|Institutional Source||Beutler Lab|
|Gene Name||integrin beta 1 (fibronectin receptor beta)|
|Synonyms||Gm9863, Fnrb, CD29, 4633401G24Rik, beta1 integrin|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R7800 (G1)|
|Chromosomal Location||128685654-128733200 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 128713237 bp|
|Amino Acid Change||Lysine to Glutamic Acid at position 136 (K136E)|
|Ref Sequence||ENSEMBL: ENSMUSP00000087457 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000090006] [ENSMUST00000124826]|
|Predicted Effect||possibly damaging
AA Change: K136E
PolyPhen 2 Score 0.890 (Sensitivity: 0.82; Specificity: 0.94)
AA Change: K136E
|Predicted Effect||probably benign
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Integrins are heterodimeric proteins made up of alpha and beta subunits. At least 18 alpha and 8 beta subunits have been described in mammals. Integrin family members are membrane receptors involved in cell adhesion and recognition in a variety of processes including embryogenesis, hemostasis, tissue repair, immune response and metastatic diffusion of tumor cells. This gene encodes a beta subunit. Multiple alternatively spliced transcript variants which encode different protein isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous targeted null mutants die at or soon after implantation. Tissue-specific knockouts exhibit skin blisters, hair-loss, brain and heart defects, and impaired immune responses, wound healing, and hematopoietic stem cell migration, respectively. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Itgb1||
(F):5'- GTTGAGGCGCTAACAAAATTCT -3'
(R):5'- CACCAACTCTAAATGCACATCTTTT -3'
(F):5'- GGCGCTAACAAAATTCTTAGATTTGG -3'
(R):5'- TTTCTAAAGCCCAGTATGGAGGC -3'