Homo sapiens (human): 51621
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Entry
51621 CDS
T01001
Symbol
KLF13, BTEB3, FKLF2, NSLP1, RFLAT-1, RFLAT1
Name
(RefSeq) Krueppel-like factor 13 isoform 1
KO
K09208
krueppel-like factor 9/13/14/16
Organism
hsa
Homo sapiens (human)
Disease
H01877
Chromosome 15q13.3 microdeletion syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
51621 (KLF13)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 SP/KLF family and related proteins
51621 (KLF13)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
zf-C2H2
zf-H2C2_2
zf-C2H2_4
zf_C2H2_ZNF292
zf-C2H2_15
B129_C2H2-zf
zf-C2H2_ZN292
zf-C2H2_8
Zap1_zf1
zf-Di19
zf-C2H2_6
PTR3_N
DUF5810
Motif
Other DBs
NCBI-GeneID:
51621
NCBI-ProteinID:
NP_057079
OMIM:
605328
HGNC:
13672
Ensembl:
ENSP00000302456.3
UniProt:
Q9Y2Y9
X5DNR2
LinkDB
All DBs
Position
15:31326835..31435665
Genome browser
AA seq
288 aa
AA seq
DB search
MAAAAYVDHFAAECLVSMSSRAVVHGPREGPESRPEGAAVAATPTLPRVEERRDGKDSAS
LFVVARILADLNQQAPAPAPAERREGAAARKARTPCRLPPPAPEPTSPGAEGAAAAPPSP
AWSEPEPEAGLEPEREPGPAGSGEPGLRQRVRRGRSRADLESPQRKHKCHYAGCEKVYGK
SSHLKAHLRTHTGERPFACSWQDCNKKFARSDELARHYRTHTGEKKFSCPICEKRFMRSD
HLTKHARRHANFHPGMLQRRGGGSRTGSLSDYSRSDASSPTISPASSP
NT seq
867 nt
NT seq
+upstream
nt +downstream
nt
atggcagccgccgcctatgtggaccacttcgccgccgagtgcctcgtgtccatgtcgagc
cgcgcggtcgtgcacgggccgcgggaggggccggagtcccggcccgagggcgcggccgtg
gccgccacccccacgctgccccgcgtcgaggagcgccgcgacggtaaggacagcgcctcg
ctcttcgtggtggcgcggatcctagcggacctcaaccagcaagcgccggcgcccgccccg
gcggagcgcagggagggcgccgcggcccggaaggcgaggaccccctgccgcctgccgccg
cccgcccccgagcccacctcccccggcgccgaaggcgcggcggccgcgccccccagcccg
gcgtggagcgagccggagcccgaggcggggctggagcccgagcgggagccggggcccgcg
gggagcggcgagcccggcctcagacaaagggtccggcggggccgaagtcgcgccgacctc
gagtccccgcagaggaagcacaagtgccactacgcgggctgcgagaaagtttacgggaaa
tcttcgcacctcaaggcgcacctgagaactcacacaggtgagaggcccttcgcctgcagc
tggcaggactgcaacaagaagttcgcgcgctccgacgagctggcgcggcactaccgcaca
cacacgggcgagaagaagttcagctgccccatctgcgagaagcgcttcatgcgcagcgac
cacctgaccaagcacgcgcgccgccacgccaacttccacccgggaatgctgcagcggcgc
ggcgggggctcgcggaccggctccctcagcgactacagccgctccgacgccagcagcccc
accatcagcccggccagctcgccctga
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