KEGG   Homo sapiens (human): 3882
Entry
3882              CDS       T01001                                 
Symbol
KRT32, HA2, HKA2, KRTHA2, hHa2
Name
(RefSeq) keratin 32
  KO
K07604  type I keratin, acidic
Organism
hsa  Homo sapiens (human)
Pathway
hsa04382  Cornified envelope formation
hsa04915  Estrogen signaling pathway
hsa05150  Staphylococcus aureus infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09152 Endocrine system
   04915 Estrogen signaling pathway
    3882 (KRT32)
  09158 Development and regeneration
   04382 Cornified envelope formation
    3882 (KRT32)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05150 Staphylococcus aureus infection
    3882 (KRT32)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    3882 (KRT32)
   04147 Exosome [BR:hsa04147]
    3882 (KRT32)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Intermediate filaments
   Intermediate filaments
    Types I and II: Acidic and basic keratins
     3882 (KRT32)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of epithelial cells
   3882 (KRT32)
  Exosomal proteins of other body fluids (saliva and urine)
   3882 (KRT32)
  Exosomal proteins of colorectal cancer cells
   3882 (KRT32)
  Exosomal proteins of melanoma cells
   3882 (KRT32)
SSDB
Motif
Pfam: Filament FKBP15 Uso1_p115_C INO80F TPR_MLP1_2 CCDC39 Lzipper-MIP1 Baculo_PEP_C CoV_S2 TMEM120A-B Spore_GerAC FliD_C Rab11-FIP3
Other DBs
NCBI-GeneID: 3882
NCBI-ProteinID: NP_002269
OMIM: 602760
HGNC: 6449
Ensembl: ENSG00000108759
UniProt: Q14532
Position
17:complement(41459513..41467386)
AA seq 448 aa
MTSSCCVTNNLQASLKSCPRPASVCSSGVNCRPELCLGYVCQPMACLPSVCLPTTFRPAS
CLSKTYLSSSCQAASGISGSMGPGSWYSEGAFNGNEKETMQFLNDRLASYLTRVRQLEQE
NAELESRIQEASHSQVLTMTPDYQSHFRTIEELQQKILCTKAENARMVVNIDNAKLAADD
FRAKYEAELAMRQLVEADINGLRRILDDLTLCKADLEAQVESLKEELMCLKKNHEEEVGS
LRCQLGDRLNIEVDAAPPVDLTRVLEEMRCQYEAMVEANRRDVEEWFNMQMEELNQQVAT
SSEQLQNYQSDIIDLRRTVNTLEIELQAQHSLRDSLENTLTESEARYSSQLAQMQCMITN
VEAQLAEIRADLERQNQEYQVLLDVRARLEGEINTYRSLLENEDCKLPCNPCSTPSCTTC
VPSPCVPRTVCVPRTVGMPCSPCPQGRY
NT seq 1347 nt   +upstreamnt  +downstreamnt
atgacatcctcctgctgtgtcaccaacaacttgcaagcctctctcaagagctgcccccgg
cctgcctcggtctgttccagcggcgtgaactgccggcctgagctgtgcctgggctatgtc
tgccagcccatggcatgcctgccttcggtctgcctgcccaccaccttccggccagccagc
tgcctctccaaaacctatctatccagttcctgccaggcagccagtggcatctccggctcc
atgggccccggcagctggtacagcgaaggggccttcaatggcaatgagaaggaaaccatg
cagttccttaacgaccgcctggccagctacctgacgagggtgcggcagctggagcaggag
aatgcggagctggagagcaggatccaagaggcctctcactcccaggtgctcaccatgact
cctgactaccagtctcatttcaggaccattgaggagctccagcagaagattctgtgtacc
aaggcagagaatgccaggatggttgtgaacattgataatgccaaactggctgccgatgac
ttcagggccaagtacgaggcagagctggccatgcggcagctggtggaggccgacatcaat
ggcctgcgcaggatcctggatgatctcactctgtgcaaggctgacctggaggcccaggtt
gagtccctgaaggaggagctgatgtgcctcaaaaagaaccatgaggaggaagtcggttcc
cttcgatgccagcttggggaccgccttaacatcgaggtggacgctgcacccccggtggac
ctgaccagggtgctggaggagatgcggtgtcagtacgaggccatggtggaggccaaccgc
agggacgtggaggaatggttcaatatgcagatggaggagcttaaccaacaggtggccaca
agctctgagcagcttcagaactaccagtcagacatcattgacctgagacgcacggtcaac
acgctggagatcgagctgcaggcccagcacagcctgagggactccctggaaaacacgctg
acggagagtgaggcccgctacagctcccagctggcccagatgcagtgcatgatcaccaac
gttgaggcccagctggctgagatccgggctgacctggagcggcagaaccaggagtaccag
gtgctgctggacgtccgggcccggctggagggcgagatcaacacgtaccggagcctgctg
gagaacgaggactgcaagctgccctgtaacccatgctccactccttcctgcaccacctgt
gtgccctccccatgcgtgccccgcaccgtctgtgtgccacgcactgttggcatgccttgc
tcaccctgcccccagggccgctactga

  All links  
Disease (1)   
   OMIM (1)   
Gene (26)   
   RefGene (21)   
   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 (7)   
   RefSeq(nuc) (3)   
   GenBank (2)   
   EMBL (2)   
Protein domain (13)   
   Pfam (13)   
All databases (50)   

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