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GENE - TERM ANNOTATION REPORT
RGD ID:
18927941
Species:
Heterocephalus glaber
RGD Object:
Gene
Symbol:
Abcc8
Name:
ATP binding cassette subfamily C member 8
Acc ID:
DOID:630
Term:
genetic disease
Definition:
A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s):
http://ghr.nlm.nih.gov/
"DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object Symbol
Qualifier
Evidence
With
Reference
Source
Notes
Original Reference(s)
Abcc8
ISO
ABCC8 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Hereditary disease | ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10204114
PMID:10447255
PMID:10487673
PMID:10923633
PMID:11272143
PMID:11999683
PMID:12941782
PMID:14692646
PMID:14715863
PMID:15356046
PMID:15562009
PMID:15579781
PMID:16357843
PMID:16429405
PMID:16860127
PMID:17378627
PMID:18339976
PMID:18414213
PMID:18493152
PMID:20672374
PMID:21716120
PMID:21851374
PMID:23345197
PMID:24401662
PMID:25306193
PMID:25972930
PMID:26467025
PMID:27175728
PMID:27754802
PMID:28492532
PMID:7716548
PMID:8923011
PMID:9618169
PMID:9648840
Abcc8
ISO
ABCC8 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10204114
PMID:10338089
PMID:10447255
PMID:10487673
PMID:10923633
PMID:11272143
PMID:11999683
PMID:12941782
PMID:14692646
PMID:14715863
PMID:15111507
PMID:15356046
PMID:15562009
PMID:15579781
PMID:15580558
PMID:15718250
PMID:15807877
PMID:15842514
PMID:16186397
PMID:16357843
PMID:16429405
PMID:16613899
PMID:16860127
PMID:16885549
PMID:17317760
PMID:17378627
PMID:17389331
PMID:17446535
PMID:17919176
PMID:18025408
PMID:18339976
PMID:18414213
PMID:18493152
PMID:18599530
PMID:18662362
PMID:18758683
PMID:18767144
PMID:18981553
PMID:19475716
PMID:20672374
PMID:20685672
PMID:20810569
PMID:20922570
PMID:20943779
PMID:21544516
PMID:21716120
PMID:21738553
PMID:21851374
PMID:21989597
PMID:22704848
PMID:22902787
PMID:23275527
PMID:23345197
PMID:24401662
PMID:24411943
PMID:24622368
PMID:24768178
PMID:24959012
PMID:25008049
PMID:25306193
PMID:25555642
PMID:25741868
PMID:25765446
PMID:25931474
PMID:25955821
PMID:25972930
PMID:26208381
PMID:26221353
PMID:26268944
PMID:26431509
PMID:26448950
PMID:26467025
PMID:27175728
PMID:27538677
PMID:27754802
PMID:27908292
PMID:27913849
PMID:28442472
PMID:28492532
PMID:29216354
PMID:30191644
PMID:31216263
PMID:31291970
PMID:31604004
PMID:32027066
PMID:32376986
PMID:32792356
PMID:32928245
PMID:33013711
PMID:33046911
PMID:33300273
PMID:33410562
PMID:33565752
PMID:34032641
PMID:34304300
PMID:34309670
PMID:34927408
PMID:35402560
PMID:36208030
PMID:36407475
PMID:38095268
PMID:38513803
PMID:7716548
PMID:8923011
PMID:9075812
PMID:9618169
PMID:9648840
Abcc8
ISO
ABCC8 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10204114
PMID:10338089
PMID:10447255
PMID:10487673
PMID:10923633
PMID:11272143
PMID:11999683
PMID:12941782
PMID:14692646
PMID:14715863
PMID:15111507
PMID:15356046
PMID:15562009
PMID:15579781
PMID:15580558
PMID:15718250
PMID:15807877
PMID:15842514
PMID:16186397
PMID:16357843
PMID:16429405
PMID:16613899
PMID:16860127
PMID:16885549
PMID:17317760
PMID:17378627
PMID:17389331
PMID:17446535
PMID:17919176
PMID:18025408
PMID:18339976
PMID:18414213
PMID:18493152
PMID:18599530
PMID:18662362
PMID:18758683
PMID:18767144
PMID:18981553
PMID:19475716
PMID:20672374
PMID:20685672
PMID:20810569
PMID:20922570
PMID:20943779
PMID:21544516
PMID:21716120
PMID:21738553
PMID:21851374
PMID:21989597
PMID:22704848
PMID:22902787
PMID:23275527
PMID:23345197
PMID:24401662
PMID:24411943
PMID:24622368
PMID:24768178
PMID:24959012
PMID:25008049
PMID:25306193
PMID:25555642
PMID:25741868
PMID:25765446
PMID:25931474
PMID:25955821
PMID:25972930
PMID:26208381
PMID:26221353
PMID:26268944
PMID:26448950
PMID:26467025
PMID:27175728
PMID:27538677
PMID:27754802
PMID:27908292
PMID:27913849
PMID:28442472
PMID:28492532
PMID:29216354
PMID:30191644
PMID:31216263
PMID:31291970
PMID:31604004
PMID:32027066
PMID:32376986
PMID:32792356
PMID:32928245
PMID:33013711
PMID:33046911
PMID:33300273
PMID:33410562
PMID:33565752
PMID:34032641
PMID:34304300
PMID:34309670
PMID:34927408
PMID:35402560
PMID:36208030
PMID:36407475
PMID:38095268
PMID:38513803
PMID:7716548
PMID:8923011
PMID:9075812
PMID:9618169
PMID:9648840
Abcc8
ISO
ABCC8 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10204114
PMID:10338089
PMID:10447255
PMID:10487673
PMID:10923633
PMID:11272143
PMID:11999683
PMID:12941782
PMID:14692646
PMID:14715863
PMID:15111507
PMID:15356046
PMID:15562009
PMID:15579781
PMID:15580558
PMID:15718250
PMID:15807877
PMID:15842514
PMID:16186397
PMID:16357843
PMID:16429405
PMID:16613899
PMID:16860127
PMID:16885549
PMID:17378627
PMID:17389331
PMID:17446535
PMID:17919176
PMID:18025408
PMID:18339976
PMID:18414213
PMID:18493152
PMID:18599530
PMID:18662362
PMID:18758683
PMID:18767144
PMID:18981553
PMID:19475716
PMID:20672374
PMID:20685672
PMID:20810569
PMID:20943779
PMID:21544516
PMID:21716120
PMID:21851374
PMID:21989597
PMID:22704848
PMID:22902787
PMID:23275527
PMID:23345197
PMID:24401662
PMID:24411943
PMID:24622368
PMID:24768178
PMID:24959012
PMID:25008049
PMID:25306193
PMID:25555642
PMID:25741868
PMID:25765446
PMID:25931474
PMID:25955821
PMID:25972930
PMID:26208381
PMID:26221353
PMID:26268944
PMID:26448950
PMID:26467025
PMID:27175728
PMID:27538677
PMID:27754802
PMID:27908292
PMID:27913849
PMID:28442472
PMID:28492532
PMID:30191644
PMID:31291970
PMID:31604004
PMID:32027066
PMID:32792356
PMID:32928245
PMID:33046911
PMID:33300273
PMID:33410562
PMID:33565752
PMID:34304300
PMID:34309670
PMID:34927408
PMID:35402560
PMID:36208030
PMID:36407475
PMID:7716548
PMID:8923011
PMID:9075812
PMID:9618169
PMID:9648840
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