ZMP
si:dkeyp-46c9.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate DENN/MADD domain containing 2C (DENND2C) [Source:UniProtKB/TrEMB
Human Orthologue:
DENND2C
Human Description:
DENN/MADD domain containing 2C [Source:HGNC Symbol;Acc:24748]
Mouse Orthologue:
Dennd2c
Mouse Description:
DENN/MADD domain containing 2C Gene [Source:MGI Symbol;Acc:MGI:3036254]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34321 | Nonsense | Available for shipment | Available now |
| sa16106 | Splice Site, Nonsense | Available for shipment | Available now |
| sa15429 | Nonsense | Available for shipment | Available now |
| sa9597 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34321
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 |
|---|---|---|---|---|---|
| ENSDART00000109877 | Nonsense | 126 | 920 | 1 | 18 |
| ENSDART00000143844 | None | None | 531 | None | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11640125)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11028999 |
| GRCz11 | 8 | 11066704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGAGATCATTTAAATAAATGTGTTACCCCAAGCACTGTATCACAAGTC[C/T]AAGTGGCTAAACCGAATGTAAAAATCAATAATATCAACTCCAGCCATTTT
Long Flanking Sequence:
CTGTCCTGCAGGAAGCAGTGTCTTGGGTGAACTTATTAACCAACTTGCACTGCAGAGGAAGGGCTTCTTCCTTGATAGGCTTGCAATGTCAGACAGTCCTGCGGTGTGACGGCAGTCTCGTCGTCATGCTGGCCCTTGGAGTGGACCATGAGAAAAAAGGAGGACCAGGAGGAAAGACGCGAGAGCCTGGCGTCAACATCAAGCAGAAAATCTCACAATGGGAGGGATTGACCCAGCAGGAGGACATCCGGAGTGGGAAAGTCCAGACCCAGCGAACCCTTGCTTCTCGCAGGCTTTCAGAGGACCTTCTTGGAAACGGACTTGACTCCAGTGATGGAGGTCGTAACAAAGCAACTGTATTTAAAGCCAAAAGCCTGGGTTTGGATTTCAGGGAAAACCTGAAGACTTTCAAACCAGTTACTCCTGAAGTCAAGCCTAATTTCCCAAGAAATCGAGATCATTTAAATAAATGTGTTACCCCAAGCACTGTATCACAAGTC[C/T]AAGTGGCTAAACCGAATGTAAAAATCAATAATATCAACTCCAGCCATTTTTCAAATGTGGAAATTACATCTCTACCTCAGTGTGTAGATTATCCAGAGCCGTCACTACCTCCGGGTAACTTTTACACCTCCAGGGGTTTCTGGAAACGACTGGAGGCGGATGAATCTTTCTGGGAGAGGGAGAAGGATTCCTCGCTAATGACTAAGGGACTTGACTTTGGACCGTCTTCTCCTCCACCTAAACCACAGCGCACATTCCAATACAAGGGTGCAAGCAGTCCTACCAACCAGTGGATCCAACCGGAGAACCAGACTCCAGCTGTCAGCAAATTGAATCAAGTGCAGAAGCATGACATCATCTTAAAGCCACCCAGCTGTCCACCTCCTCCTTGTCCAGTCAACACCGTCAATGGGTTTTCCAGACACCGAAAGAACAGGTGAATGCTTTTCCCAGCATGCATATCACATTACATAGTTAATCCCAAACTTAAGAAGGGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16106
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109877 | Splice Site, Nonsense | 313 | 920 | 3 | 18 |
| ENSDART00000143844 | None | None | 531 | None | 15 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11648867)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11020257 |
| GRCz11 | 8 | 11057962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTACAATGTTATCTATAATCTTCAACRTTTTTTAACTATTTGTTTGCAG[C/A]GGATATGCCAAAAGAAAACCCATATGAAGATATCACGCTTTCTCCCATGT
Long Flanking Sequence:
TGTGTGGAACCCAGCAGTTTTTATAATGCATATGTTTTCATTGAGGGGTGTCAAAACTTTTAAACGGTAGATCTCAATAGGCATTTCACCAGCCACCAAGTTCAAGACCTTCAGACCTTCATCAATCTATAGCTATCACTAGCAAGAGATAGCACCTAGCCTGGAACATGCTAACAACATGCTACTTCATGCTAGCAGAAGGTTAACTCATGTTAAAACATTCGAACTATAATGGTAATTTGTGTTACTTCATGCTAAAACAACCCAACAATAATTCTAAGTTATGTTAGTAACGCTAATTCATGCTAAAATTCATGTATTATAAACAAATGTGATTATAGGGTGCTTTCTCAAGACAGATAGACAGACAGACAGACAGACAGACCACTGACTTGTAGATTTACACATCCATAATTGCTATGGAGGATTTTTGTTTATTGTTTTGCATGATTTACAATGTTATCTATAATCTTCAACATTTTTTAACTATTTGTTTGCAG[C/A]GGATATGCCAAAAGAAAACCCATATGAAGATATCACGCTTTCTCCCATGTGTTTACCTATAAGGCGGCAACGAAACTACACAGTTGGACAAAGAGAAAGGCCACAGCTCAAGGTGACTGTCCTTTTAAATGAATACTGATTTGATGAGTTTTTTTAGTACATATCATATCATATCCAGTGTTGGGCAATTAGTCCTCATCATAAACTCAACAAATAAAGATATAATTTTTTGGCCTTTTTGCCTTTATTAGATAGGACAGTGTTGAGACAGGAAGCGAAGTGGGAGAGAAAGAGAGGGGGTAGGGTAGGGAAATGTCCTCGAGCCGGGATTCGAACTCGAGACGCCCTGACGTGCTATTGCACCATATGTCGGCGCTAACCACTAGGCTATTGCGCCGACGAAACTCAACAAATAAGCCGTTGATGATTTAGTGTAAAACCAGCAAATCAATCTTTTTTTCTATTTGGAAAATTACAGTTATTAATAGTTCTTATAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15429
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 |
|---|---|---|---|---|---|
| ENSDART00000109877 | Nonsense | 337 | 920 | 3 | 18 |
| ENSDART00000143844 | None | None | 531 | None | 15 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11648938)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11020186 |
| GRCz11 | 8 | 11057891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATATGAAGATATCACGCTTTCTCCCATGTGTTTACCTATAAGGCGGCAA[C/T]GAAACTACACAGTTGGACAAAGAGAAAGGCCACAGCTCAAGGTGACTGTC
Long Flanking Sequence:
TCTCAATAGGCATTTCACCAGCCACCAAGTTCAAGACCTTCAGACCTTCATCAATCTATAGCTATCACTAGCAAGAGATAGCACCTAGCCTGGAACATGCTAACAACATGCTACTTCATGCTAGCAGAAGGTTAACTCATGTTAAAACATTCGAACTATAATGGTAATTTGTGTTACTTCATGCTAAAACAACCCAACAATAATTCTAAGTTATGTTAGTAACGCTAATTCATGCTAAAATTCATGTATTATAAACAAATGTGATTATAGGGTGCTTTCTCAAGACAGATAGACAGACAGACAGACAGACAGACCACTGACTTGTAGATTTACACATCCATAATTGCTATGGAGGATTTTTGTTTATTGTTTTGCATGATTTACAATGTTATCTATAATCTTCAACATTTTTTAACTATTTGTTTGCAGCGGATATGCCAAAAGAAAACCCATATGAAGATATCACGCTTTCTCCCATGTGTTTACCTATAAGGCGGCAA[C/T]GAAACTACACAGTTGGACAAAGAGAAAGGCCACAGCTCAAGGTGACTGTCCTTTTAAATGAATACTGATTTGATGAGTTTTTTTAGTACATATCATATCATATCCAGTGTTGGGCAATTAGTCCTCATCATAAACTCAACAAATAAAGATATAATTTTTTGGCCTTTTTGCCTTTATTAGATAGGACAGTGTTGAGACAGGAAGCGAAGTGGGAGAGAAAGAGAGGGGGTAGGGTAGGGAAATGTCCTCGAGCCGGGATTCGAACTCGAGACGCCCTGACGTGCTATTGCACCATATGTCGGCGCTAACCACTAGGCTATTGCGCCGACGAAACTCAACAAATAAGCCGTTGATGATTTAGTGTAAAACCAGCAAATCAATCTTTTTTTCTATTTGGAAAATTACAGTTATTAATAGTTCTTATAAACTATCCATTTTTAACATAGCCTACATAATCTACGAATCAAACAAATCCAAAGATTTTATTGATTTTTGCATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9597
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 |
|---|---|---|---|---|---|
| ENSDART00000109877 | Essential Splice Site | 545 | 920 | 8 | 18 |
| ENSDART00000143844 | Essential Splice Site | 156 | 531 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 11663280)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11005844 |
| GRCz11 | 8 | 11043549 |
KASP Assay ID:
554-6564.1 (used for ordering genotyping assays)
KASP Sequence:
TTWGTTTTCCTGACTGTCATGACTGGYGTCCCTCCTCMGAYCACACCAGG[T/C]AACATWTCAACAWTAAACCTTTYATTATAGTTGTCTGACTAGTTCACTTT
Long Flanking Sequence:
ATTGATAGATGGATGGATGGATGGATGGATGGATTGATAAATATATAGATGGATGGATGGATGGATGGATGGATGGATGGAAAGATGGATGGATGGATGGATGGATGGATGCATGGATGAAAAGATGGATGGAAGGATAGATGGATGAAAGGGATGGATAGATAGATAGATAGATAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATGGATGGATGGATAGAAAGATAGATAAAAGATGGAAAGATAGACAGATACAATATATATTTTACTATAAATGTATGTTTAGTGTTCTTTTTCCTCTTTGGTTTGCTTATAGTTTGAGAAGTCTTCTCGTCTGTCTCGTGAGGCTGAAGACAGATTAAGAGCGATTCCCAAGTTTTGTTTTCCTGACTGTCATGACTGGCGTCCCTCCTCAGACCACACCAGG[T/C]AACATTTCAACAATAAACCTTTCATTATAGTTGTCTGACTAGTTCACTTTTCTTAGACACATTTTATCGATCACCCACAGTGAAACGTTTTCTTTTGTCCTGACGGGGGAGGATGGGAGTCGCTTATTTGGATACTGCCGCAAAATCCTGGTGAGTTTTTAATATGGATTCATTCAACAAACAAAAAACATAATTTCACTTTGTCACTTAACACTTGACACACACATCAAATGGAAAACGGAATACGGGGAGGAGCCCCGTTTAAAAAGGACTGAGGCGACAATTTAGTGTGCAGTTTATAAGCTAGCCGCAAAAATTTTAGGGCGGCTGAGTAGAAATATACAGCTACAGCCCCCCTAAAATAGGCCTAGCGACACCCATGCCAAGTAATCATGCATTCTTGATTGTTGGTGGTTTTCCCTGTTGTGAAGAGGTAAAATGGTTGGCAACATTAACACTTTAGATAGGTCTGTGCAAAAAAGTTTCTGGCTTTATATGGA
Associated Phenotype:
Not determined