GRINA
Protein lifeguard 1
Also known as: HNRGW, LFG1, LFG1_HUMAN, NMDARA1, TMBIM3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z429
- Gene
- GRINA
- Ensembl
- ENSG00000178719
- Chromosome
- 8
- Canonical length
- 371 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoli fibrillar center,Cytosol
OverviewNCBI Gene
Predicted to enable calcium channel activity. Predicted to be involved in apoptotic signaling pathway; negative regulation of extrinsic apoptotic signaling pathway via death domain receptors; and negative regulation of neuron apoptotic process. Predicted to act upstream of or within endoplasmic reticulum calcium ion homeostasis and negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway. Located in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
371 residues, UniProt reviewed canonical sequence.
>Q7Z429|GRINA
1 MSHEKSFLVS GDNYPPPNPG YPGGPQPPMP PYAQPPYPGA PYPQPPFQPS PYGQPGYPHG
61 PSPYPQGGYP QGPYPQGGYP QGPYPQEGYP QGPYPQGGYP QGPYPQSPFP PNPYGQPQVF
121 PGQDPDSPQH GNYQEEGPPS YYDNQDFPAT NWDDKSIRQA FIRKVFLVLT LQLSVTLSTV
181 SVFTFVAEVK GFVRENVWTY YVSYAVFFIS LIVLSCCGDF RRKHPWNLVA LSVLTASLSY
241 MVGMIASFYN TEAVIMAVGI TTAVCFTVVI FSMQTRYDFT SCMGVLLVSM VVLFIFAILC
301 IFIRNRILEI VYASLGALLF TCFLAVDTQL LLGNKQLSLS PEEYVFAALN LYTDIINIFL
361 YILTIIGRAK ELocalizationUniProt · AlphaFold · HPA
Whether an antibody against GRINA 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
- 7
- Mean surface accessibility (rSASA)
- 0.47
- Highest tissue expression
- 427 nTPM
Expression across tissuesHPA
Tissue
- liver: 427 nTPM
- cerebellum: 311 nTPM
- spleen: 298 nTPM
- cerebral cortex: 290 nTPM
- adipose tissue: 260 nTPM
- testis: 258 nTPM
Single-cell type
- late spermatids: 756 nCPM
- neutrophils: 397 nCPM
- syncytiotrophoblasts: 294 nCPM
- kupffer cells: 286 nCPM
- early spermatids: 283 nCPM
- hepatocytes: 228 nCPM
Immune cell
- intermediate monocyte: 36 nTPM
- non-classical monocyte: 36 nTPM
- classical monocyte: 32 nTPM
- plasmacytoid DC: 23 nTPM
- neutrophil: 19 nTPM
- total PBMC: 16 nTPM
Brain region
- thalamus: 263 nTPM
- pons: 258 nTPM
- hippocampal formation: 249 nTPM
- midbrain: 248 nTPM
- amygdala: 241 nTPM
- medulla oblongata: 239 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)
- 0.49
- gnomAD pLI
- 0.44
- gnomAD missense Z
- 1.21
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 16% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic signaling pathway
- endoplasmic reticulum calcium ion homeostasis
- negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway
- negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
- negative regulation of neuron apoptotic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GRINA as an antibody target. Whether an autoantibody or antibody against GRINA could matter depends on whether native GRINA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GRINA 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 GRINA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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