Homo sapiens (human): 51475 Help Entry 51475             CDS       T01001                                  Symbol CABP2, DFNB93 Name (RefSeq) calcium binding protein 2   KO K23531   calcium-binding protein 1/2/4/5 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    04131 Membrane trafficking [BR:hsa04131]     51475 (CABP2)   09183 Protein families: signaling and cellular processes    04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]     51475 (CABP2) Membrane trafficking [BR:hsa04131]  Exocytosis   Calcium ion-dependent exocytosis    Others     51475 (CABP2) Domain-containing proteins not elsewhere classified [BR:hsa04990]  EF-hand domain-containing proteins   Calcium binding proteins    51475 (CABP2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  EF-hand_1 EF-hand_7 EF-hand_8 EF-hand_6 EF-hand_5 AIF-1 EF-hand_9 EH DUF5580_M Dockerin_1 DIMCO_N Motif Other DBs NCBI-GeneID:  51475 NCBI-ProteinID:  NP_057450 OMIM:  607314 HGNC:  1385 Ensembl:  ENSG00000167791 UniProt:  Q9NPB3 LinkDB All DBs Position 11:complement(67518912..67523446) Genome browser AA seq 220 aa AA seqDB search MGNCAKRPWRRGPKDPLQWLGSPPRGSCPSPSSSPKEQGDPAPGVQGYSVLNSLVGPACI FLRPSIAATQLDRELRPEEIEELQVAFQEFDRDRDGYIGCRELGACMRTLGYMPTEMELI EISQQISGGKVDFEDFVELMGPKLLAETADMIGVRELRDAFREFDTNGDGRISVGELRAA LKALLGERLSQREVDEILQDVDLNGDGLVDFEEFVRMMSR NT seq 663 nt NT seq  +upstreamnt  +downstreamnt atggggaactgtgccaagcggccctggcgccggggccctaaggaccccttgcagtggctc ggctccccaccaaggggctcctgccccagccccagctccagccccaaggagcagggggac cccgcgccaggcgtccagggctactcggtgctcaacagcctggtggggcctgcctgcatc ttcctgcggcccagcattgccgccacccaactcgaccgggagctgcggcccgaggagatt gaagagctgcaggtcgccttccaggagtttgaccgagaccgggacggctacattggctgc cgggagctgggtgcctgcatgcggaccctgggctacatgcccaccgagatggagctcatc gagatctcacaacaaatcagtggcggaaaggtggactttgaagacttcgtggagctgatg ggccccaagctgctggcagagacggcagacatgatcggtgtccgggagctacgggacgcc ttccgggagttcgacaccaatggggacggccgcatcagcgtgggcgagctccgggcggcc ctcaaggccctgctgggggagcgcctcagccagcgggaggtggacgagatcctccaggac gtggacctcaatggggacggtctggtcgacttcgaagagtttgtgcgaatgatgtctcgg tga

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