ZMP
LOC568954
Ensembl ID:
Human Orthologue:
DIP2B
Human Description:
DIP2 disco-interacting protein 2 homolog B (Drosophila) [Source:HGNC Symbol;Acc:29284]
Mouse Orthologue:
Dip2b
Mouse Description:
DIP2 disco-interacting protein 2 homolog B (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2145977]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18847 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11944 | Essential Splice Site | Available for shipment | Available now |
sa15891 | Nonsense | Available for shipment | Available now |
sa31527 | Nonsense | Available for shipment | Available now |
sa38568 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15645 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18847
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 |
---|---|---|---|---|---|
ENSDART00000044276 | Essential Splice Site | 592 | 1603 | 14 | 39 |
ENSDART00000044276 | Essential Splice Site | 592 | 1603 | 14 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39492816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39564416 |
GRCz11 | 6 | 39561952 |
KASP Assay ID:
2259-7857.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGGACTTTAAGAAGGACATGGGATTGTGGCATGGAGTTCTAACGG[T/C]GAGAGGAAATAAATGTGTATATGTCATCACTGGTAATGCTGAATTCACCT
Long Flanking Sequence:
GGGCTTACATTGTTTCAGATTTAATTCATTCAGCAGTTGTTCTAATTGTGTTTCTCATAGGTTGGCCCAGATTAAAATGGGTGGTGACCGACTCCAAATACCTCACAAAGCCTTCGAAAGACTGGCAGCCTCACATCCCAACAGCCAACACAGACACGGCATACATTGAAGTAAGAGCACGTTTCATTTGTCTGAATGTGGTTATGTGTCTTCAAGGCATGTAAACCTCTTCCTGTGGTTCTTTCATGCAGTATAAGGCCAGTAAGGAGGGCACAGTGATGGGGGTTGCGGTTTCCAAAGTGGCCATGCTAACACACTGCCAGGCGCTCAGTCAGGCCTGTAACTACTGTGAGGGTGAGTGATGCTGTTGCAGCTAGTCATGCTGCTTCATGGTCTGCTCTCTTGGAGAGTTAATGAAACTGTTCTGCATGCAGGTGAGACACTGGTGAATGTTTTGGACTTTAAGAAGGACATGGGATTGTGGCATGGAGTTCTAACGG[T/C]GAGAGGAAATAAATGTGTATATGTCATCACTGGTAATGCTGAATTCACCTAAAAGCAGCTGTGTATGTGTGTTTCAGAGTGTGATGAACCGAATCCACACAATCAGCGTTCCATATGCAGTAATGAAGGCCTGTCCTCTGTCCTGGGTTCAGCGGGTTCATATACATAAAGGTTCAGAGAGACAAAACTAAATGACTATTCAGTCCTCTAGACCCATTTGCTTTGATTTCACAAACGTCTGTGGTCTTACAGCACGGGTGGCCCTGGTGAAGTGCCGTGACCTGCATTGGGCGATGATGGCGCACAGAGATCAGAGAGACACCAGTCTGGCCTCTCTGCGTATGCTAATTGTTGCTGACGGCGCCAATCCTTGTGAGTTATGCTAACAGGCCTCCTGTAGAGATGTGGCTATTTAATGTTCATATTCAAGGTTGCCACTCTTTTTAATCTCCTTTTATCTGCTTCTCTTTTGAATTTAGGGTCTGTTTCATCATGTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11944
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 |
---|---|---|---|---|---|
ENSDART00000044276 | Essential Splice Site | 592 | 1603 | 14 | 39 |
ENSDART00000044276 | Essential Splice Site | 592 | 1603 | 14 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39492816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39564416 |
GRCz11 | 6 | 39561952 |
KASP Assay ID:
2259-7857.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTYTGGACTTTAAGAAGGACATGGGATTGTGGCATGGAGTTCTAACGG[T/C]GAGAGGAAATAAATGTGTATAWGTCATCACTGGTAATGCTGAATTCACCT
Long Flanking Sequence:
GGGCTTACATTGTTTCAGATTTAATTCATTCAGCAGTTGTTCTAATTGTGTTTCTCATAGGTTGGCCCAGATTAAAATGGGTGGTGACCGACTCCAAATACCTCACAAAGCCTTCGAAAGACTGGCAGCCTCACATCCCAACAGCCAACACAGACACGGCATACATTGAAGTAAGAGCACGTTTCATTTGTCTGAATGTGGTTATGTGTCTTCAAGGCATGTAAACCTCTTCCTGTGGTTCTTTCATGCAGTATAAGGCCAGTAAGGAGGGCACAGTGATGGGGGTTGCGGTTTCCAAAGTGGCCATGCTAACACACTGCCAGGCGCTCAGTCAGGCCTGTAACTACTGTGAGGGTGAGTGATGCTGTTGCAGCTAGTCATGCTGCTTCATGGTCTGCTCTCTTGGAGAGTTAATGAAACTGTTCTGCATGCAGGTGAGACACTGGTGAATGTTTTGGACTTTAAGAAGGACATGGGATTGTGGCATGGAGTTCTAACGG[T/C]GAGAGGAAATAAATGTGTATATGTCATCACTGGTAATGCTGAATTCACCTAAAAGCAGCTGTGTATGTGTGTTTCAGAGTGTGATGAACCGAATCCACACAATCAGCGTTCCATATGCAGTAATGAAGGCCTGTCCTCTGTCCTGGGTTCAGCGGGTTCATATACATAAAGGTTCAGAGAGACAAAACTAAATGACTATTCAGTCCTCTAGACCCATTTGCTTTGATTTCACAAACGTCTGTGGTCTTACAGCACGGGTGGCCCTGGTGAAGTGCCGTGACCTGCATTGGGCGATGATGGCGCACAGAGATCAGAGAGACACCAGTCTGGCCTCTCTGCGTATGCTAATTGTTGCTGACGGCGCCAATCCTTGTGAGTTATGCTAACAGGCCTCCTGTAGAGATGTGGCTATTTAATGTTCATATTCAAGGTTGCCACTCTTTTTAATCTCCTTTTATCTGCTTCTCTTTTGAATTTAGGGTCTGTTTCATCATGTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15891
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 |
---|---|---|---|---|---|
ENSDART00000044276 | Nonsense | 948 | 1603 | 23 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39484705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39556305 |
GRCz11 | 6 | 39553841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACATCTCAGACACCAAACAGCTGTTYCTAGAGGGRGCACTACATCCCYG[C/A]AACATTCTCATGTGYCCACACACCTGYGTCACCAAMATGCCCAAACCAYG
Long Flanking Sequence:
GATTACGTTTGTCTGAGGTATTGGGTGTGCTTAACATAGTTAACCACGCCCTTCCAACTGTCAGTTTTGACAGCGCTATGACAACAAACAGAAATAGTGTGTAGTGTCTGTTAGGTTGTAATAACTCTCCCAAAAACCCTTTCACGATCTTTCTGAATGAAATGCCTACTTAACTACATCCAATCAGCTCGCAGTAGAAAAAACAAGCCACGCCCACTGTATTATCATTTAACATTTAGTTTTTCTAGGAACTGCCATCACAATAGGAAAAAAACTGTCACAGCTTCCAGTACATGCAGACTAAAAAATGTATTAATCTTTATGTTTGATTAATATTTTGTTGGTTCTTGTTTTGTTTCTCAGGCAATTGATAGTATTCATCAGGTGGGTCTGTACTGTCTAGCACTGGTTCCTGCAAACACTCTGCCTAAAACTCCCCTGGGTGGCATTCACATCTCAGACACCAAACAGCTGTTCCTAGAGGGGGCACTACATCCCTG[C/A]AACATTCTCATGTGCCCACACACCTGCGTCACCAACATGCCCAAACCACGCCAGAAACAACCAGGTGTGTTTTTTAAACCATAAATCTGCTTTTACATACACAGTAATTGCTGAAATGCATTATTAGTGATGTAAAGTAACAATGTGTTTTGTTAATCATTTTCGACATTAGCATAAGGGGCCATTTACATGTTGCATCTAAAGAAGCCTATGGAAAATGTAAAGCGTGTCGCTTCCTCTACCAGTTTCAGTGCTCCTGTGGCATTGCTAAGCAACCATCAGCTGCATTCTCTGAGGAACCACCACTGACAAACCCTTGCTGTAGCTCTGATACAAGTTTTATTTGTAGAGAAAACAACTAAGCGGCATAGTGTACTCTGCGTTTGTTTGAGTTAGTCTACTGTTATAACTGAATTGTGTGTAATACGTACAAAGTGTGAAGCTGATTGTATAGTTCTTGTCACATTTTTTCTTTTAAAAAATAGCTATAAAAATAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31527
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 |
---|---|---|---|---|---|
ENSDART00000044276 | Nonsense | 968 | 1603 | 23 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39484647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39556247 |
GRCz11 | 6 | 39553783 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGTGCCCACACACCTGCGTCACCAACATGCCCAAACCACGCCAGAAA[C/T]AACCAGGTGTGTTTTTTAAACCATAAATCTGCTTTTACATACACAGTAAT
Long Flanking Sequence:
TGTCAGTTTTGACAGCGCTATGACAACAAACAGAAATAGTGTGTAGTGTCTGTTAGGTTGTAATAACTCTCCCAAAAACCCTTTCACGATCTTTCTGAATGAAATGCCTACTTAACTACATCCAATCAGCTCGCAGTAGAAAAAACAAGCCACGCCCACTGTATTATCATTTAACATTTAGTTTTTCTAGGAACTGCCATCACAATAGGAAAAAAACTGTCACAGCTTCCAGTACATGCAGACTAAAAAATGTATTAATCTTTATGTTTGATTAATATTTTGTTGGTTCTTGTTTTGTTTCTCAGGCAATTGATAGTATTCATCAGGTGGGTCTGTACTGTCTAGCACTGGTTCCTGCAAACACTCTGCCTAAAACTCCCCTGGGTGGCATTCACATCTCAGACACCAAACAGCTGTTCCTAGAGGGGGCACTACATCCCTGCAACATTCTCATGTGCCCACACACCTGCGTCACCAACATGCCCAAACCACGCCAGAAA[C/T]AACCAGGTGTGTTTTTTAAACCATAAATCTGCTTTTACATACACAGTAATTGCTGAAATGCATTATTAGTGATGTAAAGTAACAATGTGTTTTGTTAATCATTTTCGACATTAGCATAAGGGGCCATTTACATGTTGCATCTAAAGAAGCCTATGGAAAATGTAAAGCGTGTCGCTTCCTCTACCAGTTTCAGTGCTCCTGTGGCATTGCTAAGCAACCATCAGCTGCATTCTCTGAGGAACCACCACTGACAAACCCTTGCTGTAGCTCTGATACAAGTTTTATTTGTAGAGAAAACAACTAAGCGGCATAGTGTACTCTGCGTTTGTTTGAGTTAGTCTACTGTTATAACTGAATTGTGTGTAATACGTACAAAGTGTGAAGCTGATTGTATAGTTCTTGTCACATTTTTTCTTTTAAAAAATAGCTATAAAAATAACTTAATCAAGACATACTGTTTTCCTCATTTCAAAACATTGCAAGACTAGAGAACGACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38568
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044276 | Essential Splice Site | 1083 | 1603 | 27 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39482703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39554303 |
GRCz11 | 6 | 39551839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAGTGGCATTAACATCGGAGAAAATGTGGTGCTTTTGTATCCTCCAG[G/A]TAAACAACACTCCTTTAACAATGCGTATAATGAAGGGCTATAAACAGCAC
Long Flanking Sequence:
ATATAATGGATGCAAACCATTTCTTTTATTTGAAATGCCTTGTGTGGTATTTTAATGCTCTCGTGTGGATTCAGCTGTGCATGTGGCCTACTATGATGGTGAGAGCTGAACATTATGTCACAGTCACTTGATACAATTCTGTATTCTTTTCTTTTTTTAATGTTACATATTGGGCAGTTCACATAATGACCTGTCTCTGTTTTCTTTTTTAGCATCAGTTCCTCACTGAAGCTTTACAGTGGAGAGCTCAAACAGATCCCGACCATACGCTTTATGTGCTTTTGAATGCAAAGGTAAAAATATAGAAACGCCAAAAGAAGTAGCAAAAAGACTAAACCTGCAATGCTGGCCTATAATGTGCTGTTTTTCTCTGCAGGGAGTGGCGGTGTGTACAGCTACATGTGTGCAGCTTCATAAAAGAGCAGAGAAAATCGCTGCTGCTCTCATGGAGAGAAGTGGCATTAACATCGGAGAAAATGTGGTGCTTTTGTATCCTCCAG[G/A]TAAACAACACTCCTTTAACAATGCGTATAATGAAGGGCTATAAACAGCACTCTCATTTCATATGTGTAGAGTGCGTGTATATAGAGTAAAGACAATATTTTACATACTTTTATGTTTTTATTTCATATAAATTTCATATAAAAATAGTCATTCGTAGAAATACAAACTCATATAAAATACTTCAAATACAATCTAAGACAGCAATTTTAGCCCTTGTGTTAAACTTTCTTTAGTTTTTTCAAGTATTTCTCATGTAATGTTTAATAGAGCAAGGATTTATTTCACATTATTTTCTATTAAATGTTTGTTATGGAGAATGTTCTATATCTTAGTTTGGCTGGAATAAAAAAGAGTTTAATATAAATCTGCTACGGTCAATATTATTAGCCCCCTTAAGATTTTTATTTCAGAACAACCGGCTTTCCATTAACTTGCCTTATAAATCTAACTTGCCTAATTAACCTTGATAAGCTTTCACATTGCACTTTAAGTTGAATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15645
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 |
---|---|---|---|---|---|
ENSDART00000044276 | Essential Splice Site | 1520 | 1603 | 38 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 39463149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39534749 |
GRCz11 | 6 | 39532285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGACATCGAGACCAGTGTGTCTCGTGCCCACCGCAGCATTGGTGAAAGG[T/A]AACTTTGCTTTAAGAGGGCCACATTATGCTTTCTGTACTAGTTAAACTTT
Long Flanking Sequence:
ATATCTTGATTACTTACCGAAAATGCAGAGCTGGATGCAGCATTCAAATGAGTGCATCACGTTCAATCTCCCCGCCTTGGCGCCTTCAGGAAAAAAAGTGTCTGCACATGCGCAGACCGGATAGTATATGGAAATTAAATGAAACGTATTTTTTTCTAATTACTTTTAATTGAATGAAATTAACTTGTTTTAAACAAAAGCAGTGAATTTGAAAATTAATAATAAAAAATAAGTAGGATTAAATAACACATTAAAATCAGTGAAATTAACCAGATAAAAACATGTAACATTTACAAGGGGTCAGAATCCTTTTTTTCAGTGCAGTAAATGAATGCTCATGTAAAAATATGCCTGGCTATATCTCTTTCTGTTTAGATCGCCATGATGCTCTGTTTGTGGTGGGCTATCTGGACGAGACTTTAGAACTGAGAGGTCTGCGATATCATCCAATTGACATCGAGACCAGTGTGTCTCGTGCCCACCGCAGCATTGGTGAAAGG[T/A]AACTTTGCTTTAAGAGGGCCACATTATGCTTTCTGTACTAGTTAAACTTTGTTGTAATGTGTTGTCTCAATGTCACAGATCTGCTATAGACCTTTTGAGGAATGTAAACAATAACAATGGTCCTAACATTGTCCTATTTGACATTTATTTATTTCCATAGTTTCCAAGAAAAATCCACATATCCAATGTTTTAAGACAAAGTTATGATTGAATTGCATCTTGTCACAGTTGTGAAATACATTGACAAGAAGCAGGAAATGTTGATAGGCCAACGACATCACCACATTGAAATGCTCTATACTAATACACATGCTTGTTTTTCGCTCCGCAGTGCCGTTTTCACCTGGACAAATCTGCTGGTGGTGGTGGCTGAGCTCTGTGGATCAGAGCAGGACGCTTTAGACCTGGTTCCACTGGTAACCAATGTAGTATTAGAGGAGCACCATCTGATTGTGGGAGTAGTGGTTATTGTGGACCCAGGCGTCATACCTATAAACTCC
Associated Phenotype:
Not determined