SEC23B
Protein transport protein Sec23B
Also known as: CDA-II, CDAII, CDAN2, HEMPAS, SC23B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15437
- Gene
- SEC23B
- Ensembl
- ENSG00000101310
- Chromosome
- 20
- Canonical length
- 767 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum,Vesicles,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The function of this gene product has been implicated in cargo selection and concentration. Multiple alternatively spliced transcript variants have been identified in this gene. [provided by RefSeq, Feb 2010]
Canonical amino-acid sequenceUniProt
767 residues, UniProt reviewed canonical sequence.
>Q15437|SEC23B
1 MATYLEFIQQ NEERDGVRFS WNVWPSSRLE ATRMVVPLAC LLTPLKERPD LPPVQYEPVL
61 CSRPTCKAVL NPLCQVDYRA KLWACNFCFQ RNQFPPAYGG ISEVNQPAEL MPQFSTIEYV
121 IQRGAQSPLI FLYVVDTCLE EDDLQALKES LQMSLSLLPP DALVGLITFG RMVQVHELSC
181 EGISKSYVFR GTKDLTAKQI QDMLGLTKPA MPMQQARPAQ PQEHPFASSR FLQPVHKIDM
241 NLTDLLGELQ RDPWPVTQGK RPLRSTGVAL SIAVGLLEGT FPNTGARIML FTGGPPTQGP
301 GMVVGDELKI PIRSWHDIEK DNARFMKKAT KHYEMLANRT AANGHCIDIY ACALDQTGLL
361 EMKCCANLTG GYMVMGDSFN TSLFKQTFQR IFTKDFNGDF RMAFGATLDV KTSRELKIAG
421 AIGPCVSLNV KGPCVSENEL GVGGTSQWKI CGLDPTSTLG IYFEVVNQHN TPIPQGGRGA
481 IQFVTHYQHS STQRRIRVTT IARNWADVQS QLRHIEAAFD QEAAAVLMAR LGVFRAESEE
541 GPDVLRWLDR QLIRLCQKFG QYNKEDPTSF RLSDSFSLYP QFMFHLRRSP FLQVFNNSPD
601 ESSYYRHHFA RQDLTQSLIM IQPILYSYSF HGPPEPVLLD SSSILADRIL LMDTFFQIVI
661 YLGETIAQWR KAGYQDMPEY ENFKHLLQAP LDDAQEILQA RFPMPRYINT EHGGSQARFL
721 LSKVNPSQTH NNLYAWGQET GAPILTDDVS LQVFMDHLKK LAVSSACLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC23B 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
- 67 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 67 nTPM
- pancreas: 60 nTPM
- thyroid gland: 56 nTPM
- choroid plexus: 54 nTPM
- epididymis: 51 nTPM
- parathyroid gland: 48 nTPM
Single-cell type
- neutrophils: 186 nCPM
- salivary acinar cells: 157 nCPM
- late primary spermatocytes: 128 nCPM
- monocyte progenitors: 121 nCPM
- plasma cells: 121 nCPM
- pancreatic acinar cells: 113 nCPM
Immune cell
- basophil: 149 nTPM
- myeloid DC: 108 nTPM
- eosinophil: 106 nTPM
- total PBMC: 104 nTPM
- intermediate monocyte: 96 nTPM
- non-classical monocyte: 96 nTPM
Brain region
- white matter: 78 nTPM
- choroid plexus: 58 nTPM
- medulla oblongata: 58 nTPM
- basal ganglia: 56 nTPM
- cerebellum: 52 nTPM
- spinal cord: 52 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SEC23B.
Disease | AllUniProt
Conditions SEC23B is implicated in, by any mechanism.
- Cowden syndrome 7 (CWS7) MIM:616858
- Anemia, congenital dyserythropoietic, 2 (CDAN2) MIM:224100
Disease | GeneticClinVar
99 pathogenic / likely-pathogenic of 819 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Congenital dyserythropoietic anemia, type II
- Cowden syndrome 7
- SEC23B-related disorder
- See cases
- Non-Fanconi anemia cytopenia
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)
- 0.98
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.47
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% 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
- 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 SEC23B 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 SEC23B as an antibody target. Whether an autoantibody or antibody against SEC23B could matter depends on whether native SEC23B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC23B 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 SEC23B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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