KEGG   Homo sapiens (human): 4488
Entry
4488              CDS       T01001                                 
Symbol
MSX2, CRS2, FPP, HOX8, MSH, PFM, PFM1
Name
(RefSeq) msh homeobox 2
  KO
K09341  homeobox protein MSX
Organism
hsa  Homo sapiens (human)
Pathway
hsa05166  Human T-cell leukemia virus 1 infection
Disease
H00475  Enlarged parietal foramina/cranium bifidum
H02160  Craniosynostoses
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    4488 (MSX2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4488 (MSX2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: NKL
    4488 (MSX2)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN HTH_NDX Pacs-1 DUF7645
Other DBs
NCBI-GeneID: 4488
NCBI-ProteinID: NP_002440
OMIM: 123101
HGNC: 7392
Ensembl: ENSG00000120149
UniProt: P35548
LinkDB
Position
5:174724582..174730896
AA seq 267 aa
MASPSKGNDLFSPDEEGPAVVAGPGPGPGGAEGAAEERRVKVSSLPFSVEALMSDKKPPK
EASPLPAESASAGATLRPLLLSGHGAREAHSPGPLVKPFETASVKSENSEDGAAWMQEPG
RYSPPPRHMSPTTCTLRKHKTNRKPRTPFTTSQLLALERKFRQKQYLSIAERAEFSSSLN
LTETQVKIWFQNRRAKAKRLQEAELEKLKMAAKPMLPSSFSLPFPISSPLQAASIYGASY
PFHRPVLPIPPVGLYATPVGYGMYHLS
NT seq 804 nt   +upstreamnt  +downstreamnt
atggcttctccgtccaaaggcaatgacttgttttcgcccgacgaggagggcccagcagtg
gtggccggaccaggcccggggcctgggggcgccgagggggccgcggaggagcgccgcgtc
aaggtctccagcctgcccttcagcgtggaggcgctcatgtccgacaagaagccgcccaag
gaggcgtccccgctgccggccgaaagcgcctcggccggggccaccctgcggccactgctg
ctgtcggggcacggcgctcgggaagcgcacagccccgggccgctggtgaagcccttcgag
accgcctcggtcaagtcggaaaattcagaagatggagcggcgtggatgcaggaacccggc
cgatattcgccgccgccaagacatatgagccctaccacctgcaccctgaggaaacacaag
accaatcggaagccgcgcacgccctttaccacatcccagctcctcgccctggagcgcaag
ttccgtcagaaacagtacctctccattgcagagcgtgcagagttctccagctctctgaac
ctcacagagacccaggtcaaaatctggttccagaaccgaagggccaaggcgaaaagactg
caggaggcagaactggaaaagctgaaaatggctgcaaaacctatgctgccctccagcttc
agtctccctttccccatcagctcgcccctgcaggcagcgtccatatatggagcatcctac
ccgttccatagacctgtgcttcccatcccgcctgtgggactctatgccacgccagtggga
tatggcatgtaccacctgtcctaa

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