Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	390205
Gene name Gene Name - the full gene name approved by the HGNC.	Leucine rich repeat containing 10B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	LRRC10B
Synonyms (NCBI Gene) Gene synonyms aliases	-
Chromosome Chromosome number	11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	11q12.2

Show/Hide all(29)

miRTarBase ID	miRNA	Experiments	Reference
MIRT043349	hsa-miR-331-3p	CLASH	23622248
MIRT1118754	hsa-miR-1262	CLIP-seq
MIRT1118755	hsa-miR-1321	CLIP-seq
MIRT1118756	hsa-miR-146b-3p	CLIP-seq
MIRT1118757	hsa-miR-2861	CLIP-seq
MIRT1118758	hsa-miR-3135	CLIP-seq
MIRT1118759	hsa-miR-3147	CLIP-seq
MIRT1118760	hsa-miR-3173-5p	CLIP-seq
MIRT1118761	hsa-miR-4419a	CLIP-seq
MIRT1118762	hsa-miR-4425	CLIP-seq
MIRT1118763	hsa-miR-4510	CLIP-seq
MIRT1118764	hsa-miR-4701-3p	CLIP-seq
MIRT1118765	hsa-miR-4728-5p	CLIP-seq
MIRT1118766	hsa-miR-4739	CLIP-seq
MIRT1118767	hsa-miR-4756-5p	CLIP-seq
MIRT1118768	hsa-miR-541	CLIP-seq
MIRT1118769	hsa-miR-609	CLIP-seq
MIRT1118770	hsa-miR-654-5p	CLIP-seq
MIRT1118771	hsa-miR-874	CLIP-seq
MIRT2033579	hsa-miR-3157-5p	CLIP-seq
MIRT2033580	hsa-miR-4691-3p	CLIP-seq
MIRT1118759	hsa-miR-3147	CLIP-seq
MIRT2264022	hsa-miR-4421	CLIP-seq
MIRT1118762	hsa-miR-4425	CLIP-seq
MIRT1118765	hsa-miR-4728-5p	CLIP-seq
MIRT2264023	hsa-miR-676	CLIP-seq
MIRT2563166	hsa-miR-1305	CLIP-seq
MIRT2563167	hsa-miR-2277-3p	CLIP-seq
MIRT2563168	hsa-miR-607	CLIP-seq

MIM	HGNC	e!Ensembl
HGNC	N/A	HGNC

Protein

UniProt ID

A6NIK2

Protein name

Leucine-rich repeat-containing protein 10B

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF13855	LRR_8	67 → 125	Leucine rich repeat	Repeat
PF13855	LRR_8	90 → 148	Leucine rich repeat	Repeat

Sequence

MGIAESTPDELPSDAEEQLRSGDQQLELSGRRLRRLPSAVCALSRLQKLYVSGTGLRELP
EEIEELRELRILALDFNKLERLPDGLCRLPRLTRLYLGGNRLLALPADFAQLQSLRCLWI
EGNFLRRFPRPLLRLVALQSLQMGDNRLRALPAELPRMTGLRGLWLYGNRFEEFPPALLR
MGRLHILDLDRNRLGGFPDLHPLRALRVFSYDHNPVTGPPRVADTVFLVGEGAVERMAER
DEPTPRPPPRRPARAFEDEEEEDLLIGGAGSRALGAPGGSFRALEAAPGLGT

Sequence length

292

Interactions

View interactions

Show/Hide Unknown Diseases (2)

Disease merge term	Disease name	Evidence	References	Source
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.
Coronary artery disease	Coronary artery disease	N/A	N/A	GWAS
Hypertension	High blood pressure / hypertension, Hypertension, Hypertension (PheCode 401), Essential hypertension (PheCode 401.1)	N/A	N/A	GWAS

LRRC10B (leucine rich repeat containing 10B)