Mutagenetix > Incidental Mutation

Incidental Mutation 'R3709:Tsks'

259488

Institutional Source

Beutler Lab

Gene Symbol

Tsks

Ensembl Gene

ENSMUSG00000059891

Gene Name

testis-specific serine kinase substrate

Synonyms

clone 4, Tsks, Tssks1, Stk22s1

MMRRC Submission

040702-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3709 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

44592628-44607459 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 44601309 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Leucine at position 208 (R208L)

Ref Sequence

ENSEMBL: ENSMUSP00000112673 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080233] [ENSMUST00000120929] [ENSMUST00000207719]

AlphaFold

O54887

Predicted Effect

probably benign
Transcript: ENSMUST00000080233
AA Change: R199L

PolyPhen 2 Score 0.388 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000079122
Gene: ENSMUSG00000059891
AA Change: R199L

Domain	Start	End	E-Value	Type
Pfam:TSKS	26	525	5.7e-281	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000120929
AA Change: R208L

PolyPhen 2 Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000112673
Gene: ENSMUSG00000059891
AA Change: R208L

Domain	Start	End	E-Value	Type
Pfam:TSKS	26	585	8.1e-297	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000207719

Predicted Effect

probably benign
Transcript: ENSMUST00000208475

Meta Mutation Damage Score

0.1023

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 93.9%

Validation Efficiency

98% (50/51)

MGI Phenotype

FUNCTION: This gene is a member of a small family of testis-specific serine/threonine kinases. This gene may play a role in testicular physiology or spermiogenesis. Its expression is restricted to the testis during the last stages of spermatid maturation. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9930111J21Rik2	T	G	11: 48,910,480 (GRCm39)	D651A	probably damaging	Het
Abcb1a	A	G	5: 8,788,738 (GRCm39)	N1039S	probably benign	Het
Abcc2	G	T	19: 43,786,885 (GRCm39)	V169F	possibly damaging	Het
Adcy8	T	C	15: 64,597,384 (GRCm39)		probably benign	Het
Aida	C	A	1: 183,085,610 (GRCm39)		probably null	Het
Armc8	A	G	9: 99,402,550 (GRCm39)	I333T	probably damaging	Het
B4galt3	C	A	1: 171,101,613 (GRCm39)	H196N	probably damaging	Het
Ccdc92b	C	A	11: 74,528,933 (GRCm39)	R146S	probably damaging	Het
Cdc42bpa	A	G	1: 179,892,628 (GRCm39)	D264G	probably damaging	Het
Cenpf	A	G	1: 189,381,009 (GRCm39)	S2804P	possibly damaging	Het
Cic	A	G	7: 24,986,406 (GRCm39)	D1276G	probably damaging	Het
Cldn19	T	C	4: 119,114,094 (GRCm39)	S79P	possibly damaging	Het
Ctdp1	G	A	18: 80,493,428 (GRCm39)	Q356*	probably null	Het
Cyp2c69	A	G	19: 39,839,667 (GRCm39)		probably benign	Het
Dhrs3	T	C	4: 144,620,281 (GRCm39)		probably null	Het
Fhod3	T	A	18: 25,223,815 (GRCm39)	W1054R	probably damaging	Het
Gfral	G	A	9: 76,100,725 (GRCm39)	R238*	probably null	Het
Gm10322	C	A	10: 59,451,941 (GRCm39)	D19E	possibly damaging	Het
Gprc6a	CAAA	CA	10: 51,491,776 (GRCm39)		probably null	Het
Idh3a	T	C	9: 54,493,810 (GRCm39)	S4P	possibly damaging	Het
Il15ra	G	T	2: 11,735,458 (GRCm39)		probably null	Het
Ipo8	A	T	6: 148,707,842 (GRCm39)		probably null	Het
Iqgap1	G	A	7: 80,366,835 (GRCm39)	T1595I	possibly damaging	Het
Kalrn	C	T	16: 34,212,400 (GRCm39)		probably null	Het
Klrb1a	T	C	6: 128,595,466 (GRCm39)	D96G	probably benign	Het
Lrp1b	C	T	2: 40,587,454 (GRCm39)	V165M	unknown	Het
Lrp4	A	C	2: 91,320,811 (GRCm39)	T975P	possibly damaging	Het
Lsm14a	T	A	7: 34,053,204 (GRCm39)	I283F	probably damaging	Het
Mael	T	C	1: 166,066,135 (GRCm39)	D34G	probably damaging	Het
Map2	C	T	1: 66,455,015 (GRCm39)	Q1302*	probably null	Het
Mctp1	T	C	13: 76,972,999 (GRCm39)		probably null	Het
Mlxip	T	C	5: 123,585,537 (GRCm39)	V642A	probably benign	Het
Myh9	T	C	15: 77,657,547 (GRCm39)	E1066G	possibly damaging	Het
Naa35	T	A	13: 59,765,846 (GRCm39)		probably benign	Het
Nacc1	T	A	8: 85,403,828 (GRCm39)	I16F	probably damaging	Het
Ncapd3	T	A	9: 26,963,645 (GRCm39)	N499K	probably benign	Het
Or10ab4	A	G	7: 107,655,004 (GRCm39)	M272V	possibly damaging	Het
Osbpl10	C	A	9: 115,036,655 (GRCm39)	P253Q	probably benign	Het
Ptpn21	G	T	12: 98,654,800 (GRCm39)	S722R	probably benign	Het
Rab44	C	T	17: 29,358,843 (GRCm39)	P344S	probably benign	Het
Rbms2	C	T	10: 127,979,312 (GRCm39)	R139Q	probably damaging	Het
Sh3bp2	T	C	5: 34,709,002 (GRCm39)	Y32H	probably damaging	Het
Slc6a15	A	G	10: 103,229,275 (GRCm39)	I105V	probably benign	Het
Thumpd3	A	G	6: 113,032,652 (GRCm39)	D130G	possibly damaging	Het
Trib1	A	G	15: 59,526,210 (GRCm39)	Y260C	probably damaging	Het
Ttn	G	T	2: 76,577,585 (GRCm39)	S22690*	probably null	Het
Ttyh2	T	G	11: 114,609,958 (GRCm39)	S510A	possibly damaging	Het
Was	G	T	X: 7,952,927 (GRCm39)	S271R	probably benign	Het
Zfp267	T	A	3: 36,213,725 (GRCm39)	C20S	possibly damaging	Het
Zfp472	T	A	17: 33,196,685 (GRCm39)	Y253*	probably null	Het

Other mutations in Tsks

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01292:Tsks	APN	7	44,601,982 (GRCm39)	missense	probably damaging	1.00
IGL03006:Tsks	APN	7	44,600,198 (GRCm39)	unclassified	probably benign
IGL03065:Tsks	APN	7	44,592,724 (GRCm39)	missense	probably damaging	1.00
IGL03091:Tsks	APN	7	44,607,319 (GRCm39)	missense	possibly damaging	0.54
R0139:Tsks	UTSW	7	44,603,883 (GRCm39)	missense	probably benign
R0619:Tsks	UTSW	7	44,600,258 (GRCm39)	missense	probably damaging	1.00
R4273:Tsks	UTSW	7	44,607,353 (GRCm39)	missense	probably damaging	1.00
R4982:Tsks	UTSW	7	44,593,418 (GRCm39)	missense	possibly damaging	0.69
R5664:Tsks	UTSW	7	44,603,208 (GRCm39)	missense	probably damaging	1.00
R5846:Tsks	UTSW	7	44,593,412 (GRCm39)	missense	probably damaging	1.00
R6193:Tsks	UTSW	7	44,603,263 (GRCm39)	missense	probably damaging	0.96
R6567:Tsks	UTSW	7	44,603,305 (GRCm39)	missense	probably damaging	1.00
R7044:Tsks	UTSW	7	44,593,216 (GRCm39)	missense	probably damaging	0.99
R7255:Tsks	UTSW	7	44,602,112 (GRCm39)	missense	probably benign	0.13
R7845:Tsks	UTSW	7	44,603,168 (GRCm39)	splice site	probably null
R8073:Tsks	UTSW	7	44,607,305 (GRCm39)	missense	probably benign
R8162:Tsks	UTSW	7	44,603,296 (GRCm39)	missense	probably damaging	1.00
R8307:Tsks	UTSW	7	44,607,086 (GRCm39)	missense
R8340:Tsks	UTSW	7	44,602,144 (GRCm39)	missense	probably damaging	1.00
R8474:Tsks	UTSW	7	44,600,263 (GRCm39)	missense	probably damaging	1.00
R8911:Tsks	UTSW	7	44,592,694 (GRCm39)	intron	probably benign
R9438:Tsks	UTSW	7	44,607,095 (GRCm39)	nonsense	probably null
R9623:Tsks	UTSW	7	44,605,931 (GRCm39)	missense	possibly damaging	0.85

Predicted Primers

PCR Primer
(F):5'- ATCACCTCCCGGCTCATAAG -3'
(R):5'- AAACCCTCCTCAGTTCACTG -3'

Sequencing Primer
(F):5'- ATGGTCAAAGGGGTACTGC -3'
(R):5'- CAGTTCACTGAAGGCTCTGGAG -3'

Posted On

2015-01-23