KEGG   Homo sapiens (human): 3181
Entry
3181              CDS       T01001                                 
Symbol
HNRNPA2B1, HNRNPA2, HNRNPB1, HNRPA2, HNRPA2B1, HNRPB1, IBMPFD2, OPMD2, RNPA2, SNRPB1
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein A2/B1
  KO
K13158  heterogeneous nuclear ribonucleoprotein A2/B1
Organism
hsa  Homo sapiens (human)
Pathway
hsa05014  Amyotrophic lateral sclerosis
Disease
H00704  Oculopharyngeal muscular dystrophy
H02031  Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    3181 (HNRNPA2B1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    3181 (HNRNPA2B1)
   03041 Spliceosome [BR:hsa03041]
    3181 (HNRNPA2B1)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    3181 (HNRNPA2B1)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   Factors involved in mRNA localization
    Trans-acting binding proteins
     3181 (HNRNPA2B1)
Spliceosome [BR:hsa03041]
 Other splicing related proteins
  Spliceosome associated proteins (SAPs)
   hnRNP proteins
    3181 (HNRNPA2B1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   3181 (HNRNPA2B1)
  Exosomal proteins of colorectal cancer cells
   3181 (HNRNPA2B1)
SSDB
Motif
Pfam: RRM_1 HnRNPA1_LC RRM_7
Other DBs
NCBI-GeneID: 3181
NCBI-ProteinID: NP_112533
OMIM: 600124
HGNC: 5033
Ensembl: ENSG00000122566
UniProt: P22626
Structure
Position
7:complement(26189927..26200746)
AA seq 353 aa
MEKTLETVPLERKKREKEQFRKLFIGGLSFETTEESLRNYYEQWGKLTDCVVMRDPASKR
SRGFGFVTFSSMAEVDAAMAARPHSIDGRVVEPKRAVAREESGKPGAHVTVKKLFVGGIK
EDTEEHHLRDYFEEYGKIDTIEIITDRQSGKKRGFGFVTFDDHDPVDKIVLQKYHTINGH
NAEVRKALSRQEMQEVQSSRSGRGGNFGFGDSRGGGGNFGPGPGSNFRGGSDGYGSGRGF
GDGYNGYGGGPGGGNFGGSPGYGGGRGGYGGGGPGYGNQGGGYGGGYDNYGGGNYGSGNY
NDFGNYNQQPSNYGPMKSGNFGGSRNMGGPYGGGNYGPGGSGGSGGYGGRSRY
NT seq 1062 nt   +upstreamnt  +downstreamnt
atggagaaaactttagaaactgttcctttggagaggaaaaagagagaaaaggaacagttc
cgtaagctctttattggtggcttaagctttgaaaccacagaagaaagtttgaggaactac
tacgaacaatggggaaagcttacagactgtgtggtaatgagggatcctgcaagcaaaaga
tcaagaggatttggttttgtaactttttcatccatggctgaggttgatgctgccatggct
gcaagacctcattcaattgatgggagagtagttgagccaaaacgtgctgtagcaagagag
gaatctggaaaaccaggggctcatgtaactgtgaagaagctgtttgttggcggaattaaa
gaagatactgaggaacatcaccttagagattactttgaggaatatggaaaaattgatacc
attgagataattactgataggcagtctggaaagaaaagaggctttggctttgttactttt
gatgaccatgatcctgtggataaaatcgtattgcagaaataccataccatcaatggtcat
aatgcagaagtaagaaaggctttgtctagacaagaaatgcaggaagttcagagttctagg
agtggaagaggaggcaactttggctttggggattcacgtggtggcggtggaaatttcgga
ccaggaccaggaagtaactttagaggaggatctgatggatatggcagtggacgtggattt
ggggatggctataatgggtatggaggaggacctggaggtggcaattttggaggtagcccc
ggttatggaggaggaagaggaggatatggtggtggaggacctggatatggcaaccagggt
gggggctacggaggtggttatgacaactatggaggaggaaattatggaagtggaaattac
aatgattttggaaattataaccagcaaccttctaactacggtccaatgaagagtggaaac
tttggtggtagcaggaacatggggggaccatatggtggaggaaactatggtccaggaggc
agtggaggaagtgggggttatggtgggaggagccgatactga

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