Homo sapiens (human): 3850
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Entry
3850 CDS
T01001
Symbol
KRT3, CK3, K3, MECD2
Name
(RefSeq) keratin 3
KO
K07605
type II keratin, basic
Organism
hsa
Homo sapiens (human)
Pathway
hsa04382
Cornified envelope formation
Disease
H00726
Meesmann corneal dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09158 Development and regeneration
04382 Cornified envelope formation
3850 (KRT3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
3850 (KRT3)
04147 Exosome [BR:
hsa04147
]
3850 (KRT3)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Types I and II: Acidic and basic keratins
3850 (KRT3)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of epithelial cells
3850 (KRT3)
Exosomal proteins of other body fluids (saliva and urine)
3850 (KRT3)
Exosomal proteins of colorectal cancer cells
3850 (KRT3)
Exosomal proteins of bladder cancer cells
3850 (KRT3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Filament
Keratin_2_head
CENP-F_leu_zip
ATG16
TPR_MLP1_2
DUF7260
ADIP
PUMA_CC
COG6_N
DUF948
Alanine_zipper
DUF4407
DUF7222
Motif
Other DBs
NCBI-GeneID:
3850
NCBI-ProteinID:
NP_476429
OMIM:
148043
HGNC:
6440
Ensembl:
ENSG00000186442
UniProt:
P12035
LinkDB
All DBs
Position
12:complement(52789685..52796117)
Genome browser
AA seq
628 aa
AA seq
DB search
MSRQASKTSGGGSQGFSGRSAVVSGSSRMSCVAHSGGAGGGAYGFRSGAGGFGSRSLYNL
GGNKSISISVAAGGSRAGGFGGGRSSCAFAGGYGGGFGSGYGGGFGGGFGGGRGMGGGFG
GAGGFGGAGGFGGAGGFGGPGGFGGSGGFGGPGSLGSPGGFGPGGFPGGIQEVTINQSLL
QPLNVEIDPQIGQVKAQEREQIKTLNNKFASFIDKVRFLEQQNKVLETKWNLLQQQGTSS
ISGTNNLEPLFENHINYLRSYLDNILGERGRLDSELKNMEDLVEDFKKKYEDEINKRTAA
ENEFVTLKKDVDSAYMNKVELQAKVDALIDEIDFLRTLYDAELSQMQSHISDTSVVLSMD
NNRSLDLDSIIAEVRAQYEDIAQRSKAEAEALYQTKLGELQTTAGRHGDDLRNTKSEIIE
LNRMIQRLRAEIEGVKKQNANLQTAIAEAEQHGEMALKDANAKLQELQAALQQAKDDLAR
LLRDYQELMNVKLALDVEIATYRKLLEGEEYRMSGECPSAVSISVVSSSTTSASAGGYGG
GYGGGMGGGLGGGFSAGGGSGSGFGRGGGGGIGGGFGGGSSGFSGGSGFGSISGARYGVS
GGGFSSASNRGGSIKFSQSSQSSQRYSR
NT seq
1887 nt
NT seq
+upstream
nt +downstream
nt
atgagcagacaagccagcaagacatctggtggcgggagccagggtttctccggccgctct
gctgtggtctccggcagcagcaggatgagctgtgtggcccactctgggggagctggcgga
ggggcctatggcttccggagcggagcaggtggctttggcagtcgcagcctctacaacctg
ggcggcaacaagagcatctccatcagcgtggcagctggcggctcccgggctggaggcttt
gggggagggcggagcagctgtgcctttgcaggtggctatggaggtggctttgggagcggc
tatggaggtggctttggtggtggctttggtggtggcagaggaatgggaggtggctttggt
ggagctggtggctttggaggggctggtggctttggaggggctggtggctttggtggtcct
ggtggctttggtgggtctggtggctttggtgggcctggcagcttgggcagtcctggtggc
tttggccctgggggctttcctgggggaattcaggaagtgactatcaaccagagtctcctg
cagcccctcaatgtggagatcgacccccagattgggcaagtaaaggcccaggagcgggaa
cagatcaagaccctcaacaacaagtttgcctccttcattgacaaggtgcggttcctggag
caacagaacaaagtcctggagaccaagtggaacctgctccagcagcagggcacaagttcc
atctcaggcacaaacaaccttgagcctctttttgagaatcacatcaactacctgcggagc
tacctggacaacatcctcggggagagagggcgcctggactctgagctgaagaacatggag
gacctggtggaagacttcaagaagaaatatgaggatgaaatcaataaacgtacagctgct
gagaatgaatttgtgactctgaagaaggatgtggacagtgcctatatgaacaaggtggag
cttcaggccaaagtggatgccttgatagatgagatcgacttcttaaggaccctctacgac
gctgagctatctcagatgcagagccacatcagtgacacatctgtggtgctgtccatggac
aataatcgctccctggacctggacagcatcattgctgaagttcgtgcacagtatgaggat
atcgctcagagaagcaaggccgaagctgaggccctgtaccagaccaagttgggggagctg
cagaccacggctggcaggcatggggatgacctaagaaataccaagagcgagatcatagag
ctcaacagaatgatccagaggctgcgggcagagatcgagggtgtcaagaagcagaatgcc
aacctgcagacggccattgccgaggccgagcagcatggagagatggccctcaaggatgcc
aatgccaagctccaagagctgcaggctgctctacagcaggcgaaggatgacctggcgcgg
ctgctacgtgactaccaggagctgatgaatgtcaagctggccctggacgtggagatcgcc
acctaccgcaagctgctggagggcgaggagtacaggatgtctggagagtgtccgagtgct
gtcagcatctccgtggtcagcagcagcacgacttccgcctccgcaggtggctatggagga
ggttacggcggaggcatgggcggtggtttaggaggtggcttcagtgcgggcggcggctca
ggcagtggctttggccggggaggcggcggtggaatcggcggtggatttggcggcggcagc
agcggtttcagcggtggcagcggctttggctccatctctggcgcccgctatggagtcagt
ggcgggggcttcagctcggccagcaaccggggcggcagcatcaagttctcccagtcctcc
cagtcctcccagcgctactccagataa
DBGET
integrated database retrieval system
