KEGG   Homo sapiens (human): 5626
Entry
5626              CDS       T01001                                 
Symbol
PROP1, CPHD2, PROP-1
Name
(RefSeq) PROP paired-like homeobox 1
  KO
K09327  homeobox protein prophet of Pit-1
Organism
hsa  Homo sapiens (human)
Disease
H00254  Growth hormone deficiency
H02036  Combined pituitary hormone deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5626 (PROP1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    5626 (PROP1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN
Other DBs
NCBI-GeneID: 5626
NCBI-ProteinID: NP_006252
OMIM: 601538
HGNC: 9455
Ensembl: ENSG00000175325
UniProt: O75360 A0A0G2JQ02
Position
5:complement(177992235..177996242)
AA seq 226 aa
MEAERRRQAEKPKKGRVGSNLLPERHPATGTPTTTVDSSAPPCRRLPGAGGGRSRFSPQG
GQRGRPHSRRRHRTTFSPVQLEQLESAFGRNQYPDIWARESLARDTGLSEARIQVWFQNR
RAKQRKQERSLLQPLAHLSPAAFSSFLPESTACPYSYAAPPPPVTCFPHPYSHALPSQPS
TGGAFALSHQSEDWYPTLHPAPAGHLPCPPPPPMLPLSLEPSKSWN
NT seq 681 nt   +upstreamnt  +downstreamnt
atggaagcagaaaggaggcgccaggctgagaagccaaagaaggggcgagtcggcagcaac
ctgttgcctgagagacacccggccactgggaccccgaccaccacggtggactcgagtgct
ccaccctgcagaaggctccctggtgcaggaggggggagatcaaggttctccccgcaagga
ggacagaggggccgcccgcactcccggcgccgccaccgcaccaccttcagcccagtgcag
ttggaacagctggagtcagcctttgggaggaaccagtaccccgacatctgggcccgagag
agtcttgcccgggacactggcctcagtgaggcccgaatccaggtctggttccagaaccgc
agagctaagcaacggaagcaagagcgctcactgcttcagcctctggcccatctgtctcct
gccgccttttccagcttcttgccagagtccactgcttgcccctattcttacgcagcacca
ccaccaccagtgacctgcttccctcacccctacagccatgccctcccttcccagccctcc
acaggaggcgcctttgctttgtcacaccagtctgaggactggtaccctaccttgcaccca
gcccctgccggccatctgccctgccccccaccccctcccatgctccccctcagccttgag
ccatccaagtcctggaactga

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