ZMP
si:dkeyp-118h9.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
DIP2A
Human Description:
DIP2 disco-interacting protein 2 homolog A (Drosophila) [Source:HGNC Symbol;Acc:17217]
Mouse Orthologue:
Dip2a
Mouse Description:
DIP2 disco-interacting protein 2 homolog A (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2385920]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31693 | Nonsense | Available for shipment | Available now |
sa27310 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14344 | Nonsense | Available for shipment | Available now |
sa2496 | Nonsense | F2 line generated | Not yet available |
sa11374 | Essential Splice Site | Available for shipment | Available now |
sa13406 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31693
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 |
---|---|---|---|---|---|
ENSDART00000115030 | Nonsense | 45 | 1578 | 2 | 38 |
ENSDART00000139436 | None | None | 1411 | 2 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 622117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 636845 |
GRCz11 | 9 | 636478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTTTTAATTCTCTCTCTCTCTCTCTCTTTATAGGTGACATCACGCAG[A/T]AAGGCTATGAGAAGAAAAGAGGGAAATTACTGGCGCCCTACATTCCCCAG
Long Flanking Sequence:
AGATATTAATGTAAGCTTTACATGAGGGTTACGTCTCAGTTATTGGTAACACTTTAGTGTAAGTCACAATTCACAGTGTTAACAAACCATTAACTAACACCACTAGCTGTTTATTAATAGGAAGTGAGGTAGAAGTCGGGTTTAGGTGTTGGGTTAGATTAGGGATGCAGACTGAACAGGTCATGTCTTAATAACAGGCAGGTACTCAGCCAGTGTGAATAGCAGGAGCTGTGAGCGGAAGTAGTGTCATCCTTTGTTTTGTGTCGTGGAGTCAGCCAAATTCTGCAATTCATATCAGTCGTCTTCTCAAAGTGTTGTTGATTTCAACTTTCTCAGTGTTTGGTGTTGCTGAAGAGCTTTATTTTCAGCTGTTGAGGGAGATTTGGTGTTTTCTGTATAACTCTCTCTGTAATGGGGTATCGGCTGCATAATTATGGAATTAATTGATAATCATTTTTAATTCTCTCTCTCTCTCTCTCTTTATAGGTGACATCACGCAG[A/T]AAGGCTATGAGAAGAAAAGAGGGAAATTACTGGCGCCCTACATTCCCCAGATACAAGGTAAAGCACTGAAGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACCGACACACAGACACACACATTGATTTCAGCACACAGGGTTATAAACTGCAGTTTGCCTGCGCTGGCACTGATCTGAGAACTGTGCACAGTTTGGCTTGTGTCAAGAAGACCGTCAGCTAATGGAAACAGTGTGAGTGTGTGTGTGTGTGTGCTTGTGTGTGAGTGTGTGTGTGTCTGTGGTGAACATGACTTATCCAGACTGTAAAACTACAAGCTAAGTGCAGGTTCAGACTACCGCAAACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCTGTTTGCGCTCGCTGTCTAGCCACTGCTCATATATCCACATATTTCACATGCAGAACTGACTGTTATTTATAAATGCTCATCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27310
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115030 | Essential Splice Site | 1059 | 1578 | 26 | 38 |
ENSDART00000139436 | Essential Splice Site | 892 | 1411 | 25 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 584294)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 599649 |
GRCz11 | 9 | 599282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGACGACTGAACGCTGGAGATCACGTAGCACTGCTGTATCCTCCTGG[T/C]GAGAGAGAAATATATGAGTGTGCTCTGATCAATAAAATAGGGCTATGACA
Long Flanking Sequence:
TGTTAGCTGCTTGAATCAGCACACGCCTGCTCTCTAAAATAACATGACAAGTGTCTTTCACAATGAAAGGGCGTCCGCTGCGGAAAACATGTGCTAGATAAGTTGGTGGTTCATTCCGCTGTGTCGACCCCAAATTAATAAAGGGACCAAGCCGAAAAGAAAATGAATGAATGAAGACAACTCTTTAAGGTCATGCAGCTGGTGCGCAGACAGTTTTTCCCATCCTTAATATAGCAAAAGTGCATTCAGACATGTCCTTTTGCTCCATGCATTTTAGACTTTGCGCCTAGACTGTTAACATAGAGCCCTTTCAGTGGACAGGGTGTGTGTTTCTGTCCTCTCACCGTGTGTGTGTGTGTGTGTGTGTCTCTGCAGGGCACTGTGGTCAACACTGCGTCCTGTGTGCAGCTGCACAAGCGTGCGGAGCGTGTGGCGTTAGCGCTGATGGAGAGAGGACGACTGAACGCTGGAGATCACGTAGCACTGCTGTATCCTCCTGG[T/C]GAGAGAGAAATATATGAGTGTGCTCTGATCAATAAAATAGGGCTATGACAAGATCTGACTGGTCATTTCGGGGTAATGATGTCAGAATTGACCAGTATTGTGTACTGGATGTGTGAATGGTGCTTTTGCAGGAAAACTCCGGGACGCTGTTGCCTGTGTGAACAATGTATATTTGATTGCTGGTTAAATCGACTGCTAAAGTCATCCTGGCTGTCCTTTACACATACTACAATTTATTAAAACAGTTTTTAAATGTACACATGCATTCGGTGGACTTTTGAAGTGCCATGCACGTAAGCACGGTGTTTTTCAGACACAGTTTAAAGATCATCACTGATACTGCTCATCACTGTCAGTAGAGCTTGGAGGCAGGACAACCGTTGCAAGTTCCTATCTCAGTGGCTGTGTCCAGATACATGTTTTGTCACTCCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTTTGACCTGTGCAGGTATTGATCTGATCGCCACGTTTTACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14344
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 |
---|---|---|---|---|---|
ENSDART00000115030 | Nonsense | 1069 | 1578 | 27 | 38 |
ENSDART00000139436 | Nonsense | 902 | 1411 | 26 | 37 |
ENSDART00000115030 | Nonsense | 1069 | 1578 | 27 | 38 |
ENSDART00000139436 | Nonsense | 902 | 1411 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 583789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 599156 |
GRCz11 | 9 | 598789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNGTGTNNNNTTGACCTKTGCAGGYATTGAWCTGATCGCCACGTTTTAYGRCTG[T/A]CTGYACGCYGGCTGTGTTCCCGTCACCGTCAGACCCCCACACCCGCAGAA
Long Flanking Sequence:
GAGAAATATATGAGTGTGCTCTGATCAATAAAATAGGGCTATGACAAGATCTGACTGGTCATTTCGGGGTAATGATGTCAGAATTGACCAGTATTGTGTACTGGATGTGTGAATGGTGCTTTTGCAGGAAAACTCCGGGACGCTGTTGCCTGTGTGAACAATGTATATTTGATTGCTGGTTAAATCGACTGCTAAAGTCATCCTGGCTGTCCTTTACACATACTACAATTTATTAAAACAGTTTTTAAATGTACACATGCATTCGGTGGACTTTTGAAGTGCCATGCACGTAAGCACGGTGTTTTTCAGACACAGTTTAAAGATCATCACTGATACTGCTCATCACTGTCAGTAGAGCTTGGAGGCAGGACAACCGTTGCAAGTTCCTATCTCAGTGGCTGTGTCCAGATACATGTTTTGTCACTCCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTTTGACCTGTGCAGGTATTGATCTGATCGCCACGTTTTACGGCTG[T/A]CTGTACGCCGGCTGTGTTCCCGTCACCGTCAGACCCCCACACCCGCAGAACCTGACCACAACCCTGCCCACCGTCAAGATGATTGTTGAGGTGACCCCAAACACACTTACTCACACAATCTGGAGGAATAAATACTGCTGTGGAGAAACTGTCAAGAGCAGTTCTGAAATATATCATATCGTGTATCATATCAAATATTCAATAATTTCACATATCATATCACATATATCAAATATCATATCATATCAAATCAAATACAAAATCATATCACATATCATATCATATATCATACATCACACATCATGTCATATATCATATCAAATATTAAATCATATATCAAATATCAAATATTATATATCATATGTCAAACATCATATCACATATCATATAAGATATTAAATCCTATCACATATATAAAATATCATATCATATATCATATCAAATCAAATACAAAATCATATCACATATATCAAATATTATATATCATATATCAAACATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2496
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 |
---|---|---|---|---|---|
ENSDART00000115030 | Nonsense | 1069 | 1578 | 27 | 38 |
ENSDART00000139436 | Nonsense | 902 | 1411 | 26 | 37 |
ENSDART00000115030 | Nonsense | 1069 | 1578 | 27 | 38 |
ENSDART00000139436 | Nonsense | 902 | 1411 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 583789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 599156 |
GRCz11 | 9 | 598789 |
KASP Assay ID:
554-2823.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTGTTTGACCTGTGCAGGYATTGATCTGATCGCCACGTTTTAYGGCTG[T/A]CTGTACGCYGGCTGTGTTCCCGTCACCGTCAGACCCCCACACCCGCAGAA
Long Flanking Sequence:
GAGAAATATATGAGTGTGCTCTGATCAATAAAATAGGGCTATGACAAGATCTGACTGGTCATTTCGGGGTAATGATGTCAGAATTGACCAGTATTGTGTACTGGATGTGTGAATGGTGCTTTTGCAGGAAAACTCCGGGACGCTGTTGCCTGTGTGAACAATGTATATTTGATTGCTGGTTAAATCGACTGCTAAAGTCATCCTGGCTGTCCTTTACACATACTACAATTTATTAAAACAGTTTTTAAATGTACACATGCATTCGGTGGACTTTTGAAGTGCCATGCACGTAAGCACGGTGTTTTTCAGACACAGTTTAAAGATCATCACTGATACTGCTCATCACTGTCAGTAGAGCTTGGAGGCAGGACAACCGTTGCAAGTTCCTATCTCAGTGGCTGTGTCCAGATACATGTTTTGTCACTCCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTTTGACCTGTGCAGGTATTGATCTGATCGCCACGTTTTACGGCTG[T/A]CTGTACGCCGGCTGTGTTCCCGTCACCGTCAGACCCCCACACCCGCAGAACCTGACCACAACCCTGCCCACCGTCAAGATGATTGTTGAGGTGACCCCAAACACACTTACTCACACAATCTGGAGGAATAAATACTGCTGTGGAGAAACTGTCAAGAGCAGTTCTGAAATATATCATATCGTGTATCATATCAAATATTCAATAATTTCACATATCATATCACATATATCAAATATCATATCATATCAAATCAAATACAAAATCATATCACATATCATATCATATATCATACATCACACATCATGTCATATATCATATCAAATATTAAATCATATATCAAATATCAAATATTATATATCATATGTCAAACATCATATCACATATCATATAAGATATTAAATCCTATCACATATATAAAATATCATATCATATATCATATCAAATCAAATACAAAATCATATCACATATATCAAATATTATATATCATATATCAAACATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11374
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 |
---|---|---|---|---|---|
ENSDART00000115030 | Essential Splice Site | 1099 | 1578 | 27 | 38 |
ENSDART00000139436 | Essential Splice Site | 932 | 1411 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 583697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 599064 |
GRCz11 | 9 | 598697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCGCAGAACCTGACCACAACCCTGCCYACCGTCAAGATGATTGTTGAGG[T/C]GACCCCAAAMACACTTACTCACACAATCTGGAGGAATAAATACWGCTGTG
Long Flanking Sequence:
ATTGTGTACTGGATGTGTGAATGGTGCTTTTGCAGGAAAACTCCGGGACGCTGTTGCCTGTGTGAACAATGTATATTTGATTGCTGGTTAAATCGACTGCTAAAGTCATCCTGGCTGTCCTTTACACATACTACAATTTATTAAAACAGTTTTTAAATGTACACATGCATTCGGTGGACTTTTGAAGTGCCATGCACGTAAGCACGGTGTTTTTCAGACACAGTTTAAAGATCATCACTGATACTGCTCATCACTGTCAGTAGAGCTTGGAGGCAGGACAACCGTTGCAAGTTCCTATCTCAGTGGCTGTGTCCAGATACATGTTTTGTCACTCCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTTTGACCTGTGCAGGTATTGATCTGATCGCCACGTTTTACGGCTGTCTGTACGCCGGCTGTGTTCCCGTCACCGTCAGACCCCCACACCCGCAGAACCTGACCACAACCCTGCCCACCGTCAAGATGATTGTTGAGG[T/C]GACCCCAAACACACTTACTCACACAATCTGGAGGAATAAATACTGCTGTGGAGAAACTGTCAAGAGCAGTTCTGAAATATATCATATCGTGTATCATATCAAATATTCAATAATTTCACATATCATATCACATATATCAAATATCATATCATATCAAATCAAATACAAAATCATATCACATATCATATCATATATCATACATCACACATCATGTCATATATCATATCAAATATTAAATCATATATCAAATATCAAATATTATATATCATATGTCAAACATCATATCACATATCATATAAGATATTAAATCCTATCACATATATAAAATATCATATCATATATCATATCAAATCAAATACAAAATCATATCACATATATCAAATATTATATATCATATATCAAACATCATATCATAAATCATATCAAATATTAAATCATATCTCAAATATAAAAGATCATATCATATATCATATCAAATCAAATATATAATCATATCCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13406
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 |
---|---|---|---|---|---|
ENSDART00000115030 | Nonsense | 1573 | 1578 | 38 | 38 |
ENSDART00000139436 | Nonsense | 1406 | 1411 | 37 | 37 |
Genomic Location (Zv9):
Chromosome 9 (position 570128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 585325 |
GRCz11 | 9 | 584958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCATGCACCTGCGGGACGGCTTCCTCGCGGACCAGCTCGACCCCATATA[T/A]GTGGCCTACAAMATGTGAGACTGCGGAACCTRAGGAATCTGCAGATGCAC
Long Flanking Sequence:
TGTTATACAATGACTTGCCTAATTACCCTAACTTTACTCTAATAAACCTAGTGAAGTCTTTACATGTCACTTTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGTCATCATGACAAAGAGAAAATACATCAGTTATTAAACCGAGTTAAACTTTCACTGAAGGGGCAGAATCATTTTGACTTCAACTGTATATATAAATACTTATAGTGTTTCCCCTGATGTCCGTCGTGTTGTGTGGTCTCCGCAGTGCCGTGTTCACCTGGACGAATCTGCTGGTGGTGGTGGTGGAGCTGGAGGGCTCGGAGCAGGAGGCTCTGGATCTCGTAGCACTGGTGACCAATGTGGTTCTGGAGGAGCACTACCTGATCGTGGGGGTGGTGGTGGTGGTGGACCCCGGGGTCATTCCCATCAACTCCAGAGGGGAGAAACAGCGCATGCACCTGCGGGACGGCTTCCTCGCGGACCAGCTCGACCCCATATA[T/A]GTGGCCTACAACATGTGAGACTGCGGAACCTAAGGAATCTGCAGATGCACATTTACAGAGGAAGCGTTCGGGGTGGGGGAGAGTGTGGACGGTCGCTTTTCTTCCTCCAGAAACACGAAGAGTCCTTGATGGAGCTATGCAGTTTATTTTTTATATCAGACTGACAGAATGCCTTGGAAATAAAACTCTGATTCAGTGGTCAGGCCAAACGACTCAATTACATCTCCTGTTTATCTGAGGCTGGGACACTGAACCGATGCATTGAGAATCAGGAAATCATTCTGCATTGATTATGAGATTTTATGAATGCATGGAGATTCTGTTAAATCAATTTTAAGCTTCATTTTCACCAGCAGATGGTGCTGTATGCTTTACAAACAGCCTATCTCTGCTTGCTTCTAATTGCATACACATACCACGCAAACCTAAAATGATCAATATTAAGGGTTTCATTAACAATCGAGTTCATCGTGAGTTGTTTACATTAACCGTATGACAAA
Associated Phenotype:
Not determined