Homo sapiens (human): 10750 Help 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) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SH3_1 SH3_9 SH3_2 SH2 SH3_3 SH3_10 DUF7145 SH2_1 Motif Other DBs NCBI-GeneID:  10750 NCBI-ProteinID:  NP_006604 OMIM:  604330 HGNC:  4562 Ensembl:  ENSG00000154016 UniProt:  Q13588 LinkDB All DBs Position 17:complement(19020656..19051373) Genome browser AA seq 217 aa AA seqDB search MESVALYSFQATESDELAFNKGDTLKILNMEDDQNWYKAELRGVEGFIPKNYIRVKPHPW YSGRISRQLAEEILMKRNHLGAFLIRESESSPGEFSVSVNYGDQVQHFKVLREASGKYFL WEEKFNSLNELVDFYRTTTIAKKRQIFLRDEEPLLKSPGACFAQAQFDFSAQDPSQLSFR RGDIIEVLERPDPHWWRGRSCGRVGFFPRSYVQPVHL NT seq 654 nt NT seq  +upstreamnt  +downstreamnt atggagtccgtggccctgtacagctttcaggctacagagagcgacgagctggccttcaac aagggagacacactcaagatcctgaacatggaggatgaccagaactggtacaaggccgag ctccggggtgtcgagggatttattcccaagaactacatccgcgtcaagccccatccgtgg tactcgggcaggatttcccggcagctggccgaagagattctgatgaagcggaaccatctg ggagccttcctgatccgggagagtgagagctccccaggggagttctctgtgtctgtgaac tatggagaccaggtgcagcacttcaaggtgctgcgtgaggcctcggggaagtacttcctg tgggaggagaagttcaactccctcaacgagctggtcgacttctaccgcaccaccaccatc gccaagaagcggcagatcttcctgcgcgacgaggagcccttgctcaagtcacctggggcc tgctttgcccaggcccagtttgacttctcagcccaggacccctcgcagctcagcttccgc cgtggcgacatcattgaggtcctggagcgcccagacccccactggtggcggggccggtcc tgcgggcgcgttggcttcttcccacggagttacgtgcagcccgtgcacctgtga

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