ZC3H14 - zinc finger CCCH-type containing 14 Gene

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

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79882

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

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
Others ZC3H14 NCBI