Homo sapiens (human): 8091
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Entry
8091 CDS
T01001
Symbol
HMGA2, BABL, HMGI-C, HMGIC, LIPO, SRS5, STQTL9
Name
(RefSeq) high mobility group AT-hook 2
KO
K09283
high mobility group AT-hook protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa05202
Transcriptional misregulation in cancer
hsa05206
MicroRNAs in cancer
Network
nt06240
Transcription (cancer)
Element
N00119
MLL-AF4 fusion to transcriptional activation
Disease
H00711
Russell-Silver syndrome
H01640
Uterine leiomyoma
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
8091 (HMGA2)
05206 MicroRNAs in cancer
8091 (HMGA2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
8091 (HMGA2)
03036 Chromosome and associated proteins [BR:
hsa03036
]
8091 (HMGA2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Other transcription factors
HMGI(Y)
8091 (HMGA2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Nucleosome assembly factors
HMG (high mobility group) proteins
8091 (HMGA2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AT_hook
Motif
Other DBs
NCBI-GeneID:
8091
NCBI-ProteinID:
NP_003474
OMIM:
600698
HGNC:
5009
Ensembl:
ENSG00000149948
UniProt:
P52926
LinkDB
All DBs
Position
12:65824460..65966291
Genome browser
AA seq
109 aa
AA seq
DB search
MSARGEGAGQPSTSAQGQPAAPAPQKRGRGRPRKQQQEPTGEPSPKRPRGRPKGSKNKSP
SKAAQKKAEATGEKRPRGRPRKWPQQVVQKKPAQEETEETSSQESAEED
NT seq
330 nt
NT seq
+upstream
nt +downstream
nt
atgagcgcacgcggtgagggcgcggggcagccgtccacttcagcccagggacaacctgcc
gccccagcgcctcagaagagaggacgcggccgccccaggaagcagcagcaagaaccaacc
ggtgagccctctcctaagagacccaggggaagacccaaaggcagcaaaaacaagagtccc
tctaaagcagctcaaaagaaagcagaagccactggagaaaaacggccaagaggcagacct
aggaaatggccacaacaagttgttcagaagaagcctgctcaggaggaaactgaagagaca
tcctcacaagagtctgccgaagaggactag
DBGET
integrated database retrieval system