Homo sapiens (human): 4821
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Entry
4821 CDS
T01001
Symbol
NKX2-2, NKX2.2, NKX2B
Name
(RefSeq) NK2 homeobox 2
KO
K08029
homeobox protein Nkx-2.2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04950
Maturity onset diabetes of the young
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09167 Endocrine and metabolic disease
04950 Maturity onset diabetes of the young
4821 (NKX2-2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
4821 (NKX2-2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain ANTP: NKL
4821 (NKX2-2)
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GFIT
Motif
Pfam:
Homeodomain
Homeobox_KN
Motif
Other DBs
NCBI-GeneID:
4821
NCBI-ProteinID:
NP_002500
OMIM:
604612
HGNC:
7835
Ensembl:
ENSG00000125820
UniProt:
O95096
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Position
20:complement(21511017..21522689)
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AA seq
273 aa
AA seq
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MSLTNTKTGFSVKDILDLPDTNDEEGSVAEGPEEENEGPEPAKRAGPLGQGALDAVQSLP
LKNPFYDSSDNPYTRWLASTEGLQYSLHGLAAGAPPQDSSSKSPEPSADESPDNDKETPG
GGGDAGKKRKRRVLFSKAQTYELERRFRQQRYLSAPEREHLASLIRLTPTQVKIWFQNHR
YKMKRARAEKGMEVTPLPSPRRVAVPVLVRDGKPCHALKAQDLAAATFQAGIPFSAYSAQ
SLQHMQYNAQYSSASTPQYPTAHPLVQAQQWTW
NT seq
822 nt
NT seq
+upstream
nt +downstream
nt
atgtcgctgaccaacacaaagacggggttttcggtcaaggacatcttagacctgccggac
accaacgatgaggagggctctgtggccgaaggtccggaggaagagaacgaggggcccgag
ccagccaagagggccgggccgctggggcagggcgccctggacgcggtgcagagcctgccc
ctgaagaaccccttctacgacagcagcgacaacccgtacacgcgctggctggccagcacc
gagggccttcagtactccctgcacggtctggctgccggggcgccccctcaggactcaagc
tccaagtccccggagccctcggccgacgagtcaccggacaatgacaaggagaccccgggc
ggcgggggggacgccggcaagaagcgaaagcggcgagtgcttttctccaaggcgcagacc
tacgagctggagcggcgctttcggcagcagcggtacctgtcggcgcccgagcgcgaacac
ctggccagcctcatccgcctcacgcccacgcaggtcaagatctggttccagaaccaccgc
tacaagatgaagcgcgcccgggccgagaaaggtatggaggtgacgcccctgccctcgccg
cgccgggtggccgtgcccgtcttggtcagggacggcaaaccatgtcacgcgctcaaagcc
caggacctggcagccgccaccttccaggcgggcattcccttttctgcctacagcgcgcag
tcgctgcagcacatgcagtacaacgcccagtacagctcggccagcaccccccagtacccg
acagcacaccccctggtccaggcccagcagtggacttggtga
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