HPRT1
protein-coding gene in the species Homo sapiens
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HPRT1
Summary
HPRT1 is a gene[1].
Key Facts
- HPRT1's instance of is recorded as gene[2].
- HPRT1's subclass of is recorded as protein-coding gene[3].
- HPRT1's Entrez Gene ID is recorded as 3251[4].
- HPRT1's HGNC gene symbol is recorded as HPRT1[5].
- HPRT1's HGNC ID is recorded as 5157[6].
- HPRT1's OMIM ID is recorded as 308000[7].
- HPRT1's HomoloGene ID is recorded as 56590[8].
- HPRT1's Ensembl gene ID is recorded as ENSG00000165704[9].
- HPRT1's RefSeq RNA ID is recorded as NM_000194[10].
- HPRT1's genomic start is recorded as 133594183[11].
- HPRT1's genomic start is recorded as 134460165[12].
- HPRT1's genomic end is recorded as 134520513[13].
- HPRT1's genomic end is recorded as 133654543[14].
- HPRT1's ortholog is recorded as Hprt[15].
- HPRT1's ortholog is recorded as Hprt1[16].
- HPRT1's ortholog is recorded as hprt1[17].
- HPRT1's ortholog is recorded as hprt-1[18].
- HPRT1's encodes is recorded as Hypoxanthine phosphoribosyltransferase 1[19].
- HPRT1's Gene Atlas image is recorded as PBB GE HPRT1 202854 at fs.png[20].
- HPRT1's found in taxon is recorded as Homo sapiens[21].
- HPRT1's Ensembl transcript ID is recorded as ENST00000475720[22].
- HPRT1's Ensembl transcript ID is recorded as ENST00000298556[23].
- HPRT1's Ensembl transcript ID is recorded as ENST00000462974[24].
- HPRT1's chromosome is recorded as human X chromosome[25].
- HPRT1's genetic association is recorded as Lesch-Nyhan syndrome[26].