MEIG1 is an 88 amino acid protein that is thought to function in germ cell differentiation and belongs to the MEIG1 family. The gene encoding MEIG1 maps to human chromosome 10p13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Function:
May be involved in germ cell differentiation.
Similarity:
Belongs to the MEIG1 family.
SWISS:
Q5JSS6
Gene ID:
644890
Database links:
Entrez Gene: 644890 Human
Omim: 614174 Human
SwissProt: Q5JSS6 Human
Unigene: 257249 Human
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