IMP
Process View
positive regulation of dipeptide transport
Any process that activates or increases the frequency, rate or extent of dipeptide transport.
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In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "positive regulation of dipeptide transport"
| Name | Description | Probability | Func Analog Organism | |
|---|---|---|---|---|
| Ush1g | Usher syndrome 1G homolog (human) | 0.693 | ||
| Cdh23 | cadherin 23 (otocadherin) | 0.400 | ||
| LOC100503041 | PDZ domain-containing protein 7-like | 0.352 | ||
| Thrb | thyroid hormone receptor beta | 0.268 | ||
| Tmc1 | transmembrane channel-like gene family 1 | 0.124 | ||
| Espn | espin | 0.088 | ||
| Myo7a | myosin VIIA | 0.060 | ||
| Myo15 | myosin XV | 0.058 | ||
| Clrn1 | clarin 1 | 0.055 | ||
| Kcne1 | potassium voltage-gated channel, Isk-related subfamily, member 1 | 0.053 | ||
| Slc4a4 | solute carrier family 4 (anion exchanger), member 4 | 0.044 | ||
| Ush1c | Usher syndrome 1C homolog (human) | 0.041 | ||
| Atp2b2 | ATPase, Ca++ transporting, plasma membrane 2 | 0.038 | ||
| Tecta | tectorin alpha | 0.036 | ||
| Srrm4 | serine/arginine repetitive matrix 4 | 0.030 | ||
| Pcdh15 | protocadherin 15 | 0.030 | ||
| Cdkn2d | cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4) | 0.029 | ||
| Myo6 | myosin VI | 0.027 | ||
| Gjb6 | gap junction protein, beta 6 | 0.026 | ||
| Grxcr1 | glutaredoxin, cysteine rich 1 | 0.024 | ||
| St14 | suppression of tumorigenicity 14 (colon carcinoma) | 0.022 | ||
| Tmprss3 | transmembrane protease, serine 3 | 0.020 | ||
| Ceacam16 | carcinoembryonic antigen-related cell adhesion molecule 16 | 0.020 | ||
| Gpr98 | G protein-coupled receptor 98 | 0.018 | ||
| Chd7 | chromodomain helicase DNA binding protein 7 | 0.017 | ||
| Kcnq1 | potassium voltage-gated channel, subfamily Q, member 1 | 0.015 | ||
| Foxi1 | forkhead box I1 | 0.012 | ||
| Neurod1 | neurogenic differentiation 1 | 0.012 | ||
| Otos | otospiralin | 0.011 | ||
| Kcnj10 | potassium inwardly-rectifying channel, subfamily J, member 10 | 0.011 | ||
| Bsnd | Bartter syndrome, infantile, with sensorineural deafness (Barttin) | 0.011 | ||
| Slc4a1 | solute carrier family 4 (anion exchanger), member 1 | 0.011 |