Homo sapiens (human): 4808 Help Entry 4808              CDS       T01001                                  Symbol NHLH2, HEN2, HH27, NSCL2, bHLHa34 Name (RefSeq) helix-loop-helix protein 2   KO K09075   nescient helix-loop-helix protein Organism hsa  Homo sapiens (human) Disease H00255   Hypogonadotropic hypogonadism Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     4808 (NHLH2) Transcription factors [BR:hsa03000]  Eukaryotic type   Basic helix-loop-helix (bHLH)    Tal/Twist/Atonal/Hen, HEN     4808 (NHLH2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  HLH bHLH_IRO3 bHLH_INO4 Motif Other DBs NCBI-GeneID:  4808 NCBI-ProteinID:  NP_001104531 OMIM:  162361 HGNC:  7818 UniProt:  Q02577 LinkDB All DBs Position 1:complement(115831344..115841126) Genome browser AA seq 135 aa AA seqDB search MMLSPDQAADSDHPSSAHSDPESLGGTDTKVLGSVSDLEPVEEAEGDGKGGSRAALYPHP QQLSREEKRRRRRATAKYRSAHATRERIRVEAFNLAFAELRKLLPTLPPDKKLSKIEILR LAICYISYLNHVLDV NT seq 408 nt NT seq  +upstreamnt  +downstreamnt atgatgctgagtccggaccaagcagcagattcggaccatcccagctcggcgcactcggat ccggagtccctgggcggcacggacaccaaggtgctcggcagcgtgtcggacctggagccg gtggaggaggccgagggcgacggcaagggcggcagccgagccgcgctctacccgcacccg cagcagctgagccgcgaggagaagcgccgccgccggcgcgccacggccaagtaccgctcg gcccacgccacccgcgagcgcatccgcgtggaagccttcaacttggccttcgccgagctc cgcaaattgctgcccacgctgcccccggacaagaagctctccaagatcgagatcctgcgc ctggccatctgctacatctcctatctcaaccacgtcctggacgtgtag

DBGET integrated database retrieval system