TMEM214
Transmembrane protein 214
Also known as: FLJ20254, TM214_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NUQ4
- Gene
- TMEM214
- Ensembl
- ENSG00000119777
- Chromosome
- 2
- Canonical length
- 689 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Endoplasmic reticulum,Golgi apparatus,Cytosol
OverviewNCBI Gene
Predicted to be involved in apoptotic process. Located in several cellular components, including Golgi apparatus; cytoplasmic microtubule; and endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
689 residues, UniProt reviewed canonical sequence.
>Q6NUQ4|TMEM214
1 MATKTAGVGR WEVVKKGRRP GVGAGAGGRG GGRNRRALGE ANGVWKYDLT PAIQTTSTLY
61 ERGFENIMKR QNKEQVPPPA VEPKKPGNKK QPKKVATPPN QNQKQGRFRS LEEALKALDV
121 ADLQKELDKS QSVFSGNPSI WLKDLASYLN YKLQAPLSEP TLSQHTHDYP YSLVSRELRG
181 IIRGLLAKAA GSLELFFDHC LFTMLQELDK TPGESLHGYR ICIQAILQDK PKIATANLGK
241 FLELLRSHQS RPAKCLTIMW ALGQAGFANL TEGLKVWLGI MLPVLGIKSL SPFAITYLDR
301 LLLMHPNLTK GFGMIGPKDF FPLLDFAYMP NNSLTPSLQE QLCQLYPRLK VLAFGAKPDS
361 TLHTYFPSFL SRATPSCPPE MKKELLSSLT ECLTVDPLSA SVWRQLYPKH LSQSSLLLEH
421 LLSSWEQIPK KVQKSLQETI QSLKLTNQEL LRKGSSNNQD VVTCDMACKG LLQQVQGPRL
481 PWTRLLLLLL VFAVGFLCHD LRSHSSFQAS LTGRLLRSSG FLPASQQACA KLYSYSLQGY
541 SWLGETLPLW GSHLLTVVRP SLQLAWAHTN ATVSFLSAHC ASHLAWFGDS LTSLSQRLQI
601 QLPDSVNQLL RYLRELPLLF HQNVLLPLWH LLLEALAWAQ EHCHEACRGE VTWDCMKTQL
661 SEAVHWTWLC LQDITVAFLD WALALISQQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM214 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 2
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 79 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 79 nTPM
- pancreas: 76 nTPM
- epididymis: 63 nTPM
- pituitary gland: 59 nTPM
- blood vessel: 56 nTPM
- parathyroid gland: 53 nTPM
Single-cell type
- syncytiotrophoblasts: 85 nCPM
- extravillous trophoblasts: 80 nCPM
- plasma cells: 64 nCPM
- hepatic stellate cells: 58 nCPM
- salivary acinar cells: 56 nCPM
- epididymal principal cells: 52 nCPM
Immune cell
- basophil: 5.7 nTPM
- NK-cell: 5.6 nTPM
- MAIT T-cell: 5 nTPM
- plasmacytoid DC: 5 nTPM
- gdT-cell: 3.9 nTPM
- intermediate monocyte: 3.8 nTPM
Brain region
- choroid plexus: 56 nTPM
- medulla oblongata: 36 nTPM
- midbrain: 35 nTPM
- pons: 34 nTPM
- thalamus: 33 nTPM
- hypothalamus: 31 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.73
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transmembrane protein 214
- TMEM214, C-terminal, caspase 4 activator
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM214 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM214 as an antibody target. Whether an autoantibody or antibody against TMEM214 could matter depends on whether native TMEM214 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM214 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TMEM214 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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