KEGG T01001: 56975

Homo sapiens (human): 56975

Entry

56975 CDS T01001

Gene name

FAM20C, DMP-4, DMP4, GEF-CK, RNS

Definition

family with sequence similarity 20, member C (EC:2.7.11.1)

Organism

hsa Homo sapiens (human)

Disease

H00968

Raine syndrome

Class

SSDB

Motif

Pfam:

DUF1193 FAM198

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

UniProt:

Position

7p22.3

AA seq 584 aa
MKMMLVRRFRVLILMVFLVACALHIALDLLPRLERRGARPSGEPGCSCAQPAAEVAAPGW
AQVRGRPGEPPAASSAAGDAGWPNKHTLRILQDFSSDPSSNLSSHSLEKLPPAAEPAERA
LRGRDPGALRPHDPAHRPLLRDPGPRRSESPPGPGGDASLLARLFEHPLYRVAVPPLTEE
DVLFNVNSDTRLSPKAAENPDWPHAGAEGAEFLSPGEAAVDSYPNWLKFHIGINRYELYS
RHNPAIEALLHDLSSQRITSVAMKSGGTQLKLIMTFQNYGQALFKPMKQTREQETPPDFF
YFSDYERHNAEIAAFHLDRILDFRRVPPVAGRMVNMTKEIRDVTRDKKLWRTFFISPANN
ICFYGECSYYCSTEHALCGKPDQIEGSLAAFLPDLSLAKRKTWRNPWRRSYHKRKKAEWE
VDPDYCEEVKQTPPYDSSHRILDVMDMTIFDFLMGNMDRHHYETFEKFGNETFIIHLDNG
RGFGKYSHDELSILVPLQQCCRIRKSTYLRLQLLAKEEYKLSLLMAESLRGDQVAPVLYQ
PHLEALDRRLRVVLKAVRDCVERNGLHSVVDDDLDTEHRAASAR

NT seq 1755 nt +upstreamnt +downstreamnt
atgaagatgatgctggtgcgccggttccgcgtgctcatcctgatggtgttcctggtggcc
tgcgcgctgcacatcgccctggacctgctgcccaggctggagcgacgcggcgcgcggccc
tcgggggagcccggctgttcgtgcgcgcagcccgccgccgaggtggccgcgcccggctgg
gcccaggttcggggccgccccggggagcccccggccgcctcctccgccgccggcgacgcg
ggctggcccaacaagcacacgctccgcatcctgcaggacttcagctccgacccctcctcc
aacctctcgtcccactcgctggagaaactgccgcccgcggccgagccggccgagcgcgcc
ttgcgggggcgggatcccggcgccctaagaccccacgaccccgcgcaccggccgctgctg
cgagaccccggcccgcgtcggtccgagtcgccccccggccccggcggagacgcctccctc
ctggccaggctgttcgagcacccgctttaccgggtggcggttccgccgctcacggaggag
gacgtcctgttcaatgtgaacagcgacaccaggctcagccccaaagcggcggagaacccg
gactggccgcatgcgggtgctgaaggtgcagaattcctctcccccggggaggcggccgtg
gactcctatcccaactggctcaagttccacattggtatcaaccggtacgagctgtactcc
agacacaacccggccatcgaggccctgctgcacgacctcagctcccagaggatcaccagc
gtggccatgaagtcggggggcacgcagctgaagctcatcatgaccttccagaattacggg
caagcgctgttcaaacccatgaaacaaacgagggagcaggagacaccccctgactttttt
tatttctctgactacgagaggcacaatgcggagattgctgccttccacctggacaggatc
ctggacttccgccgggtccctcccgtggccggcaggatggtcaacatgaccaaggagatc
cgggacgtcacacgggacaagaagctctggaggaccttcttcatctctccagccaacaac
atctgcttctacggcgagtgttcctactactgctccacggagcacgccctgtgcgggaag
ccagaccagatcgagggctcgctggcggccttcctgcccgacctgtccctggccaagagg
aagacctggcggaacccttggcggcgttcctaccacaagcgcaagaaggccgagtgggag
gtggaccctgactactgcgaggaggtgaagcagacaccgccctacgacagcagccaccgc
atcctggacgtcatggacatgacgatcttcgacttcctcatgggaaacatggaccgtcac
cactacgagacttttgagaagtttgggaatgaaacgttcatcatccacttagacaatgga
agagggtttgggaagtattcgcacgacgagctctccatcctggtgccgctacagcagtgc
tgcaggatccggaagtccacctacctgcgtctgcagctcctggccaaggaggagtacaag
ctgagcctgctgatggccgagtctctgcggggggaccaggtggcacccgtgctgtaccag
ccgcacctggaggccctggaccggcggctccgcgtcgtgctaaaggccgtccgggactgc
gtggagaggaacgggctccacagcgtggtggatgacgacctggacactgagcacagagcc
gcctcggcgaggtag

All links

Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   NCBI-Gene (1)   
   NCBI-GI (6)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (2)   
   RefSeq(pep) (1)   
DNA sequence (21)   
   RefSeq(nuc) (1)   
   GenBank (10)   
   EMBL (10)   
Protein domain (2)   
   Pfam (2)   
All databases (42)   

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