Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
92689
Gene name Gene Name - the full gene name approved by the HGNC.
Family with sequence similarity 114 member A1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM114A1
Synonyms (NCBI Gene) Gene synonyms aliases
Noxp20
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p14
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the FAM114 family and may play a role in neuronal cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017402 hsa-miR-335-5p Microarray 18185580
MIRT717821 hsa-miR-519a-3p HITS-CLIP 19536157
MIRT717820 hsa-miR-519b-3p HITS-CLIP 19536157
MIRT717819 hsa-miR-519c-3p HITS-CLIP 19536157
MIRT717818 hsa-miR-302a-3p 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:0005515 Function Protein binding IPI 25416956, 31515488, 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005794 Component Golgi apparatus IDA
GO:0005829 Component Cytosol 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 Q8IWE2
Protein name Protein NOXP20 (Nervous system overexpressed protein 20) (Protein FAM114A1)
Protein function May play a role in neuronal cell development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05334 DUF719 125 299 Protein of unknown function (DUF719) Family
Sequence
MSDDAGDTLATGDKAEVTEMPNSDSLPEDAEVHCDSAAVSHEPTPADPRGEGHENAAVQG
AGAAAIGPPVQPQDANALEPPLNGDVTEDTLAECIDSVSLEAEPRSEIPLQEQNYLAVDS
PPSGGGWAGWGSWGKSLLSSASATVGHGLTAVKEKAGATLRIHGVNSGSSEGAQPNTENG
VPEITDAATDQGPAESPPTSPSSASRGMLSAITNVVQNTGKSVLTGGLDALEFIGKKTMN
VLAESDPGFKRTKTLMERTVSLSQMLREAKEKEKQRLAQQLTMERTAHYGMLFDEYQGL
S
HLEALEILSNESESKVQSFLASLDGEKLELLKNDLISIKDIFAAKELENEENQEEQGLEE
KGEEFARMLTELLFELHVAATPDKLNKAMKRAHDWVEEDQTVVSVDVAKVSEEETKKEEK
EEKSQDPQEDKKEEKKTKTIEEVYMSSIESLAEVTARCIEQLHKVAELILHGQEEEKPAQ
DQAKVLIKLTTAMCNEVASLSKKFTNSLTTVGSNKKAEVLNPMISSVLLEGCNSTTYIQD
AFQLLLPVLQVSHIQTSCLKAQP
Sequence length 563
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Coronary heart disease Coronary heart disease 28753643 ClinVar
Coronary syndrome Acute Coronary Syndrome 28753643 ClinVar
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 35441810
Enteritis Associate 34837888
Lesch Nyhan Syndrome Stimulate 34837888
N syndrome Stimulate 34837888
Prostatic Neoplasms Associate 32800727
Spondylitis Ankylosing Associate 34837888
Vitiligo Associate 34837888