ZMP
CDC42BPA
Ensembl ID:
Description:
CDC42 binding protein kinase alpha (DMPK-like) [Source:HGNC Symbol;Acc:1737]
Human Orthologue:
CDC42BPA
Human Description:
CDC42 binding protein kinase alpha (DMPK-like) [Source:HGNC Symbol;Acc:1737]
Mouse Orthologue:
Cdc42bpa
Mouse Description:
CDC42 binding protein kinase alpha Gene [Source:MGI Symbol;Acc:MGI:2441841]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18095 | Nonsense | Available for shipment | Available now |
sa36323 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14618 | Essential Splice Site | Available for shipment | Available now |
sa2899 | Essential Splice Site | Available for shipment | Available now |
sa18292 | Essential Splice Site | Available for shipment | Available now |
sa39147 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36324 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18095
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081651 | Nonsense | 335 | 1757 | 8 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8259357)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8262029 |
GRCz11 | 17 | 8419207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YCCGCAGACTCATCTGCTGCAGAGAGCACAGGCTRGGGCAGAACGGCATY[G/T]AGGACTTCAAACAACACCCCTTCTTCTCTGGCATTGACTGGCAGAACATC
Long Flanking Sequence:
TTTATTCAATTTAAGTTAATTTATTTAATTGTAATTATACTTTTAGTCCATTAAAATATTAATTAATTTTATTTATTTATTTTTAATTAATTTACTTTAATTCGTTTTTTCTTAAATTTTATTTTAAATTATAATTTTTAATTTATTTTATTAATTTTTATTTTCATCTATTTAATTTATTTAATTGCAATTTATTATTATTTAATTTCAATTAAATTTTAATTAAATCTTAATTTAATTTTATATGCTTTGTTTGTATAGACTACTTTTGTGGAGTTACATACTGTTTTAAATTAAATTAAATTATATTACATTACATTTAAAAGAATCAAATAGTGTCATGAAAGCCTACCAATGTTGTGGTTTTGTGTTTGTGCTCTGTGTTCCCACAGGAACGGTTCCAGTTTCCTGCTCAAATGACGGACGTGTCTGAAAATGCCAAAGATCTGATCCGCAGACTCATCTGCTGCAGAGAGCACAGGCTAGGGCAGAACGGCATC[G/T]AGGACTTCAAACAACACCCCTTCTTCTCTGGCATTGACTGGCAGAACATCCGCAACTGTGACGCCCCCTACATCCCTGAAGTCAGCAGCCCGTCTGACACATCAAACTTTGACGTGGACGACGACTGCCTCAAGAACACGGTAAAAAACTTTGCACTCATGTTTTTAATGAAATGTAATGAATCGGATATTTCTCAGTTTAAAGAGATGGTTCACACAAAAAATGAAAATTCTCTCATTATTTACTTTGTTGAACAATAATTCTGAAGAATGTTGTAAAAACATCTGTTGATTTTTTTTCTACTATGGATGTCAATGGCTGCTAATTTCCAGCAATCTTTAAATATTGTTTTGTGTTCAACAGAAGAAAAAAATGGATAAATGTTTACAACCACTTGAGTGAGAGCAAATGTTCATTTTTGCGTGAACTATCCCTTTAAAGCTTACTTTAGGTTATATCACCTTAAGCATTTTACTAAGATGCAGCAAATGATGACCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36323
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 |
---|---|---|---|---|---|
ENSDART00000081651 | Nonsense | 688 | 1757 | 15 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8270542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8273214 |
GRCz11 | 17 | 8430392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTCCAAGCACGGGGTCGTCTGAGCAGAACCAAGAGCTTAGTAAACTA[C/T]GAGCAGACCTGGAAAAGAAGACGGTGCACTTCAAAGAAGAGCTTTCCCGC
Long Flanking Sequence:
ATTAATTCGTTATGAAATATTTATTCATTAATAATTAATTCACCGCTGCCTACGATGACAATGGCGTCGTCTATTGCAGTGTTTTACATTAGACATCTTACGATGCCAAATTGGTGGACATCGCGCAACCCTAGTTTGACGGCTTTAACCACACCCCTTTTACTGTTAGTTTCCTATAAGGGAATTTTGCACAAAGTGAAAGACCTACCCCTATACTCAATATTCAGTTTCAACGTACTTAAACAAAAGTGTCAGCAACATCCGGTTCACATGGACATGGCTTGTTTACATTTAATCAGAACATTACTTTATGGGAAAAATAAAGATAAACTATATTAACAAACCAGTCATTTGTCCAAATTATTTGTGCATAACTTTAAATGAGCCGTGTGCAAGTCTCTGAAGATCAATTTTTTTGGTCTGTCATCGAGCAGCAGAAGCATGTGGGCCGCTCTCCAAGCACGGGGTCGTCTGAGCAGAACCAAGAGCTTAGTAAACTA[C/T]GAGCAGACCTGGAAAAGAAGACGGTGCACTTCAAAGAAGAGCTTTCCCGCATAGAACAGCAACATGCCAATGAACTGAAGAGCCTGAAGAAGGAACTGAAAGAGTCAGAGGGACAGCAGCTCAGCTTGAAGAAAGAGATCATGATGCTTAAAGACAAGCTGGACAAGTCCCGCAGAGAGAGGTACGCATTTTCATTATTCTAGAAACACTGTGAATGTGAAACACTTGATAATACTACAGAGGGTCACAAAGGGTCATGTAAAACTAAATTATAATCATTTGTGGTGCACTTGGCTAACATTGTACGTGGACTTGTGAAATAATATAAAATAAAAAGTGGTGTTGAATGCACTGTAAAATGTTTAATAGCAAAAATTCAAGTCAACAAATGTTTATATGTTACTTTAATTTATTTTAATATGTAAATCAAGCTTCAATTACATTTTTTAAGTTATACATAGTTTAACTTAATGTGTTTACTCAGTTTGATTGATGGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14618
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081651 | Essential Splice Site | 895 | 1757 | 19 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8284645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8286238 |
GRCz11 | 17 | 8443416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGGATGAGCTCAACAAAGTCAAGGCATCCCATATGGCTACTGAGTGG[T/G]AAAACACACAGCTCTTCTTTAAAGTACAAGAGKKGGTAGATCTGAAAATT
Long Flanking Sequence:
ACCTGTTTGATTGAAGCTAGTCTTTGGTCTGGTGAACACAAGAGGAGATATTTTAAAGAATGTTGGTACCTGGCACCAACGTTTTTTTTTTTTACCTACTATGGAAGTCAATAGGTGTTAGCAACTTCTTCAAACTTGTCTTCTTTTTGTGTTCAATAGAATAAGGAAACTCATAAAGGTTTAAAACTGACATGAGATAAACTAAATGATGTAATTTTTGTTTATGTTTCTCTACTATCACTTTAATAATATCAAAAGCAATCTATTCAGACTTTCAATGGCGTTTATGTCAACATATCTCATTGTACAATGTGACACAGCACGTTTAAACTTTTCTTCTGGTTTTCCAGGACATGCCATGGAAGGTGAGACGTCTGGCCAAACTGGATATGTCTGCCCGTCTGGAACTGCAGTCTGCACTGGATGCTGAGATTAAAGCCAAACAAACCATCCAGGATGAGCTCAACAAAGTCAAGGCATCCCATATGGCTACTGAGTGG[T/G]AAAACACACAGCTCTTCTTTAAAGTACAAGAGTTGGTAGATCTGAAAATTAGATACCAATTATCTACTTAATGTTCCAGAATCAGTTGCGGAAAATCCCAAATGGTGGTCAGCAGATATGGGTTTGATTTGAAAGGCCTAAATTTATGCAGAAAATATAATCTGCTTATGCACAAAATATTCGCCTTATTCTCCGCGTATTAGCGGACGCAGCCATTTGAATTATTTTGAATTCCAGTCTCATTCACTTCCATTCATTTTTAGACTTTAAAAACAGCTCGTTTTGCTGCTAGATGTTGCAAACTGATATTTTCTTCTTATATTATTGTACTTTGTCTGTATAGGCATCCTAGTCATTTCTCCCATGGCGACACAGAATCAGAAGTTCTAAAACAATCGCAAAAACGAGCGCACTTCTACACTGAAGTATAAAGTCGATAGGAGCAATATATTTATTTTGTGCTATACAGCGGGGGGAAATAAGTATTGAACACATTATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2899
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 |
---|---|---|---|---|---|
ENSDART00000081651 | Essential Splice Site | 1066 | 1757 | 25 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8292652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8294258 |
GRCz11 | 17 | 8451436 |
KASP Assay ID:
554-2596.1 (used for ordering genotyping assays)
KASP Sequence:
TGTACGTCTCTGATGGTGGGGATCATCCGTCAGGGCTGCACGTGTGAAGG[T/C]GAGACAGGTCATTTACGCTGAAACTGATGGCGTTGTAAAAATGGTAACTA
Long Flanking Sequence:
TTATTCTGGAAAAAGAGATCTTGTTTGCTATTATTTTGGCTAGAGTAAAAATTGTTTCCTCTTTTTTTTAACCATTTCAAGGTCAATATTATTAGCCCTGTTAAGAAATATAATTTTGGATAGTCAACAGAACAAACCATTATTATACAATGACTTGCTAATAACACTAACTTGCCTAATTAGCCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTAATAAAATCAATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATATGTTGAAAAAACTGCTCTCTGTTAAATAGAAATTGGGGAAAACACATAAAAGGGGGGCTAATAATTCTGCATGATTTCATGTATTTACTAGTATTCTGAATTGCTCTTTTTAGCCAAAAGCCCATCAGTTTGTGGTGAAAACCTTCAACACACCTACTAAATGTAACCAGTGTACGTCTCTGATGGTGGGGATCATCCGTCAGGGCTGCACGTGTGAAGG[T/C]GAGACAGGTCATTTACGCTGAAACTGATGGCGTTGTAAAAATGGTAACTAGTATTTAGATTGGCATTCACCTTTTTCTCCTCTTGCAGTCTGTAACTTCTCCTGTCATGTGACGTGTGCGGATAAAGCTCCCGCTGTGTGCCCGATCCCACCAGATCAAACCAAAGGACCGCTCGGCATCGACCCTCAGAAGGGCATCGGCACAGCATATGAGGGCCACGTAAAGGTTAGACACTTCAGTTTAAATTACCATGAACAATTTGTGATCAAAATGAACTATTAGCACAATTAGTCATTATAGCGTGTCATTAATGGTTTTGTAGCTATATTGTTTAAATAGTAGGAATTAAATGAAAGCTTTCTTAAAATTACTAGTTCAGGAATTCAAAAATAAAATAGCCTGTCACTAAATGTAATATTCCAACATTTCAATGTAATGTTTTTCAATTTAATTTAATTTGATTTGATTTAATTAAATTGATCTGCTTCAAAAGTACAAGA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa18292
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081651 | Essential Splice Site | 1111 | 1757 | 26 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8292878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8294484 |
GRCz11 | 17 | 8451662 |
KASP Assay ID:
2261-0651.1 (used for ordering genotyping assays)
KASP Sequence:
GCATCGACCCTCARAAGGGCATCGGCACAGCATATGAGGGCCACGTAAAG[G/T]TTAGACAYTTCAGTTWAAATTACCATSAACAATTTGTGATCAAAATRAAC
Long Flanking Sequence:
ATAAAATCAATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATATGTTGAAAAAACTGCTCTCTGTTAAATAGAAATTGGGGAAAACACATAAAAGGGGGGCTAATAATTCTGCATGATTTCATGTATTTACTAGTATTCTGAATTGCTCTTTTTAGCCAAAAGCCCATCAGTTTGTGGTGAAAACCTTCAACACACCTACTAAATGTAACCAGTGTACGTCTCTGATGGTGGGGATCATCCGTCAGGGCTGCACGTGTGAAGGTGAGACAGGTCATTTACGCTGAAACTGATGGCGTTGTAAAAATGGTAACTAGTATTTAGATTGGCATTCACCTTTTTCTCCTCTTGCAGTCTGTAACTTCTCCTGTCATGTGACGTGTGCGGATAAAGCTCCCGCTGTGTGCCCGATCCCACCAGATCAAACCAAAGGACCGCTCGGCATCGACCCTCAGAAGGGCATCGGCACAGCATATGAGGGCCACGTAAAG[G/T]TTAGACACTTCAGTTTAAATTACCATGAACAATTTGTGATCAAAATGAACTATTAGCACAATTAGTCATTATAGCGTGTCATTAATGGTTTTGTAGCTATATTGTTTAAATAGTAGGAATTAAATGAAAGCTTTCTTAAAATTACTAGTTCAGGAATTCAAAAATAAAATAGCCTGTCACTAAATGTAATATTCCAACATTTCAATGTAATGTTTTTCAATTTAATTTAATTTGATTTGATTTAATTAAATTGATCTGCTTCAAAAGTACAAGACACAACAAACACTGTCATCAAATGCATGTAAACAGCCGGGATTCACATCGGAAGCGTGTGTGAAGCACGTAGGAATGGTTTTCTGAAATGCATTTAATTTAATTTACTTCAGAATCTCTGTTATTAGAAATGTTTACTTATGCCTAGTTCACACTAGAGGATTTTAAGCCTGATTTGAGCCCGATTTGGAAGTTAACGAGCTCGCCGACAGATCGGGCTGTGATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39147
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081651 | Nonsense | 1202 | 1757 | 29 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8300822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8301410 |
GRCz11 | 17 | 8458588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGACAGCATCACAGCTCTGCGCCTCCAGCAATAAAAAATGCTCCATTT[T/A]GATCCTGGCCGACAGCGATCAGGAAAGAACAAAGTGGGTCGGCCTTTTGA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATAAATATATCATTATCAGAATAGTGTTTCTTATAATTAATGTCATTCAACCATCCAGGCACCACAAAGTCAATGGTTTCATGTTTCCAGCTTTCTTCAATATATCTTTTTTAAGTGTTAAACAGACACTAGAAAGAAATAGTTTGGTACCACTCGACGGAGCAAATTTTCAGCTTTTGGTGAACTATCCCTTTTTCCCATTAGCTTTTGTGTTGTAAGTTAAGAATAATCGAGTCAAACTTGTGATGGACTTTGAAACTGCTCTGCTTTTGTTCTCCTGCAGGTGACAGCATCACAGCTCTGCGCCTCCAGCAATAAAAAATGCTCCATTT[T/A]GATCCTGGCCGACAGCGATCAGGAAAGAACAAAGTGGGTCGGCCTTTTGAAGGAGCTGCACCGGCTCTTGAAGAAAAGCAAACTGAAAGAACGCTTTGTTTACGTCCCTAAAGAAGCATATGACTGCGCACTGCCTCTCATCAAAACCACACAGTCTGCTGCTATTATAGGTAGAGTCCAACACTTCTCCTAATGTCCTAATCATAAAGTTTTTATGTAAATATCACCAAAATCTGCCTATATAAAAGATCTCATATAAGATCAGAGAACCTCGCCATATAAATAAGTGTCTTAATGGCATTTTGTTGGATCTTTGTTTTAGTTTTTGTTAGTGGTCTGGCTATACATACAGTTGAAGTCAGAATTATTAGCCCCCCTAAATTATTAGAACCGCTTGTTTATTTTTTCCCCAACTTCTGTTTAACGGAGAGCAGATTTCTTCAACGCATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTGATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36324
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081651 | Essential Splice Site | 1512 | 1757 | 32 | 38 |
Genomic Location (Zv9):
Chromosome 17 (position 8309793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8310371 |
GRCz11 | 17 | 8467549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTGATGTCAACACTATGGAGTGGATTCAAACAATTCCTTTGAAAAAG[G/A]TACATTTTTATTTTTCCTTATGAGCAAAGAAAAAAACACACAAATGCAGA
Long Flanking Sequence:
GGCATTAATGCGTCCTGATGTAAAGTGAAACGGCTATACGTCGTGTTTGCTGGCATCACACACCTGTCTGCCAGTCATCAGCATGTGAACTTAAAGGGTTAAACAAATAACGCACAGCACTACTACGGTTACAGAAAAGTTTGCGTTGTTATAATTCACTTACCTTTTAATACGTTTTGGTGCGATTATCACCCGCTATTAAAAAAAAAAAAAAACACGACTGAATGTTTTGAATGAAAAGCTGTAATGTAGCCGTAGCGGGATCAATTCTGGTGTGGCACATGGAAGAATGAATGTAGCGGAAACCATGTATATTGTCAGTTTAGTTTGTAAAGGTCAGGTTTCTGTTCCTTACACATATTCCCACACAAGTCCTTTAAAAATTGTGCTTATGTCTTGCAGGTTATAATGCACCTTATCTGTCAGTGTACAGTGAGAATGCGGTAGATGTATTTGATGTCAACACTATGGAGTGGATTCAAACAATTCCTTTGAAAAAG[G/A]TACATTTTTATTTTTCCTTATGAGCAAAGAAAAAAACACACAAATGCAGACACGTTCCAAAGAGAGTTTCTCATCTAGACATGAAATTGAGAATAGTAGGAGAAGAAGTGCGGAGTGTTAATGAGCTGTGTGTCTCCTTCATTGCAGGTCCATCCACTGAACTCTGATGGCTCTCTAAACCTGCTGGGGCTGGAGACTGTACGGCTCATCTACTTCAAGAACAAGACAGCAGGTCAGATGCTCCCTCCTGCTGCTCCAACACATATTCAGTATTCCTAGCCCTGTACTTATGAATATTCAGCAGCAAATATATGATAAAAGAAGCAAAGTTGTTTCAGAGGTGGTGAAAGCAAATGCATTTTGATTATTAGCACAAAAGTTAGTCATGTTTTCGTTTAAAGGGGCCCTGTTATGCCCATTTTTGCTTGATAAGAAATAAGAAAATAAGTATTTGGTGTTCTTAATGTGTTAATGTGAAGTTTCAGCTAAAAATAATCCAC
Associated Phenotype:
Not determined