ELL2
RNA polymerase II elongation factor ELL2
Also known as: ELL2_HUMAN, MRCCAT1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00472
- Gene
- ELL2
- Ensembl
- ENSG00000118985
- Chromosome
- 5
- Canonical length
- 640 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable cis-regulatory region sequence-specific DNA binding activity. Involved in snRNA transcription by RNA polymerase II. Located in nucleoplasm. Part of transcription elongation factor complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
640 residues, UniProt reviewed canonical sequence.
>O00472|ELL2
1 MAAGGTGGLR EEQRYGLSCG RLGQDNITVL HVKLTETAIR ALETYQSHKN LIPFRPSIQF
61 QGLHGLVKIP KNDPLNEVHN FNFYLSNVGK DNPQGSFDCI QQTFSSSGAS QLNCLGFIQD
121 KITVCATNDS YQMTRERMTQ AEEESRNRST KVIKPGGPYV GKRVQIRKAP QAVSDTVPER
181 KRSTPMNPAN TIRKTHSSST ISQRPYRDRV IHLLALKAYK KPELLARLQK DGVNQKDKNS
241 LGAILQQVAN LNSKDLSYTL KDYVFKELQR DWPGYSEIDR RSLESVLSRK LNPSQNAAGT
301 SRSESPVCSS RDAVSSPQKR LLDSEFIDPL MNKKARISHL TNRVPPTLNG HLNPTSEKSA
361 AGLPLPPAAA AIPTPPPLPS TYLPISHPPQ IVNSNSNSPS TPEGRGTQDL PVDSFSQNDS
421 IYEDQQDKYT SRTSLETLPP GSVLLKCPKP MEENHSMSHK KSKKKSKKHK EKDQIKKHDI
481 ETIEEKEEDL KREEEIAKLN NSSPNSSGGV KEDCTASMEP SAIELPDYLI KYIAIVSYEQ
541 RQNYKDDFNA EYDEYRALHA RMETVARRFI KLDAQRKRLS PGSKEYQNVH EEVLQEYQKI
601 KQSSPNYHEE KYRCEYLHNK LAHIKRLIGE FDQQQAESWSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ELL2 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)
- 0.53
- Highest tissue expression
- 96 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 96 nTPM
- salivary gland: 91 nTPM
- pancreas: 89 nTPM
- liver: 81 nTPM
- esophagus: 60 nTPM
- skin: 56 nTPM
Single-cell type
- neutrophils: 5,148 nCPM
- mast cells: 2,268 nCPM
- plasma cells: 1,499 nCPM
- monocytes: 1,492 nCPM
- pancreatic acinar cells: 1,448 nCPM
- salivary acinar cells: 1,376 nCPM
Immune cell
- basophil: 7 nTPM
- eosinophil: 5.7 nTPM
- memory B-cell: 3.5 nTPM
- neutrophil: 1.8 nTPM
- naive B-cell: 1.7 nTPM
- NK-cell: 1.6 nTPM
Brain region
- white matter: 128 nTPM
- medulla oblongata: 124 nTPM
- thalamus: 107 nTPM
- hypothalamus: 84 nTPM
- basal ganglia: 81 nTPM
- pons: 79 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)
- 0.24
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.55
- DepMap mean gene effect
- -0.15
- 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
Biological processes
- positive regulation of transcription elongation by RNA polymerase II
- snRNA transcription by RNA polymerase II
- transcription elongation by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ELL2 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 ELL2 as an antibody target. Whether an autoantibody or antibody against ELL2 could matter depends on whether native ELL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ELL2 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 ELL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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