KEGG   Homo sapiens (human): 23353
Entry
23353             CDS       T01001                                 
Symbol
SUN1, UNC84A
Name
(RefSeq) Sad1 and UNC84 domain containing 1
  KO
K19347  SUN domain-containing protein 1/2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01822  Linker of nucleoskeleton and cytoskeleton (LINC) complex
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    23353 (SUN1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    23353 (SUN1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   LINC complex
    23353 (SUN1)
SSDB
Motif
Pfam: MRP Sad1_UNC HTH_SUN2 CCDC144C Trimer_CC FapA
Other DBs
NCBI-GeneID: 23353
NCBI-ProteinID: NP_001124437
OMIM: 607723
HGNC: 18587
Ensembl: ENSG00000164828
UniProt: O94901
Structure
LinkDB
Position
7:815557..874934
AA seq 785 aa
MDFSRLHMYSPPQCVPENTGYTYALSSSYSSDALDFETEHKLDPVFDSPRMSRRSLRLAT
TACTLGDGEAVGADSGTSSAVSLKNRAARTTKQRRSTNKSAFSINHVSRQVTSSGVSHGG
TVSLQDAVTRRPPVLDESWIREQTTVDHFWGLDDDGDLKGGNKAAIQGNGDVGAAAATAH
NGFSCSNCSMLSERKDVLTAHPAAPGPVSRVYSRDRNQKCYFLLQILRRIGAVGQAVSRT
AWSALWLAVVAPGKAASGVFWWLGIGWYQFVTLISWLNVFLLTRCLRNICKFLVLLIPLF
LLLAGLSLRGQGNFFSFLPVLNWASMHRTQRVDDPQDVFKPTTSRLKQPLQGDSEAFPWH
WMSGVEQQVASLSGQCHHHGENLRELTTLLQKLQARVDQMEGGAAGPSASVRDAVGQPPR
ETDFMAFHQEHEVRMSHLEDILGKLREKSEAIQKELEQTKQKTISAVGEQLLPTVEHLQL
ELDQLKSELSSWRHVKTGCETVDAVQERVDVQVREMVKLLFSEDQQGGSLEQLLQRFSSQ
FVSKGDLQTMLRDLQLQILRNVTHHVSVTKQLPTSEAVVSAVSEAGASGITEAQARAIVN
SALKLYSQDKTGMVDFALESGGGSILSTRCSETYETKTALMSLFGIPLWYFSQSPRVVIQ
PDIYPGNCWAFKGSQGYLVVRLSMMIHPAAFTLEHIPKTLSPTGNISSAPKDFAVYGLEN
EYQEEGQLLGQFTYDQDGESLQMFQALKRPDDTAFQIVELRIFSNWGHPEYTCLYRFRVH
GEPVK
NT seq 2358 nt   +upstreamnt  +downstreamnt
atggatttttctcggcttcacatgtacagtcctccccagtgtgtgccggagaacacgggc
tacacgtatgcgctcagttccagctattcttcagatgctctggattttgagacggagcac
aaattggaccctgtatttgattctccacggatgtcccgccgtagtttgcgcctggccacg
acagcatgcaccctgggggatggtgaggctgtgggtgccgacagcggcaccagcagcgct
gtctccctgaagaaccgagcggccagaacaacaaaacagcgcagaagcacaaacaaatca
gcttttagtatcaaccacgtgtcaaggcaggtcacgtcctctggcgtcagccacggcggc
actgtcagcctgcaggatgctgtgactcgacggcctcctgtattggacgagtcttggatt
cgtgaacagaccacagtggaccacttctggggtcttgatgatgatggtgatcttaaaggt
ggaaataaagctgccattcagggaaacggggatgtgggagccgccgccgccaccgcgcac
aacggcttctcctgcagcaactgcagcatgctgtccgagcgcaaggacgtgctcacggcg
caccccgcggcccccgggcccgtgtcgagagtttattctagggacaggaatcaaaaatgt
tacttcttgctgcagattctgcgcaggatcggagctgtgggccaggctgtgtccaggacg
gcgtggtcggccctttggctggccgtggttgctccagggaaggcagcctctggagtgttc
tggtggctggggattggatggtaccagtttgttactttgatttcttggctgaatgtgttt
cttcttaccaggtgccttcgaaacatctgcaagtttttagtcttgctcatcccactcttc
cttttactagcaggtctctccttacggggccagggcaatttcttttcgttcttgcccgtg
ttgaactgggcaagcatgcatagaacacagcgggtggatgacccccaggacgtgtttaaa
cccacgacttctcgcctgaagcagcctctgcagggtgacagtgaggcttttccgtggcat
tggatgagtggcgtggagcagcaggtggcctctctgtctggacagtgccaccaccatggt
gagaatctccgagagctgaccactttgctacagaagctgcaggctcgggtggaccagatg
gaaggcggcgctgccgggccgtcagcttcggtcagagacgctgtgggacagcccccgagg
gagactgactttatggcctttcaccaagaacatgaagtgcgtatgtcacacttggaagat
attctgggaaaactgagagaaaaatctgaggccatccagaaggaactagaacagaccaag
caaaaaacaatcagtgcggttggtgagcagctcctgcccacagtcgagcacctccagctg
gagctggatcagctaaagtcagagctgtccagctggcgacacgtgaagaccggctgtgag
acagtggatgccgtacaagaaagagtggacgtgcaagtcagagaaatggtgaaactcctg
ttttccgaagatcagcaaggcggttctctggaacagctgctgcagaggttctcatcacag
tttgtgagcaaaggcgacttgcagacgatgctgcgagacctgcagctgcagatcctgcgg
aacgtcacccaccacgtttccgtgaccaagcagctcccaacctcagaagccgtggtgtct
gctgtgagcgaggcgggggcgtctggaataacagaggcgcaagcacgtgccatcgtgaac
agcgccttgaagctgtattcccaagataagaccgggatggtggactttgctctggaatct
ggtggtggcagcatcttgagtactcgctgttctgaaacttacgaaaccaaaacggcgctg
atgagtctgtttgggatcccgctgtggtacttctcgcagtccccgcgcgtggtcatccag
cctgacatttaccccggtaactgctgggcatttaaaggctcccaggggtacctggtggtg
aggctctccatgatgatccacccagccgccttcactctggagcacatccctaagacgctg
tcgccaacaggcaacatcagcagcgcccccaaggacttcgccgtctatggattagaaaat
gagtatcaggaagaagggcagcttctgggacagttcacgtatgatcaggatggggagtcg
ctccagatgttccaggccctgaaaagacccgacgacacagctttccaaatagtggaactt
cggattttttctaactggggccatcctgagtatacctgtctgtatcggttcagagttcat
ggcgaacctgtcaagtga

KEGG   Homo sapiens (human): 25777
Entry
25777             CDS       T01001                                 
Symbol
SUN2, UNC84B, rab5IP
Name
(RefSeq) Sad1 and UNC84 domain containing 2
  KO
K19347  SUN domain-containing protein 1/2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01822  Linker of nucleoskeleton and cytoskeleton (LINC) complex
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    25777 (SUN2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    25777 (SUN2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   LINC complex
    25777 (SUN2)
SSDB
Motif
Pfam: Sad1_UNC HTH_SUN2 Lipoprotein_6 DUF2096 Pox_F11 DUF2937
Other DBs
NCBI-GeneID: 25777
NCBI-ProteinID: NP_001186509
OMIM: 613569
HGNC: 14210
Ensembl: ENSG00000100242
UniProt: Q9UH99 B4E2A6
Structure
LinkDB
Position
22:complement(38734734..38755998)
AA seq 717 aa
MSRRSQRLTRYSQGDDDGSSSSGGSSVAGSQSTLFKDSPLRTLKRKSSNMKRLSPAPQLG
PSSDAHTSYYSESLVHESWFPPRSSLEELHGDANWGEDLRVRRRRGTGGSESSRASGLVG
RKATEDFLGSSSGYSSEDDYVGYSDVDQQSSSSRLRSAVSRAGSLLWMVATSPGRLFRLL
YWWAGTTWYRLTTAASLLDVFVLTRRFSSLKTFLWFLLPLLLLTCLTYGAWYFYPYGLQT
FHPALVSWWAAKDSRRPDEGWEARDSSPHFQAEQRVMSRVHSLERRLEALAAEFSSNWQK
EAMRLERLELRQGAPGQGGGGGLSHEDTLALLEGLVSRREAALKEDFRRETAARIQEELS
ALRAEHQQDSEDLFKKIVRASQESEARIQQLKSEWQSMTQESFQESSVKELRRLEDQLAG
LQQELAALALKQSSVAEEVGLLPQQIQAVRDDVESQFPAWISQFLARGGGGRVGLLQREE
MQAQLRELESKILTHVAEMQGKSAREAAASLSLTLQKEGVIGVTEEQVHHIVKQALQRYS
EDRIGLADYALESGGASVISTRCSETYETKTALLSLFGIPLWYHSQSPRVILQPDVHPGN
CWAFQGPQGFAVVRLSARIRPTAVTLEHVPKALSPNSTISSAPKDFAIFGFDEDLQQEGT
LLGKFTYDQDGEPIQTFHFQAPTMATYQVVELRILTNWGHPEYTCIYRFRVHGEPAH
NT seq 2154 nt   +upstreamnt  +downstreamnt
atgtcccgaagaagccagcgcctcacgcgctactcccagggtgacgatgacggcagcagc
agcagcggagggagctcggtggctgggagtcagagcaccctgtttaaagacagtcctctc
aggaccttgaagaggaaatccagcaacatgaagcgcctgtccccagcgccacagctgggc
ccgtcctctgatgcacacacctcctactacagtgagtcgctggtccacgagtcctggttc
ccacccaggagctccctggaggaactgcatggtgacgccaactggggtgaggacctgcgg
gtgcggaggaggagaggcacgggtggctcagagagcagcagggccagcgggcttgtgggg
cgcaaggccaccgaggacttcctgggctcttcctcgggctactcctctgaggacgactac
gtgggctactcggatgtggaccagcagagttccagctcgcggctccgaagcgccgtctca
cgggcgggctccttactctggatggtggccacttcgccaggccggctcttcagacttctc
tactggtgggctggcaccacctggtaccgcctgaccacagctgcctccctccttgacgtc
ttcgttttaaccaggcgcttctcgtccctgaagacgttcctctggttcctgctgccgctg
ctcttgctgacgtgcctgacgtatggtgcttggtatttctacccctatgggctgcagaca
ttccaccctgctttggtttcctggtgggcagcgaaggacagcaggaggccggatgagggc
tgggaagccagagactcatcgccacatttccaggctgagcagcgtgttatgtcccgggta
cactctctggagcggcgtctggaagctcttgctgctgaattttcctccaactggcagaag
gaggccatgcggctggaacgtctggagctgcggcaaggggctcctggccagggaggtggt
ggtggcctgagccacgaggacaccctggcgctgctggaggggctagtgagccgccgtgaa
gctgccctgaaggaggatttccgcagggaaactgctgctcgcatccaggaagaactgtct
gccctgagagcagagcatcagcaagactcagaagacctcttcaagaagatcgtccgggcc
tcccaggagtccgaggctcgcatccagcagctgaagtcagagtggcaaagcatgacccag
gagtccttccaggagagctctgtgaaggagctgaggcggctggaggaccagctggccggc
ctgcagcaggagctggcggctctggcactgaagcagagctcggtggcggaagaagtgggc
ctgctgccccagcagatccaggccgtgcgggacgacgtggaatctcagttcccggcctgg
atcagtcagttccttgcccgaggtggagggggccgcgtggggctccttcagagagaggag
atgcaagctcagctgcgagagctggagagcaagatcctcacccatgtggcagagatgcag
ggcaagtcggccagggaagccgcggcctccctgagcctgacgctgcagaaagaaggtgtg
attggagtgacagaggagcaggtgcaccacatcgtgaagcaggccctgcagcgctacagt
gaggaccgcatcgggctggcagactacgccctggagtcaggaggggccagcgtcatcagc
acccgatgttctgagacctacgagaccaagacggccctcctcagcctcttcggcatcccc
ctgtggtaccactcccagtcaccccgagtcatcctccagccagatgtgcacccaggcaac
tgctgggccttccaggggccacaaggcttcgccgtggtccgcctctctgcccgcatccgc
cccacagccgttaccttagagcatgtgcccaaggccttgtcacccaacagcactatctcc
agtgcccccaaggacttcgccatctttgggtttgacgaagacctgcagcaggaggggaca
ctccttggcaagttcacttacgatcaggacggcgagcctattcagacgtttcactttcag
gcccctacgatggccacgtaccaggtggtggagctgcggatcctgactaactggggccac
cccgagtacacctgcatctaccgcttcagagtgcatggggagcccgcccactag

KEGG   Homo sapiens (human): 79188
Entry
79188             CDS       T01001                                 
Symbol
TMEM43, ARVC5, ARVD5, AUNA3, EDMD7, AUNA2, LUMA
Name
(RefSeq) transmembrane protein 43
  KO
K27488  transmembrane protein 43
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01822  Linker of nucleoskeleton and cytoskeleton (LINC) complex
Disease
H00293  Arrhythmogenic right ventricular cardiomyopathy
H00563  Emery-Dreifuss muscular dystrophy
H02339  Auditory neuropathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    79188 (TMEM43)
SSDB
Motif
Pfam: TMEM43 UPF0697
Other DBs
NCBI-GeneID: 79188
NCBI-ProteinID: NP_077310
OMIM: 612048
HGNC: 28472
Ensembl: ENSG00000170876
UniProt: Q9BTV4 A0A024R2F9
LinkDB
Position
3:14125052..14143680
AA seq 400 aa
MAANYSSTSTRREHVKVKTSSQPGFLERLSETSGGMFVGLMAFLLSFYLIFTNEGRALKT
ATSLAEGLSLVVSPDSIHSVAPENEGRLVHIIGALRTSKLLSDPNYGVHLPAVKLRRHVE
MYQWVETEESREYTEDGQVKKETRYSYNTEWRSEIINSKNFDREIGHKNPSAMAVESFMA
TAPFVQIGRFFLSSGLIDKVDNFKSLSLSKLEDPHVDIIRRGDFFYHSENPKYPEVGDLR
VSFSYAGLSGDDPDLGPAHVVTVIARQRGDQLVPFSTKSGDTLLLLHHGDFSAEEVFHRE
LRSNSMKTWGLRAAGWMAMFMGLNLMTRILYTLVDWFPVFRDLVNIGLKAFAFCVATSLT
LLTVAAGWLFYRPLWALLIAGLALVPILVARTRVPAKKLE
NT seq 1203 nt   +upstreamnt  +downstreamnt
atggccgcgaattattccagtaccagtacccggagagaacatgtcaaagttaaaaccagc
tcccagccaggcttcctggaacggctgagcgagacctcgggtgggatgtttgtggggctc
atggccttcctgctctccttctacctaattttcaccaatgagggccgcgcattgaagacg
gcaacctcattggctgaggggctctcgcttgtggtgtctcccgacagcatccacagtgtg
gctccggagaatgaaggaaggctggtgcacatcattggcgccttacggacatccaagctt
ttgtctgatccaaactatggggtccatcttccggctgtgaaactgcggaggcacgtggag
atgtaccaatgggtagaaactgaggagtccagggagtacaccgaggatgggcaggtgaag
aaggagacgaggtattcctacaacactgaatggaggtcagaaatcatcaacagcaaaaac
ttcgaccgagagattggccacaaaaaccccagtgccatggcagtggagtcattcatggca
acagccccctttgtccaaattggcaggtttttcctctcgtcaggcctcatcgacaaagtc
gacaacttcaagtccctgagcctatccaagctggaggaccctcatgtggacatcattcgc
cgtggagactttttctaccacagcgaaaatcccaagtatccagaggtgggagacttgcgt
gtctccttttcctatgctggactgagcggcgatgaccctgacctgggcccagctcacgtg
gtcactgtgattgcccggcagcggggtgaccagctagtcccattctccaccaagtctggg
gataccttactgctcctgcaccacggggacttctcagcagaggaggtgtttcatagagaa
ctaaggagcaactccatgaagacctggggcctgcgggcagctggctggatggccatgttc
atgggcctcaaccttatgacacggatcctctacaccttggtggactggtttcctgttttc
cgagacctggtcaacattggcctgaaagcctttgccttctgtgtggccacctcgctgacc
ctgctgaccgtggcggctggctggctcttctaccgacccctgtgggccctcctcattgcc
ggcctggcccttgtgcccatccttgttgctcggacacgggtgccagccaaaaagttggag
tga

KEGG   Homo sapiens (human): 2010
Entry
2010              CDS       T01001                                 
Symbol
EMD, EDMD, LEMD5, STA
Name
(RefSeq) emerin
  KO
K12569  emerin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01822  Linker of nucleoskeleton and cytoskeleton (LINC) complex
Disease
H00563  Emery-Dreifuss muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    2010 (EMD)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    2010 (EMD)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    2010 (EMD)
   05414 Dilated cardiomyopathy
    2010 (EMD)
SSDB
Motif
Pfam: LEM MGC-24 DotU
Other DBs
NCBI-GeneID: 2010
NCBI-ProteinID: NP_000108
OMIM: 300384
HGNC: 3331
Ensembl: ENSG00000102119
UniProt: P50402
Structure
LinkDB
Position
X:154379295..154381523
AA seq 254 aa
MDNYADLSDTELTTLLRRYNIPHGPVVGSTRRLYEKKIFEYETQRRRLSPPSSSAASSYS
FSDLNSTRGDADMYDLPKKEDALLYQSKGYNDDYYEESYFTTRTYGEPESAGPSRAVRQS
VTSFPDADAFHHQVHDDDLLSSSEEECKDRERPMYGRDSAYQSITHYRPVSASRSSLDLS
YYPTSSSTSFMSSSSSSSSWLTRRAIRPENRAPGAGLGQDRQVPLWGQLLLFLVFVIVLF
FIYHFMQAEEGNPF
NT seq 765 nt   +upstreamnt  +downstreamnt
atggacaactacgcagatctttcggataccgagctgaccaccttgctgcgccggtacaac
atcccgcacgggcctgtagtaggatcaactcgtaggctttacgagaagaagatcttcgag
tacgagacccagaggcggcggctctcgccccccagctcgtccgccgcctcctcttatagc
ttctctgacttgaattcgactagaggggatgcagatatgtatgatcttcccaagaaagag
gacgctttactctaccagagcaagggctacaatgacgactactatgaagagagctacttc
accaccaggacttatggggagcccgagtctgccggcccgtccagggctgtccgccagtca
gtgacttcattcccagatgctgacgctttccatcaccaggtgcatgatgacgatcttttg
tcttcttctgaagaggagtgcaaggatagggaacgccccatgtacggccgggacagtgcc
taccagagcatcacgcactaccgccctgtttcagcctccaggagctccctggacctgtcc
tattatcctacttcctcctccacctcttttatgtcctcctcatcatcttcctcttcatgg
ctcacccgccgtgccatccggcctgaaaaccgtgctcctggggctgggctgggccaggat
cgccaggtcccgctctggggccagctgctgcttttcctggtctttgtgatcgtcctcttc
ttcatttaccacttcatgcaggctgaagaaggcaaccccttctag

KEGG   Homo sapiens (human): 3930
Entry
3930              CDS       T01001                                 
Symbol
LBR, C14SR, DHCR14B, LMN2R, PHA, PHASK, TDRD18
Name
(RefSeq) lamin B receptor
  KO
K19532  Delta14-sterol reductase (lamin-B receptor) [EC:1.3.1.70]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00100  Steroid biosynthesis
hsa01100  Metabolic pathways
hsa04820  Cytoskeleton in muscle cells
Module
hsa_M00101  Cholesterol biosynthesis, FPP => cholesterol
Network
nt06034  Cholesterol biosynthesis
nt06539  Cytoskeleton in muscle cells
  Element
N01624  Cholesterol biosynthesis
N01822  Linker of nucleoskeleton and cytoskeleton (LINC) complex
Disease
H00234  Pelger-Huet anomaly
H00447  HEM skeletal dysplasia
H01133  Reynolds syndrome
H02732  Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09103 Lipid metabolism
   00100 Steroid biosynthesis
    3930 (LBR)
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    3930 (LBR)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    3930 (LBR)
Enzymes [BR:hsa01000]
 1. Oxidoreductases
  1.3  Acting on the CH-CH group of donors
   1.3.1  With NAD+ or NADP+ as acceptor
    1.3.1.70  Delta14-sterol reductase
     3930 (LBR)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Heterochromatin formation proteins
   Other heterochromatin formation proteins
    3930 (LBR)
SSDB
Motif
Pfam: ERG4_ERG24 LBR_tudor DUF1295 ICMT PTM_DIR17_Tudor PEMT Tudor_3
Other DBs
NCBI-GeneID: 3930
NCBI-ProteinID: NP_002287
OMIM: 600024
HGNC: 6518
Ensembl: ENSG00000143815
UniProt: Q14739
Structure
LinkDB
Position
1:complement(225401502..225428821)
AA seq 615 aa
MPSRKFADGEVVRGRWPGSSLYYEVEILSHDSTSQLYTVKYKDGTELELKENDIKPLTSF
RQRKGGSTSSSPSRRRGSRSRSRSRSPGRPPKSARRSASASHQADIKEARREVEVKLTPL
ILKPFGNSISRYNGEPEHIERNDAPHKNTQEKFSLSQESSYIATQYSLRPRREEVKLKEI
DSKEEKYVAKELAVRTFEVTPIRAKDLEFGGVPGVFLIMFGLPVFLFLLLLMCKQKDPSL
LNFPPPLPALYELWETRVFGVYLLWFLIQVLFYLLPIGKVVEGTPLIDGRRLKYRLNGFY
AFILTSAVIGTSLFQGVEFHYVYSHFLQFALAATVFCVVLSVYLYMRSLKAPRNDLSPAS
SGNAVYDFFIGRELNPRIGTFDLKYFCELRPGLIGWVVINLVMLLAEMKIQDRAVPSLAM
ILVNSFQLLYVVDALWNEEALLTTMDIIHDGFGFMLAFGDLVWVPFIYSFQAFYLVSHPN
EVSWPMASLIIVLKLCGYVIFRGANSQKNAFRKNPSDPKLAHLKTIHTSTGKNLLVSGWW
GFVRHPNYLGDLIMALAWSLPCGFNHILPYFYIIYFTMLLVHREARDEYHCKKKYGVAWE
KYCQRVPYRIFPYIY
NT seq 1848 nt   +upstreamnt  +downstreamnt
atgccaagtaggaaatttgccgatggtgaagtggtaagaggtcgatggcctgggagttca
ctttattatgaagtagaaattctgagccacgacagcacctcccagctttacactgtgaag
tataaagatggaacagagcttgaattgaaagagaatgatattaagcctttaacttccttt
aggcaaaggaaaggtggctcaacttccagttccccttccagacgccgagggagtcgatca
aggtcacgctcccgatcccctggtcgaccacctaaaagtgcccgccgatctgcttctgct
tcccaccaggccgacattaaggaagcaaggagggaagtggaagttaaattgactccgctg
attctgaagccatttggaaatagcatcagcagatataatggggagcctgagcatattgag
agaaatgacgcacctcataaaaatacacaggaaaaattcagtttgtcacaagaaagcagt
tacatagcaacacagtatagccttcgtccaagaagagaagaagtcaaattaaaagaaata
gattctaaggaagaaaaatacgttgcaaaagaactggcagtgagaacctttgaagtgacc
cccatccgggcaaaggacttggagtttggaggagtacctggtgtgtttctcatcatgttt
ggcctgcctgtgttcctcttcctgttgctgttgatgtgtaaacagaaagatcccagtctt
ctgaatttccctcctcctttgccagctttgtatgagttatgggaaaccagagtatttggg
gtctacctcctgtggtttttgattcaagtcctgttctacctactgccaattggaaaggtt
gtagaaggaacgcctcttattgatggaagaagactcaagtatagattaaatggattctat
gcttttatcctgacatctgcagtcatcggaacatctctcttccagggcgtagagtttcat
tacgtgtacagtcattttcttcagtttgcacttgcggccactgttttttgtgtggtcttg
agtgtgtatctctacatgcgctctttgaaagcgccccggaatgacctgtcgcctgccagc
tctggaaatgctgtctatgatttcttcattggccgtgaattaaaccctcgaattggtact
tttgatctcaaatacttttgtgaattgcgccccggattgattggatgggtggttattaac
ttggtgatgcttttggctgaaatgaaaatacaggaccgcgctgttccatccttggccatg
attttagttaatagtttccagcttctctatgtggtggatgctctctggaatgaggaagcg
ttgttgacgaccatggacatcatccacgatggatttggattcatgctggcttttggagac
ttggtgtgggttccctttatttacagcttccaagccttttatttagtcagtcatccaaat
gaagtgtcttggccaatggcttctctaattattgttctgaaactttgtggttatgtaatc
ttccgaggtgcaaattctcagaaaaatgcattccggaaaaatcccagtgatccaaagctt
gcacatttaaaaaccattcatacttcaacgggaaaaaatcttctagtttctggatggtgg
ggctttgttcgccaccccaattacttgggtgatctcatcatggccttggcgtggtccctc
ccatgtggttttaaccacattctgccttatttctacataatttatttcaccatgttgctt
gtccaccgagaagctcgtgacgagtaccactgtaagaagaaatacggcgtggcttgggaa
aagtactgtcagcgtgtgccctaccgtatatttccatacatctactaa

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