KEGG   Homo sapiens (human): 3166
Entry
3166              CDS       T01001                                 
Symbol
HMX1, H6, NKX5-3
Name
(RefSeq) H6 family homeobox 1
  KO
K09349  homeobox protein Nkx-5
Organism
hsa  Homo sapiens (human)
Disease
H01012  Oculo-auricular syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    3166 (HMX1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: NKL
    3166 (HMX1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN
Other DBs
NCBI-GeneID: 3166
NCBI-ProteinID: NP_061815
OMIM: 142992
HGNC: 5017
Ensembl: ENSG00000215612
UniProt: Q9NP08
Position
4:complement(8846076..8871839)
AA seq 348 aa
MPDELTEPGRATPARASSFLIENLLAAEAKGAGRATQGDGSREDEEEDDDDPEDEDAEQA
RRRRLQRRRQLLAGTGPGGEARARALLGPGALGLGPRPPPGPGPPFALGCGGAARWYPRA
HGGYGGGLSPDTSDRDSPETGEEMGRAEGAWPRGPGPGAVQREAAELAARGPAAGTEEAS
ELAEVPAAAGETRGGVGVGGGRKKKTRTVFSRSQVFQLESTFDLKRYLSSAERAGLAASL
QLTETQVKIWFQNRRNKWKRQLAAELEAASLSPPGAQRLVRVPVLYHESPPAAAAAGPPA
TLPFPLAPAAPAPPPPLLGFSGALAYPLAAFPAAASVPFLRAQMPGLV
NT seq 1047 nt   +upstreamnt  +downstreamnt
atgcctgacgagctgacggagcccgggcgcgccacgccggcccgcgcctcctccttcctc
atcgagaacctgctggcggccgaggccaagggcgcagggcgcgcgacccagggcgacggc
agccgggaggacgaggaggaggacgacgacgaccccgaagacgaggacgccgagcaggcg
cggcggcgacggctacagcggcggcgacagttgctcgcgggcaccgggcccggcggggag
gcgcgggcccgtgcgctgctcgggccgggcgcgctgggcctcggtcctcggccgcccccc
ggtcccgggccgcccttcgctctgggctgcggaggcgcagcgcgctggtacccacgggcg
cacggtggctatggaggcggcctcagtcctgacaccagcgaccgggactcaccggagacg
ggcgaggagatgggccgtgcggagggcgcctggccgcgaggccccgggccgggagcggtg
cagcgggaggcagcggagctggcggcgcgtggcccggcggccggcacggaggaggcgtcg
gagctggccgaggtccctgcggcggctggggagacacgcggcggcgttggcgtgggcggc
ggccgaaagaagaagacgcgcacagtcttctcccgcagccaggtcttccagctggaatcc
accttcgacctgaagcgctacctgagcagcgccgagcgcgccggcctggccgcctccctg
cagctcaccgagacgcaggttaagatctggttccagaaccgccgcaacaagtggaagcgg
cagctggcagccgagctggaggcggccagcctgtccccgccgggagcgcagcgcctggtc
cgcgtgccggtgctctaccacgaaagccccccggccgcagccgccgctgggcccccggcc
accctgcccttcccgctggcgcccgccgcgcccgcgccgcccccaccgctgctcggcttc
tccggggccctcgcctacccgctggccgccttcccggccgccgcctccgtgccctttctg
cgggcgcagatgcctggcctggtgtga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (12)   
   RefSeq(nuc) (2)   
   GenBank (5)   
   EMBL (5)   
Protein domain (2)   
   Pfam (2)   
All databases (41)   

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