Ush1g (Usher syndrome 1G) - Rat Genome Database

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Keyword

Gene: Ush1g (Usher syndrome 1G) Rattus norvegicus

Symbol:

Ush1g

Name:

Usher syndrome 1G

Description:

ENCODES a protein that exhibits protein homodimerization activity (ortholog); INVOLVED IN equilibrioception (ortholog); inner ear morphogenesis (ortholog); inner ear receptor cell differentiation (ortholog); ASSOCIATED WITH Deafness (ortholog); Usher Syndrome, Type IG (ortholog); FOUND IN actin cytoskeleton (ortholog); cytoplasm (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; indole-3-methanol

Type:

protein-coding

RefSeq Status:

PROVISIONAL

Also known as:

LOC287819; Ush1g_predicted; Usher syndrome 1G; Usher syndrome 1G (autosomal recessive); Usher syndrome 1G (autosomal recessive) (predicted); Usher syndrome 1G homolog; Usher syndrome 1G homolog (human); Usher syndrome 1G homolog (human) (predicted)

Orthologs:

Homo sapiens : USH1G (Usher syndrome 1G (autosomal recessive)) HGNC
Mus musculus : Ush1g (Usher syndrome 1G) MGI

Latest Assembly:

RGSC Genome Assembly v3.4

Position:

Map	Chr	Position	Strand	Source
Rat Cytogenetic Map	10	q32.2-q32.3		NCBI
RGSC Genome Assembly v5.0	10	104,422,767 - 104,426,636	+	NCBI
RGSC Genome Assembly v3.4	10	105,395,184 - 105,399,053	-	NCBI
Rat Celera Assembly	10	99,135,313 - 99,139,182	-	NCBI
Genome Assembly 3.1	10	105,406,916 - 105,414,392	-	NCBI