Name | catenin (cadherin-associated protein), alpha 1 (102kD) |
Symbol | CTNNA1 |
Aliases | CAP102 |
Gene Product | - catenin (cadherin-associated protein), alpha 1 (102kD)
|
Category | - Gross deletion in Prostate cancer
- Mutation in Prostate cancer
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UniGene | Hs.178452 |
OMIM | 116805 |
Locus | 1495 |
Summary | Catenin alpha 1 (cadherin-associated protein); binds cadherins and links them with the actin cytoskeleton |
Gene Ontology | |
Expression | EST (1093 ESTs, 348 libraries) |
Tissue ? |
Frequency ? |
Count ? |
adrenal gland (3/15) | | 6/17521 |
blood (2/27) | | 4/40686 |
bone (4/13) | | 9/26211 |
brain (26/204) | | 80/362011 |
cervix (3/7) | | 5/28115 |
colon (25/853) | | 90/165626 |
ear (1/2) | | 3/12660 |
embryo (5/19) | | 13/37976 |
eye (5/33) | | 15/93836 |
foreskin (1/4) | | 6/20040 |
germ cell (2/7) | | 2/57383 |
head and neck (21/990) | | 66/79796 |
heart (3/22) | | 16/55494 |
intestine (1/4) | | 4/11528 |
kidney (15/86) | | 46/132968 |
liver (4/38) | | 11/46472 |
lung (27/312) | | 80/245386 |
mammary gland (1/1) | | 3/2313 |
muscle (5/21) | | 16/71297 |
nervous (6/475) | | 10/43438 |
oral cavity (1/18) | | 2/44567 |
ovary (12/144) | | 35/81880 |
pancreas (9/33) | | 38/117255 |
parathyroid (1/4) | | 13/19377 |
placenta (15/342) | | 62/157762 |
prostate (17/291) | | 37/109871 |
skin (10/31) | | 61/100815 |
spleen (2/7) | | 4/9511 |
stomach (12/312) | | 57/129930 |
testis (9/171) | | 22/117531 |
thyroid (2/24) | | 4/6853 |
uncharacterized tissue (76/1773) | | 170/713325 |
uterus (18/212) | | 99/155110 |
|
SAGE (34817208 tags, 661 libraries) |
Tissue ? |
Frequency ? |
Count ? |
blood (1/1) | | 4/194092 |
brain (19/19) | | 255/9029753 |
cerebellum (1/1) | | 5/256400 |
colon (8/8) | | 108/3393835 |
eye (5/6) | | 35/2177790 |
foreskin (2/2) | | 2/19256 |
heart (1/1) | | 15/674856 |
kidney (2/2) | | 18/527324 |
liver (1/1) | | 8/334305 |
lung (1/1) | | 19/356572 |
mammary gland (18/19) | | 183/3536979 |
muscle (2/2) | | 10/484787 |
ovary (10/10) | | 82/1663476 |
pancreas (8/8) | | 55/1185743 |
prostate (13/13) | | 107/3194793 |
skin (4/7) | | 11/167044 |
stomach (3/3) | | 36/1474660 |
uncharacterized tissue (20/22) | | 174/4475610 |
vascular (3/3) | | 53/1669933 |
|
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SNP | rs1059014 (C/G:coding-nonsyn);  rs167009 (G/C:intron);  rs3048865 (TG/-:locus-region);  rs288041 (G/T:intron);  rs2462931 (A/G:intron);  rs891995 (A/G:intron);  rs2011462 (C/T:intron);  rs884469 (C/T:intron);  rs2016720 (C/T:intron);  rs2011433 (C/T:intron);  rs442153 (T/G:intron);  rs700626 (A/C:intron);  rs495638 (A/G:intron);  rs2292268 (A/G:intron);  rs387761 (A/T:intron);  rs433260 (T/C:intron);  rs883333 (A/C:intron);  rs185956 (T/C:intron);  rs1976568 (G/T:intron);  rs1059039 (G/A:coding-nonsyn);  rs995176 (C/T:intron);  rs906695 (A/G:intron);  rs2662543 (A/T:intron);  rs1848505 (A/T:intron);  rs1508896 (G/T:intron);  rs1972072 (C/G:intron);  rs2351247 (A/G:intron);  rs423469 (C/G:intron);  rs2048221 (C/T:intron);  rs2351463 (A/G:intron);  rs373794 (C/T:intron);  rs375425 (G/T:intron);  rs1828187 (C/T:intron);  rs176381 (A/G:intron);  rs825745 (G/C:locus-region);  rs425132 (A/G:intron);  rs1030680 (C/T:intron);  rs2116809 (C/T:intron);  rs862230 (G/T:intron);  rs1039788 (A/G:intron);  rs430654 (A/G:intron);  rs288002 (T/C:intron);   |
Evidence | Gross deletion in Prostate cancer
Mutation in Prostate cancer
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