KEGG   Homo sapiens (human): 54757
Entry
54757             CDS       T01001                                 
Symbol
FAM20A, AI1G, AIGFS, FP2747
Name
(RefSeq) pseudokinase FAM20A isoform a precursor
  KO
K21957  pseudokinase FAM20A
Organism
hsa  Homo sapiens (human)
Disease
H00615  Amelogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    54757 (FAM20A)
Membrane trafficking [BR:hsa04131]
 Endoplasmic reticulum (ER) - Golgi transport
  Others
   Others
    54757 (FAM20A)
SSDB
Motif
Pfam: Fam20C FJX1_middle FAM198 PI3_PI4_kinase
Other DBs
NCBI-GeneID: 54757
NCBI-ProteinID: NP_060035
OMIM: 611062
HGNC: 23015
Ensembl: ENSP00000468308.1
UniProt: Q96MK3 L8B8N7 Q8IYA5
Structure
Position
17:complement(68535116..68601367)
AA seq 541 aa
MPGLRRDRLLTLLLLGALLSADLYFHLWPQVQRQLRPRERPRGCPCTGRASSLARDSAAA
ASDPGTIVHNFSRTEPRTEPAGGSHSGSSSKLQALFAHPLYNVPEEPPLLGAEDSLLASQ
EALRYYRRKVARWNRRHKMYREQMNLTSLDPPLQLRLEASWVQFHLGINRHGLYSRSSPV
VSKLLQDMRHFPTISADYSQDEKALLGACDCTQIVKPSGVHLKLVLRFSDFGKAMFKPMR
QQRDEETPVDFFYFIDFQRHNAEIAAFHLDRILDFRRVPPTVGRIVNVTKEILEVTKNEI
LQSVFFVSPASNVCFFAKCPYMCKTEYAVCGNPHLLEGSLSAFLPSLNLAPRLSVPNPWI
RSYTLAGKEEWEVNPLYCDTVKQIYPYNNSQRLLNVIDMAIFDFLIGNMDRHHYEMFTKF
GDDGFLIHLDNARGFGRHSHDEISILSPLSQCCMIKKKTLLHLQLLAQADYRLSDVMRES
LLEDQLSPVLTEPHLLALDRRLQTILRTVEGCIVAHGQQSVIVDGPVEQLAPDSGQANLT
S
NT seq 1626 nt   +upstreamnt  +downstreamnt
atgccggggctgcgccgggaccgcctactgactctgctgctgctgggcgcgctgctctcc
gccgacctctacttccacctctggccccaagtacagcgccagctgcggcctcgggagcgc
ccgcgggggtgcccgtgcaccggccgcgcctcctccctggcgcgggactcggccgcagct
gcctcggaccccggcacgatcgtgcacaacttttcccgaaccgagccccggactgaaccg
gctggcggcagccacagcgggtcgagctccaagttgcaggccctcttcgcccacccgctg
tacaacgtcccggaggagccgcctctcctgggagccgaggactcgctcctggccagccag
gaggcgctgcggtattaccggaggaaggtggcccgctggaacaggcgacacaagatgtac
agagagcagatgaaccttacctccctggaccccccactgcagctccgactcgaggccagc
tgggtccagttccacctgggtattaaccgccatgggctctactcccggtccagccctgtt
gtcagcaaacttctgcaagacatgaggcactttcccaccatcagtgctgattacagtcaa
gatgagaaagccttgctgggggcatgtgactgcacccagattgtgaaacccagtggggtc
cacctcaagctggtgctgaggttctcggatttcgggaaggccatgttcaaacccatgaga
cagcagcgagatgaggagacaccagtggacttcttctacttcattgactttcagagacac
aatgctgagatcgcagctttccatctggacaggattctggacttccgacgggtgccgcca
acagtggggaggatagtaaatgtcaccaaggaaatcctagaggtcaccaagaatgaaatc
ctgcagagtgttttctttgtctctccagcgagcaacgtgtgcttcttcgccaagtgtcca
tacatgtgcaagacggagtatgctgtctgtggcaacccacacctgctggagggttccctc
tctgccttcctgccgtccctcaacctggcccccaggctgtctgtgcccaacccctggatc
cgctcctacacactggcaggaaaagaggagtgggaggtcaatcccctttactgtgacaca
gtgaaacagatctacccgtacaacaacagccagcggctcctcaatgtcatcgacatggcc
atcttcgacttcttgatagggaatatggaccggcaccattatgagatgttcaccaagttc
ggggatgatgggttccttattcaccttgacaacgccagagggttcggacgacactcccat
gatgaaatctccatcctctcgcctctctcccagtgctgcatgataaaaaagaaaacactt
ttgcacctgcagctgctggcccaagctgactacagactcagcgatgtgatgcgagaatca
ctgctggaagaccagctcagccctgtcctcactgaaccccacctccttgccctggatcga
aggctccaaaccatcctaaggacagtggaggggtgcatagtggcccatggacagcagagt
gtcatagtcgacggcccagtggaacagttggccccagactctggccaggctaacttgaca
agctaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (14)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (14)   
   UniProt (3)   
   SWISS-PROT (1)   
   RefSeq(pep) (10)   
DNA sequence (43)   
   RefSeq(nuc) (19)   
   GenBank (12)   
   EMBL (12)   
3D Structure (4)   
   PDB (4)   
Protein domain (4)   
   Pfam (4)   
All databases (81)   

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