SEC24C
Protein transport protein Sec24C
Also known as: KIAA0079, SC24C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P53992
- Gene
- SEC24C
- Ensembl
- ENSG00000176986
- Chromosome
- 10
- Canonical length
- 1094 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The product of this gene may play a role in shaping the vesicle, as well as in cargo selection and concentration. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1094 residues, UniProt reviewed canonical sequence.
>P53992|SEC24C
1 MNVNQSVPPV PPFGQPQPIY PGYHQSSYGG QSGSTAPAIP YGAYNGPVPG YQQTPPQGMS
61 RAPPSSGAPP ASTAQAPCGQ AAYGQFGQGD VQNGPSSTVQ MQRLPGSQPF GSPLAPVGNQ
121 PPVLQPYGPP PTSAQVATQL SGMQISGAVA PAPPSSGLGF GPPTSLASAS GSFPNSGLYG
181 SYPQGQAPPL SQAQGHPGIQ TPQRSAPSQA SSFTPPASGG PRLPSMTGPL LPGQSFGGPS
241 VSQPNHVSSP PQALPPGTQM TGPLGPLPPM HSPQQPGYQP QQNGSFGPAR GPQSNYGGPY
301 PAAPTFGSQP GPPQPLPPKR LDPDAIPSPI QVIEDDRNNR GTEPFVTGVR GQVPPLVTTN
361 FLVKDQGNAS PRYIRCTSYN IPCTSDMAKQ AQVPLAAVIK PLARLPPEEA SPYVVDHGES
421 GPLRCNRCKA YMCPFMQFIE GGRRFQCCFC SCINDVPPQY FQHLDHTGKR VDAYDRPELS
481 LGSYEFLATV DYCKNNKFPS PPAFIFMIDV SYNAIRTGLV RLLCEELKSL LDFLPREGGA
541 EESAIRVGFV TYNKVLHFYN VKSSLAQPQM MVVSDVADMF VPLLDGFLVN VNESRAVITS
601 LLDQIPEMFA DTRETETVFV PVIQAGMEAL KAAECAGKLF LFHTSLPIAE APGKLKNRDD
661 RKLINTDKEK TLFQPQTGAY QTLAKECVAQ GCCVDLFLFP NQYVDVATLS VVPQLTGGSV
721 YKYASFQVEN DQERFLSDLR RDVQKVVGFD AVMRVRTSTG IRAVDFFGAF YMSNTTDVEL
781 AGLDGDKTVT VEFKHDDRLN EESGALLQCA LLYTSCAGQR RLRIHNLALN CCTQLADLYR
841 NCETDTLINY MAKFAYRGVL NSPVKAVRDT LITQCAQILA CYRKNCASPS SAGQLILPEC
901 MKLLPVYLNC VLKSDVLQPG AEVTTDDRAY VRQLVTSMDV TETNVFFYPR LLPLTKSPVE
961 STTEPPAVRA SEERLSNGDI YLLENGLNLF LWVGASVQQG VVQSLFSVSS FSQITSGLSV
1021 LPVLDNPLSK KVRGLIDSLR AQRSRYMKLT VVKQEDKMEM LFKHFLVEDK SLSGGASYVD
1081 FLCHMHKEIR QLLSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC24C 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)
- 0.36
- Highest tissue expression
- 66 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 66 nTPM
- parathyroid gland: 48 nTPM
- skeletal muscle: 47 nTPM
- pituitary gland: 43 nTPM
- liver: 43 nTPM
- tonsil: 41 nTPM
Single-cell type
- esophageal apical cells: 194 nCPM
- syncytiotrophoblasts: 61 nCPM
- tuft cells: 58 nCPM
- esophageal suprabasal cells: 50 nCPM
- neutrophil progenitors: 42 nCPM
- neutrophils: 41 nCPM
Immune cell
- MAIT T-cell: 36 nTPM
- basophil: 28 nTPM
- gdT-cell: 27 nTPM
- total PBMC: 23 nTPM
- NK-cell: 23 nTPM
- memory CD8 T-cell: 22 nTPM
Brain region
- cerebral cortex: 62 nTPM
- cerebellum: 47 nTPM
- thalamus: 47 nTPM
- white matter: 46 nTPM
- medulla oblongata: 45 nTPM
- pons: 44 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SEC24C.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 197 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)
- 0.17
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.5
- DepMap mean gene effect
- -0.13
- 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
- endoplasmic reticulum to Golgi vesicle-mediated transport
- in utero embryonic development
- intracellular protein transport
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
- Sec24-like, trunk domain
- SEC23/SEC24 family, SEC24 subfamily
- 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 SEC24C 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 SEC24C as an antibody target. Whether an autoantibody or antibody against SEC24C could matter depends on whether native SEC24C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC24C 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 SEC24C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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