Incidental Mutation 'IGL01625:Tesk2'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tesk2
Ensembl Gene ENSMUSG00000033985
Gene Nametestis-specific kinase 2
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.150) question?
Stock #IGL01625
Quality Score
Chromosomal Location116720948-116805956 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 116771801 bp
Amino Acid Change Phenylalanine to Leucine at position 116 (F116L)
Ref Sequence ENSEMBL: ENSMUSP00000102064 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045542] [ENSMUST00000106456] [ENSMUST00000106459]
Predicted Effect possibly damaging
Transcript: ENSMUST00000045542
AA Change: F116L

PolyPhen 2 Score 0.539 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000041009
Gene: ENSMUSG00000033985
AA Change: F116L

low complexity region 24 30 N/A INTRINSIC
Pfam:Pkinase 59 309 1.6e-48 PFAM
Pfam:Pkinase_Tyr 59 309 1.2e-50 PFAM
low complexity region 539 546 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000106456
AA Change: F116L

PolyPhen 2 Score 0.676 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000102064
Gene: ENSMUSG00000033985
AA Change: F116L

low complexity region 24 30 N/A INTRINSIC
Pfam:Pkinase_Tyr 59 291 4.5e-46 PFAM
Pfam:Pkinase 60 332 3.6e-46 PFAM
low complexity region 510 517 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106459
AA Change: F116L

PolyPhen 2 Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000102067
Gene: ENSMUSG00000033985
AA Change: F116L

low complexity region 24 30 N/A INTRINSIC
Pfam:Pkinase_Tyr 59 238 6.1e-37 PFAM
Pfam:Pkinase 60 239 4.3e-39 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142529
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product is a serine/threonine protein kinase that contains an N-terminal protein kinase domain that is structurally similar to the kinase domains of testis-specific protein kinase-1 and the LIM motif-containing protein kinases (LIMKs). Its overall structure is most related to the former, indicating that it belongs to the TESK subgroup of the LIMK/TESK family of protein kinases. This gene is predominantly expressed in testis and prostate. The developmental expression pattern of the rat gene in testis suggests an important role for this gene in meitoic stages and/or early stages of spermiogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik T A 5: 145,043,147 H37Q possibly damaging Het
2210010C04Rik A C 6: 41,032,948 S151A probably benign Het
Akr1c19 T A 13: 4,233,817 I16N probably damaging Het
Arpc1b T C 5: 145,121,745 probably null Het
Bzw1 A G 1: 58,401,440 T191A probably benign Het
Cacna1h T C 17: 25,383,485 D1523G probably damaging Het
Cacna1h G A 17: 25,385,712 T1209I possibly damaging Het
Cdc20b T C 13: 113,059,785 L148P possibly damaging Het
Cubn A G 2: 13,306,274 F3147L possibly damaging Het
Dagla A G 19: 10,251,202 probably benign Het
Dnah9 T C 11: 66,044,645 N1983D probably damaging Het
Fbxw10 G A 11: 62,860,027 D479N probably damaging Het
Fer A T 17: 64,037,626 Q630L probably damaging Het
Gbp5 A G 3: 142,503,028 N111D probably damaging Het
Gm8127 T G 14: 43,291,063 probably benign Het
Heatr1 T A 13: 12,413,528 N814K probably damaging Het
Iba57 G A 11: 59,158,949 R191W probably damaging Het
Itgae C A 11: 73,119,437 F584L probably benign Het
Kdm5b A G 1: 134,617,968 K956E possibly damaging Het
Muc4 C T 16: 32,755,544 probably benign Het
Mybpc2 T C 7: 44,516,913 K218E possibly damaging Het
Pcdh10 T C 3: 45,379,397 S49P probably damaging Het
Rai14 T C 15: 10,572,374 D889G probably benign Het
Rbpjl A G 2: 164,407,785 K102R possibly damaging Het
Retreg2 A G 1: 75,144,715 probably benign Het
Rfc4 A T 16: 23,115,823 L149Q probably damaging Het
Rft1 T A 14: 30,676,896 D274E possibly damaging Het
Rlf A T 4: 121,188,260 S143R possibly damaging Het
Rptn T A 3: 93,397,894 S845T probably benign Het
Slamf8 C A 1: 172,582,482 D267Y probably damaging Het
Smoc2 C T 17: 14,325,614 S55L probably damaging Het
Sptan1 C T 2: 30,026,114 A2038V probably damaging Het
Stx17 C A 4: 48,181,526 P210T probably damaging Het
Tbc1d5 A G 17: 50,917,573 Y317H probably benign Het
Tenm4 C A 7: 96,885,358 T1737N probably damaging Het
Tln2 T C 9: 67,370,623 S370G probably damaging Het
Tm6sf2 G T 8: 70,076,083 G162C probably null Het
Togaram2 A C 17: 71,714,698 E718D probably benign Het
Ttn A C 2: 76,747,983 F15862V probably damaging Het
Uba6 T A 5: 86,120,529 R916* probably null Het
Umodl1 A G 17: 30,996,255 M1018V probably benign Het
Wdr26 G A 1: 181,191,816 T332I possibly damaging Het
Xdh A T 17: 73,916,786 probably null Het
Other mutations in Tesk2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02051:Tesk2 APN 4 116751184 missense probably damaging 1.00
IGL02223:Tesk2 APN 4 116741825 nonsense probably null
IGL02747:Tesk2 APN 4 116802879 missense probably benign 0.31
IGL02942:Tesk2 APN 4 116771820 missense probably damaging 0.99
R1804:Tesk2 UTSW 4 116800621 unclassified probably benign
R1936:Tesk2 UTSW 4 116741824 missense probably benign 0.23
R1986:Tesk2 UTSW 4 116751193 missense probably damaging 1.00
R2414:Tesk2 UTSW 4 116801757 missense possibly damaging 0.96
R4632:Tesk2 UTSW 4 116741712 missense probably benign 0.01
R4896:Tesk2 UTSW 4 116802993 missense probably benign
R5186:Tesk2 UTSW 4 116741896 missense probably damaging 1.00
R5209:Tesk2 UTSW 4 116724698 start gained probably benign
R5278:Tesk2 UTSW 4 116805936 intron probably benign
R5769:Tesk2 UTSW 4 116802315 intron probably null
R6199:Tesk2 UTSW 4 116792170 missense probably damaging 0.98
R6464:Tesk2 UTSW 4 116802849 missense probably damaging 1.00
R6567:Tesk2 UTSW 4 116792164 missense probably damaging 1.00
R6867:Tesk2 UTSW 4 116801798 missense probably damaging 0.99
R7028:Tesk2 UTSW 4 116802687 nonsense probably null
Posted On2013-12-09