si:ch73-379f5.2

Ensembl ID:
ENSDARG00000039108
ZFIN IDs:
ZDB-GENE-050327-87, ZDB-GENE-050327-87, ZDB-GENE-091112-11
Description:
hypothetical protein LOC541547 [Source:RefSeq peptide;Acc:NP_001014382]
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 is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa40000 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa40000
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036266 Essential Splice Site 87 373 2 6
ENSDART00000138588 Essential Splice Site 99 385 2 8
Genomic Location (Zv9):
Chromosome 3 (position 8869401)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 8406868
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AAGAGTTAAAGACGAGAGGAGAGCTGGAGAAAACAGTTCAACACATCAAG[G/A]TAAGGACTGGTATCTCAACACTGAGTTATCTCACATAATTGTATGCAGAA
Associated Phenotype:
Not determined

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