RecName: Full=Interferon-induced transmembrane protein 5; AltName: Ful - Protein

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Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V. [Bone. 2021]
Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V.
Whyte MP, Aronson J, McAlister WH, Weinstein RS, Wenkert D, Clements KL, Gottesman GS, Madson KL, Stolina M, Bijanki VN, et al. Bone. 2021 Apr; 145:115835. Epub 2020 Dec 24.
A novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature. [Clin Dysmorphol. 2019]
A novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature.
Lim JY, Bhatia NS, Vasanwala RF, Chay PL, Lim KBL, Khoo PC, Schwarze U, Jamuar SS. Clin Dysmorphol. 2019 Jul; 28(3):120-125.
Dental and craniofacial characteristics caused by the p.Ser40Leu mutation in IFITM5. [Am J Med Genet A. 2019]
Dental and craniofacial characteristics caused by the p.Ser40Leu mutation in IFITM5.
Dagdeviren D, Tamimi F, Lee B, Sutton R, Rauch F, Retrouvey JM. Am J Med Genet A. 2019 Jan; 179(1):65-70. Epub 2018 Oct 5.

RefSeq protein
See the reference protein sequence for interferon-induced transmembrane protein 5 (NP_001020466.1).

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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Interferon-induced transmembrane protein 5; AltName: Full=Bone-res...
RecName: Full=Interferon-induced transmembrane protein 5; AltName: Full=Bone-restricted interferon-induced transmembrane protein-like protein; Short=BRIL; AltName: Full=Dispanin subfamily A member 1; Short=DSPA1
gi|158705851|sp|A6NNB3.1|IFM5_HUMAN

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