2. Gene
  3. ZC3H14 - zinc finger CCCH-type containing 14 Gene

ZC3H14 - zinc finger CCCH-type containing 14 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as SUT2; MRT56; UKp68; MSUT-2; NY-REN-37

Gene ID: 79882 | Gene type: protein coding

About ZC3H14

Cytogenetic location: 14q31.3 Genomic coordinates (GRCh38): 14:88,563,037-88,627,596 (from NCBI)

This gene has 26 transcripts (splice variants), 215 orthologues and is associated with 2 phenotypes. Broad expression in testis (RPKM 19.6), thyroid (RPKM 8.3) and 25 other tissues.

Summary

The protein encoded by this gene is a poly(A)-binding protein that can affect gene expression and poly(A) tail length. The encoded protein may influence mRNA stability, nuclear export, and translation. [provided by RefSeq, May 2016]

ZC3H14 Products(28)

mRNA Protein Name
NM_001160103.2 NP_001153575.1 zinc finger CCCH domain-containing protein 14 isoform 5
NM_001160104.2 NP_001153576.1 zinc finger CCCH domain-containing protein 14 isoform 6
NM_001326295.2 NP_001313224.1 zinc finger CCCH domain-containing protein 14 isoform 7
NM_001326296.2 NP_001313225.1 zinc finger CCCH domain-containing protein 14 isoform 8
NM_001326297.2 NP_001313226.1 zinc finger CCCH domain-containing protein 14 isoform 9
NM_001326298.2 NP_001313227.1 zinc finger CCCH domain-containing protein 14 isoform 10
NM_001326299.2 NP_001313228.1 zinc finger CCCH domain-containing protein 14 isoform 11
NM_001326300.2 NP_001313229.1 zinc finger CCCH domain-containing protein 14 isoform 12
NM_001326301.2 NP_001313230.1 zinc finger CCCH domain-containing protein 14 isoform 13
NM_001326302.2 NP_001313231.1 zinc finger CCCH domain-containing protein 14 isoform 14
NM_001326303.2 NP_001313232.1 zinc finger CCCH domain-containing protein 14 isoform 15
NM_001326304.2 NP_001313233.1 zinc finger CCCH domain-containing protein 14 isoform 16
NM_001326305.2 NP_001313234.1 zinc finger CCCH domain-containing protein 14 isoform 17
NM_001326306.2 NP_001313235.1 zinc finger CCCH domain-containing protein 14 isoform 18
NM_001326307.2 NP_001313236.1 zinc finger CCCH domain-containing protein 14 isoform 19
NM_001326308.2 NP_001313237.1 zinc finger CCCH domain-containing protein 14 isoform 20
NM_001326309.2 NP_001313238.1 zinc finger CCCH domain-containing protein 14 isoform 21
NM_001326310.2 NP_001313239.1 zinc finger CCCH domain-containing protein 14 isoform 22
NM_001326311.2 NP_001313240.1 zinc finger CCCH domain-containing protein 14 isoform 23
NM_001326312.2 NP_001313241.1 zinc finger CCCH domain-containing protein 14 isoform 24
NM_001326313.2 NP_001313242.1 zinc finger CCCH domain-containing protein 14 isoform 25
NM_001326314.2 NP_001313243.1 zinc finger CCCH domain-containing protein 14 isoform 26
NM_001326315.2 NP_001313244.1 zinc finger CCCH domain-containing protein 14 isoform 27
NM_001326316.2 NP_001313245.1 zinc finger CCCH domain-containing protein 14 isoform 27
NM_024824.5 NP_079100.2 zinc finger CCCH domain-containing protein 14 isoform 1
NM_207660.4 NP_997543.1 zinc finger CCCH domain-containing protein 14 isoform 2
NM_207661.3 NP_997544.1 zinc finger CCCH domain-containing protein 14 isoform 3
NM_207662.4 NP_997545.2 zinc finger CCCH domain-containing protein 14 isoform 4
Protein Preferred Names Protein Names

zinc finger CCCH domain-containing protein 14

mammalian suppressor of tau pathology-2

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Recessive 56

MRT56

Mental Retardation, Autosomal Recessive 56

Autosomal Recessive Intellectual Developmental Disorder 56
Autosomal Recessive Non-Syndromic Intellectual Disability

Ar-Nsid

Ns-Arid
Partington Syndrome

X-Linked Reticulate Pigmentary Disorder

PRTS

Partington X-Linked Mental Retardation Syndrome

Mrxs1

Mrx36

Intellectual Developmental Disorder, X-Linked, Syndromic 1

Partington Disease

Pdr

Partington-Mulley Syndrome

Russell-Silver Syndrome, X-Linked

Mental Retardation, X-Linked, Syndromic 1

Mental Retardation, X-Linked, With Dystonic Movements, Ataxia, And Seizures

Mental Retardation, X-Linked 36

X-Linked Reticulate Pigmentary Disorder With Systemic Manifestations

X-Linked Russell-Silver Syndrome

Intelectual Disability-Dystonic Movements-Ataxia-Seizures Syndrome

Intellectual Disability, X-Linked, Syndromic 1

Intellectual Disability, X-Linked, With Dystonic Movements, Ataxia, And Seizures

Partington X-Linked Intellectual Disability Syndrome

X-Linked Intellectual Deficit-Dystonia-Dysarthria

X-Linked Mental Retardation With Dystonic Movements, Ataxia, And Seizures

Familial Cutaneous Amyloidosis

X-Linked Cutaneous Amyloidosis

Xlpdr

X-Linked Intellectual Disability-Dystonia-Dysarthria Syndrome

Pigmentary Disorder, Reticulate, With Systemic Manifestations
Pontocerebellar Hypoplasia, Type 7

Pontocerebellar Hypoplasia Type 7

PCH7

Pontocerebellar Hypoplasia-46,Xy Disorder Of Sex Development Syndrome

Pontocerebellar Hypoplasia 7

Hypoplasia, Pontocerebellar, Type 7
Non-Syndromic X-Linked Intellectual Disability 90

Mrx90
Intellectual Developmental Disorder, Autosomal Dominant 4

MRD4

Autosomal Dominant Non-Syndromic Intellectual Disability 4

Mental Retardation, Autosomal Dominant 4

Autosomal Dominant Intellectual Developmental Disorder 4
Oculopharyngeal Muscular Dystrophy

OPMD

Muscular Dystrophy, Oculopharyngeal

Dystrophy, Oculopharyngeal Muscular

Oculopharyngeal Dystrophy

Progressive Muscular Dystrophy, Oculopharyngeal Type

Muscular Dystrophy Oculopharyngeal

Dystrophy, Muscular, Oculopharyngeal
Autosomal Recessive Intellectual Developmental Disorder

Mental Retardation, Autosomal Recessive

Autosomal Recessive Mental Retardation

Autosomal Recessive Non-Syndromic Mental Retardation

Autosomal Recessive Non-Syndromic Intellectual Disability
Pick Disease Of Brain

Pick Disease

Pick'S Disease

Pick Disease Of The Brain

Lobar Atrophy Of Brain

Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

Behavioral Variant Of Frontotemporal Dementia

Dementia In Pick'S Disease

Lobar Atrophy Of The Brain

Bvftd

Bv-Ftd

PIDB

Picks Disease
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS15989 ZC3H14 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris ZC3H14 VGNC VGNC:48555
Bos taurus ZC3H14 VGNC VGNC:37102
Mus musculus ZC3H14 MGD MGI:1919824
Rattus norvegicus ZC3H14 RGD RGD:621850
Macaca mulatta ZC3H14 VGNC VGNC:79255