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Rabbit Anti-MOSPD1 antibody
MOSPD1 is a 213 amino acid multi-pass membrane protein that contains one MSP domain and exists as three alternatively spliced isoforms. The gene encoding MOSPD1 maps to human chromosome Xq26.3. 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 unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and 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
Subcellular Location:
Membrane.
Similarity:
Contains 1 MSP domain.
SWISS:
Q9UJG1
Gene ID:
5636
Database links:
Entrez Gene: 5636 Human
Entrez Gene: 70380 Mouse
Entrez Gene: 317312 Rat
Omim: 300674 Human
SwissProt: Q9UJG1 Human
SwissProt: Q8VEL0 Mouse
SwissProt: Q5RJS6 Rat
Unigene: 726077 Human
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