Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54980
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 2 open reading frame 42
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C2orf42
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p13.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027207 hsa-miR-103a-3p Sequencing 20371350
MIRT032004 hsa-miR-16-5p Sequencing 20371350
MIRT728101 hsa-miR-15a-5p HITS-CLIP 22473208
MIRT728100 hsa-miR-15b-5p HITS-CLIP 22473208
MIRT032004 hsa-miR-16-5p HITS-CLIP 22473208
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0005654 Component Nucleoplasm IDA
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 Q9NWW7
Protein name Uncharacterized protein C2orf42
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14952 zf-tcix 16 57 Putative treble-clef, zinc-finger, Zn-binding Domain
Sequence
MEPNSLRTKVPAFLSDLGKATLRGIRKCPRCGTYNGTRGLSCKNKTCGTIFRYGARKQPS
VEAVKIITGSDLQVYSVRQRDRGPDYRCFVELGVSETTIQTVDGTIITQLSSGRCYVPSC
LKAATQGVVENQCQHIKLAVNCQAEATPLTLKSSVLNAMQASPETKQTIWQLATEPTGPL
VQRITKNILVVKCKASQKHSLGYLHTSFVQKVSGKSLPERRFFCSCQTLKSHKSNASKDE
TAQRCIHFFACICAFASDETLAQEFSDFLNFDSSGLKEIIVPQLGCHSESTVSACESTAS
KSKKRRKDEVSGAQMNSSLLPQDAVSSNLRKSGLKKPVVASSLKRQACGQLLDEAQVTLS
FQDWLASVTERIHQTMHYQFDGKPEPLVFHIPQSFFDALQQRISIGSAKKRLPNSTTAFV
RKDALPLGTFSKYTWHITNILQVKQILDTPEMPLEITRSFIQNRDGTYELFKCPKVEVES
IAETYGRIEKQPVLRPLELKTFLKVGNTSPDQKEPTPFIIEWIPDILPQSKIGELRIKFE
YGHHRNGHVAEYQDQRPPLDQPLELAPLTTITFP
Sequence length 574
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Welander distal myopathy Welander Distal Myopathy rs747068278 23401021, 10482271, 27282841, 28817800, 23348830
Unknown
Disease term Disease name Evidence References Source
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Endometrial Neoplasms Associate 35880269