Mutagenetix > Incidental Mutation

Incidental Mutation 'R0201:Tssk4'

23669

Institutional Source

Beutler Lab

Gene Symbol

Tssk4

Ensembl Gene

ENSMUSG00000007591

Gene Name

testis-specific serine kinase 4

Synonyms

1700020B19Rik, 4933424F08Rik

MMRRC Submission

038458-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.771) question?

Stock #

R0201 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

55650184-55652539 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 55651559 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 181 (K181*)

Ref Sequence

ENSEMBL: ENSMUSP00000154783 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000007735] [ENSMUST00000164809] [ENSMUST00000226497] [ENSMUST00000226591] [ENSMUST00000227297] [ENSMUST00000228041] [ENSMUST00000228395]

AlphaFold

Q9D411

Predicted Effect

probably null
Transcript: ENSMUST00000007735
AA Change: K181*

SMART Domains

Protein: ENSMUSP00000007735
Gene: ENSMUSG00000007591
AA Change: K181*

Domain	Start	End	E-Value	Type
Pfam:Pkinase	25	280	1.1e-54	PFAM
Pfam:Pkinase_Tyr	25	280	7.9e-34	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000164809
AA Change: K181*

SMART Domains

Protein: ENSMUSP00000127728
Gene: ENSMUSG00000007591
AA Change: K181*

Domain	Start	End	E-Value	Type
Pfam:Pkinase	25	281	4e-56	PFAM
Pfam:Pkinase_Tyr	25	281	3.3e-35	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000226497
AA Change: K177*

Predicted Effect

probably null
Transcript: ENSMUST00000226591
AA Change: K171*

Predicted Effect

probably benign
Transcript: ENSMUST00000227297

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000227568

Predicted Effect

probably null
Transcript: ENSMUST00000228041
AA Change: K171*

Predicted Effect

probably null
Transcript: ENSMUST00000228395
AA Change: K181*

Meta Mutation Damage Score

0.9756

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.7%
20x: 94.2%

Validation Efficiency

97% (91/94)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the testis-specific serine/threonine kinase family. The encoded protein is thought to be involved in spermatogenesis via stimulation of the CREB/CRE responsive pathway through phosphorylation of the cAMP responsive element binding protein transcription factor. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamdec1	A	G	14: 68,581,957		probably null	Het
Adamts16	T	A	13: 70,779,644	Q492L	possibly damaging	Het
Aplnr	A	G	2: 85,137,177	D182G	probably damaging	Het
Arnt2	G	T	7: 84,361,659	S3*	probably null	Het
Asxl3	T	C	18: 22,523,154	V1407A	probably benign	Het
Atg13	A	T	2: 91,684,762		probably null	Het
Atm	A	T	9: 53,454,279		probably benign	Het
Birc6	T	G	17: 74,609,327	V1746G	possibly damaging	Het
Cbln1	G	T	8: 87,472,113	T43K	probably benign	Het
Cbx5	T	C	15: 103,199,700	T173A	probably damaging	Het
Cc2d2a	A	G	5: 43,737,512	Y1437C	probably damaging	Het
Ccdc78	C	A	17: 25,789,236		probably benign	Het
Cd2bp2	A	G	7: 127,193,828	Y341H	probably damaging	Het
Cdhr5	T	A	7: 141,276,378	D88V	probably damaging	Het
Ces1f	T	A	8: 93,267,329	T275S	probably null	Het
Clca4a	T	C	3: 144,960,717	N458S	probably benign	Het
Cog5	A	G	12: 31,839,841	K521R	probably damaging	Het
Csf2ra	T	A	19: 61,225,568	T305S	probably benign	Het
Csmd3	T	A	15: 47,619,729		probably benign	Het
Cts6	T	A	13: 61,201,499	R132*	probably null	Het
D5Ertd579e	G	T	5: 36,616,465	N195K	probably damaging	Het
Ddx1	A	G	12: 13,223,808	V606A	probably damaging	Het
Dip2b	G	A	15: 100,186,147	D884N	probably damaging	Het
Ehhadh	A	G	16: 21,773,493		probably null	Het
Enpp1	T	A	10: 24,653,917	T608S	probably benign	Het
Fancm	T	C	12: 65,101,632	Y674H	probably damaging	Het
Fat4	T	A	3: 38,891,596	V1546D	probably damaging	Het
Fsd1	G	A	17: 55,990,522	A158T	probably benign	Het
Fzd2	T	A	11: 102,606,122	M464K	probably damaging	Het
Gjc2	A	G	11: 59,177,590	F22S	possibly damaging	Het
Gm13101	T	C	4: 143,964,890	E421G	probably damaging	Het
Gria2	T	C	3: 80,707,838	Y445C	probably damaging	Het
Hsdl1	T	A	8: 119,566,256	I147F	possibly damaging	Het
Ifi44	T	C	3: 151,745,636	Y226C	probably damaging	Het
Il16	A	G	7: 83,722,308	C97R	probably damaging	Het
Impg1	A	T	9: 80,345,561	S369T	probably damaging	Het
Jmjd1c	A	G	10: 67,219,109	T390A	unknown	Het
Lgi1	A	G	19: 38,301,293	E269G	possibly damaging	Het
Lrp6	G	T	6: 134,450,897	Y1577*	probably null	Het
Lrrc74a	G	T	12: 86,761,773		probably benign	Het
Man1c1	A	T	4: 134,640,398		probably null	Het
Map1lc3b	A	C	8: 121,590,550	Q9P	possibly damaging	Het
Mboat1	G	A	13: 30,202,375	R124H	probably benign	Het
Mcu	A	G	10: 59,456,677	L60P	probably damaging	Het
Mrs2	G	T	13: 25,018,534	Q75K	probably benign	Het
Muc2	CGTG	CGTGTG	7: 141,699,185		probably null	Het
Neb	G	A	2: 52,206,878		probably benign	Het
Nlrp2	C	T	7: 5,328,329	G356D	probably benign	Het
Notch3	A	G	17: 32,156,148		probably benign	Het
Npr2	A	C	4: 43,641,617	S474R	probably damaging	Het
Nupl1	A	G	14: 60,244,616	F100L	probably benign	Het
Osbpl6	A	C	2: 76,546,042	D87A	possibly damaging	Het
Pabpc2	A	T	18: 39,775,307	M542L	probably benign	Het
Papln	A	G	12: 83,783,027		probably benign	Het
Parpbp	T	C	10: 88,092,896	I561V	possibly damaging	Het
Pcdhb13	C	T	18: 37,442,581	A4V	probably benign	Het
Pelp1	T	C	11: 70,395,704	T533A	possibly damaging	Het
Poldip3	T	A	15: 83,135,296	M182L	probably benign	Het
Por	T	C	5: 135,731,178	S240P	possibly damaging	Het
Pramef20	A	T	4: 144,377,273		probably benign	Het
Prss22	A	T	17: 23,996,301	V167D	probably damaging	Het
Prss37	A	C	6: 40,516,349	L61R	probably damaging	Het
Psmd1	C	T	1: 86,118,616	T702M	probably benign	Het
Pxdn	G	T	12: 30,002,431	G869V	possibly damaging	Het
Rabgap1l	A	G	1: 160,453,745		probably benign	Het
Rapgef6	T	C	11: 54,619,941	V228A	probably damaging	Het
Rnf169	T	C	7: 99,926,003	R462G	possibly damaging	Het
Rnft2	A	G	5: 118,194,680		probably benign	Het
Sgo2b	T	C	8: 63,926,636	D1054G	probably benign	Het
Sh3bgr	T	C	16: 96,228,517		probably benign	Het
Slc12a4	A	G	8: 105,945,350	V910A	possibly damaging	Het
Slc6a12	A	T	6: 121,355,372	I222F	probably benign	Het
Spty2d1	G	A	7: 46,997,901	R427*	probably null	Het
Ssc5d	A	G	7: 4,944,663	T1339A	probably benign	Het
Sspo	A	C	6: 48,455,752	E854A	possibly damaging	Het
Stx7	A	G	10: 24,185,079		probably benign	Het
Styk1	A	T	6: 131,301,730		probably benign	Het
Tex33	T	A	15: 78,378,828	M209L	probably damaging	Het
Tmem163	T	G	1: 127,668,637		probably benign	Het
Tmppe	C	CT	9: 114,404,639		probably null	Het
Tmx2	A	G	2: 84,673,082	V229A	probably benign	Het
Top2b	T	C	14: 16,383,174	L54P	probably damaging	Het
Trim62	A	T	4: 128,902,550	Y280F	probably benign	Het
Ubn1	A	G	16: 5,064,614	D313G	probably damaging	Het
Ugt1a10	C	T	1: 88,215,123	P113L	probably damaging	Het
Ugt1a10	C	T	1: 88,218,249	P473L	probably damaging	Het

Other mutations in Tssk4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01627:Tssk4	APN	14	55650553	missense	probably damaging	1.00
IGL02943:Tssk4	APN	14	55651566	missense	probably damaging	1.00
IGL03082:Tssk4	APN	14	55651061	missense	probably damaging	1.00
IGL03281:Tssk4	APN	14	55650428	missense	possibly damaging	0.86
R0201:Tssk4	UTSW	14	55651560	missense	probably damaging	1.00
R1655:Tssk4	UTSW	14	55651695	missense	probably damaging	1.00
R1660:Tssk4	UTSW	14	55650572	missense	probably null	0.90
R1743:Tssk4	UTSW	14	55651031	missense	probably damaging	1.00
R2103:Tssk4	UTSW	14	55651540	missense	probably damaging	1.00
R3431:Tssk4	UTSW	14	55651695	missense	probably damaging	1.00
R3432:Tssk4	UTSW	14	55651695	missense	probably damaging	1.00
R4113:Tssk4	UTSW	14	55650373	missense	probably benign	0.00
R4870:Tssk4	UTSW	14	55651815	missense	probably benign	0.38
R4957:Tssk4	UTSW	14	55651809	missense	probably damaging	1.00
R5147:Tssk4	UTSW	14	55650973	missense	possibly damaging	0.56
R6785:Tssk4	UTSW	14	55650475	missense	probably damaging	1.00
R6917:Tssk4	UTSW	14	55652407	missense	probably benign	0.13
R7748:Tssk4	UTSW	14	55651112	missense	probably damaging	1.00
R9043:Tssk4	UTSW	14	55651754	missense	probably damaging	0.99
R9189:Tssk4	UTSW	14	55650447	missense	probably benign	0.00
Z1088:Tssk4	UTSW	14	55650923	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CACAATGGTGAACTAGTGGTCCTCAG -3'
(R):5'- TGCTCCAGGTGTCAGACAGGAAAG -3'

Sequencing Primer
(F):5'- TTGGGCTCTGCTCACAAC -3'
(R):5'- TGTCAGACAGGAAAGGGTTGTAG -3'

Posted On

2013-04-16