Busch Lab

ZMP

caprin2

Ensembl ID:
ENSDARG00000020749
ZFIN ID:
ZDB-GENE-040812-2
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
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.
Availability:
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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:
sa12256
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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