KEGG   Homo sapiens (human): 338917
Entry
338917            CDS       T01001                                 
Symbol
VSX2, CHX10, HOX10, MCOP2, MCOPCB3, RET1
Name
(RefSeq) visual system homeobox 2
  KO
K09336  visual system homeobox protein 2
Organism
hsa  Homo sapiens (human)
Disease
H01027  Microphthalmia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    338917 (VSX2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    338917 (VSX2)
SSDB
Motif
Pfam: Homeodomain OAR Homeobox_KN
Other DBs
NCBI-GeneID: 338917
NCBI-ProteinID: NP_878314
OMIM: 142993
HGNC: 1975
Ensembl: ENSG00000119614
UniProt: P58304
Position
14:74239449..74262738
AA seq 361 aa
MTGKAGEALSKPKSETVAKSTSGGAPARCTGFGIQEILGLNKEPPSSHPRAALDGLAPGH
LLAARSVLSPAGVGGMGLLGPGGLPGFYTQPTFLEVLSDPQSVHLQPLGRASGPLDTSQT
ASSDSEDVSSSDRKMSKSALNQTKKRKKRRHRTIFTSYQLEELEKAFNEAHYPDVYAREM
LAMKTELPEDRIQVWFQNRRAKWRKREKCWGRSSVMAEYGLYGAMVRHSIPLPESILKSA
KDGIMDSCAPWLLGMHKKSLEAAAESGRKPEGERQALPKLDKMEQDERGPDAQAAISQEE
LRENSIAVLRAKAQEHSTKVLGTVSGPDSLARSTEKPEEEEAMDEDRPAERLSPPQLEDM
A
NT seq 1086 nt   +upstreamnt  +downstreamnt
atgacggggaaagcaggggaagcgctgagcaagcccaaatccgagacagtggccaagagt
acctcggggggcgccccggccaggtgcactgggttcggcatccaggagatcctgggcttg
aacaaggagcccccgagctcccacccgcgggcagcgctcgacggcctggcccccgggcac
ttgctggcggcgcgctcagtgctcagccccgcgggggtgggcggcatggggcttctgggg
cccggggggctccctggcttctacacgcagcccaccttcctggaagtgctgtccgacccg
cagagcgtccacttgcagccattgggcagagcatcggggccgctggacaccagccagacg
gccagctcggattctgaagatgtttcctccagcgatcgaaaaatgtccaaatctgcttta
aaccagaccaagaaacggaagaagcggcgacacaggacaatctttacctcctaccagcta
gaggagctggagaaggcattcaacgaagcccactacccagacgtctatgcccgggagatg
ctggccatgaaaacggagctgccggaagacaggatacaggtctggttccagaaccgtcga
gccaagtggaggaagcgggagaagtgctggggccggagcagtgtcatggcggagtatggg
ctctacggggccatggtgcggcactccatccccctgcccgagtccatcctcaagtcagcc
aaggatggcatcatggactcctgtgccccgtggctactggggatgcacaaaaagtcgctg
gaggcagcagccgagtcggggaggaagcccgagggggaacgccaggccctgcccaagctc
gacaagatggagcaggacgagcggggccccgacgctcaggcggccatctcccaggaggaa
ctgagggagaacagcattgcggtgctccgggccaaagctcaggagcacagcaccaaagtg
ctggggactgtgtctgggccggacagcctggcccggagtaccgagaagccagaggaggag
gaggccatggatgaagacaggccggcggagaggctcagtccaccgcagctggaggacatg
gcttag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (7)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   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 (5)   
   RefSeq(nuc) (1)   
   GenBank (2)   
   EMBL (2)   
Protein domain (3)   
   Pfam (3)   
All databases (25)   

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