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NM_001319238.2 - NP_001306167.1
NM_001376338.1 - NP_001363267.1
NM_001376367.1 - NP_001363296.1
NM_001376358.1 - NP_001363287.1
NM_001319239.2 - NP_001306168.1
NM_001350261.2 - NP_001337190.1
NM_001376346.1 - NP_001363275.1
NM_001376356.1 - NP_001363285.1
NM_001376343.1 - NP_001363272.1
NM_001376363.1 - NP_001363292.1
NM_001376361.1 - NP_001363290.1
NM_001376334.1 - NP_001363263.1
NM_001376362.1 - NP_001363291.1
NM_001376351.1 - NP_001363280.1
NM_001350262.2 - NP_001337191.1
NM_001376357.1 - NP_001363286.1
NM_001376342.1 - NP_001363271.1 (MANE)
NM_001376366.1 - NP_001363295.1
NM_001376337.1 - NP_001363266.1
NM_001376352.1 - NP_001363281.1
NM_001376341.1 - NP_001363270.1
NM_001350265.2 - NP_001337194.1
NM_001376347.1 - NP_001363276.1
NM_001350263.2 - NP_001337192.1
NM_001350264.2 - NP_001337193.1
NM_001376349.1 - NP_001363278.1
NM_001376364.1 - NP_001363293.1
NM_001376336.1 - NP_001363265.1
NM_001376339.1 - NP_001363268.1
NM_001376353.1 - NP_001363282.1
NM_014827.6 - NP_055642.3
NM_001350266.2 - NP_001337195.1
NM_001376348.1 - NP_001363277.1
NM_001376344.1 - NP_001363273.1
NM_001376340.1 - NP_001363269.1
NM_001376359.1 - NP_001363288.1
NM_001376335.1 - NP_001363264.1
NM_001376345.1 - NP_001363274.1
NM_001376360.1 - NP_001363289.1
NM_001376354.1 - NP_001363283.1
NM_001376355.1 - NP_001363284.1
NM_001376350.1 - NP_001363279.1
NM_001376365.1 - NP_001363294.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
1
Location
Chr1:203,795,123-203,854,624
LOEUF
0.186
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Pathogenic/ Likely pa...
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ToMMo
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Rare [<1%]
By consequences
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
9877
Ensembl
ENSG00000058673
GeneCards
ZC3H11A
UniProt
O75152
KEGG
hsa:9877
gnomAD
ENSG00000058673
ICGC
ENSG00000058673
RefDIC
9877
RefEx
9877
DTX
ZC3H11A
AS-ALPS
ZC3H11A
ZC3H11A
zinc finger CCCH-type containing 11A
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