KEGG   Homo sapiens (human): 79827
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)
SSDB
Motif
Pfam: V-set Ig_3 I-set Ig_2 ig Syndecan Sp38 TM_ErbB1 V-set_CD47 Ctr Ig_C17orf99 Miga
Other DBs
NCBI-GeneID: 79827
NCBI-ProteinID: NP_079045
OMIM: 611693
HGNC: 24039
Ensembl: ENSG00000166250
UniProt: Q9H6B4 B4E3S3
Position
11:complement(123069872..123195248)
AA seq 373 aa
MSLLLLLLLVSYYVGTLGTHTEIKRVAEEKVTLPCHHQLGLPEKDTLDIEWLLTDNEGNQ
KVVITYSSRHVYNNLTEEQKGRVAFASNFLAGDASLQIEPLKPSDEGRYTCKVKNSGRYV
WSHVILKVLVRPSKPKCELEGELTEGSDLTLQCESSSGTEPIVYYWQRIREKEGEDERLP
PKSRIDYNHPGRVLLQNLTMSYSGLYQCTAGNEAGKESCVVRVTVQYVQSIGMVAGAVTG
IVAGALLIFLLVWLLIRRKDKERYEEEERPNEIREDAEAPKARLVKPSSSSSGSRSSRSG
SSSTRSTANSASRSQRTLSTDAAPQPGLATQAYSLVGPEVRGSEPKKVHHANLTKAETTP
SMIPSQSRAFQTV
NT seq 1122 nt   +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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