Homo sapiens (human): 285498 Help Entry 285498            CDS       T01001                                  Symbol RNF212, SPGF62, ZHP3 Name (RefSeq) ring finger protein 212   KO K25662   E3 SUMO-protein ligase RNF212 [EC:2.3.2.-] 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]     285498 (RNF212)    03036 Chromosome and associated proteins [BR:hsa03036]     285498 (RNF212) Ubiquitin system [BR:hsa04121]  Ubiquitin ligases (E3)   UBL E3 ligases    285498 (RNF212) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Meiosis-specific proteins    Others     285498 (RNF212) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  zf-RING_5 Prok-RING_4 Fib_alpha zf-RING_UBOX STX17_N Motif Other DBs NCBI-GeneID:  285498 NCBI-ProteinID:  NP_001124506 OMIM:  612041 HGNC:  27729 Ensembl:  ENSG00000178222 UniProt:  Q495C1 LinkDB All DBs Position 4:complement(1056251..1113710) Genome browser AA seq 297 aa AA seqDB search MANWVFCNRCFQPPHRTSCFSLTNCGHVYCDACLGKGKKNECLICKAPCRTVLLSKHTDA DIQAFFMSIDSLCKKYSRETSQILEFQEKHRKRLLAFYREKISRLEESLRKSVLQIEQLQ SMRSSQQTAFSTIKSSVSTKPHGCLLPPHSSAPDRLESMEVDLSPSPIRKSEIAAGPARI SMISPPQDGRMGPHLTASFCFIPWLTLSKPPVPGECVISRGSPCFCIDVCPHWLLLLAFS SGRHGELTNSKTLPIYAEVQRAVLFPFQQAEGTLDTFRTPAVSVVFPLCQFERKKSF NT seq 894 nt NT seq  +upstreamnt  +downstreamnt atggccaactgggtgttctgtaatcgctgcttccagccgccccacaggacgtcgtgcttc agcctcaccaactgcgggcacgtgtactgcgacgcctgcctcggcaaaggtaaaaagaat gaatgcttgatttgtaaagctccttgtcgtacagttttgctttcaaagcataccgacgca gatatccaggcattcttcatgagcatagacagtctgtgtaagaagtactccagggaaacc tcccagattttagaatttcaagaaaaacacaggaagagattgttagccttctatagagaa aagatttctaggttggaagaatcccttaggaagtcagtgctgcagatagaacaactacaa agtatgagatcatcacaacaaacagctttcagcacaataaaaagttcagtttcaacaaaa ccacacggatgcctgctgccacctcactcatcagcccccgacagactggagtcgatggaa gttgatctctctccttctccgattagaaaatctgagatagcagccggccctgcgagaatc tccatgattagtccacctcaagatggacgaatggggccacatctaacagcttctttctgt ttcatcccatggttgaccttgtctaagccccctgtgcccggagagtgtgtcatttccaga ggttcaccatgtttctgcatagacgtctgtcctcactggctgctcctcctagcgttcagt tctggaaggcacggggaactcaccaactctaaaacacttccaatatatgctgaggtacaa agggccgtcttgtttccgttccagcaggctgagggcaccctggacacgttcagaacaccc gctgtgtctgttgtgtttcctctttgccaatttgaaaggaaaaagtcattttga

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