STBD1
Starch-binding domain-containing protein 1
Also known as: FLJ41801, GENX-3414, STBD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95210
- Gene
- STBD1
- Ensembl
- ENSG00000118804
- Chromosome
- 4
- Canonical length
- 358 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Transporters
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
Enables enzyme binding activity and glycogen binding activity. Involved in glycophagy and intracellular transport. Located in T-tubule; endoplasmic reticulum; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
358 residues, UniProt reviewed canonical sequence.
>O95210|STBD1
1 MGAVWSALLV GGGLAGALFV WLLRGGPGDT GKDGDAEQEK DAPLGGAAIP GGHQSGSSGL
61 SPGPSGQELV TKPEHLQESN GHLISKTKDL GKLQAASWRL QNPSREVCDN SREHVPSGQF
121 PDTEAPATSE TSNSRSYSEV SRNESLESPM GEWGFQKGQE ISAKAATCFA EKLPSSNLLK
181 NRAKEEMSLS DLNSQDRVDH EEWEMVPRHS SWGDVGVGGS LKAPVLNLNQ GMDNGRSTLV
241 EARGQQVHGK MERVAVMPAG SQQVSVRFQV HYVTSTDVQF IAVTGDHECL GRWNTYIPLH
301 YNKDGFWSHS IFLPADTVVE WKFVLVENGG VTRWEECSNR FLETGHEDKV VHAWWGIHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STBD1 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)
- 0.6
- Highest tissue expression
- 233 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 233 nTPM
- tongue: 144 nTPM
- liver: 122 nTPM
- adipose tissue: 103 nTPM
- heart muscle: 53 nTPM
- small intestine: 29 nTPM
Single-cell type
- enterocytes: 15 nCPM
- colonocytes: 7.1 nCPM
- urothelial cells: 5 nCPM
- fallopian tube ciliated cells: 4.5 nCPM
- other brain neurons: 3.8 nCPM
- goblet cells: 3.5 nCPM
Immune cell
- eosinophil: 5.7 nTPM
- NK-cell: 4.4 nTPM
- intermediate monocyte: 3.1 nTPM
- classical monocyte: 2.6 nTPM
- myeloid DC: 2.5 nTPM
- memory CD4 T-cell: 2.4 nTPM
Brain region
- hypothalamus: 9.4 nTPM
- medulla oblongata: 8.7 nTPM
- pons: 7.9 nTPM
- spinal cord: 6.5 nTPM
- thalamus: 6.3 nTPM
- white matter: 6.3 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.
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Carbohydrate binding module family 20
- Immunoglobulin-like fold
- Carbohydrate-binding-like fold
- Starch binding domain
- Starch-binding domain-containing protein 1, CBM20 domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STBD1 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 STBD1 as an antibody target. Whether an autoantibody or antibody against STBD1 could matter depends on whether native STBD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STBD1 is annotated at the cell surface, where native STBD1 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 STBD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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