RIC1
Guanine nucleotide exchange factor subunit RIC1
Also known as: bA207C16.1, KIAA1432, RIC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4ADV7
- Gene
- RIC1
- Ensembl
- ENSG00000107036
- Chromosome
- 9
- Canonical length
- 1423 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
Enables guanyl-nucleotide exchange factor activity and small GTPase binding activity. Involved in several processes, including positive regulation of GTPase activity; regulation of extracellular matrix constituent secretion; and retrograde transport, endosome to Golgi. Located in cytosol and membrane. Part of Ric1-Rgp1 guanyl-nucleotide exchange factor complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1423 residues, UniProt reviewed canonical sequence.
>Q4ADV7|RIC1
1 MYFLSGWPKR LLCPLGSPAE APFHVQSDPQ RAFFAVLAAA RLSIWYSRPS VLIVTYKEPA
61 KSSTQFGSYK QAEWRPDSTM IAVSTANGYI LFFHITSTRG DKYLYEPVYP KGSPQMKGTP
121 HFKEEQCAPA LNLEMRKILD LQAPIMSLQS VLEDLLVATS DGLLHLIHWE GMTNGRKAIN
181 LCTVPFSVDL QSSRVGSFLG FTDVHIRDME YCATLDGFAV VFNDGKVGFI TPVSSRFTAE
241 QLHGVWPQDV VDGTCVAVNN KYRLMAFGCV SGSVQVYTID NSTGAMLLSH KLELTAKQYP
301 DIWNKTGAVK LMRWSPDNSV VIVTWEYGGL SLWSVFGAQL ICTLGGDFAY RSDGTKKDPL
361 KINSMSWGAE GYHLWVISGF GSQNTEIESD LRSVVKQPSI LLFQFIKSVL TVNPCMSNQE
421 QVLLQGEDRL YLNCGEASQT QNPRSSSTHS EHKPSREKSP FADGGLESQG LSTLLGHRHW
481 HVVQISSTYL ESNWPIRFSA IDKLGQNIAV VGKFGFAHYS LLTKKWKLFG NITQEQNMIV
541 TGGLAWWNDF MVLACYNIND RQEELRVYLR TSNLDNAFAH VTKAQAETLL LSVFQDMVIV
601 FRADCSICLY SIERKSDGPN TTAGIQVLQE VSMSRYIPHP FLVVSVTLTS VSTENGITLK
661 MPQQARGAES IMLNLAGQLI MMQRDRSGPQ IREKDSNPNN QRKLLPFCPP VVLAQSVENV
721 WTTCRANKQK RHLLEALWLS CGGAGMKVWL PLFPRDHRKP HSFLSQRIML PFHINIYPLA
781 VLFEDALVLG AVNDTLLYDS LYTRNNAREQ LEVLFPFCVV ERTSQIYLHH ILRQLLVRNL
841 GEQALLLAQS CATLPYFPHV LELMLHEVLE EEATSREPIP DPLLPTVAKF ITEFPLFLQT
901 VVHCARKTEY ALWNYLFAAV GNPKDLFEEC LMAQDLDTAA SYLIILQNME VPAVSRQHAT
961 LLFNTALEQG KWDLCRHMIR FLKAIGSGES ETPPSTPTAQ EPSSSGGFEF FRNRSISLSQ
1021 SAENVPASKF SLQKTLSMPS GPSGKRWSKD SDCAENMYID MMLWRHARRL LEDVRLKDLG
1081 CFAAQLGFEL ISWLCKERTR AARVDNFVIA LKRLHKDFLW PLPIIPASSI SSPFKNGKYR
1141 TVGEQLLKSQ SADPFLNLEM DAGISNIQRS QSWLSNIGPT HHEIDTASSH GPQMQDAFLS
1201 PLSNKGDECS IGSATDLTES SSMVDGDWTM VDENFSTLSL TQSELEHISM ELASKGPHKS
1261 QVQLRYLLHI FMEAGCLDWC IVIGLILRES SIINQILVIT QSSEVDGEML QNIKTGLHAV
1321 DRWASTDCPG YKPFLNIIKP QLQKLSEITE EQVQPDAFQP ITMGKTPEQT SPRAEESRGS
1381 SSHGSIPQGE VGSSNMVSRK EEDTAQAEEE EPFQDGTYDC SVSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RIC1 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)
- 0.35
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 16 nTPM
- lymph node: 16 nTPM
- tonsil: 16 nTPM
- tongue: 15 nTPM
- thymus: 14 nTPM
- placenta: 13 nTPM
Single-cell type
- myonuclei: 334 nCPM
- plasma cells: 298 nCPM
- thymic myoid cells: 279 nCPM
- cardiomyocytes: 276 nCPM
- mast cells: 256 nCPM
- epicardial cells: 252 nCPM
Immune cell
- intermediate monocyte: 1 nTPM
- NK-cell: 1 nTPM
- memory B-cell: 0.7 nTPM
- plasmacytoid DC: 0.7 nTPM
- classical monocyte: 0.6 nTPM
- eosinophil: 0.5 nTPM
Brain region
- choroid plexus: 36 nTPM
- cerebellum: 33 nTPM
- white matter: 32 nTPM
- medulla oblongata: 28 nTPM
- pons: 28 nTPM
- basal ganglia: 27 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about RIC1.
Disease | AllUniProt
Conditions RIC1 is implicated in, by any mechanism.
- CATIFA syndrome (CATIFA) MIM:618761
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 261 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Catifa syndrome
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)
- 0.4
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.55
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cranial skeletal system development
- intracellular protein transport
- negative regulation of protein catabolic process
- positive regulation of GTPase activity
- retrograde transport, endosome to Golgi
- regulation of extracellular matrix constituent secretion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- WD40/YVTN repeat-like-containing domain superfamily
- WD40-repeat-containing domain superfamily
- RIC1, C-terminal alpha solenoid region
- RAB6A-GEF complex partner protein 1
- RIC1 C-terminal alpha solenoid region
- RIC1 second beta propeller domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RIC1 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 RIC1 as an antibody target. Whether an autoantibody or antibody against RIC1 could matter depends on whether native RIC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RIC1 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 RIC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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