G2D: Candidate Genes to Inherited Diseases
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Welcome to the G2D web server (version 5.0). Here you can use our algorithms to scan a human genomic region for genes related to an inherited disease.

Candidate priorities are automatically established by data mining algorithms that evaluate genes in the chromosomal region where the disease is mapped, and prioritize them for a possible relation to the disease based on the phenotype of the disorder or their similarity to an already known related gene. If the phenotype have been linked to more than one locus, known or inferred interactions between proteins from two loci can be also examined. To know more about g2d.

PHENOTYPE KNOWN GENES INTERACTIONS

PHENOTYPE BOX

Type one MIM number defining the disease picked from this list (e.g. 131244)


LOCUS BOX

Type a locus and select format
and chromosome (maximum 100 Mb)

format:
chromosome:

Band(s) e.g. q13.2

Marker(s) e.g. D9S201 D9S298

Positions e.g. 63950000 73950000