Homo sapiens (human): 317719 Help Entry 317719            CDS       T01001                                  Symbol KLHL10, SPGF11 Name (RefSeq) kelch like family member 10   KO K10448   kelch-like protein 10 Organism hsa  Homo sapiens (human) Disease H01282   Spermatogenic failure Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04121 Ubiquitin system [BR:hsa04121]     317719 (KLHL10) Ubiquitin system [BR:hsa04121]  Ubiquitin ligases (E3)   Multi subunit type E3    Cul3 complex     Adoptor and target recognizing subunit (BTB)      317719 (KLHL10) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Kelch_1 Kelch_KLHDC2_KLHL20_DRC7 Kelch_2 BACK BTB Kelch_FKB95 Beta-prop_Calicin Beta-prop_FBX42 Beta-prop_ATRN-LZTR1 NANM BTB_KLHL33 INTS1_R4 Motif Other DBs NCBI-GeneID:  317719 NCBI-ProteinID:  NP_001316524 OMIM:  608778 HGNC:  18829 Ensembl:  ENSG00000161594 UniProt:  Q6JEL2 A0A140VJM8 LinkDB All DBs Position 17:41835685..41848384 Genome browser AA seq 608 aa AA seqDB search MEMESAAASTRFHQPHMERKMSAMACEIFNELRLEGKLCDVVIKVNGFEFSAHKNILCSC SSYFRALFTSGWNNTEKKVYNIPGISPDMMKLIIEYAYTRTVPITPDNVEKLLAAADQFN IMGIVRGCCEFLKSELCLDNCIGICKFTDYYYCPELRQKAYMFILHNFEEMVKVSAEFLE LSVTELKDIIEKDELNVKQEDAVFEAILKWISHDPQNRKQHISILLPKVRLALMHAEYFM NNVKMNDYVKDSEECKPVIINALKAMYDLNMNGPSNSDFTNPLTRPRLPYAILFAIGGWS GGSPTNAIEAYDARADRWVNVTCEEESPRAYHGAAYLKGYVYIIGGFDSVDYFNSVKRFD PVKKTWHQVAPMHSRRCYVSVTVLGNFIYAMGGFDGYVRLNTAERYEPETNQWTLIAPMH EQRSDASATTLYGKVYICGGFNGNECLFTAEVYNTESNQWTVIAPMRSRRSGIGVIAYGE HVYAVGGFDGANRLRSAEAYSPVANTWRTIPTMFNPRSNFGIEVVDDLLFVVGGFNGFTT TFNVECYDEKTDEWYDAHDMSIYRSALSCCVVPGLANVEEYAARRDNFPGLALRDEVKYS ASTSTLPV NT seq 1827 nt NT seq  +upstreamnt  +downstreamnt atggagatggagagcgcggcggcctccacacgtttccaccagcctcacatggagaggaag atgagtgcgatggcctgtgagatcttcaacgagcttagactagagggcaagctctgcgac gtggtcatcaaggtcaatggctttgagttcagtgcccataagaacatcctctgtagctgc agttcctactttagagctttgtttacaagtggctggaacaacactgaaaagaaggtatac aacatccctggcatttctcccgacatgatgaagctaatcattgagtatgcatacacccgg accgtgcctatcacaccggacaatgtggagaaactgcttgctgctgcagaccagtttaac atcatgggtatcgtcaggggttgctgcgagttcctcaagtcagagctgtgcttggataat tgtatcggcatctgtaagttcacggactactactactgtcctgagctgaggcagaaggcc tacatgttcatactgcacaactttgaggagatggtgaaagtctcggcagaatttttagag ctctcggtcactgaacttaaggatatcattgagaaagatgagctcaatgtcaaacaggaa gatgctgtatttgaggccattttaaagtggatttctcatgacccccaaaatagaaagcag cacatttcaattttgcttcctaaggttcgcctggccctaatgcatgctgagtacttcatg aacaatgttaagatgaatgactatgtcaaagacagtgaggaatgcaaaccagtcatcatt aatgccctaaaggccatgtatgacctcaacatgaatggaccctctaattctgatttcacc aacccactcaccagaccacgcttgccctatgccatcctctttgcaattggtggctggagt ggtgggagccccaccaatgccattgaggcatatgacgctcgggcagacagatgggtgaat gttacttgtgaggaagagagtccccgtgcctaccatggggcagcctatttgaaaggctat gtgtatatcattggggggtttgatagtgtagactatttcaatagtgttaagcgttttgac ccagtcaagaaaacttggcatcaggtggccccgatgcactccagacgttgctatgtcagt gtgacagtcctcggcaattttatttatgccatgggaggatttgatggctacgtgcgtcta aacactgctgaacgttatgagccagagaccaatcaatggacactcatcgcccccatgcac gaacagaggagtgatgcaagcgccacaacactttatgggaaggtctacatatgtggtggg tttaatggaaacgagtgcctgttcacagcagaagtgtataacactgaaagtaatcagtgg acagtcatagcacccatgagaagcaggaggagtggaataggcgtgattgcttatggagaa catgtatatgcggtaggtggctttgatggagctaatcgacttaggagtgccgaagcctac agccctgtggctaacacttggcgcacaatccccactatgtttaatcctcgtagcaatttt ggcatcgaggtggtggatgacctcttgtttgtggtgggtggctttaatggttttaccacc acctttaatgttgagtgctatgatgaaaagaccgatgagtggtatgatgctcatgacatg agtatataccgcagtgctctgagctgctgtgtagtaccagggctggccaatgttgaggaa tatgcagctagacgggacaacttcccaggattagcactgcgagatgaagtaaaatattct gcttcgacaagtaccctacctgtatga

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