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14 records found for search term Lins1
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1308792Lins1lines homolog 1INVOLVED IN cognition (ortholog); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog); INTERACTS WITH amphetamine; bisphenol A; endosulfan1129677815129705399Rat40symbol , PhenoGengene, protein-coding, VALIDATED [RefSeq]
1602699LINS1lines homolog 1The Drosophila segment polarity gene lin encodes a protein, lines, which plays important roles in development of the epidermis and hindgut. This gene encodes a protein containing a lines-like domain. This gene is located on chromosome 15 and clustered with the gene encoding ankyrin repeat and SOCS b15100566924100602184Human69symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1615057Lins1lines homolog 1Predicted to be involved in cognition. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 27. Orthologous to human LINS1 (lines homolog 1). [provided by Alliance of Genome Resources, Jul 2025]76633956566367004Mouse45symbol , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
8948031Lins1lines homolog 1INVOLVED IN cognition (ortholog); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)NW_0049554162758517227609780Chinchilla7symbolgene, protein-coding, MODEL [RefSeq]
11858729LINS1lines homolog 1INVOLVED IN cognition (inferred); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)157929342679328691Bonobo7symbolgene, protein-coding, MODEL [RefSeq]
12375317LINS1lines homolog 1INVOLVED IN cognition (inferred); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)34041559940437075Dog7symbolgene, protein-coding, MODEL [RefSeq]
18904028Lins1lines homolog 1INVOLVED IN cognition (inferred); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)Naked Mole-Rat7symbolgene, protein-coding, MODEL [RefSeq]
155259229lins1Tropical Clawed Frogsymbolgene, null
18423629LINS1lines homolog 1INVOLVED IN cognition (inferred); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)Green Monkey7symbolgene, protein-coding, MODEL [RefSeq]
14209311LINS1lines homolog 1INVOLVED IN cognition (inferred); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)Pig7symbolgene, protein-coding, MODEL [RefSeq]
626134239Lins1lines homolog 1INVOLVED IN cognition (ortholog); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive intellectual developmental disorder 27 (ortholog); genetic disease (ortholog)Black Rat7symbolgene, protein-coding, MODEL [RefSeq]
155244094lins1.LAfrican Clawed Frogsymbolgene, null
12659265LOC101958833ceramide synthase 3ENCODES a protein that exhibits DNA binding (inferred); sphingosine N-acyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN sphingolipid biosynthetic process (ortholog); ASSOCIATED WITH autosomal recessive congenital ichthyosis (ortholog); autosomal recessive congenital iNW_00493648332765193365054Squirrel34old_gene_symbolgene, protein-coding, MODEL [RefSeq]
16562262AC027020.1novel transcript, antisense to LINS115100558666100559799Humannamegene, ncrna, VALIDATED [RefSeq]