CTR9
RNA polymerase-associated protein CTR9 homolog
Also known as: CTR9_HUMAN, KIAA0155, p150TSP, SH2BP1, TSBP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6PD62
- Gene
- CTR9
- Ensembl
- ENSG00000198730
- Chromosome
- 11
- Canonical length
- 1173 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The protein encoded by this gene is a component of the PAF1 complex, which associates with RNA polymerase II and functions in transcriptional regulation and elongation. This complex also plays a role in the modification of histones. [provided by RefSeq, Oct 2016]
Canonical amino-acid sequenceUniProt
1173 residues, UniProt reviewed canonical sequence.
>Q6PD62|CTR9
1 MSRGSIEIPL RDTDEVIELD FDQLPEGDEV ISILKQEHTQ LHIWIALALE YYKQGKTEEF
61 VKLLEAARID GNLDYRDHEK DQMTCLDTLA AYYVQQARKE KNKDNKKDLI TQATLLYTMA
121 DKIIMYDQNH LLGRACFCLL EGDKMDQADA QFHFVLNQSP NNIPALLGKA CISFNKKDYR
181 GALAYYKKAL RTNPGCPAEV RLGMGHCFVK LNKLEKARLA FSRALELNSK CVGALVGLAV
241 LELNNKEADS IKNGVQLLSR AYTIDPSNPM VLNHLANHFF FKKDYSKVQH LALHAFHNTE
301 VEAMQAESCY QLARSFHVQE DYDQAFQYYY QATQFASSSF VLPFFGLGQM YIYRGDKENA
361 SQCFEKVLKA YPNNYETMKI LGSLYAASED QEKRDIAKGH LKKVTEQYPD DVEAWIELAQ
421 ILEQTDIQGA LSAYGTATRI LQEKVQADVP PEILNNVGAL HFRLGNLGEA KKYFLASLDR
481 AKAEAEHDEH YYNAISVTTS YNLARLYEAM CEFHEAEKLY KNILREHPNY VDCYLRLGAM
541 ARDKGNFYEA SDWFKEALQI NQDHPDAWSL IGNLHLAKQE WGPGQKKFER ILKQPSTQSD
601 TYSMLALGNV WLQTLHQPTR DREKEKRHQD RALAIYKQVL RNDAKNLYAA NGIGAVLAHK
661 GYFREARDVF AQVREATADI SDVWLNLAHI YVEQKQYISA VQMYENCLRK FYKHQNTEVV
721 LYLARALFKC GKLQECKQTL LKARHVAPSD TVLMFNVALV LQRLATSVLK DEKSNLKEVL
781 NAVKELELAH RYFSYLSKVG DKMRFDLALA ATEARQCSDL LSQAQYHVAR ARKQDEEERE
841 LRAKQEQEKE LLRQKLLKEQ EEKRLREKEE QKKLLEQRAQ YVEKTKNILM FTGETEATKE
901 KKRGGGGGRR SKKGGEFDEF VNDDTDDDLP ISKKKKRRKG SGSEQEGEDE EGGERKKKKR
961 RRHPKGEEGS DDDETENGPK PKKRRPPKAE KKKAPKPERL PPSMKGKIKS KAIISSSDDS
1021 SDEDKLKIAD EGHPRNSNSN SDSDEDEQRK KCASSESDSD ENQNKSGSEA GSPRRPRRQR
1081 SDQDSDSDQP SRKRRPSGSE QSDNESVQSG RSHSGVSEND SRPASPSAES DHESERGSDN
1141 EGSGQGSGNE SEPEGSNNEA SDRGSEHGSD DSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CTR9 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)
- 0.37
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 45 nTPM
- parathyroid gland: 28 nTPM
- thymus: 28 nTPM
- retina: 27 nTPM
- testis: 25 nTPM
- lymph node: 25 nTPM
Single-cell type
- epicardial cells: 205 nCPM
- cardiomyocytes: 183 nCPM
- platelets: 164 nCPM
- basal keratinocytes: 160 nCPM
- innate lymphoid cells: 149 nCPM
- epididymal principal cells: 149 nCPM
Immune cell
- basophil: 55 nTPM
- eosinophil: 31 nTPM
- NK-cell: 27 nTPM
- MAIT T-cell: 26 nTPM
- memory CD4 T-cell: 22 nTPM
- naive CD4 T-cell: 20 nTPM
Brain region
- choroid plexus: 25 nTPM
- midbrain: 22 nTPM
- hypothalamus: 19 nTPM
- white matter: 19 nTPM
- pons: 19 nTPM
- thalamus: 18 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CTR9.
Disease | GeneticClinVar
17 pathogenic / likely-pathogenic of 789 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- CTR9-related neurodevelopmental disorder
- Inborn genetic diseases
- Neurodevelopmental disorder
- See cases
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)
- 0.14
- gnomAD pLI
- 1
- gnomAD missense Z
- 4.3
- DepMap mean gene effect
- -1.02
- DepMap dependency class
- common
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
- blastocyst growth
- blastocyst hatching
- cell surface receptor signaling pathway via JAK-STAT
- cellular response to lipopolysaccharide
- endodermal cell fate commitment
- inner cell mass cell differentiation
- interleukin-6-mediated signaling pathway
- negative regulation of gene expression, epigenetic
- negative regulation of myeloid cell differentiation
- negative regulation of transcription by RNA polymerase II
- positive regulation of transcription by RNA polymerase II
- stem cell population maintenance
- transcription elongation by RNA polymerase II
- trophectodermal cell differentiation
- Wnt signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CTR9 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 CTR9 as an antibody target. Whether an autoantibody or antibody against CTR9 could matter depends on whether native CTR9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CTR9 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 CTR9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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