GRAMD1A
Protein Aster-A
Also known as: ASTRA_HUMAN, FLJ90346, KIAA1533
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96CP6
- Gene
- GRAMD1A
- Ensembl
- ENSG00000089351
- Chromosome
- 19
- Canonical length
- 724 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
Predicted to enable cholesterol binding activity and cholesterol transfer activity. Predicted to be involved in cellular response to cholesterol and intracellular sterol transport. Located in several cellular components, including cytosol; endoplasmic reticulum membrane; and organelle membrane contact site. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
724 residues, UniProt reviewed canonical sequence.
>Q96CP6|GRAMD1A
1 MFDTTPHSGR STPSSSPSLR KRLQLLPPSR PPPEPEPGTM VEKGSDSSSE KGGVPGTPST
61 QSLGSRNFIR NSKKMQSWYS MLSPTYKQRN EDFRKLFSKL PEAERLIVDY SCALQREILL
121 QGRLYLSENW ICFYSNIFRW ETTISIQLKE VTCLKKEKTA KLIPNAIQIC TESEKHFFTS
181 FGARDRCFLL IFRLWQNALL EKTLSPRELW HLVHQCYGSE LGLTSEDEDY VSPLQLNGLG
241 TPKEVGDVIA LSDITSSGAA DRSQEPSPVG SRRGHVTPNL SRASSDADHG AEEDKEEQVD
301 SQPDASSSQT VTPVAEPPST EPTQPDGPTT LGPLDLLPSE ELLTDTSNSS SSTGEEADLA
361 ALLPDLSGRL LINSVFHVGA ERLQQMLFSD SPFLQGFLQQ CKFTDVTLSP WSGDSKCHQR
421 RVLTYTIPIS NPLGPKSASV VETQTLFRRG PQAGGCVVDS EVLTQGIPYQ DYFYTAHRYC
481 ILGLARNKAR LRVSSEIRYR KQPWSLVKSL IEKNSWSGIE DYFHHLEREL AKAEKLSLEE
541 GGKDARGLLS GLRRRKRPLS WRAHGDGPQH PDPDPCARAG IHTSGSLSSR FSEPSVDQGP
601 GAGIPSALVL ISIVICVSLI ILIALNVLLF YRLWSLERTA HTFESWHSLA LAKGKFPQTA
661 TEWAEILALQ KQFHSVEVHK WRQILRASVE LLDEMKFSLE KLHQGITVSD PPFDTQPRPD
721 DSFSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GRAMD1A 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
- 1
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 87 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 87 nTPM
- lung: 63 nTPM
- salivary gland: 52 nTPM
- skeletal muscle: 51 nTPM
- spleen: 46 nTPM
- ovary: 43 nTPM
Single-cell type
- neutrophils: 680 nCPM
- pancreatic acinar cells: 167 nCPM
- monocytes: 122 nCPM
- alveolar cells type 1: 116 nCPM
- hofbauer cells: 112 nCPM
- vascular endothelial cells: 98 nCPM
Immune cell
- basophil: 23 nTPM
- non-classical monocyte: 20 nTPM
- neutrophil: 13 nTPM
- intermediate monocyte: 9.6 nTPM
- MAIT T-cell: 7.3 nTPM
- classical monocyte: 5.7 nTPM
Brain region
- medulla oblongata: 51 nTPM
- cerebral cortex: 51 nTPM
- pons: 51 nTPM
- thalamus: 50 nTPM
- midbrain: 49 nTPM
- hypothalamus: 44 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)
- 0.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.29
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GRAMD1A 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 GRAMD1A as an antibody target. Whether an autoantibody or antibody against GRAMD1A could matter depends on whether native GRAMD1A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GRAMD1A is annotated at the cell surface, where native GRAMD1A 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 GRAMD1A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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