Homo sapiens (human): 4604
Help
Entry
4604 CDS
T01001
Symbol
MYBPC1, CMYO16, CMYP16, LCCS4, MYBPCC, MYBPCS, MYOTREM, ssMyBP-C
Name
(RefSeq) myosin binding protein C1
KO
K12557
myosin-binding protein C, slow-type
Organism
hsa
Homo sapiens (human)
Pathway
hsa04820
Cytoskeleton in muscle cells
Network
nt06539
Cytoskeleton in muscle cells
Element
N01817
Myosin thick filament
Disease
H00811
Distal arthrogryposis
H00865
Lethal congenital contractural syndrome
H01810
Congenital myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04820 Cytoskeleton in muscle cells
4604 (MYBPC1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
4604 (MYBPC1)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Cross-linking proteins
4604 (MYBPC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
I-set
Ig_3
fn3
ig
Ig_2
THB
V-set
C2-set_2
Pur_ac_phosph_N
Motif
Other DBs
NCBI-GeneID:
4604
NCBI-ProteinID:
NP_996556
OMIM:
160794
HGNC:
7549
Ensembl:
ENSG00000196091
Pharos:
Q00872
(Tbio)
UniProt:
Q00872
Q86TA8
A8KAB1
Structure
PDB
PDBj
LinkDB
All DBs
Position
12:101594971..101695841
Genome browser
AA seq
1141 aa
AA seq
DB search
MPEPTKKEENEVPAPAPPPEEPSKEKEAGTTPAKDWTLVETPPGEEQAKQNANSQLSILF
IEKPQGGTVKVGEDITFIAKVKAEDLLRKPTIKWFKGKWMDLASKAGKHLQLKETFERHS
RVYTFEMQIIKAKDNFAGNYRCEVTYKDKFDSCSFDLEVHESTGTTPNIDIRSAFKRSGE
GQEDAGELDFSGLLKRREVKQQEEEPQVDVWELLKNAKPSEYEKIAFQYGITDLRGMLKR
LKRMRREEKKSAAFAKILDPAYQVDKGGRVRFVVELADPKLEVKWYKNGQEIRPSTKYIF
EHKGCQRILFINNCQMTDDSEYYVTAGDEKCSTELFVREPPIMVTKQLEDTTAYCGERVE
LECEVSEDDANVKWFKNGEEIIPGPKSRYRIRVEGKKHILIIEGATKADAAEYSVMTTGG
QSSAKLSVDLKPLKILTPLTDQTVNLGKEICLKCEISENIPGKWTKNGLPVQESDRLKVV
HKGRIHKLVIANALTEDEGDYVFAPDAYNVTLPAKVHVIDPPKIILDGLDADNTVTVIAG
NKLRLEIPISGEPPPKAMWSRGDKAIMEGSGRIRTESYPDSSTLVIDIAERDDSGVYHIN
LKNEAGEAHASIKVKVVDFPDPPVAPTVTEVGDDWCIMNWEPPAYDGGSPILGYFIERKK
KQSSRWMRLNFDLCKETTFEPKKMIEGVAYEVRIFAVNAIGISKPSMPSRPFVPLAVTSP
PTLLTVDSVTDTTVTMRWRPPDHIGAAGLDGYVLEYCFEGSTSAKQSDENGEAAYDLPAE
DWIVANKDLIDKTKFTITGLPTDAKIFVRVKAVNAAGASEPKYYSQPILVKEIIEPPKIR
IPRHLKQTYIRRVGEAVNLVIPFQGKPRPELTWKKDGAEIDKNQINIRNSETDTIIFIRK
AERSHSGKYDLQVKVDKFVETASIDIQIIDRPGPPQIVKIEDVWGENVALTWTPPKDDGN
AAITGYTIQKADKKSMEWFTVIEHYHRTSATITELVIGNEYYFRVFSENMCGLSEDATMT
KESAVIARDGKIYKNPVYEDFDFSEAPMFTQPLVNTYAIAGYNATLNCSVRGNPKPKITW
MKNKVAIVDDPRYRMFSNQGVCTLEIRKPSPYDGGTYCCKAVNDLGTVEIECKLEVKVIA
Q
NT seq
3426 nt
NT seq
+upstream
nt +downstream
nt
atgccagaacccactaagaaagaggaaaatgaagtgccagccccagccccacccccggaa
gaaccaagtaaagagaaggaggccggaactacaccagcaaaagactggacccttgtcgaa
actcctcctggggaggaacaagccaagcagaatgccaactcccagctgtccatcttgttc
attgaaaaacctcaaggaggaacagtgaaagttggtgaagatatcaccttcatagccaaa
gtcaaggctgaagatcttctgagaaaacccactatcaaatggttcaaaggaaaatggatg
gacctggccagcaaagccgggaagcaccttcagctgaaggaaacctttgagaggcacagt
cgggtgtacacatttgagatgcagatcatcaaggccaaagataactttgcaggaaattac
agatgcgaggtcacctataaggataagtttgacagctgttcatttgatcttgaagtgcac
gaatctactgggactactccaaacattgacatcagatctgctttcaagagaagtggagaa
ggtcaagaggatgcaggagaacttgactttagtggtctcctgaaacgtagggaggtgaag
cagcaggaggaagaaccccaggtggacgtatgggagttgctgaagaacgcgaaacccagt
gagtacgagaagatcgccttccagtatggaatcaccgacctgcgcggcatgctcaagcga
ctcaagcgcatgcgcagagaggagaagaagagcgcagcttttgcaaaaattcttgatcct
gcatatcaggttgacaaaggaggcagagtgaggtttgttgtggagctggcagatccaaag
ttggaggtgaaatggtataaaaatggtcaagaaattcgacccagtaccaaatacatcttt
gaacacaaaggatgccagagaatcctgtttatcaataactgtcagatgacagatgattca
gagtattatgtgacagccggtgatgagaaatgttccactgagctcttcgtaagagagcct
ccaattatggtgaccaaacagctggaagatacaactgcttattgtggggagagagtggaa
ttagaatgtgaggtgtctgaagatgatgccaatgtaaaatggtttaagaatggtgaagag
attatccctggtccaaaatcaagataccgaattagagttgagggtaaaaaacacatcttg
atcatagagggagcaacaaaggctgatgctgcagaatattcagtaatgacaacaggagga
caatcatctgctaaacttagtgttgacttgaaacctctgaagattttgacacctctgact
gatcagactgtaaatcttggaaaagaaatctgcctgaagtgtgaaatctctgaaaacata
ccaggaaaatggactaaaaatggcctacctgttcaggagagtgaccgtctaaaggtggtt
cacaagggaaggatccacaagttagtgatagccaatgccctcactgaagatgaaggtgat
tatgtatttgcacctgatgcctacaatgttactctgcctgccaaagttcatgttattgat
cctcctaagatcatcctggatggtcttgatgctgacaacacagtgacagtgattgcagga
aacaagcttcgtcttgagatccccatcagcggagaaccacctcctaaagccatgtggagc
cggggagataaggctattatggaaggcagtggccggataagaacagaatcttaccctgat
agcagcactctggtcattgatatagctgaaagagatgactctggtgtttaccacatcaat
ctgaaaaacgaagctggagaggcacatgcaagcatcaaggttaaagttgtggacttccct
gatcctccagtggcaccgactgtgacagaggtgggagatgactggtgtatcatgaactgg
gagcctcctgcctacgacggaggctctccaatcctaggatattttattgagaggaagaag
aaacaaagctccaggtggatgaggctgaattttgatctctgcaaagaaacaacttttgag
cccaagaagatgattgaaggtgtggcctatgaggtccgcatctttgcagtcaatgccatt
ggcatctccaagcccagtatgccctccaggccttttgttcctttggctgtaacaagccct
cctactcttctgactgtggactctgtcactgacacgactgtcacgatgaggtggcgcccc
ccagaccacattggtgcagcaggtttagatggctatgtgctagagtattgctttgaagga
agtacatcagcaaaacagtctgatgaaaatggggaggctgcctatgatctgccagctgag
gactggatagttgcaaacaaagatctgattgacaagacgaagttcaccatcacaggtctg
ccaacagatgcaaagatctttgtgcgtgtgaaggctgttaatgcagctggtgccagcgag
cccaagtactattctcagcccattctcgtgaaggaaatcatagaacctccaaagattcgc
attccaagacacctgaagcaaacctatatccgcagagttggagaagctgtcaatctggtt
atacctttccagggaaaaccaagaccagaattaacttggaagaaggatggtgcagaaatt
gataagaatcaaataaacattcgcaactctgagactgatacaatcatatttattagaaaa
gcagagaggagccactctgggaaatatgatctgcaagtcaaagtggacaaattcgtggag
accgcatcaattgacatccagatcattgaccgtccaggtccaccccaaattgtgaagatt
gaggatgtctggggagaaaatgtcgctctcacatggactccaccaaaggatgatggaaat
gctgctatcacaggctataccattcagaaggctgacaagaagagcatggaatggtttact
gtcattgagcattatcatcgaaccagtgccaccattactgaattggtcatagggaatgaa
tattacttccgggtcttttctgaaaacatgtgtggcctcagtgaggatgccaccatgact
aaagagagtgcagtgatcgccagggatggtaaaatctacaaaaatccagtgtatgaagac
tttgatttctcagaggcacccatgtttactcagcctttggttaacacctatgccatagct
ggttacaatgccaccctaaactgcagtgtgagaggaaatcctaagcctaaaataacctgg
atgaaaaacaaagttgctattgtggatgatccaagatacaggatgttcagcaaccaggga
gtctgtaccctggaaattcgcaagcccagcccctatgatggaggcacttactgctgcaaa
gcagtcaatgaccttgggacagtggagattgaatgcaaactggaggtgaaagtcattgca
caataa
Homo sapiens (human): 4606
Help
Entry
4606 CDS
T01001
Symbol
MYBPC2, MYBPC, MYBPCF, fsMyBP-C
Name
(RefSeq) myosin binding protein C2
KO
K12558
myosin-binding protein C, fast-type
Organism
hsa
Homo sapiens (human)
Pathway
hsa04820
Cytoskeleton in muscle cells
Network
nt06539
Cytoskeleton in muscle cells
Element
N01817
Myosin thick filament
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04820 Cytoskeleton in muscle cells
4606 (MYBPC2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
4606 (MYBPC2)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Cross-linking proteins
4606 (MYBPC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
I-set
Ig_3
fn3
ig
Ig_2
THB
V-set
Pur_ac_phosph_N
Receptor_2B4
Motif
Other DBs
NCBI-GeneID:
4606
NCBI-ProteinID:
NP_004524
OMIM:
160793
HGNC:
7550
Ensembl:
ENSG00000086967
Pharos:
Q14324
(Tbio)
UniProt:
Q14324
A0A140VJQ0
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:50432892..50466321
Genome browser
AA seq
1141 aa
AA seq
DB search
MPEAKPAAKKAPKGKDAPKGAPKEAPPKEAPAEAPKEAPPEDQSPTAEEPTGVFLKKPDS
VSVETGKDAVVVAKVNGKELPDKPTIKWFKGKWLELGSKSGARFSFKESHNSASNVYTVE
LHIGKVVLGDRGYYRLEVKAKDTCDSCGFNIDVEAPRQDASGQSLESFKRTSEKKSDTAG
ELDFSGLLKKREVVEEEKKKKKKDDDDLGIPPEIWELLKGAKKSEYEKIAFQYGITDLRG
MLKRLKKAKVEVKKSAAFTKKLDPAYQVDRGNKIKLMVEISDPDLTLKWFKNGQEIKPSS
KYVFENVGKKRILTINKCTLADDAAYEVAVKDEKCFTELFVKEPPVLIVTPLEDQQVFVG
DRVEMAVEVSEEGAQVMWMKDGVELTREDSFKARYRFKKDGKRHILIFSDVVQEDRGRYQ
VITNGGQCEAELIVEEKQLEVLQDIADLTVKASEQAVFKCEVSDEKVTGKWYKNGVEVRP
SKRITISHVGRFHKLVIDDVRPEDEGDYTFVPDGYALSLSAKLNFLEIKVEYVPKQEPPK
IHLDCSGKTSENAIVVVAGNKLRLDVSITGEPPPVATWLKGDEVFTTTEGRTRIEKRVDC
SSFVIESAQREDEGRYTIKVTNPVGEDVASIFLQVVDVPDPPEAVRITSVGEDWAILVWE
PPMYDGGKPVTGYLVERKKKGSQRWMKLNFEVFTETTYESTKMIEGILYEMRVFAVNAIG
VSQPSMNTKPFMPIAPTSEPLHLIVEDVTDTTTTLKWRPPNRIGAGGIDGYLVEYCLEGS
EEWVPANTEPVERCGFTVKNLPTGARILFRVVGVNIAGRSEPATLAQPVTIREIAEPPKI
RLPRHLRQTYIRKVGEQLNLVVPFQGKPRPQVVWTKGGAPLDTSRVHVRTSDFDTVFFVR
QAARSDSGEYELSVQIENMKDTATIRIRVVEKAGPPINVMVKEVWGTNALVEWQAPKDDG
NSEIMGYFVQKADKKTMEWFNVYERNRHTSCTVSDLIVGNEYYFRVYTENICGLSDSPGV
SKNTARILKTGITFKPFEYKEHDFRMAPKFLTPLIDRVVVAGYSAALNCAVRGHPKPKVV
WMKNKMEIREDPKFLITNYQGVLTLNIRRPSPFDAGTYTCRAVNELGEALAECKLEVRVP
Q
NT seq
3426 nt
NT seq
+upstream
nt +downstream
nt
atgcctgaggcaaaaccagcggccaaaaaggcccccaaaggcaaagatgcccccaaagga
gcccccaaggaggctccccctaaggaggctcctgcagaggcccccaaagaagccccaccc
gaggaccagtccccgactgcagaggagcccaccggcgttttcctgaagaagccggactcc
gtctcagtggagactgggaaggacgcagtggtcgtggccaaggtgaacgggaaggagctc
ccagacaaaccgaccatcaagtggttcaaggggaagtggctggagctgggcagcaagagt
ggcgcccgcttctccttcaaggagtcccacaactccgccagcaatgtgtacaccgtggag
ctgcacattgggaaggtggtactgggggaccgtgggtattaccgcctcgaggtcaaagcc
aaggacacctgtgacagctgtggcttcaacatcgatgtggaggcaccccgtcaggatgcc
tctgggcagagtctagaaagcttcaagcgtacgagtgaaaagaagtcggatactgcaggt
gagctggatttcagtggcctgttgaagaagagggaggtggtggaggaggagaagaagaag
aaaaagaaagatgacgatgacctaggcatccccccggagatttgggagctcctgaaaggg
gcaaagaagagcgagtacgagaaaatcgccttccagtatggcatcaccgacctccggggc
atgctgaagcggctgaaaaaggctaaggtcgaggtcaagaagagtgcagcattcacaaag
aagctggatccagcctaccaagtggacagaggcaacaagatcaagttgatggtagagatc
agcgacccagacctgaccctcaagtggttcaagaacggccaggagatcaaaccaagcagc
aagtacgtgtttgagaacgttggtaagaagcgaattcttaccatcaacaagtgcacgctg
gcggatgacgctgcctatgaagtagctgtcaaggatgagaagtgtttcaccgagctcttc
gtcaaagaacctccagtcctaattgtcacacctcttgaggaccagcaggtgtttgtgggt
gaccgggtggaaatggcagtggaggtgtcagaagagggtgcccaggtgatgtggatgaaa
gatggtgtggaactgactcgggaggattccttcaaggcccggtaccgcttcaagaaggac
gggaagcgccacatcctcatcttctcagacgtggtccaggaggacaggggtcgctatcag
gtcataaccaatggcggccagtgtgaggccgagctgattgtggaagagaaacagctggag
gtcctgcaggacatcgcggatctgacggtgaaggcctcagaacaagctgtgttcaagtgc
gaggtgtctgatgagaaagtgacgggcaagtggtataagaatggggtcgaggtgcggccc
agcaagaggatcaccatttcccatgtaggcaggttccacaagctggtgatcgatgacgtc
cgccccgaggatgagggagactacacgtttgtgcctgacggctacgccctgtcgctctcg
gccaagctcaacttcctggaaatcaaggtggagtacgttcccaagcaagagccaccaaag
atccacttggattgctcggggaagacctcagagaatgcgattgtggttgtggctggaaac
aagctgaggcttgacgtgtccatcacaggggagccccctcccgtcgctacctggctgaag
ggagatgaggtattcacgaccaccgagggcaggacccgcatcgagaagcgggtggactgc
agcagctttgtgattgagagtgcgcagcgggaagacgagggccgctacaccatcaaggtc
accaaccccgtcggcgaggacgtggcttccatcttcctgcaagttgtagatgtcccagac
cccccggaggctgtgcgcatcacctcggttggagaggattgggccatccttgtctgggag
ccaccaatgtacgatggggggaagccagtcaccgggtacctcgtagagcggaagaagaag
ggctctcagcgctggatgaagctgaactttgaggtcttcacagagaccacctatgagtcc
accaagatgatcgagggcatcctctatgagatgcgtgtcttcgccgtcaatgctataggg
gtctcccagcccagcatgaacaccaagccttttatgcctattgcacccacgagtgaaccc
ctgcacctgatagtggaggatgtgacagacaccaccaccacactcaagtggaggcctccg
aacaggatcggggcaggtggcatcgatgggtacctggtggagtactgcctggaaggctcc
gaggaatgggtccctgccaacaccgagcccgtggagcgctgtggcttcaccgtcaagaat
ctcccgaccggagccagaatcctcttccgagtagttggggtcaacatcgcggggcgcagc
gagccggccaccctggcccagccggtcaccatcagggagattgcggagccacccaagatc
cggcttccccgccatctccgccagacctacatccgcaaagtgggcgagcagctcaacctt
gtcgtccccttccagggaaagccccggccccaggtggtgtggaccaagggcggggccccg
ctggacacctcccgcgtgcacgtgcggaccagcgacttcgacaccgtgttcttcgtgcgc
caggcggcccgctccgactccggggagtacgagctgagcgtgcagatcgagaacatgaag
gacaccgccaccatccgcatccgcgttgtggaaaaggctgggccccccataaacgtgatg
gtgaaggaggtgtggggcacgaacgcgctggtggagtggcaggcccccaaagatgatggg
aacagtgagatcatggggtatttcgtccagaaagcagacaaaaaaaccatggagtggttc
aacgtctatgaacgtaacaggcacactagctgtactgtgtccgaccttatcgtgggcaat
gaatactatttccgagtttacaccgagaacatctgtgggctcagtgactcacctggtgtc
tccaagaacacggcccgcatcctcaagacaggaatcaccttcaaaccgttcgagtataag
gagcatgacttccggatggctcccaagttcctgacacctctcatagaccgcgtggtcgtg
gctgggtactcggcagccctcaactgtgctgtcagaggccacccgaagccgaaggtggtc
tggatgaagaacaagatggaaatccgtgaagatcccaagttcctgataaccaattaccaa
ggagtcctgacgctgaacatccgtcgcccctcgcccttcgacgctgggacttacacctgc
cgggccgtcaacgagctgggcgaggcgctggctgagtgcaagctggaggtccgagtgccg
cagtga
Homo sapiens (human): 4607
Help
Entry
4607 CDS
T01001
Symbol
MYBPC3, CMD1MM, CMH4, FHC, LVNC10, MYBP-C, cMyBP-C
Name
(RefSeq) myosin binding protein C3
KO
K12568
myosin-binding protein C, cardiac-type
Organism
hsa
Homo sapiens (human)
Pathway
hsa04820
Cytoskeleton in muscle cells
hsa05410
Hypertrophic cardiomyopathy
hsa05414
Dilated cardiomyopathy
Network
nt06539
Cytoskeleton in muscle cells
Element
N01817
Myosin thick filament
Disease
H00292
Hypertrophic cardiomyopathy
H00294
Dilated cardiomyopathy
H01216
Left ventricular noncompaction
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04820 Cytoskeleton in muscle cells
4607 (MYBPC3)
09160 Human Diseases
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
4607 (MYBPC3)
05414 Dilated cardiomyopathy
4607 (MYBPC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
I-set
Ig_3
fn3
ig
Ig_2
THB
V-set
C2-set_2
PKD_3
Herpes_gE_N
Motif
Other DBs
NCBI-GeneID:
4607
NCBI-ProteinID:
NP_000247
OMIM:
600958
HGNC:
7551
Ensembl:
ENSG00000134571
Pharos:
Q14896
(Tbio)
UniProt:
Q14896
A5YM48
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:complement(47331406..47352702)
Genome browser
AA seq
1274 aa
AA seq
DB search
MPEPGKKPVSAFSKKPRSVEVAAGSPAVFEAETERAGVKVRWQRGGSDISASNKYGLATE
GTRHTLTVREVGPADQGSYAVIAGSSKVKFDLKVIEAEKAEPMLAPAPAPAEATGAPGEA
PAPAAELGESAPSPKGSSSAALNGPTPGAPDDPIGLFVMRPQDGEVTVGGSITFSARVAG
ASLLKPPVVKWFKGKWVDLSSKVGQHLQLHDSYDRASKVYLFELHITDAQPAFTGSYRCE
VSTKDKFDCSNFNLTVHEAMGTGDLDLLSAFRRTSLAGGGRRISDSHEDTGILDFSSLLK
KRDSFRTPRDSKLEAPAEEDVWEILRQAPPSEYERIAFQYGVTDLRGMLKRLKGMRRDEK
KSTAFQKKLEPAYQVSKGHKIRLTVELADHDAEVKWLKNGQEIQMSGSKYIFESIGAKRT
LTISQCSLADDAAYQCVVGGEKCSTELFVKEPPVLITRPLEDQLVMVGQRVEFECEVSEE
GAQVKWLKDGVELTREETFKYRFKKDGQRHHLIINEAMLEDAGHYALCTSGGQALAELIV
QEKKLEVYQSIADLMVGAKDQAVFKCEVSDENVRGVWLKNGKELVPDSRIKVSHIGRVHK
LTIDDVTPADEADYSFVPEGFACNLSAKLHFMEVKIDFVPRQEPPKIHLDCPGRIPDTIV
VVAGNKLRLDVPISGDPAPTVIWQKAITQGNKAPARPAPDAPEDTGDSDEWVFDKKLLCE
TEGRVRVETTKDRSIFTVEGAEKEDEGVYTVTVKNPVGEDQVNLTVKVIDVPDAPAAPKI
SNVGEDSCTVQWEPPAYDGGQPILGYILERKKKKSYRWMRLNFDLIQELSHEARRMIEGV
VYEMRVYAVNAIGMSRPSPASQPFMPIGPPSEPTHLAVEDVSDTTVSLKWRPPERVGAGG
LDGYSVEYCPEGCSEWVAALQGLTEHTSILVKDLPTGARLLFRVRAHNMAGPGAPVTTTE
PVTVQEILQRPRLQLPRHLRQTIQKKVGEPVNLLIPFQGKPRPQVTWTKEGQPLAGEEVS
IRNSPTDTILFIRAARRVHSGTYQVTVRIENMEDKATLVLQVVDKPSPPQDLRVTDAWGL
NVALEWKPPQDVGNTELWGYTVQKADKKTMEWFTVLEHYRRTHCVVPELIIGNGYYFRVF
SQNMVGFSDRAATTKEPVFIPRPGITYEPPNYKALDFSEAPSFTQPLVNRSVIAGYTAML
CCAVRGSPKPKISWFKNGLDLGEDARFRMFSKQGVLTLEIRKPCPFDGGIYVCRATNLQG
EARCECRLEVRVPQ
NT seq
3825 nt
NT seq
+upstream
nt +downstream
nt
atgcctgagccggggaagaagccagtctcagcttttagcaagaagccacggtcagtggaa
gtggccgcaggcagccctgccgtgttcgaggccgagacagagcgggcaggagtgaaggtg
cgctggcagcgcggaggcagtgacatcagcgccagcaacaagtacggcctggccacagag
ggcacacggcatacgctgacagtgcgggaagtgggccctgccgaccagggatcttacgca
gtcattgctggctcctccaaggtcaagttcgacctcaaggtcatagaggcagagaaggca
gagcccatgctggcccctgcccctgcccctgctgaggccactggagcccctggagaagcc
ccggccccagccgctgagctgggagaaagtgccccaagtcccaaagggtcaagctcagca
gctctcaatggtcctacccctggagcccccgatgaccccattggcctcttcgtgatgcgg
ccacaggatggcgaggtgaccgtgggtggcagcatcaccttctcagcccgcgtggccggc
gccagcctcctgaagccgcctgtggtcaagtggttcaagggcaaatgggtggacctgagc
agcaaggtgggccagcacctgcagctgcacgacagctacgaccgcgccagcaaggtctat
ctgttcgagctgcacatcaccgatgcccagcctgccttcactggcagctaccgctgtgag
gtgtccaccaaggacaaatttgactgctccaacttcaatctcactgtccacgaggccatg
ggcaccggagacctggacctcctatcagccttccgccgcacgagcctggctggaggtggt
cggcggatcagtgatagccatgaggacactgggattctggacttcagctcactgctgaaa
aagagagacagtttccggaccccgagggactcgaagctggaggcaccagcagaggaggac
gtgtgggagatcctacggcaggcacccccatctgagtacgagcgcatcgccttccagtac
ggcgtcactgacctgcgcggcatgctaaagaggctcaagggcatgaggcgcgatgagaag
aagagcacagcctttcagaagaagctggagccggcctaccaggtgagcaaaggccacaag
atccggctgaccgtggaactggctgaccatgacgctgaggtcaaatggctcaagaatggc
caggagatccagatgagcggcagcaagtacatctttgagtccatcggtgccaagcgtacc
ctgaccatcagccagtgctcattggcggacgacgcagcctaccagtgcgtggtgggtggc
gagaagtgtagcacggagctctttgtgaaagagccccctgtgctcatcacgcgccccttg
gaggaccagctggtgatggtggggcagcgggtggagtttgagtgtgaagtatcggaggag
ggggcgcaagtcaaatggctgaaggacggggtggagctgacccgggaggagaccttcaaa
taccggttcaagaaggacgggcagagacaccacctgatcatcaacgaggccatgctggag
gacgcggggcactatgcactgtgcactagcgggggccaggcgctggctgagctcattgtg
caggaaaagaagctggaggtgtaccagagcatcgcagacctgatggtgggcgcaaaggac
caggcggtgttcaaatgtgaggtctcagatgagaatgttcggggtgtgtggctgaagaat
gggaaggagctggtgcccgacagccgcataaaggtgtcccacatcgggcgggtccacaaa
ctgaccattgacgacgtcacacctgccgacgaggctgactacagctttgtgcccgagggc
ttcgcctgcaacctgtcagccaagctccacttcatggaggtcaagattgacttcgtaccc
aggcaggaacctcccaagatccacctggactgcccaggccgcataccagacaccattgtg
gttgtagctggaaataagctacgtctggacgtccctatctctggggaccctgctcccact
gtgatctggcagaaggctatcacgcaggggaataaggccccagccaggccagccccagat
gccccagaggacacaggtgacagcgatgagtgggtgtttgacaagaagctgctgtgtgag
accgagggccgggtccgcgtggagaccaccaaggaccgcagcatcttcacggtcgagggg
gcagagaaggaagatgagggcgtctacacggtcacagtgaagaaccctgtgggcgaggac
caggtcaacctcacagtcaaggtcatcgacgtgccagacgcacctgcggcccccaagatc
agcaacgtgggagaggactcctgcacagtacagtgggagccgcctgcctacgatggcggg
cagcccatcctgggctacatcctggagcgcaagaagaagaagagctaccggtggatgcgg
ctgaacttcgacctgattcaggagctgagtcatgaagcgcggcgcatgatcgagggcgtg
gtgtacgagatgcgcgtctacgcggtcaacgccatcggcatgtccaggcccagccctgcc
tcccagcccttcatgcctatcggtccccccagcgaacccacccacctggcagtagaggac
gtctctgacaccacggtctccctcaagtggcggcccccagagcgcgtgggagcaggaggc
ctggatggctacagcgtggagtactgcccagagggctgctcagagtgggtggctgccctg
caggggctgacagagcacacatcgatactggtgaaggacctgcccacgggggcccggctg
cttttccgagtgcgggcacacaatatggcagggcctggagcccctgttaccaccacggag
ccggtgacagtgcaggagatcctgcaacggccacggcttcagctgcccaggcacctgcgc
cagaccattcagaagaaggtcggggagcctgtgaaccttctcatccctttccagggcaag
ccccggcctcaggtgacctggaccaaagaggggcagcccctggcaggcgaggaggtgagc
atccgcaacagccccacagacaccatcctgttcatccgggccgctcgccgcgtgcattca
ggcacttaccaggtgacggtgcgcattgagaacatggaggacaaggccacgctggtgctg
caggttgttgacaagccaagtcctccccaggatctccgggtgactgacgcctggggtctt
aatgtggctctggagtggaagccaccccaggatgtcggcaacacggagctctgggggtac
acagtgcagaaagccgacaagaagaccatggagtggttcaccgtcttggagcattaccgc
cgcacccactgcgtggtgccagagctcatcattggcaatggctactacttccgcgtcttc
agccagaatatggttggctttagtgacagagcggccaccaccaaggagcccgtctttatc
cccagaccaggcatcacctatgagccacccaactataaggccctggacttctccgaggcc
ccaagcttcacccagcccctggtgaaccgctcggtcatcgcgggctacactgctatgctc
tgctgtgctgtccggggtagccccaagcccaagatttcctggttcaagaatggcctggac
ctgggagaagacgcccgcttccgcatgttcagcaagcagggagtgttgactctggagatt
agaaagccctgcccctttgacgggggcatctatgtctgcagggccaccaacttacagggc
gaggcacggtgtgagtgccgcctggaggtgcgagtgcctcagtga
DBGET
integrated database retrieval system