Gene: ZNF142
Alternate names for this Gene: HA4654|NEDISHM|pHZ-49
Gene Summary: The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene.
Gene is located in Chromosome: 2
Location in Chromosome : 2q35
Description of this Gene: zinc finger protein 142
Type of Gene: protein-coding
rs10187066 in
ZNF142 gene and
Body Height
PMID 20881960 2010 Hundreds of variants clustered in genomic loci and biological pathways affect human height.
rs1447313633 in
ZNF142 gene and
Delayed speech and language development
PMID 31036918 2019 Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
rs1447313633 in
ZNF142 gene and
Dystonia
PMID 31036918 2019 Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
rs1447313633 in
ZNF142 gene and
Global developmental delay
PMID 31036918 2019 Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
rs10187066 in
ZNF142 gene and
Height
PMID 20881960 2010 Hundreds of variants clustered in genomic loci and biological pathways affect human height.
rs1447313633 in
ZNF142 gene and
Poor school performance
PMID 31036918 2019 Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
rs546151500 in
ZNF142 gene and
Tonic - clonic seizures
PMID 31036918 2019 Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.