Protein name: TMEM165 Aliases: N/D Substrates: Ca2+, H+ [PMID: 23569283]; or Mn2+ [PMID: 27008884] [PMID: 28270545] Transport type: Exchanger / Ca2+:H+ Tissue and cellular expression: N/D Subcellular expression: Golgi, lysosomes, endosomes, plasma membrane (PM) [PMID: 23575229] Disease: Congenital disorder of glycosylation (CDG) type II [PMID: 22683087] [PMID: 23430531] Locus: 4q12 Sequence ID: NP_060945.2, NM_018475.4 XP_016863901.1, XM_017008412.1 Gene ID: 55858 Splice variants: N/D

TM165_HUMAN (UniProt)

Gene names: TMEM165, TPARL
Protein names and data: TM165_HUMAN, Full=Transmembrane protein 165, Full=Transmembrane protein PT27; Full=Transmembrane protein TPARL Length: 324 a.a., Mass: 34906 Da,
fasta formatted sequence

Database cross-references

UniProt: Q9HC07
OMIM: 614726 614727
Ensembl: ENST00000381334
GeneCard: TMEM165
TCDB: 2.A.106.2.2
HGNC: HGNC:30760

Genetic variants

See also Ensembl:ENST00000381334