|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 #||R1654 (G1)|
|Chromosomal Location||25317164-25365917 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 25338486 bp|
|Amino Acid Change||Leucine to Proline at position 809 (L809P)|
|Ref Sequence||ENSEMBL: ENSMUSP00000122192 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000128119]|
|Predicted Effect||possibly damaging
AA Change: L809P
PolyPhen 2 Score 0.563 (Sensitivity: 0.88; Specificity: 0.91)
AA Change: L809P
|Coding Region Coverage||
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'- GGCAGCTTCCCAAAGTCTAGGAAC -3'
(R):5'- GAGGTCCAAGGCTGAAGTCAGAATC -3'
(F):5'- TTCCCAAAGTCTAGGAACCCTTG -3'
(R):5'- GGCTGAAGTCAGAATCAAGTG -3'