RFTN2
protein-coding gene in the species Homo sapiens
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RFTN2
Summary
RFTN2 is a gene[1].
Key Facts
- RFTN2's instance of is recorded as gene[2].
- RFTN2 is a type of protein-coding gene[3].
- RFTN2's HomoloGene ID is recorded as 16954[4].
- RFTN2's genomic start is recorded as 197568224[5].
- RFTN2's genomic start is recorded as 198432948[6].
- RFTN2's genomic end is recorded as 197676045[7].
- RFTN2's genomic end is recorded as 198540769[8].
- RFTN2's ortholog is recorded as Rftn2[9].
- RFTN2's ortholog is recorded as Rftn2[10].
- RFTN2's ortholog is recorded as rftn2[11].
- RFTN2's encodes is recorded as Raftlin family member 2[12].
- RFTN2's found in taxon is recorded as Homo sapiens[13].
- RFTN2's chromosome is recorded as human chromosome 2[14].
- RFTN2's strand orientation is recorded as reverse strand[15].
- RFTN2's exact match is recorded as http://identifiers.org/ncbigene/130132[16].
- RFTN2's cytogenetic location is recorded as 2q33.1[17].
- RFTN2's expressed in is recorded as ventricular zone[18].
- RFTN2's expressed in is recorded as C1 segment[19].
- RFTN2's expressed in is recorded as internal globus pallidus[20].
- RFTN2's expressed in is recorded as corpus callosum[21].
- RFTN2's expressed in is recorded as Achilles tendon[22].
- RFTN2's expressed in is recorded as tendon of biceps brachii[23].
- RFTN2's expressed in is recorded as amygdala[24].
- RFTN2's expressed in is recorded as caudate nucleus[25].
- RFTN2's expressed in is recorded as substantia nigra[26].