Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84138
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 7 member 6 opposite strand
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC7A6OS
Synonyms (NCBI Gene) Gene synonyms aliases
EPM12, Iwr1
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT664723 hsa-miR-6887-3p HITS-CLIP 23824327
MIRT664722 hsa-miR-4780 HITS-CLIP 23824327
MIRT664721 hsa-miR-6780b-3p HITS-CLIP 23824327
MIRT664720 hsa-miR-4287 HITS-CLIP 23824327
MIRT664719 hsa-miR-4685-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002244 Process Hematopoietic progenitor cell differentiation IEA
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IEA
GO:0015031 Process Protein transport IEA
GO:0032502 Process Developmental process IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619192 25807 ENSG00000103061
Protein
UniProt ID Q96CW6
Protein name Probable RNA polymerase II nuclear localization protein SLC7A6OS (ADAMS proteinase-related protein) (Solute carrier family 7 member 6 opposite strand transcript)
Protein function Directs RNA polymerase II nuclear import.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08574 Iwr1 194 257 Transcription factor Iwr1 Family
Sequence
MEAARTAVLRVKRKRSAEPAEALVLACKRLRSDAVESAAQKTSEGLERAAENNVFHLVAT
VCSQEEPVQPLLREVLRPSRDSQQRVRRNLRASAREVRQEGRYRVLSSRRSLGTTSSGQE
SEYTPGNPEAAGNSGFQLLDLVHEEGEPEAASAGSCKTSDPDVILCNSVELIRERLTVSE
DGPGVRRQEEQKHDDYVYDIYYLETATPGWIENILSVQPYSQEWELVNDDQEPEDIYDDE
DDENSENNWRNEYPEEE
SSDGDEDSRGSADYNSLSEEERGSSRQRMWSKYPLDVQKEFGY
DSPHDLDSD
Sequence length 309
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Epilepsy epilepsy, progressive myoclonic, 12, epilepsy N/A N/A GenCC
Schizophrenia Schizophrenia N/A N/A GWAS