Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26010
Gene name Gene Name - the full gene name approved by the HGNC.
Spermatogenesis associated serine rich 2 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SPATS2L
Synonyms (NCBI Gene) Gene synonyms aliases
DNAPTP6, SGNP
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q33.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004812 hsa-miR-21-5p Quantitative proteomic approach 19253296
MIRT021247 hsa-miR-146a-5p Microarray 18057241
MIRT027221 hsa-miR-103a-3p Sequencing 20371350
MIRT666141 hsa-miR-548ae-3p HITS-CLIP 23824327
MIRT666140 hsa-miR-548ah-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:0003723 Function RNA binding HDA 22658674, 22681889
GO:0005654 Component Nucleoplasm IDA
GO:0005730 Component Nucleolus IDA
GO:0005737 Component Cytoplasm IBA 21873635
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
613817 24574 ENSG00000196141
Protein
UniProt ID Q9NUQ6
Protein name SPATS2-like protein (DNA polymerase-transactivated protein 6) (Stress granule and nucleolar protein) (SGNP)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07139 DUF1387 59 368 Protein of unknown function (DUF1387) Family
Sequence
MAELNTHVNVKEKIYAVRSVVPNKSNNEIVLVLQQFDFNVDKAVQAFVDGSAIQVLKEWN
MTGKKKNNKRKRSKSKQHQGNKDAKDKVERPEAGPLQPQPPQIQNGPMNGCEKDSSSTDS
ANEKPALIPREKKISILEEPSKALRGVTEGNRLLQQKLSLDGNPKPIHGTTERSDGLQWS
AEQPCNPSKPKAKTSPVKSNTPAAHLEIKPDELAKKRGPNIEKSVKDLQRCTVSLTRYRV
MIKEEVDSSVKKIKAAFAELHNCIIDKEVSLMAEMDKVKEEAMEILTARQKKAEELKRLT
DLASQMAEMQLAELRAEIKHFVSERKYDEELGKAARFSCDIEQLKAQIMLCGEITHPKNN
YSSRTPCS
SLLPLLNAHAATSGKQSNFSRKSSTHNKPSEGKAANPKMVSSLPSTADPSHQ
TMPANKQNGSSNQRRRFNPQYHNNRLNGPAKSQGSGNEAEPLGKGNSRHEHRRQPHNGFR
PKNKGGAKNQEASLGMKTPEAPAHSEKPRRRQHAADTSEARPFRGSVGRVSQCNLCPTRI
EVSTDAAVLSVPAVTLVA
Sequence length 558
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
29892015, 30061737
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
28991256, 30285260
Unknown
Disease term Disease name Evidence References Source
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation 30061737, 29892015 ClinVar
Pelvic Organ Prolapse Pelvic Organ Prolapse GWAS
Atrial Fibrillation Atrial Fibrillation GWAS
Bipolar Disorder Bipolar Disorder GWAS
Associations from Text Mining
Disease Name Relationship Type References
Abdominal Pain Associate 25358868
Diabetes Mellitus Associate 35320353
Lupus Erythematosus Systemic Associate 36405750
Pain Associate 25358868
Philadelphia Chromosome Associate 37819686
Precursor Cell Lymphoblastic Leukemia Lymphoma Associate 37819686
Psoriasis Stimulate 24267790
Respiratory Distress Syndrome Associate 30665420
Sleep Wake Disorders Associate 25358868
Squamous Cell Carcinoma of Head and Neck Associate 34974809