KEGG   Homo sapiens (human): 60529
Entry
60529             CDS       T01001                                 
Symbol
ALX4, CRS5, FND2, PFM2
Name
(RefSeq) ALX homeobox 4
  KO
K09451  homeobox protein aristaless-like 4
Organism
hsa  Homo sapiens (human)
Disease
H00475  Enlarged parietal foramina/cranium bifidum
H00528  Frontonasal dysplasia
H02160  Craniosynostoses
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    60529 (ALX4)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain Paired-related
    60529 (ALX4)
SSDB
Motif
Pfam: Homeodomain OAR Homeobox_KN
Other DBs
NCBI-GeneID: 60529
NCBI-ProteinID: NP_068745
OMIM: 605420
HGNC: 450
Ensembl: ENSG00000052850
UniProt: Q9H161
Structure
Position
11:complement(44260440..44310139)
AA seq 411 aa
MNAETCVSYCESPAAAMDAYYSPVSQSREGSSPFRAFPGGDKFGTTFLSAAAKAQGFGDA
KSRARYGAGQQDLATPLESGAGARGSFNKFQPQPSTPQPQPPPQPQPQQQQPQPQPPAQP
HLYLQRGACKTPPDGSLKLQEGSSGHSAALQVPCYAKESSLGEPELPPDSDTVGMDSSYL
SVKEAGVKGPQDRASSDLPSPLEKADSESNKGKKRRNRTTFTSYQLEELEKVFQKTHYPD
VYAREQLAMRTDLTEARVQVWFQNRRAKWRKRERFGQMQQVRTHFSTAYELPLLTRAENY
AQIQNPSWLGNNGAASPVPACVVPCDPVPACMSPHAHPPGSGASSVTDFLSVSGAGSHVG
QTHMGSLFGAASLSPGLNGYELNGEPDRKTSSIAALRMKAKEHSAAISWAT
NT seq 1236 nt   +upstreamnt  +downstreamnt
atgaatgctgagacttgcgtctcttactgcgagtcgccggccgctgccatggacgcctac
tacagcccggtgtcgcagagtcgggagggctcgtcgccttttagggcatttcccggaggc
gacaagttcggcacaactttcctgtcggccgccgccaaagcacagggattcggggacgcc
aagagccgggcccgttacggcgctgggcagcaggacctggcgacacccctggagagtgga
gctggggcgcggggctcctttaacaagttccagccccagccgtcgaccccgcagccccag
ccgccgccgcagccgcagccgcagcagcagcagccgcagccccagccgcccgcgcaaccg
catctttacttgcagcgaggcgcctgcaagacgcccccggacggcagcctcaaactccag
gaaggcagcagcggccacagcgcggccttgcaggttccctgctacgctaaagagagctcc
ctgggtgagccagagttaccccctgactctgacactgtggggatggacagcagctacctg
agtgtcaaggaggctggggtgaaggggccccaggaccgggccagctcagacctccccagc
ccattggagaaggccgactcagagagcaacaagggcaagaagcggcggaaccggaccacc
ttcaccagctaccagctggaggagctggagaaggtcttccagaagacccactacccagac
gtgtatgcgcgggaacagctggccatgaggacagacctcactgaggcccgcgtgcaggtc
tggttccagaaccgaagggccaagtggaggaagcgggagcgttttgggcagatgcagcag
gttcgaacccacttctccactgcatatgagctgcccctcctcacccgagctgagaactac
gcccagattcagaacccgtcctggctcggcaacaacggggctgcctcaccagtgccagcc
tgcgtggtcccctgcgacccggtgcctgcctgcatgtcccctcatgcccacccccctggc
tctggggccagcagcgtcaccgacttcctgagtgtgtctggggctggcagtcacgtgggc
cagacgcacatgggcagcctgtttggagcagccagcctcagcccaggcctcaatggctac
gagctcaacggcgagccggaccgcaagacctcgagcatcgcggccctccgcatgaaggcc
aaggagcacagtgcggccatttcctgggccacatga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (7)   
   KEGG DISEASE (3)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (9)   
   RefSeq(nuc) (1)   
   GenBank (4)   
   EMBL (4)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (40)   

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