Search Result
Gene id | 57569 | ||||||||||||||||||||||||||||||||
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Gene Summary Protein Summary Gene ontology Diseases PubMed | |||||||||||||||||||||||||||||||||
Gene Summary |
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Gene Symbol | ARHGAP20 Gene UCSC Ensembl | ||||||||||||||||||||||||||||||||
Aliases | RARHOGAP | ||||||||||||||||||||||||||||||||
Gene name | Rho GTPase activating protein 20 | ||||||||||||||||||||||||||||||||
Alternate names | rho GTPase-activating protein 20, RA and RhoGAP domain containing protein, rho GTPase activating protein 20 variant 2, rho-type GTPase-activating protein 20, | ||||||||||||||||||||||||||||||||
Gene location |
11q22.3-q23.1 (110713188: 110577034) Exons: 20 NC_000011.10 |
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Gene summary(Entrez) |
The protein encoded by this gene is an activator of RHO-type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth. [provided by RefSeq, Sep 2016] |
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OMIM | 615951 | ||||||||||||||||||||||||||||||||
Protein Summary |
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Protein general information | Q9P2F6 Name: Rho GTPase activating protein 20 (Rho type GTPase activating protein 20) Length: 1191 Mass: 132608 Tissue specificity: Expressed predominantly in the brain. Lower expression is found in lymph nodes. {ECO | ||||||||||||||||||||||||||||||||
Sequence |
MEAMSPQQETLGGQPGRSSSLTGVSRLAGGSCTKKKMKTLAERRRSAPSLILDKALQKRPTTRDSPSASVDTCTF LSSLVCSNRTLLIDGRAELKRGLQRQERHLFLFNDLFVVAKIKYNNNFKIKNKIKLTDMWTASCVDEVGEGNTNA MKSFVLGWPTVNFVATFSSPEQKDKWLSLLQRYINLEKEKDYPKSIPLKIFAKDIGNCAYSKTITVMNSDTANEV INMSLPMLGITGSERDYQLWVNSGKEEAPYPLIGHEYPYGIKMSHLRDSALLTPGSKDSTTPFNLQEPFLMEQLP REMQCQFILKPSRLAAAQQLSDSGHKTFKRRRSIINWAFWRGSSTHLDNLPSSPTSPMPGQLFGISLPNICENDN LPKPVLDMLFFLNQKGPLTKGIFRQSANVKSCRELKEKLNSGVEVHLDCESIFVIASVLKDFLRNIPGSIFSSDL YDHWVSVMDQGNDEEKINTVQRLLDQLPRANVVLLRYLFGVLHNIEQHSSSNQMTAFNLAVCVAPSILWPPASSS PELENEFTKKVSLLIQFLIENCLRIFGEEITSLFREVSVRCDTRENASDISCFQLNDSSYDSLENELNEDVDAPC SDLVKKLGQGSRSMDSVLTLSDYDLDQPEVEGLLTLSDFDLAHSKDEDVQMKRPLESKPVNILVYTKIPLRDHAR APSAMCTPSYLSTAAANAAKSLRRHRRCSEPSIDYLDSKLSYLREFYQKKLRKSSCDAILSQKDEDYLKQNQPLQ EEGKTCFKQSLVTGTDVSKKNATTQNTKKKSLSGSEGNHVKLFPKSKPVAISVASYSPMSSQDHSKNQPFDVNTS GYSPPHTADALKGPRTHRRCSEPNIEDQNRKLTYLRGIYSKKQHKTSCEAGLLHGEEDYLKRHKSLQMEGQKLIN QSLVMGIEVGKSSATNQNTEKVLPPRLNLCPRTSYSSLSSPGTSPSGSSVSSQDSAFSQISEHSVFTPTETSSPI DCTFQAQRKREDLSPDFSNASHVSGMPGPSSGQACSRPAYTKKDTMEWHSQMHSVTLHPSTWLRNGVASLKNWSL KKKAKAARPEEEKIASPKGPLEPPPHASGVPEANSLQEEQKDLPLRAAEGLSPVQSAQRCSSSPFQDSERHCSSP FSLVESRLKLCMKSHEEIEPGSQSSSGSLPWERASASSWTLEDATSPDSGPTVVCDIEDRYLTKDI | ||||||||||||||||||||||||||||||||
Structural information |
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Other Databases | GeneCards: ARHGAP20  Malacards: ARHGAP20 | ||||||||||||||||||||||||||||||||
Gene ontology
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Diseases
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PubMed references
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