Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 6833 |
Gene Name: | ATP binding cassette subfamily C member 8 |
Gene Aliases: |
ABC36, HHF1, HI, HRINS, MRP8, PHHI, SUR, SUR1, SUR1delta2, TNDM2 |
Location: |
Chr.11:17392885-17476870 on Build GRCh38 |
Assay Gene Location: | Within Exon 39 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ABCC8 | NM_000352.4 | 39 | 4840 | NP_000343.2 |
| NM_001287174.1 | 39 | 4843 | NP_001274103.1 | |
| XM_011520331.2 | 39 | 4865 | XP_011518633.1 | |
| XM_017018197.1 | 39 | 4903 | XP_016873686.1 | |
| XM_017018198.1 | 39 | 4900 | XP_016873687.1 | |
| XM_017018199.1 | 39 | 4908 | XP_016873688.1 | |
| XM_017018200.1 | 39 | 4858 | XP_016873689.1 | |
| XM_017018202.1 | 38 | 4704 | XP_016873691.1 | |
| XM_017018204.1 | 33 | 3816 | XP_016873693.1 | |
| AF087138.1 | AAC36724.1 | |||
| BM313666.1 | 1 | 96 | ||
| L40625.1 | 11 | 1214 | AAA99227.1 | |
| L78207.1 | 39 | 4809 | AAB02278.1 | |
| U63421.1 | 39 | 4771 | AAB36699.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv553583 | Chr.11:17372097 - 17396930 on Build GRCh38 | Loss |
 ABCC8
KCNJ11
NCR3LG1
|
| nsv553567 | Chr.11:16890704 - 17946708 on Build GRCh38 | Gain |
LOC102723330
KCNC1
SERGEF
NUCB2
MYOD1
OTOG
RPS13
PIK3C2A
SNORD14B
NCR3LG1
ABCC8
USH1C
KCNJ11
SNORD14A
PLEKHA7
OR7E14P
LOC105376575
|
| dgv59n21 | Chr.11:17379587 - 17413667 on Build GRCh38 | Loss |
ABCC8
KCNJ11
|
| nsv467713 | Chr.11:17386478 - 17418926 on Build GRCh38 | Loss |
ABCC8
KCNJ11
|
| nsv469895 | Chr.11:17346723 - 17562673 on Build GRCh38 | Loss |
ABCC8
USH1C
KCNJ11
OTOG
LOC105376575
NCR3LG1
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top