Homo sapiens (human): 4000
Help
Entry
4000 CDS
T01001
Symbol
LMNA, CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1
Name
(RefSeq) lamin A/C
KO
K12641
lamin A/C
Organism
hsa
Homo sapiens (human)
Pathway
hsa04210
Apoptosis
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
H00264
Charcot-Marie-Tooth disease
H00294
Dilated cardiomyopathy
H00420
Familial partial lipodystrophy
H00563
Emery-Dreifuss muscular dystrophy
H00590
Congenital muscular dystrophies (CMD/MDC)
H00601
Hutchinson-Gilford progeria syndrome
H00663
Restrictive dermopathy
H00665
Mandibuloacral dysplasia
H02677
Progeroid laminopathy
H02725
Heart-hand syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
4000 (LMNA)
09142 Cell motility
04820 Cytoskeleton in muscle cells
4000 (LMNA)
09160 Human Diseases
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
4000 (LMNA)
05412 Arrhythmogenic right ventricular cardiomyopathy
4000 (LMNA)
05414 Dilated cardiomyopathy
4000 (LMNA)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
4000 (LMNA)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Type V: Nuclear lamins
4000 (LMNA)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Filament
LTD
TPR_MLP1_2
HAUS-augmin3
TolA_bind_tri
Cnn_1N
CENP-F_leu_zip
Tht1
DUF4407
Motif
Other DBs
NCBI-GeneID:
4000
NCBI-ProteinID:
NP_733821
OMIM:
150330
HGNC:
6636
Ensembl:
ENSG00000160789
UniProt:
P02545
A0A384MQX1
Structure
PDB
LinkDB
All DBs
Position
1:156082573..156140081
Genome browser
AA seq
664 aa
AA seq
DB search
METPSQRRATRSGAQASSTPLSPTRITRLQEKEDLQELNDRLAVYIDRVRSLETENAGLR
LRITESEEVVSREVSGIKAAYEAELGDARKTLDSVAKERARLQLELSKVREEFKELKARN
TKKEGDLIAAQARLKDLEALLNSKEAALSTALSEKRTLEGELHDLRGQVAKLEAALGEAK
KQLQDEMLRRVDAENRLQTMKEELDFQKNIYSEELRETKRRHETRLVEIDNGKQREFESR
LADALQELRAQHEDQVEQYKKELEKTYSAKLDNARQSAERNSNLVGAAHEELQQSRIRID
SLSAQLSQLQKQLAAKEAKLRDLEDSLARERDTSRRLLAEKEREMAEMRARMQQQLDEYQ
ELLDIKLALDMEIHAYRKLLEGEEERLRLSPSPTSQRSRGRASSHSSQTQGGGSVTKKRK
LESTESRSSFSQHARTSGRVAVEEVDEEGKFVRLRNKSNEDQSMGNWQIKRQNGDDPLLT
YRFPPKFTLKAGQVVTIWAAGAGATHSPPTDLVWKAQNTWGCGNSLRTALINSTGEEVAM
RKLVRSVTVVEDDEDEDGDDLLHHHHGSHCSSSGDPAEYNLRSRTVLCGTCGQPADKASA
SGSGAQVGGPISSGSSASSVTVTRSYRSVGGSGGGSFGDNLVTRSYLLGNSSPRTQSPQN
CSIM
NT seq
1995 nt
NT seq
+upstream
nt +downstream
nt
atggagaccccgtcccagcggcgcgccacccgcagcggggcgcaggccagctccactccg
ctgtcgcccacccgcatcacccggctgcaggagaaggaggacctgcaggagctcaatgat
cgcttggcggtctacatcgaccgtgtgcgctcgctggaaacggagaacgcagggctgcgc
cttcgcatcaccgagtctgaagaggtggtcagccgcgaggtgtccggcatcaaggccgcc
tacgaggccgagctcggggatgcccgcaagacccttgactcagtagccaaggagcgcgcc
cgcctgcagctggagctgagcaaagtgcgtgaggagtttaaggagctgaaagcgcgcaat
accaagaaggagggtgacctgatagctgctcaggctcggctgaaggacctggaggctctg
ctgaactccaaggaggccgcactgagcactgctctcagtgagaagcgcacgctggagggc
gagctgcatgatctgcggggccaggtggccaagcttgaggcagccctaggtgaggccaag
aagcaacttcaggatgagatgctgcggcgggtggatgctgagaacaggctgcagaccatg
aaggaggaactggacttccagaagaacatctacagtgaggagctgcgtgagaccaagcgc
cgtcatgagacccgactggtggagattgacaatgggaagcagcgtgagtttgagagccgg
ctggcggatgcgctgcaggaactgcgggcccagcatgaggaccaggtggagcagtataag
aaggagctggagaagacttattctgccaagctggacaatgccaggcagtctgctgagagg
aacagcaacctggtgggggctgcccacgaggagctgcagcagtcgcgcatccgcatcgac
agcctctctgcccagctcagccagctccagaagcagctggcagccaaggaggcgaagctt
cgagacctggaggactcactggcccgtgagcgggacaccagccggcggctgctggcggaa
aaggagcgggagatggccgagatgcgggcaaggatgcagcagcagctggacgagtaccag
gagcttctggacatcaagctggccctggacatggagatccacgcctaccgcaagctcttg
gagggcgaggaggagaggctacgcctgtcccccagccctacctcgcagcgcagccgtggc
cgtgcttcctctcactcatcccagacacagggtgggggcagcgtcaccaaaaagcgcaaa
ctggagtccactgagagccgcagcagcttctcacagcacgcacgcactagcgggcgcgtg
gccgtggaggaggtggatgaggagggcaagtttgtccggctgcgcaacaagtccaatgag
gaccagtccatgggcaattggcagatcaagcgccagaatggagatgatcccttgctgact
taccggttcccaccaaagttcaccctgaaggctgggcaggtggtgacgatctgggctgca
ggagctggggccacccacagcccccctaccgacctggtgtggaaggcacagaacacctgg
ggctgcgggaacagcctgcgtacggctctcatcaactccactggggaagaagtggccatg
cgcaagctggtgcgctcagtgactgtggttgaggacgacgaggatgaggatggagatgac
ctgctccatcaccaccacggctcccactgcagcagctcgggggaccccgctgagtacaac
ctgcgctcgcgcaccgtgctgtgcgggacctgcgggcagcctgccgacaaggcatctgcc
agcggctcaggagcccaggtgggcggacccatctcctctggctcttctgcctccagtgtc
acggtcactcgcagctaccgcagtgtggggggcagtgggggtggcagcttcggggacaat
ctggtcacccgctcctacctcctgggcaactccagcccccgaacccagagcccccagaac
tgcagcatcatgtaa
Homo sapiens (human): 4001
Help
Entry
4001 CDS
T01001
Symbol
LMNB1, ADLD, LMN, LMN2, LMNB, MCPH26
Name
(RefSeq) lamin B1
KO
K07611
lamin B
Organism
hsa
Homo sapiens (human)
Pathway
hsa04210
Apoptosis
hsa04820
Cytoskeleton in muscle cells
Network
nt06539
Cytoskeleton in muscle cells
Element
N01822
Linker of nucleoskeleton and cytoskeleton (LINC) complex
Disease
H00269
Primary microcephaly
H01230
Adult-onset autosomal dominant leukodystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
4001 (LMNB1)
09142 Cell motility
04820 Cytoskeleton in muscle cells
4001 (LMNB1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
4001 (LMNB1)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Type V: Nuclear lamins
4001 (LMNB1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Filament
LTD
Motif
Other DBs
NCBI-GeneID:
4001
NCBI-ProteinID:
NP_005564
OMIM:
150340
HGNC:
6637
Ensembl:
ENSG00000113368
UniProt:
P20700
Structure
PDB
LinkDB
All DBs
Position
5:126776623..126837020
Genome browser
AA seq
586 aa
AA seq
DB search
MATATPVPPRMGSRAGGPTTPLSPTRLSRLQEKEELRELNDRLAVYIDKVRSLETENSAL
QLQVTEREEVRGRELTGLKALYETELADARRALDDTARERAKLQIELGKCKAEHDQLLLN
YAKKESDLNGAQIKLREYEAALNSKDAALATALGDKKSLEGDLEDLKDQIAQLEASLAAA
KKQLADETLLKVDLENRCQSLTEDLEFRKSMYEEEINETRRKHETRLVEVDSGRQIEYEY
KLAQALHEMREQHDAQVRLYKEELEQTYHAKLENARLSSEMNTSTVNSAREELMESRMRI
ESLSSQLSNLQKESRACLERIQELEDLLAKEKDNSRRMLTDKEREMAEIRDQMQQQLNDY
EQLLDVKLALDMEISAYRKLLEGEEERLKLSPSPSSRVTVSRASSSRSVRTTRGKRKRVD
VEESEASSSVSISHSASATGNVCIEEIDVDGKFIRLKNTSEQDQPMGGWEMIRKIGDTSV
SYKYTSRYVLKAGQTVTIWAANAGVTASPPTDLIWKNQNSWGTGEDVKVILKNSQGEEVA
QRSTVFKTTIPEEEEEEEEAAGVVVEEELFHQQGTPRASNRSCAIM
NT seq
1761 nt
NT seq
+upstream
nt +downstream
nt
atggcgactgcgacccccgtgccgccgcggatgggcagccgcgctggcggccccaccacg
ccgctgagccccacgcgcctgtcgcggctccaggagaaggaggagctgcgcgagctcaat
gaccggctggcggtgtacatcgacaaggtgcgcagcctggagacggagaacagcgcgctg
cagctgcaggtgacggagcgcgaggaggtgcgcggccgtgagctcaccggcctcaaggcg
ctctacgagaccgagctggccgacgcgcgacgcgcgctcgacgacacggcccgcgagcgc
gccaagctgcagatcgagctgggcaagtgcaaggcggaacacgaccagctgctcctcaac
tatgctaagaaggaatctgatcttaatggcgcccagatcaagcttcgagaatatgaagca
gcactgaattcgaaagatgcagctcttgctactgcacttggtgacaaaaaaagtttagag
ggagatttggaggatctgaaggatcagattgcccagttggaagcctccttagctgcagcc
aaaaaacagttagcagatgaaactttacttaaagtagatttggagaatcgttgtcagagc
cttactgaggacttggagtttcgcaaaagcatgtatgaagaggagattaacgagaccaga
aggaagcatgaaacgcgcttggtagaggtggattctgggcgtcaaattgagtatgagtac
aagctggcgcaagcccttcatgagatgagagagcaacatgatgcccaagtgaggctgtat
aaggaggagctggagcagacttaccatgccaaacttgagaatgccagactgtcatcagag
atgaatacttctactgtcaacagtgccagggaagaactgatggaaagccgcatgagaatt
gagagcctttcatcccagctttctaatctacagaaagagtctagagcatgtttggaaagg
attcaagaattagaggacttgcttgctaaagaaaaagacaactctcgtcgcatgctgaca
gacaaagagagagagatggcggaaataagggatcaaatgcagcaacagctgaatgactat
gaacagcttcttgatgtaaagttagccctggacatggaaatcagtgcttacaggaaactc
ttagaaggcgaagaagagaggttgaagctgtctccaagcccttcttcccgtgtgacagta
tcccgagcatcctcaagtcgtagtgtacgtacaactagaggaaagcggaagagggttgat
gtggaagaatcagaggcgagtagtagtgttagcatctctcattccgcctcagccactgga
aatgtttgcatcgaagaaattgatgttgatgggaaatttatccgcttgaagaacacttct
gaacaggatcaaccaatgggaggctgggagatgatcagaaaaattggagacacatcagtc
agttataaatatacctcaagatatgtgctgaaggcaggccagactgttacaatttgggct
gcaaacgctggtgtcacagccagccccccaactgacctcatctggaagaaccagaactcg
tggggcactggcgaagatgtgaaggttatattgaaaaattctcagggagaggaggttgct
caaagaagtacagtctttaaaacaaccatacctgaagaagaggaggaggaggaagaagca
gctggagtggttgttgaggaagaacttttccaccagcagggaaccccaagagcatccaat
agaagctgtgcaattatgtaa
Homo sapiens (human): 84823
Help
Entry
84823 CDS
T01001
Symbol
LMNB2, EPM9, LAMB2, LMN2, MCPH27
Name
(RefSeq) lamin B2
KO
K07611
lamin B
Organism
hsa
Homo sapiens (human)
Pathway
hsa04210
Apoptosis
hsa04820
Cytoskeleton in muscle cells
Network
nt06539
Cytoskeleton in muscle cells
Element
N01822
Linker of nucleoskeleton and cytoskeleton (LINC) complex
Disease
H00269
Primary microcephaly
H00420
Familial partial lipodystrophy
H00810
Progressive myoclonic epilepsy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
84823 (LMNB2)
09142 Cell motility
04820 Cytoskeleton in muscle cells
84823 (LMNB2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
84823 (LMNB2)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Intermediate filaments
Intermediate filaments
Type V: Nuclear lamins
84823 (LMNB2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Filament
LTD
BRE1
Atg11_middle
Motif
Other DBs
NCBI-GeneID:
84823
NCBI-ProteinID:
NP_116126
OMIM:
150341
HGNC:
6638
Ensembl:
ENSG00000176619
UniProt:
Q03252
Structure
PDB
LinkDB
All DBs
Position
19:complement(2428166..2456959)
Genome browser
AA seq
620 aa
AA seq
DB search
MSPPSPGRRREQRRPRAAATMATPLPGRAGGPATPLSPTRLSRLQEKEELRELNDRLAHY
IDRVRALELENDRLLLKISEKEEVTTREVSGIKALYESELADARRVLDETARERARLQIE
IGKLRAELDEVNKSAKKREGELTVAQGRVKDLESLFHRSEVELAAALSDKRGLESDVAEL
RAQLAKAEDGHAVAKKQLEKETLMRVDLENRCQSLQEELDFRKSVFEEEVRETRRRHERR
LVEVDSSRQQEYDFKMAQALEELRSQHDEQVRLYKLELEQTYQAKLDSAKLSSDQNDKAA
SAAREELKEARMRLESLSYQLSGLQKQASAAEDRIRELEEAMAGERDKFRKMLDAKEQEM
TEMRDVMQQQLAEYQELLDVKLALDMEINAYRKLLEGEEERLKLSPSPSSRVTVSRATSS
SSGSLSATGRLGRSKRKRLEVEEPLGSGPSVLGTGTGGSGGFHLAQQASASGSVSIEEID
LEGKFVQLKNNSDKDQSLGNWRIKRQVLEGEEIAYKFTPKYILRAGQMVTVWAAGAGVAH
SPPSTLVWKGQSSWGTGESFRTVLVNADGEEVAMRTVKKSSVMRENENGEEEEEEAEFGE
EDLFHQQGDPRTTSRGCYVM
NT seq
1863 nt
NT seq
+upstream
nt +downstream
nt
atgagcccgccgagcccgggccgccgtcgggagcagcgcaggccgcgagccgccgccacc
atggccacgccgctgcccggccgcgcgggcgggcccgccacgccgctgtcgcccacgcgc
ctgtcgcggctgcaggagaaggaggagctgcgcgagctcaacgaccgcctggcgcactac
atcgaccgcgtccgcgcgctggagctggagaacgaccggctcctgctcaagatctcagag
aaggaggaggtgaccacgcgcgaggtgagtggcatcaaggcgctgtacgagtcggagctg
gccgatgcccggagagtcctggatgagacggctcgagagcgtgcccggctgcagatagag
attgggaagctgagggcagagttggacgaggtcaacaagagcgccaagaagagggagggc
gagcttacggtggcccagggccgtgtgaaggacctggagtccctgttccaccggagcgag
gtggagctggcagctgccctcagcgacaagcgcggcctggagagtgacgtggctgagctg
cgggcccagctggccaaggccgaggacggtcatgcagtggccaaaaagcagctggagaag
gagacgctgatgcgtgtggacctggagaaccgctgccagagcctgcaggaggagctggac
ttccggaagagtgtgttcgaggaggaggtgcgggagacgcggcggcggcacgagcggcgc
ctggtggaggtggacagcagccggcagcaggagtacgacttcaagatggcacaggcgctg
gaggagctgcggagccagcacgacgagcaagtgcggctctacaagctggagctggagcag
acctaccaggccaagctggacagcgccaagctgagctctgaccagaacgacaaggcggcc
agtgcggctcgcgaggagctgaaggaggcccgcatgcgcctggagtccctcagctaccag
ctctccggcctccagaagcaggccagtgccgctgaagatcgcattcgggagctggaggag
gccatggccggggagcgggacaagttccggaagatgctggacgccaaggagcaggagatg
acggagatgcgggacgtgatgcagcagcagctggccgagtaccaggagctgctggacgtg
aagctggccctggacatggagatcaacgcctaccggaagctcctggagggcgaggaggag
aggctgaagctgtcccccagcccatcctcgcgcgtcaccgtctcacgagccacctcgagc
agcagcggcagcttgtccgccaccgggcgcctgggccgcagtaagcggaagcggctggag
gtggaggagcccttgggcagcggcccaagcgtcctgggcacgggcacgggtggcagcggt
ggcttccacctggcccagcaggcctcggcctcgggtagcgtcagcatcgaggagatcgac
ctggagggcaagtttgtgcagctcaagaacaactcggacaaggatcagtctctggggaac
tggagaatcaagaggcaggtcttggagggggaggagatcgcctacaagttcacgcccaag
tacatcctgcgcgccggccagatggtcacggtgtgggcagctggtgcgggggtggcccac
agccccccctcgacgctggtgtggaagggccagagcagctggggcacgggcgagagcttc
cgcaccgtcctggttaacgcggatggcgaggaagtggccatgaggactgtgaagaagtcc
tcggtgatgcgtgagaatgagaatggggaggaagaggaggaggaagccgagtttggcgag
gaggatcttttccaccaacagggggacccgaggaccacctcaagaggctgctacgtgatg
tga
DBGET
integrated database retrieval system