Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
138046
Gene name Gene Name - the full gene name approved by the HGNC.
RALY RNA binding protein like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RALYL
Synonyms (NCBI Gene) Gene synonyms aliases
HNRPCL3
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q21.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT735412 hsa-miR-483-3p Western blotting, qRT-PCR 33219048
MIRT1289317 hsa-miR-208a CLIP-seq
MIRT1289318 hsa-miR-208b CLIP-seq
MIRT1289319 hsa-miR-23a CLIP-seq
MIRT1289320 hsa-miR-23b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674
GO:0003723 Function RNA binding IBA 21873635
GO:0005515 Function Protein binding IPI 16189514, 19447967, 25416956
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
614648 27036 ENSG00000184672
Protein
UniProt ID Q86SE5
Protein name RNA-binding Raly-like protein (hRALYL) (Heterogeneous nuclear ribonucleoprotein C-like 3) (hnRNP core protein C-like 3)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00076 RRM_1 23 86 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, with highest levels in brain. {ECO:0000269|PubMed:12688537}.
Sequence
MTGKTQTSNVTNKNDPKSINSRVFIGNLNTAIVKKVDIEAIFSKYGKIVGCSVHKGYAFV
QYMSERHARAAVAGENARVIAGQPLD
INMAGEPKPYRPKPGNKRPLSALYRLESKEPFLS
VGGYVFDYDYYRDDFYNRLFDYHGRVPPPPRAVIPLKRPRVAVTTTRRGKGVFSMKGGSR
STASGSTGSKLKSDELQTIKKELTQIKTKIDSLLGRLEKIEKQQKAEAEAQKKQLEESLV
LIQEECVSEIADHSTEEPAEGGPDADGEEMTDGIEEDFDEDGGHELFLQIK
Sequence length 291
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
21466612
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
21466612
Marfan syndrome Mammary Carcinoma, Human rs137854456, rs137854457, rs267606796, rs137854458, rs137854459, rs137854460, rs137854470, rs137854471, rs267606797, rs137854461, rs137854462, rs137854463, rs869025419, rs137854464, rs137854465
View all (942 more)
21466612
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 33298176, 40631452
Atrial Fibrillation Associate 37960721
Carcinoma Hepatocellular Associate 35765089
Carcinoma Renal Cell Associate 22994768
Colorectal Neoplasms Associate 35065650
Metabolic Syndrome Associate 26507551
Neoplasms Associate 22994768
Ovarian Neoplasms Inhibit 33437214
Small Cell Lung Carcinoma Associate 37399175