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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

Search Results for ‘hsa-mir-143’ Sorted by GIFtS

 
showing 1-20
675 GeneCards for hsa-mir-143   • Click + below for hit context (minicards)   • Click symbol for GeneCard

  Symbol   Description   Category   GIFtS   GC id   Score  
1 ARPC4-TTLL3 ARPC4-TTLL3 readthrough protein-coding 25  GC03P009838  -0.08 
2 KLLN killin, p53-regulated DNA replication inhibitor protein-coding 33  GC10M089619  -0.08 
3 ANKRD33B ankyrin repeat domain 33B protein-coding 34  GC05P010564  -1.40 
4 PABPC1L2B poly(A) binding protein, cytoplasmic 1-like 2B protein-coding 36  GC0XP072223  0.60 
5 TMEM167B transmembrane protein 167B protein-coding 36  GC01P109630  -0.81 
6 KIAA1211 KIAA1211 protein-coding 36  GC04P057036  -1.59 
7 PRCD progressive rod-cone degeneration protein-coding 37  GC17P074523  -0.59 
8 TMEM121 transmembrane protein 121 protein-coding 38  GC14P105992  -0.08 
9 VWC2L von Willebrand factor C domain containing protein 2-like protein-coding 38  GC02P215275  -1.40 
10 CCDC149 coiled-coil domain containing 149 protein-coding 38  GC04M024809  -1.59 
11 C1orf115 chromosome 1 open reading frame 115 protein-coding 38  GC01P220863  -0.81 
12 C7orf60 chromosome 7 open reading frame 60 protein-coding 39  GC07M112459  -1.40 
13 RGSL1 regulator of G-protein signaling like 1 protein-coding 39  GC01P182419  -1.40 
14 QSER1 glutamine and serine rich 1 protein-coding 39  GC11P032905  -1.08 
15 CECR6 cat eye syndrome chromosome region, candidate 6 protein-coding 40  GC22M017597  -0.08 
16 SMCR8 Smith-Magenis syndrome chromosome region, candidate 8 protein-coding 40  GC17P018218  -0.40 
17 PABPC1L2A poly(A) binding protein, cytoplasmic 1-like 2A protein-coding 40  GC0XM072297  0.60 
18 FADS6 fatty acid desaturase 6 protein-coding 40  GC17M072873  -0.59 
19 KCTD21 potassium channel tetramerization domain containing 21 protein-coding 40  GC11M077882  -0.40 
20 C12orf68 chromosome 12 open reading frame 68 protein-coding 40  GC12P048577  -0.40 
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Developed at the Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science

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