dbn1

Ensembl ID:
ENSDARG00000069113
ZFIN ID:
ZDB-GENE-091204-284
Human Orthologue:
DBN1
Human Description:
drebrin 1 [Source:HGNC Symbol;Acc:2695]
Mouse Orthologue:
Dbn1
Mouse Description:
drebrin 1 Gene [Source:MGI Symbol;Acc:MGI:1931838]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa24003 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24003
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
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100310 Nonsense 256 553 8 14
ENSDART00000133115   None 85 None 3
ENSDART00000138222   None 145 None 3
Genomic Location (Zv9):
Chromosome 21 (position 36157144)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 37149358
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACAGGAAGAAGATTCTGGAGGAGGAAGAGGCCAAAGAGAGGACAAGGAAT[C/T]AACCTTTGATTGTAAGAGTGCGTACGCTTTCAGTACGGTAAACCAGGTTT
Associated Phenotype:
Not determined

GWAS

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

  • Prothrombin time: Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. (View Study)

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

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