ZMP
DSP (2 of 2)
Ensembl ID:
Description:
desmoplakin [Source:HGNC Symbol;Acc:3052]
Human Orthologue:
DSP
Human Description:
desmoplakin [Source:HGNC Symbol;Acc:3052]
Mouse Orthologue:
Dsp
Mouse Description:
desmoplakin Gene [Source:MGI Symbol;Acc:MGI:109611]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37182 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37181 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43550 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43549 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39311 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37182
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 |
---|---|---|---|---|---|
ENSDART00000111078 | Nonsense | 40 | 1491 | 2 | 7 |
ENSDART00000126556 | None | None | 640 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 53203857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53055467 |
GRCz11 | 20 | 52861073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATGCTGCTTTATTATAATGCGTTTTTGTGTCCTTCAGGTGTCTTCTT[T/A]AAATGCGCACTACTTGGAACTGCTCACCCGCTCAAGCGATTACTACAAAC
Long Flanking Sequence:
TTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGTTGAAGAGAAAATAAATCAGTGATTACAGATGAGTTATTAAAACTATTATGTTTAGAGATGTGTTGAAGAAATCTGCTCCCCATTAAACAAAAAATGGGGGGAAAAATGTACAAGAGGGCGAATTATTCTGACTGTACATTATTGAAATGGAATAAAAGTCAGCAACTTCTAGTCCACACAGACTATATTAAGCGTTTTCAGTGTAAAAAGCACTGTTTTAAATATAAATGGTTAATCCCGTGACGTGTTTTTGTGTAGAATTACGAGCTTGAGTTGGCCACTTACAGCGCTGGACTGGAGACTCTGCTCAACATCCCGATCAAGAGGACCGTTCTGCAGTCTCCATCATCCTCCATCGCTGAAGAGGTACAGCGGAGACATTAAAAACTCCACAGGCATTAGTTTTATCACAATGCTGCTTTATTATAATGCGTTTTTGTGTCCTTCAGGTGTCTTCTT[T/A]AAATGCGCACTACTTGGAACTGCTCACCCGCTCAAGCGATTACTACAAACTTCTTTTGGCATCCCAGAAAAACATGGAGGAGCTGAAGGTAACACTTGAATGGGGATTAGTCGAAACATGAACGCTTTAAATGACGACTTTAATTGTTACTCAAGTCAGCAAACAGCATATTAAAGCTTCATTATTTAATTGTAAAGGTTTGTCCAAAACCATGATTTATAGGGGAATTGGGTAAGTTCAAATTGTCCATAGTGTATGAGTGTGTGAATGAGTGTGTTTGGATGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCAAGTTAAAATTGTCCGTAGTAAATAATAAATATTAAAATAAATGAATAATAATTAAATCGCTTGAACTGATTATAACAATGAATAAAACTGTAAAAATAAATAAATGAATAATAATAATAAAAAATAAATATTAAAATAAATTACAAATATTTAAATAAGTAAATTATAAATTTTATAATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37181
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 |
---|---|---|---|---|---|
ENSDART00000111078 | Nonsense | 100 | 1491 | 3 | 7 |
ENSDART00000126556 | None | None | 640 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 53200448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53052078 |
GRCz11 | 20 | 52857684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAACTGAGGGATGCCATCAAAGACCAAACTGCCAACAATGCATCTTTA[C/T]AGGATGCTCTTCTGCAATACCAGCAAGAGCTGAACAATTCCCAAAGCCAC
Long Flanking Sequence:
TATGTTTTACACAGAGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAACCCAAATTTATATGTTACAGAAAAATATTAAACACAATTTAAAATTTTTTTAATTTTGTTAAAATTTTGTAGGTTGTAATTTTTTGTTGTTGCAATATTTAGCTTGAATTTAATTGTATTATCCTTAAATTTCTAAATATGTTTGGTGGCTATAATATTGTCATAAACATTTCTGTTTAATAAATCTGTTTTGTTTAAATGCACCAAAATACATTGCCTATTTTCACTGAGAAATTGAGAAAAACATTAATCTTCAAAATGGGTTGTACTCCATTATGCTGAGTACTGCATATATTTTTGAATAATAATAATAATAATAATAATAAAGAATTAACAAATCTCACAATGTGTTTTCTGCAGATACGAAATACCAGAATTGAGCTGCTGGAGGAGGAGCTTGAGCAACTGAGGGATGCCATCAAAGACCAAACTGCCAACAATGCATCTTTA[C/T]AGGATGCTCTTCTGCAATACCAGCAAGAGCTGAACAATTCCCAAAGCCACCTACTCTCTCTGGAAGAGGTGAAAAGGACTGAAACCATGAAGTGCATGGCCACTCAGGAGAGCCTGGACTCCTCTAAAGACCGCCTCGAGGAGCTTACAGAGGAAGTACGTCGCCTGAAACTCCAACTGGAGGACATGGAGAGAAAAAAGAAAATCGTGGAAGAGCGCTACACATTTCTGCAAGAAGAACATGATGAAACTATGCGCAAGAAACTCAAGGAACTGGAACAAGCTAGCTGGGCTAAAATGGAGCTGGAGAAAACCGTATCCGAACGGAACCGAGAGTTGGAGCGTCTGCGCAAGGAGTTGGAAGACGAGGCTCGGCGCATAAAGGAGGCGCAAACAGAGCTAGCTAAGGTAAGACAGGAGCACAGCACAGAGATTCGAGAGGTAAAACAAACCTACGAGTCTCAAATCCTCGTAGCGCAATCCAGCATGCAGAAGCTTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43550
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 |
---|---|---|---|---|---|
ENSDART00000111078 | Nonsense | 816 | 1491 | 4 | 7 |
ENSDART00000126556 | None | None | 640 | None | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 53197412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53049042 |
GRCz11 | 20 | 52854648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGCTCTTGCAGAACTTTGAACAAGAGAGAACAGAGATGCAGGCACTT[C/T]GAGACTCGAAGCAGGAGTTGCTGAGACTGCAGCAGAAACCAGATGGTGCT
Long Flanking Sequence:
TTGCAACAAATCTGTTAAATAACATATACAGAATTATCACTCTTGAATAATATTTAACATTATGTTTCTTATTTGTCTTTTTGTTGCAGACTTCCTCTGTAATCCAGACGTCCCAGTCTCAGTGCAGCAGCCTGAGTCAAGAAAGGGATGACCTCCTCAAGAAGATTACAACCATGGAACAGGAAATTGTGCGCTTGAAAAGGCTTGAAGATGAGCTAGCCCGTATAAAACTCTCACTGGAGTCAGAACTGCGATTTAAATCACAGCTGCAGGAGGAGAACAACAAGATCAAGAAGGATTTTACGCAGTGGAAGACCAAGTGTGCATCTCATGAGGAGCAACTTCGACAGCACGCCTCAGAACGCTCCGGCCTGGAGAGTCAGTTTAGCTCTGTCCGGACTGAGTTGGAGAGGCTGAGGACTCAACTCAGAGAAGCTGAAGAACGTTACAGGTTGCTCTTGCAGAACTTTGAACAAGAGAGAACAGAGATGCAGGCACTT[C/T]GAGACTCGAAGCAGGAGTTGCTGAGACTGCAGCAGAAACCAGATGGTGCTACCAAATATACTCAAACAGACCAAACTGATCCCTCCTCTTTGGTCTTCGAAGGTGTCCGCAAGAACATCACGGCACAACAGCTGCAAGACTGTGGTGTGATTGACAAGGTGATATTTGAGCAATTGATGACTGGCAAGAGGACTGTCCAGGATGTGTCTGTTGACATCAGGCTGAATCTGAAAGGGACAGGAGCTATTGCAGGGCTGGCAGCAGGACCTAAAGGCAAGATGACCTTCACCGAGGCTAAGAAACAAAACTTGATTTCAGACAAGAGTGGAAACATGTTGTTGGAGGCTCAAGCTGCCACAGGGTACATCATAGATCCCCAGGCTAATACAAAGATGACTGTTGAGGAGGCTTGCTTGAATGGAGTTGTGGATGAAGCTGACAAGAAACAACTGTTGATTGCAGAGGCCGCATGTGTTGGGTTTAGGGATCCCAAAACTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43549
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 > A
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111078 | Missense | 1231 | 1491 | 7 | 7 |
ENSDART00000126556 | Nonsense | 371 | 640 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 53195377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53047007 |
GRCz11 | 20 | 52852613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGCATTGAGAGCACCTCAGAGTACCTTCAGCAAGATCAATCCTCAG[C/A]AAACTCCTCCAAGCACATTTCCAGCATGTCAGTCAAACTATCCCCATTAG
Long Flanking Sequence:
AAAAGCACAGCAGAAGAACTCGACAAGGAAGAGACGTGTACTTATCGTTGATCCTGACAGTAATAAAGAGATGACAGTGCGTGAAGCTTATGAGAAGAAACTCATAGACTACGAGACCTTTCTGGAATTATCTCAGCAAGAGTGTGAGTGGGAAGAAACGACCATCACTGCCCCGGATGGCTCAACCAGTACTGCTATAATGGACATGCAAACCGGCATTCAGTACAACCTGAAAGAATTGCTCGCTCAAGGAGTGATTGACCAAGATGTATTCAATAAATATCGTTCCGGAGGTATATCTGTTACAGAGTTGGCTGGTATGATCACCAAGAAGACAAAGATGCTAACTAATCCTGTTAGCTCCTCCTCCTCTTCATCATTATCATCATCATCATCATCATTTACATCCCAGACAACAACGAAAAGCCAAATAGTCAAAACTGAAACCATAAAAAGCATTGAGAGCACCTCAGAGTACCTTCAGCAAGATCAATCCTCAG[C/A]AAACTCCTCCAAGCACATTTCCAGCATGTCAGTCAAACTATCCCCATTAGTAGAATCGATTGAAGAACAGAATCCAGTTGGAGCGATCTTTGACACTGAAAAGCTGGAGAAAATCACTGTTTGTGACGCCCTTAAGCGAGGAATGATTGATTCCATCACTGCACAACGACTTTTAGAGGCACAAGCTTGTACCGGTGGGATTGTAAGCCCTGATAATGGTCGTCGTATGTCTATTCAGGAGGCGACCAGAGTCGGTGTTCTGGATGACGAAATGGCTAACCGAATAAAACCTGCACAGAAGGCGTATATTGGATTTGAAGATGTGAAAACCAAACGTAAGATGTCTGCTGCAGAGGCTGTCAAAGAGAAGTGGCTGCCGTATGAAGCTGGCCAACGCTTTCTTGAATTTCAATACTTAACCGGAGGTCTCTTCGACCCTGAGCTTGGGTGCAGACGCTCACTTGAGGAGGCCTTGCAGATGGGTTGGCTGGATATGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39311
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 |
---|---|---|---|---|---|
ENSDART00000111078 | Nonsense | 1247 | 1491 | 7 | 7 |
ENSDART00000126556 | Nonsense | 387 | 640 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 53195329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53046959 |
GRCz11 | 20 | 52852565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAAACTCCTCCAAGCACATTTCCAGCATGTCAGTCAAACTATCCCCAT[T/A]AGTAGAATCGATTGAAGAACAGAATCCAGTTGGAGCGATCTTTGACACTG
Long Flanking Sequence:
TGATCCTGACAGTAATAAAGAGATGACAGTGCGTGAAGCTTATGAGAAGAAACTCATAGACTACGAGACCTTTCTGGAATTATCTCAGCAAGAGTGTGAGTGGGAAGAAACGACCATCACTGCCCCGGATGGCTCAACCAGTACTGCTATAATGGACATGCAAACCGGCATTCAGTACAACCTGAAAGAATTGCTCGCTCAAGGAGTGATTGACCAAGATGTATTCAATAAATATCGTTCCGGAGGTATATCTGTTACAGAGTTGGCTGGTATGATCACCAAGAAGACAAAGATGCTAACTAATCCTGTTAGCTCCTCCTCCTCTTCATCATTATCATCATCATCATCATCATTTACATCCCAGACAACAACGAAAAGCCAAATAGTCAAAACTGAAACCATAAAAAGCATTGAGAGCACCTCAGAGTACCTTCAGCAAGATCAATCCTCAGCAAACTCCTCCAAGCACATTTCCAGCATGTCAGTCAAACTATCCCCAT[T/A]AGTAGAATCGATTGAAGAACAGAATCCAGTTGGAGCGATCTTTGACACTGAAAAGCTGGAGAAAATCACTGTTTGTGACGCCCTTAAGCGAGGAATGATTGATTCCATCACTGCACAACGACTTTTAGAGGCACAAGCTTGTACCGGTGGGATTGTAAGCCCTGATAATGGTCGTCGTATGTCTATTCAGGAGGCGACCAGAGTCGGTGTTCTGGATGACGAAATGGCTAACCGAATAAAACCTGCACAGAAGGCGTATATTGGATTTGAAGATGTGAAAACCAAACGTAAGATGTCTGCTGCAGAGGCTGTCAAAGAGAAGTGGCTGCCGTATGAAGCTGGCCAACGCTTTCTTGAATTTCAATACTTAACCGGAGGTCTCTTCGACCCTGAGCTTGGGTGCAGACGCTCACTTGAGGAGGCCTTGCAGATGGGTTGGCTGGATATGAGAGCGGCTCAGAGGCTCCAGGATACTCGCCACCACCCGAAGACCCTGACCT
Associated Phenotype:
Not determined