Sarcophilus harrisii (Tasmanian devil): 100925503
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Entry
100925503 CDS
T02286
Name
(RefSeq) Ig heavy chain Mem5 isoform X1
Organism
shr
Sarcophilus harrisii (Tasmanian devil)
Pathway
shr04020
Calcium signaling pathway
shr04064
NF-kappa B signaling pathway
shr04072
Phospholipase D signaling pathway
shr04145
Phagosome
shr04151
PI3K-Akt signaling pathway
shr04613
Neutrophil extracellular trap formation
shr04640
Hematopoietic cell lineage
shr04650
Natural killer cell mediated cytotoxicity
shr04662
B cell receptor signaling pathway
shr04664
Fc epsilon RI signaling pathway
shr04666
Fc gamma R-mediated phagocytosis
shr04672
Intestinal immune network for IgA production
shr05135
Yersinia infection
shr05140
Leishmaniasis
shr05143
African trypanosomiasis
shr05146
Amoebiasis
shr05150
Staphylococcus aureus infection
shr05152
Tuberculosis
shr05169
Epstein-Barr virus infection
shr05171
Coronavirus disease - COVID-19
shr05202
Transcriptional misregulation in cancer
shr05310
Asthma
shr05320
Autoimmune thyroid disease
shr05322
Systemic lupus erythematosus
shr05323
Rheumatoid arthritis
shr05330
Allograft rejection
shr05340
Primary immunodeficiency
shr05414
Dilated cardiomyopathy
shr05416
Viral myocarditis
Brite
KEGG Orthology (KO) [BR:
shr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04064 NF-kappa B signaling pathway
100925503
04020 Calcium signaling pathway
100925503
04072 Phospholipase D signaling pathway
100925503
04151 PI3K-Akt signaling pathway
100925503
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
100925503
09150 Organismal Systems
09151 Immune system
04640 Hematopoietic cell lineage
100925503
04613 Neutrophil extracellular trap formation
100925503
04650 Natural killer cell mediated cytotoxicity
100925503
04662 B cell receptor signaling pathway
100925503
04664 Fc epsilon RI signaling pathway
100925503
04666 Fc gamma R-mediated phagocytosis
100925503
04672 Intestinal immune network for IgA production
100925503
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
100925503
09172 Infectious disease: viral
05171 Coronavirus disease - COVID-19
100925503
05169 Epstein-Barr virus infection
100925503
09171 Infectious disease: bacterial
05135 Yersinia infection
100925503
05150 Staphylococcus aureus infection
100925503
05152 Tuberculosis
100925503
09174 Infectious disease: parasitic
05146 Amoebiasis
100925503
05140 Leishmaniasis
100925503
05143 African trypanosomiasis
100925503
09163 Immune disease
05310 Asthma
100925503
05322 Systemic lupus erythematosus
100925503
05323 Rheumatoid arthritis
100925503
05320 Autoimmune thyroid disease
100925503
05330 Allograft rejection
100925503
05340 Primary immunodeficiency
100925503
09166 Cardiovascular disease
05414 Dilated cardiomyopathy
100925503
05416 Viral myocarditis
100925503
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C1-set
V-set
I-set
Ig_3
Peptidase_A25
Defensin_big
Motif
Other DBs
NCBI-GeneID:
100925503
NCBI-ProteinID:
XP_012399578
Ensembl:
ENSSHAG00000002867
LinkDB
All DBs
Position
1:complement(645542492..645549057)
Genome browser
AA seq
282 aa
AA seq
DB search
MNVLSLLTLFSSLLYSMEQPVPKESGGGSHTAGNSLNLKCETSDFQFKTSKLGWYLWAPG
HIPLGLTNFDSISTDATEDRIITSREDSGSRIFLQIKDLGLRDSGQYHCVRRVGTGDDRD
KLFFGLGTDVTVEPGTRTPLTPNVFLVRSQDVVACLIRNFYPKEIHVSLASPGALISAQT
YVMAPMANGIYSAVQIGRIGENDTVTCTVEHLGKEIHVSHKPEPTGPNPGIAPNQKQSCS
GQDLLEGNEQRNKLLLSVLGLRLLFMRIMIINIFFTAMALIF
NT seq
849 nt
NT seq
+upstream
nt +downstream
nt
atgaatgtattatctctgcttactctattctcatctctgctttattcaatggaacaacca
gtgccgaaagaatcagggggaggctctcacacagctggaaacagcctgaacctcaaatgt
gaaacctctgatttccaattcaagacaagcaaacttggctggtacctttgggcacctggt
catatcccactaggactgaccaatttcgacagtatttctacagatgccactgaagaccga
atcatcacctctagagaggacagtgggagcagaattttcctacagattaaggacttgggc
ctaagagattctggccaataccattgtgtaaggagggtgggcactggagatgacagagac
aagttattctttggtcttgggacagatgtgactgtggagcctggaactcgaaccccactg
acacctaatgtgttcttggtgaggagccaggatgttgtggcttgcctgatcaggaacttc
taccccaaggaaatccatgtgtccttggcttcccctggggctttgatctcagcccagacc
tatgttatggctcccatggccaatggcatctatagtgctgtacagattggcaggattggt
gagaatgatacagtaacatgcacagtggagcatcttgggaaagagatacatgtatcccac
aagccagagcctactggaccaaaccctggaattgcccctaatcagaaacagtcttgttct
gggcaggatctcttggaaggaaatgagcagaggaataagctgctactcagtgttctgggc
ctgagactactattcatgaggattatgatcatcaacatcttcttcactgccatggccttg
atcttctga
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