SEC61A2
Protein transport protein Sec61 subunit alpha isoform 2
Also known as: FLJ10578, S61A2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H9S3
- Gene
- SEC61A2
- Ensembl
- ENSG00000065665
- Chromosome
- 10
- Canonical length
- 476 aa
- Protein class
- Predicted membrane proteins, Transporters
OverviewNCBI Gene
The protein encoded by this gene has similarity to a mouse protein which suggests a role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum. It may also be required for the assembly of membrane and secretory proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
Canonical amino-acid sequenceUniProt
476 residues, UniProt reviewed canonical sequence.
>Q9H9S3|SEC61A2
1 MGIKFLEVIK PFCAVLPEIQ KPERKIQFRE KVLWTAITLF IFLVCCQIPL FGIMSSDSAD
61 PFYWMRVILA SNRGTLMELG ISPIVTSGLI MQLLAGAKII EVGDTPKDRA LFNGAQKLFG
121 MIITIGQAIV YVMTGMYGDP AEMGAGICLL IIIQLFVAGL IVLLLDELLQ KGYGLGSGIS
181 LFIATNICET IVWKAFSPTT INTGRGTEFE GAVIALFHLL ATRTDKVRAL REAFYRQNLP
241 NLMNLIATVF VFAVVIYFQG FRVDLPIKSA RYRGQYSSYP IKLFYTSNIP IILQSALVSN
301 LYVISQMLSV RFSGNFLVNL LGQWADVSGG GPARSYPVGG LCYYLSPPES MGAIFEDPVH
361 VVVYIIFMLG SCAFFSKTWI EVSGSSAKDV AKQLKEQQMV MRGHRDTSMV HELNRYIPTA
421 AAFGGLCIGA LSVLADFLGA IGSGTGILLA VTIIYQYFEI FVKEQAEVGG MGALFFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC61A2 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
- 10
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 32 nTPM
- hypothalamus: 31 nTPM
- cerebral cortex: 26 nTPM
- hippocampal formation: 24 nTPM
- cerebellum: 24 nTPM
- midbrain: 22 nTPM
Single-cell type
- neutrophils: 89 nCPM
- retinal horizontal cells: 80 nCPM
- other brain neurons: 63 nCPM
- oligodendrocytes: 56 nCPM
- brain inhibitory neurons: 56 nCPM
- cardiomyocytes: 55 nCPM
Immune cell
- plasmacytoid DC: 2.5 nTPM
- neutrophil: 1.7 nTPM
- naive CD4 T-cell: 1 nTPM
- NK-cell: 0.9 nTPM
- gdT-cell: 0.8 nTPM
- MAIT T-cell: 0.7 nTPM
Brain region
- white matter: 67 nTPM
- cerebral cortex: 66 nTPM
- hypothalamus: 64 nTPM
- pons: 62 nTPM
- midbrain: 61 nTPM
- basal ganglia: 59 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)
- 0.56
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 3
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- post-translational protein targeting to membrane, translocation
- SRP-dependent cotranslational protein targeting to membrane, translocation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SEC61A2 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 SEC61A2 as an antibody target. Whether an autoantibody or antibody against SEC61A2 could matter depends on whether native SEC61A2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC61A2 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 SEC61A2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...