KEGG   Homo sapiens (human): 83986
Entry
83986             CDS       T01001                                 
Symbol
FAM234A, C16orf9, ITFG3, gs19
Name
(RefSeq) family with sequence similarity 234 member A
  KO
K17258  integrin alpha FG-GAP repeat containing protein 3
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    83986 (FAM234A)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   83986 (FAM234A)
SSDB
Motif
Pfam: FG-GAP_3 FG-GAP DUF6766 PQQ_2
Other DBs
NCBI-GeneID: 83986
NCBI-ProteinID: NP_001271426
HGNC: 14163
Ensembl: ENSG00000167930
UniProt: Q9H0X4
Position
16:234821..269963
AA seq 552 aa
MLDHKDLEAEIHPLKNEERKSQENLGNPSKNEDNVKSAPPQSRLSRCRAAAFFLSLFLCL
FVVFVVSFVIPCPDRPASQRMWRIDYSAAVIYDFLAVDDINGDRIQDVLFLYKNTNSSNN
FSRSCVDEGFSSPCTFAAAVSGANGSTLWERPVAQDVALVECAVPQPRGSEAPSACILVG
RPSSFIAVNLFTGETLWNHSSSFSGNASILSPLLQVPDVDGDGAPDLLVLTQEREEVSGH
LYSGSTGHQIGLRGSLGVDGESGFLLHVTRTGAHYILFPCASSLCGCSVKGLYEKVTGSG
GPFKSDPHWESMLNATTRRMLSHSSGAVRYLMHVPGNAGADVLLVGSEAFVLLDGQELTP
RWTPKAAHVLRKPIFGRYKPDTLAVAVENGTGTDRQILFLDLGTGAVLCSLALPSLPGGP
LSASLPTADHRSAFFFWGLHELGSTSETETGEARHSLYMFHPTLPRVLLELANVSTHIVA
FDAVLFEPSRHAAYILLTGPADSEAPGLVSVIKHKVRDLVPSSRVVRLGEGGPDSDQAIR
DRFSRLRYQSEA
NT seq 1659 nt   +upstreamnt  +downstreamnt
atgttggaccacaaggacttagaggccgaaatccaccccttgaaaaatgaagaaagaaaa
tcgcaggaaaatctgggaaatccatcaaaaaatgaggataacgtgaaaagcgcgcctcca
cagtcccggctctcccggtgccgagcggcggcgttttttctttcattgtttctctgcctt
tttgtggtgttcgtcgtctcattcgtcatcccgtgtccagaccggccggcgtcacagcga
atgtggaggatagactacagtgccgctgttatctatgactttctggctgtggatgatata
aacggggacaggatccaagatgttctttttctttataaaaacaccaacagcagcaacaat
ttcagccgatcctgtgtggacgaaggcttttcctctccctgcacctttgcagctgctgtg
tcgggggccaacggcagcacgctctgggagagacctgtggcccaagacgtggccctcgtg
gagtgtgctgtgccccagccaagaggcagtgaggcaccttctgcctgcatcctggtgggc
agacccagttctttcattgcagtcaacttgttcacaggggaaaccctgtggaaccacagc
agcagcttcagcgggaatgcgtccatcctgagccctctgctgcaggtgcctgatgtggac
ggcgatggggccccagacctgctggttctcacccaggagcgggaggaggttagtggccac
ctctactccggcagcaccgggcaccagattggcctcagaggcagccttggtgtggacggg
gaaagtggcttcctccttcacgtcaccaggacaggtgcccactacatcctctttccctgc
gcaagctccctctgcggctgctctgtgaagggtctctacgagaaggtgaccgggagcggc
ggcccgttcaagagtgacccgcactgggagagcatgctcaatgccaccacccgcaggatg
ctttcccacagctctggagcagtgcgctacctgatgcatgtcccagggaacgccggtgca
gatgtgcttcttgtgggctcagaggccttcgtgctgctggacgggcaggagctgacgcct
cgctggacacccaaggcagcccatgtcctgagaaaacccatcttcggccgctacaaacca
gacaccttggctgtagccgttgaaaacggaactggcaccgacagacagatcctgtttctg
gaccttggcactggagccgtcctgtgtagcctagccctcccgagcctccctgggggtcca
ctgtccgccagcctgccgaccgcagaccaccgctcagccttcttcttctggggcctccac
gagctggggagcaccagcgagacggagaccggggaggcccggcacagcctgtacatgttc
caccccaccctgccgcgcgtgctgctggagctggccaatgtctctacccacattgtcgcc
tttgacgccgtcctgtttgagccaagccgccacgccgcctacatccttctgacaggcccg
gcagactcagaggcacccggcctggtctctgtgatcaagcacaaggtgcgggaccttgtc
ccaagcagcagggtggtccgcctgggtgagggtgggccagacagtgaccaagccatcagg
gaccggttctcccggctgcggtaccagagtgaggcgtag

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