Gene Gene information from NCBI Gene database.
Entrez ID 84918
Gene name LDL receptor related protein 11
Gene symbol LRP11
Synonyms (NCBI Gene)
MANSC3bA350J20.3
Chromosome 6
Chromosome location 6q25.1
miRNA miRNA information provided by mirtarbase database.
137
miRTarBase ID miRNA Experiments Reference
MIRT023392 hsa-miR-122-5p Microarray 17612493
MIRT039310 hsa-miR-425-5p CLASH 23622248
MIRT037854 hsa-miR-455-3p CLASH 23622248
MIRT1117787 hsa-miR-1178 CLIP-seq
MIRT1117788 hsa-miR-1200 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IC 17620599
GO:0009408 Process Response to heat IEA
GO:0009409 Process Response to cold IEA
GO:0009414 Process Response to water deprivation IEA
GO:0009612 Process Response to mechanical stimulus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86VZ4
Protein name Low-density lipoprotein receptor-related protein 11 (LRP-11)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07502 MANEC 87 183 MANEC domain Domain
PF00057 Ldl_recept_a 308 344 Low-density lipoprotein receptor domain class A Repeat
Sequence
MASVAQESAGSQRRLPPRHGALRGLLLLCLWLPSGRAALPPAAPLSELHAQLSGVEQLLE
EFRRQLQQERPQEELELELRAGGGPQEDCPGPGSGGYSAMPDAIIRTKDSLAAGASFLRA
PAAVRGWRQCVAACCSEPRCSVAVVELPRRPAPPAAVLGCYLFNCTARGRNVCKFALHSG
YSS
YSLSRAPDGAALATARASPRQEKDAPPLSKAGQDVVLHLPTDGVVLDGRESTDDHAI
VQYEWALLQGDPSVDMKVPQSGTLKLSHLQEGTYTFQLTVTDTAGQRSSDNVSVTVLRAA
YSTGGCLHTCSRYHFFCDDGCCIDITLACDGVQQCPDGSDEDFCQNLGLDRKMVTHTAAS
PALPRTTGPSEDAGGDSLVEKSQKATAPNKPPALSNTEKRNHSAFWGPESQIIPVMPDSS
SSGKNRKEESYIFESKGDGGGGEHPAPETGAVLPLALGLAITALLLLMVACRLRLVKQKL
KKARPITSEESDYLINGMYL
Sequence length 500
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CONNECTIVE TISSUE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTROPHIC CARDIOMYOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIGRAINE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIXED CONNECTIVE TISSUE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 34868337
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 30008265, 36930084
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Associate 38203854
★☆☆☆☆
Found in Text Mining only
Renal Insufficiency Chronic Associate 37816758
★☆☆☆☆
Found in Text Mining only
Uterine Cervical Neoplasms Associate 36930084
★☆☆☆☆
Found in Text Mining only