ZMP
caprin2
Ensembl ID:
ZFIN ID:
Description:
Caprin-2 [Source:UniProtKB/Swiss-Prot;Acc:Q5RJ80]
Human Orthologue:
CAPRIN2
Human Description:
caprin family member 2 [Source:HGNC Symbol;Acc:21259]
Mouse Orthologue:
Caprin2
Mouse Description:
caprin family member 2 Gene [Source:MGI Symbol;Acc:MGI:2448541]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12716 | Nonsense | Available for shipment | Available now |
sa6049 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12256 | Nonsense | Available for shipment | Available now |
sa14869 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12716
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040708 | Nonsense | 200 | 914 | 5 | 21 |
ENSDART00000064009 | None | None | 331 | None | 6 |
ENSDART00000125323 | None | None | 329 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 15694236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16637076 |
GRCz11 | 4 | 16626052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTGCTACATGTCCACTCAAGACATGGAGGGTTTGATGGATTTGGCRT[C/G]ACTGGTGGGATGYAAAAGGGATTACAGCATTAGGTTTGCACTATTGGATA
Long Flanking Sequence:
CTGAAGAAGGGGGAAAAGCTGAATGAAGACCAACTGGTAACTGACTTTCATATCATATGTTGCATCTTAGGAAATCTTGTTTGTGTCGCTAACATGGGTTGTCATTGTAGGAAGCTGTGGGCAAGTACGATGAGGTGGTCCATAATCTGAAGTTTGCCAAAGAGCTCCAGAAGACCATCGGCTCCCTCACTCAAGATGCAAGTCTTGTGTCTTTGTGAAGTATAGCATAAAATTAGGTTAAAAAAATACTTGAGTGTTGTACTGAATTTCCTTTTTTTCCCCCCCTACTCTGTAGTTGCTGAAGGCTCAGCGTAAAGCCGTTCGCCAAGAGAAGCAAATGAAGACTGATGAGGAGAAGAGCCGTTTGAGTCTAATGCTCCAGGTGCAGTACGTCCTCCATAGTCTGCAGAGAGAGGACGTCCGGAAGAACTTCTGCAACACCAGACAATATTCCTGCTACATGTCCACTCAAGACATGGAGGGTTTGATGGATTTGGCAT[C/G]ACTGGTGGGATGTAAAAGGGATTACAGCATTAGGTTTGCACTATTGGATACTGCAATCTGTTTTTGCATTGTGCATACAATTATTTATCGGTATCCCCCATACCCCCCAAGTTATTGTAGCTAACTCAGAATTGCTATGCGTTTTACAATGTCAACCTTGTCCAAACATGTTTTTTGATGCAAAAGGACACAGCTCTCATGTAGGCACATTCAAGTGGAGCTTAAGTATGACATTAAGTGATGTATAATAAACTTCTTAATTAGTGGGAGGGGTTTACCGATAGGTCAACTATGCAACTATGCAGTTATCTATGGCTATAGCTTTGGATGCTTTCAGGTTTCATGTTGCAGTATTTGGTGTTTATCCTGTTGATTTAGCATGGTCTTCCTGTTGTTTCATGCTCTAGTTTGGAGGATCAGATGCGACGGGCTGCTATTGTTTACTGGGAGCTGCTGGAAGGGAATGAAAAACCGGTTGCTGGCTCGACATGTGAGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6049
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 |
---|---|---|---|---|---|
ENSDART00000040708 | Nonsense | 384 | 914 | 10 | 21 |
ENSDART00000064009 | None | None | 331 | None | 6 |
ENSDART00000125323 | None | None | 329 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 15692089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16634929 |
GRCz11 | 4 | 16623905 |
KASP Assay ID:
554-3814.1 (used for ordering genotyping assays)
KASP Sequence:
CATACTGTAGAGAAAATKTGTTAAACTTCTGTCTCTTTTTCTAGAAACGT[C/T]AAAGAAAGAAGGCTGAGCAAGACTCCAAATCTGTGAGTTTTTGATCAGAG
Long Flanking Sequence:
TTTTTTTTTTGCAAAAGTCTATTCACATTCTTATATCAATCGTTAAATGAAGTGGTCAACATTTAACATTTTGTTATTGTAATTACGAACTACTATAAAGTTCTCTTTACTGAAAGTTACTTGATGTATGATGTTTAGTGCACATTCAGGACATGTGGATTTGTATGGTCCTTTTTATTTCATTTATTTATTTTAGTGCAATTAAACTAACATTTCCATACTACAAAGACCCCCTGATGCACATTTGAAAGCAAATATAAATTGCTATTATTTGTGCTGTTCAATTAAATGACCCAATTAACTAATATGAATATAAAAAGAAATAATTTTTACTTATTTACAATATTCTCTGATGCTATAACATTTTTAAAACCTGTTGAAGATGTTGCTGTTTTACAACTTAGCATGTTGGTGGTTTACTCAGCTGTCAAGCTATTTGCAGCCTGCATGCATACTGTAGAGAAAATGTGTTAAACTTCTGTCTCTTTTTCTAGAAACGT[C/T]AAAGAAAGAAGGCTGAGCAAGACTCCAAATCTGTGAGTTTTTGATCAGAGGATCCAAACCTTTGTAAAATCATCAGTCAAGTGTAAAATTATTTTTTTTTTTTGGATTATATTTTCAGATGCCCGTTGCAGTGGAAGTCTTCAGTTCTCCATCTCCGTTACCAAAAGATCCCGTTCAGCGCCGGCAGCAGCTGGAGACACTGATGGACCAGATCTCTGGCTCCTTCAGTTTCATGCAGGCAAGCATTAAAGCAAGCAACTGTTTAATTTAAACAATCAGTGTTTTTTAAATCCCCAATATAATCCGTGTTTGCAGGAGTCTCTTTTGGATGGAGAATCTTCACCTGTCAACACTCAAACAAAAAGATGCCGTCCATCTCCAGGCTCCTCCACTCCAATCGGTACAGGAATGTTTCATATTAACACCGTAAGAATAGAATGGTGTTAAATTCACAGTTTGCTTGCATAGAACGGTAGTGATTATTACAGGATTTATCTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12256
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 |
---|---|---|---|---|---|
ENSDART00000040708 | Nonsense | 390 | 914 | 10 | 21 |
ENSDART00000064009 | None | None | 331 | None | 6 |
ENSDART00000125323 | None | None | 329 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 15692071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16634911 |
GRCz11 | 4 | 16623887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTAAACTTCTGTCTCTTTTTCTAGAAACGTYAAAGAAAGAAGGCTGAG[C/T]AAGACTCCAAATCTGTGAGTTTTTGATCAGAGGATCCANNNNAACCTTKGTAAA
Long Flanking Sequence:
CTATTCACATTCTTATATCAATCGTTAAATGAAGTGGTCAACATTTAACATTTTGTTATTGTAATTACGAACTACTATAAAGTTCTCTTTACTGAAAGTTACTTGATGTATGATGTTTAGTGCACATTCAGGACATGTGGATTTGTATGGTCCTTTTTATTTCATTTATTTATTTTAGTGCAATTAAACTAACATTTCCATACTACAAAGACCCCCTGATGCACATTTGAAAGCAAATATAAATTGCTATTATTTGTGCTGTTCAATTAAATGACCCAATTAACTAATATGAATATAAAAAGAAATAATTTTTACTTATTTACAATATTCTCTGATGCTATAACATTTTTAAAACCTGTTGAAGATGTTGCTGTTTTACAACTTAGCATGTTGGTGGTTTACTCAGCTGTCAAGCTATTTGCAGCCTGCATGCATACTGTAGAGAAAATGTGTTAAACTTCTGTCTCTTTTTCTAGAAACGTCAAAGAAAGAAGGCTGAG[C/T]AAGACTCCAAATCTGTGAGTTTTTGATCAGAGGATCCAAACCTTTGTAAAATCATCAGTCAAGTGTAAAATTATTTTTTTTTTTTGGATTATATTTTCAGATGCCCGTTGCAGTGGAAGTCTTCAGTTCTCCATCTCCGTTACCAAAAGATCCCGTTCAGCGCCGGCAGCAGCTGGAGACACTGATGGACCAGATCTCTGGCTCCTTCAGTTTCATGCAGGCAAGCATTAAAGCAAGCAACTGTTTAATTTAAACAATCAGTGTTTTTTAAATCCCCAATATAATCCGTGTTTGCAGGAGTCTCTTTTGGATGGAGAATCTTCACCTGTCAACACTCAAACAAAAAGATGCCGTCCATCTCCAGGCTCCTCCACTCCAATCGGTACAGGAATGTTTCATATTAACACCGTAAGAATAGAATGGTGTTAAATTCACAGTTTGCTTGCATAGAACGGTAGTGATTATTACAGGATTTATCTAGGCACATCATTAGTTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14869
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 |
---|---|---|---|---|---|
ENSDART00000040708 | Nonsense | 438 | 914 | 12 | 21 |
ENSDART00000064009 | None | None | 331 | None | 6 |
ENSDART00000125323 | None | None | 329 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 15691763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16634603 |
GRCz11 | 4 | 16623579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTGTTTTTTAAATSCCCAATATAATNNNNGTTTGCAGGAGTCTCTTT[T/A]GGATGGAGAATCTTCACCTGYSAACWCTCAAACAAAAAGATGCCGTCCAT
Long Flanking Sequence:
TTTTTACTTATTTACAATATTCTCTGATGCTATAACATTTTTAAAACCTGTTGAAGATGTTGCTGTTTTACAACTTAGCATGTTGGTGGTTTACTCAGCTGTCAAGCTATTTGCAGCCTGCATGCATACTGTAGAGAAAATGTGTTAAACTTCTGTCTCTTTTTCTAGAAACGTCAAAGAAAGAAGGCTGAGCAAGACTCCAAATCTGTGAGTTTTTGATCAGAGGATCCAAACCTTTGTAAAATCATCAGTCAAGTGTAAAATTATTTTTTTTTTTTGGATTATATTTTCAGATGCCCGTTGCAGTGGAAGTCTTCAGTTCTCCATCTCCGTTACCAAAAGATCCCGTTCAGCGCCGGCAGCAGCTGGAGACACTGATGGACCAGATCTCTGGCTCCTTCAGTTTCATGCAGGCAAGCATTAAAGCAAGCAACTGTTTAATTTAAACAATCAGTGTTTTTTAAATCCCCAATATAATCCGTGTTTGCAGGAGTCTCTTT[T/A]GGATGGAGAATCTTCACCTGTCAACACTCAAACAAAAAGATGCCGTCCATCTCCAGGCTCCTCCACTCCAATCGGTACAGGAATGTTTCATATTAACACCGTAAGAATAGAATGGTGTTAAATTCACAGTTTGCTTGCATAGAACGGTAGTGATTATTACAGGATTTATCTAGGCACATCATTAGTTTTAAATTGATTGTTCCCCCATTATAGGGCTGGGCGATTTTGCCCTAATCAATCTCTATTAATTGAACATTTGAACTATTACGATTAATGAAGGTTTGTTTTATTTATTAAATTTTGCCCTCATAGTTCACTGACCGATTTTGTACAGGAAATATGTAAGCATATTTTAAGTGAGATTGCTGAATGAAGGGTGCATTACTTAATTTTTTAATTAAAGGAAACGCACAGTCTACTATCTATGATTATTTATTGAACATCAACATTGAGTAACTGAAATTAAACCACACATTGCCACATTTTTGTCTTTAATAAAT
Associated Phenotype:
Not determined