ZMP
tfdp1b
Ensembl ID:
ZFIN ID:
Description:
transcription factor Dp-1, b [Source:RefSeq peptide;Acc:NP_957070]
Human Orthologues:
TFDP1, TFDP3
Human Descriptions:
transcription factor Dp family, member 3 [Source:HGNC Symbol;Acc:24603]
transcription factor Dp-1 [Source:HGNC Symbol;Acc:11749]
transcription factor Dp-1 [Source:HGNC Symbol;Acc:11749]
Mouse Orthologue:
Tfdp1
Mouse Description:
transcription factor Dp 1 Gene [Source:MGI Symbol;Acc:MGI:101934]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39526 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39526
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000003317 | Nonsense | 167 | 385 | 7 | 12 |
| ENSDART00000137356 | None | None | 148 | None | 6 |
| ENSDART00000145758 | Nonsense | 163 | 266 | 7 | 9 |
| ENSDART00000146722 | Nonsense | 163 | 346 | 7 | 11 |
| ENSDART00000146971 | Nonsense | 160 | 254 | 7 | 9 |
The following transcripts of ENSDARG00000016304 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 111545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 241675 |
| GRCz11 | 1 | 236854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTCCTGCAGCACGTGTACGACCAGAAGAACATCCGGCGGCGGGTTTA[C/A]GACGCCCTCAACGTCCTCATGGCCATGAACATCATCTCCAAAGACAAGAA
Long Flanking Sequence:
AGCATCTCCCCCAATGATGCGGTCAGTTCCTGTGTGTGTGTGTGTGTGTGTGTGTATGTTTAAGTGTGCCCTGACCTGTGTGTGTATGCAGATGTGTTACCTGACCTGTATGTGTAATTGTATGGGTATATTTGGGTGTGTGTCTTTACCCTTGTGTGTGTGTGTGTGTGTCCAGATCTGTGTGTCTTGACCTGTTTTTTGTGTGTTTGTGAATGTGCTCCTGTTTCTTGCCTTGTTCAAGTGTGTGTGTTTGTTTTAAAGTATGTTCCCACTTGTGTTTTTGTTTTAAGTGTGGGTTGTGAGTCTGCACCAATGGCCTAGTGGTTGGTGCATCAATCCTCCCCTGTCTCTGCTCCCCGCGCTTTCCTGTCTGTGGATCTCCACTGTCCTATCAATAAAGGTGAAAACGGCTAATAAATTCCATATTTAAAAAAAAAAGAATGGGTTGTGTGTGTCCTGCAGCACGTGTACGACCAGAAGAACATCCGGCGGCGGGTTTA[C/A]GACGCCCTCAACGTCCTCATGGCCATGAACATCATCTCCAAAGACAAGAAGGAGATCAAGTGGATTGGCTTTCCCACCAACTCAGCGCAGGAGTGTGAGGATCTGAAGGTGTGTGTGCGCTTCTGTGTGATAGTAATGCTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTTGCTGTCTGATGGTAATGCTGAATCCTCCTGCAGGCTGAGCGTCAGAGGCGACAGGAGAGAATCAAGCAGAAGCAGTCTCAGCTGCAGGAGCTCATTGTGCAGGTACAGCACCGCATCTTGATATTGTTCAGTCACGTGAGAATTGAATAATAATAATTTCAGTAATGTGAAAGATCGAGTAATGATGCTGTTTCACTTGTGTTTTTCAGCAAATCGCCTTCAAGAACCTGGTTCAGCGTAACCGTGAGGTGGAGCAGCAGAGTAAGAGATCTCCATCTGCAAACACCATCA
Associated Phenotype:
Not determined