|Institutional Source||Beutler Lab|
|Gene Name||Fraser extracellular matrix complex subunit 1|
|Essential gene?||Non essential (E-score: 0.000)|
|Stock #||R9779 (G1)|
|Chromosomal Location||96373955-96784728 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to A at 96569494 bp (GRCm38)|
|Amino Acid Change||Threonine to Asparagine at position 389 (T389N)|
|Ref Sequence||ENSEMBL: ENSMUSP00000043250 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000036019]|
|AlphaFold||no structure available at present|
AA Change: T389N
PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
AA Change: T389N
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for mutations at this locus display a significant amount of embryonic lethality due to hemorrhaging of embryonic blisters. Survival is variable on genetic backgrounds. Kidney development is severely affected and syndactyly is common. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Fras1||
(F):5'- TGAAGGCATGCATCTCCTG -3'
(R):5'- TAGGCCTTGGTGAGTCCTTC -3'
(F):5'- GGCATGCATCTCCTGGTCTTTG -3'
(R):5'- ACACTGAGGGTCAATGACTTGCC -3'