Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	100130311
Gene name Gene Name - the full gene name approved by the HGNC.	Chromosome 17 open reading frame 107
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	C17orf107
Synonyms (NCBI Gene) Gene synonyms aliases	-
Chromosome Chromosome number	17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	17p13.2

Show/Hide all(27)

miRTarBase ID	miRNA	Experiments
MIRT835971	hsa-miR-1275	CLIP-seq
MIRT835972	hsa-miR-2277-3p	CLIP-seq
MIRT835973	hsa-miR-24	CLIP-seq
MIRT835974	hsa-miR-3660	CLIP-seq
MIRT835975	hsa-miR-4313	CLIP-seq
MIRT835976	hsa-miR-4525	CLIP-seq
MIRT835977	hsa-miR-4526	CLIP-seq
MIRT835978	hsa-miR-4665-5p	CLIP-seq
MIRT835979	hsa-miR-4723-5p	CLIP-seq
MIRT835980	hsa-miR-625	CLIP-seq
MIRT835981	hsa-miR-635	CLIP-seq
MIRT1947682	hsa-miR-3943	CLIP-seq
MIRT1947683	hsa-miR-4435	CLIP-seq
MIRT1947684	hsa-miR-4455	CLIP-seq
MIRT1947685	hsa-miR-4787-5p	CLIP-seq
MIRT1947686	hsa-miR-644	CLIP-seq
MIRT1947687	hsa-miR-663b	CLIP-seq
MIRT2185661	hsa-miR-1293	CLIP-seq
MIRT2185662	hsa-miR-3622a-5p	CLIP-seq
MIRT2185663	hsa-miR-4423-3p	CLIP-seq
MIRT2185664	hsa-miR-4483	CLIP-seq
MIRT2185665	hsa-miR-4648	CLIP-seq
MIRT2185666	hsa-miR-4651	CLIP-seq
MIRT2185667	hsa-miR-4755-3p	CLIP-seq
MIRT2185668	hsa-miR-541	CLIP-seq
MIRT2185669	hsa-miR-608	CLIP-seq
MIRT2185670	hsa-miR-654-5p	CLIP-seq

MIM	HGNC	e!Ensembl
HGNC	N/A	HGNC

Protein

UniProt ID

Q6ZR85

Protein name

Uncharacterized protein C17orf107

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF17688	DUF5536	1 → 186	Family of unknown function (DUF5536)	Family

Sequence

MKGTPSSLDTLMWIYHFHSSTEVALQPPLLSSLELSVAAAHEYLEQRFRELKSLEPPEPK
MQGMLPAPKPTLGLVLREATASLVSFGTTLLEISALWLQQEARRLDGSAGPAPDGRDPGA
ALSRVAQAAGQGVRQAGAAVGASARLLVQGAWLCLCGRGLQGSASFLRQSQQQLGLGIPG
EPVSSGHGVS

Sequence length

190

Interactions

View interactions

Show/Hide Causal Diseases (1)

Disease term	Disease name	dbSNP ID	References
Causal
Myasthenic syndrome	Myasthenic Syndromes, Congenital, MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL, MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL, MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL	rs606231128, rs606231129, rs606231130, rs606231131, rs606231132, rs118203994, rs118203995, rs863223277, rs606231133, rs121908547, rs121908553, rs121908557, rs104893733, rs104893734, rs121908922 View all (237 more)	20562457, 9708546, 21150643, 29054425, 29383513, 9158150, 27717316, 22678886, 7538206, 21822932, 8755487, 14592868, 27779167, 8872460

C17orf107 (chromosome 17 open reading frame 107)