LongevityMap variant group

Entry Details

Longevity Association
Non-significant
Population
American (Caucasian)
Study Design
Genome-wide association study for longevity-related traits in up to 1345 Framingham Study participants from 330 families; 713 participants achieved age 65 years or greater. A total of 79 potential candidate genes and regions associated with longevity were also studied.
Conclusions
Although no genome-wide associations were significant, mutiple SNPs and genes had suggestive associations with age at death

Variants (9)

No gene

1.
Identifier
rs1528753
Cytogenetic Location
2.
Identifier
rs2371208
Cytogenetic Location
3.
Identifier
rs10489006
Cytogenetic Location
4.
Identifier
rs10493515
In Other Studies (IDs)
1354
Cytogenetic Location
5.
Identifier
rs1915501
Cytogenetic Location

LOC105374956

1.
Identifier
rs6459623
Cytogenetic Location
6p22.3
UCSC Genome Browser
View 6p22.3 on the UCSC genome browser

Gene details

HGNC symbol
LOC105374956
Aliases
 
Common name
uncharacterized LOC105374956 
Description
OMIM
Ensembl
UniProt/Swiss-Prot
Entrez Gene
105374956
UniGene
561599
HapMap
View on HapMap

Homologs in model organisms

No homologs found

MYLIP

1.
Identifier
rs3757354
Cytogenetic Location
6p22.3
UCSC Genome Browser
View 6p22.3 on the UCSC genome browser

Gene details

HGNC symbol
MYLIP
Aliases
MIR; IDOL 
Common name
myosin regulatory light chain interacting protein 
Description
The ERM protein family members ezrin, radixin, and moesin are cytoskeletal effector proteins linking actin to membrane-bound proteins at the cell surface. Myosin regulatory light chain interacting protein (MYLIP) is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth. [provided by RefSeq, Jul 2008]
OMIM
610082
Ensembl
ENSG00000007944
UniProt/Swiss-Prot
MYLIP_HUMAN
Entrez Gene
29116
UniGene
484738
HapMap
View on HapMap

Homologs in model organisms

Danio rerio
mylipa
Mus musculus
Mylip
Rattus norvegicus
Mylip

NXPH2

1.
Identifier
rs10496799
Cytogenetic Location
2q22.1
UCSC Genome Browser
View 2q22.1 on the UCSC genome browser

Gene details

HGNC symbol
NXPH2
Aliases
NPH2 
Common name
neurexophilin 2 
Description
OMIM
604635
Ensembl
ENSG00000144227
UniProt/Swiss-Prot
NXPH2_HUMAN
Entrez Gene
11249
UniGene
435019
HapMap
View on HapMap

Homologs in model organisms

Danio rerio
nxph2a
Mus musculus
Nxph2
Rattus norvegicus
Nxph2

OR4Q3

1.
Identifier
rs10498263
Cytogenetic Location
14q11.2
UCSC Genome Browser
View 14q11.2 on the UCSC genome browser

Gene details

HGNC symbol
OR4Q3
Aliases
HSA6; OR4Q4; OR14-3; C14orf13; c14_5008 
Common name
olfactory receptor family 4 subfamily Q member 3 
Description
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
OMIM
Ensembl
ENSG00000182652
UniProt/Swiss-Prot
A0A126GW32_HUMAN
Entrez Gene
441669
UniGene
553828
HapMap
View on HapMap

Homologs in model organisms

Mus musculus
Olfr735

References

Lunetta et al. (2007)

Other variants which are also part of this study