Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55684
Gene name Gene Name - the full gene name approved by the HGNC.
RAB, member RAS oncogene family like 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RABL6
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf86, PARF, RBEL1, pp8875
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q34.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the Ras superfamily of small GTPases. The encoded protein binds to both GTP and GDP and may play a role in cell growth and survival. Overexpression of this gene may play a role in breast cancer tumorigenesis, and pseudogenes
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT051536 hsa-let-7e-5p CLASH 23622248
MIRT051536 hsa-let-7e-5p CLASH 23622248
MIRT047585 hsa-miR-10a-5p CLASH 23622248
MIRT046592 hsa-miR-222-3p CLASH 23622248
MIRT045800 hsa-miR-191-5p CLASH 23622248
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 12646258, 12970870, 16189514
GO:0005525 Function GTP binding IBA 21873635
GO:0005525 Function GTP binding IDA 17962191
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus IDA 17962191
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610615 24703 ENSG00000196642
Protein
UniProt ID Q3YEC7
Protein name Rab-like protein 6 (GTP-binding protein Parf) (Partner of ARF) (Rab-like protein 1) (RBEL1)
Protein function May enhance cellular proliferation. May reduce growth inhibitory activity of CDKN2A.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08477 Roc 45 111 Domain
Sequence
MFSALKKLVGSDQAPGRDKNIPAGLQSMNQALQRRFAKGVQYNMKIVIRGDRNTGKTALW
HRLQGRPFVEEYIPTQEIQVTSIHWSYKTTDDIVKVEVWDVVDKGKCKKRG
DGLKMENDP
QEAESEMALDAEFLDVYKNCNGVVMMFDITKQWTFNYILRELPKVPTHVPVCVLGNYRDM
GEHRVILPDDVRDFIDNLDRPPGSSYFRYAESSMKNSFGLKYLHKFFNIPFLQLQRETLL
RQLETNQLDMDATLEELSVQQETEDQNYGIFLEMMEARSRGHASPLAANGQSPSPGSQSP
VVPAGAVSTGSSSPGTPQPAPQLPLNAAPPSSVPPVPPSEALPPPACPSAPAPRRSIISR
LFGTSPATEAAPPPPEPVPAAEGPATVQSVEDFVPDDRLDRSFLEDTTPARDEKKVGAKA
AQQDSDSDGEALGGNPMVAGFQDDVDLEDQPRGSPPLPAGPVPSQDITLSSEEEAEVAAP
TKGPAPAPQQCSEPETKWSSIPASKPRRGTAPTRTAAPPWPGGVSVRTGPEKRSSTRPPA
EMEPGKGEQASSSESDPEGPIAAQMLSFVMDDPDFESEGSDTQRRADDFPVRDDPSDVTD
EDEGPAEPPPPPKLPLPAFRLKNDSDLFGLGLEEAGPKESSEEGKEGKTPSKEKKKKKKK
GKEEEEKAAKKKSKHKKSKDKEEGKEERRRRQQRPPRSRERTAADELEAFLGGGAPGGRH
PGGGDYEEL
Sequence length 729
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Mental retardation Profound Mental Retardation, Mental deficiency, Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
21937992
Unknown
Disease term Disease name Evidence References Source
Neurodevelopmental Disorders neurodevelopmental disorder GenCC
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 17962191
Colorectal Neoplasms Associate 34262080
Esophageal Squamous Cell Carcinoma Associate 32600359
Neoplasms Associate 32600359
Polycystic Ovary Syndrome Stimulate 38243290