Homo sapiens (human): 10362
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Entry
10362 CDS
T01001
Symbol
HMG20B, BRAF25, BRAF35, HMGX2, HMGXB2, PP7706, SMARCE1r, SOXL, pp8857
Name
(RefSeq) high mobility group 20B
KO
K24650
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
10362 (HMG20B)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HDAC complexes
BRAF-HDAC complex
10362 (HMG20B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HMG_box
HMG_box_2
WHAMM-JMY_N
MlaC
DASH_Duo1
PI3K_P85_iSH2
Motif
Other DBs
NCBI-GeneID:
10362
NCBI-ProteinID:
NP_006330
OMIM:
605535
HGNC:
5002
Ensembl:
ENSG00000064961
UniProt:
Q9P0W2
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All DBs
Position
19:3572944..3579083
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AA seq
317 aa
AA seq
DB search
MSHGPKQPGAAAAPAGGKAPGQHGGFVVTVKQERGEGPRAGEKGSHEEEPVKKRGWPKGK
KRKKILPNGPKAPVTGYVRFLNERREQIRTRHPDLPFPEITKMLGAEWSKLQPTEKQRYL
DEAEREKQQYMKELRAYQQSEAYKMCTEKIQEKKIKKEDSSSGLMNTLLNGHKGGDCDGF
STFDVPIFTEEFLDQNKAREAELRRLRKMNVAFEEQNAVLQRHTQSMSSARERLEQELAL
EERRTLALQQQLQAVRQALTASFASLPVPGTGETPTLGTLDFYMARLHGAIERDPAQHEK
LIVRIKEILAQVASEHL
NT seq
954 nt
NT seq
+upstream
nt +downstream
nt
atgtcccacggccccaagcagcccggcgcggccgccgcgccggcgggcggcaaggctccg
ggccagcatgggggcttcgtggtgactgtcaagcaagagcgcggcgagggtccacgcgcg
ggcgagaaggggtcccacgaggaggagccggtgaagaaacgcggctggcccaagggcaag
aagcggaagaagattctgccgaatgggcccaaggcaccggtcacgggctacgtgcgcttc
ctgaacgagcggcgcgagcagatccgcacgcgccacccggatctgccctttcccgagatc
accaagatgctgggcgccgagtggagcaagctgcagccaacggaaaagcagcggtacctg
gatgaggccgagagagagaagcagcagtacatgaaggagctgcgggcgtaccagcagtct
gaagcctataagatgtgcacggagaagatccaggagaagaagatcaagaaagaagactcg
agctctgggctcatgaacactctcctgaatggacacaagggtggggactgcgatggcttc
tccaccttcgatgttcccatcttcactgaagagttcttggaccaaaacaaagcgcgtgag
gcggagcttcggcgcttgcggaagatgaatgtggccttcgaggagcagaacgcggtactg
cagaggcacacgcagagcatgagcagcgcgcgcgagcgtctggagcaggagctggcgctg
gaggagcggaggacgctggcgctgcagcagcagctccaggccgtgcgccaggcgctcacc
gccagcttcgcctcactgccggtgccgggcacgggcgaaacgcccacgctgggcactctg
gacttctacatggcccggcttcacggagccatcgagcgcgaccccgcccagcacgagaag
ctcatcgtccgcatcaaggaaatcctggcccaggtcgccagcgagcacctgtga
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