GPRIN2
G protein-regulated inducer of neurite outgrowth 2
Also known as: GRIN2_HUMAN, KIAA0514, MGC15171
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60269
- Gene
- GPRIN2
- Ensembl
- ENSG00000204175
- Chromosome
- 10
- Canonical length
- 458 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Microtubules,Cytokinetic bridge,Mitotic spindle
OverviewNCBI Gene
Predicted to be involved in neuron projection development. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
458 residues, UniProt reviewed canonical sequence.
>O60269|GPRIN2
1 MSSSRPEPGP WAPLSPRLQP LSQSSSSLLG EGREQRPELR KTASSTVWQA QLGEASTRPQ
61 APEEEGNPPE SMKPARASGP KARPSAGGHW WSSTVGNVST MGGSDLCRLR APSAAAMQRS
121 HSDLVRSTQM RGHSGARKAS LSCSALGSSP VHRAQLQPGG TSGQGGQAPA GLERDLAPED
181 ETSNSAWMLG ASQLSVPPLD LGDTTAHSSS AQAEPKAAEQ LATTTCHALP PAALLCGMRE
241 VRAGGCCHAL PATGILAFPK LVASVSESGL QAQHGVKIHC RLSGGLPGHS HCCAHLWGPA
301 GLVPEPGSRT KDVWTMTSAN DLAPAEASPL SAQDAGVQAA PVAACKAVAT SPSLEAPAAL
361 HVFPEVTLGS SLEEVPSPVR DVRWDAEGMT WEVYGAAVDL EVLGVAIQKH LEMQFEQLQR
421 APASEDSLSV EGRRGPLRAV MQSLRRPSCC GCSGAAPELocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPRIN2 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.73
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- skin: 14 nTPM
- cerebellum: 9.1 nTPM
- lung: 7.4 nTPM
- small intestine: 5.9 nTPM
- rectum: 4.7 nTPM
- hypothalamus: 4.6 nTPM
Single-cell type
- alveolar cells type 1: 50 nCPM
- goblet cells: 48 nCPM
- late spermatids: 29 nCPM
- paneth cells: 27 nCPM
- colonocytes: 20 nCPM
- enterocytes: 19 nCPM
Immune cell
- neutrophil: 0.2 nTPM
- basophil: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- hypothalamus: 23 nTPM
- cerebellum: 21 nTPM
- pons: 17 nTPM
- thalamus: 14 nTPM
- midbrain: 14 nTPM
- medulla oblongata: 12 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)
- 1.49
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.56
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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
InteractionsUniProt · HPA
Protein binding partners of GPRIN2 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 GPRIN2 as an antibody target. Whether an autoantibody or antibody against GPRIN2 could matter depends on whether native GPRIN2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPRIN2 is annotated at the cell surface, where native GPRIN2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label GPRIN2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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