KEGG   Homo sapiens (human): 8820
Entry
8820              CDS       T01001                                 
Symbol
HESX1, ANF, CPHD5, RPX
Name
(RefSeq) HESX homeobox 1
  KO
K09354  homeobox protein expressed in ES cells 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04550  Signaling pathways regulating pluripotency of stem cells
Disease
H00254  Growth hormone deficiency
H00544  Septo-optic dysplasia
H02036  Combined pituitary hormone deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    8820 (HESX1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    8820 (HESX1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    8820 (HESX1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN HTH_NDX
Other DBs
NCBI-GeneID: 8820
NCBI-ProteinID: NP_003856
OMIM: 601802
HGNC: 4877
Ensembl: ENSG00000163666
UniProt: Q9UBX0
Structure
LinkDB
Position
3:complement(57197838..57227615)
AA seq 185 aa
MSPSLQEGAQLGENKPSTCSFSIERILGLDQKKDCVPLMKPHRPWADTCSSSGKDGNLCL
HVPNPPSGISFPSVVDHPMPEERASKYENYFSASERLSLKRELSWYRGRRPRTAFTQNQI
EVLENVFRVNCYPGIDIREDLAQKLNLEEDRIQIWFQNRRAKLKRSHRESQFLMAKKNFN
TNLLE
NT seq 558 nt   +upstreamnt  +downstreamnt
atgtctcccagccttcaggaaggcgctcagctcggggaaaacaaaccctcaacttgctcc
ttttcaattgagagaatcttaggactggaccagaagaaagactgtgttccattaatgaaa
ccccacaggccctgggcagacacctgcagctcatcagggaaagatggtaacttatgtcta
catgtcccaaatcctcccagtgggatttcattccctagcgtggtggatcacccaatgcca
gaagaaagagcttcgaaatatgaaaattacttttcagcctcagaaagactgtctttgaaa
agagagttgagttggtatagaggccgaagaccaagaactgcttttactcaaaaccagatt
gaagtgttagaaaatgtctttagagtaaactgctatcctggtatcgatattagagaagac
ttagctcaaaaattgaatctagaggaagacagaatccagatttggtttcaaaatcggcgt
gcaaaactgaaaaggtcccatagagaatcacagtttctaatggcgaaaaaaaatttcaac
acaaatctgctggaatag

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