KEGG   Homo sapiens (human): 1300
Entry
1300              CDS       T01001                                 
Symbol
COL10A1
Name
(RefSeq) collagen type X alpha 1 chain
  KO
K19479  collagen type X alpha
Organism
hsa  Homo sapiens (human)
Pathway
hsa04974  Protein digestion and absorption
Disease
H00479  Metaphyseal dysplasias
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    1300 (COL10A1)
SSDB
Motif
Pfam: Collagen C1q BclA_C
Other DBs
NCBI-GeneID: 1300
NCBI-ProteinID: NP_000484
OMIM: 120110
HGNC: 2185
Ensembl: ENSG00000123500
UniProt: Q03692 A0A650AXN9
Structure
Position
6:complement(116118909..116217144)
AA seq 680 aa
MLPQIPFLLLVSLNLVHGVFYAERYQMPTGIKGPLPNTKTQFFIPYTIKSKGIAVRGEQG
TPGPPGPAGPRGHPGPSGPPGKPGYGSPGLQGEPGLPGPPGPSAVGKPGVPGLPGKPGER
GPYGPKGDVGPAGLPGPRGPPGPPGIPGPAGISVPGKPGQQGPTGAPGPRGFPGEKGAPG
VPGMNGQKGEMGYGAPGRPGERGLPGPQGPTGPSGPPGVGKRGENGVPGQPGIKGDRGFP
GEMGPIGPPGPQGPPGERGPEGIGKPGAAGAPGQPGIPGTKGLPGAPGIAGPPGPPGFGK
PGLPGLKGERGPAGLPGGPGAKGEQGPAGLPGKPGLTGPPGNMGPQGPKGIPGSHGLPGP
KGETGPAGPAGYPGAKGERGSPGSDGKPGYPGKPGLDGPKGNPGLPGPKGDPGVGGPPGL
PGPVGPAGAKGMPGHNGEAGPRGAPGIPGTRGPIGPPGIPGFPGSKGDPGSPGPPGPAGI
ATKGLNGPTGPPGPPGPRGHSGEPGLPGPPGPPGPPGQAVMPEGFIKAGQRPSLSGTPLV
SANQGVTGMPVSAFTVILSKAYPAIGTPIPFDKILYNRQQHYDPRTGIFTCQIPGIYYFS
YHVHVKGTHVWVGLYKNGTPVMYTYDEYTKGYLDQASGSAIIDLTENDQVWLQLPNAESN
GLYSSEYVHSSFSGFLVAPM
NT seq 2043 nt   +upstreamnt  +downstreamnt
atgctgccacaaataccctttttgctgctagtatccttgaacttggttcatggagtgttt
tacgctgaacgataccaaatgcccacaggcataaaaggcccactacccaacaccaagaca
cagttcttcattccctacaccataaagagtaaaggtatagcagtaagaggagagcaaggt
actcctggtccaccaggccctgctggacctcgagggcacccaggtccttctggaccacca
ggaaaaccaggctacggaagtcctggactccaaggagagccagggttgccaggaccaccg
ggaccatcagctgtagggaaaccaggtgtgccaggactcccaggaaaaccaggagagaga
ggaccatatggaccaaaaggagatgttggaccagctggcctaccaggaccccggggccca
ccaggaccacctggaatccctggaccggctggaatttctgtgccaggaaaacctggacaa
cagggacccacaggagccccaggacccaggggctttcctggagaaaagggtgcaccagga
gtccctggtatgaatggacagaaaggggaaatgggatatggtgctcctggtcgtccaggt
gagaggggtcttccaggccctcagggtcccacaggaccatctggccctcctggagtggga
aaaagaggtgaaaatggggttccaggacagccaggcatcaaaggtgatagaggttttccg
ggagaaatgggaccaattggcccaccaggtccccaaggccctcctggggaacgagggcca
gaaggcattggaaagccaggagctgctggagccccaggccagccagggattccaggaaca
aaaggtctccctggggctccaggaatagctgggcccccagggcctcctggctttgggaaa
ccaggcttgccaggcctgaagggagaaagaggacctgctggccttcctgggggtccaggt
gccaaaggggaacaagggccagcaggtcttcctgggaagccaggtctgactggaccccct
gggaatatgggaccccaaggaccaaaaggcatcccgggtagccatggtctcccaggccct
aaaggtgagacagggccagctgggcctgcaggataccctggggctaagggtgaaaggggt
tcccctgggtcagatggaaaaccagggtacccaggaaaaccaggtctcgatggtcctaag
ggtaacccagggttaccaggtccaaaaggtgatcctggagttggaggacctcctggtctc
ccaggccctgtgggcccagcaggagcaaagggaatgcccggacacaatggagaggctggc
ccaagaggtgcccctggaataccaggtactagaggccctattgggccaccaggcattcca
ggattccctgggtctaaaggggatccaggaagtcccggtcctcctggcccagctggcata
gcaactaagggcctcaatggacccaccgggccaccagggcctccaggtccaagaggccac
tctggagagcctggtcttccagggccccctgggcctccaggcccaccaggtcaagcagtc
atgcctgagggttttataaaggcaggccaaaggcccagtctttctgggacccctcttgtt
agtgccaaccagggggtaacaggaatgcctgtgtctgcttttactgttattctctccaaa
gcttacccagcaataggaactcccataccatttgataaaattttgtataacaggcaacag
cattatgacccaaggactggaatctttacttgtcagataccaggaatatactatttttca
taccacgtgcatgtgaaagggactcatgtttgggtaggcctgtataagaatggcacccct
gtaatgtacacctatgatgaatacaccaaaggctacctggatcaggcttcagggagtgcc
atcatcgatctcacagaaaatgaccaggtgtggctccagcttcccaatgccgagtcaaat
ggcctatactcctctgagtatgtccactcctctttctcaggattcctagtggctccaatg
tga

  All links  
Disease (2)   
   OMIM (2)   
Gene (16)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (17)   
   RefSeq(nuc) (5)   
   GenBank (6)   
   EMBL (6)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (47)   

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