Homo sapiens (human): 353288
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Entry
353288 CDS
T01001
Symbol
KRT26, CK26, K25B, K25IRS2, K26, KRT25B
Name
(RefSeq) keratin, type I cytoskeletal 26
KO
K07604
type I keratin, acidic
Organism
hsa
Homo sapiens (human)
Pathway
hsa04382
Cornified envelope formation
hsa04519
Cadherin signaling
hsa04915
Estrogen signaling pathway
hsa05150
Staphylococcus aureus infection
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04519 Cadherin signaling
353288 (KRT26)
09150 Organismal Systems
09152 Endocrine system
04915 Estrogen signaling pathway
353288 (KRT26)
09158 Development and regeneration
04382 Cornified envelope formation
353288 (KRT26)
09160 Human Diseases
09171 Infectious disease: bacterial
05150 Staphylococcus aureus infection
353288 (KRT26)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
353288 (KRT26)
04147 Exosome [BR:
hsa04147
]
353288 (KRT26)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Types I and II: Acidic and basic keratins
353288 (KRT26)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of epithelial cells
353288 (KRT26)
Exosomal proteins of other body fluids (saliva and urine)
353288 (KRT26)
Exosomal proteins of colorectal cancer cells
353288 (KRT26)
Exosomal proteins of melanoma cells
353288 (KRT26)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Filament
SSNA1
TPR_MLP1_2
BRE1B
CERLI2_mid_2nd
Prefoldin
Bacillus_HBL
Astrin_C
FlaC_arch
V_ATPase_I
Motif
Other DBs
NCBI-GeneID:
353288
NCBI-ProteinID:
NP_853517
OMIM:
616675
HGNC:
30840
Ensembl:
ENSP00000334798.4
UniProt:
Q7Z3Y9
LinkDB
All DBs
Position
17:complement(40766238..40772201)
Genome browser
AA seq
468 aa
AA seq
DB search
MSFRLSGGSRRICSRTGSGRLSGGGTGFVAGNVCVGSGARSSFSCTLEGISSGGSFCNSG
GGLGSGACAGFLGNEHSLLSGNEKVTMQNLNDRLASYLDHVHALEEANADLEQKIKGWYE
KCEPGSSREHDHDYSRYFSVIEDLKRQIISATICNASIVLQNDNARLTADDFRLKYENEL
ALHHSVEADTSGLRRVLDELTLCTTDLEIQCETLSEELTYLKKSHEEEMEVLQYTAGGNV
NVEMNATPGVDLTVLLNNMRAEYEDLAEQNRKDAEAWFNERSATLQQQISDHEGAATAAR
NELTELKRNLQTLEIELQSLMAVKHSYECSLAETEGNYCNQLQQIQDQIGVMEEQLQQIR
TETEGQKLEYEQLLDVKIFLEKEIDIYCNLLDGEERKSKSTCYKSKGYRPVNSGNQAKDS
TEETIVKTVVEELDQIGNLLSLRVHSVEEKSSKISNITVEQRVPSKAP
NT seq
1407 nt
NT seq
+upstream
nt +downstream
nt
atgtcttttcgactttctggtggatccaggaggatctgctcgcgaactgggtctggtagg
ctgtccggtggaggaacaggcttcgtggctgggaatgtgtgtgttggatcgggagcaaga
agcagcttttcttgtactcttgagggcatctcttctggaggaagcttctgcaatagcggt
ggagggttgggaagtggtgcctgtgctggttttcttggcaatgagcacagcctcctctct
gggaatgaaaaggtgaccatgcagaatctcaacgaccgcctggcatcctacctggaccat
gtgcatgctctagaggaggccaacgcagacctggagcagaagatcaagggctggtacgag
aaatgtgagcctggctcttcccgggaacacgatcatgactatagcagatacttctcagtc
atagaagatcttaaaaggcagattatttctgcgaccatctgcaatgccagcattgttcta
caaaatgacaatgccagactgaccgctgatgacttcaggctgaagtatgaaaatgagctg
gctctgcaccacagtgttgaggccgacaccagtggtcttcgcagagtgttggatgaactg
accctttgtacaaccgacctggagatacagtgtgagaccctcagtgaggaattgacctac
ctcaaaaaaagtcatgaggaggaaatggaagtcttgcaatatacagctggggggaacgtg
aacgtggagatgaatgcaaccccaggagtggacctaactgtcctgttgaacaacatgagg
gctgagtatgaggacttggctgagcagaaccgcaaagatgctgaagcctggttcaacgag
aggagtgcaacgctgcaacaacagatttccgatcatgagggagcagccacagcagccaga
aatgagctgaccgaattaaaacgcaatctgcaaaccctggaaatagaacttcagtccctc
atggctgtgaaacattcctatgaatgctccttggctgagactgaaggaaattactgcaat
caactccagcaaattcaggatcagataggggtgatggaggaacaactgcaacagattcga
acagaaacagaaggccagaagctggagtatgaacagcttcttgatgtaaaaatattttta
gaaaaagaaattgacatttattgcaacttactagatggagaagaaagaaaaagcaaatcc
acatgttacaaatcaaaaggatacaggcctgtgaattctggaaatcaagccaaagactca
acagaagaaactattgttaaaacagtggttgaggaactggatcaaattggcaatctcctt
tcactgagagtccactcagttgaagaaaagtcctctaaaataagcaacattacagtagag
caacgagtaccttctaaagcaccataa
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