ZMP
dopey2
Ensembl ID:
ZFIN ID:
Human Orthologue:
DOPEY2
Human Description:
dopey family member 2 [Source:HGNC Symbol;Acc:1291]
Mouse Orthologue:
Dopey2
Mouse Description:
dopey family member 2 Gene [Source:MGI Symbol;Acc:MGI:1917278]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16432 | Essential Splice Site | Available for shipment | Available now |
sa21523 | Nonsense | Available for shipment | Available now |
sa13946 | Nonsense | Available for shipment | Available now |
sa17692 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16432
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078256 | Essential Splice Site | 302 | 2260 | 7 | 41 |
ENSDART00000131910 | None | None | 1485 | None | 23 |
ENSDART00000132465 | Essential Splice Site | 302 | 542 | 8 | 13 |
The following transcripts of ENSDARG00000055857 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34198219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33354165 |
GRCz11 | 9 | 33164911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGCAATATTAAGGAATTCATYTTTATTTTATTTGTGTGTGACTTGTCA[G/T]GCTTGGACATTAAAGGAGGAAYGGGGGCTGCAGACTCCAGTCACTACAGC
Long Flanking Sequence:
TGTACACCTTCTTATCTTGCTCTGCTCCAGGTGAAAGCTGTTTGTCTTGCTTTACAAGACTCTAATGTTCTGGTCCAGAGGAACACGCTGGAAATTCTTCTCTACTTCTTCCCCTTCACGACCTTCCAGGTTATACCTTTAATTCCTGTCTTCGCTGCCAATTACATTTGAGTAAATCCTAGACCTGCCCCAAATTGAATAGTCTGTTTAAATGATCCTGTGTGTAGGATCCTGGCGAGTGTGCAATTCCATTAAAACAAGATGAGATGATCAGTGTTGTGTCTGCTGCCTCGCTCACACTGCTCAGGAGAGACATGTCTCTCAACCGCCGCCTCTATGCATGGATGCTTGGTATTAAAGATTTGTGTTCAGAACATTACAGAAATATAAATATATTTATTTTTTAATTGTATGGAAATGAAAGTTGTAATATACATTTAAACACATGTTTGAGCAATATTAAGGAATTCATCTTTATTTTATTTGTGTGTGACTTGTCA[G/T]GCTTGGACATTAAAGGAGGAATGGGGGCTGCAGACTCCAGTCACTACAGCACTGTGGAGGAATACACTGCATTCTACTTCAATACACACTCCAGAGAATTATTGGTGCAGGTGTGGATGATAACACTCACTCTAAGTCACATTACATCATATAACATCTTATTCAATGGCAAAGTAGAGCTTTGCATTTAGAAATGCAGGTGTTGCATTTAACATGTTCCCTATATAGGGATTTCCCAAACTGGAGTTCAGATTTTTTTGTGTATCCCTGGAAGAACTGCAGCTTGTTCATAAGTTAATGAAGTGCTAATAATTATTACGTTTAAATATAAGTTGTAAAGGGATAGTTTATCCAAAAAATGAAAATTTCCCAACCATTAGCTTACTCAAGTGTTTATAAACTGTTGTGAATTTCATTCTTCTGCTGAACATAAAACAAAATATTCAAAATAAATCATTCATTGACGTTGTCTTTAGTAGGAACAACAATATTATTAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21523
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 |
---|---|---|---|---|---|
ENSDART00000078256 | Nonsense | 663 | 2260 | 14 | 41 |
ENSDART00000131910 | None | None | 1485 | None | 23 |
ENSDART00000132465 | None | None | 542 | None | 13 |
The following transcripts of ENSDARG00000055857 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34206437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33362383 |
GRCz11 | 9 | 33173129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAGATATAGTGGATCCAGAGAAGAAGAAGAAACAGGAAGAAGCAAAT[C/T]AGCTTGATGCTAATGCGTCTCCTAAAAGCAGCAAGCGGTCTCCACTAAAA
Long Flanking Sequence:
TACAGTATGCATCTGCAAACCATTTGTTATATTTAAAATGGTTCCTACTTTGACTTCTAAATAATTGGTGATTTAGTGTAGAATTATTAATGTACACATGATTGGCATAATTTGGCATAAAATGCACATTTATAATTGTTTTTTTTTCAATCTTTCATTAACTGACAACTGTTTTTAGTCTGTCTTTCTGGGTTTTCAATTAGTCTTATTTATATAATCATGTTATATTAATTTTGGCCTATTTTTACTCTTCTGTTATATTTTAAGCATTTTAAATTACCTTAAGGCCCCTAGAGGACCAGGACCCCTTGTTTTAAATGCTACTTTAGGCTATCTACTAGTATTCTTCTCTTGCCCTGAAACTAGCAGTATGCATACTCACTATATTTGCTTTCTCTTTTTCTATATCTGTGTCTTATTTGCATTCACTTCTTGTATCTTGCAGACATTTGTTAGATATAGTGGATCCAGAGAAGAAGAAGAAACAGGAAGAAGCAAAT[C/T]AGCTTGATGCTAATGCGTCTCCTAAAAGCAGCAAGCGGTCTCCACTAAAACGGAAAGGCAGCCGAGACCTGGGTTTGATCAAAGACAGGCTTGCAGAGTTTTTCAACCCCAGTAAACTGAGGATTCATGCCCTTCACGGGTTATCTAGAGATGGGGGTAAAGACCACAGACCAGCACAGCTGGAGTGGATGGGAAGTTTTCAGTCAAAGAGCAAAGGGGAGATATCAGAGTCATGCCGTCAGGCCTTTACTGTGATCTGCCAGCTTCTTCTGGAGTGTACAACGTTTCCTGTCTATTTCACTGAGGAAGAAAATCAAGAGCTGCACACATCCATGTTCAACAAGACAGGTATGTAAAGGAACTGTATTGCACTGTGTTAAATAGTGCTTTCTTGTGGATGTGTTCTCTTAGGCACTCATTTTTTTCTCTCATCAGGGATTGAGGGAACTCTTCCTGACTGGCTGAGGTCTTTGATGACTCTGTGTTGCTTAACTAAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13946
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078256 | Nonsense | 798 | 2260 | 15 | 41 |
ENSDART00000131910 | None | None | 1485 | None | 23 |
ENSDART00000132465 | None | None | 542 | None | 13 |
The following transcripts of ENSDARG00000055857 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34206927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33362873 |
GRCz11 | 9 | 33173619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGGAACTCTTCCTGACTGGCTGAGGTCTTTGATGACTCWGTGTTGCT[T/G]RACTAAAGACTACCAGGTACCAGTTCACAAGCACTCAAAATGTAAAYATT
Long Flanking Sequence:
AGAAGCAAATCAGCTTGATGCTAATGCGTCTCCTAAAAGCAGCAAGCGGTCTCCACTAAAACGGAAAGGCAGCCGAGACCTGGGTTTGATCAAAGACAGGCTTGCAGAGTTTTTCAACCCCAGTAAACTGAGGATTCATGCCCTTCACGGGTTATCTAGAGATGGGGGTAAAGACCACAGACCAGCACAGCTGGAGTGGATGGGAAGTTTTCAGTCAAAGAGCAAAGGGGAGATATCAGAGTCATGCCGTCAGGCCTTTACTGTGATCTGCCAGCTTCTTCTGGAGTGTACAACGTTTCCTGTCTATTTCACTGAGGAAGAAAATCAAGAGCTGCACACATCCATGTTCAACAAGACAGGTATGTAAAGGAACTGTATTGCACTGTGTTAAATAGTGCTTTCTTGTGGATGTGTTCTCTTAGGCACTCATTTTTTTCTCTCATCAGGGATTGAGGGAACTCTTCCTGACTGGCTGAGGTCTTTGATGACTCTGTGTTGCT[T/G]AACTAAAGACTACCAGGTACCAGTTCACAAGCACTCAAAATGTAAATATTTAATTCTAATAGTGGTGTCTACTGTCTTAATATATAAGAAAGACTAATTTCCTTTCTTATTAATGGTAAATGAATATAGTATATGATATGATATGTTATGATATGATATGATATGATATGATATGATATGATATGATATGATATGATATGATATAGAAAAAACAAACTTTGAGTCCTGCTTTACTATTTAACAGTATTCTCCAAATTCATACAGGATAGGAATAGTTTGATTGCGCATTCATTTACACCATTTAGGAGTGTCAAACTATCAATGGCTTTATTAGAGTTGCCTTTGCACAGTGATTTGGGATAGGACAAATGATATTGACATAGAAAAATGACTTTTCCCTAATCTAAGTCCTTTTCAAACACATTTTCTTTTACATTTTTGTAGGTCCAACATACTGCCATCTCCTCTTTGCTAGAGATGATCAACCACTCTCAGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17692
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 |
---|---|---|---|---|---|
ENSDART00000078256 | Nonsense | 2018 | 2260 | 36 | 41 |
ENSDART00000131910 | Nonsense | 1243 | 1485 | 18 | 23 |
ENSDART00000132465 | None | None | 542 | None | 13 |
The following transcripts of ENSDARG00000055857 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34220640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33376586 |
GRCz11 | 9 | 33187332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGACAGGCTTTTGCCATGTTTAGYGGAGAAAATGACCAGTACCACTTCTA[T/A]TTGCCTCTMATTCAAGGTATCACTCAGTTTGTRTGGAAAACAAATACAAT
Long Flanking Sequence:
CTGTTCAAATTTTACATTAAAAACTATTAGGCTAAGTGGCAAACACGAACTGGCTAGCACATTCATCTTTCCCCAGTCACGCCGAAGCAATAGCCCGCACAGGATTCCGCTTGGTCTTAAATCCTTTTTCAATGGGTTATTTTCACAATTTATTATGGCATAGCAGTCAAAATAGGACAAATGAGCTTGTGTATGGGAACAATTCTTAAGCTTTTTCAGTGAGGGGTGGGTACAAAAACATTGCGCAATGATGACAAAATTCAAACTATTCAAAATATGTGGACTCTCATGTATGCATAAAACTGGGGTATCTTTTGGGCTTTTACTGTCATTTGTTGTATGATCAATGCATTACATGGATTGTGTGGGTTCATGTTGTAATACGCAGGTATGCAGAGCAGTTCTTTAAAACTCTTCAACAGCGCTGAGCAGAAGCCCATGTTACTGAAACGACAGGCTTTTGCCATGTTTAGTGGAGAAAATGACCAGTACCACTTCTA[T/A]TTGCCTCTAATTCAAGGTATCACTCAGTTTGTGTGGAAAACAAATACAATTGTCATAGAATATGAAAATATGTAGCTAATTCCTTTTTTTAACATATATTGTAGAGCGTCTGACAGAGAACCTGCGTGTAGGACAGAGCCCATCAGTGTCAGCTCAGATGTTTCTCATGTTTCGTGTTCTCCTTTTGAGGATCTCACCACAACATCTCACCTCCCTCTGGCCAATCATGGTGACTGAGCTGGTAAGAAATAAACCCACAGTCCTCTTTTGATTTTTTGTAGTGCTCTGTGCAACATGAGTAATTAAAAAAACAAATGTAATTTGTTTACAGTGATTTAGAATGCTGAAGTTAAAGATCCTTTTTTTTAGCAGTGCTTCTGCCAGTTATTCTGCTTAGAGATGTGTGTTCTGTGTCAGCCAGTCTGATAAAAAAGCAGACCCTAGTTTGCCAGTTGGCAGAAAACTGTGTATTTTTCCAACAGCAAACAAACTGGGGTGAA
Associated Phenotype:
Not determined