SEC23A
Protein transport protein Sec23A
Also known as: SC23A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15436
- Gene
- SEC23A
- Ensembl
- ENSG00000100934
- Chromosome
- 14
- Canonical length
- 765 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family. It is part of a protein complex and found in the ribosome-free transitional face of the endoplasmic reticulum (ER) and associated vesicles. This protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The encoded protein is suggested to play a role in the ER-Golgi protein trafficking. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
765 residues, UniProt reviewed canonical sequence.
>Q15436|SEC23A
1 MTTYLEFIQQ NEERDGVRFS WNVWPSSRLE ATRMVVPVAA LFTPLKERPD LPPIQYEPVL
61 CSRTTCRAVL NPLCQVDYRA KLWACNFCYQ RNQFPPSYAG ISELNQPAEL LPQFSSIEYV
121 VLRGPQMPLI FLYVVDTCME DEDLQALKES MQMSLSLLPP TALVGLITFG RMVQVHELGC
181 EGISKSYVFR GTKDLSAKQL QEMLGLSKVP LTQATRGPQV QQPPPSNRFL QPVQKIDMNL
241 TDLLGELQRD PWPVPQGKRP LRSSGVALSI AVGLLECTFP NTGARIMMFI GGPATQGPGM
301 VVGDELKTPI RSWHDIDKDN AKYVKKGTKH FEALANRAAT TGHVIDIYAC ALDQTGLLEM
361 KCCPNLTGGY MVMGDSFNTS LFKQTFQRVF TKDMHGQFKM GFGGTLEIKT SREIKISGAI
421 GPCVSLNSKG PCVSENEIGT GGTCQWKICG LSPTTTLAIY FEVVNQHNAP IPQGGRGAIQ
481 FVTQYQHSSG QRRIRVTTIA RNWADAQTQI QNIAASFDQE AAAILMARLA IYRAETEEGP
541 DVLRWLDRQL IRLCQKFGEY HKDDPSSFRF SETFSLYPQF MFHLRRSSFL QVFNNSPDES
601 SYYRHHFMRQ DLTQSLIMIQ PILYAYSFSG PPEPVLLDSS SILADRILLM DTFFQILIYH
661 GETIAQWRKS GYQDMPEYEN FRHLLQAPVD DAQEILHSRF PMPRYIDTEH GGSQARFLLS
721 KVNPSQTHNN MYAWGQESGA PILTDDVSLQ VFMDHLKKLA VSSAALocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC23A 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
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- smooth muscle: 84 nTPM
- liver: 76 nTPM
- tongue: 55 nTPM
- duodenum: 54 nTPM
- blood vessel: 53 nTPM
- skeletal muscle: 51 nTPM
Single-cell type
- enterocytes: 189 nCPM
- hepatocytes: 179 nCPM
- lactotrophs: 178 nCPM
- somatotrophs: 164 nCPM
- gonadotrophs: 144 nCPM
- neutrophil progenitors: 138 nCPM
Immune cell
- basophil: 70 nTPM
- NK-cell: 42 nTPM
- eosinophil: 39 nTPM
- MAIT T-cell: 38 nTPM
- T-reg: 38 nTPM
- naive CD4 T-cell: 35 nTPM
Brain region
- choroid plexus: 101 nTPM
- hypothalamus: 74 nTPM
- cerebellum: 72 nTPM
- cerebral cortex: 69 nTPM
- pons: 68 nTPM
- midbrain: 65 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SEC23A.
Disease | AllUniProt
Conditions SEC23A is implicated in, by any mechanism.
- Craniolenticulosutural dysplasia (CLSD) MIM:607812
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 264 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.74
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.79
- DepMap mean gene effect
- -0.17
- 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
- COPII-coated vesicle cargo loading
- intracellular protein transport
- protein localization to plasma membrane
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, Sec23/Sec24-type
- Sec23/Sec24, trunk domain
- Sec23/Sec24, helical domain
- Gelsolin-like domain
- Sec23/Sec24, beta-sandwich
- ADF-H/Gelsolin-like domain superfamily
- Zinc finger, Sec23/Sec24-type superfamily
- Sec23/Sec24 helical domain superfamily
- Gelsolin-like domain superfamily
- von Willebrand factor A-like domain superfamily
- Protein transport protein Sec23
- Sec23, C-terminal
- Gelsolin repeat
- Sec23/Sec24 zinc finger
- Sec23/Sec24 trunk domain
- Sec23/Sec24 helical domain
- Sec23/Sec24 beta-sandwich domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SEC23A 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 SEC23A as an antibody target. Whether an autoantibody or antibody against SEC23A could matter depends on whether native SEC23A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC23A 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 SEC23A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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