TSSK6 (testis specific serine kinase 6) - Rat Genome Database

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Gene: TSSK6 (testis specific serine kinase 6) Homo sapiens
Analyze
Symbol: TSSK6
Name: testis specific serine kinase 6
RGD ID: 1605019
HGNC Page HGNC:30410
Description: Enables ATP binding activity; magnesium ion binding activity; and protein serine/threonine kinase activity. Predicted to be involved in sperm DNA condensation. Located in nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cancer/testis antigen 72; CT72; FKSG82; FLJ24002; serine/threonine protein kinase SSTK; serine/threonine-protein kinase SSTK; small serine/threonine kinase; SSTK; testis secretory sperm-binding protein Li 205a; testis-specific kinase 6; testis-specific serine kinase 6; testis-specific serine/threonine-protein kinase 6; TSK-6; TSSK-6; TSSK4
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381919,514,219 - 19,515,548 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1919,512,418 - 19,515,548 (-)EnsemblGRCh38hg38GRCh38
GRCh371919,625,028 - 19,626,357 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361919,486,028 - 19,487,469 (-)NCBINCBI36Build 36hg18NCBI36
Celera1919,529,087 - 19,530,528 (-)NCBICelera
Cytogenetic Map19p13.11NCBI
HuRef1919,187,321 - 19,188,762 (-)NCBIHuRef
CHM1_11919,625,724 - 19,627,165 (-)NCBICHM1_1
T2T-CHM13v2.01919,651,706 - 19,653,035 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IEA)
nucleus  (HDA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15044604   PMID:15489334   PMID:15870294   PMID:20037600   PMID:20829357   PMID:21630459   PMID:21832049   PMID:21873635   PMID:22939624   PMID:23974872  
PMID:25036637   PMID:25056061   PMID:25852190   PMID:32707033   PMID:33961781  


Genomics

Comparative Map Data
TSSK6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381919,514,219 - 19,515,548 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1919,512,418 - 19,515,548 (-)EnsemblGRCh38hg38GRCh38
GRCh371919,625,028 - 19,626,357 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361919,486,028 - 19,487,469 (-)NCBINCBI36Build 36hg18NCBI36
Celera1919,529,087 - 19,530,528 (-)NCBICelera
Cytogenetic Map19p13.11NCBI
HuRef1919,187,321 - 19,188,762 (-)NCBIHuRef
CHM1_11919,625,724 - 19,627,165 (-)NCBICHM1_1
T2T-CHM13v2.01919,651,706 - 19,653,035 (-)NCBIT2T-CHM13v2.0
Tssk6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39870,354,834 - 70,356,168 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl870,354,834 - 70,356,168 (+)EnsemblGRCm39 Ensembl
GRCm38869,902,184 - 69,903,518 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl869,902,184 - 69,903,518 (+)EnsemblGRCm38mm10GRCm38
MGSCv37872,426,114 - 72,427,417 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36872,831,204 - 72,832,507 (+)NCBIMGSCv36mm8
Celera872,462,020 - 72,463,323 (+)NCBICelera
Cytogenetic Map8B3.3NCBI
cM Map834.05NCBI
Tssk6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81619,551,757 - 19,559,918 (-)NCBIGRCr8
mRatBN7.21619,523,626 - 19,526,074 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1619,517,334 - 19,526,090 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1619,565,417 - 19,566,718 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01620,703,631 - 20,704,932 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01619,618,400 - 19,619,701 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01621,272,282 - 21,274,756 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1621,273,387 - 21,274,688 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01621,189,471 - 21,190,772 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41620,009,499 - 20,010,800 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1619,713,817 - 19,715,118 (-)NCBICelera
Cytogenetic Map16p14NCBI
Tssk6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555242,433,955 - 2,434,776 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555242,433,855 - 2,434,864 (+)NCBIChiLan1.0ChiLan1.0
TSSK6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22024,368,803 - 24,377,963 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11923,376,046 - 23,384,379 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01918,952,643 - 18,954,101 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11919,948,494 - 19,951,687 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1919,950,614 - 19,951,435 (-)Ensemblpanpan1.1panPan2
TSSK6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12043,730,769 - 43,732,179 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2043,730,907 - 43,731,728 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2043,648,310 - 43,649,731 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02044,218,731 - 44,220,145 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2044,218,873 - 44,219,694 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12043,456,322 - 43,457,736 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02043,865,730 - 43,867,144 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02044,141,362 - 44,142,783 (+)NCBIUU_Cfam_GSD_1.0
Tssk6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118202,405,185 - 202,406,630 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365961,954,517 - 1,955,338 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365961,953,797 - 1,955,753 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TSSK6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl258,411,122 - 58,411,943 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1258,411,122 - 58,411,943 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2258,286,057 - 58,286,878 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TSSK6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1617,974,174 - 17,975,996 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl617,974,913 - 17,975,734 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660741,325,901 - 1,327,361 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tssk6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249082,310,872 - 2,311,693 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249082,310,456 - 2,311,803 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TSSK6
4 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3 copy number gain See cases [RCV000050635] Chr19:17176767..34924150 [GRCh38]
Chr19:17287576..35415054 [GRCh37]
Chr19:17148576..40106894 [NCBI36]
Chr19:19p13.11-q13.11
pathogenic
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3 copy number gain See cases [RCV000052912] Chr19:13974677..27839676 [GRCh38]
Chr19:14085489..28330584 [GRCh37]
Chr19:13946489..33022424 [NCBI36]
Chr19:19p13.12-q11
pathogenic
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31
pathogenic
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3 copy number gain See cases [RCV000136696] Chr19:15133594..24193591 [GRCh38]
Chr19:15244405..24376393 [GRCh37]
Chr19:15105405..24168233 [NCBI36]
Chr19:19p13.12-12
pathogenic|likely pathogenic
chr19:19230868-24115369 complex variant complex Breast ductal adenocarcinoma [RCV000207223] Chr19:19230868..24115369 [GRCh37]
Chr19:19p13.11-12
uncertain significance
GRCh37/hg19 19p13.11-11(chr19:16526787-24631604)x3 copy number gain not provided [RCV000752593] Chr19:16526787..24631604 [GRCh37]
Chr19:19p13.11-11
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.11(chr19:19560981-19962412)x3 copy number gain not provided [RCV000849580] Chr19:19560981..19962412 [GRCh37]
Chr19:19p13.11
uncertain significance
GRCh37/hg19 19p13.12-12(chr19:14286624-20956753)x3 copy number gain not provided [RCV001259370] Chr19:14286624..20956753 [GRCh37]
Chr19:19p13.12-12
pathogenic
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3 copy number gain Specific learning disability [RCV001801194] Chr19:19546923..41313229 [GRCh37]
Chr19:19p13.11-q13.2
pathogenic
NM_032037.4(TSSK6):c.434C>G (p.Pro145Arg) single nucleotide variant Inborn genetic diseases [RCV002956273] Chr19:19514994 [GRCh38]
Chr19:19625803 [GRCh37]
Chr19:19p13.11
uncertain significance
NM_032037.4(TSSK6):c.679G>A (p.Gly227Ser) single nucleotide variant Inborn genetic diseases [RCV003180291] Chr19:19514749 [GRCh38]
Chr19:19625558 [GRCh37]
Chr19:19p13.11
uncertain significance
NM_032037.4(TSSK6):c.736G>A (p.Glu246Lys) single nucleotide variant Inborn genetic diseases [RCV003201027] Chr19:19514692 [GRCh38]
Chr19:19625501 [GRCh37]
Chr19:19p13.11
uncertain significance
NM_032037.4(TSSK6):c.606C>T (p.Leu202=) single nucleotide variant not provided [RCV003415161] Chr19:19514822 [GRCh38]
Chr19:19625631 [GRCh37]
Chr19:19p13.11
likely benign
GRCh37/hg19 19p13.11-12(chr19:18926463-21100330)x1 copy number loss not specified [RCV003986109] Chr19:18926463..21100330 [GRCh37]
Chr19:19p13.11-12
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1705
Count of miRNA genes:525
Interacting mature miRNAs:610
Transcripts:ENST00000360913, ENST00000585580, ENST00000587522, ENST00000602623
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
TSSK6  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371919,625,619 - 19,625,788UniSTSGRCh37
Celera1919,529,678 - 19,529,847UniSTS
HuRef1919,187,912 - 19,188,081UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High 8
Medium 6 7 3 20 3 7 9 4 3 415 5 5
Low 2360 2167 1645 570 1710 413 3749 1259 3375 408 1013 1513 169 1089 2204 3
Below cutoff 66 816 71 49 214 48 593 919 329 7 12 89 1 114 574 1

Sequence


RefSeq Acc Id: ENST00000585580   ⟹   ENSP00000466477
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1919,514,219 - 19,515,548 (-)Ensembl
RefSeq Acc Id: ENST00000587522   ⟹   ENSP00000466056
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1919,512,418 - 19,515,548 (-)Ensembl
RefSeq Acc Id: ENST00000602623   ⟹   ENSP00000473413
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1919,512,456 - 19,514,935 (-)Ensembl
RefSeq Acc Id: NM_032037   ⟹   NP_114426
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381919,514,219 - 19,515,548 (-)NCBI
GRCh371919,625,028 - 19,626,469 (-)RGD
Build 361919,486,028 - 19,487,469 (-)NCBI Archive
Celera1919,529,087 - 19,530,528 (-)RGD
HuRef1919,187,321 - 19,188,762 (-)RGD
CHM1_11919,625,724 - 19,627,165 (-)NCBI
T2T-CHM13v2.01919,651,706 - 19,653,035 (-)NCBI
Sequence:
RefSeq Acc Id: NP_114426   ⟸   NM_032037
- UniProtKB: Q6ZMC4 (UniProtKB/Swiss-Prot),   B2R9F8 (UniProtKB/Swiss-Prot),   Q96LJ4 (UniProtKB/Swiss-Prot),   Q9BXA6 (UniProtKB/Swiss-Prot),   A0A024R7Q5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000466477   ⟸   ENST00000585580
RefSeq Acc Id: ENSP00000466056   ⟸   ENST00000587522
RefSeq Acc Id: ENSP00000473413   ⟸   ENST00000602623
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BXA6-F1-model_v2 AlphaFold Q9BXA6 1-273 view protein structure

Promoters
RGD ID:6795842
Promoter ID:HG_KWN:29367
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000360913,   UC002NMS.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361919,487,731 - 19,488,231 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30410 AgrOrtholog
COSMIC TSSK6 COSMIC
Ensembl Genes ENSG00000178093 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000585580 ENTREZGENE
  ENST00000585580.4 UniProtKB/Swiss-Prot
  ENST00000587522.3 UniProtKB/Swiss-Prot
  ENST00000602623.1 UniProtKB/TrEMBL
Gene3D-CATH Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000178093 GTEx
HGNC ID HGNC:30410 ENTREZGENE
Human Proteome Map TSSK6 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TSSK6_STKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:83983 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 83983 ENTREZGENE
OMIM 610712 OMIM
PANTHER MAP/MICROTUBULE AFFINITY-REGULATING KINASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TESTIS-SPECIFIC SERINE_THREONINE-PROTEIN KINASE 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142670682 PharmGKB
PIRSF Integrin-linked_kinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R7Q5 ENTREZGENE, UniProtKB/TrEMBL
  B2R9F8 ENTREZGENE
  Q6ZMC4 ENTREZGENE
  Q96LJ4 ENTREZGENE
  Q9BXA6 ENTREZGENE
  R4GMZ2_HUMAN UniProtKB/TrEMBL
  TSSK6_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2R9F8 UniProtKB/Swiss-Prot
  Q6ZMC4 UniProtKB/Swiss-Prot
  Q96LJ4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 TSSK6  testis specific serine kinase 6    testis-specific serine kinase 6  Symbol and/or name change 5135510 APPROVED