IMP

Process View

Mus musculus

0 genes annotated in mouse

fundus dystrophy

DOID:8501

Loading network...

In addition to gene-name show these genes:

Known genes in the process in mouse Include functional analogs

Network Filters

Minimum relationship confidence:

Maximum number of genes:

Highlight known relationships in gold.

Graphical Options

Adjust edge length:

Adjust node size:

Fixed layout

Black background

Low confidence color:

Med confidence color:

High confidence color:

Hide the legend in the network

Save Options

Gene Predictions

Disease predictions are made from cross-annotation of human disease genes to the identified functional analogs in mouse and predicted with the mouse functional network.

Show only novel predictions Show only unknown genes Highlight genes with functional analogs involved in "fundus dystrophy" (in gray)

Name	Description	Probability
Olfr70	olfactory receptor 70	0.023
Kcnj6	potassium inwardly-rectifying channel, subfamily J, member 6	0.020
Sspo	SCO-spondin	0.018
Pou2f3	POU domain, class 2, transcription factor 3	0.018
Kcnq2	potassium voltage-gated channel, subfamily Q, member 2	0.017
Pax1	paired box gene 1	0.017
Ghrhr	growth hormone releasing hormone receptor	0.015
Tacr1	tachykinin receptor 1	0.015
Igdcc3	immunoglobulin superfamily, DCC subclass, member 3	0.013
Hoxb1	homeobox B1	0.012
Wnt1	wingless-related MMTV integration site 1	0.012
Pitx3	paired-like homeodomain transcription factor 3	0.011
Foxl1	forkhead box L1	0.011
Fshr	follicle stimulating hormone receptor	0.011
Foxh1	forkhead box H1	0.010
Tacr2	tachykinin receptor 2	0.010
Lhb	luteinizing hormone beta	0.010