Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
414152
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 10 open reading frame 105
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C10orf105
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT025760 hsa-miR-7-5p Microarray 17612493
MIRT716353 hsa-miR-5007-5p HITS-CLIP 19536157
MIRT716352 hsa-miR-520g-5p HITS-CLIP 19536157
MIRT716351 hsa-miR-432-5p HITS-CLIP 19536157
MIRT716350 hsa-miR-539-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q8TEF2
Protein name Uncharacterized protein C10orf105
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17665 DUF5527 1 133 Family of unknown function (DUF5527) Family
Sequence
Sequence length 133
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Deafness Deafness, Autosomal Recessive 12 rs267607135, rs387906219, rs387906220, rs387906221, rs387906222, rs606231120, rs267606855, rs121918370, rs137853185, rs137853186, rs137853187, rs137853188, rs587776522, rs587776523, rs200781822
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Multiple congenital anomalies Multiple congenital anomalies rs1057517732 11138009, 11090341
Pituitary adenoma PITUITARY ADENOMA 5, MULTIPLE TYPES rs5030861, rs104894194, rs121908356, rs121908347, rs727502931, rs121908348, rs121908349, rs111033271, rs121908351, rs121917839, rs121917840, rs587776681, rs193922688, rs121917841, rs587776682
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Usher syndrome USHER SYNDROME, TYPE ID rs80338903, rs397518008, rs111033367, rs121912598, rs121912599, rs80338902, rs111033364, rs111033272, rs121912600, rs587776538, rs111033334, rs137852839, rs137852840, rs2133130286, rs104894651
View all (734 more)