Homo sapiens (human): 79827 Help Entry 79827             CDS       T01001                                  Symbol CLMP, ACAM, ASAM, CSBM, CSBS Name (RefSeq) CXADR like membrane protein   KO K06789   adipocyte-specific adhesion molecule Organism hsa  Homo sapiens (human) Disease H01477   Congenital short bowel syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99995 Signaling proteins     79827 (CLMP) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  V-set Ig_3 I-set Ig_2 ig Syndecan DUF7269 Sp38 TM_ErbB1 Ig_CD22 V-set_CD47 Ctr Ig_C17orf99 Miga Motif Other DBs NCBI-GeneID:  79827 NCBI-ProteinID:  NP_079045 OMIM:  611693 HGNC:  24039 Ensembl:  ENSG00000166250 UniProt:  Q9H6B4 B4E3S3 LinkDB All DBs Position 11:complement(123069872..123195248) Genome browser AA seq 373 aa AA seqDB search MSLLLLLLLVSYYVGTLGTHTEIKRVAEEKVTLPCHHQLGLPEKDTLDIEWLLTDNEGNQ KVVITYSSRHVYNNLTEEQKGRVAFASNFLAGDASLQIEPLKPSDEGRYTCKVKNSGRYV WSHVILKVLVRPSKPKCELEGELTEGSDLTLQCESSSGTEPIVYYWQRIREKEGEDERLP PKSRIDYNHPGRVLLQNLTMSYSGLYQCTAGNEAGKESCVVRVTVQYVQSIGMVAGAVTG IVAGALLIFLLVWLLIRRKDKERYEEEERPNEIREDAEAPKARLVKPSSSSSGSRSSRSG SSSTRSTANSASRSQRTLSTDAAPQPGLATQAYSLVGPEVRGSEPKKVHHANLTKAETTP SMIPSQSRAFQTV NT seq 1122 nt NT seq  +upstreamnt  +downstreamnt atgtccctcctccttctcctcttgctagtttcctactatgttggaaccttggggactcac actgagatcaagagagtggcagaggaaaaggtcactttgccctgccaccatcaactgggg cttccagaaaaagacactctggatattgaatggctgctcaccgataatgaagggaaccaa aaagtggtgatcacttactccagtcgtcatgtctacaataacttgactgaggaacagaag ggccgagtggcctttgcttccaatttcctggcaggagatgcctccttgcagattgaacct ctgaagcccagtgatgagggccggtacacctgtaaggttaagaattcagggcgctacgtg tggagccatgtcatcttaaaagtcttagtgagaccatccaagcccaagtgtgagttggaa ggagagctgacagaaggaagtgacctgactttgcagtgtgagtcatcctctggcacagag cccattgtgtattactggcagcgaatccgagagaaagagggagaggatgaacgtctgcct cccaaatctaggattgactacaaccaccctggacgagttctgctgcagaatcttaccatg tcctactctggactgtaccagtgcacagcaggcaacgaagctgggaaggaaagctgtgtg gtgcgagtaactgtacagtatgtacaaagcatcggcatggttgcaggagcagtgacaggc atagtggctggagccctgctgattttcctcttggtgtggctgctaatccgaaggaaagac aaagaaagatatgaggaagaagagagacctaatgaaattcgagaagatgctgaagctcca aaagcccgtcttgtgaaacccagctcctcttcctcaggctctcggagctcacgctctggt tcttcctccactcgctccacagcaaatagtgcctcacgcagccagcggacactgtcaact gacgcagcaccccagccagggctggccacccaggcatacagcctagtggggccagaggtg agaggttctgaaccaaagaaagtccaccatgctaatctgaccaaagcagaaaccacaccc agcatgatccccagccagagcagagccttccaaacggtctga

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