InnateDB Protein
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IDBP-32042.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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LINS
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Protein Name
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lines homolog (Drosophila)
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000318423
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InnateDB Gene
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IDBG-32040 (LINS)
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Protein Structure
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Function |
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Subcellular Localization |
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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.
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Tissue Specificity |
Expressed in adult testis, prostate, prostate, spleen, thymus, skeletal muscle, fetal kidney and brain. {ECO:0000269PubMed:12119551}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
1
[view]
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Protein-Protein |
1
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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PDB ID |
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InterPro |
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PFAM |
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q8NG48
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PhosphoSite |
PhosphoSite-Q8NG48
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TrEMBL |
H3BNS6
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UniProt Splice Variant |
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Entrez Gene |
55180
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UniGene |
Hs.709044
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RefSeq |
NP_001035706
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HUGO |
HGNC:30922
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OMIM |
610350
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CCDS |
CCDS10385
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HPRD |
17280
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IMGT |
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EMBL |
AB083157
AC027020
AC090695
AK001445
AK292972
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GenPept |
BAA91696
BAB93864
BAF85661
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