Homo sapiens (human): 83893 Help Entry 83893             CDS       T01001                                  Symbol SPATA16, NYD-SP12, SPGF6 Name (RefSeq) spermatogenesis associated 16   KO K26121   spermatogenesis-associated protein 16 Organism hsa  Homo sapiens (human) Disease H01208   Globozoospermia H01282   Spermatogenic failure Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     83893 (SPATA16) Cilium and associated proteins [BR:hsa03037]  Motile cilia and associated proteins   Sperm associated proteins    83893 (SPATA16) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  NYD-SP12_N TPR_2 DUF3856 Motif Other DBs NCBI-GeneID:  83893 NCBI-ProteinID:  NP_114161 OMIM:  609856 HGNC:  29935 Ensembl:  ENSG00000144962 UniProt:  Q9BXB7 A0A140VJV8 LinkDB All DBs Position 3:complement(172889357..173141235) Genome browser AA seq 569 aa AA seqDB search MDAGSSRSLENAVNRIYHDQLVPKINTSKKMSTLAHPPNILEMSQEIKKNCGGKQVEITL ERTKMTKGIKEKQSNDLEKAAFKRKAEGEEKPTRKKQAKITELDNQLITMPLPHIPLKNI MDVEMKLVYIDEMGVRYEFVESFMSTGSQPTCQAAEIVDPLSVHNFSFLPQIDKWLQVAL KDASSCYRQKKYALAAGQFRTALELCSKGAVLGEPFDAPAEDIASVASFIETKLVTCYLR MRKPDLALNHAHRSIVLNPAYFRNHLRQATVFRCLERYSEAARSAMIADYMFWLGGGREE SISKLIKLYWQAMIEEAITRAESFSVMYTPFATKIRADKIEKVKDAFTKTHPAYAEYMYT DLQALHMLPQTVDWSSFPPQQYLLTLGFKNKDDGKFLEKISSRKLPIFTEHKTPFGLTRE DTVRQMETMGKRILPILDFIRSTQLNGSFPASSGVMEKLQYASLLSQLQRVKEQSQVINQ AMAELATIPYLQDISQQEAELLQSLMADAMDTLEGRRNNNERVWNMIQKVGQIEDFLYQL EDSFLKTKKLRTARRQKTKMKRLQTVQQR NT seq 1710 nt NT seq  +upstreamnt  +downstreamnt atggatgcaggaagcagtaggagtttggagaatgcagtgaataggatctatcatgatcag cttgttccaaagataaacacaagcaagaaaatgtccaccttagcgcacccacctaacatc ctggaaatgtcacaagagattaagaaaaactgtggaggtaaacaggtagaaatcacactt gaaagaacaaaaatgacaaagggcatcaaagaaaaacaaagcaatgatttagagaaagca gcctttaaacggaaggcagaaggtgaagaaaagccaactagaaagaaacaggcaaagata acagaacttgacaatcagttaatcaccatgcctctgcctcacatccccttaaagaacata atggatgtggaaatgaagttggtctacattgatgaaatgggtgttcgctatgagtttgta gagtccttcatgtctactgggagtcagccaacatgccaagctgctgaaatagtagaccct ttgagtgtacataatttcagctttctgcctcagattgacaaatggcttcaggtagcctta aaggatgccagctcttgctatagacaaaagaaatacgccttggcagcaggacagttcaga acagcacttgagctttgcagcaaaggagcagttctgggagaaccatttgatgcacctgct gaagatatagcaagcgtggcaagtttcattgagacaaagcttgttacctgttatctacgg atgaggaaaccagatcttgccctgaatcatgcacacaggagcattgttttaaacccagcc tatttccggaatcatcttcgtcaagcaacagtgtttagatgtctggagaggtattcagag gctgcccggagtgccatgattgctgactacatgttctggcttggtggaggaagggaagag agcataagcaagctcatcaaactgtattggcaggccatgattgaggaagccatcaccaga gctgaatctttctcggttatgtacacaccatttgcgacaaaaataagagctgataaaata gaaaaagtaaaagatgctttcacaaaaactcatcctgcatatgcagagtatatgtacaca gatcttcaagcactccacatgttgcctcagacagttgactggtcatcttttcctccccaa caatatctcttgactcttgggttcaaaaacaaagatgatggaaaatttttggaaaaaata tcaagcaggaagctgccgatattcacagagcataaaacacctttcggtctgaccagagaa gatacagtgaggcaaatggagacaatggggaagcgaatcttgccaatattggattttatt agaagcacccaattgaatgggagttttcctgcatcctcaggtgtgatggagaagttgcaa tatgccagcctcctcagccagctgcagagagtaaaggagcagtcccaggtgattaatcaa gcaatggcagagctagcaaccattccctacctacaggacatcagtcaacaggaggcagaa ttgctgcagtcactaatggcagatgctatggacacccttgaaggaagaagaaacaataat gaacgtgtgtggaatatgatccaaaaggttggacaaattgaagattttctataccaatta gaggacagtttcttaaaaactaaaaaactgagaactgctcgaaggcaaaaaacaaaaatg aagcgacttcaaactgttcagcaaaggtag

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