Fine module 74 - -


Module's content:

Genes:

SYMBOLTITLEMINMAXNCBI human gene summary
2610002M06RIKRIKEN cDNA 2610002M06 gene5.688.96NCBI mm gene  
2810422O20RIKRIKEN cDNA 2810422O20 gene4.867.43NCBI mm gene  
3110001D03RIKRIKEN cDNA 3110001D03 gene6.039.31NCBI mm gene  
5730469M10RIKRIKEN cDNA 5730469M10 gene5.5810.04NCBI mm gene  
ALDOAaldolase A, fructose-bisphosphate8.8912.72NCBI mm gene  Summary: This gene product, Aldolase A (fructose-bisphosphate aldolase) is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants which encode the same protein. [provided by RefSeq].
B3GNT2UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 26.5711.11NCBI mm gene  
CCDC109Acoiled-coil domain containing 109A5.559.49NCBI mm gene  
CCDC125coiled-coil domain containing 1255.0110.33NCBI mm gene  
ERO1LERO1-like (S. cerevisiae)7.1710.85NCBI mm gene  
FBXO9f-box protein 96.358.96NCBI mm gene  
HCFC2host cell factor C26.019.21NCBI mm gene  
HRSP12heat-responsive protein 124.878.90NCBI mm gene  
ICAM2intercellular adhesion molecule 26.0011.24NCBI mm gene  
KLHDC2kelch domain containing 25.289.55NCBI mm gene  
KLHL12kelch-like 12 (Drosophila)4.818.69NCBI mm gene  
PGM1phosphoglucomutase 17.019.89NCBI mm gene  
PGM2phosphoglucomutase 26.609.50NCBI mm gene  Summary: The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.
RABIFRAB interacting factor6.869.52NCBI mm gene  
RDH14retinol dehydrogenase 14 (all-trans and 9-cis)4.326.49NCBI mm gene  
TEX2testis expressed gene 26.1811.49NCBI mm gene  
TMEM60transmembrane protein 605.617.73NCBI mm gene  
TMX4thioredoxin-related transmembrane protein 47.0710.49NCBI mm gene  
TSPAN5tetraspanin 55.629.78NCBI mm gene  
TTLL1tubulin tyrosine ligase-like 15.888.39NCBI mm gene