ZMP
LOC565254
Ensembl ID:
Human Orthologue:
PKDCC
Human Description:
protein kinase domain containing, cytoplasmic homolog (mouse) [Source:HGNC Symbol;Acc:25123]
Mouse Orthologue:
Pkdcc
Mouse Description:
protein kinase domain containing, cytoplasmic Gene [Source:MGI Symbol;Acc:MGI:2147077]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14501 | Nonsense | Available for shipment | Available now |
sa15337 | Nonsense | Available for shipment | Available now |
sa18146 | Essential Splice Site | Available for shipment | Available now |
sa42961 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14501
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 |
---|---|---|---|---|---|
ENSDART00000055754 | Nonsense | 21 | 463 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 31223214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 31147141 |
GRCz11 | 17 | 31164104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAAGTCCGTTTTGCGYTTTYGTCCTCYTTGCTTTGTTGTTTTTGTCTT[T/A]AACGCTTAWTGTGAAAAAGTGGCACTTYGGTCTCCARGAGAACGAGCCTT
Long Flanking Sequence:
GATACATATTAATAGTAATAACGATGTAATAGGGGTTGTTAGTTAGGGTTTAATTAACAATTTATATTTAAATAAATAACGTTTATAATATTCGATGTATTCATTTATTTATTTAGAAAATAAAATAAATCAATTCACACCTCAGCATGAACTTTATCAGTTTTATTTTAAAACTCATAACGTTTTAGCCTTTGATGATATGTATATTAAAACGCATAGGCTCTTTTATCTGTGTGTGTGTGTGTTAATGGAGGTTGCATTGTGTGGGAGGTGATTATTTGGCCATGAGCAGTAAGACACGCCCACTGGGCGTTACCGCAGCTCACACTTACTACACTAAATTACAGTACGCACGTACTCAAAGCGCCAGAGTGAAGTATGAACAGAGACGCTGTCGTACTTTGACAGTACACAAAAAGGACCTACACTTAAACTTGCCATGACTTTCCAAAGAAGTCCGTTTTGCGCTTTCGTCCTCCTTGCTTTGTTGTTTTTGTCTT[T/A]AACGCTTATTGTGAAAAAGTGGCACTTTGGTCTCCAGGAGAACGAGCCTTTTGGTGATGCTGCCCGCTCAGATGGTTCTGCTCCACAGCGCGACACATTGCGCCAACAACTTCAGGAAAGACAACAAGAACTTGTGCTCCTGGACATCACTTTTGAAGACATACAACAACAAGAAGGATTTAATGGGAAAATTAGTTTGGATAATCCAACTGCAGCTGACATTGGTTGTGAAGAACTTGGTGGCGTGAAAGCTGTTGACTTTCTTGGTTCAGGTTACACCAAAACAGTGTTAAAAGCAGCACTGCCAAACGGATTATTTGTGGCACTGAAATCTGTAAACCATCAAGGCACTGACATGAGATTATGCTTGGATGTTTTCCAAGATTCCCAGGGATGCCTTGAGCTGGTGTCGTTCAAGCTGAGGAAGGAGATTGTGTTATTGCAGAAACTTCAGCACCCTAATATTGTAGAGGTAAAAACAGCCTACAGTTTGTCTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15337
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 |
---|---|---|---|---|---|
ENSDART00000055754 | Nonsense | 63 | 463 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 31223089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 31147016 |
GRCz11 | 17 | 31163979 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCTGCTCCACAGCGCGAYACATTGCGCCAACAACTTCWGGAAAGACAA[C/T]AAGAACTTGTGCTYCTGGACATCACTTTTGAAGACATACAACAACAAGAA
Long Flanking Sequence:
TAAATCAATTCACACCTCAGCATGAACTTTATCAGTTTTATTTTAAAACTCATAACGTTTTAGCCTTTGATGATATGTATATTAAAACGCATAGGCTCTTTTATCTGTGTGTGTGTGTGTTAATGGAGGTTGCATTGTGTGGGAGGTGATTATTTGGCCATGAGCAGTAAGACACGCCCACTGGGCGTTACCGCAGCTCACACTTACTACACTAAATTACAGTACGCACGTACTCAAAGCGCCAGAGTGAAGTATGAACAGAGACGCTGTCGTACTTTGACAGTACACAAAAAGGACCTACACTTAAACTTGCCATGACTTTCCAAAGAAGTCCGTTTTGCGCTTTCGTCCTCCTTGCTTTGTTGTTTTTGTCTTTAACGCTTATTGTGAAAAAGTGGCACTTTGGTCTCCAGGAGAACGAGCCTTTTGGTGATGCTGCCCGCTCAGATGGTTCTGCTCCACAGCGCGACACATTGCGCCAACAACTTCAGGAAAGACAA[C/T]AAGAACTTGTGCTCCTGGACATCACTTTTGAAGACATACAACAACAAGAAGGATTTAATGGGAAAATTAGTTTGGATAATCCAACTGCAGCTGACATTGGTTGTGAAGAACTTGGTGGCGTGAAAGCTGTTGACTTTCTTGGTTCAGGTTACACCAAAACAGTGTTAAAAGCAGCACTGCCAAACGGATTATTTGTGGCACTGAAATCTGTAAACCATCAAGGCACTGACATGAGATTATGCTTGGATGTTTTCCAAGATTCCCAGGGATGCCTTGAGCTGGTGTCGTTCAAGCTGAGGAAGGAGATTGTGTTATTGCAGAAACTTCAGCACCCTAATATTGTAGAGGTAAAAACAGCCTACAGTTTGTCTCATTGTGTTATGTAAAGTATTAGACATGCATAGGTTAAAATGTTTAATATGTGCCCTAATTGATCTTGTTGTGCTCTTTCTAGCTGAAAGGTCAATGTCAGGACAGCGTCCTGGTTGGTGGCATCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18146
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 |
---|---|---|---|---|---|
ENSDART00000055754 | Essential Splice Site | 217 | 463 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 31222516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 31146443 |
GRCz11 | 17 | 31163406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTCAGATGATCCAGCTCCTGCAGAGCCCCTGGGAAGAGCGCTTTCGGG[T/C]AAGARCACCACCCCCAGGCCTCCTATGGAGTGTTAATCAGAGATTCYCCA
Long Flanking Sequence:
TGGATAATCCAACTGCAGCTGACATTGGTTGTGAAGAACTTGGTGGCGTGAAAGCTGTTGACTTTCTTGGTTCAGGTTACACCAAAACAGTGTTAAAAGCAGCACTGCCAAACGGATTATTTGTGGCACTGAAATCTGTAAACCATCAAGGCACTGACATGAGATTATGCTTGGATGTTTTCCAAGATTCCCAGGGATGCCTTGAGCTGGTGTCGTTCAAGCTGAGGAAGGAGATTGTGTTATTGCAGAAACTTCAGCACCCTAATATTGTAGAGGTAAAAACAGCCTACAGTTTGTCTCATTGTGTTATGTAAAGTATTAGACATGCATAGGTTAAAATGTTTAATATGTGCCCTAATTGATCTTGTTGTGCTCTTTCTAGCTGAAAGGTCAATGTCAGGACAGCGTCCTGGTTGGTGGCATCACAGCAGTTCTGGAGCAGGGGATGCCACTTCAGATGATCCAGCTCCTGCAGAGCCCCTGGGAAGAGCGCTTTCGGG[T/C]AAGAGCACCACCCCCAGGCCTCCTATGGAGTGTTAATCAGAGATTCCCCACCCACTGTCCCCCCACAGGGCATACCTGAGGTGGGGGTGGATGAAATTCTTCAGCTTTAGCTGGATTAACTGGAGCCCCATCTCCATACCAACTGAGCCTGATCAAATAGTACAGAGGGGACAGATGTCTGTCTCAGATGTCCATCCTTTTACTCTTCTTTACCCTGATCAGTTCTTGGCACTGTTTGAGGGAGCGAGGTGATACTGAGTTTCACTACACCATGGAGTGTTTCATGTTCACGTTGGTGTGCAATAAGCAGGTGCTGATATTGTGTGCCTTTGATTTTTGATGATGACAAATGTGTTTAAGCTAAAGGGCTGTAATCGAGTGTCTCTTTGACATTCTTACCTTCTCTGAAAAGTCTTAACACGTGGTCGAGAGTTATTCAAGAAGGTGTTTGGTTTCATCCACCTCTGCTTTTGGAGAGCTGCTGTGGCTATATAGTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42961
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 |
---|---|---|---|---|---|
ENSDART00000055754 | Nonsense | 224 | 463 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 31218261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 31142188 |
GRCz11 | 17 | 31159151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGTTCCTTTTGATTGTGTTATCCCACAGGTCTGTCTTGGTTTGGTG[C/T]GACTCCTTCAATACCTGTCTGTCTCACCTCTGGGATCAGTTGCCCTGCTG
Long Flanking Sequence:
CACACACTTTTCTCCCTTGTGAGTTGAGTGCGCCTCCATCGCCGTGTGCGCGTTTTATTTACGGGCGCACCTTACCTGACGCGGACGCGCTGTGACCGGATCTCTCGACTATAGGATAACTTTATCCCCACAATTTTTCATAATTTAATTGCTATGTCATATATTTTAAAATATTTAAATGTGTGTTCTAAAGGTTGAAACAACGGGAGTGTTTGTAATTAAAGACAGAAAGAATTTTCAGTTTTGAGTGAACAAGCCTTTATAAAAACTGGGTAAAAAAAAAAACCCGTAGCGCCGGGCCTGGTTACACACATACTGTTTGCTATATGGAATGCAAAATCTTTGAAGCTCAATATCTCAAAATCATTCAGAAAGCAGATAAAACCTTATAATTCCTAGGTGAGGATGAACTGTCTGACAATTACAGCTAAATAGTCTTATTATTTTATTAAAAAGTTCCTTTTGATTGTGTTATCCCACAGGTCTGTCTTGGTTTGGTG[C/T]GACTCCTTCAATACCTGTCTGTCTCACCTCTGGGATCAGTTGCCCTGCTGGATTTCCAGCCTCGACAGTTTGTAATGGTGTCTGGAGAACTCAAGTTAACAGACTTGGATGATGCAAGTATTCATGAACCGGTCTGTCAAGAGGACTCTGACTGCCTGCTGCAGTTTCCCCTCCGCAACTTCACCCTGCGATGCTCCCCGTCCCAAACTTGCAAGGGTCTGAATGAGATGAGAAACCTCTACAATGCCTACAGGTGAGCACTTTTATTGTCTGAGCCACAGATAATGAAAAAAAGTTGTGTTACAAGAGTCTCAAGTCTCCCCTCATGTGTCTGTTATGATTAATTATCCACCCCGCTGAGTGTCGGGGCAGCAGTTGTAGTATATTGATCTCGCAGCATGAATCTCCACTCTGCTGGATGAATTATATGAAATATTTCCCCTACAGGTATTTTTTCACCTACCTGCTGCCTCATCAGGCTCCCCCGTTGCTGAAACCTC
Associated Phenotype:
Not determined