Homo sapiens (human): 8820
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Homeobox_KN
HTH_NDX
Motif
Other DBs
NCBI-GeneID:
8820
NCBI-ProteinID:
NP_003856
OMIM:
601802
HGNC:
4877
Ensembl:
ENSG00000163666
UniProt:
Q9UBX0
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:complement(57197838..57227615)
Genome browser
AA seq
185 aa
AA seq
DB search
MSPSLQEGAQLGENKPSTCSFSIERILGLDQKKDCVPLMKPHRPWADTCSSSGKDGNLCL
HVPNPPSGISFPSVVDHPMPEERASKYENYFSASERLSLKRELSWYRGRRPRTAFTQNQI
EVLENVFRVNCYPGIDIREDLAQKLNLEEDRIQIWFQNRRAKLKRSHRESQFLMAKKNFN
TNLLE
NT seq
558 nt
NT seq
+upstream
nt +downstream
nt
atgtctcccagccttcaggaaggcgctcagctcggggaaaacaaaccctcaacttgctcc
ttttcaattgagagaatcttaggactggaccagaagaaagactgtgttccattaatgaaa
ccccacaggccctgggcagacacctgcagctcatcagggaaagatggtaacttatgtcta
catgtcccaaatcctcccagtgggatttcattccctagcgtggtggatcacccaatgcca
gaagaaagagcttcgaaatatgaaaattacttttcagcctcagaaagactgtctttgaaa
agagagttgagttggtatagaggccgaagaccaagaactgcttttactcaaaaccagatt
gaagtgttagaaaatgtctttagagtaaactgctatcctggtatcgatattagagaagac
ttagctcaaaaattgaatctagaggaagacagaatccagatttggtttcaaaatcggcgt
gcaaaactgaaaaggtcccatagagaatcacagtttctaatggcgaaaaaaaatttcaac
acaaatctgctggaatag
DBGET
integrated database retrieval system