si:dkey-266f7.1

Ensembl ID:
ENSDARG00000094283
ZFIN ID:
ZDB-GENE-061207-67
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WUS6]
Human Orthologue:
C8orf80
Human Description:
chromosome 8 open reading frame 80 [Source:HGNC Symbol;Acc:33550]
Mouse Orthologue:
Gm600
Mouse Description:
predicted gene 600 Gene [Source:MGI Symbol;Acc:MGI:2685446]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa13249 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13249
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000145695 Nonsense 184 314 6 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 8533180)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 7991719
GRCz11 19 7910644
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GATGTAGAGATKSCATTGCAAAAATKAAYGAGATGGASAAAGACAAAAGA[A/T]GAAAGGAAACYATTGGTGTTTTTGGMAAAACAGGAGAAGGAAAAAGCTCT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

  • Cardiac Troponin-T levels: Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. (View Study)

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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