ZMP
si:ch211-203l9.3
Ensembl ID:
ZFIN ID:
Description:
tumor protein D52 [Source:RefSeq peptide;Acc:NP_001038486]
Human Orthologue:
TPD52
Human Description:
tumor protein D52 [Source:HGNC Symbol;Acc:12005]
Mouse Orthologue:
Tpd52
Mouse Description:
tumor protein D52 Gene [Source:MGI Symbol;Acc:MGI:107749]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36869 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36870 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36869
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 |
|---|---|---|---|---|---|
| ENSDART00000088340 | Essential Splice Site | 7 | 187 | 1 | 6 |
| ENSDART00000121829 | Essential Splice Site | 7 | 187 | 1 | 6 |
| ENSDART00000128465 | None | None | 222 | None | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 33149939)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 32317746 |
| GRCz11 | 19 | 31905059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACAACATCAAGAGTCCTCAAAGACAGGATGGAGGAGAACGATAAAGG[T/C]AGTTGAATTCTTCTGCAAATGTGATGTGACATGTCGGCACAGATTAGAAA
Long Flanking Sequence:
CCTATTTGCAGGGCAAATAGAACTAGAAATTATTTTATGATGGTGGCCATTAGGTCATTAAATGAGTGCAGGGGTAAGGGAGATGCACTCATAAATGATGTATGTTGTGGTAATATTTTTTTATTGTGTACATGGAACTTAGCCTGTGTTAAATGGCACCTTGCTGCAATTTTTGTTGCCCTAAACGGGATAATAAAGTTGAGTCTGAGTCTTAGCTTATCAATGTTTTACTATTTAACGTTTTTTCTAAAGTAATTTTTGAGCTTTAAAACCCGTCAGGTGGGACAGCGTGCCCTTCTCTCGCTCTGTTTACATATTTACGTACTGTGCGTGCTGACGTCACAGACGACCCCACCCCATCTCGCGCAGCAGCCCAGGGTTGCAGTGGCAGCTTTGAGCTGAATTTTGAGAGGTTGAAGTGGGAACGCGGGACCGCAAGAATCAGAATAACTCACAACATCAAGAGTCCTCAAAGACAGGATGGAGGAGAACGATAAAGG[T/C]AGTTGAATTCTTCTGCAAATGTGATGTGACATGTCGGCACAGATTAGAAATGCAACAAAACTCAACTTTCAGAAGTTAGCTAGCTTGTTTGGTTAGCAAAGCCAGCAGCTGGTGACAGAATAATGGTTGATTAATTTTATTAATCCGATGAATATAGATAACGTGACACTCATTCAGAATAAATATTGACGGGAATTTCTTTCGAGCTTGAGCAGTTTTGCCAATTATAATTAGTTCGTCGTGGGCTAATTAATAATGTTTATAAACACTGAGGGAAATTAACCGTTACCACAACACAATAATTTAGTCTGGTAAAATATTTTTGGTGTTTTTGTTACAAAAAAACTATTTATTTAATTTTCGTGGTTTTAACTTGCAGCATCGTTGAACCATATGTTAGCTCTTAACACCTGCAGTAAATGTGATGCTAATGATTCATGCTTTAACCGTTATTTCAGTTCTGCCTTTTCATCGAGGCAATTCCGTTAACTATTGTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36870
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088340 | Nonsense | 146 | 187 | 5 | 6 |
| ENSDART00000121829 | Nonsense | 146 | 187 | 5 | 6 |
| ENSDART00000128465 | Nonsense | 182 | 222 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 33183469)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 32351276 |
| GRCz11 | 19 | 31938589 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGGAACACACCCTCCTTCAAGTCATTTGAGGAGAAAGTGGAAACCT[T/G]AAAGGTAAACCCACAAGCATAATATCAACACTGTGTGTGTGATCTAAACA
Long Flanking Sequence:
GAATACTATAATTTTTAAAGAACATAATCTGATAATTAATGACAAGTGAAATGAAAAATTCGGATGAATAGAATTTAAAAGCAATTAAATTAATTGTTTCACTGTTATAATTAATAATTGCTAAAAAATAAACAATTATTTCTAATACACTAACAAAAAACTAAAATATTACTCTTAACAAGTTAATTAAGTTAAAATGAAATTAAGTTAACTTTTAAAATCCTTAACATATGGAACATTTTTATTTATCATTCTGCAAAGTTTTTTCAATAAATAAGTGTTTCTATCAACAAAATTTTCAATGTGTAATACTTTTTTCATTTGACGTTTGCCATCTAGGTTGAAAATTTGATTTTTGCCACTAAACATTATCAAGCTTAGCAAAACATTATTCTGACAACCTGTGAGTGTGACACATGAAGTGTTTAGTGAATTTTACATCATCATTTTTTTCAGGAACACACCCTCCTTCAAGTCATTTGAGGAGAAAGTGGAAACCT[T/G]AAAGGTAAACCCACAAGCATAATATCAACACTGTGTGTGTGATCTAAACATGTTAAAAACCCCAAGCCTCATTGCTGGTTTACAGACTAAGATGAGCCCCAAACCATCGACAAGCGATATTGAAGAGGTTTCAGACTCCACACCTGATGGAGAGCCCATGATTAAACAACCAGACGACACGTTTTCACCAGATCAGCAACCGCACTGAGAATCAGCCCTCAAACTCTTCTCTTTTTCCACTTTTCTTTTGGTACTTCAGCATAGTCACAGTGAGTTTGCTTCTGTATAACTGGAGTCTCAGTGATCTCCAGATGGGACGGGGTAGTCCTACACTGGAACAGACACGTCAAAATGTCATTACTGTAAGAGCATGTTACTAGTTCCGTTTTCATCCATAACTTCAGTGCCATTGAATTAGCCAAAATAAAAAGACTTTAAATGTCTGTTTGTTAATTTTTTTAAGAATGTATTCAGAATTCATCATATAATATATATATATA
Associated Phenotype:
Not determined