KEGG   Homo sapiens (human): 10661
Entry
10661             CDS       T01001                                 
Symbol
KLF1, EKLF, EKLF/KLF1
Name
(RefSeq) KLF transcription factor 1
  KO
K09204  krueppel-like factor 1
Organism
hsa  Homo sapiens (human)
Disease
H00917  Congenital dyserythropoietic anemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    10661 (KLF1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Zinc finger
   Cys2His2 SP/KLF family and related proteins
    10661 (KLF1)
SSDB
Motif
Pfam: EKLF_TAD1 zf-C2H2 EKLF_TAD2 zf-H2C2_2 zf-C2H2_4 zf-C2H2_8
Other DBs
NCBI-GeneID: 10661
NCBI-ProteinID: NP_006554
OMIM: 600599
HGNC: 6345
Ensembl: ENSG00000105610
UniProt: Q13351
Structure
Position
19:complement(12884422..12887201)
AA seq 362 aa
MATAETALPSISTLTALGPFPDTQDDFLKWWRSEEAQDMGPGPPDPTEPPLHVKSEDQPG
EEEDDERGADATWDLDLLLTNFSGPEPGGAPQTCALAPSEASGAQYPPPPETLGAYAGGP
GLVAGLLGSEDHSGWVRPALRARAPDAFVGPALAPAPAPEPKALALQPVYPGPGAGSSGG
YFPRTGLSVPAASGAPYGLLSGYPAMYPAPQYQGHFQLFRGLQGPAPGPATSPSFLSCLG
PGTVGTGLGGTAEDPGVIAETAPSKRGRRSWARKRQAAHTCAHPGCGKSYTKSSHLKAHL
RTHTGEKPYACTWEGCGWRFARSDELTRHYRKHTGQRPFRCQLCPRAFSRSDHLALHMKR
HL
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggccacagccgagaccgccttgccctccatcagcacactgaccgccctgggccccttc
ccggacacacaggatgacttcctcaagtggtggcgctccgaagaggcgcaggacatgggc
ccgggtcctcctgaccccacggagccgcccctccacgtgaagtctgaggaccagcccggg
gaggaagaggacgatgagaggggcgcggacgccacctgggacctggatctcctcctcacc
aacttctcgggcccggagcccggtggcgcgccccagacctgcgctctggcgcccagcgag
gcctccggggcgcaatatccgccgccgcccgagactctgggcgcatatgctggcggcccg
gggctggtggctgggcttttgggttcggaggatcactcgggttgggtgcgccctgccctg
cgagcccgggctcccgacgccttcgtgggcccagccctggctccagccccggcccccgag
cccaaggcgctggcgctgcaaccggtgtacccggggcccggcgccggctcctcgggtggc
tacttcccgcggaccgggctttcagtgcctgcggcgtcgggcgccccctacgggctactg
tccgggtaccccgcgatgtacccggcgcctcagtaccaagggcacttccagctcttccgc
gggctccagggacccgcgcccggtcccgccacgtccccctccttcctgagttgtttggga
cccgggacggtgggcactggactcggggggactgcagaggatccaggtgtgatagccgag
accgcgccatccaagcgaggccgacgttcgtgggcgcgcaagaggcaggcagcgcacacg
tgcgcgcacccgggttgcggcaagagctacaccaagagctcccacctgaaggcgcatctg
cgcacgcacacaggggagaagccatacgcctgcacgtgggaaggctgcggctggagattc
gcgcgctcggacgagctgacccgccactaccggaaacacacggggcagcgccccttccgc
tgccagctctgcccacgtgctttttcgcgctctgaccacctggccttgcacatgaagcgc
cacctttga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (1)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (27)   
   KEGG ORTHOLOGY (1)   
   RefGene (17)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (7)   
   RefSeq(nuc) (1)   
   GenBank (3)   
   EMBL (3)   
3D Structure (3)   
   PDB (3)   
Protein domain (6)   
   Pfam (6)   
All databases (54)   

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