Homo sapiens (human): 6658 Help Entry 6658              CDS       T01001                                  Symbol SOX3, GHDX, MRGH, PHP, PHPX, SOXB Name (RefSeq) SRY-box transcription factor 3   KO K09267   transcription factor SOX1/3/14/21 (SOX group B) Organism hsa  Homo sapiens (human) Disease H00254   Growth hormone deficiency H00544   Septo-optic dysplasia H00598   46,XX testicular disorder of sex development H00658   X-linked syndromic intellectual developmental disorder H02038   X-linked panhypopituitarism Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     6658 (SOX3) Transcription factors [BR:hsa03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    HMG SOX     6658 (SOX3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SOXp HMG_box HMG_box_2 HMG_WDHD1 Motif Other DBs NCBI-GeneID:  6658 NCBI-ProteinID:  NP_005625 OMIM:  313430 HGNC:  11199 Ensembl:  ENSG00000134595 UniProt:  P41225 LinkDB All DBs Position X:complement(140502985..140505069) Genome browser AA seq 446 aa AA seqDB search MRPVRENSSGARSPRVPADLARSILISLPFPPDSLAHRPPSSAPTESQGLFTVAAPAPGA PSPPATLAHLLPAPAMYSLLETELKNPVGTPTQAAGTGGPAAPGGAGKSSANAAGGANSG GGSSGGASGGGGGTDQDRVKRPMNAFMVWSRGQRRKMALENPKMHNSEISKRLGADWKLL TDAEKRPFIDEAKRLRAVHMKEYPDYKYRPRRKTKTLLKKDKYSLPSGLLPPGAAAAAAA AAAAAAAASSPVGVGQRLDTYTHVNGWANGAYSLVQEQLGYAQPPSMSSPPPPPALPPMH RYDMAGLQYSPMMPPGAQSYMNVAAAAAAASGYGGMAPSATAAAAAAYGQQPATAAAAAA AAAAMSLGPMGSVVKSEPSSPPPAIASHSQRACLGDLRDMISMYLPPGGDAADAASPLPG GRLHGVHQHYQGAGTAVNGTVPLTHI NT seq 1341 nt NT seq  +upstreamnt  +downstreamnt atgcgacctgttcgagagaactcatcaggtgcgagaagcccgcgggttcctgctgatttg gcgcggagcattttgataagcctacccttcccgccggactcgctggcccacaggccccca agctccgctccgacggagtcccagggccttttcaccgtggccgctccagccccgggagcg ccttctcctcccgccacgctggcgcaccttcttcccgccccggcaatgtacagccttctg gagactgaactcaagaaccccgtagggacacccacacaagcggcgggcaccggcggcccc gcagccccgggaggcgcaggcaagagtagtgcgaacgcagccggcggcgcgaactcgggc ggcggcagcagcggtggtgcgagcggaggtggcgggggtacagaccaggaccgtgtgaaa cggcccatgaacgccttcatggtatggtcccgcgggcagcggcgcaaaatggccctggag aaccccaagatgcacaattctgagatcagcaagcgcttgggcgccgactggaaactgctg accgacgccgagaagcgaccattcatcgacgaggccaagcgacttcgcgccgtgcacatg aaggagtatccggactacaagtaccgaccgcgccgcaagaccaagacgctgctcaagaaa gataagtactccctgcccagcggcctcctgcctcccggtgccgcggccgccgccgccgct gccgcggccgcagccgctgccgccagcagtccggtgggcgtgggccagcgcctggacacg tacacgcacgtgaacggctgggccaacggcgcgtactcgctggtgcaggagcagctgggc tacgcgcagcccccgagcatgagcagcccgccgccgccgcccgcgctgccgccgatgcac cgctacgacatggccggcctgcagtacagcccaatgatgccgcccggcgctcagagctac atgaacgtcgctgccgcggccgccgccgcctcgggctacgggggcatggcgccctcagcc acagcagccgcggccgccgcctacgggcagcagcccgccaccgccgcggccgcagctgcg gccgcagccgccatgagcctgggccccatgggctcggtagtgaagtctgagcccagctcg ccgccgcccgccatcgcatcgcactctcagcgcgcgtgcctcggcgacctgcgcgacatg atcagcatgtacctgccacccggcggggacgcggccgacgccgcctctccgctgcccggc ggtcgcctgcacggcgtgcaccagcactaccagggcgccgggactgcagtcaacggaacg gtgccgctgacccacatctga

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