Homo sapiens (human): 100653049
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Entry
100653049 CDS
T01001
Name
(RefSeq) keratin, type I cuticular Ha4 isoform X1
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
100653049
09150 Organismal Systems
09152 Endocrine system
04915 Estrogen signaling pathway
100653049
09158 Development and regeneration
04382 Cornified envelope formation
100653049
09160 Human Diseases
09171 Infectious disease: bacterial
05150 Staphylococcus aureus infection
100653049
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
100653049
04147 Exosome [BR:
hsa04147
]
100653049
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Types I and II: Acidic and basic keratins
100653049
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of epithelial cells
100653049
Exosomal proteins of other body fluids (saliva and urine)
100653049
Exosomal proteins of colorectal cancer cells
100653049
Exosomal proteins of melanoma cells
100653049
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Filament
SSNA1
SGL_GH162
Motif
Other DBs
NCBI-GeneID:
100653049
NCBI-ProteinID:
XP_003403930
UniProt:
O76011
A0A140TA62
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Position
17:49141..55289
Genome browser
AA seq
436 aa
AA seq
DB search
MLYAKPPPTINGIKGLQRKERLKPAHIHLQQLTCFSITCSSTMSYSCCLPSLGCRTSCSS
RPCVPPSCHGYTLPGACNIPANVSNCNWFCEGSFNGSEKETMQFLNDRLASYLEKVRQLE
RDNAELEKLIQERSQQQEPLLCPSYQSYFKTIEELQQKILCAKAENARLVVNIDNAKLAS
DDFRSKYQTEQSLRLLVESDINSIRRILDELTLCKSDLESQVESLREELICLKKNHEEEV
NTLRSQLGDRLNVEVDTAPTVDLNQVLNETRSQYEALVETNRREVEQWFATQTEELNKQV
VSSSEQLQSCQAEIIELRRTVNALEIELQAQHNLRDSLENTLTESEAHYSSQLSQVQSLI
TNVESQLAEIRCDLERQNQEYQVLLDVRARLECEINTYRSLLESEDCKLPCNPCATTNAS
GNSCGPCGTSQKGCCN
NT seq
1311 nt
NT seq
+upstream
nt +downstream
nt
atgctgtatgccaagcccccacccacaattaatggtataaaaggactgcagaggaaggag
agactcaaacctgcccacatccacctccagcagcttacctgcttttccattacctgttcc
agcaccatgtcttacagttgttgcctgcccagcctgggctgccgcaccagctgctcctcc
cggccctgcgtgccccccagctgccacggctacaccctgcctggggcctgcaacatcccc
gccaatgtgagcaactgcaactggttctgtgagggctccttcaatggcagcgagaaggag
actatgcagttcctgaacgaccgcctggccagctacctggagaaggtgcgtcagctggag
cgggacaacgcggagctggagaaactcatccaggagcggtcccagcagcaggagcccttg
ctgtgccccagctaccagtcgtacttcaagaccattgaggagctccagcagaagattctg
tgtgccaaggctgagaatgccaggctggtggtgaacattgacaatgccaagctggcctct
gacgacttcagaagcaagtaccagacggagcagtccctgaggctgttggtggagtcggac
atcaacagcatacgcaggatcctggatgagctgaccctctgcaagtctgacctggagtcc
caggtggagtccctgagggaggagctgatctgcttgaagaagaaccatgaggaggaggtt
aacaccctgcgctcccagcttggagaccgcctcaacgtggaggtggacactgcccccact
gtggacctgaaccaggtcctgaacgagaccaggagtcagtatgaggctctggtggaaact
aaccgcagggaagtggagcaatggttcgccacgcagaccgaggagctgaacaagcaggtg
gtatccagctcagagcagctgcagtcctgccaggcggagatcatcgagctgagacgcaca
gtcaacgccctggagatcgagctgcaggcccagcacaacctgcgagactctctggaaaac
acgctgacggagagcgaggcccactacagctcccagctgtcccaggtgcagagcctgatc
accaacgtggagtctcagctggcagagatccgctgtgacctggagcggcagaaccaggag
taccaggtgctgctggacgtgcgtgcccggctggagtgtgagatcaacacgtaccggagc
ctcctggagagtgaggactgcaagctcccctgcaacccatgcgccaccaccaatgctagt
ggcaactcctgtggaccctgtggcacctctcaaaagggttgctgtaattga
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