KEGG   Homo sapiens (human): 442444
Entry
442444            CDS       T01001                                 
Symbol
FAM47C
Name
(RefSeq) family with sequence similarity 47 member C
Organism
hsa  Homo sapiens (human)
SSDB
Motif
Pfam: FAM47 Drf_FH1
Other DBs
NCBI-GeneID: 442444
NCBI-ProteinID: NP_001013758
OMIM: 301067
HGNC: 25301
Ensembl: ENSG00000198173
UniProt: Q5HY64
Position
X:37008366..37011664
AA seq 1035 aa
MGDQRPQDRPSSPGMDSTPWYCDKPPSKYFAKRKHRRLRFPPVDTQNWVFVTEGMDDFRY
GCQSPEDTLVCRRDEFLLPKISLRGPQADPKSRKKKLLKKAALFSKLSPAQPARKAFVEE
VEAQLMTKHPLAMYPNLGEDMPPDLLLQVLKPLDPERKLEDAGSCEGQEKTTDEPTEPGK
YPCGEFSPRPPETRVSCLPPEPPKTPVSSLRPEPPETGVSHLRPQPPKTQVSSLHLEPPE
TGVSHLRPEPPKTQVSSLHLEPPETGVSHLYLEPPGTGVSHLCPEPPKTRVSHLHREPPE
TGVPDLCLEPPKSRVSHLRPEPSETGVSHLHPEPPKTLVSSLHPEPPETGVSHLCPEPPE
TRVSPLRQLPPEAGVSHLCPEPPKTRVPPLRPETPKNGVSPLFPEPPKTRISNLRSEPPK
IGVSHLCLEPPKTRGSHLRPEPPETGVSHLRPEPPKTRVSSLHLEPPETGVSHLCPEPPE
KDVSHLRPEPPDTGVSHLCPEPPKTRVSHLRPEPSETGVSHLRPEPPKILVSSLHQAPPE
SSVSHLRPEPPETGVSHLRPEPPKTRMYSLRPEPPDTGVSHLCPEPPKTRVSSLPPEPPE
TGVSHLCPEPPETRVSHLRPEPPETGVSHLRPEPPKTRMYSLRPEPPNTGVSHLCPEPPK
TRVSSLPPEPPETGVSHLCPEPPETRVSHLRPEPPETGVSRLHPEPPKTRVSSLHAEPPE
SRVSHLCPEPPETGVSHLRPEPPKPRVSSLRPEPLETRVSHLRPEPPETGVSHLHPELPK
PRVSSLHLEPPKTRRVSSLRLEPPKTGRVSSLCPEPTKTGASHLKELFQEGTSSTMECVS
DSLQRRHTSRKLRDFKWAGDLGVNEESISSLFDFTPECRATYQDQKNKKANECSSGLKYS
MELDEMDEVKFFSQEKDLDGKIQNAPNSHSAQHVKMGYGAWYLKPKLGKKLRSDEPLIDP
KLVLEKPDEPDILDGLYGPIAFKDFILSKGYEMPGIIQRLFARRGWTYDSVKTPIQRAMQ
VYKYKEDVTDASEED
NT seq 3108 nt   +upstreamnt  +downstreamnt
atgggggaccagaggccgcaggaccggcccagttccccgggcatggactccacgccctgg
tactgtgacaaaccgccttccaagtacttcgcgaagcgcaagcacaggcgcctgaggttc
ccgcctgtggacacccagaactgggtatttgtgacggagggcatggacgacttccgctac
ggctgtcagtctcctgaagatacgcttgtttgtcgccgtgacgagtttttactccccaaa
atatctctcagaggtccccaagctgaccccaaaagcaggaagaaaaagctgctcaagaaa
gcggccctgttttccaagctctcgccagcacagccagcacggaaggcgttcgtagaggaa
gtggaagcccagctgatgaccaagcatcccttggccatgtaccccaatctgggagaagat
atgcctccagatctcctactacaggtactgaaaccgctggaccctgagaggaagctggag
gacgcaggctcttgtgagggccaggagaagacaactgacgaacccacggagcctggtaaa
tacccctgtggggaattctcccctcggcctcccgagactcgggtgtcctgtctccccccg
gagcctcccaagactccggtgtccagtctccgcccggagcctccagagactggagtgtcc
catctccgcccacagcctcccaagactcaggtgtccagtctccacctggagcctccagag
actggagtgtcccatctccgcccagagcctcccaagactcaggtgtccagtctccacctg
gagcctcccgagactggagtgtcccatctctacctggagcctcctgggactggagtgtct
catctctgcccagagcctcccaagactcgcgtatctcatctccatcgggagcctcctgag
actggagtgcctgatctctgcctggagcctcccaagtcacgcgtatctcatctccgccca
gagccttctgagactggagtgtcccatctccacccagagcctcccaagactctggtgtcc
agtctccacccagagcctcccgagactggagtgtcccatctctgcccggaacctccagag
actcgcgtatctcctctccgccagctgcctcccgaggctggagtgtcccatctctgcccg
gaacctcccaagactcgcgtacctcctctccgcccagagacccccaagaatggagtgtct
cctctcttcccggagcctcccaagactcgcatatctaatctccgctcggagcctcccaag
attggagtgtcccatctctgcctggagcctcccaagactcgcggatctcatctccgcccg
gaacctcctgagactggagtgtcccatctccgcccagagcctcccaagactcgggtgtcc
agtctccacctggagcctcctgagactggagtgtcccatctctgcccggagcctccagag
aaggacgtatctcatctccgcccagagcctcccgacactggagtgtcccatctctgccca
gagccccccaagacacgcgtatctcatctccgcccagagccttctgagactggagtgtcc
catctccgcccagagcctcccaagattctggtgtccagtctccaccaggcacctcctgag
agtagcgtatctcatctccgcccagagcctcctgagactggagtgtcccatctccgccca
gagcctcccaagactcggatgtacagtctccgcccggagcctcccgatactggagtgtcc
catctctgcccagagcctcccaagactcgggtgtccagtctccccccggagccccccgag
actggagtgtcccatctctgcccggagcctccagagactcgcgtatctcatctccgccca
gagcctcctgagactggagtgtcccatctccgcccagagcctcccaagactcggatgtac
agtctccgcccggagcctcccaatactggagtgtcccatctctgcccagagcctcccaag
actcgggtgtccagtctccccccggagccccccgagactggagtgtcccatctctgcccg
gagcctccagagactcgcgtatctcatctccgcccagagcctcctgagactggagtgtcc
cgtctccacccagagcctcccaagactcgggtgtccagtctccacgcggagcctcctgag
agtcgcgtatctcatctctgcccggagcctcctgagactggagtgtcccatctccgccca
gagcctcccaagcctcgggtttccagtctccgcccagagcctcttgagactcgcgtatct
catctccgcccggagcctcctgagactggagtgtcccatctccacccagagcttcccaag
cctcgggtatccagtctccacctggagcctcccaagactcgtcgagtgtccagtctccgc
ctggagcctcccaagactggtcgggtgtccagtctctgcccggagcctaccaagaccgga
gcgtcccatctaaaagaactgtttcaggaaggtacatcaagcacaatggagtgtgtttct
gactctcttcaacgtagacacacatcgagaaaactccgtgacttcaagtgggctggagac
ctaggagttaatgaagaatccatcagcagtctgtttgactttacccctgagtgcagagca
acctatcaagaccaaaagaataagaaggcaaacgagtgttcctcagggctgaagtacagc
atggagctagacgaaatggatgaggtcaaattcttctcacaggaaaaagacttggacggg
aaaatccagaatgcaccaaattctcatagtgcacagcatgtgaagatggggtatggagca
tggtacctcaagcctaagttggggaaaaagctaagaagtgatgaacctttgattgacccc
aagctcgtacttgaaaagcctgatgaacccgacattcttgacggtctttatggaccaatc
gcctttaaggatttcattctaagcaagggctatgaaatgcctggcatcattcaaaggctg
tttgccaggaggggatggacttatgactctgttaagactcctattcaacgtgcaatgcaa
gtttacaagtacaaagaagacgtcacagatgcatcggaagaagattag

  All links  
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (74)   
   RefGene (69)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (5)   
   RefSeq(nuc) (1)   
   GenBank (2)   
   EMBL (2)   
Protein domain (2)   
   Pfam (2)   
All databases (86)   

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