ZMP
si:dkey-76b14.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate DENN/MADD domain containing 1 family [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
DENND1C
Human Description:
DENN/MADD domain containing 1C [Source:HGNC Symbol;Acc:26225]
Mouse Orthologue:
Dennd1c
Mouse Description:
DENN/MADD domain containing 1C Gene [Source:MGI Symbol;Acc:MGI:1918035]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13858 | Essential Splice Site | Available for shipment | Available now |
| sa9160 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13858
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 |
|---|---|---|---|---|---|
| ENSDART00000062505 | Essential Splice Site | 361 | 561 | 16 | 24 |
| ENSDART00000137237 | None | None | 192 | None | 9 |
| ENSDART00000142505 | Essential Splice Site | 363 | 424 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 56744051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55527984 |
| GRCz11 | 1 | 56197280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYATGCGGGAGTTTCTGGAGAGCGCCGTCCAWCTGCAGTGTTTCAAAGAG[G/A]TAAAACACAACATCACTCACTRTTRTGACAGATTTATGATGAGTTCTGTK
Long Flanking Sequence:
ACTGTGCAGAGCTGCGGCAGGAGTCCAGTTTGACACCTATGCACTAGAGCCTGTTCCTGACACACACAATAACACAATAATAATATCACCTTTTCCCCAAGGTTGCGAATTTGTATCTCACAACTTCAAGTTTTACATTTGCAGTTGTGTAATGATGAGTTTATTTCTCAGAATTGACACTGTTTACTGTTGCAGGTGGCGGGTCTGAAAGTCCGTCTGAAGCGGCAGGCAGCGGCGGCAGGATCAGGAGTCGCTCATGCATTTCTCAGAGCGCAGGCGCTGCTGTTCGGAGGATACAGAGATGCTTTACAGGCTCCTGCTGTAAATACACACACTGAGTGATACACAATTACACACACAGATGAACACACAGCTAAAGCAGTTCCCTCTGTCTAAAGGATGGGCCCGTGGTGTTCTGTACTGAGCTGTTTCTCAATCATAAATCTCCAAGCATGCGGGAGTTTCTGGAGAGCGCCGTCCATCTGCAGTGTTTCAAAGAG[G/A]TAAAACACAACATCACTCACTATTGTGACAGATTTATGATGAGTTCTGTTGTCTTGGTGATGTCGAGTTGTCATGAAAAGGACAAAAGCAGGTTGTGAAGTATTTGTTTATGTCAAGTTGTCATAACAAACAATGTCATCTTTGCATTTAACACGTCTAACTGACAGTATGACAGTTGTTATAAGTGTAACCCCGCCGATCCTACGCCACCCAACCCGCTCCGAGCTGGGATCGATCTGGCGACCTTCCGCATGGGAGTCGGTTGCTCTAACAAGGAGGCTAAAGACCATGGCTTCTAGCGACTGTCGCTAGAGCACCTTTAGAGGTCAGAGGAGTGGGGTTTACCTGCACAGCACTTACTAGCTGGCCTCCATTACACTCAACCCCCTAAACCTCACTCCCATCCGGGTCATGGCACCAATGTAACCCCGCCGATCCTGCGCCACCCAACCCGCTCCGAGCTGGGATCGATCCGGTGACCTTCCGCATGGGAGTCGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9160
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 |
|---|---|---|---|---|---|
| ENSDART00000062505 | Essential Splice Site | 428 | 561 | 20 | 24 |
| ENSDART00000137237 | None | None | 192 | None | 9 |
| ENSDART00000142505 | None | None | 424 | None | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 56742178)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55526111 |
| GRCz11 | 1 | 56195407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTTTRCCATTTACAGTRWCTGGTTTCCAAGTAAACTTGTTGTCAAAT[G/A]TAATTTAATCCTGTTATGTAGARCTGAACTTTCAGYATCATTACTCCGGT
Long Flanking Sequence:
TCTATAAGAGTTTCTTTCTTCTGTTTAACACTAAAGAAAATATTTAAAAAATGTTCAATAGCTGTAACCATTAAATTGCATAATAGGAAAAACAAATATTGGATTATTATTAACTTATTTTGACATATTATATCTAAAAATGAGACCATATGTTAATGCTTCTTGATTTAGGAATTTGAAGATATTTCGACTCATTTGCAGTGTCCCTTATGTATATAAAATTAGAGCATACTCTGTGGTTTGATTGACTGGTGTTTTAACACAATGCTGGCTTTAAGATGCATTTTTTAATGGTTTCTTTTTTATTTTATTTTTAACCACAGAAAGGCGGAGGAGCTCTGATTGTGACCTGGAAGTCTACAGCTAACAAAGCAGTGAGTATTTGTACATTCATTTTCGGGGTTTTTAAGGCTGTATTTATCTGATCACAATGCAGTGTAAAATTGTAAATATTTTTACCATTTACAGTATCTGGTTTCCAAGTAAACTTGTTGTCAAAT[G/A]TAATTTAATCCTGTTATGTAGAACTGAACTTTCAGTATCATTACTCCGGTATTGATTCACATGATTCTAAAATAATGAAGAGAAATAGATGGATGGATGGATGGACTGACAGATAGAGATAGACAGACAGACAGATGGATGGATGGATGGACGGATGGATAAATATACAGATAGATAGACAGACGGACAGTTAGATGAATGGATGGAGGGATGGACAGACAGACAGATAGACGGACGGATGGACAGACAGACAGAGAGACAGAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACGGATAGATAGACGGATAGATAGACGGACGGACGGACGGACGGATGGATGGATGGACATACGGACAGACAGACAGACAGACAAATAGATAAACAGACAAATAGATAGATGGATGGATGGATGGATAG
Associated Phenotype:
Not determined