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Rabbit Anti-FUNDC2 antibody
FUNDC2 is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. 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. 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.
Function:
The function of FUNDC2 (FUN14 domain-containing protein 2) is unknown.
Subcellular Location:
Mitochondrial
Similarity:
Belongs to the FUN14 family.
SWISS:
Q9BWH2
Gene ID:
65991
Database links:
Entrez Gene: 65991 Human
Entrez Gene: 67391 Mouse
SwissProt: Q9BWH2 Human
SwissProt: Q9D6K8 Mouse
Unigene: 356050 Human
Unigene: 121284 Mouse
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