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NR_148982.2 - -
NR_148986.2 - -
NR_148981.2 - -
NR_148987.2 - -
NR_148983.2 - -
NR_148985.2 - -
NR_148984.2 - -
NM_001354827.2 - NP_001341756.1
NM_001354825.2 - NP_001341754.1
NM_001330752.2 - NP_001317681.1
NM_001354826.2 - NP_001341755.1
NM_001330751.2 - NP_001317680.1
NM_013261.5 - NP_037393.1 (MANE)
NM_001330753.2 - NP_001317682.1
NM_001354828.2 - NP_001341757.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
4
Location
Chr4:23,791,521-24,473,405
LOEUF
0.267
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ClinVar
Pathogenic/ Likely pa...
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GnomAD
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Rare [<1%]
ToMMo
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Rare [<1%]
By consequences
Missense
Loss-of-function
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
10891
Ensembl
ENSG00000109819
GeneCards
PPARGC1A
UniProt
Q9UBK2
KEGG
hsa:10891
gnomAD
ENSG00000109819
ICGC
ENSG00000109819
RefDIC
10891
RefEx
10891
DTX
PPARGC1A
AS-ALPS
PPARGC1A
PPARGC1A
PPARG coactivator 1 alpha
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Amino Acid Sequence
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