|Institutional Source||Beutler Lab|
|Gene Name||laminin, alpha 1|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R0312 (G1)|
|Chromosomal Location||67697265-67822645 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 67775851 bp (GRCm38)|
|Amino Acid Change||Leucine to Proline at position 1368 (L1368P)|
|Ref Sequence||ENSEMBL: ENSMUSP00000043957 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000035471]|
|AlphaFold||no structure available at present|
AA Change: L1368P
PolyPhen 2 Score 0.453 (Sensitivity: 0.89; Specificity: 0.90)
AA Change: L1368P
|Meta Mutation Damage Score||0.1795|
|Coding Region Coverage||
|Validation Efficiency||100% (60/60)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome. [provided by RefSeq, Sep 2014]
PHENOTYPE: Homozygous null mice display embryonic lethality before somite formation with impaired formation of Reichert's membrane. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Lama1||
(F):5'- TCGGCTCAGGACAGATGTAAATGC -3'
(R):5'- TCCCCAGAACTGTAAGCACATGGC -3'
(F):5'- GGACAGATGTAAATGCTAAACCTTG -3'
(R):5'- CACTCAAAAGTTGATGGAGTCC -3'