KEGG   Homo sapiens (human): 10750
Entry
10750             CDS       T01001                                 
Symbol
GRAP, DFNB114
Name
(RefSeq) GRB2 related adaptor protein
  KO
K23694  GRB2-related adapter protein
Organism
hsa  Homo sapiens (human)
Disease
H00605  Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]
    10750 (GRAP)
Domain-containing proteins not elsewhere classified [BR:hsa04990]
 Src homology (SH) domain-containing proteins
  Signal transducing adaptor proteins
   10750 (GRAP)
SSDB
Motif
Pfam: SH3_1 SH3_9 SH3_2 SH2 SH3_3 SH3_10
Other DBs
NCBI-GeneID: 10750
NCBI-ProteinID: NP_006604
OMIM: 604330
HGNC: 4562
Ensembl: ENSG00000154016
UniProt: Q13588
Position
17:complement(19020656..19051373)
AA seq 217 aa
MESVALYSFQATESDELAFNKGDTLKILNMEDDQNWYKAELRGVEGFIPKNYIRVKPHPW
YSGRISRQLAEEILMKRNHLGAFLIRESESSPGEFSVSVNYGDQVQHFKVLREASGKYFL
WEEKFNSLNELVDFYRTTTIAKKRQIFLRDEEPLLKSPGACFAQAQFDFSAQDPSQLSFR
RGDIIEVLERPDPHWWRGRSCGRVGFFPRSYVQPVHL
NT seq 654 nt   +upstreamnt  +downstreamnt
atggagtccgtggccctgtacagctttcaggctacagagagcgacgagctggccttcaac
aagggagacacactcaagatcctgaacatggaggatgaccagaactggtacaaggccgag
ctccggggtgtcgagggatttattcccaagaactacatccgcgtcaagccccatccgtgg
tactcgggcaggatttcccggcagctggccgaagagattctgatgaagcggaaccatctg
ggagccttcctgatccgggagagtgagagctccccaggggagttctctgtgtctgtgaac
tatggagaccaggtgcagcacttcaaggtgctgcgtgaggcctcggggaagtacttcctg
tgggaggagaagttcaactccctcaacgagctggtcgacttctaccgcaccaccaccatc
gccaagaagcggcagatcttcctgcgcgacgaggagcccttgctcaagtcacctggggcc
tgctttgcccaggcccagtttgacttctcagcccaggacccctcgcagctcagcttccgc
cgtggcgacatcattgaggtcctggagcgcccagacccccactggtggcggggccggtcc
tgcgggcgcgttggcttcttcccacggagttacgtgcagcccgtgcacctgtga

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