KAT14 - lysine acetyltransferase 14 Gene

Also Known as ATAC2; CRP2BP; CSRP2BP; PRO1194; dJ717M23.1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57325

About KAT14

Cytogenetic location: 20p11.23 Genomic coordinates (GRCh38): 20:18,137,153-18,188,372 (from NCBI)

This gene has 13 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in brain (RPKM 8.7), testis (RPKM 8.1) and 25 other tissues.

Summary

CSRP2 is a protein containing two LIM domains, which are double zinc finger motifs found in proteins of diverse function. CSRP2 and some related proteins are thought to act as protein adapters, bridging two or more proteins to form a larger protein complex. The protein encoded by this gene binds to one of the LIM domains of CSRP2 and contains an acetyltransferase domain. Although the encoded protein has been detected in the cytoplasm, it is predominantly a nuclear protein. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2011]

KAT14 Products (15)

mRNA Protein Name
NM_001384192.3 NP_001371121.2 cysteine-rich protein 2-binding protein isoform 1
NM_001392069.1 NP_001378998.1 cysteine-rich protein 2-binding protein isoform 1
NM_001392070.1 NP_001378999.1 cysteine-rich protein 2-binding protein isoform 1
NM_001392071.1 NP_001379000.1 cysteine-rich protein 2-binding protein isoform 1
NM_001392072.1 NP_001379001.1 cysteine-rich protein 2-binding protein isoform 1
NM_001392073.1 NP_001379002.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392074.1 NP_001379003.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392075.1 NP_001379004.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392076.1 NP_001379005.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392077.1 NP_001379006.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392078.1 NP_001379007.1 cysteine-rich protein 2-binding protein isoform 2
NM_001392079.1 NP_001379008.1 cysteine-rich protein 2-binding protein isoform 3
NM_001392080.1 NP_001379009.1 cysteine-rich protein 2-binding protein isoform 4
NM_001392081.1 NP_001379010.1 cysteine-rich protein 2-binding protein isoform 5
NM_020536.7 NP_065397.4 cysteine-rich protein 2-binding protein isoform 1
Molecular Function GO Annotation Evidence References Source
enables histone acetyltransferase activity IDA
IDA: Inferred from direct assay
19103755 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
18838386 GOA
involved in regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
19936620 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
19103755 GOA
involved in regulation of cell division IDA
IDA: Inferred from direct assay
20562830 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
22055187 GOA
involved in regulation of tubulin deacetylation IMP
IMP: Inferred from mutant phenotype
20562830 GOA
Cellular Component GO Annotation Evidence References Source
part of ATAC complex IDA
IDA: Inferred from direct assay
18838386 GOA
located in nucleus IPI
IPI: Inferred from physical interaction
10924333 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KAT14 Protein Structure

Acetyltransf_1

Acetyltransf_1: Acetyltransferase (GNAT) family (684 - 752)

  • 0
  • 200
  • 400
  • 600
  • 782 a.a.
Protein Preferred Names Protein Names

cysteine-rich protein 2-binding protein

  • ADA2A-containing complex subunit 2

KAT14 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73-5 25416956
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73-5 25416956
Intra
KAT14 Q9H8E8 ZFY Homo sapiens P08048 32296183
Intra
KAT14 Q9H8E8 ZFY Homo sapiens P08048 32296183
Intra
KAT14 Q9H8E8 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
KAT14 Q9H8E8 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
KAT14 Q9H8E8 DPPA4 Homo sapiens Q7L190 32296183
Intra
KAT14 Q9H8E8 DPPA4 Homo sapiens Q7L190 32296183
Intra
KAT14 Q9H8E8 TRIM27 Homo sapiens P14373 25416956
Intra
KAT14 Q9H8E8 TRIM27 Homo sapiens P14373 32296183
Intra
KAT14 Q9H8E8 TRIM27 Homo sapiens P14373 32296183
Intra
KAT14 Q9H8E8 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
KAT14 Q9H8E8 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73 32296183
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73 32296183
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73 19060904
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73 19060904
Intra
KAT14 Q9H8E8 MBIP Homo sapiens Q9NS73 32296183
Intra
KAT14 Q9H8E8 SERTAD1 Homo sapiens Q9UHV2 32296183
Intra
KAT14 Q9H8E8 SERTAD1 Homo sapiens Q9UHV2 32296183
Intra
KAT14 Q9H8E8 SERTAD1 Homo sapiens Q9UHV2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Mitochondrial Complex Iv Deficiency, Nuclear Type 19
  • MC4DN19

  • Mitochondrial Complex 4 Deficiency, Nuclear Type 19

Buruli Ulcer
  • Buruli Ulcer, Susceptibility To

  • Buruli Ulcer Disease

  • Mycobacterium Ulcerans

  • Mycobacterium Ulcerans, Susceptibility To

  • Bairnsdale Ulcer

  • Daintree Ulcer

  • Mossman Ulcer

  • Searl Ulcer

  • Searle'S Ulcer

  • Bud

Filippi Syndrome
  • Scott Craniodigital Syndrome With Mental Retardation

  • Type 1 Syndactyly-Microcephaly-Intellectual Disability Syndrome

  • FLPIS

  • Scott Bryant Graham Syndrome

  • Craniodigital-Intellectual Disability Syndrome

  • Scott Craniodigital Syndrome

  • Scott-Bryant-Graham Syndrome

  • Syndactyly, Type I, With Microcephaly And Mental Retardation

  • Syndactyly Type I With Microcephaly And Intellectual Disability

  • Unusual Facial Appearance, Microcephaly, Growth And Intellectual Disability And Syndactyly

  • Craniodigital Syndrome With Intellectual Disability

  • Craniodigital Syndrome-Intellectual Disability Syndrome

  • Craniodigital Syndrome-Intellectual Disability, Scott Type

  • Intellectual Disability-Craniodigital Syndrome

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
Rattus norvegicus KAT14 RGD RGD:1309538
Bos taurus KAT14 VGNC VGNC:30397
Felis catus KAT14 VGNC VGNC:63022
Mus musculus KAT14 MGD MGI:1917264
Canis familiaris KAT14 VGNC VGNC:42208
Others KAT14 NCBI