trappc3

Ensembl ID:
ENSDARG00000045364
ZFIN ID:
ZDB-GENE-040801-120
Description:
trafficking protein particle complex subunit 3 [Source:RefSeq peptide;Acc:NP_001003601]
Human Orthologue:
TRAPPC3
Human Description:
trafficking protein particle complex 3 [Source:HGNC Symbol;Acc:19942]
Mouse Orthologue:
Trappc3
Mouse Description:
trafficking protein particle complex 3 Gene [Source:MGI Symbol;Acc:MGI:1351486]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa43319 Essential Splice Site Mutation detected in F1 DNA During 2016
sa14418 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa43319
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 2016.
Mutation:
T > G
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066712 Essential Splice Site 14 180 1 5
Genomic Location:
Chromosome 19 (position 37281596)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGACAACATGTCTAGGCAGTCAAACAGAGCCACGGACAGCAAGAAGATGG[T/G]GAGTGTGTATCGTGTTGTTTCAGTTACTACATAAACCCAAGGCTGCTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14418
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066712 Essential Splice Site 47 180 2 5
Genomic Location:
Chromosome 19 (position 37277847)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GTAAGGACTATGAAAATGATGAAGAGGTCAACAAACAACTGGATAAAATG[T/G]RAGTCTGCCTTTCCCTTGCTTTCATTCTGATTTAGYCCTCTCATCAYYAG
Associated Phenotype:
Not determined

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