LURAP1L (leucine rich adaptor protein 1 like)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
286343
Gene name Gene Name - the full gene name approved by the HGNC.
Leucine rich adaptor protein 1 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LURAP1L
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf150, HYST0841, LRAP35b, bA3L8.2
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9p23
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(43)
miRTarBase ID miRNA Experiments Reference
MIRT017481 hsa-miR-335-5p Microarray 18185580
MIRT556389 hsa-miR-381-3p PAR-CLIP 21572407
MIRT556388 hsa-miR-300 PAR-CLIP 21572407
MIRT556387 hsa-miR-424-5p PAR-CLIP 21572407
MIRT556386 hsa-miR-15b-5p PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(2)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0043123 Process Positive regulation of I-kappaB kinase/NF-kappaB signaling IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
616130 31452 ENSG00000153714
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q8IV03
Protein name Leucine rich adaptor protein 1-like
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14854 LURAP 80 → 196 Leucine rich adaptor protein Family
Sequence 
MEDSPLPDLRDIELKLGRKVPESLVRSLRGEEPVPRERDRDPCGGSGGGGGGGGGGGGCS
SSSSYCSFPPSLSSSSSSSPTSGSPRGSHSSALERLETKLHLLRQEMVNLRATDVRLMRQ
LLVINESIESIKWMIEEKATITSRGSSLSGSLCSLLESQSTSLRGSYNSLHDGSDGLDGI
SVGSYLDTLADDVPGHQTPSDLDQFSDSSLIEDSQALHKRPKLDSEYYCFG
Sequence length 231
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Causal Diseases (5)
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 26301688
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs869025224 26301688
Common variable immunodeficiency Common Variable Immunodeficiency rs72553883, rs121908379, rs104894650, rs587776775, rs398122863, rs398122864, rs397514332, rs397514331, rs727502786, rs727502787, rs72553882, rs869320688, rs869320689, rs869320754, rs773694113
View all (35 more)		 26301688
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)		 26301688
Show/Hide Unknown Diseases (3)
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac Disease 26301688 ClinVar
Crohn disease Crohn Disease 26301688 ClinVar
Asthma Asthma GWAS
Show/Hide Text Mining Associations (1)
Associations from Text Mining
Disease Name Relationship Type References
Dermatitis Atopic Associate 39245941