KEGG   Homo sapiens (human): 3199
Entry
3199              CDS       T01001                                 
Symbol
HOXA2, HOX1K, MCOHI
Name
(RefSeq) homeobox A2
  KO
K09302  homeobox protein HoxA/B2
Organism
hsa  Homo sapiens (human)
Disease
H01286  Microtia hearing impairment and cleft palate
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    3199 (HOXA2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: HOXL
    3199 (HOXA2)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN
Other DBs
NCBI-GeneID: 3199
NCBI-ProteinID: NP_006726
OMIM: 604685
HGNC: 5103
Ensembl: ENSG00000105996
UniProt: O43364
Position
7:complement(27100354..27102683)
AA seq 376 aa
MNYEFEREIGFINSQPSLAECLTSFPPVADTFQSSSIKTSTLSHSTLIPPPFEQTIPSLN
PGSHPRHGAGGRPKPSPAGSRGSPVPAGALQPPEYPWMKEKKAAKKTALLPAAAAAATAA
ATGPACLSHKESLEIADGSGGGSRRLRTAYTNTQLLELEKEFHFNKYLCRPRRVEIAALL
DLTERQVKVWFQNRRMKHKRQTQCKENQNSEGKCKSLEDSEKVEEDEEEKTLFEQALSVS
GALLEREGYTFQQNALSQQQAPNGHNGDSQSFPVSPLTSNEKNLKHFQHQSPTVPNCLST
MGQNCGAGLNNDSPEALEVPSLQDFSVFSTDSCLQLSDAVSPSLPGSLDSPVDISADSLD
FFTDTLTTIDLQHLNY
NT seq 1131 nt   +upstreamnt  +downstreamnt
atgaattacgaatttgagcgagagattggttttatcaatagccagccgtcgctcgctgag
tgcctgacatcttttccccctgtcgctgatacatttcaaagttcatcaatcaagacctcg
acgctttcacactcgacactgattcctcctccttttgagcagaccattcccagcctgaac
cccggcagtcaccctcgccacggcgctggcggccgccccaagccgagccccgcgggcagc
cgcggcagcccggtgcccgccggcgccctgcagccgcccgagtacccctggatgaaggag
aagaaggcggccaagaaaaccgcacttctgccggccgccgccgccgccgccaccgccgca
gccaccggccctgcttgcctcagccacaaagaatccctggaaatcgccgatggcagcggc
gggggatcgcggcgcctgagaactgcttacaccaacacacagcttctagagctggaaaaa
gaatttcatttcaacaagtacctttgcagaccccgaagggtggagattgcagcgctgctg
gatttgactgagagacaagtgaaagtgtggtttcagaaccggaggatgaagcacaagagg
cagacccagtgcaaggaaaaccaaaacagcgaagggaaatgtaaaagccttgaggactcc
gagaaagtagaggaggacgaggaagagaagacgctctttgagcaagcccttagcgtctct
ggggcccttctggagagggaaggctacacttttcagcaaaatgccctctctcagcagcag
gctcccaatggacacaatggcgactcccaaagtttcccagtctcgcctttaaccagcaat
gagaaaaatctgaaacattttcagcaccagtcacccactgttcccaactgcttgtcaaca
atgggccagaactgtggagctggcctaaacaatgacagtcctgaggcccttgaggtcccc
tctttgcaggactttagcgttttctccacagattcctgcctgcagctttcagatgcagtt
tcacccagtttgccaggttccctcgacagtcccgtagatatttcagctgacagcttagac
ttttttacagacacactcaccacaatcgacttgcagcatctgaattactaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (23)   
   RefSeq(nuc) (1)   
   GenBank (11)   
   EMBL (11)   
Protein domain (2)   
   Pfam (2)   
All databases (48)   

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