Homo sapiens (human): 81562 Help Entry 81562             CDS       T01001                                  Symbol LMAN2L, MRD69, MRT52, VIPL Name (RefSeq) lectin, mannose binding 2 like   KO K10083   lectin, mannose-binding 2-like Organism hsa  Homo sapiens (human) Disease H00768   Autosomal recessive intellectual developmental disorder H00773   Autosomal dominant intellectual developmental disorder Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04091 Lectins [BR:hsa04091]     81562 (LMAN2L) Lectins [BR:hsa04091]  L-type lectins   81562 (LMAN2L) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Lectin_leg-like Bact_lectin PMP1_2 Motif Other DBs NCBI-GeneID:  81562 NCBI-ProteinID:  NP_110432 OMIM:  609552 HGNC:  19263 Ensembl:  ENSG00000114988 UniProt:  Q9H0V9 LinkDB All DBs Position 2:complement(96705929..96740064) Genome browser AA seq 348 aa AA seqDB search MAATLGPLGSWQQWRRCLSARDGSRMLLLLLLLGSGQGPQQVGAGQTFEYLKREHSLSKP YQGVGTGSSSLWNLMGNAMVMTQYIRLTPDMQSKQGALWNRVPCFLRDWELQVHFKIHGQ GKKNLHGDGLAIWYTKDRMQPGPVFGNMDKFVGLGVFVDTYPNEEKQQERVFPYISAMVN NGSLSYDHERDGRPTELGGCTAIVRNLHYDTFLVIRYVKRHLTIMMDIDGKHEWRDCIEV PGVRLPRGYYFGTSSITGDLSDNHDVISLKLFELTVERTPEEEKLHRDVFLPSVDNMKLP EMTAPLPPLSGLALFLIVFFSLVFSVFAIVIGIILYNKWQEQSRKRFY NT seq 1047 nt NT seq  +upstreamnt  +downstreamnt atggcggcgactctgggaccccttgggtcgtggcagcagtggcggcgatgtttgtcggct cgggatgggtccaggatgttactccttcttcttttgttggggtctgggcaggggccacag caagtcggggcgggtcaaacgttcgagtacttgaaacgggagcactcgctgtcgaagccc taccagggtgtgggcacaggcagttcctcactgtggaatctgatgggcaatgccatggtg atgacccagtatatccgccttaccccagatatgcaaagtaaacagggtgccttgtggaac cgggtgccatgtttcctgagagactgggagttgcaggtgcacttcaaaatccatggacaa ggaaagaagaatctgcatggggatggcttggcaatctggtacacaaaggatcggatgcag ccagggcctgtgtttggaaacatggacaaatttgtggggctgggagtatttgtagacacc taccccaatgaggagaagcagcaagagcgggtattcccctacatctcagccatggtgaac aacggctccctcagctatgatcatgagcgggatgggcggcctacagagctgggaggctgc acagccattgtccgcaatcttcattacgacaccttcctggtgattcgctacgtcaagagg catttgacgataatgatggatattgatggcaagcatgagtggagggactgcattgaagtg cccggagtccgcctgccccgcggctactacttcggcacctcctccatcactggggatctc tcagataatcatgatgtcatttccttgaagttgtttgaactgacagtggagagaacccca gaagaggaaaagctccatcgagatgtgttcttgccctcagtggacaatatgaagctgcct gagatgacagctccactgccgcccctgagtggcctggccctcttcctcatcgtctttttc tccctggtgttttctgtatttgccatagtcattggtatcatactctacaacaaatggcag gaacagagccgaaagcgcttctactga

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