Homo sapiens (human): 23111 Help Entry 23111             CDS       T01001                                  Symbol SPART, SPG20, TAHCCP1 Name (RefSeq) spartin   KO K19366   spartin Organism hsa  Homo sapiens (human) Pathway hsa04144   Endocytosis Disease H00266   Hereditary spastic paraplegia Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04144 Endocytosis     23111 (SPART) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Senescence MIT TPR_8 Motif Other DBs NCBI-GeneID:  23111 NCBI-ProteinID:  NP_001135766 OMIM:  607111 HGNC:  18514 Ensembl:  ENSG00000133104 UniProt:  Q8N0X7 A0A024RDV9 Structure PDB LinkDB All DBs Position 13:complement(36301638..36370180) Genome browser AA seq 666 aa AA seqDB search MEQEPQNGEPAEIKIIREAYKKAFLFVNKGLNTDELGQKEEAKNYYKQGIGHLLRGISIS SKESEHTGPGWESARQMQQKMKETLQNVRTRLEILEKGLATSLQNDLQEVPKLYPEFPPK DMCEKLPEPQSFSSAPQHAEVNGNTSTPSAGAVAAPASLSLPSQSCPAEAPPAYTPQAAE GHYTVSYGTDSGEFSSVGEEFYRNHSQPPPLETLGLDADELILIPNGVQIFFVNPAGEVS APSYPGYLRIVRFLDNSLDTVLNRPPGFLQVCDWLYPLVPDRSPVLKCTAGAYMFPDTML QAAGCFVGVVLSSELPEDDRELFEDLLRQMSDLRLQANWNRAEEENEFQIPGRTRPSSDQ LKEASGTDVKQLDQGNKDVRHKGKRGKRAKDTSSEEVNLSHIVPCEPVPEEKPKELPEWS EKVAHNILSGASWVSWGLVKGAEITGKAIQKGASKLRERIQPEEKPVEVSPAVTKGLYIA KQATGGAAKVSQFLVDGVCTVANCVGKELAPHVKKHGSKLVPESLKKDKDGKSPLDGAMV VAASSVQGFSTVWQGLECAAKCIVNNVSAETVQTVRYKYGYNAGEATHHAVDSAVNVGVT AYNINNIGIKAMVKKTATQTGHTLLEDYQIVDNSQRENQEGAANVNVRGEKDEQTKEVKE AKKKDK NT seq 2001 nt NT seq  +upstreamnt  +downstreamnt atggagcaagagccacaaaatggagaacctgctgaaattaagatcatcagagaagcatat aagaaggcctttttatttgttaacaaaggtctgaatacagatgaattaggtcagaaggaa gaagcaaagaactactataagcaaggaataggacacctgctcagagggatcagcatttca tcaaaagagtctgaacacacaggtcctgggtgggaatctgctagacagatgcaacagaaa atgaaagaaactctacagaatgtacgcaccaggctggaaattctagagaagggtcttgcc acttctctgcagaatgatcttcaggaggtgcccaagttatatccagaatttccacctaaa gacatgtgtgaaaaattaccagagcctcagtcttttagttcagctcctcagcatgctgaa gtaaatggaaacacctcaactccaagtgcaggggcagttgctgcacctgcttctctgtct ttaccatcacaaagttgtccagcagaagctcctcctgcttatactcctcaagctgctgaa ggtcactacactgtatcctatggaacagattctggggagttttcatcagttggagaggag ttttataggaatcattctcagccaccgcctcttgagaccttagggctggatgcagatgaa ttgattttgataccaaatggagtacagattttttttgtaaatcctgcaggggaggttagt gcaccttcgtatcctgggtaccttcgaattgtgaggtttttggataattctctcgatacg gttctaaaccgtcctcccgggtttcttcaggtttgtgactggttatatcctctagttcct gatagatctccggttctgaaatgtactgcgggagcctacatgtttcctgatacaatgcta caagcagcaggatgctttgtgggggtcgtcctgtcctctgagttaccagaggatgataga gagctctttgaggatctgttaaggcaaatgtctgaccttcggctccaggccaactggaac agagcagaagaagaaaatgaattccaaatccctggaagaactagaccctcctctgaccaa ctaaaagaagcctctggcactgatgtgaaacagttggaccaaggcaataaggatgtacgt cataaaggaaaacgtggaaaaagggctaaagatacttcaagtgaagaagttaacctgagt cacattgtaccatgtgagccagttccagaagaaaagccaaaagaattacctgaatggagt gaaaaagtggctcacaacattttgtcaggtgcttcctgggtgagttggggtttagtcaaa ggtgctgagattactggtaaggcaatccagaaaggtgcttctaaactccgagagcggatt caaccagaagaaaaacccgtggaagttagtccagctgtcaccaagggactttatatagcg aagcaagctacaggaggagcagcaaaagtcagtcagttcctggttgatggagtttgcact gtagcaaattgcgttggaaaagaactagctccacatgtcaagaagcatggaagcaaactt gttccagaatctcttaaaaaagacaaagatgggaaatctcctctggatggtgctatggtt gtagcagcaagtagtgttcaaggattttcaactgtctggcaaggattggaatgtgcagct aaatgcatcgttaacaatgtttcagcagaaactgtacaaactgtcagatacaaatacgga tataatgcaggagaagctacccaccatgcggtggattctgcggtcaatgttggcgtaact gcctacaatattaacaacattggtatcaaagcaatggtgaagaaaactgcaacacaaaca ggacacactctccttgaggactatcagatagttgataattctcagagggaaaatcaagaa ggagcagcaaatgtcaacgtgagaggggagaaggatgagcagacgaaggaagtaaaggag gcaaagaagaaagataaatga

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