KEGG   Homo sapiens (human): 9901
Entry
9901              CDS       T01001                                 
Symbol
SRGAP3, ARHGAP14, MEGAP, SRGAP2, WRP
Name
(RefSeq) SLIT-ROBO Rho GTPase activating protein 3
  KO
K07526  SLIT-ROBO Rho GTPase activating protein
Organism
hsa  Homo sapiens (human)
Pathway
hsa04360  Axon guidance
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09158 Development and regeneration
   04360 Axon guidance
    9901 (SRGAP3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    9901 (SRGAP3)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Bin/Amphiphysin/Rvs (BAR) family proteins
   F-BAR proteins
    9901 (SRGAP3)
 Others
  Rho GTPase associated proteins
   Rho GTPase-activating proteins
    9901 (SRGAP3)
SSDB
Motif
Pfam: RhoGAP FCH SH3_1 SH3_2 SH3_9 Flg_hook FlaC_arch
Other DBs
NCBI-GeneID: 9901
NCBI-ProteinID: NP_055665
OMIM: 606525
HGNC: 19744
Ensembl: ENSG00000196220
UniProt: O43295
Position
3:complement(8980591..9363027)
AA seq 1099 aa
MSSQTKFKKDKEIIAEYEAQIKEIRTQLVEQFKCLEQQSESRLQLLQDLQEFFRRKAEIE
LEYSRSLEKLAERFSSKIRSSREHQFKKDQYLLSPVNCWYLVLHQTRRESRDHATLNDIF
MNNVIVRLSQISEDVIRLFKKSKEIGLQMHEELLKVTNELYTVMKTYHMYHAESISAESK
LKEAEKQEEKQFNKSGDLSMNLLRHEDRPQRRSSVKKIEKMKEKRQAKYSENKLKCTKAR
NDYLLNLAATNAAISKYYIHDVSDLIDCCDLGFHASLARTFRTYLSAEYNLETSRHEGLD
VIENAVDNLDSRSDKHTVMDMCNQVFCPPLKFEFQPHMGDEVCQVSAQQPVQTELLMRYH
QLQSRLATLKIENEEVRKTLDATMQTLQDMLTVEDFDVSDAFQHSRSTESVKSAASETYM
SKINIAKRRANQQETEMFYFTKFKEYVNGSNLITKLQAKHDLLKQTLGEGERAECGTTRP
PCLPPKPQKMRRPRPLSVYSHKLFNGSMEAFIKDSGQAIPLVVESCIRYINLYGLQQQGI
FRVPGSQVEVNDIKNSFERGEDPLVDDQNERDINSVAGVLKLYFRGLENPLFPKERFQDL
ISTIKLENPAERVHQIQQILVTLPRVVIVVMRYLFAFLNHLSQYSDENMMDPYNLAICFG
PTLMHIPDGQDPVSCQAHINEVIKTIIIHHEAIFPSPRELEGPVYEKCMAGGEEYCDSPH
SEPGAIDEVDHDNGTEPHTSDEEVEQIEAIAKFDYMGRSPRELSFKKGASLLLYHRASED
WWEGRHNGVDGLIPHQYIVVQDMDDAFSDSLSQKADSEASSGPLLDDKASSKNDLQSPTE
HISDYGFGGVMGRVRLRSDGAAIPRRRSGGDTHSPPRGLGPSIDTPPRAAACPSSPHKIP
LTRGRIESPEKRRMATFGSAGSINYPDKKALSEGHSMRSTCGSTRHSSLGDHKSLEAEAL
AEDIEKTMSTALHELRELERQNTVKQAPDVVLDTLEPLKNPPGPVSSEPASPLHTIVIRD
PDAAMRRSSSSSTEMMTTFKPALSARLAGAQLRPPPMRPVRPVVQHRSSSSSSSGVGSPA
VTPTEKMFPNSSADKSGTM
NT seq 3300 nt   +upstreamnt  +downstreamnt
atgtcatctcaaactaagttcaagaaagacaaagagatcattgctgaatatgaagcccaa
ataaaagagatccgcacgcagctggtggagcagttcaaatgtctggagcagcaatcagag
tcgcgactgcagctgcttcaagacctccaggagtttttccgccggaaagctgagattgag
ctcgagtactcccgcagcctggagaagctggctgagcgcttctcctccaaaatccgcagc
tcccgggagcaccagttcaagaaggaccagtacctcctctcgcctgtgaactgttggtat
ctggttctgcatcagacccggcgggagagccgagaccatgccaccctcaatgacatcttc
atgaacaatgtcatcgtccgcctctcccagatcagtgaggatgtcatcagactcttcaaa
aagagcaaggagattggcctgcagatgcacgaggagctcctgaaggtgaccaatgagctc
tacacagtcatgaaaacctaccacatgtaccatgcagagagcatcagtgcggaaagcaag
ctgaaggaggctgagaagcaggaggagaagcagttcaataagtcaggagacctcagcatg
aacctgctccggcacgaggaccggccccagcgccgcagctctgtgaagaagattgagaag
atgaaggagaagaggcaggccaagtactctgagaacaagctgaaatgcacaaaggcccgg
aatgactacttgctcaatctggcagccaccaacgcagctataagcaaatactacatccat
gatgtctctgatctgatcgattgctgtgatttgggcttccatgccagcctggcccgcacc
ttccggacctatctctcagctgaatacaacctggagacctctcgccacgaagggctggat
gtcattgagaatgcagtggacaacctggattcccgaagtgacaagcacacagtcatggac
atgtgcaatcaagtcttctgccctccactcaagttcgagttccagccccacatgggggat
gaggtctgccaggtcagcgctcagcagcccgtccagacagaactgctcatgcgttatcac
cagctgcagtccagactggccaccctcaagatagagaatgaggaggttaggaaaaccctg
gatgccaccatgcagacattacaggacatgctgactgtggaggactttgatgtctccgat
gccttccaacacagtcgatcgacagagtccgtcaagtcggctgcctctgagacctacatg
agcaagatcaacattgccaagaggagagccaaccagcaggaaacagaaatgttttatttt
acaaaatttaaagagtatgtgaatggcagtaacctcatcaccaagctgcaggccaagcac
gatttactcaagcagaccctgggcgaaggggaaagagcagaatgcggcaccaccaggccc
ccctgtcttccccctaaaccacagaaaatgaggagacctaggcctctctcagtgtatagc
cataaactctttaacggcagtatggaagcattcattaaggattcaggacaagctataccg
cttgtagtcgagagctgcatccgttacatcaatttatatggactccagcagcaggggatc
ttcagagtgccaggatctcaggtggaagtcaatgacatcaaaaattcctttgagagaggt
gaagacccccttgtggacgatcaaaatgaacgagatatcaattcagtcgctggtgtttta
aaactgtatttccgaggactggaaaacccactctttcctaaggaaaggtttcaagatttg
atatctactattaaactggagaacccagccgagagggtgcaccagatccaacaaatcctc
gtcacccttccccgcgtggtcattgtggtcatgagatacctcttcgctttcctcaaccac
ctctcccagtatagcgacgagaacatgatggatccctacaacctggccatctgcttcggg
cctaccctcatgcacatccctgatgggcaggaccctgtgtcctgccaggcacacatcaat
gaagtcatcaaaaccatcatcatccatcatgaagccatcttccccagcccccgggagcta
gagggacctgtgtatgaaaaatgcatggctggaggggaagaatattgtgacagcccacac
agcgagccaggggccatcgatgaagttgaccatgacaatggcactgagcctcataccagc
gatgaagaagtggagcagatcgaggctattgccaagtttgactacatggggcggtccccg
cgtgagctatccttcaagaagggggcctcgctgctcctgtaccaccgcgcctcggaggac
tggtgggagggccggcacaacggcgtggatggactcatcccccatcagtacatagttgta
caggacatggatgatgccttctccgacagcctgagccagaaggctgacagcgaggccagc
agtgggccattgctggatgacaaggcctcttccaaaaacgacctccagtcccccacggag
cacatctcggattacggctttgggggggtgatgggccgagtgcggttacgatctgatgga
gcagccatccccagacgccgaagcgggggcgacacacacagcccgccccggggcctgggc
cccagcatagacacaccaccccgggctgctgcctgccccagcagcccccacaaaatcccc
ctcacccgggggaggatcgagagccctgagaagcggaggatggcgacgttcgggagcgct
ggcagcatcaactaccctgacaagaaggcgctctccgaagggcactcgatgaggtcgacc
tgcggttccaccaggcacagcagcctaggggaccacaagtccctggaggccgaggccctg
gcagaagacatcgagaagaccatgagcacggctctgcacgagttgcgggaactcgagagg
cagaacacggtcaagcaggcgccagatgtggtgctggacaccctggagcccctgaagaac
ccgccaggccccgtcagctcggagcccgccagtccccttcacaccatcgtcatccgcgac
cccgatgccgccatgcgccgcagcagcagctcctccaccgagatgatgaccaccttcaag
ccagccctgtccgcccgcctggctggcgcccagctccgcccgccccccatgcggcccgtg
cggccggtggtccagcaccggtccagcagcagcagcagctcgggcgtgggcagcccggcc
gtgacgcccaccgagaagatgttccccaacagctcagcggacaagtcgggcaccatgtga

  All links  
Disease (1)   
   OMIM (1)   
Gene (19)   
   RefGene (14)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (32)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (30)   
DNA sequence (55)   
   RefSeq(nuc) (31)   
   GenBank (12)   
   EMBL (12)   
Protein domain (7)   
   Pfam (7)   
All databases (114)   

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