KEGG   Homo sapiens (human): 7478
Entry
7478              CDS       T01001                                 

Gene name
WNT8A, WNT8D
Definition
(RefSeq) Wnt family member 8A
  KO
K00714  wingless-type MMTV integration site family, member 8
Organism
hsa  Homo sapiens (human)
Pathway
hsa04150  mTOR signaling pathway
hsa04310  Wnt signaling pathway
hsa04390  Hippo signaling pathway
hsa04550  Signaling pathways regulating pluripotency of stem cells
hsa04916  Melanogenesis
hsa04934  Cushing syndrome
hsa05010  Alzheimer disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05165  Human papillomavirus infection
hsa05200  Pathways in cancer
hsa05205  Proteoglycans in cancer
hsa05217  Basal cell carcinoma
hsa05224  Breast cancer
hsa05225  Hepatocellular carcinoma
hsa05226  Gastric cancer
Network
nt06115  WNT signaling (viruses and bacteria)
nt06164  Kaposi sarcoma-associated herpesvirus (KSHV)
nt06215  WNT signaling
nt06217  HH signaling
nt06260  Colorectal cancer
nt06261  Gastric cancer
nt06263  Hepatocellular carcinoma
nt06269  Basal cell carcinoma
nt06270  Breast cancer
nt06271  Endometrial cancer
nt06274  Thyroid cancer
  Element
N00010  Mutation-inactivated PTCH1 to Hedgehog signaling pathway
N00017  Mutation-activated SMO to Hedgehog signaling pathway
N00056  Wnt signaling pathway
N00059  FZD7-overexpression to Wnt signaling pathway
N00060  LRP6-overexpression to Wnt signaling pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    7478 (WNT8A)
   04390 Hippo signaling pathway
    7478 (WNT8A)
   04150 mTOR signaling pathway
    7478 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    7478 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    7478 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    7478 (WNT8A)
   05205 Proteoglycans in cancer
    7478 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    7478 (WNT8A)
   05226 Gastric cancer
    7478 (WNT8A)
   05217 Basal cell carcinoma
    7478 (WNT8A)
   05224 Breast cancer
    7478 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    7478 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    7478 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    7478 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    7478 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:hsa00536]
    7478 (WNT8A)
Glycosaminoglycan binding proteins [BR:hsa00536]
 Heparan sulfate / Heparin
  Morphogens
   7478 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 7478
NCBI-ProteinID: NP_490645
OMIM: 606360
HGNC: 12788
Ensembl: ENSG00000061492
Vega: OTTHUMG00000129196
Pharos: Q9H1J5(Tbio)
UniProt: Q9H1J5
LinkDB
Position
5q31.2
AA seq 351 aa
MGNLFMLWAALGICCAAFSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYIITKNCSMGDFENCGCDGSNNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLAEFREMGDYLKAKYDQALKIEMDKRQLRAGNSAEGHWVPAEA
FLPSAEAELIFLEESPDYCTCNSSLGIYGTEGRECLQNSHNTSRWERRSCGRLCTECGLQ
VEERKTEVISSCNCKFQWCCTVKCDQCRHVVSKYYCARSPGSAQSLGKGSA
NT seq 1056 nt   +upstreamnt  +downstreamnt
atggggaacctgtttatgctctgggcagctctgggcatatgctgtgctgcattcagtgcc
tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctacacg
actagtgtggccttgggtgcccagagtggcatcgaggagtgcaagttccagtttgcttgg
gaacgctggaactgccctgaaaatgctcttcagctctccacccacaacaggctgagaagt
gctaccagagagacttccttcatacatgctatcagctctgctggagtcatgtacatcatc
accaagaactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaacaatgga
aaaacaggaggccatggctggatctggggaggctgcagcgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg
aatcttcacaacaacagggccggcagactggcagtgagagccaccatgaaaaggacatgc
aaatgtcatggcatctctgggagctgcagcatacagacatgctggctgcagctggctgaa
ttccgggagatgggagactacctaaaggccaagtatgaccaggcgctgaaaattgaaatg
gataagcggcagctgagagctgggaacagcgccgagggccactgggtgcccgctgaggcc
ttccttcctagcgcagaggcggaactgatctttttagaggaatcaccagattactgtacc
tgcaattccagcctgggcatctatggcacagagggtcgtgagtgcctacagaacagccac
aacacatccaggtgggagcgacgtagctgtgggcgcctgtgcactgagtgtgggctgcag
gtggaagagaggaaaactgaggtcataagcagctgtaactgcaaattccagtggtgctgt
acggtcaagtgtgaccagtgtaggcatgtggtgagcaagtattactgcgcacgctcccca
ggcagtgcccagtccctgggtaagggcagtgcctga

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