ZMP
jup
Ensembl ID:
ZFIN ID:
Description:
junction plakoglobin [Source:RefSeq peptide;Acc:NP_571252]
Human Orthologue:
JUP
Human Description:
junction plakoglobin [Source:HGNC Symbol;Acc:6207]
Mouse Orthologues:
AC165274.1, Jup
Mouse Description:
junction plakoglobin Gene [Source:MGI Symbol;Acc:MGI:96650]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12961 | Essential Splice Site | Available for shipment | Available now |
sa31818 | Nonsense | Available for shipment | Available now |
sa14171 | Essential Splice Site | Available for shipment | Available now |
sa12692 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12961
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003891 | Essential Splice Site | 580 | 729 | 12 | 16 |
ENSDART00000081018 | None | None | 390 | None | 11 |
ENSDART00000130644 | Essential Splice Site | None | 390 | 13 | 17 |
The following transcripts of ENSDARG00000070787 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 11894981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11789984 |
GRCz11 | 11 | 11773605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCYATCCGGACATGGTTAGAGTATAAGACATGCTTTCTGTTCGTGCA[G/A]CTGTTGTATTCTCCACTGGATAACRTCAAGCGTGTGGCAGCTGGTGTTCT
Long Flanking Sequence:
CAGATAATCTTTTTTTTTTCATTTTAAAATGAGATTATTTAGCCTGCTTTAAGAAAAAACTCATTTAATTTTGACATACTATTTCCCAAAACAAGTTAATTTTTTTTTTCCTGTCCAGAAAATGCTTGGACTAGAAATGAGACATTATAATCCAAGTTAAAAAAACAAACATTTCTTGCAGTGTAGAGATACTATTTTGTTAGTGAATTATAATAATGACACATTGTTTTTCCACCGTTTTTCAGGATGGGGTAAGAATGGAGGAGATTGTTGAGGGCTGCACTGGTGCTCTTCATATCATGGCCAGAGATCCTATGAACAGAGGCACCATTGCCAGCATGGACACCATTCCTCTGTTTGTTCAGGTAACGTTTACATTTTCTCACTGTTGTGCTATTTTATGACCGTTTTTATGTACACGTCTGTGAGCGGTTTTGTAAATAGTGTTTGTTCTCCATCCGGACATGGTTAGAGTATAAGACATGCTTTCTGTTCGTGCA[G/A]CTGTTGTATTCTCCACTGGATAACGTCAAGCGTGTGGCAGCTGGTGTTCTGTGTGAACTGGCTCTTGATAAACAGTCGGCTGAGATCATCGATGCGGAAGGAGCCAGTGCTCCTCTCATGGAGCTCCTTCACTCCAGCAACGAAGGGATCGGTGAGTGAGAGAGAATCGTCTAAAGCCTAACAGAGCAATTCAAGTTTCAGTTTAAGCATTGTATATACAGTTGAAGTCAAAAAGCCCTCCTGTCAATTTTTGTTTTTATGTTTCCCAAATGATGTTAAACAGAGCAAAGAATTTTTCATAGTATTTCCTATAATATTTTTTTCTTTAGAAGGAAGTCTTATTTGTTTGATTTAGGCTAGAATAAAATCAGTTTTTCATTTTTTTAAAAGTCATTTTAAGGGCAATCGTATTAGTCCCCTTAAGCATTTTTTTTTTCAAATTGTTCACCGAACAAGCCATCATTATACAATGATTAATAATTAACCTAGTTAAGCCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31818
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 |
---|---|---|---|---|---|
ENSDART00000003891 | Nonsense | 620 | 729 | 12 | 16 |
ENSDART00000081018 | None | None | 390 | None | 11 |
ENSDART00000130644 | None | None | 390 | 13 | 17 |
The following transcripts of ENSDARG00000070787 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 11895102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11790105 |
GRCz11 | 11 | 11773726 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGTCGGCTGAGATCATCGATGCGGAAGGAGCCAGTGCTCCTCTCATG[G/T]AGCTCCTTCACTCCAGCAACGAAGGGATCGGTGAGTGAGAGAGAATCGTC
Long Flanking Sequence:
ATGCTTGGACTAGAAATGAGACATTATAATCCAAGTTAAAAAAACAAACATTTCTTGCAGTGTAGAGATACTATTTTGTTAGTGAATTATAATAATGACACATTGTTTTTCCACCGTTTTTCAGGATGGGGTAAGAATGGAGGAGATTGTTGAGGGCTGCACTGGTGCTCTTCATATCATGGCCAGAGATCCTATGAACAGAGGCACCATTGCCAGCATGGACACCATTCCTCTGTTTGTTCAGGTAACGTTTACATTTTCTCACTGTTGTGCTATTTTATGACCGTTTTTATGTACACGTCTGTGAGCGGTTTTGTAAATAGTGTTTGTTCTCCATCCGGACATGGTTAGAGTATAAGACATGCTTTCTGTTCGTGCAGCTGTTGTATTCTCCACTGGATAACGTCAAGCGTGTGGCAGCTGGTGTTCTGTGTGAACTGGCTCTTGATAAACAGTCGGCTGAGATCATCGATGCGGAAGGAGCCAGTGCTCCTCTCATG[G/T]AGCTCCTTCACTCCAGCAACGAAGGGATCGGTGAGTGAGAGAGAATCGTCTAAAGCCTAACAGAGCAATTCAAGTTTCAGTTTAAGCATTGTATATACAGTTGAAGTCAAAAAGCCCTCCTGTCAATTTTTGTTTTTATGTTTCCCAAATGATGTTAAACAGAGCAAAGAATTTTTCATAGTATTTCCTATAATATTTTTTTCTTTAGAAGGAAGTCTTATTTGTTTGATTTAGGCTAGAATAAAATCAGTTTTTCATTTTTTTAAAAGTCATTTTAAGGGCAATCGTATTAGTCCCCTTAAGCATTTTTTTTTTCAAATTGTTCACCGAACAAGCCATCATTATACAATGATTAATAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGCATCTTAAAAACGTCTAGTAAAATATGATCTACTGTCATTATGGCAAAAATAAAAAGAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14171
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003891 | Essential Splice Site | 670 | 729 | None | 16 |
ENSDART00000081018 | None | None | 390 | None | 11 |
ENSDART00000130644 | Essential Splice Site | None | 390 | None | 17 |
The following transcripts of ENSDARG00000070787 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 11896953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11791956 |
GRCz11 | 11 | 11775577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACTCACACACTCACTCTTCAAACAYGACCCTGAGGCTTGGGAAATGG[T/A]GAGTTTGCCCTCTRSTGCTGTGGAGCTGTCATAACAGAAATATGTTAGTG
Long Flanking Sequence:
ATCAATGTCAGACAAAATTGTAATTTTAGTGCATCTTTAAAATTAGTCATATAATTAATTTATGTTTTAAAAATATATTTGATTAAAACTTTGTTTGCACAACCTTTAAAATCTAAAAAGTACAGGAAAAAGCAGAATAAAAGTGACTTGCAGAAGCACTTTGCTTCTGTCAAAAATGTCCTTTTTCCATTTTTCCTGCACTCTTCAGTTGTAATGGTTATGGTCTTGGTTAAAATGTGTAAAAAGATATTTTTGCTCTTAAGATCTGTAGAAAATGCCAGTTTGGATTTTTTTAGTGTTGTGTATGTAGTGTAAAGTATAAAACTATAAACCTTTGAGCTTAAGAGTGTAACAAAGCATCTTTTTTTTCCCTTCAGCCACCTATGCTGCTGCTGTTCTCTACAGAACTGCTGAGGACAAAAACCCAGACTATAAGAAAAGAGTTTCAGTAGAACTCACACACTCACTCTTCAAACACGACCCTGAGGCTTGGGAAATGG[T/A]GAGTTTGCCCTCTGGTGCTGTGGAGCTGTCATAACAGAAATATGTTAGTGTGTTATTTGAATGCAATGTTACGCAAGTCTGAATAAAAATAACTAGACTATTACTTTAAATGTATAACCCATCACAGTTGCATAATGTTACATATTGCCCATGGAAAAGATATTTTGCAAGATAGAAAAAGTTCTTACTTCATTGGTCAAAATTTAATTCCTATCAACTATCATTCACTTCAATATCAAACTTATTTGCTAGGCAGGTAGGTAGGTGGGTATATGGATGGATGGATGGATGGATGAATGGATGGATGGTTGGTAGGTTGTATGGTTGGTTTGTTGGTTGGGTGGGTGGGTGGTAGGTAGGTAGGTAGGTAGGTAAGTAGGTAAGTAAATGAGTAAGTAAGTAAGTAAGTCAGTAATGGAATTTTGACATGGCATTTTCCAGGCCTGAAAAGTTTTGGAAAAGCAGAAAAACCCACAAAGTTTTGGAAAAGTCATGGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12692
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 |
---|---|---|---|---|---|
ENSDART00000003891 | Essential Splice Site | 684 | 729 | None | 16 |
ENSDART00000081018 | None | None | 390 | None | 11 |
ENSDART00000130644 | Essential Splice Site | None | 390 | None | 17 |
The following transcripts of ENSDARG00000070787 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 11898677)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11793680 |
GRCz11 | 11 | 11777301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATTTTAGGCACACAACACTGTGATGGATCCCGTCCTTGGCGATGAAGG[T/G]CAGTAGTGTCCTTATCAAGAATGTTCCATTCAGTTCTCTCCATGTSTGTC
Long Flanking Sequence:
ATTTTTATAGTAATAATGTGTATAAACCCGATGGATGGATGGATGGATGGATGGATGGATGGAAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAAATAGATAGATAGATTACAAGTAACACCAACTTTATGCTTGCAAAATTAAAACTGTATTAAATCTTTCTTTATCATAAGCACTAAATATAACATGTAATTGTGATATTGTGCTTGAAATTAGCCAAAAATGCTGAATATTTATACTTTTAAGAATTAAAATTTCCAAAAAAAAAAAGCCAAATGGTAACAGCACAATGGCATAAATCTCAACACACATGCTAATTTATCAAAGAAACCTGTACATGGACTACAGGTATTGACCGTTTTCTTGTTACATTTTAGGCACACAACACTGTGATGGATCCCGTCCTTGGCGATGAAGG[T/G]CAGTAGTGTCCTTATCAAGAATGTTCCATTCAGTTCTCTCCATGTCTGTCACTTAACAGTCTGAAATGCATTGCTCACTCTGCAGAGATCAGATCATTGTACAGACAGCTAACATTTTGATATTTATTTTGTCTTTTGCGATACAGAGCTTGATGGCTACGGTCCTGCAGGATACGGTGGATATGCTGATGGCATGCATATGGATCCTCTAGATCCAGAAATGCAAGACGATTATAGGGGCGGCATGCCCTACAACTCCATGGCCAGAGTCTACCATGATTACTAACAGGTTAGTTTAACTCTTTATACCTTATTCACACGTGGTATTACCATTTCATTTTTGTTGATCTGATCACAAGTGGACAAAACAAGTCACATCACTGTTCATTTAAAGGTTCTGTGAAATTAAAAGAAAGTTTTTAAGATTTTACAATCAGTATGCTAGCTTAAATGATGTCTGTGAGCTAGTGTGCTCCAAAACTGTGACAATTTGCGTTTAG
Associated Phenotype:
Not determined