Gene name: SMIM14 (HGNC Symbol) Synonyms: C4orf34, FLJ13289: Description: Small integral membrane protein 14 (HGNC Symbol) Chromosome: 4: Cytoband: p14: Chromosome location (bp) 39546330 - 39639090: Number of transcripts i

cell lines with high or low copy number of SMIM14 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. CTD Gene-Chemical Interactions chemicals interacting with SMIM14 gene/protein from the curated CTD Gene-Chemical Interactions dataset.

Additional gene information for SMIM14 Gene HGNC (27321) small integral membrane protein 14 GeneRIFs: Gene References Into Functions hC4orf34 is an endoplasmic reticulum-resident type I transmembrane protein. The SMIM14 gene is located on the minus strand at cytogenetic band 4p14 and is 92,567 base pairs in length. The gene has five exons, four of which constitute the open-reading frame for SMIM14. The Kozak sequence, which functions as the protein translation initiation site in most eukaryotic mRNA transcripts, is considered a strong motif.

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C4orf34, FLJ13289 small integral membrane protein 14 Entrez Gene | BioGRID | HGNC | Alliance of Genome Resources | VEGA | Ensembl | RefSeq | GenBank | Uniprot . SMIM14 participant CRISPR screens (3 hits / 957 screens) Download Results . Filter Reset . C4orf34 (SMIM14) Human Recombinant Protein JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser. HUGO Gene Nomenclature Committee (HGNC) approved gene symbol report Toggle navigation Menu Try our new and improved search & tell us what you think : Take me there The dysregulated genes were mainly involved in metabolic and biosynthetic processes. We constructed a potential miRNA-gene regulatory network from the differentially expressed genes PCK2, HMGCS1, and SMIM14 and downregulation of two genes, BATF3 and WFDC2 were confirmed.

[3] SMIM14 Gene, Drug Resistance, Tissue Distribution, Mutation Distribution, Variants, SMIM14 Genome Browser, SMIM14 References SMIM14 - Explore an overview of SMIM14, with a histogram displaying coding mutations, full tabulated details of all associated variants, tissue distribution and any drug resistance data. Gene name: SMIM14 (HGNC Symbol) Synonyms: C4orf34, FLJ13289: Description: Small integral membrane protein 14 (HGNC Symbol) Chromosome: 4: Cytoband: p14: Chromosome location (bp) 39546330 - 39639090: Number of transcripts i SMIM14 - Small integral membrane protein 14 - Homo sapiens (Human) - SMIM14 gene & protein UniProtKB - Q96QK8 (SIM14_HUMAN) Gene information about ENSG00000163683 / SMIM14 - small integral membrane protein 14 Gene information about ENSG00000163683 / SMIM14 - small integral membrane protein 14 We use cookies to enhance the usability of our website.

Detailed information about SMIM14 gene function, sequence, synonyms and expression tissues.

Detailed information about SMIM14 gene function, sequence, synonyms and expression tissues. MOCS3 (Molybdenum Cofactor Synthesis 3) is a Protein Coding gene. Diseases associated with MOCS3 include Molybdenum Cofactor Deficiency and Molybdenum Cofactor Deficiency, Complementation Group C.Among its related pathways are Metabolism of water-soluble vitamins and cofactors and Sulfur relay system.Gene Ontology (GO) annotations related to this gene include nucleotidyltransferase activity Human Gene SMIM14 (uc003guo.3) Description and Page Index Description: Homo sapiens small integral membrane protein 14 (SMIM14), mRNA. Transcript (Including UTRs) Complete information for SMIM14 gene (protein-coding), small integral membrane protein 14, including: function, proteins, disorders, pathways, orthologs, and expression.

Products listing by gene. By Gene. Search Genes By Alphabetical Order: 0 1 2 3 4 5 6 7 8 9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. 1 

KLRG1. TNFSF4. ENTPD1. DHRS3. Nov 19, 2019 Background: Myocardial ischemia-reperfusion injury always happened after Off- pump coronary artery bypass graft(OPCABG), and this can not  Nov 20, 2018 Genes such as MALAT1, H19, and MIR29C – whose links to hepatotoxicity Furthermore, genes such as Smim14 and Thyn1 were included in  SMG9 · SMIM1 · SMIM10 · SMIM10L1 · SMIM11A · SMIM11B · SMIM12 · SMIM13 · SMIM14 · SMIM15 · SMIM18 · SMIM19 · SMIM2 · SMIM20 · SMIM22 · Therefore, we consider FCRLA, SMIM14, CD22, FCER2 and LINC00926 for further biological interpretation.

Please select a position: Gencode Genes SMIM14 (ENST00000295958.10) at chr4:39546336-39638865 - Homo sapiens small integral membrane protein 14 (SMIM14), transcript variant 2, mRNA. (from RefSeq NM_174921) SMIM14 (ENST00000630374.1) at chr4:39547836-39549812 - small integral membrane protein 14 (from HGNC SMIM14) SMIM14 … Rank scores of expression calls are normalized across genes, conditions and species. Low score means that the gene is highly expressed in the condition. Max rank score in all spec Results for query: SMIM14. Gene-Specific Resources.
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Diseases associated with SMIM14 include Mitochondrial Complex Iii Deficiency and  Up- or down- regulated genes only in 4-1BBpos PD-1high CD39+ CD8. TILs compared to PD-1+ CD39-.

If you continue, we'll assume that you are happy to receive all cookies. Gene. Small integral membrane protein 15 (SMIM15) is a protein in humans that is encoded by the SMIM15 gene.
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Homo sapiens (human): 201895: Help: Entry: 201895 CDS T01001

Choose parameters to search by Term: Qualifier: Evidence: With: Reference: Notes: Source: Original Reference(s) 1,2-dimethylhydrazine : multiple interactions: ISO: RGD:1322412: 6480464 [1, 2 Fusion gene INTS6--SMIM14 is not found in the list of known false positive fusion genes.