ZMP
si:ch211-63o20.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC566703 [Source:RefSeq peptide;Acc:NP_001038580]
Human Orthologue:
ZNF395
Human Description:
zinc finger protein 395 [Source:HGNC Symbol;Acc:18737]
Mouse Orthologue:
Zfp395
Mouse Description:
zinc finger protein 395 Gene [Source:MGI Symbol;Acc:MGI:2682318]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17836 | Essential Splice Site | Available for shipment | Available now |
| sa37100 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39292 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17836
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 |
|---|---|---|---|---|---|
| ENSDART00000034332 | Essential Splice Site | 71 | 387 | 2 | 9 |
| ENSDART00000148066 | Essential Splice Site | 71 | 387 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 34774268)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34846781 |
| GRCz11 | 20 | 34749660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAAACCTAATGTCCTTCCCAAGGTCTTCCGGCATGGAYTTACCTTACAG[G/A]TTAACATGCACAYCCATTTAATCTCTGYWGTATGTTGTCYTACCAAGGCA
Long Flanking Sequence:
ATATTTATTTAGTTAATATTGTAGCACGTTCTCGTGGCCTCATGGCGCTGTCGCAGAGCTCGCGTGTTGTTTCAATCCTCACAATAACACTGTTTTAAACAAGTTTACCTTCTTTCTAGCTGTTTTTTGTGCGGACTCAGTCAAAGCCGACTGTTTTAGCTGAGAGGACACAGTATGGCAGCGGTAGGATCCCGAGCAGGACTTGACACGATGGGCATTGACGGCCAGGATGGACTGGTATGTGTGAATTTCATTCAGTTGTCGAAATATGCTCTTTTAAGTTACAAGTTAAATGAGAAAAGGGTAGCTAGTGTGTATGTTAGCGTTAAGTGGTTGTTTTTAATCCTGTAGGTCTACATGCAGTGTTGTGGGCAAGGAGAAGGGGTGCAGAAGAAGCTGAATGCAGGATCTGCCACCACAGACTGGTCTGTCGATGCCAACACACAGCAAACAAACCTAATGTCCTTCCCAAGGTCTTCCGGCATGGACTTACCTTACAG[G/A]TTAACATGCACATCCATTTAATCTCTGCAGTATGTTGTCCTACCAAGGCAAAAACGATTCATTTTCTAAAACGTTTCATTTTTTAGCTCTGTCTGATGAGTATTGCTCTGTTTTCATGAACTGTTGTGTTTTTTTACTGCCATGGCGCAGAAGTCCTGAATCAGTGGAGATGGATGAGATCATGGCTGCGATGGTGCTCACCAGTCTGTCCTGCAGTCCAGTGGTCCAAAGCCCCCCGCAAAAAGACCTCCTACCAGGTGAATTTCACTTTTTGGAAATCTTAAAAGAACAAAGGCTAATTTTGCAACTCCCCTAGGCATTTTAAAATCCACTCAGTTGCTCTCCGGGTCTGACAGGAGCACTTTTAGCTTAGCTTAGCATAAATCATTGAATTGGATTAGACCATTAGCATCTCGCTCAAAAATGTCTATATGGAGTTTAGGCAATTTTCCTTTTAAAAGCTTGACTATTCTGCAGTTGCAGCCGGTACTAAGACTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37100
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034332 | Nonsense | 127 | 387 | 4 | 9 |
| ENSDART00000148066 | Nonsense | 127 | 387 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 34771784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34844297 |
| GRCz11 | 20 | 34747176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGTGGAGGTGATCTATCTGACAGTGGCAGCAGTGGTTACTGGAGTT[G/A]GGACCATGGAAATGTAAGCCCAGCCCCGTCTCCATCGGTCAATGAGATGG
Long Flanking Sequence:
TTTTTGCAGAGCAACACAAACAGCATGAAGAAGTATAAATGCATGACTCGACGCAGAAGTATAAACCAGGTTTAAGACTGGTTTTGTGGTCCAGGGTTACGTATATGATCATTATGTAATATTTTGAAAAAACATTGTAACACAACGCAACAATCATACATTATGTTGCTTTTTATTATAAATATATTTGATTTTCTAAATATTAAATTATTGTTTTACGCTGTTTTTTTACATAAATCCCAACAATTCGTTTCTATAATTGTATGGTTTATTCACCAGATATAATTTTATGAATTTCTATTTTTGACTGTGCACTTATTGAATTATATGACTATTAAATCGTATTATCTTATTAAACAGTGTAATGCACAACCCAACCATGAATTTGAGTAATCCCACTGTTTAAGCCTGTGTTGTTGACTCTGCTTCTGTAACTGTAGGGGACATGGAGTGTTGTGGAGGTGATCTATCTGACAGTGGCAGCAGTGGTTACTGGAGTT[G/A]GGACCATGGAAATGTAAGCCCAGCCCCGTCTCCATCGGTCAATGAGATGGACAGGAGCCCCGGCCGACCCACAGACGAGGGCCTGCACATGGAGCTGGACCAAGGTGCATGTGAGGAGCCTGAGGCCCGGAGGTGCAAGGTGAGAAAGAGACGACTGTCAGATTGCTGACCCAGAGGGCGAACATGCAGCACTTTAAGCTGATGCTTTCAAAATTTGTGTGACTCACTTGTTGTTTTACTTTCTTGCTCTCAGAGCTTGAGCCGGGGAGCATACAGGTGTTTGTGGCCGGGCTGTGGAAAAGTGCTGACATCGCGTGTCGGCATGAAGCGGCATATTCGCATTCTTCACCTCGGGTGAGTATGCTTGCGCAAACCCAAATGATACATCTTTAACACCTAAAGGCCAGTTTATACTTCTGCATGCTTATGGTAGGATTAGGGTCGCATACCGTTCACCATACCCTGACTTGCAGCTTTTAAAAAATAAAACTACAGGTCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39292
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 |
|---|---|---|---|---|---|
| ENSDART00000034332 | Essential Splice Site | 311 | 387 | 7 | 9 |
| ENSDART00000148066 | Essential Splice Site | 311 | 387 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 34767421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 34839934 |
| GRCz11 | 20 | 34742813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATTTTGCAGCTGGACTCCGCCTGGAGACGTCCAGCAGAAACCTCAG[G/A]TTAGTCTGATATCCACAAGCACTCCTCATCTTAAAGTGTATTAAGAACCT
Long Flanking Sequence:
AATTCACAGGAGGGCAATCATTTTACTATCAACAGTCTTTGAATAAATTTTACAACAAATTATTACAGCCATTGTTTAAATATTTTACCATCAAAGTAAAATGGAAATATCATTCAATTTTCATTTTTTCATTTCAATTAATTTTTGGTACAAATCAGTTTTGTTTGCTTTAATTCAATATAATTAAGTGATGATAATAAATAACACCTATATTAAATATATTGTTTGGGTAAAATCTCGTTACAATTTTCCAAAATAATTACTAAAATAAACAATAAAATAAAATAAAGTCATTTCTGGGTATGATTTTCAGCATCTTAAACATTGTTTCTGCCTAGTCTGAAATCTTGTTCAAGTAATATACACTATAGTTGTGTCAATAGTGTGTTTACTTGTGTCATTCCCTGCAGGCCTGTTCACCCATTCAGGTGACGGTCTCTCCGGGCAGCCCCACATTTTGCAGCTGGACTCCGCCTGGAGACGTCCAGCAGAAACCTCAG[G/A]TTAGTCTGATATCCACAAGCACTCCTCATCTTAAAGTGTATTAAGAACCTGAATCACTTATGGCATCTGGCCTTTTGTCACTGTATTGATGTGTAGATTCCAGCCCCTCGCAGCCGGTCGGTGAGTGTGGGAGAGCAGTGGCTCCAGAGGAACAGCACCTCCACCAGATCACACACCATCAGTGCGTCTCCATCCAGAGGACACTGCTCATTCAGGTACTGCACACGATGCTGCCCTCTAGAGGAACAGCGTGAAAAAATCCTATTAGGTCTTAAAGCATAAAATTTTTTTTTTTTTTTAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTGTATTCTTGTTATTATAAGAATTGGGCCTTCTGTATGCCTTTTTGGTTTTTTTTAGATAAAACATTTCTTATAGTTAGTAGGTGAGAGCAGAGCAAAACCCACAAACAAAACAAAAACACTTTTGAATTTCTCA
Associated Phenotype:
Not determined