TSEN15 - tRNA splicing endonuclease subunit 15 Gene

Also Known as PCH2F; sen15; C1orf19

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 116461

About TSEN15

Cytogenetic location: 1q25.3 Genomic coordinates (GRCh38): 1:184,051,730-184,097,485 (from NCBI)

This gene has 20 transcripts (splice variants), 191 orthologues and is associated with 3 phenotypes. Ubiquitous expression in thyroid (RPKM 5.4), brain (RPKM 4.2) and 25 other tissues.

Summary

This gene encodes a subunit of the tRNA splicing Endonuclease, which catalyzes the removal of introns from tRNA precursors. Alternative splicing results in multiple transcript variants. There is a pseudogene of this gene on chromosome 17. [provided by RefSeq, Jul 2014]

TSEN15 Products (5)

mRNA Protein Name
NM_001127394.4 NP_001120866.1 tRNA-splicing endonuclease subunit Sen15 isoform 2
NM_001300764.2 NP_001287693.1 tRNA-splicing endonuclease subunit Sen15 isoform 3
NM_001300766.2 NP_001287695.1 tRNA-splicing endonuclease subunit Sen15 isoform 4
NM_001363643.2 NP_001350572.1 tRNA-splicing endonuclease subunit Sen15 isoform 5
NM_052965.4 NP_443197.1 tRNA-splicing endonuclease subunit Sen15 isoform 1
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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

TSEN15 Protein Structure

Sen15

Sen15: Sen15 protein (65 - 164)

  • 0
  • 100
  • 171 a.a.
Protein Preferred Names Protein Names

tRNA-splicing endonuclease subunit Sen15

  • TSEN15 tRNA splicing endonuclease subunit

TSEN15 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
TSEN15 Q8WW01 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
TSEN15 Q8WW01 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
TSEN15 Q8WW01 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
TSEN15 Q8WW01 PBX4 Homo sapiens Q9BYU1 32296183
Intra
TSEN15 Q8WW01 PBX4 Homo sapiens Q9BYU1 32296183
Intra
TSEN15 Q8WW01 PBX4 Homo sapiens Q9BYU1 32296183
Intra
TSEN15 Q8WW01 PLB1 Homo sapiens Q6P1J6-2 32296183
Intra
TSEN15 Q8WW01 PLB1 Homo sapiens Q6P1J6-2 32296183
Intra
TSEN15 Q8WW01 REL Homo sapiens Q04864-2 32296183
Intra
TSEN15 Q8WW01 REL Homo sapiens Q04864-2 32296183
Intra
TSEN15 Q8WW01 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSEN15 Q8WW01 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSEN15 Q8WW01 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSEN15 Q8WW01 TLE5 Homo sapiens Q08117-2 32296183
Intra
TSEN15 Q8WW01 TLE5 Homo sapiens Q08117-2 32296183
Intra
TSEN15 Q8WW01 LMO2 Homo sapiens P25791-3 32296183
Intra
TSEN15 Q8WW01 LMO2 Homo sapiens P25791-3 32296183
Intra
TSEN15 Q8WW01 USP54 Homo sapiens Q70EL1-9 32296183
Intra
TSEN15 Q8WW01 USP54 Homo sapiens Q70EL1-9 32296183
Intra
TSEN15 Q8WW01 POU6F2 Homo sapiens P78424 32296183
Intra
TSEN15 Q8WW01 POU6F2 Homo sapiens P78424 32296183
Intra
TSEN15 Q8WW01 AIF1L Homo sapiens Q9BQI0-4 32296183
Intra
TSEN15 Q8WW01 AIF1L Homo sapiens Q9BQI0-4 32296183
Intra
TSEN15 Q8WW01 AIF1L Homo sapiens Q9BQI0-4 32296183
Intra
TSEN15 Q8WW01 ASB12 Homo sapiens Q8WXK4-2 32296183
Intra
TSEN15 Q8WW01 ASB12 Homo sapiens Q8WXK4-2 32296183
Intra
TSEN15 Q8WW01 ASB12 Homo sapiens Q8WXK4-2 32296183
Intra
TSEN15 Q8WW01 ZNF554 Homo sapiens Q86TJ5 32296183
Intra
TSEN15 Q8WW01 ZNF554 Homo sapiens Q86TJ5 32296183
Intra
TSEN15 Q8WW01 MEI4 Homo sapiens A8MW99 32296183
Intra
TSEN15 Q8WW01 MEI4 Homo sapiens A8MW99 32296183
Intra
TSEN15 Q8WW01 MIPOL1 Homo sapiens Q8TD10 32296183
Intra
TSEN15 Q8WW01 MIPOL1 Homo sapiens Q8TD10 32296183
Intra
TSEN15 Q8WW01 ZMAT2 Homo sapiens Q96NC0 32296183
Intra
TSEN15 Q8WW01 ZMAT2 Homo sapiens Q96NC0 32296183
Intra
TSEN15 Q8WW01 ZMAT2 Homo sapiens Q96NC0 32296183
Intra
TSEN15 Q8WW01 POLR2G Homo sapiens P62487 32296183
Intra
TSEN15 Q8WW01 POLR2G Homo sapiens P62487 32296183
Intra
TSEN15 Q8WW01 ZNF620 Homo sapiens Q6ZNG0 32296183
Intra
TSEN15 Q8WW01 ZNF620 Homo sapiens Q6ZNG0 32296183
Intra
TSEN15 Q8WW01 LRIF1 Homo sapiens Q5T3J3 32296183
Intra
TSEN15 Q8WW01 LRIF1 Homo sapiens Q5T3J3 32296183
Intra
TSEN15 Q8WW01 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSEN15 Q8WW01 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSEN15 Q8WW01 HSF2BP Homo sapiens O75031 32296183
Intra
TSEN15 Q8WW01 HSF2BP Homo sapiens O75031 32296183
Intra
TSEN15 Q8WW01 GORASP2 Homo sapiens Q9H8Y8 32296183
Intra
TSEN15 Q8WW01 GORASP2 Homo sapiens Q9H8Y8 32296183
Intra
TSEN15 Q8WW01 GORASP2 Homo sapiens Q9H8Y8 32296183
Intra
TSEN15 Q8WW01 DDIT4L Homo sapiens Q96D03 32296183
Intra
TSEN15 Q8WW01 DDIT4L Homo sapiens Q96D03 32296183
Intra
TSEN15 Q8WW01 DDIT4L Homo sapiens Q96D03 32296183
Intra
TSEN15 Q8WW01 ENKD1 Homo sapiens Q9H0I2 32296183
Intra
TSEN15 Q8WW01 ENKD1 Homo sapiens Q9H0I2 32296183
Intra
TSEN15 Q8WW01 ENKD1 Homo sapiens Q9H0I2 32296183
Intra
TSEN15 Q8WW01 TASOR2 Homo sapiens Q5VWN6 32296183
Intra
TSEN15 Q8WW01 TASOR2 Homo sapiens Q5VWN6 32296183
Intra
TSEN15 Q8WW01 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSEN15 Q8WW01 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSEN15 Q8WW01 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSEN15 Q8WW01 TSSK2 Homo sapiens Q96PF2 32296183
Intra
TSEN15 Q8WW01 ARID5A Homo sapiens Q03989 32296183
Intra
TSEN15 Q8WW01 ARID5A Homo sapiens Q03989 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Pontocerebellar Hypoplasia, Type 2f
  • PCH2F

  • Pontocerebellar Hypoplasia Type 2f

  • Pontocerebellar Hypoplasia 2f

  • Doid:0112329

  • Hypoplasia, Pontocerebellar, Type 2f

Pontocerebellar Hypoplasia, Type 2e
  • Pontocerebellar Hypoplasia Type 2

  • Pontocerebellar Hypoplasia Type 2e

  • Pch2

  • PCH2E

  • Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy

  • Pontocerebellar Hypoplasia 2e

  • Pcca2

  • Progressive Cerebello-Cerebral Atrophy Type 2

  • Doid:0112328

  • Hypoplasia, Pontocerebellar, Type 2e

  • Pontocerebellar Hypoplasia, Type 2d

  • Pontocerebellar Hypoplasia Type 2a

Primary Microcephaly
  • True Microcephaly

  • Microcephaly, Primary

Pontocerebellar Hypoplasia
  • Pch

  • Congenital Pontocerebellar Hypoplasia

  • Opch

  • Hypoplasia, Pontocerebellar

  • Pontoneocerebellar Hypoplasia

  • Nonsyndromic Pontocerebellar Hypoplasia

Acromesomelic Dysplasia 2b
  • Fibular Hypoplasia And Complex Brachydactyly

  • Du Pan Syndrome

  • AMD2B

  • Dupans

  • Acromesomelic Dysplasia-2b

  • Fibular Aplasia-Complex Brachydactyly Syndrome

Pontocerebellar Hypoplasia, Type 1d
  • PCH1D

  • Pontocerebellar Hypoplasia Type 1d

  • Pontocerebellar Hypoplasia 1d

  • Doid:0112323

  • Hypoplasia, Pontocerebellar, Type 1d

Pontocerebellar Hypoplasia, Type 4
  • Pontocerebellar Hypoplasia Type 4

  • PCH4

  • Olivopontocerebellar Hypoplasia

  • Encephalopathy Fatal Infantile With Olivopontocerebellar Hypoplasia

  • Encephalopathy, Fatal Infantile, With Olivopontocerebellar Hypoplasia

  • Fatal Infantile Encephalopathy With Olivopontocerebellar Hypoplasia

  • Pontocerebellar Hypoplasia 4

  • Young Mckeever Squier Syndrome

  • Hypoplasia, Pontocerebellar, Type 4

Pontocerebellar Hypoplasia, Type 10
  • Pontocerebellar Hypoplasia Type 10

  • PCH10

  • Clp1-Related Pontocerebellar Hypoplasia

  • Pontocerebellar Hypoplasia 10

  • Hypoplasia, Pontocerebellar, Type 10

Immunodeficiency 36
  • IMD36

  • Activated Phosphoinositide 3-Kinase Delta Syndrome 2

  • Immunodeficiency, Type 36

Pontocerebellar Hypoplasia, Type 3
  • Pontocerebellar Hypoplasia Type 3

  • Cerebellar Atrophy With Progressive Microcephaly

  • PCH3

  • Clam

  • Pch With Optic Atrophy

  • Pontocerebellar Hypoplasia 3

  • Hypoplasia, Pontocerebellar, Type 3

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Pontocerebellar Hypoplasia, Type 1e
  • Pontocerebellar Hypoplasia Type 1

  • PCH1E

  • Norman Disease

  • Pch1

  • Pontocerebellar Hypoplasia With Anterior Horn Cell Disease

  • Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy

  • Pontocerebellar Hypoplasia Type 1e

  • Pontocerebellar Hypoplasia 1e

  • Doid:0112322

  • Doid:0112330

Joubert Syndrome 1
  • Joubert Syndrome

  • Jbts

  • Cerebellooculorenal Syndrome 1

  • JBTS1

  • Joubert-Boltshauser Syndrome

  • Cerebelloparenchymal Disorder Iv

  • Cpd4

  • Cors1

  • Joubert Syndrome And Related Disorders

  • Jsrd

  • Familial Aplasia Of The Vermis

  • Joubert Syndrome Related Disorders

  • Js

  • Cerebellar Vermis Agenesis

  • Cerebelloparenchymal Disorder 4

  • Agenesis Of Cerebellar Vermis

  • Cerebello-Oculo-Renal Syndrome

  • Cors

  • Joubert-Bolthauser Syndrome

  • Cpd Iv

  • Classic Joubert Syndrome

  • Joubert Syndrome Type A

  • Pure Joubert Syndrome

  • Cerebello-Oculo-Renal Syndrome 1

  • Joubert Syndrome-1

  • Joubert Syndrome, Type 1

  • Joubert'S Syndrome

Primary Autosomal Recessive Microcephaly
  • Autosomal Recessive Primary Microcephaly

  • Mcph

  • True Microcephaly

  • Microcephalia Vera

  • Microcephaly Vera

  • Microcephaly Primary Hereditary

  • Microcephaly, Primary, Autosomal Recessive

  • Primary Microcephaly

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

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
Mus musculus TSEN15 MGD MGI:1913887
Felis catus TSEN15 VGNC VGNC:107958
Bos taurus TSEN15 VGNC VGNC:36410
Macaca mulatta TSEN15 VGNC VGNC:106525
Rattus norvegicus TSEN15 RGD RGD:1308584
Canis familiaris TSEN15 VGNC VGNC:47895
Others TSEN15 NCBI