Homo sapiens (human): 120766137 Help Entry 120766137         CDS       T01001                                  Symbol HRURF, HMU, MUHH, U2HR Name (RefSeq) HR upstream open reading frame   KO K28373   protein HRURF Organism hsa  Homo sapiens (human) Disease H00786   Hypotrichosis Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09192 Unclassified: genetic information processing    99974 Translation     120766137 (HRURF) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Other DBs NCBI-GeneID:  120766137 NCBI-ProteinID:  NP_001381061 OMIM:  619257 HGNC:  55085 Ensembl:  ENSG00000288677 UniProt:  P0DUH7 A0A7P0T8H1 LinkDB All DBs Position 8:complement(22130458..22131010) Genome browser AA seq 34 aa AA seqDB search MAQPTASAQKLVRPIRAVCRILQIPESDPSNLRP NT seq 105 nt NT seq  +upstreamnt  +downstreamnt atggcgcaacctacggcctcggcccagaagctggtgcggccgatccgcgccgtgtgccgc atcctgcagatcccggagtccgacccctccaacctgcggccctag

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