ARHGAP44
Rho GTPase-activating protein 44
Also known as: KIAA0672, RHG44_HUMAN, RICH-2, RICH2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q17R89
- Gene
- ARHGAP44
- Ensembl
- ENSG00000006740
- Chromosome
- 17
- Canonical length
- 818 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables phospholipid binding activity. Predicted to be involved in negative regulation of Rac protein signal transduction; regulation of actin cytoskeleton organization; and regulation of plasma membrane bounded cell projection organization. Located in leading edge membrane. Implicated in acquired immunodeficiency syndrome and skin melanoma. Biomarker of hepatocellular carcinoma and lung carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
818 residues, UniProt reviewed canonical sequence.
>Q17R89|ARHGAP44
1 MKKQFNRMRQ LANQTVGRAE KTEVLSEDLL QVEKRLELVK QVSHSTHKKL TACLQGQQGA
61 EADKRSKKLP LTTLAQCLME GSAILGDDTL LGKMLKLCGE TEDKLAQELI HFELQVERDV
121 IEPLFLLAEV EIPNIQKQRK HLAKLVLDMD SSRTRWQQTS KSSGLSSSLQ PAGAKADALR
181 EEMEEAANRV EICRDQLSAD MYSFVAKEID YANYFQTLIE VQAEYHRKSL TLLQAVLPQI
241 KAQQEAWVEK PSFGKPLEEH LTISGREIAF PIEACVTMLL ECGMQEEGLF RVAPSASKLK
301 KLKAALDCCV VDVQEYSADP HAIAGALKSY LRELPEPLMT FELYDEWIQA SNVQEQDKKL
361 QALWNACEKL PKANHNNIRY LIKFLSKLSE YQDVNKMTPS NMAIVLGPNL LWPQAEGNIT
421 EMMTTVSLQI VGIIEPIIQH ADWFFPGEIE FNITGNYGSP VHVNHNANYS SMPSPDMDPA
481 DRRQPEQARR PLSVATDNMM LEFYKKDGLR KIQSMGVRVM DTNWVARRGS SAGRKVSCAP
541 PSMQPPAPPA ELAAPLPSPL PEQPLDSPAA PALSPSGLGL QPGPERTSTT KSKELSPGSA
601 QKGSPGSSQG TACAGTQPGA QPGAQPGASP SPSQPPADQS PHTLRKVSKK LAPIPPKVPF
661 GQPGAMADQS AGQPSPVSLS PTPPSTPSPY GLSYPQGYSL ASGQLSPAAA PPLASPSVFT
721 STLSKSRPTP KPRQRPTLPP PQPPTVNLSA SSPQSTEAPM LDGMSPGESM STDLVHFDIP
781 SIHIELGSTL RLSPLEHMRR HSVTDKRDSE EESESTALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGAP44 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 24 nTPM
- cerebral cortex: 22 nTPM
- hippocampal formation: 17 nTPM
- basal ganglia: 17 nTPM
- parathyroid gland: 16 nTPM
- colon: 14 nTPM
Single-cell type
- retinal horizontal cells: 1,130 nCPM
- thyrotrophs: 553 nCPM
- retinal amacrine cells: 442 nCPM
- lactotrophs: 435 nCPM
- mesothelial cells: 417 nCPM
- brain excitatory neurons: 323 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 125 nTPM
- hippocampal formation: 91 nTPM
- white matter: 90 nTPM
- thalamus: 82 nTPM
- amygdala: 81 nTPM
- pons: 76 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)
- 0.22
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.39
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
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
- exocytosis
- modification of postsynaptic structure
- modulation of chemical synaptic transmission
- negative regulation of filopodium assembly
- negative regulation of Rac protein signal transduction
- regulation of actin cytoskeleton organization
- regulation of dendritic spine morphogenesis
- regulation of GTPase activity
- regulation of neurotransmitter receptor transport, endosome to postsynaptic membrane
- regulation of small GTPase mediated signal transduction
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARHGAP44 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 ARHGAP44 as an antibody target. Whether an autoantibody or antibody against ARHGAP44 could matter depends on whether native ARHGAP44 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGAP44 is annotated at the cell surface, where native ARHGAP44 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ARHGAP44 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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