ZMP
tfdp2
Ensembl ID:
ZFIN ID:
Description:
transcription factor Dp-2 [Source:RefSeq peptide;Acc:NP_937851]
Human Orthologue:
TFDP2
Human Description:
transcription factor Dp-2 (E2F dimerization partner 2) [Source:HGNC Symbol;Acc:11751]
Mouse Orthologue:
Tfdp2
Mouse Description:
transcription factor Dp 2 Gene [Source:MGI Symbol;Acc:MGI:107167]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6362 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19100 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6362
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062868 | Essential Splice Site | 56 | 414 | 4 | 13 |
| ENSDART00000128602 | Essential Splice Site | 56 | 408 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 4331990)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 4475865 |
| GRCz11 | 15 | 4467012 |
KASP Assay ID:
554-4126.1 (used for ordering genotyping assays)
KASP Sequence:
GCATAARTTCCCTAAACTGCTTGCTTTTTTNGTGTATTATTTGTGTCTGC[A/T]GATTTTAAGCACACCACAGAGAGTCTCTCACTCTGGAAATATCCTCATCG
Long Flanking Sequence:
AGGATCAATGGTGTGTAGCGCAGCGCTGATGGATGAGGATGTCCTTGCTGTGCTGTTCTGGGCTGCAGCAGGAGGTTTGGCTCTCCCCGGGGGCTGCTGCACACGCTCTCTGTGAGAGATTCAGGTTAACAGAGAAGAAGAGAGAGAGAAATGAACACCGGGATGCCCTCATATATACCATCAGTGCTCATGTGGAGCATAACAGCGCAATGAAAAGAGTTGTGCTGCACCTGGAGGATCTGTTCGCTTTCCCATCCATCTCAGTGGCAGTTGTTGTGTGCTGGAAGTGCATAAGAGAGAGAGAGAGAGTTTGATGTTTCATAGTAATGATGCAGTTACAGGATCTGCCAGCAGGGGCTGACTTCCAAAACACAATAAACTTTCTCAATATTGCACAAGTGACTCTTTCTACAAGTCTTGACTTGTCACAAAACTGTTTGGTTATGATTTGCATAAGTTCCCTAAACTGCTTGCTTTTTTTGTGTATTATTTGTGTCTGC[A/T]GATTTTAAGCACACCACAGAGAGTCTCTCACTCTGGAAATATCCTCATCGGCAGCCCGTTTACGCCCCACACAACGCCGGTTGCCATGGTTACTCAGGCACACCCACCCGAAGGCAACGAGTGGACCCCGGGGTGAGCAAAACACACCCATGATTTGAATGTTTAAAAGTTAATGATGGATTACCGGCTTCATGTTGAGGCTTTTGAAACTGGTAGGTGTTTATGGAGAACATTATTAAAGTTTATTGATGGATGCGTGTTGTCAAGAGGTGTTGAAAAATCTAGTTAATAAATGTGATTTTATTAAATATTTATCAAATACATTTTTAACTCGCATGTCCTACTGCACCCAACCTGCTCTGATCCTGATCAAATTGGCAATTCTTTGATTGAGAGTTGGTTGCTCTAACATGGAGGGTAAAGACCATGGCTTGTAGAGTCACTCGCTAGAGCGCCTTTTGAGGTCAGAGGAGTGAGGTTTATCTGCACAGTACTTCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19100
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 |
|---|---|---|---|---|---|
| ENSDART00000062868 | Essential Splice Site | 99 | 414 | 4 | 13 |
| ENSDART00000128602 | Essential Splice Site | 99 | 408 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 4331856)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 4475731 |
| GRCz11 | 15 | 4466878 |
KASP Assay ID:
2260-8095.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGGTTACTCAGGCACACCCACCCGAAGGCAACGAGTGGACCCCGGGG[T/C]GAGCAAAACACACCCATGATTTGAATGTTTAAAAGTTAATGATGGATTAC
Long Flanking Sequence:
AAGAAGAGAGAGAGAAATGAACACCGGGATGCCCTCATATATACCATCAGTGCTCATGTGGAGCATAACAGCGCAATGAAAAGAGTTGTGCTGCACCTGGAGGATCTGTTCGCTTTCCCATCCATCTCAGTGGCAGTTGTTGTGTGCTGGAAGTGCATAAGAGAGAGAGAGAGAGTTTGATGTTTCATAGTAATGATGCAGTTACAGGATCTGCCAGCAGGGGCTGACTTCCAAAACACAATAAACTTTCTCAATATTGCACAAGTGACTCTTTCTACAAGTCTTGACTTGTCACAAAACTGTTTGGTTATGATTTGCATAAGTTCCCTAAACTGCTTGCTTTTTTTGTGTATTATTTGTGTCTGCAGATTTTAAGCACACCACAGAGAGTCTCTCACTCTGGAAATATCCTCATCGGCAGCCCGTTTACGCCCCACACAACGCCGGTTGCCATGGTTACTCAGGCACACCCACCCGAAGGCAACGAGTGGACCCCGGGG[T/C]GAGCAAAACACACCCATGATTTGAATGTTTAAAAGTTAATGATGGATTACCGGCTTCATGTTGAGGCTTTTGAAACTGGTAGGTGTTTATGGAGAACATTATTAAAGTTTATTGATGGATGCGTGTTGTCAAGAGGTGTTGAAAAATCTAGTTAATAAATGTGATTTTATTAAATATTTATCAAATACATTTTTAACTCGCATGTCCTACTGCACCCAACCTGCTCTGATCCTGATCAAATTGGCAATTCTTTGATTGAGAGTTGGTTGCTCTAACATGGAGGGTAAAGACCATGGCTTGTAGAGTCACTCGCTAGAGCGCCTTTTGAGGTCAGAGGAGTGAGGTTTATCTGCACAGTACTTCGCTAGCTGGCCTCTGTTACACTCACCCCCCTAAACCTCACTCCCATCCCGGATGAGTCCCCATGTGTAACTCCACGGTCCTACTGCACCCAATTTGGTCTGAGCTGGGATCGAATTGGCGATTCTTTGTATGCGAGT
Associated Phenotype:
Not determined