KEGG   Homo sapiens (human): 342035
Entry
342035            CDS       T01001                                 
Symbol
GLDN, CLOM, COLM, CRG-L2, CRGL2, LCCS11, UNC-112, UNC-122
Name
(RefSeq) gliomedin
  KO
K16364  gliomedin
Organism
hsa  Homo sapiens (human)
Disease
H00865  Lethal congenital contractural syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    342035 (GLDN)
SSDB
Motif
Pfam: OLF Collagen
Other DBs
NCBI-GeneID: 342035
NCBI-ProteinID: NP_861454
OMIM: 608603
HGNC: 29514
Ensembl: ENSG00000186417
UniProt: Q6ZMI3
Structure
Position
15:51341655..51413365
AA seq 551 aa
MARGAEGGRGDAGWGLRGALAAVALLSALNAAGTVFALCQWRGLSSALRALEAQRGREQR
EDSALRSFLAELSRAPRGASAPPQDPASSARNKRSHSGEPAPHIRAESHDMLMMMTYSMV
PIRVMVDLCNSTKGICLTGPSGPPGPPGAGGLPGHNGLDGQPGPQGPKGEKGANGKRGKM
GIPGAAGNPGERGEKGDHGELGLQGNEGPPGQKGEKGDKGDVSNDVLLAGAKGDQGPPGP
PGPPGPPGPPGPPGSRRAKGPRQPSMFNGQCPGETCAIPNDDTLVGKADEKASEHHSPQA
ESMITSIGNPVQVLKVTETFGTWIRESANKSDDRIWVTEHFSGIMVKEFKDQPSLLNGSY
TFIHLPYYFHGCGHVVYNNSLYYHKGGSNTLVRFEFGQETSQTLKLENALYFDRKYLFAN
SKTYFNLAVDEKGLWIIYASSVDGSSILVAQLDERTFSVVQHVNTTYPKSKAGNAFIARG
ILYVTDTKDMRVTFAFDLLGGKQINANFDLRTSQSVLAMLAYNMRDQHLYSWEDGHLMLY
PVQFLSTTLNQ
NT seq 1656 nt   +upstreamnt  +downstreamnt
atggcccgaggcgctgagggaggccgtggggacgcgggttggggcctgcgtggcgccctg
gcggccgtggcgctgctctcggcgctcaacgctgcgggcacggtgttcgcgctgtgccag
tggcgcgggctgagctcggcgctgcgggctttggaggcgcagcggggccgggagcagcgc
gaggacagtgccctgcgctccttcctggccgagttgagccgcgcgccgcgcggggcgtcc
gcaccaccccaagacccggccagctcagctcgcaacaagcgcagccacagcggcgagccc
gcgccgcatatccgcgccgagagccatgacatgctgatgatgatgacctactccatggtg
ccgatccgagtgatggtggacctgtgcaacagcaccaagggcatctgcctcacaggacct
tctggaccaccaggacctccgggagccggcgggttgccaggacacaacggattggatgga
cagcctggtcctcagggcccaaaaggagaaaaaggagcaaatggaaaaagaggaaaaatg
gggatacctggagctgcaggaaatccaggggaaaggggagaaaagggagaccatggtgaa
ctgggcctgcagggaaatgagggcccaccagggcagaagggagaaaagggtgacaaagga
gatgtgtccaacgacgtgctcctggcaggtgccaaaggtgaccaaggcccacccggtcca
cctgggcccccaggccctccaggtcctccagggccccctggaagcagaagagccaaaggc
cctcggcagccaagcatgttcaacggccagtgcccaggtgagacttgtgccataccaaat
gatgataccttggttggaaaagctgatgagaaagccagtgaacaccattccccacaagca
gaatccatgatcacttccattggaaacccagtgcaagtactgaaagtgacagagacattt
gggacttggataagagagtctgctaacaagagtgatgaccggatttgggtgacagagcat
ttttcaggcatcatggttaaggaattcaaggatcagccctcacttctgaatggcagttac
acgttcatccaccttccatactatttccatggctgtgggcacgttgtttacaacaactct
ctctactaccacaaagggggttctaataccctagtgagatttgaatttggccaggaaaca
tcccaaactctgaagcttgaaaatgccttgtattttgatcgaaaatacctttttgcaaat
tccaaaacttacttcaatctagctgtagatgaaaagggcctttggattatctatgcgtca
agtgtggacggctcgagcattcttgtagcacaactggatgagaggacattctcagtggtg
caacacgtcaataccacgtaccctaaatccaaggctggcaacgccttcattgcccgagga
atcctctatgtcacagacaccaaagatatgagggtcacatttgcctttgatttgttagga
gggaaacagatcaatgcaaactttgatttaagaacttcccagtctgttcttgccatgtta
gcatacaacatgagagatcagcatttatattcatgggaagatggccatttaatgctttat
cctgtgcagtttttgtcaactaccttaaatcagtga

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Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   KEGG ORTHOLOGY (1)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (20)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (40)   
   RefSeq(nuc) (18)   
   GenBank (11)   
   EMBL (11)   
3D Structure (1)   
   PDB (1)   
Protein domain (2)   
   Pfam (2)   
All databases (80)   

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