KEGG   Homo sapiens (human): 1605
Entry
1605              CDS       T01001                                 
Symbol
DAG1, 156DAG, A3a, AGRNR, DAG, LGMDR16, MDDGA9, MDDGC7, MDDGC9
Name
(RefSeq) dystroglycan 1
  KO
K06265  dystroglycan 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04512  ECM-receptor interaction
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N00465  Deleted DMD to dystrophin-associated protein complex
N01816  Costamere
Disease
H00120  Muscular dystrophy-dystroglycanopathy type A
H00593  Limb-girdle muscular dystrophy
H01959  Muscular dystrophy-dystroglycanopathy type C
H02307  Muscular dystrophy-dystroglycanopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03268 Virion - Orthopoxvirus
    1605 (DAG1)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04512 ECM-receptor interaction
    1605 (DAG1)
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    1605 (DAG1)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    1605 (DAG1)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    1605 (DAG1)
   05414 Dilated cardiomyopathy
    1605 (DAG1)
   05416 Viral myocarditis
    1605 (DAG1)
SSDB
Motif
Pfam: DAG1 a_DG1_N2 He_PIG DUF4064 ATP1G1_PLM_MAT8
Other DBs
NCBI-GeneID: 1605
NCBI-ProteinID: NP_001159400
OMIM: 128239
HGNC: 2666
Ensembl: ENSG00000173402
UniProt: Q14118
Structure
LinkDB
Position
3:49468948..49535615
AA seq 895 aa
MRMSVGLSLLLPLSGRTFLLLLSVVMAQSHWPSEPSEAVRDWENQLEASMHSVLSDLHEA
VPTVVGIPDGTAVVGRSFRVTIPTDLIASSGDIIKVSAAGKEALPSWLHWDSQSHTLEGL
PLDTDKGVHYISVSATRLGANGSHIPQTSSVFSIEVYPEDHSELQSVRTASPDPGEVVSS
ACAADEPVTVLTVILDADLTKMTPKQRIDLLHRMRSFSEVELHNMKLVPVVNNRLFDMSA
FMAGPGNAKKVVENGALLSWKLGCSLNQNSVPDIHGVEAPAREGAMSAQLGYPVVGWHIA
NKKPPLPKRVRRQIHATPTPVTAIGPPTTAIQEPPSRIVPTPTSPAIAPPTETMAPPVRD
PVPGKPTVTIRTRGAIIQTPTLGPIQPTRVSEAGTTVPGQIRPTMTIPGYVEPTAVATPP
TTTTKKPRVSTPKPATPSTDSTTTTTRRPTKKPRTPRPVPRVTTKVSITRLETASPPTRI
RTTTSGVPRGGEPNQRPELKNHIDRVDAWVGTYFEVKIPSDTFYDHEDTTTDKLKLTLKL
REQQLVGEKSWVQFNSNSQLMYGLPDSSHVGKHEYFMHATDKGGLSAVDAFEIHVHRRPQ
GDRAPARFKAKFVGDPALVLNDIHKKIALVKKLAFAFGDRNCSTITLQNITRGSIVVEWT
NNTLPLEPCPKEQIAGLSRRIAEDDGKPRPAFSNALEPDFKATSITVTGSGSCRHLQFIP
VVPPRRVPSEAPPTEVPDRDPEKSSEDDVYLHTVIPAVVVAAILLIAGIIAMICYRKKRK
GKLTLEDQATFIKKGVPIIFADELDDSKPPPSSSMPLILQEEKAPLPPPEYPNQSVPETT
PLNQDTMGEYTPLRDEDPNAPPYQPPPPFTAPMEGKGSRPKNMTPYRSPPPYVPP
NT seq 2688 nt   +upstreamnt  +downstreamnt
atgaggatgtctgtgggcctctcgctgctgctgcccctctcggggaggacctttctcctc
ctgctctctgtggttatggctcagtcccactggcccagtgaaccctcagaggctgtcagg
gactgggaaaaccagcttgaggcatccatgcactcagtgctctcagacctccacgaggct
gttcccacagtggttggcattcctgatggcacggctgtcgtcgggcgctcatttcgagtg
accattccaacagatttgattgcctccagtggagatatcatcaaggtatcagcggcaggg
aaggaggctttgccatcttggctgcactgggactcacagagccacaccctggagggcctc
ccccttgacactgataagggtgtgcattacatttcagtgagcgctacacggctgggggcc
aacgggagccacatcccccagacctccagtgtgttctccatcgaggtctaccctgaagac
cacagtgagctgcagtcggtgaggacagcctccccagaccctggtgaggtggtatcatct
gcctgtgctgcggatgaacctgtgactgttttgacggtgattttggatgccgacctcacc
aagatgaccccaaagcaaaggattgacctcctgcacaggatgcggagcttctcagaagta
gagcttcacaacatgaaattagtgccggtggtgaataacagactatttgacatgtcggcc
ttcatggctggcccgggaaatgcaaaaaaggtggtggagaatggggcccttctctcctgg
aagctgggctgctccctgaaccagaacagtgtgcctgacattcatggtgtagaggcccct
gccagggagggcgcaatgtctgctcagcttggctaccctgtggtgggttggcacatcgcc
aataagaagccccctcttcccaaacgcgtccggaggcagatccatgctacacccacacct
gtcactgccattgggcccccaaccacggctatccaggagcccccatccaggatcgtgcca
acccccacatctccagccattgctcctccaacagagaccatggctcctccagtcagggat
cctgttcctgggaaacccacggtcaccatccggactcgaggcgccattattcaaacccca
accctaggccccatccagcctactcgggtgtcagaagctggcaccacagttcctggccag
attcgcccaacgatgaccattcctggctatgtggagcctactgcagttgctacccctccc
acaaccaccaccaagaagccacgagtatccacaccaaaaccagcaacgccttcaactgac
tccaccaccaccacgactcgcaggccaaccaagaaaccacggacaccccggccagtgccc
cgggtcaccaccaaagtttccatcaccagattggaaactgcctcaccgcctactcgtatt
cgcaccaccaccagtggagtgccccgtggcggagaacccaaccagcgcccagagctcaag
aaccatattgacagggtagatgcctgggttggcacctactttgaggtgaagatcccgtca
gacactttctatgaccatgaggacaccaccactgacaagctgaagctgaccctgaaactg
cgggagcagcagctggtgggcgagaagtcctgggtacagttcaacagcaacagccagctc
atgtatggccttcccgacagcagccacgtgggcaaacacgagtatttcatgcatgccaca
gacaaggggggcctgtcggctgtggatgccttcgagatccacgtccacaggcgcccccaa
ggggatagggctcctgcaaggttcaaggccaagtttgtgggtgacccggcactggtgttg
aatgacatccacaagaagattgccttggtaaagaaactggccttcgcctttggagaccga
aactgtagcaccatcaccctgcagaatatcacccggggctccatcgtggtggaatggacc
aacaacacactgcccttggagccctgccccaaggagcagatcgctgggctgagccgccgg
atcgctgaggatgatggaaaacctcggcctgccttctccaacgccctagagcctgacttt
aaggccacaagcatcactgtgacgggctctggcagttgtcggcacctacagtttatccct
gtggtaccacccaggagagtgccctcagaggcgccgcccacagaagtgcctgacagggac
cctgagaagagcagtgaggatgatgtctacctgcacacagtcattccggccgtggtggtc
gcagccatcctgctcattgctggcatcattgccatgatctgctaccgcaagaagcggaag
ggcaagcttacccttgaggaccaggccaccttcatcaagaagggggtgcctatcatcttt
gcagacgaactggacgactccaagcccccaccctcctccagcatgccactcattctgcag
gaggagaaggctcccctaccccctcctgagtaccccaaccagagtgtgcccgagaccact
cctctgaaccaggacaccatgggagagtacacgcccctgcgggatgaggatcccaatgcg
cctccctaccagcccccaccgcccttcacagcacccatggagggcaagggctcccgtccc
aagaacatgaccccataccggtcacctcctccctatgtcccaccttaa

KEGG   Homo sapiens (human): 6442
Entry
6442              CDS       T01001                                 
Symbol
SGCA, 50DAG, ADL, DAG2, DMDA2, LGMD2D, LGMDR3, SCARMD1, adhalin
Name
(RefSeq) sarcoglycan alpha
  KO
K12565  alpha-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Disease
H00565  Sarcoglycanopathies
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    6442 (SGCA)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    6442 (SGCA)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    6442 (SGCA)
   05414 Dilated cardiomyopathy
    6442 (SGCA)
   05416 Viral myocarditis
    6442 (SGCA)
SSDB
Motif
Pfam: Sarcoglycan_2 Sarcoglycan_2_C
Other DBs
NCBI-GeneID: 6442
NCBI-ProteinID: NP_000014
OMIM: 600119
HGNC: 10805
Ensembl: ENSG00000108823
UniProt: Q16586 A0A0S2Z4Q1
LinkDB
Position
17:50166005..50175928
AA seq 387 aa
MAETLFWTPLLVVLLAGLGDTEAQQTTLHPLVGRVFVHTLDHETFLSLPEHVAVPPAVHI
TYHAHLQGHPDLPRWLRYTQRSPHHPGFLYGSATPEDRGLQVIEVTAYNRDSFDTTRQRL
VLEIGDPEGPLLPYQAEFLVRSHDAEEVLPSTPASRFLSALGGLWEPGELQLLNVTSALD
RGGRVPLPIEGRKEGVYIKVGSASPFSTCLKMVASPDSHARCAQGQPPLLSCYDTLAPHF
RVDWCNVTLVDKSVPEPADEVPTPGDGILEHDPFFCPPTEAPDRDFLVDALVTLLVPLLV
ALLLTLLLAYVMCCRREGRLKRDLATSDIQMVHHCTIHGNTEELRQMAASREVPRPLSTL
PMFNVHTGERLPPRVDSAQVPLILDQH
NT seq 1164 nt   +upstreamnt  +downstreamnt
atggctgagacactcttctggactcctctcctcgtggttctcctggcagggctgggggac
accgaggcccagcagaccacgctacacccacttgtgggccgtgtctttgtgcacaccttg
gaccatgagacgtttctgagccttcctgagcatgtcgctgtcccacccgctgtccacatc
acctaccacgcccacctccagggacacccagacctgccccggtggctccgctacacccag
cgcagcccccaccaccctggcttcctctacggctctgccaccccagaagatcgtgggctc
caggtcattgaggtcacagcctacaatcgggacagctttgataccactcggcagaggctg
gtgctggagattggggacccagaaggccccctgctgccataccaagccgagttcctggtg
cgcagccacgatgcggaggaggtgctgccctcaacacctgccagccgcttcctctcagcc
ttggggggactctgggagcccggagagcttcagctgctcaacgtcacctctgccttggac
cgtgggggccgtgtcccccttcccattgagggccgaaaagaaggggtatacattaaggtg
ggttctgcctcacctttttctacttgcctgaagatggtggcatcccccgatagccacgcc
cgctgtgcccagggccagcctccacttctgtcttgctacgacaccttggcaccccacttc
cgcgttgactggtgcaatgtgaccctggtggataagtcagtgccggagcctgcagatgag
gtgcccaccccaggtgatgggatcctggagcatgacccgttcttctgcccacccactgag
gccccagaccgtgacttcttggtggatgctctggtcaccctcctggtgcccctgctggtg
gccctgcttctcaccttgctgctggcctatgtcatgtgctgccggcgggagggaaggctg
aagagagacctggctacctccgacatccagatggtccaccactgcaccatccacgggaac
acagaggagctgcggcagatggcggccagccgcgaggtgccccggccactctccaccctg
cccatgttcaatgtgcacacaggtgagcggctgcctccccgcgtggacagcgcccaggtg
cccctcattctggaccagcactga

KEGG   Homo sapiens (human): 8910
Entry
8910              CDS       T01001                                 
Symbol
SGCE, DYT11, ESG, epsilon-SG
Name
(RefSeq) sarcoglycan epsilon
  KO
K27061  epsilon-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Disease
H00831  Primary dystonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    8910 (SGCE)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    8910 (SGCE)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    8910 (SGCE)
   05414 Dilated cardiomyopathy
    8910 (SGCE)
   05416 Viral myocarditis
    8910 (SGCE)
SSDB
Motif
Pfam: Sarcoglycan_2 Sarcoglycan_2_C Het-C
Other DBs
NCBI-GeneID: 8910
NCBI-ProteinID: NP_003910
OMIM: 604149
HGNC: 10808
Ensembl: ENSG00000127990
UniProt: O43556 A0A0S2Z4P5
LinkDB
Position
7:complement(94584980..94656133)
AA seq 437 aa
MQLPRWWELGDPCAWTGQGRGTRRMSPATTGTFLLTVYSIFSKVHSDRNVYPSAGVLFVH
VLEREYFKGEFPPYPKPGEISNDPITFNTNLMGYPDRPGWLRYIQRTPYSDGVLYGSPTA
ENVGKPTIIEITAYNRRTFETARHNLIINIMSAEDFPLPYQAEFFIKNMNVEEMLASEVL
GDFLGAVKNVWQPERLNAINITSALDRGGRVPLPINDLKEGVYVMVGADVPFSSCLREVE
NPQNQLRCSQEMEPVITCDKKFRTQFYIDWCKISLVDKTKQVSTYQEVIRGEGILPDGGE
YKPPSDSLKSRDYYTDFLITLAVPSAVALVLFLILAYIMCCRREGVEKRNMQTPDIQLVH
HSAIQKSTKELRDMSKNREIAWPLSTLPVFHPVTGEIIPPLHTDNYDSTNMPLMQTQQNL
PHQTQIPQQQTTGKWYP
NT seq 1314 nt   +upstreamnt  +downstreamnt
atgcaattgccccggtggtgggagctgggagacccctgtgcttggacgggacagggtcgg
gggacacgcaggatgagccccgcgaccactggcacattcttgctgacagtgtacagtatt
ttctccaaggtacactccgatcggaatgtatacccatcagcaggtgtcctctttgttcat
gttttggaaagagaatattttaagggggaatttccaccttacccaaaacctggcgagatt
agtaatgatcccataacatttaatacaaatttaatgggttacccagaccgacctggatgg
cttcgatatatccaaaggacaccatatagtgatggagtcctatatgggtccccaacagct
gaaaatgtggggaagccaacaatcattgagataactgcctacaacaggcgcacctttgag
actgcaaggcataatttgataattaatataatgtctgcagaagacttcccgttgccatat
caagcagaattcttcattaagaatatgaatgtagaagaaatgttggccagtgaggttctt
ggagactttcttggcgcagtgaaaaatgtgtggcagccagagcgcctgaacgccataaac
atcacatcggccctagacaggggtggcagggtgccacttcccattaatgacctgaaggag
ggcgtttatgtcatggttggtgcagatgtcccgttttcttcttgtttacgagaagttgaa
aatccacagaatcaattgagatgtagtcaagaaatggagcctgtaataacatgtgataaa
aaatttcgtactcaattttacattgactggtgcaaaatttcattggttgataaaacaaag
caagtgtccacctatcaggaagtgattcgtggagaggggattttacctgatggtggagaa
tacaaacccccttctgattctttgaaaagcagagactattacacggatttcctaattaca
ctggctgtgccctcggcagtggcactggtcctttttctaatacttgcttatatcatgtgc
tgccgacgggaaggcgtggaaaagagaaacatgcaaacaccagacatccaactggtccat
cacagtgctattcagaaatctaccaaggagcttcgagacatgtccaagaatagagagata
gcatggcccctgtcaacgcttcctgtgttccaccctgtgactggggaaatcatacctcct
ttacacacagacaactatgatagcacaaacatgccattgatgcaaacgcagcagaacttg
ccacatcagactcagattccccaacagcagactacaggtaaatggtatccctga

KEGG   Homo sapiens (human): 6443
Entry
6443              CDS       T01001                                 
Symbol
SGCB, A3b, LGMD2E, LGMDR4, SGC
Name
(RefSeq) sarcoglycan beta
  KO
K12566  beta-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Disease
H00565  Sarcoglycanopathies
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    6443 (SGCB)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    6443 (SGCB)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    6443 (SGCB)
   05414 Dilated cardiomyopathy
    6443 (SGCB)
   05416 Viral myocarditis
    6443 (SGCB)
SSDB
Motif
Pfam: Sarcoglycan_1
Other DBs
NCBI-GeneID: 6443
NCBI-ProteinID: NP_000223
OMIM: 600900
HGNC: 10806
Ensembl: ENSG00000163069
UniProt: Q16585 Q5U0N0
LinkDB
Position
4:complement(52020706..52038299)
AA seq 318 aa
MAAAAAAAAEQQSSNGPVKKSMREKAVERRSVNKEHNSNFKAGYIPIDEDRLHKTGLRGR
KGNLAICVIILLFILAVINLIITLVIWAVIRIGPNGCDSMEFHESGLLRFKQVSDMGVIH
PLYKSTVGGRRNENLVITGNNQPIVFQQGTTKLSVENNKTSITSDIGMQFFDPRTQNILF
STDYETHEFHLPSGVKSLNVQKASTERITSNATSDLNIKVDGRAIVRGNEGVFIMGKTIE
FHMGGNMELKAENSIILNGSVMVSTTRLPSSSSGDQLGSGDWVRYKLCMCADGTLFKVQV
TSQNMGCQISDNPCGNTH
NT seq 957 nt   +upstreamnt  +downstreamnt
atggcggcagcggcggcggcggctgcagaacagcaaagttccaatggtcctgtaaagaag
tccatgcgtgagaaggctgttgagagaaggagtgtcaataaagagcacaacagtaacttt
aaagctggatacattccgattgatgaagatcgtctccacaaaacagggttgagaggaaga
aagggcaatttagccatctgtgtgattatcctcttgtttatcctggctgtcatcaattta
ataataacacttgttatttgggccgtgattcgcattggaccaaatggctgtgatagtatg
gagtttcatgaaagtggcctgcttcgatttaagcaagtatctgacatgggagtgatccac
cctctttataaaagcacagtaggaggaaggcgaaatgaaaatttggtcatcactggcaac
aaccagcctattgtttttcagcaagggacaacaaagctcagtgtagaaaacaacaaaact
tctattacaagtgacatcggcatgcagttttttgacccgaggactcaaaatatcttattc
agcacagactatgaaactcatgagtttcatttgccaagtggagtgaaaagtttgaatgtt
caaaaggcatctactgaaaggattaccagcaatgctaccagtgatttaaatataaaagtt
gatgggcgtgctattgtgcgtggaaatgaaggtgtattcattatgggcaaaaccattgaa
tttcacatgggtggtaatatggagttaaaggcggaaaacagtatcatcctaaatggatct
gtgatggtcagcaccacccgcctacccagttcctccagtggagaccagttgggtagtggt
gactgggtacgctacaagctctgcatgtgtgctgatgggacgctcttcaaggtgcaagta
accagccagaacatgggctgccaaatctcagacaacccctgtggaaacactcattaa

KEGG   Homo sapiens (human): 6444
Entry
6444              CDS       T01001                                 
Symbol
SGCD, 35DAG, CMD1L, DAGD, LGMDR6, SG-delta, SGCDP, SGD
Name
(RefSeq) sarcoglycan delta
  KO
K12563  delta-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Disease
H00294  Dilated cardiomyopathy
H00565  Sarcoglycanopathies
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    6444 (SGCD)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    6444 (SGCD)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    6444 (SGCD)
   05414 Dilated cardiomyopathy
    6444 (SGCD)
   05416 Viral myocarditis
    6444 (SGCD)
SSDB
Motif
Pfam: Sarcoglycan_1 DUF2345
Other DBs
NCBI-GeneID: 6444
NCBI-ProteinID: NP_001121681
OMIM: 601411
HGNC: 10807
Ensembl: ENSG00000170624
UniProt: Q92629
LinkDB
Position
5:155727832..156767788
AA seq 289 aa
MPQEQYTHHRSTMPGSVGPQVYKVGIYGWRKRCLYFFVLLLMILILVNLAMTIWILKVMN
FTIDGMGNLRITEKGLKLEGDSEFLQPLYAKEIQSRPGNALYFKSARNVTVNILNDQTKV
LTQLITGPKAVEAYGKKFEVKTVSGKLLFSADNNEVVVGAERLRVLGAEGTVFPKSIETP
NVRADPFKELRLESPTRSLVMEAPKGVEINAEAGNMEATCRTELRLESKDGEIKLDAAKI
RLPRLPHGSYTPTGTRQKVFEICVCANGRLFLSQAGAGSTCQINTSVCL
NT seq 870 nt   +upstreamnt  +downstreamnt
atgcctcaggagcagtacactcaccaccggagcaccatgcctggctctgtggggccacag
gtatacaaggtggggatttatggctggcggaaacgatgcctgtatttctttgtcctgctc
ctcatgattttaatactggtgaacttggccatgaccatctggattctcaaagtcatgaac
ttcacaattgatggaatgggaaacctgaggatcacagaaaaaggtctaaagctagaagga
gactctgaattcttacaacctctctacgccaaagaaatccagtcccgaccaggtaatgcc
ctgtacttcaagtctgccagaaatgttacagtgaacattctcaatgaccagactaaagtg
ctaactcagcttataacaggtccaaaagccgtagaagcttatggtaaaaaatttgaggta
aaaactgtttctggaaaattgctcttctctgcagacaataatgaagtggtagtaggagct
gaaagattacgagttttaggagcggagggcacagtgttccctaaatctatagaaacacct
aatgtcagggcagaccccttcaaagaactaaggttggagtccccaacccggtctctagtg
atggaggccccaaaaggagtggaaatcaatgcagaagctggcaatatggaagccacctgc
aggacagagctgagactggaatccaaagatggagagattaagttagatgctgcgaaaatc
aggctacctagactgcctcatggatcctacacgcctacaggaacgaggcagaaggtcttc
gagatctgcgtctgcgccaatgggagattattcctgtctcaggcaggagctgggtccact
tgtcagataaacacaagtgtctgcctctga

KEGG   Homo sapiens (human): 6445
Entry
6445              CDS       T01001                                 
Symbol
SGCG, 35DAG, A4, DAGA4, DMDA, DMDA1, LGMD2C, LGMDR5, MAM, SCARMD2, SCG3, gamma-SG
Name
(RefSeq) sarcoglycan gamma
  KO
K12564  gamma-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Disease
H00565  Sarcoglycanopathies
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    6445 (SGCG)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    6445 (SGCG)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    6445 (SGCG)
   05414 Dilated cardiomyopathy
    6445 (SGCG)
   05416 Viral myocarditis
    6445 (SGCG)
SSDB
Motif
Pfam: Sarcoglycan_1 DUF2345 TRAM
Other DBs
NCBI-GeneID: 6445
NCBI-ProteinID: NP_000222
OMIM: 608896
HGNC: 10809
Ensembl: ENSG00000102683
UniProt: Q13326
LinkDB
Position
13:23160508..23325162
AA seq 291 aa
MVREQYTTATEGICIERPENQYVYKIGIYGWRKRCLYLFVLLLLIILVVNLALTIWILKV
MWFSPAGMGHLCVTKDGLRLEGESEFLFPLYAKEIHSRVDSSLLLQSTQNVTVNARNSEG
EVTGRLKVGPKMVEVQNQQFQINSNDGKPLFTVDEKEVVVGTDKLRVTGPEGALFEHSVE
TPLVRADPFQDLRLESPTRSLSMDAPRGVHIQAHAGKIEALSQMDILFHSSDGMLVLDAE
TVCLPKLVQGTWGPSGSSQSLYEICVCPDGKLYLSVAGVSTTCQEHNHICL
NT seq 876 nt   +upstreamnt  +downstreamnt
atggtgcgtgagcagtacactacagccacagaaggcatctgcatagagaggccagagaat
cagtatgtctacaaaattggcatttatggctggagaaagcgctgtctctacttgtttgtt
cttcttttactcatcatcctcgttgtgaatttagctcttacaatttggattcttaaagtg
atgtggttttctccagcaggaatgggccacttgtgtgtaacaaaagatggactgcgcttg
gaaggggaatcagaatttttattcccattgtatgccaaagaaatacactccagagtggac
tcatctctgcttctacaatcaacccagaatgtgactgtaaatgcgcgcaactcagaaggg
gaggtcacaggcaggttaaaagtcggtcccaaaatggtagaagtccagaatcaacagttt
cagatcaactccaacgacggcaagccactatttactgtagatgagaaggaagttgtggtt
ggtacagataaacttcgagtaactgggcctgaaggggctctttttgaacattcagtggag
acaccccttgtcagagccgacccgtttcaagaccttagattagaatcccccactcggagt
ctaagcatggatgccccaaggggtgtgcatattcaagctcacgctgggaaaattgaggcg
ctttctcaaatggatattctttttcatagtagtgatggaatgcttgtgcttgatgctgaa
actgtgtgcttacccaagctggtgcaggggacgtggggtccctctggcagctcacagagc
ctctacgaaatctgtgtgtgtccagatgggaagctgtacctgtctgtggccggtgtgagc
accacgtgccaggagcacaaccacatctgcctctga

KEGG   Homo sapiens (human): 137868
Entry
137868            CDS       T01001                                 
Symbol
SGCZ, ZSG1
Name
(RefSeq) sarcoglycan zeta
  KO
K27062  zeta-sarcoglycan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    137868 (SGCZ)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    137868 (SGCZ)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    137868 (SGCZ)
   05414 Dilated cardiomyopathy
    137868 (SGCZ)
   05416 Viral myocarditis
    137868 (SGCZ)
SSDB
Motif
Pfam: Sarcoglycan_1 DUF2345
Other DBs
NCBI-GeneID: 137868
NCBI-ProteinID: NP_631906
OMIM: 608113
HGNC: 14075
Ensembl: ENSG00000185053
UniProt: Q96LD1
LinkDB
Position
8:complement(14084845..15238431)
AA seq 312 aa
MDRSTNLDIEELKMTREQYILATQQNNLPRTENAQLYPVGIYGWRKRCLYFFVLLLLVTM
IVNLAMTIWILKVMNFTVDGMGNLRVTKKGIRLEGISEFLLPLYVKEIHSRKDSPLVLQS
DRNVTVNARNHMGQLTGQLTIGADAVEAQCKRFEVRASEDGRVLFSADEDEITIGAEKLK
VTGTEGAVFGHSVETPHIRAEPSQDLRLESPTRSLIMEAPRGVQVSAAAGDFKATCRKEL
HLQSTEGEIFLNAETIKLGNLPTGSFSSSSPSSSSSRQTVYELCVCPNGKLYLSPAGVGS
TCQSSSNICLWS
NT seq 939 nt   +upstreamnt  +downstreamnt
atggacagatcaacgaacctggacattgaggagctcaagatgacacgagaacaatacata
ctagcaacccaacagaataacctgccaaggactgagaatgcacaactttacccagtggga
atttatggatggcgaaagaggtgcttatacttctttgtccttctgctgttggttaccatg
atagttaacttagccatgacaatatggatattgaaagttatgaatttcactgtggatggt
atgggaaatctgagagtcaccaagaagggaatccgacttgaaggtatatctgagtttcta
cttccattgtatgtgaaagaaattcattctcgaaaggatagtccgctggtcttacagtct
gacaggaatgtcacagtgaatgcaagaaatcacatggggcagttaaccggacagctgacc
ataggagctgatgctgtggaagctcagtgtaaaagatttgaagtgagagccagtgaagat
ggcagggtgctgttttctgcagatgaagatgagattaccattggggctgaaaagctgaaa
gttacaggcactgaaggagccgtatttgggcactctgtggagacgccgcacatcagagca
gagccatcccaagatctcaggcttgaatcacccaccagatccttgatcatggaagctccc
cgtggggtccaggtgagtgctgctgcaggagacttcaaggccacctgcaggaaggagctc
catctgcaatctacagaaggggagatatttttaaatgcagagacaatcaagctgggaaat
ctaccaactggctccttctcatcttcttcacccagctcctcaagttctcgacagacagtg
tatgaactctgcgtctgccccaatggcaaactttacctttctccagcaggagtaggttcc
acttgtcagtccagtagcaacatctgcctgtggagctga

KEGG   Homo sapiens (human): 8082
Entry
8082              CDS       T01001                                 
Symbol
SSPN, DAGA5, KRAG, NSPN, SPN1, SPN2
Name
(RefSeq) sarcospan
  KO
K22194  sarcospan
Organism
hsa  Homo sapiens (human)
Pathway
hsa04820  Cytoskeleton in muscle cells
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
hsa05416  Viral myocarditis
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01816  Costamere
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04820 Cytoskeleton in muscle cells
    8082 (SSPN)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    8082 (SSPN)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    8082 (SSPN)
   05414 Dilated cardiomyopathy
    8082 (SSPN)
   05416 Viral myocarditis
    8082 (SSPN)
SSDB
Motif
Pfam: CD20 Wzy_C_2 Sensor
Other DBs
NCBI-GeneID: 8082
NCBI-ProteinID: NP_005077
OMIM: 601599
HGNC: 11322
Ensembl: ENSG00000123096
UniProt: Q14714
LinkDB
Position
12:26121991..26234777
AA seq 243 aa
MGKNKQPRGQQRQGGPPAADAAGPDDMEPKKGTGAPKECGEEEPRTCCGCRFPLLLALLQ
LALGIAVTVVGFLMASISSSLLVRDTPFWAGIIVCLVAYLGLFMLCVSYQVDERTCIQFS
MKLLYFLLSALGLTVCVLAVAFAAHHYSQLTQFTCETTLDSCQCKLPSSEPLSRTFVYRD
VTDCTSVTGTFKLFLLIQMILNLVCGLVCLLACFVMWKHRYQVFYVGVRICSLTASEGPQ
QKI
NT seq 732 nt   +upstreamnt  +downstreamnt
atgggcaagaacaagcagccacgcggccagcagaggcaggggggcccgccggccgcggac
gccgctgggcccgacgacatggagccgaagaagggcacgggggcccccaaggagtgcggg
gaggaggagccccggacctgctgcggctgccggttcccgctgctgctcgccctgctgcag
ctggccctgggcatcgccgtgaccgtggtgggcttcctcatggcgagcatcagctcctcc
ctgctagtcagggacactccattttgggctgggatcattgtctgcttagtggcctatctt
ggcttgtttatgctttgtgtctcatatcaggttgacgaacggacatgtattcaattttct
atgaaactgttatactttctgctgagtgccctgggcctgacggtctgtgtgctggccgtg
gcctttgccgcccaccactattcgcagctcacacagtttacctgtgagaccacactcgac
tcttgccagtgcaaactgccctcctcggagccgctcagcaggacctttgtttaccgggat
gtgacggactgtaccagcgtcactggcactttcaaactgttcttactcatccagatgatt
cttaatttggtctgcggccttgtgtgcttgttggcctgctttgtgatgtggaaacatagg
taccaggtcttctatgtgggtgtcaggatatgctccctcacggcttccgaaggcccccag
caaaagatctaa

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