Assay Details
Target Gene Details
Entrez Gene ID: | 1066 |
Gene Name: | carboxylesterase 1 |
Gene Aliases: |
ACAT, CE-1, CEH, CES2, HMSE, HMSE1, PCE-1, REH, SES1, TGH, hCE-1 |
Location: |
Chr.16:55802851-55833186 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CES1 | NM_001025194.1 | NP_001020365.1 | ||
NM_001025195.1 | NP_001020366.1 | |||
NM_001266.4 | NP_001257.4 | |||
XM_005255774.1 | XP_005255831.1 | |||
AB025026.1 | BAA84995.1 | |||
AB119995.1 | BAC87748.1 | |||
AB119996.1 | BAC87749.1 | |||
AF177775.1 | AAD53175.1 | |||
AK290623.1 | ||||
AK292209.1 | ||||
AK301651.1 | ||||
AY268104.1 | AAP20868.1 | |||
BC012418.1 | AAH12418.1 | |||
BC110338.1 | AAI10339.1 | |||
L07764.1 | AAA16036.1 | |||
L07765.1 | AAA35711.1 | |||
M55509.1 | AAA35650.1 | |||
M65261.1 | AAA83932.1 | |||
M73499.1 | AAA35649.1 | |||
S73751.1 | AAC60631.2 | |||
X52973.1 | CAA37147.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv442724 | Chr.16:55808470 - 55828798 on Build GRCh38 | Gain | CES1 |
dgv5137n54 | Chr.16:55808492 - 55835816 on Build GRCh38 | Gain | CES1 |
dgv840e212 | Chr.16:55790795 - 55834514 on Build GRCh38 | Gain | CES1 |
dgv5135n54 | Chr.16:55787063 - 55830540 on Build GRCh38 | Gain | CES1 |
nsv820205 | Chr.16:55793542 - 55832100 on Build GRCh38 | Gain | CES1 |
dgv842e212 | Chr.16:55806374 - 55834514 on Build GRCh38 | Gain | CES1 |
nsv1077830 | Chr.16:55806987 - 55830388 on Build GRCh38 | Duplication | CES1 |
esv3638688 | Chr.16:55798295 - 55830609 on Build GRCh38 | Loss | CES1 |
dgv841e212 | Chr.16:55805923 - 55825046 on Build GRCh38 | Loss | CES1 |
nsv827676 | Chr.16:55821542 - 55831399 on Build GRCh38 | Gain | CES1 |
dgv52e203 | Chr.16:55750518 - 55837223 on Build GRCh38 | Gain+Loss | CES1 CES1P1 |
nsv9446 | Chr.16:55806461 - 55833345 on Build GRCh38 | Gain | CES1 |
nsv572687 | Chr.16:55798655 - 55827882 on Build GRCh38 | Gain | CES1 |
esv32573 | Chr.16:55809091 - 55831223 on Build GRCh38 | Gain+Loss | CES1 |
dgv479n67 | Chr.16:55808461 - 55832982 on Build GRCh38 | Gain | CES1 |
dgv2987n100 | Chr.16:55782722 - 55845205 on Build GRCh38 | Gain | CES1 |
esv28619 | Chr.16:55808213 - 55831467 on Build GRCh38 | Gain | CES1 |
nsv977981 | Chr.16:55776220 - 55830390 on Build GRCh38 | Duplication | CES1 |
esv2937123 | Chr.16:55808088 - 55828088 on Build GRCh38 | Duplication | CES1 |
dgv843e212 | Chr.16:55808590 - 55825046 on Build GRCh38 | Gain | CES1 |
nsv572632 | Chr.16:55759783 - 55829137 on Build GRCh38 | Gain | CES1 CES1P1 |
nsv471382 | Chr.16:55787588 - 55830150 on Build GRCh38 | Gain | CES1 |
esv2758649 | Chr.16:55635484 - 55949678 on Build GRCh38 | Gain | CES1 CES1P2 CES5A CES1P1 SLC6A2 |
nsv572693 | Chr.16:55809206 - 55844051 on Build GRCh38 | Loss | CES1 |
nsv1110287 | Chr.16:55808388 - 55827188 on Build GRCh38 | Duplication | CES1 |
More Information
Additional Information:
For this assay, SNP(s) [rs114765581,rs116621568] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |