KEGG   Homo sapiens (human): 3198
Entry
3198              CDS       T01001                                 
Symbol
HOXA1, BSAS, HOX1, HOX1F
Name
(RefSeq) homeobox A1
  KO
K09301  homeobox protein HoxA/B/D1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04550  Signaling pathways regulating pluripotency of stem cells
Disease
H00727  Athabascan brainstem dysgenesis syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    3198 (HOXA1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    3198 (HOXA1)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: HOXL
    3198 (HOXA1)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN PHC2_SAM_assoc
Other DBs
NCBI-GeneID: 3198
NCBI-ProteinID: NP_005513
OMIM: 142955
HGNC: 5099
Ensembl: ENSG00000105991
Pharos: P49639(Tbio)
UniProt: P49639
Position
7:complement(27092993..27096000)
AA seq 335 aa
MDNARMNSFLEYPILSSGDSGTCSARAYPSDHRITTFQSCAVSANSCGGDDRFLVGRGVQ
IGSPHHHHHHHHRHPQPATYQTSGNLGVSYSHSSCGPSYGSQNFSAPYSPYALNQEADVS
GGYPQCAPAVYSGNLSSPMVQHHHHHQGYAGGAVGSPQYIHHSYGQEHQSLALATYNNSL
SPLHASHQEACRSPASETSSPAQTFDWMKVKRNPPKTGKVGEYGYLGQPNAVRTNFTTKQ
LTELEKEFHFNKYLTRARRVEIAASLQLNETQVKIWFQNRRMKQKKREKEGLLPISPATP
PGNDEKAEESSEKSSSSPCVPSPGSSTSDTLTTSH
NT seq 1008 nt   +upstreamnt  +downstreamnt
atggacaatgcaagaatgaactccttcctggaataccccatacttagcagtggcgactcg
gggacctgctcagcccgagcctacccctcggaccataggattacaactttccagtcgtgc
gcggtcagcgccaacagttgcggcggcgacgaccgcttcctagtgggcaggggggtgcag
atcggttcgccccaccaccaccaccaccaccaccatcgccacccccagccggctacctac
cagacttccgggaacctgggggtgtcctactcccactcaagttgtggtccaagctatggc
tcacagaacttcagtgcgccttacagcccctacgcgttaaatcaggaagcagacgtaagt
ggtgggtacccccagtgcgctcccgctgtttactctggaaatctctcatctcccatggtc
cagcatcaccaccaccaccagggttatgctgggggcgcggtgggctcgcctcaatacatt
caccactcatatggacaggagcaccagagcctggccctggctacgtataataactccttg
tcccctctccacgccagccaccaagaagcctgtcgctcccccgcatcggagacatcttct
ccagcgcagacttttgactggatgaaagtcaaaagaaaccctcccaaaacagggaaagtt
ggagagtacggctacctgggtcaacccaacgcggtgcgcaccaacttcactaccaagcag
ctcacggaactggagaaggagttccacttcaacaagtacctgacgcgcgcccgcagggtg
gagatcgctgcatccctgcagctcaacgagacccaagtgaagatctggttccagaaccgc
cgaatgaagcaaaagaaacgtgagaaggagggtctcttgcccatctctccggccaccccg
ccaggaaacgacgagaaggccgaggaatcctcagagaagtccagctcttcgccctgcgtt
ccttccccggggtcttctacctcagacactctgactacctcccactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (19)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
   PHAROS (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (20)   
   RefSeq(nuc) (2)   
   GenBank (9)   
   EMBL (9)   
Protein domain (3)   
   Pfam (3)   
All databases (53)   

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