Nov 10, 2025 · The knowledgebase automatically integrates gene-centric data from ~200 web sources, including genomic, transcriptomic, proteomic, genetic, clinical and functional information.

Nov 14, 2025 · This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters.

Nov 13, 2025 · This gene, a Kirsten ras oncogene homolog from the mammalian ras gene family, encodes a protein that is a member of the small GTPase superfamily. A single amino acid …

Nov 13, 2025 · HBB (Hemoglobin Subunit Beta) is a Protein Coding gene. Diseases associated with HBB include Sickle Cell Disease and Beta-Thalassemia, Dominant Inclusion Body Type.

Nov 14, 2025 · This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, …

Nov 13, 2025 · This gene is a member of the immunoglobulin superfamily and encodes a protein which transmits an inhibitory signal to T cells. The protein contains a V domain, a transmembrane domain, …

Nov 13, 2025 · Complete information for CXCL12 gene (Protein Coding), C-X-C Motif Chemokine Ligand 12, including: function, proteins, disorders, pathways, orthologs, and expression.

Nov 14, 2025 · This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis-determining factor (TDF), …

Nov 14, 2025 · SIM1 (SIM BHLH Transcription Factor 1) is a Protein Coding gene. Diseases associated with SIM1 include Obesity Due To Sim1 Deficiency and Sim1-Related Prader-Willi-Like Syndrome.

Nov 13, 2025 · A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants …