ZMP
ENSDARG00000039665
Ensembl ID:
Human Orthologues:
DSG1, DSG2, DSG3, DSG4
Human Descriptions:
desmoglein 1 [Source:HGNC Symbol;Acc:3048]
desmoglein 2 [Source:HGNC Symbol;Acc:3049]
desmoglein 3 [Source:HGNC Symbol;Acc:3050]
desmoglein 4 [Source:HGNC Symbol;Acc:21307]
desmoglein 2 [Source:HGNC Symbol;Acc:3049]
desmoglein 3 [Source:HGNC Symbol;Acc:3050]
desmoglein 4 [Source:HGNC Symbol;Acc:21307]
Mouse Orthologues:
Dsg1a, Dsg1b, Dsg1c, Dsg2, Dsg3, Dsg4
Mouse Descriptions:
desmoglein 1 alpha Gene [Source:MGI Symbol;Acc:MGI:94930]
desmoglein 1 beta Gene [Source:MGI Symbol;Acc:MGI:2664357]
desmoglein 1 gamma Gene [Source:MGI Symbol;Acc:MGI:2664358]
desmoglein 2 Gene [Source:MGI Symbol;Acc:MGI:1196466]
desmoglein 3 Gene [Source:MGI Symbol;Acc:MGI:99499]
desmoglein 4 Gene [Source:MGI Symbol;Acc:MGI:2661061]
desmoglein 1 beta Gene [Source:MGI Symbol;Acc:MGI:2664357]
desmoglein 1 gamma Gene [Source:MGI Symbol;Acc:MGI:2664358]
desmoglein 2 Gene [Source:MGI Symbol;Acc:MGI:1196466]
desmoglein 3 Gene [Source:MGI Symbol;Acc:MGI:99499]
desmoglein 4 Gene [Source:MGI Symbol;Acc:MGI:2661061]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa3086 | Nonsense | F2 line generated | Not yet available |
sa23638 | Nonsense | Available for shipment | Available now |
sa32274 | Essential Splice Site | Available for shipment | Available now |
sa45688 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16750 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa3086
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057981 | Nonsense | 130 | 1418 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 7540134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7374693 |
GRCz11 | 20 | 7364572 |
KASP Assay ID:
554-3322.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCAGGAATAAACGAGCGCCCTGTTGGTTGCTTCATGGTAGAAGAGTAC[A/T]AAGGATTAGTTCGCATCATACAGCCTCTGGATCGTGAAGAGAGGAATAAC
Long Flanking Sequence:
CTTTTTCCATGCCTGCATAAATAATCACAAATTACAAGCAAAAATAAATAAATAAACTGTGATATATGGTTTTCCAGGGAGTCTAACCAGTACTCAAGTACAGACATTGAACAATCAAAAGAAACATAACTTGATCATTATTGTATAAATATTAAAAACAAAAATTATCACGACTTAATATTATCTTTATATTTTAATCTCTAATAAATAATCTAATCCTTGCGATGTGACTATTGCAGATACAAACATTGCAATATCAATGCTTAAACTTTATATTGTTTAGCCCTATCAGTGTGTTGTCTGATTTCAATAGTTATCTGTGATTTAGAACTGGCCATCTTTTACATTTATCTGTGGTTCCAGCAATCTAACCAGGATTACTGCTCTGTCAACTTCTTCAGATACGCTCAGACATGGACGATAAAGTGGCATTACGCTACACGCTAAGGGGTCCAGGAATAAACGAGCGCCCTGTTGGTTGCTTCATGGTAGAAGAGTAC[A/T]AAGGATTAGTTCGCATCATACAGCCTCTGGATCGTGAAGAGAGGAATAACTACACTGTAAGTATAACAAACACACATATTTAGGATACAAAGCATTCAAACAGCACACTGTGGCATGTCCTATGGTAGACCACAACTGTAGTCACCTCATTAACTTTGAAGGTTTTGAGAAACACTTGCCTTTCTGACTTTGGAGGCAGTCTGAACACCAAGACACCACATACAACTGAGTTAGGACAAACCTCTTGAAGCAGTGTAATGGGTTTATCATATCCAATAAACTAGAGAGAGCACATAAAAATATAATAAATATGAATTAAATAAAGTACAATTTATTCATGACCAGTGAATTTTAATGTTTAAAAGTTTAACAAAGTCAGGTATGAGCTACCTGGACTTATTTAGCTATTATATGAATTTATTTACATGCATACTAATATTTTTTACAATTTATTGTTACAAACAACCAAGTCCTGAATTCTATAATGAATTTGAAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23638
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057981 | Nonsense | 328 | 1418 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 7547764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7382035 |
GRCz11 | 20 | 7371914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTGAGGATCCAGGCACTGGATATTGATGAAGTACAAACAGACAATTG[G/A]TTGGCTGAGTTCACAATTGTGACAGGGAACGAAGATGGACATTTCAGTAT
Long Flanking Sequence:
TTTAAGACATTTAAAACTTTTTAAGACCCAGCAGACACCCTGGTCACTAAAGAGTTTATGTTTGAAATTTTTGACACTCTCAACAAAAGTCTATGGGATTTTATAGCTTTATTAAGTCAACAAACATTATGAAATTATATACAGAGTTAACCTACTTAAACTGATCAAAAAAACAGTCAAATGTTAAAACGTATAAAAATCATCAAGCATTCAAATCAAACTAATCGCATGTAATATTAGTATTTAAACTAAATACATTTTCATCATTAGTAGCATGAGGTTGCGTGAAACATAACTTTTAATTTTCTTTTAAAGGGAAAGTTCGCTCAAAAATTTAATTTGCATGAGTATATATGCATACTTCACATAATCATACTTCATAAGTGCAGACACCTATTGTTGGTTTTATAGTTTTCAGTAAGTATCGATGAGAATGAGGCACCTATCGAGGTTTTGAGGATCCAGGCACTGGATATTGATGAAGTACAAACAGACAATTG[G/A]TTGGCTGAGTTCACAATTGTGACAGGGAACGAAGATGGACATTTCAGTATTAAGACTGATCCAAGGACTAATATGGGGGTTTTGTACCTGAACAAGGTCAGAGCTTATTTTGTATACAGTTCTGAGAACTGCTGTAATATTTGTGTCTTTTAATTTGTATTTTTGTAATGGGGTTTGCAAAAAGTAAGTAAATGTATCTTGATCTTTTCTCAGCCTGTTGACTATGAGTCAGCATCTAATCTGGACCTAAGCCTCGTTGTTGCAAACAGAGCTCCTCCAGGAGCTCCTCTGGGGAATGGAGTAGGGGCAGGTAGTGCAGCTGGAGCTTCTGGAGCTGGTGGTCAATCTGGAGTTGGTGGTCAGTCTGGATCTTTTGGAGCTGGTGGTCAATCTGGATCTTCTGGAACTGGTGGTCAAGCTGGTGCTACTGGAGCTGGTGGTCAGTCTGGATCTTCTGGAGCCAGCGGTCAATCTGGAGCCTCTGGGGCAGGTTCTCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32274
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 |
---|---|---|---|---|---|
ENSDART00000057981 | Essential Splice Site | 360 | 1418 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 7547862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7382133 |
GRCz11 | 20 | 7372012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAAGACTGATCCAAGGACTAATATGGGGGTTTTGTACCTGAACAAGG[T/C]CAGAGCTTATTTTGTATACAGTTCTGAGAACTGCTGTAATATTTGTGTCT
Long Flanking Sequence:
TTTTATAGCTTTATTAAGTCAACAAACATTATGAAATTATATACAGAGTTAACCTACTTAAACTGATCAAAAAAACAGTCAAATGTTAAAACGTATAAAAATCATCAAGCATTCAAATCAAACTAATCGCATGTAATATTAGTATTTAAACTAAATACATTTTCATCATTAGTAGCATGAGGTTGCGTGAAACATAACTTTTAATTTTCTTTTAAAGGGAAAGTTCGCTCAAAAATTTAATTTGCATGAGTATATATGCATACTTCACATAATCATACTTCATAAGTGCAGACACCTATTGTTGGTTTTATAGTTTTCAGTAAGTATCGATGAGAATGAGGCACCTATCGAGGTTTTGAGGATCCAGGCACTGGATATTGATGAAGTACAAACAGACAATTGGTTGGCTGAGTTCACAATTGTGACAGGGAACGAAGATGGACATTTCAGTATTAAGACTGATCCAAGGACTAATATGGGGGTTTTGTACCTGAACAAGG[T/C]CAGAGCTTATTTTGTATACAGTTCTGAGAACTGCTGTAATATTTGTGTCTTTTAATTTGTATTTTTGTAATGGGGTTTGCAAAAAGTAAGTAAATGTATCTTGATCTTTTCTCAGCCTGTTGACTATGAGTCAGCATCTAATCTGGACCTAAGCCTCGTTGTTGCAAACAGAGCTCCTCCAGGAGCTCCTCTGGGGAATGGAGTAGGGGCAGGTAGTGCAGCTGGAGCTTCTGGAGCTGGTGGTCAATCTGGAGTTGGTGGTCAGTCTGGATCTTTTGGAGCTGGTGGTCAATCTGGATCTTCTGGAACTGGTGGTCAAGCTGGTGCTACTGGAGCTGGTGGTCAGTCTGGATCTTCTGGAGCCAGCGGTCAATCTGGAGCCTCTGGGGCAGGTTCTCAATTGATGCCTTTTGGAGGAAGCAGTAACCCAGGCTTCAATGTGTCCAAGCTAAAGTCATATTTAGTTAAGGTCAATGTAAAAAACAAACCAGATGCCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45688
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 |
---|---|---|---|---|---|
ENSDART00000057981 | Nonsense | 442 | 1418 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 7548221)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7382492 |
GRCz11 | 20 | 7372371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTGGTCAAGCTGGTGCTACTGGAGCTGGTGGTCAGTCTGGATCTTCT[G/T]GAGCCAGCGGTCAATCTGGAGCCTCTGGGGCAGGTTCTCAATTGATGCCT
Long Flanking Sequence:
GGATCCAGGCACTGGATATTGATGAAGTACAAACAGACAATTGGTTGGCTGAGTTCACAATTGTGACAGGGAACGAAGATGGACATTTCAGTATTAAGACTGATCCAAGGACTAATATGGGGGTTTTGTACCTGAACAAGGTCAGAGCTTATTTTGTATACAGTTCTGAGAACTGCTGTAATATTTGTGTCTTTTAATTTGTATTTTTGTAATGGGGTTTGCAAAAAGTAAGTAAATGTATCTTGATCTTTTCTCAGCCTGTTGACTATGAGTCAGCATCTAATCTGGACCTAAGCCTCGTTGTTGCAAACAGAGCTCCTCCAGGAGCTCCTCTGGGGAATGGAGTAGGGGCAGGTAGTGCAGCTGGAGCTTCTGGAGCTGGTGGTCAATCTGGAGTTGGTGGTCAGTCTGGATCTTTTGGAGCTGGTGGTCAATCTGGATCTTCTGGAACTGGTGGTCAAGCTGGTGCTACTGGAGCTGGTGGTCAGTCTGGATCTTCT[G/T]GAGCCAGCGGTCAATCTGGAGCCTCTGGGGCAGGTTCTCAATTGATGCCTTTTGGAGGAAGCAGTAACCCAGGCTTCAATGTGTCCAAGCTAAAGTCATATTTAGTTAAGGTCAATGTAAAAAACAAACCAGATGCCCCTAAGTTCATGCCAAAGGTCAAGCCTATATCTATATCTGAGAACAAAAAAAATTCCATTCCAAGAGTAATTGATACCTACACTGCTACAGAAGAAGACACAGGCAGACCTGCAGAAAATGTGAAGTAGGTGTTCTCTTCGTCTTAATAAATCAATTTGAAAATTTTAAATTCAAAATGAGGTACATTAAAACAATTCAATAAGCCATCTGTGTCAATGATATTACGCTTATAATACATTTTTTACCTGCATAACTTAAAATTCTAAATTTCTAAACAAAATGAGGATTTAAAAATTGCATTTCAATAACAGTCCAGTTTTGTTTAGATATGCAAAGGGATACGACCCTGACAACTGGATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16750
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057981 | Nonsense | 695 | 1418 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 7549853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7384124 |
GRCz11 | 20 | 7374003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGCCTGCCCCACAGAGCAASTCCTCAATTTAGAGGTTTGCACATGCT[C/A]AGAAGGGGTGGGTTGTGGTTCAAAAATTGSAGAAGTTCATACAAGTTCAT
Long Flanking Sequence:
GAGGATCTGAATGATAACTGCCCCATACTCCTTAATAATATGCAGATTGTCTGCAGTCATACCAAAGTAGTGAATGTCACAGCTGAAGATATAGATTCCGATCCCAATGGAACTCCATTGGAGTTCAGTTTAATACAAGAGAAGACTAGGGGCAAATGGAACTTGCAGAGAATAAATGGTAACAGCACACACAACAACAAGCTAACCTTATCAATCATACTGTAATCTAATATTTATCAAAAGTTTTACATAGTTTATTTTCAATGGTTAGAACTATTAAAAAAAATACACAGCACAAACAATTAGTAGATATTGCTTGTTCACCTTTGAGTAGGAAGTAACCTCATAGTCAGGTCTCTGCTTCTCAGATGTAAGTGCTTCACTGCTTGCTGAAGATGACTTATGGCCTGGGTTTTACCAAATCACCATGGAAATCAGAGACAAGCAAGGGCTGGCCTGCCCCACAGAGCAAGTCCTCAATTTAGAGGTTTGCACATGCT[C/A]AGAAGGGGTGGGTTGTGGTTCAAAAATTGGAGAAGTTCATACAAGTTCATCAGCAAATTTTGGATTACCAGGGATTGGTTTCCTGGTATTAGGATTCCTCTCCCTTATATGTGAGTATGATGACTAAAGTTCACGAGCAAATTTGGTCTGCAACTTTTTTTGTGGTAGCACTAAAAATAAGTCACACATTTAACATGCATTTGACTGTCTTTACATTTAGTGATGCTCTTGTTCTTGATAAAATGTGAATGTGGAAGCACTGGAAATAAGTTTATTGACTTGCCATTTGAATCCAAGCAACACCTCATCTCCTACAGCACAGAGACAAGAGAAGAACACAGGGTAAAATAATCTCACACATCTCATAATTGCCTTCAGATATTTTGACAATATGAAAGCATGTGATAATTCATTTTGTTCTCCAGGGTGTCCCTCTGATGTGGCCCCCACCAAACCTTGACAATAAAGGGGGCTGTGAAATGTCCAATGGACATTTAAGA
Associated Phenotype:
Not determined