SEC24B
Protein transport protein Sec24B
Also known as: SC24B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95487
- Gene
- SEC24B
- Ensembl
- ENSG00000138802
- Chromosome
- 4
- Canonical length
- 1268 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,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 is thought to be a cargo-binding component of the COPII vesicle, and is thought to be involved in the transport of secretory proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in this gene have been associated with neural tube defects, and are thought to be a result of a disruption in interactions with the protein encoded by the VANGL planar cell polarity protein 2 (VANGL2) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
1268 residues, UniProt reviewed canonical sequence.
>O95487|SEC24B
1 MSAPAGSSHP AASARIPPKF GGAAVSGAAA PAGPGAGPAP HQQNGPAQNQ MQVPSGYGLH
61 HQNYIAPSGH YSQGPGKMTS LPLDTQCGDY YSALYTVPTQ NVTPNTVNQQ PGAQQLYSRG
121 PPAPHIVGST LGSFQGAASS ASHLHTSASQ PYSSFVNHYN SPAMYSASSS VASQGFPSTC
181 GHYAMSTVSN AAYPSVSYPS LPAGDTYGQM FTSQNAPTVR PVKDNSFSGQ NTAISHPSPL
241 PPLPSQQHHQ QQSLSGYSTL TWSSPGLPST QDNLIRNHTG SLAVANNNPT ITVADSLSCP
301 VMQNVQPPKS SPVVSTVLSG SSGSSSTRTP PTANHPVEPV TSVTQPSELL QQKGVQYGEY
361 VNNQASSAPT PLSSTSDDEE EEEEDEEAGV DSSSTTSSAS PMPNSYDALE GGSYPDMLSS
421 SASSPAPDPA PEPDPASAPA PASAPAPVVP QPSKMAKPFG YGYPTLQPGY QNATAPLISG
481 VQPSNPVYSG FQQYPQQYPG VNQLSSSIGG LSLQSSPQPE SLRPVNLTQE RNILPMTPVW
541 APVPNLNADL KKLNCSPDSF RCTLTNIPQT QALLNKAKLP LGLLLHPFRD LTQLPVITSN
601 TIVRCRSCRT YINPFVSFID QRRWKCNLCY RVNDVPEEFM YNPLTRSYGE PHKRPEVQNS
661 TVEFIASSDY MLRPPQPAVY LFVLDVSHNA VEAGYLTILC QSLLENLDKL PGDSRTRIGF
721 MTFDSTIHFY NLQEGLSQPQ MLIVSDIDDV FLPTPDSLLV NLYESKELIK DLLNALPNMF
781 TNTRETHSAL GPALQAAFKL MSPTGGRVSV FQTQLPSLGA GLLQSREDPN QRSSTKVVQH
841 LGPATDFYKK LALDCSGQQT AVDLFLLSSQ YSDLASLACM SKYSAGCIYY YPSFHYTHNP
901 SQAEKLQKDL KRYLTRKIGF EAVMRIRCTK GLSMHTFHGN FFVRSTDLLS LANINPDAGF
961 AVQLSIEESL TDTSLVCFQT ALLYTSSKGE RRIRVHTLCL PVVSSLADVY AGVDVQAAIC
1021 LLANMAVDRS VSSSLSDARD ALVNAVVDSL SAYGSTVSNL QHSALMAPSS LKLFPLYVLA
1081 LLKQKAFRTG TSTRLDDRVY AMCQIKSQPL VHLMKMIHPN LYRIDRLTDE GAVHVNDRIV
1141 PQPPLQKLSA EKLTREGAFL MDCGSVFYIW VGKGCDNNFI EDVLGYTNFA SIPQKMTHLP
1201 ELDTLSSERA RSFITWLRDS RPLSPILHIV KDESPAKAEF FQHLIEDRTE AAFSYYEFLL
1261 HVQQQICKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC24B 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)
- 0.42
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- liver: 43 nTPM
- retina: 30 nTPM
- bone marrow: 26 nTPM
- skeletal muscle: 26 nTPM
- thymus: 25 nTPM
- tongue: 21 nTPM
Single-cell type
- neutrophils: 418 nCPM
- neutrophil progenitors: 246 nCPM
- choroid plexus epithelial cells: 203 nCPM
- retinal pigment epithelial cells: 196 nCPM
- adrenal cortex cells: 187 nCPM
- thyrotrophs: 182 nCPM
Immune cell
- myeloid DC: 12 nTPM
- eosinophil: 12 nTPM
- NK-cell: 12 nTPM
- naive CD4 T-cell: 11 nTPM
- non-classical monocyte: 11 nTPM
- intermediate monocyte: 10 nTPM
Brain region
- choroid plexus: 47 nTPM
- cerebellum: 46 nTPM
- cerebral cortex: 35 nTPM
- white matter: 34 nTPM
- pons: 32 nTPM
- medulla oblongata: 32 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)
- 0.19
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.23
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- aorta morphogenesis
- auditory receptor cell stereocilium organization
- cochlear nucleus development
- COPII-coated vesicle cargo loading
- coronary artery morphogenesis
- endoplasmic reticulum to Golgi vesicle-mediated transport
- intracellular protein transport
- lung lobe morphogenesis
- neural tube closure
- outflow tract morphogenesis
- pulmonary artery morphogenesis
- regulation of cargo loading into COPII-coated vesicle
- regulation of establishment of planar polarity involved in neural tube closure
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 SEC24B 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 SEC24B as an antibody target. Whether an autoantibody or antibody against SEC24B could matter depends on whether native SEC24B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC24B 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 SEC24B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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