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Immunogen sequence: AFLMAGQVA EQLRGFNAQL QRTRQMIRAA EESASQIQSS AQRLETQVSA SRSQMEEDVR RTRLLIQQVR DFLTDPDTDA ATIQEVSEAV LALWLPTDSA TVLQKMNEIQ AIAARLPNVD LVLSQTKQDI ARARRLQAEA EEARSRAHAV EGQVEDVVGN LRQGTVALQE AQDTMQGTSR SLRLIQDRVA EVQQVLRPAE KLVTSMTKQL GDFWTRMEEL RHQARQQGAE AVQAQQLAEG ASEQALSAQE GFERIKQKYA ELKDRLGQSS MLGEQGARIQ SVKTEAEELF GETMEMMDRM KDMELELLRG SQAIMLRSAD LTGLEKRVEQ IRDHINGRVL YYATCK (828-1172 aa encoded by BC075838 )
The product encoded by this gene is a laminin that belongs to a family of basement membrane proteins. This protein is a beta subunit laminin, which together with an alpha and a gamma subunit, forms laminin-5. Mutations in this gene cause epidermolysis bullosa junctional Herlitz type, and generalized atrophic benign epidermolysis bullosa, diseases that are characterized by blistering of the skin. Multiple alternatively spliced transcript variants that encode the same protein have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Epiligrin subunit bata; Kalinin B1 chain; Kalinin subunit beta; kalinin-140kDa; Laminin B1k chain; laminin beta 3; laminin S B3 chain; Laminin subunit beta-3; laminin, beta 3 (nicein (125kD), kalinin (140kD), BM600 (125kD)); Laminin-5 subunit beta; Nicein subunit beta; nicein-125k; nicein-125kDa; RP1-272L16.3
Gene Aliases: AI1A; BM600-125KDA; LAM5; LAMB3; LAMNB1
UniProt ID: (Human) Q13751
Entrez Gene ID: (Human) 3914
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