ZMP
CASKIN1 (1 of 3)
Ensembl ID:
Description:
CASK interacting protein 1 [Source:HGNC Symbol;Acc:20879]
Human Orthologue:
CASKIN1
Human Description:
CASK interacting protein 1 [Source:HGNC Symbol;Acc:20879]
Mouse Orthologue:
Caskin1
Mouse Description:
CASK interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:2442952]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9831 | Essential Splice Site | Available for shipment | Available now |
sa45143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33234 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20076 | Nonsense | Available for shipment | Available now |
sa14718 | Nonsense | Available for shipment | Available now |
sa20075 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9831
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 |
---|---|---|---|---|---|
ENSDART00000031390 | Essential Splice Site | 81 | 1347 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35768880)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35554076 |
GRCz11 | 3 | 35683584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTCAGATCCCCCTGCACCTGGCTGCTCAGCACGGACACTATGACGTGG[T/C]GAGTACACTGTACACACTGCTTCAGCTCCAGACCCGCTGTTCTTCAAAGA
Long Flanking Sequence:
GGAATAAGACTTTCTGCTGCAATCTTTTGAAAACTTCTATATAAGATGTACAAAGAGGACCAAAAGAACAAACAAACAGTGATCTCAAAAGAGCTTTGGCCTCAGTTATGATACTAATGTCACATAAAATAACAAGTGTAAAGTTTTTTCATTATAGATAAAAATAAATCACAAAATGAAACTCATCTCACAATATGTTGATCATTTGTAGTGCATTTGAAGCATTTATTTCAGATATTGTTAACGGAAATTTACCCAACTGGAAGCACATCCAATAACTTTAAATGCAGTAGTCACGTGTGGGCAAATGTTTTGAGTTAGCTTATATAACGTGTTTTTCTGTCATGTTTCAGGGATGCGTCCTCTACATTATGCAGCGTGGCAGGGGAAGTCGGAGCCCATGAAGCTACTGCTGAAGTCGGGCTCTTCAGTGAACGGTCAGTCGGATGAGGGTCAGATCCCCCTGCACCTGGCTGCTCAGCACGGACACTATGACGTGG[T/C]GAGTACACTGTACACACTGCTTCAGCTCCAGACCCGCTGTTCTTCAAAGACACCATACGAGCAGACCTGTATGATAAAAGAGCTGCAACACCTTTATAGATACTGACAACTTGGAAGCAGAAACTTACGAGAAAATGCTTTGAAGCTCCATCAACCCACACACATGCGTTTAATGAAACGCACAAGGCACACACTTCAACCCTTTTTCTGTCAGAGTTTCAACCACTTAGTGAAGAGGCAGTTTGAAGTAGATAGTGTGGCTTTTATTCTTTGTTCTTTTCCAGAAATAGACATGGGAAATAAATATGGCGTTCATGTGTTCAGGTTAAAGTGTGGTGTGGTGTGGTGTGTGTGTATTATATAGTCAGAATGTTTAGCCCCTCTGAATTATTATCCCCTTGATTATTTTGTTCCCCAGTTTCTCTTTAACGGAGAGAGGATTTTTTCAACACATTTCTAAACATAATAGTTTTAATAGCTAATTTCTAATAACTGATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45143
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031390 | Nonsense | 325 | 1347 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35738637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35523833 |
GRCz11 | 3 | 35653341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGTCCAGTCCACATGGCTCACCCACCCCAGCTGGTGGACCCCAGGGT[G/T]GAAGTAGCGAGGAGATCTGGGTGCTGCGCAAGCCTGTGGCAGGTAACAGC
Long Flanking Sequence:
AAACAAATTAACGTACACTTGTGTGTACACTTGTGATGTTTTGGAGACCCCAATGAACTATGCTCCTGTAATGCACTGCAACTCCTTTTGTTGTTATATATATATATATATTTACATATATAATCATATATTCCTGTATATATTATATATGTTTTACCTATGTGTATGTGTAAATCAAGGCATATATATATGTATATAAAGTACATGTTTCTGCTTAAATATTTCATGTACCTCTGTATATATCAATGTTCATATATATTTGTGTTAGATATACAGTATATATATGCGTGCTTGCCTTGTGTGGGTGTTTGAAAGAGAAAGTGGTTAGAGCGCATAGACATAGTTTAGCTTTCCTCTTGCTTGACCTCTCCAGAACACCTATGATCCCGGGCAGGCGGCGAAGCCAGGGCACAGTTAATGATGGTTTCTGTGTTAAAGGTTCTCGTGGCTCAGAGTCCAGTCCACATGGCTCACCCACCCCAGCTGGTGGACCCCAGGGT[G/T]GAAGTAGCGAGGAGATCTGGGTGCTGCGCAAGCCTGTGGCAGGTAACAGCAGGGCTGCCCCTTCCTCCACTTCCCTCTCATAACTCTCCCTGCTTTGCCACGCTCTTGGTGCAGCTGCTGTCGCCTGACCTCAGACCTCCTCAGCTGCAGGCGTGTAGGCGCGCATTGAGAGACTCTCATCCGCTCTGTTAAAGTAACATCCATGGAGTCGTTCCTTCAAGAACACACATCCAGACAATCAACAGATGTGTGTAGACGGCATTTTCAATAAAGCCAGTGTAGACCTGTGTGTGTTTGTAGTAGTGAGTAAGCTAACATGTCTCGTGTTCATTGGTCACCTTGTCTGTGGTCATCATTGTCATGTACGTTTCTGTCATCCCGCGTATCAGATCAGTGCATTGCAGAGGGGAAGTTCATAGTGGTGTGTTTAAAGGGTTCGGGGCAGAGATGTCCAAAGGGGCTGACTGTGTGTGTGTTTGTTGGGGGTTTGTTGTTCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33234
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 |
---|---|---|---|---|---|
ENSDART00000031390 | Essential Splice Site | 435 | 1347 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35735676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35520872 |
GRCz11 | 3 | 35650380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGGAGGCGGTGTCCCAGAGGAAAGGGGAGGCACCGCCTGAGGGGAAGG[T/C]AAGAAGACTACTCCGACTTGAAACACACTGACCCCTTGCCTTTCCCACAA
Long Flanking Sequence:
TTATGTTTTTCTTTATTTGATGATCTTTGTTTATCCTGTAGCTTCTGGCCACGGTTTTGTCTCAGTCTGCCAAAGCAAAAGAACACCTGCTGGAGCAGACCAAGTCTTTGGACCACCCGTCTCATGCTTCCAGCAACAAGGGTTAGTAGCAGTTTTAAGCAACTCTTCTGAAAAGAAATCACATGACAGTTCCCTGTCACAAAGAAGTATCTCCATCCAAAATGTTAATTTGGCTGCATTTTTTTGTGCCAGATGGTTGCACTAATATTTGTGGGTGGGAGCATCACAAAGATCTGATTGGTTCAGCTTGAGTTGTTGGTCAGAAAATCATTAAAGGAATTGGTTGTGCAATAGCAATGCTCCAATGTGAATGAATGATCTCATGGCTGTTCTAGGACCCTCCTCGCGCAGTCAGAGTTTGTCAAGCTGTCCACTTCACGAGCAGCCATATGGGGAGGCGGTGTCCCAGAGGAAAGGGGAGGCACCGCCTGAGGGGAAGG[T/C]AAGAAGACTACTCCGACTTGAAACACACTGACCCCTTGCCTTTCCCACAAACAAGCATACACTCATTCTTACGCACATACACATACATGCACTGGCATCTGCACATCCAGGATGCTTTCCCAGCACTTTCTCTCACAGCTGGCATCTTCCGTATTGCGTGCTCTTGGTTGTCGTCAGGACACGGTGAGTGCGCTTCTCAGCAGGCTTCAATCACGCTGTCCTCAGCTTCAGGCTTCATTCAGCCACTCTGTTTAATATTGACTATCTCTTTGATCATTCATTTCATTTTTTGTGCTGCATTTTTAAGTCCATTACGATTCTTTGCCTTCTTTGCAGTGTCTTTCATCTTATGATTTCTTTTCAGAGAGTACCCAACAATGTAGATGTGATTGAATGCTAAGTGTAACAGATTATACAGTAAAAGGAGAATGATCAAGATTTTTGTCAGTCCACGTAGGGACTTGTTGAACAGTTTTAGGTATAAAGGAATTGAGACTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20076
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 |
---|---|---|---|---|---|
ENSDART00000031390 | Nonsense | 830 | 1347 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35732068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35517264 |
GRCz11 | 3 | 35646772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGGATGAGCTGAATGTGCCTGATTCAGGAGGAAAATATGCTACAGTA[C/T]AGCCTAGGGTGGGTCGCAGCAACTCAATGAAGGGACAGGCAGACAAGAAT
Long Flanking Sequence:
GACCACCCAAAAAGGAGGCACGTACCATGCGACAGAGCAGCCAGGGAGGACAGAGAAATGTTTCATCATCGCAGCCAAAACCACGTCAGTCTTATCCCCAAGGTACAGGTCCTCCCTATACTCCACCTCAAACGCCCACCAAAACAAAGCCTCCCGCCTCACAGACAACAAGCAACCCCCCAGGAAAACCGAAACCTAGTCCGCAGATTGTCCAGCAAACAGAAAAACCTATAACACCTCGTGGTCACCCGCAATCCCCAACTCAAAGGTCCCATCCACACCCTGCTGCCCAGCCTGTTGAATCAATAGAAGCTCCTCCCCAAGGACCTGCTGTTTCAGTGCCACTCTTGTGCCTGCCACCAGATGGCGATGAAGCTTGTGATGAGTATGGTCTGCCTAAAAAACGTGCCCATAGCCTAAATCGCTATGCTGTGTCTGATGGTGAGCAGGAGCGGGATGAGCTGAATGTGCCTGATTCAGGAGGAAAATATGCTACAGTA[C/T]AGCCTAGGGTGGGTCGCAGCAACTCAATGAAGGGACAGGCAGACAAGAATGTCAACCGAAGCCAGTCTTTTGCACTCAGACAAAAAAAGAAGGGTCCTCCTCCACCTCCTCCTAAACGATCTAGTTCAGCCATCTCAAGCTCCAGTAGTAATCTGACAGAAGTGCCCAAGGAGACTAACAGTGGACCTCTTCTGGATATTCCCTATCAACCACAAAGGCGTGCCAGTGACCTGGGTGGCACTGTAGACACAGGCAGTGCAGGTAGTGTGAGAAGCATTGCAGCCATGTTAGAAATGTCCTCTATTGGTGGAGGTGCAAAGGGTCTCGCTTTGCAGAAATCTGCTGGTCACTATCTGCAGGTAAGTTTGTTGTCATAGTGCTTTTTTTTATAAAAATGTCCATTATATGGTGCTGTAAATCATGGCTTTTTCTCTACAGGTGGGTTCAGGAGCAAAGCAACGTGATGCCATTGGACTAGATGGGGAAGTAGTGAACCGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14718
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 |
---|---|---|---|---|---|
ENSDART00000031390 | Nonsense | 898 | 1347 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35731862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35517058 |
GRCz11 | 3 | 35646566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGAMGTGCCCAAGGAGACTAACAGTGGAYCTCYTCTGGATATTCCCTA[T/A]CAACCACAAAGGCGTGCCAGTGACCTGGGTGGCACTGTAGACACAGGCAG
Long Flanking Sequence:
ATTGTCCAGCAAACAGAAAAACCTATAACACCTCGTGGTCACCCGCAATCCCCAACTCAAAGGTCCCATCCACACCCTGCTGCCCAGCCTGTTGAATCAATAGAAGCTCCTCCCCAAGGACCTGCTGTTTCAGTGCCACTCTTGTGCCTGCCACCAGATGGCGATGAAGCTTGTGATGAGTATGGTCTGCCTAAAAAACGTGCCCATAGCCTAAATCGCTATGCTGTGTCTGATGGTGAGCAGGAGCGGGATGAGCTGAATGTGCCTGATTCAGGAGGAAAATATGCTACAGTACAGCCTAGGGTGGGTCGCAGCAACTCAATGAAGGGACAGGCAGACAAGAATGTCAACCGAAGCCAGTCTTTTGCACTCAGACAAAAAAAGAAGGGTCCTCCTCCACCTCCTCCTAAACGATCTAGTTCAGCCATCTCAAGCTCCAGTAGTAATCTGACAGAAGTGCCCAAGGAGACTAACAGTGGACCTCTTCTGGATATTCCCTA[T/A]CAACCACAAAGGCGTGCCAGTGACCTGGGTGGCACTGTAGACACAGGCAGTGCAGGTAGTGTGAGAAGCATTGCAGCCATGTTAGAAATGTCCTCTATTGGTGGAGGTGCAAAGGGTCTCGCTTTGCAGAAATCTGCTGGTCACTATCTGCAGGTAAGTTTGTTGTCATAGTGCTTTTTTTTATAAAAATGTCCATTATATGGTGCTGTAAATCATGGCTTTTTCTCTACAGGTGGGTTCAGGAGCAAAGCAACGTGATGCCATTGGACTAGATGGGGAAGTAGTGAACCGCCGCAGGACCATTAGTGGACCTGTGACTGATTTAGTAGCAGCTGCTAAGCGAGGACCAGAGTTAATTCAGGACAGACAATGCACTGAAGCCCAGCCTAGTTCTAGTGGGAGTTCCGCTGAGAATCTTCCATTTGCTGAAGATGGAAATCTCACTATCAAACAAAGACCTAGACAAGGAAAGGACGAGGCTGAAGAAGGCCTAGAAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20075
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 |
---|---|---|---|---|---|
ENSDART00000031390 | Nonsense | 1083 | 1347 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35731185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35516381 |
GRCz11 | 3 | 35645889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGCCGTCCCAAGAGCAAAGACAAAGATGCAGAGGAACTTCAAGATGGA[C/T]AGATGCCTGTACCATATGAGAATGGGACAGGCACAATTAAAAGGCGTCCT
Long Flanking Sequence:
TTTTTTATAAAAATGTCCATTATATGGTGCTGTAAATCATGGCTTTTTCTCTACAGGTGGGTTCAGGAGCAAAGCAACGTGATGCCATTGGACTAGATGGGGAAGTAGTGAACCGCCGCAGGACCATTAGTGGACCTGTGACTGATTTAGTAGCAGCTGCTAAGCGAGGACCAGAGTTAATTCAGGACAGACAATGCACTGAAGCCCAGCCTAGTTCTAGTGGGAGTTCCGCTGAGAATCTTCCATTTGCTGAAGATGGAAATCTCACTATCAAACAAAGACCTAGACAAGGAAAGGACGAGGCTGAAGAAGGCCTAGAAATTTCATATTCTTTACCCCATGAAGATCTTTCTCGTGCCGATTCCACAGCCTCATTGAAAAGGAGTGTCCAGACCACCAGGCACCAACCAAATGGCACCAAGTTCCATCTCACAGAGTCAAACACAGTTAAGCGCCGTCCCAAGAGCAAAGACAAAGATGCAGAGGAACTTCAAGATGGA[C/T]AGATGCCTGTACCATATGAGAATGGGACAGGCACAATTAAAAGGCGTCCTGCGTCAGATGTGACTGTTTCAGAGCAGCCAAGGCCCCAAGAACATCCTGAGAACTCGCCCCGTCGAGACAGTGCCGACCTGGAAGGCCATGTCACAGAAAGTACCCCTCGCAAGTCTGTCAAACCTCCAGTGTCTCCCAAACCTGTTCTGGCCCAGCACATGAAGAAGCAGGGACCAACAGCTGCCATCACCAAGAAAGCCCCCTTTCCTGGACCAGCTGGGGCACCTGGCAGCCCAGGTACTACACAGTGCGGCCCTTTCACTTGCCCTGTCTTTACACAATTATGTGAGTATCCCGTAGACCCCTGTAGTGTTTACTCTGTTGAATCAAAGTCAGCTCAGTCAGTGTCTCTTCCCATCTCTCTCTCTCTCTATCTCTATTCTCTTCTCTTTACAGTTGAAGGAAAAAAAGTACCTCCTCCGATTTCACCAAAACCTACACCCCCTCCC
Associated Phenotype:
Not determined