SIMC1
SUMO-interacting motif-containing protein 1
Also known as: C5orf25, FLJ44216, OOMA1, PLEIAD, SIMC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NDZ2
- Gene
- SIMC1
- Ensembl
- ENSG00000170085
- Chromosome
- 5
- Canonical length
- 872 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center
OverviewNCBI Gene
Enables SUMO polymer binding activity and peptidase inhibitor activity. Located in PML body and sarcomere. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
872 residues, UniProt reviewed canonical sequence.
>Q8NDZ2|SIMC1
1 MAPASASGED LRKLPTMAEV NGEQDFIDLT RETRPRTKDR SGLYVIDLTR AEGENRPIAT
61 LDLTLEPVTP SQKEPTSLQT CASLSGKAVM EGHVDRSSQP TARRIINSDP VDLDLVEENT
121 FVGPPPATSI SGGSVYPTEP NCSSATFTGN LSFLASLQLS SDVSSLSPTS NNSRSSSSSS
181 NQKAPLPCPQ QDVSRPPQAL PCPLRPLPCP PRASPCPPRA SSCPPRALSC PSQTMQCQLP
241 ALTHPPQEVP CPRQNIPGPP QDSLGLPQDV PGLPQSILHP QDVAYLQDMP RSPGDVPQSP
301 SDVSPSPDAP QSPGGMPHLP GDVLHSPGDM PHSSGDVTHS PRDIPHLPGD RPDFTQNDVQ
361 NRDMPMDISA LSSPSCSPSP QSETPLEKVP WLSVMETPAR KEISLSEPAK PGSAHVQSRT
421 PQGGLYNRPC LHRLKYFLRP PVHHLFFQTL IPDKDTRENK GQKLEPIPHR RLRMVTNTIE
481 ENFPLGTVQF LMDFVSPQHY PPREIVAHII QKILLSGSET VDVLKEAYML LMKIQQLHPA
541 NAKTVEWDWK LLTYVMEEEG QTLPGRVLFL RYVVQTLEDD FQQTLRRQRQ HLQQSIANMV
601 LSCDKQPHNV RDVIKWLVKA VTEDGLTQPP NGNQTSSGTG ILKASSSHPS SQPNLTKNTN
661 QLIVCQLQRM LSIAVEVDRT PTCSSNKIAE MMFGFVLDIP ERSQREMFFT TMESHLLRCK
721 VLEIIFLHSC ETPTRLPLSL AQALYFLNNS TSLLKCQSDK SQWQTWDELV EHLQFLLSSY
781 QHVLREHLRS SVIDRKDLII KRIKPKPQQG DDITVVDVEK QIEAFRSRLI QMLGEPLVPQ
841 LQDKVHLLKL LLFYAADLNP DAEPFQKGWS GSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SIMC1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 39 nTPM
Expression across tissuesHPA
Tissue
- ovary: 39 nTPM
- testis: 31 nTPM
- adrenal gland: 22 nTPM
- pituitary gland: 12 nTPM
- fallopian tube: 12 nTPM
- cervix: 11 nTPM
Single-cell type
- adrenal cortex cells: 291 nCPM
- sertoli cells: 185 nCPM
- early primary spermatocytes: 173 nCPM
- ovarian stromal cells: 154 nCPM
- gonadotrophs: 143 nCPM
- choroid plexus epithelial cells: 137 nCPM
Immune cell
- NK-cell: 7.3 nTPM
- basophil: 7.1 nTPM
- eosinophil: 7.1 nTPM
- myeloid DC: 5.2 nTPM
- memory B-cell: 4.4 nTPM
- naive B-cell: 4.2 nTPM
Brain region
- hypothalamus: 19 nTPM
- choroid plexus: 18 nTPM
- cerebellum: 16 nTPM
- basal ganglia: 16 nTPM
- cerebral cortex: 16 nTPM
- amygdala: 14 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.54
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SIMC1 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 SIMC1 as an antibody target. Whether an autoantibody or antibody against SIMC1 could matter depends on whether native SIMC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SIMC1 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 SIMC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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