Homo sapiens (human): 1749
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Entry
1749 CDS
T01001
Symbol
DLX5, SHFM1, SHFM1D
Name
(RefSeq) distal-less homeobox 5
KO
K18489
homeobox protein DLX5
Organism
hsa
Homo sapiens (human)
Pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
Disease
H00471
Split-hand/foot malformation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
1749 (DLX5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
1749 (DLX5)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain ANTP: NKL
1749 (DLX5)
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DLL_N
Homeodomain
Homeobox_KN
YdaS_toxin
Motif
Other DBs
NCBI-GeneID:
1749
NCBI-ProteinID:
NP_005212
OMIM:
600028
HGNC:
2918
Ensembl:
ENSG00000105880
UniProt:
P56178
Q53Y73
Structure
PDB
PDBj
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Position
7:complement(97020396..97024831)
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AA seq
289 aa
AA seq
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MTGVFDRRVPSIRSGDFQAPFQTSAAMHHPSQESPTLPESSATDSDYYSPTGGAPHGYCS
PTSASYGKALNPYQYQYHGVNGSAGSYPAKAYADYSYASSYHQYGGAYNRVPSATNQPEK
EVTEPEVRMVNGKPKKVRKPRTIYSSFQLAALQRRFQKTQYLALPERAELAASLGLTQTQ
VKIWFQNKRSKIKKIMKNGEMPPEHSPSSSDPMACNSPQSPAVWEPQGSSRSLSHHPHAH
PPTSNQSPASSYLENSASWYTSAASSINSHLPPPGSLQHPLALASGTLY
NT seq
870 nt
NT seq
+upstream
nt +downstream
nt
atgacaggagtgtttgacagaagggtccccagcatccgatccggcgacttccaagctccg
ttccagacgtccgcagctatgcaccatccgtctcaggaatcgccaactttgcccgagtct
tcagctaccgattctgactactacagccctacggggggagccccgcacggctactgctct
cctacctcggcttcctatggcaaagctctcaacccctaccagtatcagtatcacggcgtg
aacggctccgccgggagctacccagccaaagcttatgccgactatagctacgctagctcc
taccaccagtacggcggcgcctacaaccgcgtcccaagcgccaccaaccagccagagaaa
gaagtgaccgagcccgaggtgagaatggtgaatggcaaaccaaagaaagttcgtaaaccc
aggactatttattccagctttcagctggccgcattacagagaaggtttcagaagactcag
tacctcgccttgccggaacgcgccgagctggccgcctcgctgggattgacacaaacacag
gtgaaaatctggtttcagaacaaaagatccaagatcaagaagatcatgaaaaacggggag
atgcccccggagcacagtcccagctccagcgacccaatggcgtgtaactcgccgcagtct
ccagcggtgtgggagccccagggctcgtcccgctcgctcagccaccaccctcatgcccac
cctccgacctccaaccagtccccagcgtccagctacctggagaactctgcatcctggtac
acaagtgcagccagctcaatcaattcccacctgccgccgccgggctccttacagcacccg
ctggcgctggcctccgggacactctattag
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