCGGCTCTAGATTATTCATGGGATGCTTGTCACCTCACATTTTTTCCACATATACTGTTTTTTTTTTAAGATGAGGCAAAAAAGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29071
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098889 | Essential Splice Site | 632 | 695 | 16 | 18 |
| ENSDART00000139519 | None | None | 87 | None | 3 |
| ENSDART00000143016 | None | None | 127 | None | 5 |
The following transcripts of ENSDARG00000054272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 36692899)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 38274602 |
| GRCz11 | 18 | 38255610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACGCGGCATCATTAACGGCTACAGAGGACCATCCAATGGCTTCAGAGG[T/C]ACACAACAGCATGCGTTAGTAGGGAGTTCAGTTCACACTTATTCCCTGCA
Long Flanking Sequence:
AATCCTGTAAATCTGCACTGCTCAAGTGAAAGCAATATATGGGCCTGCATAATATCTACTGTGGCAATAGAAACTGTTAGAGTAACCATAATAAAATTTATGCGTTATGCTCTGTATACATTTATTTTCATACTCATTTATAATATTTATAGTAATAGTTGTTAAGTTGTAACCACCATTGTTTATACATATTTCTTTGATAATGTCATCAATAGTTACTATTAATATTAAATGACGATGATGACTCTAGTAACAGTTACTTAACTAAGCTATTTTATCCTTGTTTTAACAGTAGTTGGTGCCTTCCATTCTCAAGATCAGTCTCTCCAGAACTCAGCTGCTCATCAGGTCATGTCTCAGCAGCAGGCAGGTGTTCAGGGCAATGGCTTCGGTCGCCAGGCTCAGTCCTTCTACAACAGCAGAGGCATGTCTCGTGGCGGCCCCCGCAACTCACGCGGCATCATTAACGGCTACAGAGGACCATCCAATGGCTTCAGAGG[T/C]ACACAACAGCATGCGTTAGTAGGGAGTTCAGTTCACACTTATTCCCTGCATCGATCATAGTTTAAATTAGTTATTGATTATTCATTACTAGGGATATAACGGTATCAGAATTTCACGGTACGATAATACCTCGGTATGAATGGCACGGTACGGTATTTATTGAATATTTTACAGGAAAAACAAAATTAATGAAAAGACTCAAAGTGCTAAAAGTGTTTATTTACCTTAGCACTGAACATATTAATGACATACAAATTAGCCATCTATCTGTAAGTTTCGAAACAGGAACTTCAATTTTCCAATTTTAATAACAAAAAACTATTAAACCATGTAAAAAAAATAAAGTTTCAATTTAGTATTGTTGAAAACTCATCACATTCAAAGTTTAATCACTCACTCACTTAGATAGAGATGGGTTTTTTAGGAAAAATGATCATATAACTATAATCTGGTAAAAGCTGGGATCTCTAGGCATGTCCCCTGCAACAGAAAAAAAAAAA
Associated Phenotype:
Not determined