KEGG   Homo sapiens (human): 29899
Entry
29899             CDS       T01001                                 
Symbol
GPSM2, CMCS, DFNB82, LGN, PINS
Name
(RefSeq) G protein signaling modulator 2
  KO
K15837  G-protein signaling modulator 2
Organism
hsa  Homo sapiens (human)
Disease
H00605  Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    29899 (GPSM2)
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    29899 (GPSM2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   Spindle formation proteins
    29899 (GPSM2)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   29899 (GPSM2)
SSDB
Motif
Pfam: TPR_12 GoLoco TPR_1 TPR_7 TPR_2 TPR_8 TPR_10 TPR_4 TPR_16 TPR_MalT TPR_11
Other DBs
NCBI-GeneID: 29899
NCBI-ProteinID: NP_001307967
OMIM: 609245
HGNC: 29501
Ensembl: ENSG00000121957
UniProt: P81274 B4DIF1
Structure
Position
1:108876985..108934545
AA seq 684 aa
MEENLISMREDHSFHVRYRMEASCLELALEGERLCKSGDCRAGVSFFEAAVQVGTEDLKT
LSAIYSQLGNAYFYLHDYAKALEYHHHDLTLARTIGDQLGEAKASGNLGNTLKVLGNFDE
AIVCCQRHLDISRELNDKVGEARALYNLGNVYHAKGKSFGCPGPQDVGEFPEEVRDALQA
AVDFYEENLSLVTALGDRAAQGRAFGNLGNTHYLLGNFRDAVIAHEQRLLIAKEFGDKAA
ERRAYSNLGNAYIFLGEFETASEYYKKTLLLARQLKDRAVEAQSCYSLGNTYTLLQDYEK
AIDYHLKHLAIAQELNDRIGEGRACWSLGNAYTALGNHDQAMHFAEKHLEISREVGDKSG
ELTARLNLSDLQMVLGLSYSTNNSIMSENTEIDSSLNGVRPKLGRRHSMENMELMKLTPE
KVQNWNSEILAKQKPLIAKPSAKLLFVNRLKGKKYKTNSSTKVLQDASNSIDHRIPNSQR
KISADTIGDEGFFDLLSRFQSNRMDDQRCCLQEKNCHTASTTTSSTPPKMMLKTSSVPVV
SPNTDEFLDLLASSQSRRLDDQRASFSNLPGLRLTQNSQSVLSHLMTNDNKEADEDFFDI
LVKCQGSRLDDQRCAPPPATTKGPTVPDEDFFSLILRSQGKRMDEQRVLLQRDQNRDTDF
GLKDFLQNNALLEFKNSGKKSADH
NT seq 2055 nt   +upstreamnt  +downstreamnt
atggaggaaaatttgataagcatgagagaagaccattcttttcatgttcgttacagaatg
gaagcttcttgcctagagctggccttggaaggggaacgtctatgtaaatcaggagactgc
cgcgctggcgtgtcattctttgaagctgcagttcaagttggaactgaagacctaaaaaca
cttagcgctatttacagccagttgggcaatgcttatttctatttgcatgattatgccaaa
gcattagaatatcaccatcatgatttaacccttgcaaggactattggagaccagctgggg
gaagcgaaagctagtggtaatctgggaaacaccttaaaagttcttgggaattttgacgaa
gccatagtttgttgtcagcgacacctagatatttccagagagcttaatgacaaggtggga
gaagcaagagcactttacaatcttgggaatgtgtatcatgccaaagggaaaagttttggt
tgccctggtccccaggatgtaggagaatttccagaagaagtgagagatgctctgcaggca
gccgtggatttttatgaggaaaacctatcattagtgactgctttgggtgaccgagcggca
caaggacgtgcctttggaaatcttggaaacacacattacctccttggcaacttcagggat
gcagttatagctcatgagcagcgtctccttattgcaaaagaatttggagataaagcagct
gaaagaagagcatatagcaaccttggaaatgcatatatatttcttggtgaatttgaaact
gcctcggaatactacaagaagacactactgttggcccgacagcttaaagaccgagctgta
gaagcacagtcttgttacagtcttggaaatacatatactttacttcaagactatgaaaag
gccattgattatcatctgaagcacttagcaattgctcaagagctgaatgatagaattggt
gaaggaagagcatgttggagcttaggaaatgcatacacagcactaggaaatcatgatcaa
gcaatgcattttgctgaaaagcacttggaaatttcaagagaggttggggataaaagtggt
gaactaacagcacgacttaatctctcagaccttcaaatggttcttggtctgagctacagc
acaaataactccataatgtctgaaaatactgaaattgatagcagtttgaatggtgtacgc
cccaagttgggacgccggcatagtatggaaaatatggaacttatgaagttaacaccagaa
aaggtacagaactggaacagtgaaattcttgctaagcaaaaacctcttattgccaaacct
tctgcaaagctactctttgtcaacagactgaaggggaaaaaatacaaaacgaattcctcc
actaaagttctccaagatgccagtaattctattgaccaccgaattccaaattctcagagg
aaaatcagtgcagatactattggagatgaagggttctttgacttattaagccgatttcaa
agcaataggatggatgatcagagatgttgcttacaagaaaagaactgccatacagcttca
acaacaacttcttccactccccctaaaatgatgctaaaaacatcatctgttcctgtggta
tcccccaacacggatgagtttttagatcttcttgccagctcacagagtcgccgtctggat
gaccagagggctagtttcagtaatttgccagggcttcgtctaacacaaaacagccagtcg
gtacttagccacctgatgactaatgacaacaaagaggctgatgaagatttctttgacatc
cttgtaaaatgtcaaggatccagattagatgatcaaagatgtgctccaccacctgctacc
acaaagggtccgacagtaccagatgaagactttttcagccttattttacggtcccaggga
aagagaatggatgaacagagagttcttttacaaagagatcaaaacagagacactgacttt
gggctaaaggactttttgcaaaataatgctttgttggagtttaaaaattcagggaaaaaa
tcggcagaccattag

  All links  
Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (20)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (17)   
DNA sequence (41)   
   RefSeq(nuc) (17)   
   GenBank (12)   
   EMBL (12)   
3D Structure (7)   
   PDB (7)   
Protein domain (11)   
   Pfam (11)   
All databases (103)   

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