Gene: Abcc8 (ATP binding cassette subfamily C member 8) Rattus norvegicus
Analyze
Symbol:
Abcc8
Name:
ATP binding cassette subfamily C member 8
Description:
ENCODES a protein that exhibits ion channel binding (ortholog); potassium channel activity (ortholog); INVOLVED IN cellular glucose homeostasis; cellular response to organic substance; female pregnancy; PARTICIPATES IN diabetes mellitus pathway; acebutolol pharmacodynamics pathway; adrenergic beta receptor agonist and beta-blocker pharmacodynamics pathway; ASSOCIATED WITH brain edema; Brain Injuries; cardiac arrest; FOUND IN inward rectifying potassium channel; mitochondrion; sarcolemma; INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene
Type:
protein-coding
RefSeq Status:
PROVISIONAL
Also known as:
ATP-binding cassette sub-family C (CFTR/MRP) member 8; ATP-binding cassette sub-family C member 8; ATP-binding cassette subfamily C (CFTR/MRP) member 8; ATP-binding cassette transporter sub-family C member 8; ATP-binding cassette, sub-family C (CFTR/MRP), member 8; ATP-binding cassette, subfamily C (CFTR/MRP), member 8; sulfonylurea receptor; sulfonylurea receptor 1; sulphonylurea receptor 1; Sur; Sur1
Orthologs:
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
ABCC8 (ATP binding cassette subfamily C member 8) HGNC
EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Mus musculus (house mouse):
Abcc8 (ATP-binding cassette, sub-family C (CFTR/MRP), member 8) HGNC
Treefam, EggNOG, NCBI, OMA, HomoloGene, Inparanoid, Panther, OrthoDB, Ensembl
Chinchilla lanigera (long-tailed chinchilla):
Abcc8 (ATP binding cassette subfamily C member 8) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):
ABCC8 (ATP binding cassette subfamily C member 8) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Canis lupus familiaris (dog):
ABCC8 (ATP binding cassette subfamily C member 8) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):
Abcc8 (ATP binding cassette subfamily C member 8) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Alliance orthologs 3
Homo sapiens (human):
ABCC8 (ATP binding cassette subfamily C member 8) Alliance
DIOPT (OrthoInspector, HGNC, OMA, Compara, Hieranoid, Phylome, TreeFam, Inparanoid, Panther, OrthoFinder)
Mus musculus (house mouse):
Abcc8 (ATP-binding cassette, sub-family C (CFTR/MRP), member 8) Alliance
DIOPT (OrthoInspector, OMA, Compara, Hieranoid, Phylome, TreeFam, Inparanoid, Panther, OrthoFinder)
Latest Assembly:
Rnor_6.0 - RGSC Genome Assembly v6.0
NCBI Annotation Information:
Annotation category: suggests misassembly
Position:
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl Rnor_6.0 1 102,110,708 - 102,191,287 (-) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_5.0 1 103,194,473 - 103,275,508 (-) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 1 96,622,574 - 96,703,723 (-) NCBI RGSC3.4 rn4 RGSC3.4 RGSC_v3.1 1 96,700,590 - 96,781,880 (-) NCBI Celera 1 90,849,685 - 90,928,224 (-) NCBI Celera Cytogenetic Map 1 q22 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Disease Annotations
RGD Manual Annotations
brain edema IMP 1598635 associated with Cerebrovascular Accident RGD brain edema treatment IMP 12791991 associated with Neoplasms, Experimental RGD Brain Injuries treatment IMP 12791995 RGD cardiac arrest treatment IMP 12791997 RGD Congenital Hyperinsulinism ISO RGD:733938 11069847 DNA:missense mutations, nonsense mutations, splice-site mutations:CDS:multiple RGD Congenital Hyperinsulinism ISO RGD:733938 12790596 DNA:missense mutations:exon:p.G1485E (c.4454G>A), p.D1506E (c.4518C>A), p.M1544K (c.4541T>A) (human) RGD Congenital Hyperinsulinism ISO RGD:733938 12790587 DNA:mutations:exon, intron:multiple RGD Congenital Hyperinsulinism ISO RGD:733938 12743628 DNA:deletion: :p.S1387del (human) RGD Congenital Hyperinsulinism ISO RGD:733938 11070657 DNA:mutations:exon, intron:multiple RGD Congenital Hyperinsulinism ISO RGD:733938 11067821 DNA:mutations:exon, intron:multiple RGD Congenital Hyperinsulinism ISO RGD:733938 704365 RGD Congenital Hyperinsulinism ISO RGD:733938 12790723 DNA:mutations:exon:multiple RGD diabetes mellitus ISO RGD:733938 1625279 RGD Endotoxemia IEP 2301914 RGD hyperinsulinism ISO RGD:733938 1625279 RGD hyperinsulinism susceptibility ISO RGD:733938 1598639 RGD Hyperplasia ISO RGD:733938 2325205 associated with Hyperinsulinism;DNA:missense mutations:exon:p.R1353P, p.R1421C, p.R1494W (human) RGD hypertension ISO RGD:733938 737749 associated with obesity;DNA:polymorphism:exon: RGD hypoglycemia IMP 2301896 RGD middle cerebral artery infarction treatment IMP 12791996 RGD middle cerebral artery infarction treatment IMP 12790979 RGD Myocardial Reperfusion Injury ISO RGD:736889 2301903 RGD Necrosis IMP 2301913 associated with Spinal Cord Injuries RGD Parkinsonian Disorders IEP 1598645 RGD sciatic neuropathy IEP 12791994 protein:decreased expression:spinal cord RGD Spinal Cord Injuries ISO RGD:736889 12790978 RGD Spinal Cord Injuries treatment IMP 12790978 RGD Spinal Cord Injuries ISO RGD:733938 12790978 mRNA:increased expression:spinal cord RGD Spinal Cord Injuries treatment IEP 12791993 RGD status epilepticus IEP 5686281 mRNA:decreased expression:hippocampus RGD Stroke ISO RGD:733938 2301906 associated with Diabetes Mellitus, Non-Insulin-Dependent RGD Subarachnoid Hemorrhage treatment IMP 10003028 RGD Subarachnoid Hemorrhage, Traumatic treatment IMP 2325137 RGD type 2 diabetes mellitus susceptibility ISO RGD:733938 2301901 DNA:missense mutations: :p.R248Q, p.K1521N, p.Y356C (human) RGD type 2 diabetes mellitus ISO RGD:733938 2301897 DNA:polymorphism:intron:IVS16-3T>C (human) RGD type 2 diabetes mellitus susceptibility ISO RGD:733938 1598640 RGD type 2 diabetes mellitus ISO RGD:733938 2301898 DNA:polymorphism: :p.S1369A (human) RGD type 2 diabetes mellitus ISO RGD:733938 737749 DNA:polymorphism:exon: RGD type 2 diabetes mellitus ISO RGD:733938 2313628 DNA:missense mutation::A1369S (human) RGD visual epilepsy IEP 2301911 mRNA, protein:altered expression:dentate gyrus RGD
Imported Annotations - ClinVar
atrial heart septal defect ISO RGD:733938 8554872 ClinVar Annotator: match by term: Atrial septal defect ClinVar PMID:25741868 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10993895 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:12784138 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Familial hyperinsulinism ClinVar PMID:14764815 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10720932 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Familial hyperinsulinism ClinVar PMID:14715863 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:14715863 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:23275527 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:12166651 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Familial hyperinsulinism ClinVar PMID:16357843 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Familial hyperinsulinism ClinVar PMID:20685672 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: familial hyperinsulinism ClinVar PMID:16429405 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:7716548 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:7716548 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:12199344 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:16429405 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:16429405 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10204114 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinemic hypoglycemia familial 2 ClinVar PMID:11872696 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Congenital Hyperinsulinism ClinVar Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinemic hypoglycemia, familial, 1 ClinVar PMID:10426386 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10923633 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:19475716 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10447255 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10447255 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:25741868 PMID:26467025 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinemic hypoglycemia, familial, 1 ClinVar PMID:18414213 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:15579781 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:23345197 PMID:24401662 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:26545876 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:14692646 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:10204114 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:12941782 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:24044690 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:20573158 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:8751851 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:15579781 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:21378087 PMID:21978130 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:8923011 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:10334322 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: familial hyperinsulinism ClinVar PMID:18073294 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:23275527 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:16429405 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: familial hyperinsulinism ClinVar PMID:14715863 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:11018078 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:20685672 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:18414213 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:10202168 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:25741868 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Persistent hyperinsulinemic hypoglycemia of infancy ClinVar PMID:14692646 more ... Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:9769320 Congenital Hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:256450 ClinVar PMID:23273570 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Monogenic diabetes ClinVar PMID:25741868 PMID:9648840 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Monogenic diabetes ClinVar PMID:18346985 PMID:25741868 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:25741868 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Diabetes mellitus ClinVar PMID:18414213 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:24033266 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:26467025 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:18414213 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:12166651 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:18767144 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:25741868 PMID:26467025 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:11872696 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:10426386 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:18414213 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:10338089 more ... hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:20943779 PMID:25741868 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:19475716 PMID:25741868 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:25741868 hyperinsulinism ISO RGD:733938 8554872 ClinVar Annotator: match by term: Hyperinsulinism, Dominant/Recessive ClinVar PMID:18414213 PMID:25741868 Hypoglycemia, Leucine-Induced ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:240800 ClinVar PMID:15356046 maturity-onset diabetes of the young ISO RGD:733938 8554872 ClinVar Annotator: match by term: Maturity onset diabetes of the young ClinVar PMID:11872696 more ... maturity-onset diabetes of the young ISO RGD:733938 8554872 ClinVar Annotator: match by term: Maturity-onset diabetes of the young ClinVar PMID:18414213 PMID:25741868 maturity-onset diabetes of the young ISO RGD:733938 8554872 ClinVar Annotator: match by term: Maturity-onset diabetes of the young ClinVar PMID:25741868 maturity-onset diabetes of the young ISO RGD:733938 8554872 ClinVar Annotator: match by term: Maturity-onset diabetes of the young ClinVar neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:17389331 PMID:18436707 neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:16885549 more ... neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:17919176 more ... neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:10338089 more ... neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:26467025 neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Neonatal diabetes mellitus ClinVar PMID:25741868 Nesidioblastosis ISO RGD:733938 8554872 ClinVar Annotator: match by term: Nesidioblastosis ClinVar PMID:11872696 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:24033266 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:26467025 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:18414213 PMID:25741868 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:20943779 PMID:25741868 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar PMID:12166651 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:19475716 PMID:25741868 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar PMID:18414213 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:10338089 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:25741868 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:18767144 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:16885549 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:14715863 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:25741868 PMID:26467025 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Diabetes mellitus, permanent neonatal ClinVar PMID:11872696 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:10426386 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Permanent neonatal diabetes mellitus ClinVar PMID:18414213 more ... permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar PMID:16613899 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar PMID:16885549 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar PMID:17668386 permanent neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:606176 ClinVar Permanent Neonatal Diabetes Mellitus, with Neurologic Features ISO RGD:733938 8554872 ClinVar Annotator: match by null ClinVar PMID:16613899 Retrognathia ISO RGD:733938 8554872 ClinVar Annotator: match by term: Retrognathia ClinVar PMID:25741868 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:26467025 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:12166651 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:10426386 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:18414213 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:11872696 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:18767144 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:18414213 PMID:25741868 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:19475716 PMID:25741868 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:18414213 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:24033266 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:20943779 PMID:25741868 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:10338089 more ... transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:25741868 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar PMID:25741868 PMID:26467025 transient neonatal diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient Neonatal Diabetes, Dominant ClinVar Transient Neonatal Diabetes Mellitus, 2 ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient neonatal diabetes mellitus 2 ClinVar PMID:16885549 more ... Transient Neonatal Diabetes Mellitus, 2 ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:610374 ClinVar PMID:16885549 Transient Neonatal Diabetes Mellitus, 2 ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:610374 ClinVar PMID:25741868 Transient Neonatal Diabetes Mellitus, 2 ISO RGD:733938 8554872 ClinVar Annotator: match by term: Transient neonatal diabetes mellitus 2 ClinVar PMID:16885549 more ... type 2 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Diabetes mellitus type 2 ClinVar PMID:16885549 more ... type 2 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: DIABETES MELLITUS, TYPE II, SUSCEPTIBILITY TO ClinVar PMID:11872696 more ... type 2 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by OMIM:125853 ClinVar PMID:16885549 type 2 diabetes mellitus ISO RGD:733938 8554872 ClinVar Annotator: match by term: Diabetes mellitus type 2 ClinVar PMID:25741868 PMID:9519757 
Gene-Chemical Interaction Annotations
