Homo sapiens (human): 120766137 Help Entry 120766137         CDS       T01001                                  Symbol HRURF, HMU, MUHH, U2HR Name (RefSeq) protein HRURF   KO K28373   protein HRURF Organism hsa  Homo sapiens (human) Disease H00786   Hypotrichosis H00858   Marie-Unna hereditary hypotrichosis Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09192 Unclassified: genetic information processing    99974 Translation     120766137 (HRURF) SSDB OrthologParalogGFIT Other DBs NCBI-GeneID:  120766137 NCBI-ProteinID:  NP_001381061 OMIM:  619257 HGNC:  55085 Ensembl:  ENSP00000505144.1 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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