ZMP
dspa
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate desmoplakin (DSP) [Source:UniProtKB/TrEMBL;Acc:A2AVI3]
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19650 | Nonsense | Available for shipment | Available now |
sa30809 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13356 | Nonsense | Available for shipment | Available now |
sa302 | Nonsense | F2 line generated | Not yet available |
sa38306 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19651 | Nonsense | Available for shipment | Available now |
sa39744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19650
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 595 | 2244 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1952320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1807406 |
GRCz11 | 2 | 2150212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCAGGCCGAGGACATCATTAAAGTCCACGAGGCTCGTCTGACCGAG[A/T]AAGAAACCTCTTCTCTTGACCTGAACGAAGTGGAAAAGTACTGCATGACT
Long Flanking Sequence:
ATGAGAGAGCTGGAGGGCAGCAGTGACCCTGAGCAGAGCCGATACCTGCGCGCAGAACTGGACCTGATCAACCAGAAACTGGGCAGCCTGCAGGGCTTCTCCAGCGCATACATCCAGAGGCAAGAACATTTATATAACAACCTGAAGTATCAGTGCTAGAAATGCATTGGCTCCTAGACACTGTAGATTAGGTTTCCTCTTGAAATGTAAATGGACCTTGATAAATAGCAGATTTTAAGGGGTTTGTATTGGCAGCGGGCGGCACGGTGGCTCATTTATTAAAAATGAGACTAAAAATAAATATGGGTTGTACAGATCATAATTTTTATCAATAGAGATTTGTAATCCGTTACACCACTAGAGAAATGTAATAGAGATAATAGAGAAATGTAACATGATGTTTGATGTCTGTTTTCAGGCTCGGTGCTCTACAAGCTCTGCTCCAGCACCTCCTGCAGGCCGAGGACATCATTAAAGTCCACGAGGCTCGTCTGACCGAG[A/T]AAGAAACCTCTTCTCTTGACCTGAACGAAGTGGAAAAGTACTGCATGACTCTCAAGGTGAAGTTCTTTGACATATCTAAAGTTTTTTTAAAGGCACAGTGTGTAATTTTGGCCACTAGAGGGCAGGTTTTAACAACACACATATGCATCGTTTGATGATTCCCTTACTGAGTGTGGAATCATGGGAGTTGTGGTCGTCAGTATCTTATGAGGCTCCTGGAGAAACCATGTTGATGGATGAGTAAAGTATTTAACACTTATTATCAGGGTAGTGTAGAGCAGAGTAAGAAAACGAGAGAAATGCAGAAGGAATTGCTGATGAGAGATGATGTTTGGTATTATGCTACAGTGCACCACTTCCTATCCTTACACTCGTGATCATGTGGAGAAGAAGCAGCGCTGTTTATTAGACTAAATACATGTTAGACTTCTGTTATAATGCTGCTCTGTGCAGTCGAATAAAACACACCGCATATATTTAATTAAGAGTGTGTGACGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30809
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 |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 621 | 2244 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1954635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1809721 |
GRCz11 | 2 | 2152527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGAATCTGATGTCTTGTTTTCTGTAGACTATGAAAGCAGAGCTGGAG[C/T]AGAAGAAGGGTGTTTTGAAGGCGATGGAGACGGAGCTGTCTAAAGCTGTG
Long Flanking Sequence:
TCTTTTTGTGTTCGACAGAGTTGTTTAATACAAAAGAAGATATTTTGAATAATGTTGGAAACCTGTAACCATTGACTTGAATCTGCATTTGTTTTTTTCTACCATGGATGTCATTGGTTACAATTTTTCAGCTTTCCTAAAAATATCTTCTTTGTGTTTGACATAATTGTTTAATACAAAAGAAGATATTTTGAAAAATGCCGGAAACCTGTAACCATTGACTTTCATTGTTTTTGTTTTTTTCTTATATTGAAATCAATGGTTACAGGTTTCCAGCATTCTTCAAAATATCTTCTTTTAGTGTTCGACATAACCGTTTAACACAAAAGAAGATATTTTGAAAAATGTTGTAAACCTGTGACCATTGACTTCCATGGTTCCAGTAGACAGTGATTAATGTTAAGTGAACCACTATGAAAGCATGTCAAGTACTGTACACACAGTATTTGTAATTGAATCTGATGTCTTGTTTTCTGTAGACTATGAAAGCAGAGCTGGAG[C/T]AGAAGAAGGGTGTTTTGAAGGCGATGGAGACGGAGCTGTCTAAAGCTGTGCACTGGAACAGTCAGATTGACCAGTCTTTCCATCAGTGTGATGTTGACCTGTCCAGATACACTGAGCTGGTCGGACAGATGACTGACCGCTGGCGCAGGATTGTGACTCAGATTGATAGCAGGTACAGAGCACTTATTGCACTGGTCCTCAATCTGGTGTCCGGAATTCACATCTCCTCTTCAAGGAGGTCTTGGTATGCTTTTTTGGTCCGCTTTTGGTGCGCACTCGAGTATGATTGCTAGATTTTCACCTGCCCAAACGAACCGCACCAAGAAGGAGAGCGAACTCTAGTGCGATTCAACCGAACTAAATAAGGCAGGTGTGAAAGCACCCTTAGTAAGTGTAATACAAATACAAATTTACTCTATATATTAAACTCAATTGCATCTAATTAATCTGTAGTGAAAACTTTAGCAGCAATAAATCGATGATCATGAAAAATTGCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13356
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 |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 960 | 2244 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1960075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1815161 |
GRCz11 | 2 | 2157967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGCGCAAGAGACAGAAAGAACTGGAGGAGCTCACTTTGTCCAAAAGT[C/T]AATTTGAAAGAGCCATCAAAGASAAAGAGCGRGAGATTGAACGGCTGAAA
Long Flanking Sequence:
TTTCCCCATTCAAAACTATACAAGTGACACATCTTGTGTATTCTGTAGTCTTCATTATTGTTACAGTTGGTTTATTGTCACTAACTACTGCTATTCCACTTTTTATTCAGATGCGGAACACCAAAATTGAGCTTTTGGAGGAGGAACTGAGACGCCTCAAGGACAACCTCAAAGATCAAAACCAGAAGAACAAATCACTGGAGGACAGTTTGACTCGCTTCCGCCTGGAGCTGACCCAGTCCAAAGAGCAGCTCATATCTATGGAGGAGGTGAAGAGAACCCAGGCCAGGCAGTGCAACACTGCTCAGGAAAGCCTGGATAGTACTCAGAACCAGCTGAAGAGTTTACAAGATGAGATGTCCCGCCTTACATTCCTCATCGAGGAGGAAAAGCGCAAGCGAAGGCTGGCCGAGGAGCGTTACACCAACCAGCAGGAGGAGTATGAGCTGGCCATGCGCAAGAGACAGAAAGAACTGGAGGAGCTCACTTTGTCCAAAAGT[C/T]AATTTGAAAGAGCCATCAAAGAGAAAGAGCGGGAGATTGAACGGCTGAAATTACAGCTGCAGGATGAGGCCTCCCGACGCTCGGCAGCAGAACTGGAGACCTCAAAGGTAAGAACCCAGTTGAACCAGGACATAAGTAGCCTAAAGCAAACATATGAATCTGAGATCCACGTCACCAAGACCACAGTGCTCAAGTCGGCACAGCAGAAGGATGAGGAATCGGCATCTCTGAGACTTCAGGTGGACAGGTTAACCTCTGAGAAGAGAGATCTGGAAGAGGAGCTAAGGAAACTGCAGCTTTCTTTCTCCCAGACGGAAGCGGCACGACGGAAAGCAGAAGAGGACGCGCATCAGAAGAGATCTATGGCTGCAGATGAAAGCAGATCCAAGAAGGAACTGGAGTCACAGATTCAGATCATAATTCGTCAAAGGGAAGACATTGAAACTAGACACAAGATGGACCTGGCTGATGCAAACAGAGTTGCTCAGGAAAAGACCCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa302
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 1197 | 2244 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1960787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1815873 |
GRCz11 | 2 | 2158679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCRTTATAAAGAGAGAGTTGGATGTACARAAAAGTGATAAGATGAAGT[T/A]GGAGCAGAATGCCACCAGGTTGCAGAGTCGCATAAATGAACTGCAGTCCA
Long Flanking Sequence:
TGAGGAATCGGCATCTCTGAGACTTCAGGTGGACAGGTTAACCTCTGAGAAGAGAGATCTGGAAGAGGAGCTAAGGAAACTGCAGCTTTCTTTCTCCCAGACGGAAGCGGCACGACGGAAAGCAGAAGAGGACGCGCATCAGAAGAGATCTATGGCTGCAGATGAAAGCAGATCCAAGAAGGAACTGGAGTCACAGATTCAGATCATAATTCGTCAAAGGGAAGACATTGAAACTAGACACAAGATGGACCTGGCTGATGCAAACAGAGTTGCTCAGGAAAAGACCCGTGAGATCACATTGCTGACGCAAAATTTGCAAGACGAGACCAGGCGGAGGAAAGCAATGGAGGTTGAGAATCAAAGCCTCAGACAGTCTCAGGCTGAAATACTAGCCAAGCAGACTTCAACCACAGAGGTCATCAACAAATTAAAGGTCTCTGAGCAAGAGGTTCTCATTATAAAGAGAGAGTTGGATGTACAGAAAAGTGATAAGATGAAGT[T/A]GGAGCAGAATGCCACCAGGTTGCAGAGTCGCATAAATGAACTGCAGTCCAAGGTGAACGAGTTGCAGGCTGAACTGGAGAAAGAGAGAAGGAATAATCAGGATGAGCTCACGAGGAGGAAACGCATGGAAACTGAGTTGGATAGGGTAAATCAGACGTGCCGTGAATACACCACTACCATCAGCACTCTGCGGGTCCAACAAGAGAAAGAAAGTTCTTCTGGACGGAGGTACGAGCAGGAGCTTCGCAGTGCAAAAGACGAGTTGGAGAGAAGCCTGAAAGAGTATAAAATCACAGTAGAGAATCTGACCAAAGTCAATGCAGAACTGAAGGCTTTGCAACAGCAGCTTGTACGGGAGCAGGGCCTGGTCCGAGAGGCTAATCAGCGAAATGATTCCCTCTACAAGACTATTGAGGAGAAGAGTCGACTACTAAATGAGAGCACTAGCGAGGTTGAAAAGTTGCAGACCCTCACCCAGAATCTTACCAAAGAGCGCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38306
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 1293 | 2244 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1961074)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1816160 |
GRCz11 | 2 | 2158966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCTTCGCAGTGCAAAAGACGAGTTGGAGAGAAGCCTGAAAGAGTAT[A/T]AAATCACAGTAGAGAATCTGACCAAAGTCAATGCAGAACTGAAGGCTTTG
Long Flanking Sequence:
GTGAGATCACATTGCTGACGCAAAATTTGCAAGACGAGACCAGGCGGAGGAAAGCAATGGAGGTTGAGAATCAAAGCCTCAGACAGTCTCAGGCTGAAATACTAGCCAAGCAGACTTCAACCACAGAGGTCATCAACAAATTAAAGGTCTCTGAGCAAGAGGTTCTCATTATAAAGAGAGAGTTGGATGTACAGAAAAGTGATAAGATGAAGTTGGAGCAGAATGCCACCAGGTTGCAGAGTCGCATAAATGAACTGCAGTCCAAGGTGAACGAGTTGCAGGCTGAACTGGAGAAAGAGAGAAGGAATAATCAGGATGAGCTCACGAGGAGGAAACGCATGGAAACTGAGTTGGATAGGGTAAATCAGACGTGCCGTGAATACACCACTACCATCAGCACTCTGCGGGTCCAACAAGAGAAAGAAAGTTCTTCTGGACGGAGGTACGAGCAGGAGCTTCGCAGTGCAAAAGACGAGTTGGAGAGAAGCCTGAAAGAGTAT[A/T]AAATCACAGTAGAGAATCTGACCAAAGTCAATGCAGAACTGAAGGCTTTGCAACAGCAGCTTGTACGGGAGCAGGGCCTGGTCCGAGAGGCTAATCAGCGAAATGATTCCCTCTACAAGACTATTGAGGAGAAGAGTCGACTACTAAATGAGAGCACTAGCGAGGTTGAAAAGTTGCAGACCCTCACCCAGAATCTTACCAAAGAGCGCCTGCGACTTGAGGAGGAACTAAGGAATGTGCGGCTCGAGCGGGATGATGCTAAAAGAAGTCTGGGCACCATTGAGAGTGAAAGTGCTTCACGATTGTCTGCCATTCAGTTTCAGTTACAAACCAGCAATAACAGAGCAGTGGAACTGCAGGAGCTAATCAATGAACTGACAAAAGAGAGGGAAAGTTTAAGGGTGGAAATCGCCCAAATCCAAAAGCAGTTCTCAGAGGTATTTTATCCTGAGTGACACAAGCAATTTTCTTCTGTATCAGCTGAATCAAAAATACATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19651
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 |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 1882 | 2244 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1963207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1818293 |
GRCz11 | 2 | 2161099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTACCATCGAGAGTTAATCGACTATGACACCTTTCTGGAACTTTCCGAA[C/T]AAGAGTGCGAGTGGGAGGAGATCACGATTGAAACATCTGATGGAAACAAG
Long Flanking Sequence:
AGAAGGCTGTGACGGGATACAAAGATCCTGCAACAGGAAAGATCATCTCACTCTTCCAAGCTATTGAGAAAGAGATCATTGAGAAAGGCCATGGAATCAGACTGCTGGAAGCTCAGATAGCCAGCGGTGGGATTATTGATCCCAAAGGTAGCCATCGAATTGATGTGGAAGTAGCTTACAGGAAGGGTTACTTTGACCGTGAGATGAATGAGATTTTGTCCTATGAAGGGGATGACACCAAAGGTTTCTTTGATCCCAACACCCATGAAAACCTCACATATCTAGAGTTGAAAAAGAGGTGCATTAAAGATCCCAAGACTGGGCTCATGCTTTTGCCTTTAAATGACAAGCAGAAACCAAAGCAGACGACAACCCAGAAGAACACACTACGCAAAAGAAGAGTAGTGATCGTAGACCCTGACACTGGTAAAGAGATGACTGTACGAGAAGCGTACCATCGAGAGTTAATCGACTATGACACCTTTCTGGAACTTTCCGAA[C/T]AAGAGTGCGAGTGGGAGGAGATCACGATTGAAACATCTGATGGAAACAAGCGTTTACTTATTGTCGATCGCAAAACTGGAATCCAGTATGACATTCAGGAGTCCCTACAGAGGGGAATTATCAATAAACAAACTTTGGAAAAGTACCGTGCAGGGACTATGACGCTCACCGAGTTTGCAGCTCTGATCACTAGTAAAAGCAACAGCTCTGAGCTTGCCATCTTCTCCAGCAGTCCTGAGGATGTAGCCACCTGCAGCAGTCCCACACAGCCATCATCCCCAACCGTCCGCAAACGATTTGCAAGTGTTTCCATAACTCTATCCCCTCCATCTGATATTTTTGACGACCAGAGCCCTGTGGGAGCAATATTCGATACGGAGACCCTTGAGAAGATAACCATCCCCGAGGCTCAGCGACGTGGAATAGTGGACAACATCACCGCTCAGCGTCTTCTTGAAGCGCAGGTTTGCTCCGGAGGAATTATCAATCCCGCTACAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39744
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 |
---|---|---|---|---|---|
ENSDART00000029371 | Nonsense | 1918 | 2244 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 1963315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1818401 |
GRCz11 | 2 | 2161207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGTCGATCGCAAAACTGGAATCCAGTATGACATTCAGGAGTCCCTA[C/T]AGAGGGGAATTATCAATAAACAAACTTTGGAAAAGTACCGTGCAGGGACT
Long Flanking Sequence:
AAGCTCAGATAGCCAGCGGTGGGATTATTGATCCCAAAGGTAGCCATCGAATTGATGTGGAAGTAGCTTACAGGAAGGGTTACTTTGACCGTGAGATGAATGAGATTTTGTCCTATGAAGGGGATGACACCAAAGGTTTCTTTGATCCCAACACCCATGAAAACCTCACATATCTAGAGTTGAAAAAGAGGTGCATTAAAGATCCCAAGACTGGGCTCATGCTTTTGCCTTTAAATGACAAGCAGAAACCAAAGCAGACGACAACCCAGAAGAACACACTACGCAAAAGAAGAGTAGTGATCGTAGACCCTGACACTGGTAAAGAGATGACTGTACGAGAAGCGTACCATCGAGAGTTAATCGACTATGACACCTTTCTGGAACTTTCCGAACAAGAGTGCGAGTGGGAGGAGATCACGATTGAAACATCTGATGGAAACAAGCGTTTACTTATTGTCGATCGCAAAACTGGAATCCAGTATGACATTCAGGAGTCCCTA[C/T]AGAGGGGAATTATCAATAAACAAACTTTGGAAAAGTACCGTGCAGGGACTATGACGCTCACCGAGTTTGCAGCTCTGATCACTAGTAAAAGCAACAGCTCTGAGCTTGCCATCTTCTCCAGCAGTCCTGAGGATGTAGCCACCTGCAGCAGTCCCACACAGCCATCATCCCCAACCGTCCGCAAACGATTTGCAAGTGTTTCCATAACTCTATCCCCTCCATCTGATATTTTTGACGACCAGAGCCCTGTGGGAGCAATATTCGATACGGAGACCCTTGAGAAGATAACCATCCCCGAGGCTCAGCGACGTGGAATAGTGGACAACATCACCGCTCAGCGTCTTCTTGAAGCGCAGGTTTGCTCCGGAGGAATTATCAATCCCGCTACAGGCCAGAGACTATCTCTGAAAGACGCCGTACAGCAAAGCCTCATCGATGAAGACATGAGCGTCAAGCTAAAACCAGCGCAGAAGGCTTATGACGGTTTTGAGGATGTGAAG
Associated Phenotype:
Not determined