INS-IGF2
protein-coding gene in the species Homo sapiens
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INS-IGF2
Summary
INS-IGF2 is a gene[1].
Key Facts
- INS-IGF2's instance of is recorded as gene[2].
- INS-IGF2 is a type of protein-coding gene[3].
- INS-IGF2's genomic start is recorded as 2153768[4].
- INS-IGF2's genomic start is recorded as 2132538[5].
- INS-IGF2's genomic end is recorded as 2161209[6].
- INS-IGF2's genomic end is recorded as 2182439[7].
- INS-IGF2's encodes is recorded as INS-IGF2 readthrough[8].
- INS-IGF2's found in taxon is recorded as Homo sapiens[9].
- INS-IGF2's chromosome is recorded as human chromosome 11[10].
- INS-IGF2's strand orientation is recorded as reverse strand[11].
- INS-IGF2's exact match is recorded as http://identifiers.org/ncbigene/723961[12].
- INS-IGF2's cytogenetic location is recorded as 11p15.5[13].
- INS-IGF2's expressed in is recorded as islet of Langerhans[14].
- INS-IGF2's expressed in is recorded as body of pancreas[15].
- INS-IGF2's expressed in is recorded as liver[16].
- INS-IGF2's expressed in is recorded as urinary bladder[17].
- INS-IGF2's expressed in is recorded as blood[18].
- INS-IGF2's expressed in is recorded as kidney[19].
- INS-IGF2's expressed in is recorded as stomach[20].
- INS-IGF2's expressed in is recorded as small intestine[21].
- INS-IGF2's expressed in is recorded as tonsil[22].
- INS-IGF2's expressed in is recorded as lactiferous gland[23].