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NM_001393986.1 - NP_001380915.1 (MANE)
NM_001135610.2 - NP_001129082.1
NM_012231.5 - NP_036363.2
NM_015866.6 - NP_056950.2
NM_001393987.1 - NP_001380916.1
NM_001393988.1 - NP_001380917.1
NM_001007257.3 - NP_001007258.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
1
Location
Chr1:13,699,688-13,825,579
LOEUF
0.222
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Pathogenic/ Likely pa...
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GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
7799
Ensembl
ENSG00000116731
GeneCards
PRDM2
UniProt
Q13029
KEGG
hsa:7799
gnomAD
ENSG00000116731
ICGC
ENSG00000116731
RefDIC
7799
RefEx
7799
DTX
PRDM2
AS-ALPS
PRDM2
PRDM2
PR/SET domain 2
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