KEGG   Bison bison bison (American bison): 104991829
Entry
104991829         CDS       T08726                                 
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a
  KO
K00714  wingless-type MMTV integration site family, member 8
Organism
bbis  Bison bison bison (American bison)
Pathway
bbis04150  mTOR signaling pathway
bbis04310  Wnt signaling pathway
bbis04390  Hippo signaling pathway
bbis04550  Signaling pathways regulating pluripotency of stem cells
bbis04916  Melanogenesis
bbis04934  Cushing syndrome
bbis05010  Alzheimer disease
bbis05022  Pathways of neurodegeneration - multiple diseases
bbis05165  Human papillomavirus infection
bbis05200  Pathways in cancer
bbis05205  Proteoglycans in cancer
bbis05217  Basal cell carcinoma
bbis05224  Breast cancer
bbis05225  Hepatocellular carcinoma
bbis05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:bbis00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    104991829 (WNT8A)
   04390 Hippo signaling pathway
    104991829 (WNT8A)
   04150 mTOR signaling pathway
    104991829 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    104991829 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    104991829 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    104991829 (WNT8A)
   05205 Proteoglycans in cancer
    104991829 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    104991829 (WNT8A)
   05226 Gastric cancer
    104991829 (WNT8A)
   05217 Basal cell carcinoma
    104991829 (WNT8A)
   05224 Breast cancer
    104991829 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    104991829 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104991829 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    104991829 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    104991829 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:bbis00536]
    104991829 (WNT8A)
Glycosaminoglycan binding proteins [BR:bbis00536]
 Heparan sulfate / Heparin
  Morphogens
   104991829 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 104991829
NCBI-ProteinID: XP_010842755
Ensembl: ENSBBBG00000020026
UniProt: A0A6P3HW42
LinkDB
Position
Unknown
AA seq 351 aa
MGDLLILRVAVGICYVTFSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDESKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLANFRELGNYLKAKYERALKIEMDKQQLRAGNSAEGHWIPTEA
FLPSAEAELIFLEESPDYCTRNSSLGIYGTEGRECLQNSRNTSRWEQCSCGRLCTECGLQ
VEERRTEAISSCNCKFQWCCTVKCEQCRHVVNKYYCTRSPGSAQSWGKGSA
NT seq 1056 nt   +upstreamnt  +downstreamnt
atgggggacctacttattctcagagtggctgtgggcatatgctatgtaaccttcagtgcc
tctgcttggtcagtgaacaatttcctgataacagggcccaaggcctatctgacctatacc
accagtgtggccctgggcgcccagagtggcatcgaggagtgcaaattccaatttgcttgg
gaacgttggaactgtcctgaaaatgctctccagctctccactcacaacaggctaagaagt
gctaccagggagacttctttcattcacgctatcagctctgctggagtcatgtacaccatt
accaagaactgtagcatgggtgactttgaaaactgtggctgtgatgagtcaaaaaatggt
aaaacaggaggccatggctggatctggggaggttgtagtgacaatgttgaatttggggaa
agaatctccaaactctttgtggacagcctggagaaagggaaggatgccagagccctgatg
aatcttcataacaacagagcaggcaggctggcagtgagagccaccatgaagagaacttgc
aaatgtcatggcatctcaggcagctgtagcatccagacatgctggctacagctagctaac
ttcagggagttgggcaactacctaaaggccaagtacgaacgggcactgaaaattgagatg
gataaacagcagctaagggctgggaacagtgccgagggccactggatacccaccgaggcc
ttccttcctagtgcagaagctgagctgatctttttagaggaatcacctgattactgtacc
cgcaattccagcttgggcatctatggcacagaaggtcgggagtgtctgcagaacagccgc
aacacatccagatgggagcaatgcagctgtgggcgcctctgcacagaatgtggcctgcag
gtggaagagagaagaaccgaggctatcagcagctgtaactgcaaattccagtggtgctgc
actgtcaagtgtgagcagtgtcggcatgtggtgaacaagtactactgcacgcgctcccca
ggcagtgctcagtcctggggcaagggcagtgcctga

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