ZMP
znf593
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 593 [Source:RefSeq peptide;Acc:NP_957111]
Human Orthologue:
ZNF593
Human Description:
zinc finger protein 593 [Source:HGNC Symbol;Acc:30943]
Mouse Orthologue:
Zfp593
Mouse Description:
zinc finger protein 593 Gene [Source:MGI Symbol;Acc:MGI:1915290]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39163 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36412 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39163
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064754 | Nonsense | 32 | 55 | 3 | 5 |
| ENSDART00000082237 | Nonsense | 69 | 129 | 4 | 5 |
| ENSDART00000146309 | Nonsense | 69 | 129 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 24514277)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24667719 |
| GRCz11 | 17 | 24686120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACATGTTTTATATAATATTTTTTTCCACCAAAAACATTTTAGGAGATA[T/A]TTTGTTGACTTGAAAACCTTAAAGGAGCATTTCAAATCCAAACCCCACAA
Long Flanking Sequence:
TGGGCATATCTGTATAAGGGGAAGGTTAGGACAGCAAAATTTACTCGCAATTATATTACATCATTTATTGAAATTATATCATCTTTTGGGGTATTGCAGTTCTTTTATTTATCGTTGAACTCACTCTGCTTTAAGTTTGAGAACAGAATTTGGAAATTGTCCTCTTGTTTTCAGATCATGGGTAAGTCCAAACAGGTAGGAAACCACAACAATGGAAAGAAGAAGAATATCGCCAAGACATGGAAGACTAAGCGCAGGACAAAAGACCTTGACCAGATTCATGCAGACATGATCCCTACAAATGCTGCCAAGTTGCTAAAGCAAGATGTAGATTATGATGTTACAGGCTGTGGCCAGCATTACTGTCTGCACTGCGCGTAAGTCACACTTTAACACTCCTAAACACACAACACATTACTTCTATTCAATTTTTTTAAATGTAAATCCTTTATACATGTTTTATATAATATTTTTTTCCACCAAAAACATTTTAGGAGATA[T/A]TTTGTTGACTTGAAAACCTTAAAGGAGCATTTCAAATCCAAACCCCACAAAAAACGGTACGTCAAAATTTTATTTTATTTTTTTCAGATTTGCAAAAGATAATGCATGTTTGGTTATTCAGATTTTCATCCTATGTGTTGTTTGTGTGTTGTATTGTAGATTAAAGCAGCTTAGGGAAGAGCCATACACACAGGCTGAAGCTGAGCGAGCAGCAGGAATGGGCTCCTACATCCCACCAAAAACCCTAGAGGTTCACACACAGCAGGTCGAGGAAGATATGGACTGAAAAGTTACTTGTCTACCTCTTTATGGACTGGTTTAAACTATTAGGTCTGGACTGAGACCAATTTAACTTCTTTCAGAGTTGATGTTAATTTATGGAGATGGAAAGTCTACATGTAAAGGTCCTCAGCTGGCACAGTGTCAATAAAGTGTTCACTGTTGTGAACGTTGACATGTTTTTTTGCTTTCAGCAAGCAACCTTCTGCGACTGAAAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36412
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 > T
Consequence:
Missense, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064754 | Missense | 54 | 55 | 5 | 5 |
| ENSDART00000082237 | Nonsense | 91 | 129 | 5 | 5 |
| ENSDART00000146309 | Nonsense | 91 | 129 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 24514444)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24667886 |
| GRCz11 | 17 | 24686287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGATTTTCATCCTATGTGTTGTTTGTGTGTTGTATTGTAGATTAAAG[C/T]AGCTTAGGGAAGAGCCATACACACAGGCTGAAGCTGAGCGAGCAGCAGGA
Long Flanking Sequence:
TTTTCAGATCATGGGTAAGTCCAAACAGGTAGGAAACCACAACAATGGAAAGAAGAAGAATATCGCCAAGACATGGAAGACTAAGCGCAGGACAAAAGACCTTGACCAGATTCATGCAGACATGATCCCTACAAATGCTGCCAAGTTGCTAAAGCAAGATGTAGATTATGATGTTACAGGCTGTGGCCAGCATTACTGTCTGCACTGCGCGTAAGTCACACTTTAACACTCCTAAACACACAACACATTACTTCTATTCAATTTTTTTAAATGTAAATCCTTTATACATGTTTTATATAATATTTTTTTCCACCAAAAACATTTTAGGAGATATTTTGTTGACTTGAAAACCTTAAAGGAGCATTTCAAATCCAAACCCCACAAAAAACGGTACGTCAAAATTTTATTTTATTTTTTTCAGATTTGCAAAAGATAATGCATGTTTGGTTATTCAGATTTTCATCCTATGTGTTGTTTGTGTGTTGTATTGTAGATTAAAG[C/T]AGCTTAGGGAAGAGCCATACACACAGGCTGAAGCTGAGCGAGCAGCAGGAATGGGCTCCTACATCCCACCAAAAACCCTAGAGGTTCACACACAGCAGGTCGAGGAAGATATGGACTGAAAAGTTACTTGTCTACCTCTTTATGGACTGGTTTAAACTATTAGGTCTGGACTGAGACCAATTTAACTTCTTTCAGAGTTGATGTTAATTTATGGAGATGGAAAGTCTACATGTAAAGGTCCTCAGCTGGCACAGTGTCAATAAAGTGTTCACTGTTGTGAACGTTGACATGTTTTTTTGCTTTCAGCAAGCAACCTTCTGCGACTGAAAGACTCACGATGTTCATTCTGAGTGTGTGAATAACGATCTGTGATGAAATCATTAATCCATAAGTACTTAGAAGTCAAGTGTCCACATCTATAGTATGCCAAGGTCATTTAGGTTAGTGACACACTTGTACGTGTTAAACATGCATTTAATTGTAAAGTATAAATTACTCTG
Associated Phenotype:
Not determined