Homo sapiens Protein: LINS
Summary
InnateDB Protein IDBP-32042.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LINS
Protein Name lines homolog (Drosophila)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000318423
InnateDB Gene IDBG-32040 (LINS)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations Mental retardation, autosomal recessive 27 (MRT27) [MIM:614340]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. {ECO:0000269PubMed:21937992, ECO:0000269PubMed:23773660}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in adult testis, prostate, prostate, spleen, thymus, skeletal muscle, fetal kidney and brain. {ECO:0000269PubMed:12119551}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8NG48
PhosphoSite PhosphoSite-Q8NG48
TrEMBL H3BNS6
UniProt Splice Variant
Entrez Gene 55180
UniGene Hs.709044
RefSeq NP_001035706
HUGO HGNC:30922
OMIM 610350
CCDS CCDS10385
HPRD 17280
IMGT
EMBL AB083157 AC027020 AC090695 AK001445 AK292972
GenPept BAA91696 BAB93864 BAF85661