KIAA0195 [Homo sapiens]

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Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94. [Genes (Basel). 2020]
Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94.
Al-Hamed MH, Alsahan N, Tulbah M, Kurdi W, Ali W, Sayer JA, Imtiaz F. Genes (Basel). 2020 Aug 20; 11(9). Epub 2020 Aug 20.
Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism. [Am J Hum Genet. 2018]
Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism.
Stephen J, Maddirevula S, Nampoothiri S, Burke JD, Herzog M, Shukla A, Steindl K, Eskin A, Patil SJ, Joset P, et al. Am J Hum Genet. 2018 Dec 6; 103(6):948-967.
ERMA (TMEM94) is a P-type ATPase transporter for Mg(2+) uptake in the endoplasmic reticulum. [Mol Cell. 2024]
ERMA (TMEM94) is a P-type ATPase transporter for Mg(2+) uptake in the endoplasmic reticulum.
Vishnu N, Venkatesan M, Madaris TR, Venkateswaran MK, Stanley K, Ramachandran K, Chidambaram A, Madesh AK, Yang W, Nair J, et al. Mol Cell. 2024 Apr 4; 84(7):1321-1337.e11. Epub 2024 Mar 20.

RefSeq genomic sequence
See the genomic reference sequence for the TMEM94 gene (NG_054884.1).
RefSeq protein isoforms
See 95 reference sequence protein isoforms for the TMEM94 gene.

Nucleotide
Nucleotide sequence from coding region
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein