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