si:ch211-175l6.1

Ensembl ID:
ENSDARG00000093464
ZFIN ID:
ZDB-GENE-060503-861
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1MT13]
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 Estimate
sa45130 Nonsense Mutation detected in F1 DNA During 2018
sa11620 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa45130
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 2018.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000146637 Nonsense 34 319 2 5
Genomic Location (Zv9):
Chromosome 3 (position 8078913)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 8126689
GRCz11 3 8012529
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTGTGTTTTGACTCAGATTATTAAATGTGTCTGTGATTTACTTTCAGTTT[C/T]AAGCTGATCACACAGAGCGTCAGATTAAACATGAGTTTGAGAAGCTTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11620
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000146637 Nonsense 149 319 4 5
Genomic Location (Zv9):
Chromosome 3 (position 8079409)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 8126193
GRCz11 3 8012033
KASP Assay ID:
2259-3046.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TGATTCATGTGTGKCGCTACTTGGGGAACCTGCCGTTCAGAGTCTGGAAG[A/T]AGATGCAGGACATCGTCCACTACAGTAAGAGTCCCTACAACATCTCTACT
Associated Phenotype:
Not determined

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