Homo sapiens
Taxonomy:
AnimaliaChordataMammaliaPrimatesHominidaeHomoHomo sapiens
Lifespan:
122 years
Source:
HAGR:AnAge
| Symbol | Secondary Symbol | Name | Description | Source |
|---|---|---|---|---|
| MYST4 | MYST histone acetyltransferase (monocytic leukemia) 4 | Genbank | ||
| WRN | Werner syndrome | |||
| CETP | cholesteryl ester transfer protein, plasma | |||
| APP | amyloid beta (A4) precursor protein (peptidase nexin-II, Alzheimer disease) | |||
| HSPA9 | heat shock 70kDa protein 9 (mortalin) | |||
| PARK2 | Parkinson disease (autosomal recessive, juvenile) 2, parkin | |||
| PSEN2 | presenilin 2 (Alzheimer disease 4) | |||
| MT1B | metallothionein 1B | |||
| ATM | ataxia telangiectasia mutated | |||
| BLM | Bloom syndrome | |||
| NR3C1 | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) | |||
| APOE | apolipoprotein E | |||
| PSEN1 | presenilin 1 (Alzheimer disease 3) | |||
| APBB1 | amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65) | |||
| LMNA | RP11-54H19.1 | lamin A/C | ||
| ERCC8 | excision repair cross-complementing rodent repair deficiency, complementation group 8 | |||
| UCHL1 | ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) | |||
| SNCA | synuclein, alpha (non A4 component of amyloid precursor) | |||
| SIRT3 | sirtuin (silent mating type information regulation 2 homolog) 3 (S. cerevisiae) | |||
| Homo sapiens chromosome 5 clone RP11-47L17, complete sequence | Genbank | |||
| TP53 | Homo sapiens p53 protein (TP53) mRNA, complete cds, alternatively spliced | Genbank | ||
| Homo sapiens p51 gene, exon 4 | Genbank | |||
| Homo sapiens, clone RP11-115N12, complete sequence | Genbank | |||
| Homo sapiens p51 gene, exon 5 | Genbank | |||
| SLCO1A2 | HSU21943 Human organic anion transporting polypeptide (OATP) mRNA: U21943 | This gene encodes a sodium-independent transporter which mediates cellular uptake of organic ions in the liver. Its substrates include bile acids, bromosulphophthalein, and some steroidal compounds. The protein is a member of the SLC21A family of solute carriers. Alternate splicing of this gene results in three transcript variants encoding two different isoforms. | Genbank | |
| Homo sapiens p51 gene, exon 6 | Genbank | |||
| Homo sapiens isolate 27 insulin receptor gene, exon 14 and partial cds | Genbank | |||
| Homo sapiens genomic DNA of 21q22.1, APP related, B2291C14-T1533 region, segment 5/7 | Genbank | |||
| TOP3B | Homo sapiens TOP3B full length open reading frame (ORF) cDNA clone (cDNA clone C22ORF:pGEM.TOP3B.V4) | Genbank | ||
| Homo sapiens p51 gene, exon 7 | Genbank |