Posts Tagged ‘keyabbrev’

Catechol-O-methyltransferase – Wikipedia

Saturday, October 12th, 2019


Catechol-O-methyltransferase – Wikipedia
Intelligence gene

XIST – Wikipedia

Saturday, October 12th, 2019
also XIC

Xist (X-inactive specific transcript) is an RNA gene on the X chromosome of the placental mammals that acts as a major effector of the X inactivation process.[4] It is a component of the Xic – X-chromosome inactivation centre[5] – along with two other RNA genes (Jpx and Ftx) and two protein genes (Tsx and Cnbp2).[6]

Wikipedia:Too long; didn’t read – Wikipedia

Saturday, October 12th, 2019;_didn%27t_read
abbreviated TL;DR and tl;dr

Sodium/potassium/calcium exchanger 5 – Wikipedia

Monday, October 7th, 2019

Sodium/potassium/calcium exchanger 5 (NCKX5), also known as solute carrier family 24 member 5 (SLC24A5), is a protein that in humans is encoded by the SLC24A5 gene that has a major influence on natural skin colour variation.[5] The NCKX5 protein is a member of the
potassium-dependent sodium/calcium exchanger family. Sequence variation in the SLC24A5 gene, particularly a non-synonymous SNP changing the amino acid at position 111 in NCKX5 from alanine to threonine, has been associated with differences in skin

Cc2d2a Chemically induced Allele Detail MGI Mouse (MGI:5311382)

Monday, August 19th, 2019

b2b1035Clo = Blue meanie mutation

Cc2d2ab2 ^ b1035Clo
Name:coiled-coil and C2 domain containing 2A; Bench to Bassinet Program (B2B/CVDC), mutation 1035 Cecilia Lo
MGI ID:MGI:5311382
Synonyms:Blue meanie
Gene:Cc2d2a Location: Chr5:43662373-43740975 bp, + strand Genetic Position: Chr5, 23.78 cM
Heterotaxy indicated by left lung isomerism with left sided IVC and TGA (observed by EFIC imaging)

Mutation details: This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. The molecular lesion is a C to T substitution at coding nucleotide 2845 in exon 23 of the cDNA (c.2845C>T, NM_172274). This changes the arginine residue to a translation stop at position 949 of the encoded protein (p.R949*). (J:175213) Additional incidental mutations were detected in sequencing for the causative mutation, Cc2d2ab2b1035Clo, and may be present in stocks carrying this mutation.

SHANK3 | Spectrum | Autism Research News

Saturday, July 20th, 2019

From Zhu et al. Science (’18)
Further analysis revealed that the ASD-associated genes SHANK2 and SHANK3, which encode synaptic scaffolding proteins at the postsynaptic density of excitatory glutamatergic synapses, exhibited earlier expression in the macaque NCX and other brain regions relative to humans (Fig. 7B).

time – Why is a second equal to the duration of exactly 9,192,631,770 periods of radiations? – Physics Stack Exchange

Sunday, May 26th, 2019


Ideal gas law – Wikipedia – PV=nRT

Sunday, April 14th, 2019

ROBO4 Gene – GeneCards | ROBO4 Protein | ROBO4 Antibody

Sunday, April 7th, 2019

The highly pleiotropic gene SLC39A8 as an opportunity to gain insight into the molecular pathogenesis of schizophrenia – Costas – 2018 – American Journal of Medical Genetics Part B: Neuropsychiatric Genetics – Wiley Online Library

Sunday, April 7th, 2019

assoc w. SCZ+Chron’s
protective to Parkinson’s