KEGG   Homo sapiens (human): 1501
Entry
1501              CDS       T01001                                 
Symbol
CTNND2, GT24, NPRAP
Name
(RefSeq) catenin delta 2
  KO
K23491  catenin delta-2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
Disease
H00764  Chromosome 5p deletion syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    1501 (CTNND2)
SSDB
Motif
Pfam: Arm HEAT_2 HEAT Adaptin_N Atx10homo_assoc
Other DBs
NCBI-GeneID: 1501
NCBI-ProteinID: NP_001323
OMIM: 604275
HGNC: 2516
Ensembl: ENSG00000169862
UniProt: Q9UQB3
Position
5:complement(10971836..11904446)
AA seq 1225 aa
MFARKPPGAAPLGAMPVPDQPSSASEKTSSLSPGLNTSNGDGSETETTSAILASVKEQEL
QFERLTRELEAERQIVASQLERCKLGSETGSMSSMSSAEEQFQWQSQDGQKDIEDELTTG
LELVDSCIRSLQESGILDPQDYSTGERPSLLSQSALQLNSKPEGSFQYPASYHSNQTLAL
GETTPSQLPARGTQARATGQSFSQGTTSRAGHLAGPEPAPPPPPPPREPFAPSLGSAFHL
PDAPPAAAAAALYYSSSTLPAPPRGGSPLAAPQGGSPTKLQRGGSAPEGATYAAPRGSSP
KQSPSRLAKSYSTSSPINIVVSSAGLSPIRVTSPPTVQSTISSSPIHQLSSTIGTYATLS
PTKRLVHASEQYSKHSQELYATATLQRPGSLAAGSRASYSSQHGHLGPELRALQSPEHHI
DPIYEDRVYQKPPMRSLSQSQGDPLPPAHTGTYRTSTAPSSPGVDSVPLQRTGSQHGPQN
AAAATFQRASYAAGPASNYADPYRQLQYCPSVESPYSKSGPALPPEGTLARSPSIDSIQK
DPREFGWRDPELPEVIQMLQHQFPSVQSNAAAYLQHLCFGDNKIKAEIRRQGGIQLLVDL
LDHRMTEVHRSACGALRNLVYGKANDDNKIALKNCGGIPALVRLLRKTTDLEIRELVTGV
LWNLSSCDALKMPIIQDALAVLTNAVIIPHSGWENSPLQDDRKIQLHSSQVLRNATGCLR
NVSSAGEEARRRMRECDGLTDALLYVIQSALGSSEIDSKTVENCVCILRNLSYRLAAETS
QGQHMGTDELDGLLCGEANGKDAESSGCWGKKKKKKKSQDQWDGVGPLPDCAEPPKGIQM
LWHPSIVKPYLTLLSECSNPDTLEGAAGALQNLAAGSWKWSVYIRAAVRKEKGLPILVEL
LRIDNDRVVCAVATALRNMALDVRNKELIGKYAMRDLVHRLPGGNNSNNTASKAMSDDTV
TAVCCTLHEVITKNMENAKALRDAGGIEKLVGISKSKGDKHSPKVVKAASQVLNSMWQYR
DLRSLYKKDGWSQYHFVASSSTIERDRQRPYSSSRTPSISPVRVSPNNRSASAPASPREM
ISLKERKTDYECTGSNATYHGAKGEHTSRKDAMTAQNTGISTLYRNSYGAPAEDIKHNQV
SAQPVPQEPSRKDYETYQPFQNSTRNYDESFFEDQVHHRPPASEYTMHLGLKSTGNYVDF
YSAARPYSELNYETSHYPASPDSWV
NT seq 3678 nt   +upstreamnt  +downstreamnt
atgtttgcgaggaagccgccgggcgccgcgcctttgggagctatgcctgttccagaccag
ccttcatcagcctcagagaagacgagttccctgagccccggcttaaacacctccaacggg
gatggctctgaaacagaaaccacctctgccatcctcgcctcagtcaaagaacaggaatta
cagtttgaaaggctgacccgagagctggaggctgaacggcagatcgtagccagccagctg
gagcgatgcaagctcggatccgagactggcagcatgagcagcatgagttcagcagaagag
cagtttcagtggcagtcacaagatggtcaaaaagatatcgaagatgagcttacaacaggt
ctcgagctggtggactcctgtattaggtcactacaggaatcaggaatacttgacccacag
gattattctacaggtgaaaggcccagcctgctctcccagagtgcacttcagctcaattcc
aaacctgaagggtctttccagtatccggccagctaccatagcaaccagaccctggccctg
ggggaaaccaccccttcacagctcccggcccgaggcacacaagcccgagctacgggccag
agcttcagccagggcacgaccagccgcgccggccacctggcggggcccgagcccgcgccg
ccgccgccgccgccgccgcgggagccgttcgcgcccagcctgggcagcgccttccacctg
cccgacgcgccgcccgccgccgccgccgccgcgctctactactccagctccacgctgccc
gcgccgccgcgcgggggctccccgctggccgcgccccagggcggttcgcccaccaagctg
cagcgcggcggctcggcccccgagggcgccacctacgccgcgccgcgcggctcctcgccc
aagcagtcgcccagccgcctggccaagtcctacagcaccagctcgcccatcaacatcgtc
gtgtcctcggccggcctgtccccgatccgcgtgacctcgccccccaccgtgcagtccacc
atctcctcctcgcccatccaccagctgagctccaccatcggcacgtacgccaccctgtcg
cccaccaagcgcctggtccacgcgtccgagcagtacagcaagcactcgcaggagctgtat
gccacggccaccctccagaggccgggcagcctggcagctggttcccgagcctcatacagc
agccagcatgggcacctgggcccagagttgcgggccctgcagtccccagaacaccacata
gatcccatctatgaagaccgcgtctatcagaagccccctatgaggagtctcagccagagc
cagggggaccctctgccgccagcacacaccggcacctaccgcacgagcacagccccatct
tcccctggtgtcgactccgtccccttgcagcgcacaggcagccagcacggcccacagaat
gccgccgcggccaccttccagagggccagctatgccgccggcccagcctccaattacgcg
gacccctaccgacagctgcagtattgtccctctgttgagtctccatacagcaaatccggc
cctgctctcccgcctgaaggcaccttggccaggtccccgtccattgatagcattcagaaa
gatcccagagaatttggatggagagacccggaactgccggaagtgattcagatgttgcag
caccagtttccctcggtccagtctaacgcggcagcctacttgcaacacctctgttttgga
gacaacaaaattaaagccgagataaggagacaaggaggcatccagctcctggtggacctg
ttggatcatcggatgaccgaagtccaccgtagtgcctgtggagctctgagaaacctggtg
tatgggaaggccaacgatgataacaaaattgccctgaaaaactgtggtggcatcccagca
ctggtgaggttactccgcaagacgactgacctggagatccgggagctggtcacaggagtc
ctttggaacctctcctcatgcgatgcactcaaaatgccaatcatccaggatgccctagca
gtactgaccaacgcggtgattatcccccactcaggctgggaaaattcgcctcttcaggat
gatcggaaaatacagctgcattcatcacaggtgctgcgtaacgccaccgggtgcctaagg
aatgttagttcggccggagaggaggcccgcagaaggatgagagagtgtgatgggcttacg
gatgccttgctgtacgtgatccagtctgcgctggggagcagtgagatcgatagcaagacc
gttgaaaactgtgtgtgcattttaaggaacctctcgtaccggctggcggcagaaacgtct
cagggacagcacatgggcacggacgagctggacgggctactctgtggcgaggccaatggc
aaggatgctgagagctctgggtgctggggcaagaagaagaagaaaaagaaatcccaagat
cagtgggatggagtaggacctcttccagactgtgctgaaccaccaaaagggatccagatg
ctgtggcacccatcaatagtcaaaccctacctcacactgctctctgagtgctcaaatcca
gacacgctggaaggggcggcaggcgccctgcagaacttggctgcagggagctggaagtgg
tcagtatatatccgagccgctgtccgaaaagagaaaggcctgcccatcctcgtggagctg
ctccgaatagacaatgaccgtgtggtgtgcgcggtggccactgcgctgcggaacatggcc
ttggacgtcagaaataaggagctcatcggcaaatacgccatgcgagacctagtccacagg
cttccaggagggaacaacagcaacaacactgcaagcaaggccatgtcggatgacacagtg
acagctgtctgctgcacactgcacgaagtgattaccaagaacatggagaacgccaaggcc
ttacgggatgccggtggcatcgagaagttggtcggcatctccaaaagcaaaggagataaa
cactctccaaaagtggtcaaggctgcatctcaggtcctcaacagcatgtggcagtaccga
gatctgaggagtctctacaaaaaggatggatggtcacaataccactttgtagcctcgtct
tcaaccatcgagagggaccggcaaaggccctactcctcctcccgcacgccctccatctcc
cctgtgcgcgtgtctcccaacaaccgctcagcaagtgccccagcttcacctcgggaaatg
atcagcctcaaagaaaggaaaacagactacgagtgcaccggcagcaacgccacctaccac
ggagctaaaggcgaacacacttccaggaaagatgccatgacagctcaaaacactggaatt
tcaactttgtataggaattcttatggtgcgcccgctgaagacatcaaacacaaccaggtt
tcagcacagccagtcccacaggagcccagcagaaaagattacgagacctaccagccattt
cagaattccacaagaaattacgatgagtccttcttcgaggaccaggtccaccatcgccct
cccgccagcgagtacaccatgcacctgggtctcaagtccaccggcaactacgttgacttc
tactcagctgcccgtccctacagtgaactgaactatgaaacgagccactacccggcctcc
cccgactcctgggtgtga

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Ontology (1)   
   KEGG BRITE (1)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (2)   
   KEGG DISEASE (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (20)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (55)   
   RefSeq(nuc) (19)   
   GenBank (18)   
   EMBL (18)   
Protein domain (5)   
   Pfam (5)   
All databases (99)   

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