KEGG   Homo sapiens (human): 2018
Entry
2018              CDS       T01001                                 
Symbol
EMX2
Name
(RefSeq) empty spiracles homeobox 2
  KO
K09317  homeobox protein EMX
Organism
hsa  Homo sapiens (human)
Disease
H01160  Schizencephaly
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    2018 (EMX2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: NKL
    2018 (EMX2)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN DUF874
Other DBs
NCBI-GeneID: 2018
NCBI-ProteinID: NP_004089
OMIM: 600035
HGNC: 3341
Ensembl: ENSG00000170370
UniProt: Q04743
Position
10:117542746..117549546
AA seq 252 aa
MFQPAPKRCFTIESLVAKDSPLPASRSEDPIRPAALSYANSSPINPFLNGFHSAAAAAAG
RGVYSNPDLVFAEAVSHPPNPAVPVHPVPPPHALAAHPLPSSHSPHPLFASQQRDPSTFY
PWLIHRYRYLGHRFQGNDTSPESFLLHNALARKPKRIRTAFSPSQLLRLEHAFEKNHYVV
GAERKQLAHSLSLTETQVKVWFQNRRTKFKRQKLEEEGSDSQQKKKGTHHINRWRIATKQ
ASPEEIDVTSDD
NT seq 759 nt   +upstreamnt  +downstreamnt
atgttccagccggcgcccaagcgctgcttcaccatcgagtcgctggtggccaaggacagt
cccctgcccgcctcgcgctccgaggaccccatccgtcccgcggcactcagctacgctaac
tccagccccataaatccgttcctcaacggcttccactcggccgccgccgccgccgccggt
aggggcgtctactccaacccggacttggtgttcgccgaggcggtctcgcacccgcccaac
cccgccgtgccagtgcacccggtgccgccgccgcacgccctggccgcccaccccctaccc
tcctcgcactcgccacaccccctattcgcctcgcagcagcgggatccgtccaccttctac
ccctggctcatccaccgctaccgatatctgggtcatcgcttccaagggaacgacactagc
cccgagagtttccttttgcacaacgcgctggcccgaaagcccaagcggatccgaaccgcc
ttctccccgtcccagcttctaaggctggaacacgcctttgagaagaatcactacgtggtg
ggcgccgaaaggaagcagctggcacacagcctcagcctcacggaaactcaggtaaaagta
tggtttcagaaccgaagaacaaagttcaaaaggcagaagctggaggaagaaggctcagat
tcgcaacaaaagaaaaaagggacgcaccatattaaccggtggagaatcgccaccaagcag
gcgagtccggaggaaatagacgtgacctcagatgattaa

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