KEGG   Monodelphis domestica (gray short-tailed opossum): 100024816
Entry
100024816         CDS       T01031                                 
Symbol
WNT8A
Name
(RefSeq) Wnt family member 8A
  KO
K00714  wingless-type MMTV integration site family, member 8
Organism
mdo  Monodelphis domestica (gray short-tailed opossum)
Pathway
mdo04150  mTOR signaling pathway
mdo04310  Wnt signaling pathway
mdo04390  Hippo signaling pathway
mdo04550  Signaling pathways regulating pluripotency of stem cells
mdo04916  Melanogenesis
mdo04934  Cushing syndrome
mdo05010  Alzheimer disease
mdo05022  Pathways of neurodegeneration - multiple diseases
mdo05165  Human papillomavirus infection
mdo05200  Pathways in cancer
mdo05205  Proteoglycans in cancer
mdo05217  Basal cell carcinoma
mdo05224  Breast cancer
mdo05225  Hepatocellular carcinoma
mdo05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mdo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100024816 (WNT8A)
   04390 Hippo signaling pathway
    100024816 (WNT8A)
   04150 mTOR signaling pathway
    100024816 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100024816 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100024816 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100024816 (WNT8A)
   05205 Proteoglycans in cancer
    100024816 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100024816 (WNT8A)
   05226 Gastric cancer
    100024816 (WNT8A)
   05217 Basal cell carcinoma
    100024816 (WNT8A)
   05224 Breast cancer
    100024816 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100024816 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100024816 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    100024816 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100024816 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mdo00536]
    100024816 (WNT8A)
Glycosaminoglycan binding proteins [BR:mdo00536]
 Heparan sulfate / Heparin
  Morphogens
   100024816 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100024816
NCBI-ProteinID: XP_007474469
LinkDB
Position
1:329000579..329002764
AA seq 190 aa
MPRALMAVRATMKRTCKCHGISGSCSIQTCWLQLADFREMGDYLKAKYNQALKIEMDKQR
LRAGNSAESRWAPAEAFHPNAEAELIFLEESPDYCIHNSSLGIYGTEGRECLQSGRNLSQ
WERRNCARLCMDCGLRVEERRTEAVNSCNCKFQWCCTVRCDQCWQVVTKYYCTRAPGSSR
ARAKGSSSAS
NT seq 573 nt   +upstreamnt  +downstreamnt
atgccaagggctctgatggctgtaagggctaccatgaagaggacctgtaaatgtcatggc
atctcaggtagctgtagcatccagacttgttggctgcagctagctgacttccgtgagatg
ggggattacctgaaggccaagtacaaccaggccttgaagatagagatggataagcagcgg
ctccgggctgggaacagtgctgagagccggtgggccccagcagaggcctttcatcccaat
gccgaggctgagctgattttcctggaggagtcccctgactactgtatccataactccagc
ctgggcatctacgggactgagggccgggagtgcttgcagagtggccgcaatctgtcccag
tgggagcggcgcaactgtgcgcgcctgtgtatggactgtggacttcgagtggaagagagg
aggacagaggctgtcaacagctgcaattgcaagtttcagtggtgctgcacagttaggtgt
gaccagtgctggcaagtagtgaccaagtactactgcacccgagctccaggaagctctcga
gctcgggccaagggcagttccagtgccagctaa

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