EGFLAM (1 of 2)

Ensembl ID:
ENSDARG00000059416
Description:
EGF-like, fibronectin type III and laminin G domains [Source:HGNC Symbol;Acc:26810]
Human Orthologue:
EGFLAM
Human Description:
EGF-like, fibronectin type III and laminin G domains [Source:HGNC Symbol;Acc:26810]
Mouse Orthologue:
Egflam
Mouse Description:
EGF-like, fibronectin type III and laminin G domains Gene [Source:MGI Symbol;Acc:MGI:2146149]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa40360 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa40360
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:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082542 Nonsense 209 793 6 19
Genomic Location (Zv9):
Chromosome 5 (position 8367351)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 7449743
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CAATGTTAATGTTAATGTTAATTTACAATGTCCCGCTTTAAAAACAGGTT[C/A]AGTGGACACAGGCAGTGGAGACTATGACGTCTACATCTCAAACTCTGATA
Associated Phenotype:
Not determined

GWAS

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

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

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