The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM104B gene product has been provisionally designated FAM104B pending further characterization.
Similarity:
Belongs to the FAM104 family.
SWISS:
Q5XKR9
Gene ID:
90268
Database links:
Entrez Gene: 90268 Human
Entrez Gene: 432940 Mouse
Entrez Gene: 100362554 Rat
SwissProt: Q96BN8 Human
SwissProt: Q3UCV8 Mouse
Unigene: 406335 Human
Unigene: 309164 Mouse
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Sample: PSLC3 Cell (Human) Lysate at 40 ug
Primary: Anti-FAM104B (SL8231R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 13 kD
Observed band size: 13 kD
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