ZMP
si:ch1073-352h10.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein with Zinc finger, C3HC4 type (RING finger) and B-box zinc finger domains [Source:UniPr
Human Orthologue:
TRIM35
Human Description:
tripartite motif-containing 35 [Source:HGNC Symbol;Acc:16285]
Mouse Orthologue:
Trim35
Mouse Description:
tripartite motif-containing 35 Gene [Source:MGI Symbol;Acc:MGI:1914104]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19306 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29835 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19306
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 |
---|---|---|---|---|---|
ENSDART00000086144 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000146662 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000086144 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000146662 | Nonsense | 380 | 453 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39595869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36744619 |
GRCz11 | 22 | 36713628 |
KASP Assay ID:
554-6172.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAGAGGAAGGGAGGGGGTTTCTTTAACTCTGATGTCTGGAGTGTGT[G/A]GTATGACCCTGATAAACTGTTTGAGTCTGGTTTTCATGTTGATCAGGCTC
Long Flanking Sequence:
TAACACTGTTAATACAGAATATTTATGATACAATACTATTAAAAATTTATGAAAACAATATTTTATGATCATCACATCATAACACTCAAACACACACACACACTCAAACACACACACACTCAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACATTATATGAACATCAGAATAACAGCAGCTGTTGATTGTGTCTCTTCAGCTCCTGTCATCCTGGATCCAAACACGGCAAATCCACGACTCCGCCTGTCTGATGATCTGACCAGAGTGACAATCAGAAGAAAACAACCAGTTCTTGATAATCCAGAGAGATTTGACTGTTATCGCTGTGTTCTGGGTTCAGAGGGTTTTAACTCAGGAAAACACTGCTGGATCGTGGAGGTTAAAAAGAGTAAAATCTGGAGTCTTGGAGTAACAACAGCATCAAACCAGAGGAAGGGAGGGGGTTTCTTTAACTCTGATGTCTGGAGTGTGT[G/A]GTATGACCCTGATAAACTGTTTGAGTCTGGTTTTCATGTTGATCAGGCTCTTGATCGAGTGCGAGTTGATCTGGATTATGACAGAGGAACAGTGTCTTTCTCTGATCCTGTAAATAACAAACATCTACACACTTACACAACCACCTTCACTCACACTCTCTACCCTTTCTTCATGTGTTATAACAATTTCTTTTCATACTCTTCTTCCTCTCTAAAGATTTTGCCGTCCAGTATTCAGTAGCATTACAGCTGTACAGTGAGTCTCTGTTTTTATCAAGTCTCTAATATAAAATGTTTTTTAAAAGAGATTAATCATTTCATTCAGCAAAGCTAAAATTTAAAACTCAGTTGATGAAAATGACTACACACACACACAGTCTCTTATTTCTATTTTAATTAGTGTTTAATAAATTGTTCAAATCAATCTCTAGAAATATGTTAAATTATAATATAATGATAAGTTTATTACAATAAATACAAAAGCATCAAAATCAGGGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29835
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 |
---|---|---|---|---|---|
ENSDART00000086144 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000146662 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000086144 | Nonsense | 380 | 453 | 6 | 7 |
ENSDART00000146662 | Nonsense | 380 | 453 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39595869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36744619 |
GRCz11 | 22 | 36713628 |
KASP Assay ID:
554-6172.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAGAGGAAGGGAGGGGGTTTCTTTAACTCTGATGTCTGGAGTGTGT[G/A]GTATGACCCTGATAAACTGTTTGAGTCTGGTTTTCATGTTGATCAGGCTC
Long Flanking Sequence:
TAACACTGTTAATACAGAATATTTATGATACAATACTATTAAAAATTTATGAAAACAATATTTTATGATCATCACATCATAACACTCAAACACACACACACACTCAAACACACACACACTCAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACATTATATGAACATCAGAATAACAGCAGCTGTTGATTGTGTCTCTTCAGCTCCTGTCATCCTGGATCCAAACACGGCAAATCCACGACTCCGCCTGTCTGATGATCTGACCAGAGTGACAATCAGAAGAAAACAACCAGTTCTTGATAATCCAGAGAGATTTGACTGTTATCGCTGTGTTCTGGGTTCAGAGGGTTTTAACTCAGGAAAACACTGCTGGATCGTGGAGGTTAAAAAGAGTAAAATCTGGAGTCTTGGAGTAACAACAGCATCAAACCAGAGGAAGGGAGGGGGTTTCTTTAACTCTGATGTCTGGAGTGTGT[G/A]GTATGACCCTGATAAACTGTTTGAGTCTGGTTTTCATGTTGATCAGGCTCTTGATCGAGTGCGAGTTGATCTGGATTATGACAGAGGAACAGTGTCTTTCTCTGATCCTGTAAATAACAAACATCTACACACTTACACAACCACCTTCACTCACACTCTCTACCCTTTCTTCATGTGTTATAACAATTTCTTTTCATACTCTTCTTCCTCTCTAAAGATTTTGCCGTCCAGTATTCAGTAGCATTACAGCTGTACAGTGAGTCTCTGTTTTTATCAAGTCTCTAATATAAAATGTTTTTTAAAAGAGATTAATCATTTCATTCAGCAAAGCTAAAATTTAAAACTCAGTTGATGAAAATGACTACACACACACACAGTCTCTTATTTCTATTTTAATTAGTGTTTAATAAATTGTTCAAATCAATCTCTAGAAATATGTTAAATTATAATATAATGATAAGTTTATTACAATAAATACAAAAGCATCAAAATCAGGGGGC
Associated Phenotype:
Not determined