|Institutional Source||Beutler Lab|
|Gene Name||multiple EGF-like-domains 8|
|Synonyms||Egfl4, b2b1702Clo, m687Ddg, b2b288Clo|
|Is this an essential gene?||Probably essential (E-score: 0.929)|
|Stock #||R7427 (G1)|
|Chromosomal Location||25317164-25365917 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to T at 25338371 bp|
|Amino Acid Change||Arginine to Cysteine at position 771 (R771C)|
|Ref Sequence||ENSEMBL: ENSMUSP00000122192 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000128119]|
|Predicted Effect||probably benign
AA Change: R771C
PolyPhen 2 Score 0.436 (Sensitivity: 0.89; Specificity: 0.90)
AA Change: R771C
|Coding Region Coverage||
|Validation Efficiency||100% (78/78)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
PHENOTYPE: Mice homozygous for an ENU mutation exhibit varying degrees of heterotaxia and congenital heart defects. Mice homozygous for another ENU-induced mutation exhibit abnormal development and patterning of the peripheral nervous system. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Megf8||
(F):5'- TTGAGTGACAAGTGCGATTTC -3'
(R):5'- AGGCTAGACACTCACACTGC -3'
(F):5'- ACAAGTGCGATTTCCCTGAG -3'
(R):5'- CTCACACTGCCACCCGG -3'