RIN2
protein-coding gene in the species Homo sapiens
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RIN2
Summary
RIN2 is a gene[1].
Key Facts
- RIN2's instance of is recorded as gene[2].
- RIN2 is a type of protein-coding gene[3].
- RIN2's HomoloGene ID is recorded as 32430[4].
- RIN2's genomic start is recorded as 19867165[5].
- RIN2's genomic start is recorded as 19757606[6].
- RIN2's genomic end is recorded as 19983101[7].
- RIN2's genomic end is recorded as 20002457[8].
- RIN2's ortholog is recorded as Rin2[9].
- RIN2's ortholog is recorded as Rin2[10].
- RIN2's ortholog is recorded as rin2a[11].
- RIN2's encodes is recorded as Ras and Rab interactor 2[12].
- RIN2's found in taxon is recorded as Homo sapiens[13].
- RIN2's chromosome is recorded as human chromosome 20[14].
- RIN2's genetic association is recorded as obesity[15].
- RIN2's genetic association is recorded as bipolar disorder[16].
- RIN2's genetic association is recorded as schizophrenia[17].
- RIN2's genetic association is recorded as RIN2 syndrome[18].
- RIN2's strand orientation is recorded as forward strand[19].
- RIN2's exact match is recorded as http://identifiers.org/ncbigene/54453[20].
- RIN2's cytogenetic location is recorded as 20p11.23[21].
- RIN2's expressed in is recorded as Epithelium of choroid plexus[22].
- RIN2's expressed in is recorded as tendon of biceps brachii[23].
- RIN2's expressed in is recorded as hair follicle[24].
- RIN2's expressed in is recorded as parotid gland[25].
- RIN2's expressed in is recorded as Achilles tendon[26].