KEGG   Homo sapiens (human): 120766137
Entry
120766137         CDS       T01001                                 
Symbol
HRURF, HMU, MUHH, U2HR
Name
(RefSeq) HR upstream open reading frame
Organism
hsa  Homo sapiens (human)
Disease
H00786  Hypotrichosis
SSDB
Other DBs
NCBI-GeneID: 120766137
NCBI-ProteinID: NP_001381061
OMIM: 619257
HGNC: 55085
Ensembl: ENSG00000288677
Position
8:complement(22130458..22131010)
AA seq 34 aa
MAQPTASAQKLVRPIRAVCRILQIPESDPSNLRP
NT seq 105 nt   +upstreamnt  +downstreamnt
atggcgcaacctacggcctcggcccagaagctggtgcggccgatccgcgccgtgtgccgc
atcctgcagatcccggagtccgacccctccaacctgcggccctag

  All links  
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
Protein sequence (1)   
   RefSeq(pep) (1)   
DNA sequence (1)   
   RefSeq(nuc) (1)   
All databases (10)   

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