Homo sapiens

Gene : FTH1P2 - ENSG00000234975 - Homo sapiens (human)

General information

Gene identifier

ENSG00000234975

Name

FTH1P2

Description

ferritin heavy chain 1 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:3989]

Synonym(s)

fthl2

Expression

80%

Reported absence of expression

Show

entries

Anatomical entity
Expression score
FDR
Link to source data
Sources
CL:0002092bone marrow cell36.161See source data
RSCAIE
UBERON:0003053ventricular zone36.481See source data
RSCAIE
UBERON:0000397colonic epithelium37.201See source data
RSCAIE
UBERON:0015488sural nerve38.390.589See source data
RSCAIE

Sources

A Affimetrix
E EST
I In Situ
R RNA-Seq
SC scRNA-Seq
datano data

Expression scores

3.25e4 lightgrey: low confidence scores

important score variation

Expression scores of expression calls is based on the rank of a gene in a condition according to its expression levels (non-parametric statistics), normalized using the minimum and maximum Rank of the species. Values of Expression scores are between 0 and 100. Low score means that the gene is lowly expressed in the condition compared to other genes. Scores are normalized and comparable across genes, conditions and species.

Sources of annotations to anatomy and development:

Sources of raw data:

Cross-references

Ensembl

HGNC

HGNC:3989 (FTH1P2)