Human cDNA
| Basic Informations | Advanced Informations |
| Clone information |
Clone ID | hMU002108 |
| Korean Unigene Clone | IRAT-22-H08 | |
| Original Clone | IRAK-32-A05 | |
| Vector | pBluescriptR | |
| Gene | FZD9 | |
| Gene Description | frizzled class receptor 9 | |
| Clone sequence size | 2352 (bp) | |
| Fullness | F | |
| Mutation | 824,1571,1799,1895 | |
| Amino acid - mutation | CCC(P)-> CGC(R),ATC(I)-> GTC(V),AGC(S)-> AAC(N),CGC(R)-> CAC(H) | |
| Price | \77,000 (부가세 포함가) |
| Clone information |
5' end sequenced Length | 2352 |
| Sequence | TGGTTCAGCGGCGGCTCCGGTGGCAGCGGCGGTGGCGGCTAGGCG GGCTCGGCGGCTCCTGTCCCTCGGGCGGCTGCCCGCTCGCTGCCC AGGGCGCCCGGACACACGTGGGCGGCTCAGCGATGGCCCGCGCCC CGCGACGTGGCGGGCAGGCACCGGGGCGCGGGACCGCTGAGCCCA AGTGAGCCGGGGCCGCGCTCCCGCCTTCGGCCCGGGCCTCCCGGG ATGGCCGTGGCGCCTCTGCGGGGGGCGCTGCTGCTGTGGCAGCTG CTGGCGGCGGGCGGCGCGGCACTGGAGATCGGCCGCTTCGACCCG GAGCGCGGGCGCGGGGCTGCGCCGTGCCAGGCGGTGGAGATCCCC ATGTGCCGCGGCATCGGCTACAACCTGACCCGCATGCCCAACCTG CTGGGCCACACGTCGCAGGGCGAGGCGGCTGCCGAGCTAGCGGAG TTCGCGCCGCTGGTGCAGTACGGCTGCCACAGCCACCTGCGCTTC TTCCTGTGCTCGCTCTACGCGCCCATGTGCACCGACCAGGTCTCG ACGCCCATTCCCGCCTGCCGGCCCATGTGCGAGCAGGCGCGCCTG CGCTGCGCGCCCATCATGGAGCAGTTCAACTTCGGCTGGCCGGAC TCGCTCGACTGCGCCCGGCTGCCCACGCGCAACGACCCGCACGCG CTGTGCATGGAGGCGCCCGAGAACGCCACGGCCGGCCCCGCGGAG CCCCACAAGGGCCTGGGCATGCTGCCCGTGGCGCCGCGGCCCGCG CGCCCTCCCGGAGACCTGGGCCCGGGCGCGGGCGGCAGTGGCACC TGCGAGAACCGCGAGAAGTTCCAGTACGTGGAGAAGAGCCGCTCG TGCGCACCGCGCTGCGGGCCCGGCGTCGAGGTGTTCTGGTCCCGG CGCGACAAGGACTTCGCGCTGGTCTGGATGGCCGTGTGGTCGGCG CTGTGCTTCTTCTCCACCGCCTTCACTGTGCTCACCTTCTTGCTG GAGCCCCACCGCTTCCAGTACCCCGAGCGCCCCATCATCTTCCTC TCCATGTGCTACAACGTCTACTCGCTGGCCTTCCTGATCCGTGCG GTGGCCGGAGCGCAGAGCGTGGCCTGTGACCAGGAGGCGGGCGCG CTCTACGTGATCCAGGAGGGCCTGGAGAACACGGGCTGCACGCTG GTCTTCCTACTGCTCTACTACTTCGGCATGGCCAGCTCGCTCTGG TGGGTGGTCCTGACGCTCACCTGGTTCCTGGCTGCCGGGAAGAAA TGGGGCCACGAGGCCATCGAGGCCCACGGCAGCTATTTCCACATG GCTGCCTGGGGCCTGCCCGCGCTCAAGACCATCGTCATCCTGACC CTGCGCAAGGTGGCGGGTGATGAGCTGACTGGGCTTTGCTACGTG GCCAGCACGGATGCAGCAGCGCTCACGGGCTTCGTGCTGGTGCCC CTCTCTGGCTACCTGGTGCTGGGCAGTAGTTTCCTCCTGACCGGC TTCGTGGCCCTCTTCCACATCCGCAAGATCATGAAGACGGGCGGC ACCAACACAGAGAAGCTGGAGAAGCTCATGGTCAAGGTCGGGGTC TTCTCCATCCTCTACACGGTGCCCGCCACCTGCGTCATCGTTTGC TATGTCTACGAACGCCTCAACATGGACTTCTGGCGCCTTCGGGCC ACAGAGCAGCCATGCGCAGCGGCCGCGGGGCCCGGAGGCCGGAGG GACTGCTCGCTGCCAGGGGGCTCGGTGCCCACCGTGGCGGTCTTC ATGCTCAAAATTTTCATGTCACTGGTGGTGGGGATCACCAACGGC GTCTGGGTGTGGAGCTCCAAGACTTTCCAGACCTGGCAGAGCCTG TGCTACCGCAAGATAGCAGCTGGCCGGGCCCGGGCCAAGGCCTGC CACGCCCCCGGGAGCTACGGACGTGGCACGCACTGCCACTATAAG GCTCCCACCGTGGTCTTGCACATGACTAAGACGGACCCCTCTTTG GAGAACCCCACACACCTCTAGCCACACAGGCCTGGCGCGGGGTGG CTGCTGCCCCCTCCTTGCCCTCCACGCCCTGCCCCCTGCATCCCC TAGAGACAGCTGACTAGCAGCTGCCCAGCTGTCAAGGTCAGGCAA GTGAGCACCGGGGACTGAGGATCAGGGCGGGACCCCGTGAGGCTC ATTAGGGGAGATGGGGGTCTCCCCTAATGCGGGGGCTGGACCAGG CTGAGTCCCCACAGGGTCCTAGTGGAGGATGTGGAGGGGCGGGGC AGAGGGGTCCAGCCGGAGTTTATTTAATGATGTAATTTATTGTTG CGTTCCTCTGGAAGCTGTGACTGGAATAAACCCCCGCGTGGCAAA AAAAAAAAAAAA |
| vector name | |
| vector source | |
| enzyme site(DNA insert) | |
| sequencing primer | |
| vector sequence | |
| Gene Location | Chromosome | 7 | |||||||||||
| Location | 7q11.23 | ||||||||||||
| Strand |
|
||||||||||||
| Database links | RefSeq | NM_003508 | |||||||||||
| KEGG Genes | 8326 | ||||||||||||
| GeneCard | FZD9 |
| sequence | sequence of CDS | ATGGCCGTGGCGCCTCTGCGGGGGGCGCTGCTGCTGTGGCAGCTGCTGGCGGCGGGCGGCGCGGCACTGGAGATCGGCCGCTTCGACCCGGAGCGCGGGCGCGGGGCTGCGCCGTGCCAGGCGGTGGAGATCCCCATGTGCCGCGGCATCGGCTACAACCTGACCCGCATGCCCAACCTGCTGGGCCACACGTCGCAGGGCGAGGCGGCTGCCGAGCTAGCGGAGTTCGCGCCGCTGGTGCAGTACGGCTGCCACAGCCACCTGCGCTTCTTCCTGTGCTCGCTCTACGCGCCCATGTGCACCGACCAGGTCTCGACGCCCATTCCCGCCTGCCGGCCCATGTGCGAGCAGGCGCGCCTGCGCTGCGCGCCCATCATGGAGCAGTTCAACTTCGGCTGGCCGGACTCGCTCGACTGCGCCCGGCTGCCCACGCGCAACGACCCGCACGCGCTGTGCATGGAGGCGCCCGAGAACGCCACGGCCGGCCCCGCGGAGCCCCACAAGGGCCTGGGCATGCTGCCCGTGGCGCCGCGGCCCGCGCGCCCTCCCGGAGACCTGGGCCCGGGCGCGGGCGGCAGTGGCACCTGCGAGAACCCCGAGAAGTTCCAGTACGTGGAGAAGAGCCGCTCGTGCGCACCGCGCTGCGGGCCCGGCGTCGAGGTGTTCTGGTCCCGGCGCGACAAGGACTTCGCGCTGGTCTGGATGGCCGTGTGGTCGGCGCTGTGCTTCTTCTCCACCGCCTTCACTGTGCTCACCTTCTTGCTGGAGCCCCACCGCTTCCAGTACCCCGAGCGCCCCATCATCTTCCTCTCCATGTGCTACAACGTCTACTCGCTGGCCTTCCTGATCCGTGCGGTGGCCGGAGCGCAGAGCGTGGCCTGTGACCAGGAGGCGGGCGCGCTCTACGTGATCCAGGAGGGCCTGGAGAACACGGGCTGCACGCTGGTCTTCCTACTGCTCTACTACTTCGGCATGGCCAGCTCGCTCTGGTGGGTGGTCCTGACGCTCACCTGGTTCCTGGCTGCCGGGAAGAAATGGGGCCACGAGGCCATCGAGGCCCACGGCAGCTATTTCCACATGGCTGCCTGGGGCCTGCCCGCGCTCAAGACCATCGTCATCCTGACCCTGCGCAAGGTGGCGGGTGATGAGCTGACTGGGCTTTGCTACGTGGCCAGCACGGATGCAGCAGCGCTCACGGGCTTCGTGCTGGTGCCCCTCTCTGGCTACCTGGTGCTGGGCAGTAGTTTCCTCCTGACCGGCTTCGTGGCCCTCTTCCACATCCGCAAGATCATGAAGACGGGCGGCACCAACACAGAGAAGCTGGAGAAGCTCATGGTCAAGATCGGGGTCTTCTCCATCCTCTACACGGTGCCCGCCACCTGCGTCATCGTTTGCTATGTCTACGAACGCCTCAACATGGACTTCTGGCGCCTTCGGGCCACAGAGCAGCCATGCGCAGCGGCCGCGGGGCCCGGAGGCCGGAGGGACTGCTCGCTGCCAGGGGGCTCGGTGCCCACCGTGGCGGTCTTCATGCTCAAAATTTTCATGTCACTGGTGGTGGGGATCACCAGCGGCGTCTGGGTGTGGAGCTCCAAGACTTTCCAGACCTGGCAGAGCCTGTGCTACCGCAAGATAGCAGCTGGCCGGGCCCGGGCCAAGGCCTGCCGCGCCCCCGGGAGCTACGGACGTGGCACGCACTGCCACTATAAGGCTCCCACCGTGGTCTTGCACATGACTAAGACGGACCCCTCTTTGGAGAACCCCACACACCTCTAG |
| sequence of protein | MAVAPLRGALLLWQLLAAGGAALEIGRFDPERGRGAAPCQAVEIPMCRGIGYNLTRMPNLLGHTSQGEAAAELAEFAPLVQYGCHSHLRFFLCSLYAPMCTDQVSTPIPACRPMCEQARLRCAPIMEQFNFGWPDSLDCARLPTRNDPHALCMEAPENATAGPAEPHKGLGMLPVAPRPARPPGDLGPGAGGSGTCENPEKFQYVEKSRSCAPRCGPGVEVFWSRRDKDFALVWMAVWSALCFFSTAFTVLTFLLEPHRFQYPERPIIFLSMCYNVYSLAFLIRAVAGAQSVACDQEAGALYVIQEGLENTGCTLVFLLLYYFGMASSLWWVVLTLTWFLAAGKKWGHEAIEAHGSYFHMAAWGLPALKTIVILTLRKVAGDELTGLCYVASTDAAALTGFVLVPLSGYLVLGSSFLLTGFVALFHIRKIMKTGGTNTEKLEKLMVKIGVFSILYTVPATCVIVCYVYERLNMDFWRLRATEQPCAAAAGPGGRRDCSLPGGSVPTVAVFMLKIFMSLVVGITSGVWVWSSKTFQTWQSLCYRKIAAGRARAKACRAPGSYGRGTHCHYKAPTVVLHMTKTDPSLENPTHL | |
| Database link | RefSeq | NM_003508 |
| UniProt | ||
| CCDS |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Gene Ontology Provided by GOA (www.ebi.ac.uk/GOA)
|
| Disease | Summary |
| Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008] |
|
|||||||||||
