FTHL17

Entrez Summary: This gene encodes a ferritin heavy chain-like protein. This gene is primarily expressed in embryonic germ cells. The encoded protein may lack ferroxidase activity. Multiple pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Oct 2016].
UniProt Summary: N/A

Pfam Domains GO Terms

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

Global Fraction of Cell Lines Where Essential: 0/694

Tissue	Fraction Of Cell Lines Where Essential
1290807.0	0/1
909776.0	0/1
bile duct	0/28
blood	0/26
bone	0/26
breast	0/30
central nervous system	0/49
cervix	0/4
colorectal	0/17
esophagus	0/11
fibroblast	0/1
gastric	0/14
kidney	0/18
liver	0/19
lung	0/72
lymphocyte	0/16
ovary	0/25
pancreas	0/22
peripheral nervous system	0/15
plasma cell	0/12
prostate	0/1
skin	0/20
soft tissue	0/9
thyroid	0/2
upper aerodigestive	0/22
urinary tract	0/28
uterus	0/5

Expression Distribution

intracellular sequestering of iron ion
sequestering of iron ion
ferroxidase activity
ferric iron binding
sequestering of metal ion
ferrous iron binding
cellular iron ion homeostasis
iron ion transport
iron ion homeostasis
maintenance of location in cell
cellular transition metal ion homeostasis
transition metal ion transport
transition metal ion homeostasis
iron ion binding
maintenance of location
cellular metal ion homeostasis
metal ion homeostasis
cellular cation homeostasis
metal ion transport
cellular ion homeostasis
cation homeostasis
inorganic ion homeostasis
cellular chemical homeostasis
ion homeostasis
cation transport
cellular homeostasis
oxidation-reduction process
identical protein binding
chemical homeostasis
ion transport
homeostatic process