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211986 Ensembl ENSG00000151353 ENSMUSG00000043061 UniProt Q96B42 Q3TUD9 RefSeq (mRNA) NM_152834 NM_001352680 NM_001352681 NM_172049 RefSeq (protein) NP_690047 NP_001339609 NP_001339610 NP_742046 Location (UCSC) Chr 2: 0.66 – 0.68 Mb Chr 12: 30.63 – 30.64 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Transmembrane protein 18 also known as TMEM18 is a protein which in humans is ...
Christ by Heinrich Hofmann, 1889, digitally edited to include a MAGA Cap.. Republican Jesus or GOP Jesus is a meme satirizing Republican socially conservative and libertarian Christians whose values appear antithetical to the Gospels, [1] a Jesus who "loves borders, guns, unborn babies, and economic prosperity and hates homosexuality, taxes, welfare, and universal healthcare", [2] and for whom ...
16p11.2 deletion syndrome is a rare genetic condition caused by microdeletion on the short arm of chromosome 16. Most affected individuals experience global developmental delay and intellectual disability, as well as childhood-onset obesity. [1] 16p11.2 deletion is estimated to account for approximately 1% of autism spectrum disorder cases. [3] [4]
The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms. This number, along with the visual appearance of the chromosome, is known as the karyotype , [ 1 ] [ 2 ] [ 3 ] and can be found by looking at the chromosomes through a microscope .
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.
Turner syndrome (TS), commonly known as 45,X, or 45,XO, [note 1] is a chromosomal disorder in which cells have only one X chromosome or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome.
Facial features (A), left hand and feet showing broad thumb and big toes (B, C) and X-ray of both hands showing short broad thumbs (D). (Limb Malformations & Skeletal Dysplasia) Rubinstein–Taybi syndrome presents itself from birth, and is usually hallmarked by delayed physical and cognitive growth. [citation needed]
A karyotype of an individual with trisomy 21, showing three copies of chromosome 21. An abnormal number of chromosomes is known as aneuploidy, and occurs when an individual is either missing a chromosome from a pair (resulting in monosomy) or has more than two chromosomes of a pair (trisomy, tetrasomy, etc.).