Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
92129
Gene name Gene Name - the full gene name approved by the HGNC.
Ripply transcriptional repressor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RIPPLY1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein similar to a zebrafish protein which acts as a transcriptional repressor in and is required for somite segmentation in zebrafish embryos (PMID: 16326386). Multiple transcript variants encoding different isoforms have been found
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1307649 hsa-miR-1237 CLIP-seq
MIRT1307650 hsa-miR-1248 CLIP-seq
MIRT1307651 hsa-miR-4777-5p CLIP-seq
MIRT1307652 hsa-miR-518d-5p CLIP-seq
MIRT1307653 hsa-miR-519b-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IBA 21873635
GO:0001757 Process Somite specification ISS
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300575 25117 ENSG00000147223
Protein
UniProt ID Q0D2K3
Protein name Protein ripply1
Protein function Plays a role in somitogenesis. Essential for transcriptional repression of the segmental patterning genes, thus terminating the segmentation program in the presomitic mesoderm, and also required for the maintenance of rostrocaudal polarity in so
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14998 Ripply 56 140 Transcription Regulator Family
Sequence
MDSAACAAAATPVPALALALAPDLAQAPLALPGLLSPSCLLSSGQEVNGSERGTCLWRPW
LSSTNDSPRQMRKLVDLAAGGATAAEVTKAESKFHHPVRLFWPKSRSFDYLYSAGEILLQ
NFPVQATINLYEDSDSEEEE
EDEEQEDEEEK
Sequence length 151
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Pancreatitis Pancreatitis 23143602 ClinVar
Mental retardation cerebellar ataxia, intellectual disability, and dysequilibrium GenCC
Associations from Text Mining
Disease Name Relationship Type References
Scoliosis Associate 32815649