Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
723961
Gene name Gene Name - the full gene name approved by the HGNC.
INS-IGF2 readthrough
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
INS-IGF2
Synonyms (NCBI Gene) Gene synonyms aliases
INSIGF
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.5
Summary Summary of gene provided in NCBI Entrez Gene.
This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5` region and to the IGF2 gene in the 3` region. One transcript is predicted to encode a protein which shares the N-terminus with the INS pro
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1067729 hsa-miR-1205 CLIP-seq
MIRT1067730 hsa-miR-2467-5p CLIP-seq
MIRT1067731 hsa-miR-3183 CLIP-seq
MIRT1067732 hsa-miR-3188 CLIP-seq
MIRT1067733 hsa-miR-3975 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005179 Function Hormone activity IEA
GO:0005576 Component Extracellular region IEA
GO:0007165 Process Signal transduction IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID F8WCM5
Protein name Insulin, isoform 2 (INS-IGF2 readthrough transcript protein)
PDB 7YQ3 , 7YQ4 , 7YQ5 , 8GUY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00049 Insulin 28 168 Insulin/IGF/Relaxin family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in pancreas, eye and, to a lower extent, in limb. {ECO:0000269|PubMed:16531418}.
Sequence
Sequence length 200
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 26301688
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs869025224 26301688
Common variable immunodeficiency Common Variable Immunodeficiency rs72553883, rs121908379, rs104894650, rs587776775, rs398122863, rs398122864, rs397514332, rs397514331, rs727502786, rs727502787, rs72553882, rs869320688, rs869320689, rs869320754, rs773694113
View all (35 more)
26301688
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent, Diabetes Mellitus, Non-Insulin-Dependent, Neonatal diabetes mellitus, DIABETES MELLITUS, PERMANENT NEONATAL, DIABETES MELLITUS, INSULIN-DEPENDENT, 2 rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
17632545, 26301688, 21829393, 17554260, 25751624, 31152121, 28838971, 30254083, 25102180, 21592955, 20133622
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac Disease 26301688 ClinVar
Crohn disease Crohn Disease 26301688 ClinVar