Homo sapiens (human): 5630 Help Entry 5630              CDS       T01001                                  Symbol PRPH, NEF4, PRPH1 Name (RefSeq) peripherin   KO K07607   peripherin Organism hsa  Homo sapiens (human) Pathway hsa05014   Amyotrophic lateral sclerosis hsa05022   Pathways of neurodegeneration - multiple diseases Network nt06541  Cytoskeleton in neurons   Element N01853   Neurofilament structure Disease H00058   Amyotrophic lateral sclerosis (ALS) Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     5630 (PRPH)    05022 Pathways of neurodegeneration - multiple diseases     5630 (PRPH)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     5630 (PRPH) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Intermediate filaments    Intermediate filaments     Type III      5630 (PRPH) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Filament Filament_head BLOC1_2 Spc29 Laminin_II DUF3944 Motif Other DBs NCBI-GeneID:  5630 NCBI-ProteinID:  NP_006253 OMIM:  170710 HGNC:  9461 Ensembl:  ENSG00000135406 UniProt:  P41219 B3KWQ6 LinkDB All DBs Position 12:49295147..49298686 Genome browser AA seq 470 aa AA seqDB search MSHHPSGLRAGFSSTSYRRTFGPPPSLSPGAFSYSSSSRFSSSRLLGSASPSSSVRLGSF RSPRAGAGALLRLPSERLDFSMAEALNQEFLATRSNEKQELQELNDRFANFIEKVRFLEQ QNAALRGELSQARGQEPARADQLCQQELRELRRELELLGRERDRVQVERDGLAEDLAALK QRLEEETRKREDAEHNLVLFRKDVDDATLSRLELERKIESLMDEIEFLKKLHEEELRDLQ VSVESQQVQQVEVEATVKPELTAALRDIRAQYESIAAKNLQEAEEWYKSKYADLSDAANR NHEALRQAKQEMNESRRQIQSLTCEVDGLRGTNEALLRQLRELEEQFALEAGGYQAGAAR LEEELRQLKEEMARHLREYQELLNVKMALDIEIATYRKLLEGEESRISVPVHSFASLNIK TTVPEVEPPQDSHSRKTVLIKTIETRNGEVVTESQKEQRSELDKSSAHSY NT seq 1413 nt NT seq  +upstreamnt  +downstreamnt atgagccaccacccgtcgggcctccgggccggcttcagctccacctcataccgccgtacc ttcggtccaccgccctcactatcccccggggccttctcctactcgtccagctcccgcttc tccagcagccgcctgctgggctccgcgtccccgagctcctcggtgcgcctgggcagcttc cgtagcccccgagcgggagcgggcgccctcctgcgcctgccctcggagcgcctcgacttc tccatggccgaggccctcaaccaggagttcctggccacgcgcagcaacgagaagcaggag ctgcaggagctcaacgaccgcttcgccaacttcatcgagaaggtacgctttctggagcag cagaacgcggccctgcgcggggagctgagccaagcccggggccaggagccggcgcgcgcc gaccagctgtgccagcaggagctgcgcgagctgcggcgagagctggagctgttgggccgc gagcgtgaccgggtgcaggtggagcgcgacgggctggcggaggacctggcggcgctcaag cagaggttggaggaggagacgcgcaagcgggaggacgcggagcacaacctcgtgctcttc cgcaaggacgtggacgatgccactctgtcccgcctggaactagagcgcaagattgagtct ctgatggatgagattgagttcctcaagaagctgcacgaggaggagctgcgagacctgcag gtgagtgtggagagccagcaggtgcagcaggtggaggtggaagccacggtgaagcccgag ctgacggcagcgctgagggacatccgcgcgcagtacgagagcatcgccgcgaagaacctg caggaggcggaggagtggtacaagtccaagtacgcggacctgtccgacgctgccaaccgg aaccacgaggccctgcgccaggccaagcaggagatgaacgagtcccgacgccagatccag agtctaacgtgcgaggtggacgggctgcgcggcacgaacgaggcgctgctcaggcagttg agagagctggaggagcagttcgccctggaggcggggggctaccaggcgggcgctgcgcgg ctcgaggaggagctgcgacagctaaaagaggagatggcgcggcacctgagggagtaccag gagctcctcaacgtcaagatggccctggacatcgagatcgccacctaccgcaagctgctg gagggcgaggagagccggatctccgtgcccgtccattcttttgcctccttaaatataaag acgactgtgcctgaggtggagcctccccaggacagccacagccggaagacggttctgatc aagaccattgagacccggaatggggaggtggtgacagagtcccagaaggagcagcgcagt gagctggacaagtcttctgcccacagttactga

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