Homo sapiens (human): 3208 Help Entry 3208              CDS       T01001                                  Symbol HPCA, BDR2, DYT2 Name (RefSeq) hippocalcin   KO K23846   neuron-specific calcium-binding protein hippocalcin Organism hsa  Homo sapiens (human) Disease H00831   Primary dystonia 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]     3208 (HPCA) Domain-containing proteins not elsewhere classified [BR:hsa04990]  EF-hand domain-containing proteins   Calcium binding proteins    3208 (HPCA) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  EF-hand_7 EF-hand_1 EF-hand_6 EF-hand_5 EF-hand_8 EH SPARC_Ca_bdg FCaBP_EF-hand WEF-hand SPEF2_C Motif Other DBs NCBI-GeneID:  3208 NCBI-ProteinID:  NP_002134 OMIM:  142622 HGNC:  5144 Ensembl:  ENSG00000121905 UniProt:  P84074 Structure PDBPDBj LinkDB All DBs Position 1:32885996..32894646 Genome browser AA seq 193 aa AA seqDB search MGKQNSKLRPEMLQDLRENTEFSELELQEWYKGFLKDCPTGILNVDEFKKIYANFFPYGD ASKFAEHVFRTFDTNSDGTIDFREFIIALSVTSRGRLEQKLMWAFSMYDLDGNGYISREE MLEIVQAIYKMVSSVMKMPEDESTPEKRTEKIFRQMDTNNDGKLSLEEFIRGAKSDPSIV RLLQCDPSSASQF NT seq 582 nt NT seq  +upstreamnt  +downstreamnt atgggcaagcagaacagcaagctgcggcccgagatgttgcaggacctgcgagagaacaca gagttctcagagctggagctgcaggagtggtacaagggcttcctcaaggactgccccaca ggaatcctcaatgtggatgagttcaagaagatctacgccaacttctttccctatggtgac gcctccaagtttgccgagcacgtcttccgcacctttgacaccaacagcgatggcaccata gactttcgggagttcatcattgcgctgagcgtgacctcgcgcggccgcctggagcagaag ctcatgtgggccttcagcatgtatgacctggacggcaacggctacatcagccgggaggag atgctggagatcgtgcaggccatttacaagatggtttcgtccgtgatgaagatgccggag gacgagtcgaccccggaaaagaggactgagaaaatcttccgccaaatggacacaaacaac gacggcaagctgtccttggaggagttcatccgcggggccaaaagcgacccgtccatcgtg cgtctgctgcagtgcgaccccagcagcgcctcccagttctga

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