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Protein-coding gene in the species Homo sapiens
channel-like protein 6 is a protein that in humans is encoded by the TMC6 gene. In vivo, TMC6 and its homolog TMC8, interact and form a complex with the zinc
TMC6
Medical condition
biallelic loss-of-function mutations of transmembrane channel-like protein 6 (TMC6; also called EV protein 1, EVER1), TMC8 (also called EVER2), or calcium-
Epidermodysplasia verruciformis
Epidermodysplasia_verruciformis
Human chromosome
pyrophosphatase/phosphodiesterase 7 (17q25.3) RHBDF2: Rhomboid family member 2 (17q25.3) TMC6 and TMC8: Transmembrane channel-like 6 and 8 (epidermodysplasia verruciformis)
Chromosome_17
Mammalian protein found in humans
MBP TNFRSF14 IRF4 RBM35A PLA1A APOLD1 KCNN2 INPP4B CAPN3 LGALS3 GREB1 FRMD4B SLC1A4 TBC1D16 GMPR ASAH1 MICAL1 TMC6 ITPKB SLC7A8
Microphthalmia-associated transcription factor
Microphthalmia-associated_transcription_factor
type 1 ERCC6 (CSB) Cockayne syndrome ERCC8 (CSA) Cockayne syndrome EVER1 (TMC6) Epidermodysplasia verruciformis EVER2 (TCM8) Epidermodysplasia verruciformis
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Q7Z5M5 16807 TMC4 HGNC:22998; Q7Z404 16808 TMC5 HGNC:22999; Q6UXY8 16809 TMC6 HGNC:18021; Q7Z403 16810 TMC7 HGNC:23000; Q7Z402 16811 TMC8 HGNC:20474; Q8IU68
List of human protein-coding genes 8
List_of_human_protein-coding_genes_8
peroxidase deficiency; 261500; EPX Epidermodysplasia verruciformis; 226400; TMC6 Epidermodysplasia verruciformis; 226400; TMC8 Epidermolysis bullosa dystrophica
List_of_OMIM_disorder_codes
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