Mutagenetix > Incidental Mutation

Incidental Mutation 'R9269:Tes'

702747

Institutional Source

Beutler Lab

Gene Symbol

Tes

Ensembl Gene

ENSMUSG00000029552

Gene Name

testis derived transcript

Synonyms

D6Ertd352e, Tes1, Tes2, testin, testin2

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.211) question?

Stock #

R9269 (G1)

Quality Score

117.008

Status

Not validated

Chromosome

Chromosomal Location

17065149-17105828 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 17100342 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 325 (C325S)

Ref Sequence

ENSEMBL: ENSMUSP00000111127 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076654] [ENSMUST00000115467] [ENSMUST00000154266]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000076654
AA Change: C316S

PolyPhen 2 Score 0.250 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000075950
Gene: ENSMUSG00000029552
AA Change: C316S

Domain	Start	End	E-Value	Type
Pfam:PET	82	187	9.6e-46	PFAM
LIM	224	281	9.54e-12	SMART
LIM	289	341	5.35e-15	SMART
LIM	349	404	1.69e-12	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000115467
AA Change: C325S

PolyPhen 2 Score 0.250 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000111127
Gene: ENSMUSG00000029552
AA Change: C325S

Domain	Start	End	E-Value	Type
Pfam:PET	96	194	2.1e-44	PFAM
LIM	233	290	9.54e-12	SMART
LIM	298	350	5.35e-15	SMART
LIM	358	413	1.69e-12	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000154266

SMART Domains

Protein: ENSMUSP00000118791
Gene: ENSMUSG00000029552

Domain	Start	End	E-Value	Type
Pfam:PET	6	79	4e-33	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Cancer-associated chromosomal changes often involve regions containing fragile sites. This gene maps to a commom fragile site on chromosome 7q31.2 designated FRA7G. This gene is similar to mouse Testin, a testosterone-responsive gene encoding a Sertoli cell secretory protein containing three LIM domains. LIM domains are double zinc-finger motifs that mediate protein-protein interactions between transcription factors, cytoskeletal proteins and signaling proteins. This protein is a negative regulator of cell growth and may act as a tumor suppressor. This scaffold protein may also play a role in cell adhesion, cell spreading and in the reorganization of the actin cytoskeleton. Multiple protein isoforms are encoded by transcript variants of this gene.[provided by RefSeq, Mar 2011]
PHENOTYPE: Homozygous and heterozygous null mice display small forestomachs with thickened epithelium and increased tumor incidence and malignancy. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	A	C	15: 8,219,016	Q1683P	probably damaging	Het
A2m	T	C	6: 121,660,906	S845P	probably benign	Het
Actn1	T	A	12: 80,172,971	N709Y	probably benign	Het
Alox5ap	A	G	5: 149,279,196	Y64C	probably damaging	Het
Anapc4	T	A	5: 52,861,278	S521T	possibly damaging	Het
Ap3b1	C	A	13: 94,404,062	P164Q	probably damaging	Het
Arhgef26	A	G	3: 62,340,499	N335D	probably damaging	Het
Arrdc2	G	A	8: 70,836,329	A354V	probably benign	Het
Atg2b	A	G	12: 105,652,100	S898P	probably damaging	Het
Atxn1	T	A	13: 45,557,204	T751S	probably benign	Het
Begain	T	A	12: 109,033,193	R551W	possibly damaging	Het
Borcs8	C	A	8: 70,141,871	D15E	probably benign	Het
Btbd16	C	T	7: 130,815,786	R344C	probably damaging	Het
Card11	A	T	5: 140,906,761	M183K	probably damaging	Het
Cldn3	T	C	5: 134,986,725	L94P	probably damaging	Het
Clvs2	A	T	10: 33,543,426	Y211N	probably damaging	Het
Col15a1	G	C	4: 47,288,200		probably benign	Het
Cop1	C	T	1: 159,288,983	P409L	probably benign	Het
Crhbp	C	A	13: 95,436,516	A241S	probably benign	Het
Cyfip1	C	A	7: 55,907,431	S794*	probably null	Het
D17Wsu92e	A	C	17: 27,786,075	Y169*	probably null	Het
Dlg5	T	A	14: 24,192,813	H172L	probably damaging	Het
Doc2a	T	A	7: 126,850,987	I199N	probably benign	Het
Dock3	T	C	9: 106,941,323	T1191A	probably benign	Het
Efcab8	G	C	2: 153,804,941	V397L	unknown	Het
Fcgr1	C	T	3: 96,285,838	R281H	probably benign	Het
Fndc10	T	C	4: 155,694,748	V83A	possibly damaging	Het
Galnt2	T	A	8: 124,338,463	I444K	probably benign	Het
Gcnt3	T	C	9: 70,034,008	Y426C	probably damaging	Het
Gm5580	C	T	6: 116,552,356	T398I	probably damaging	Het
Gtpbp1	C	T	15: 79,717,654	R533C	probably damaging	Het
Hid1	T	C	11: 115,361,676	E60G	probably damaging	Het
Ighv1-81	A	T	12: 115,920,541	L30Q	possibly damaging	Het
Ighv5-8	TATATATATATATATATATATA	TATATATATATATATATATATATA	12: 113,654,945		probably null	Het
Klf10	A	G	15: 38,297,758	L44P	probably damaging	Het
Lamc3	T	C	2: 31,923,005	V1001A	probably benign	Het
Lamc3	C	A	2: 31,928,896	S1211*	probably null	Het
Lmx1a	T	A	1: 167,830,625	H192Q	probably benign	Het
Nkx2-4	T	C	2: 147,084,264	H226R	possibly damaging	Het
Olfr1046	T	C	2: 86,216,903	H269R	probably damaging	Het
Olfr1179	G	A	2: 88,402,242	R231C	probably benign	Het
Olfr1240	T	A	2: 89,439,932	M116L	probably damaging	Het
Olfr1281	T	C	2: 111,328,952	F178L	probably damaging	Het
Olfr1453	T	C	19: 13,027,630	H233R	probably benign	Het
Olfr1468-ps1	A	T	19: 13,375,640	N226I	unknown	Het
Olfr472	T	A	7: 107,903,320	I201N	possibly damaging	Het
Olfr715	T	C	7: 107,128,626	I256V	probably benign	Het
Olfr869	T	C	9: 20,137,461	M115T	probably damaging	Het
Orai3	G	T	7: 127,774,022	A232S	probably benign	Het
Pak1ip1	G	A	13: 41,009,251	G177R	probably benign	Het
Pcp4l1	T	C	1: 171,174,406	R62G	possibly damaging	Het
Phox2b	T	A	5: 67,098,721	Q74L	probably benign	Het
Pi4kb	A	G	3: 94,984,486	Y159C	probably damaging	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 109,624,195		probably benign	Het
Plxna1	T	C	6: 89,329,559	R1430G	probably null	Het
Plxna4	T	C	6: 32,178,380	H1543R	probably benign	Het
Prcc	A	T	3: 87,869,731	F312Y	probably damaging	Het
Ranbp6	A	G	19: 29,809,988	L988P	probably damaging	Het
Rbm27	A	G	18: 42,327,507	T840A	probably benign	Het
Rchy1	G	T	5: 91,957,972	T39N	probably benign	Het
Rmi1	C	T	13: 58,409,026	T363I	probably benign	Het
Rnpc3	A	C	3: 113,611,246	I420S	probably damaging	Het
Rsph4a	T	A	10: 33,909,398	V435E	probably benign	Het
Rwdd1	T	C	10: 34,012,099	T38A	probably damaging	Het
S100a13	G	T	3: 90,515,863	D54Y	unknown	Het
Sel1l3	T	C	5: 53,154,286	Y619C	probably damaging	Het
Sf3b3	T	C	8: 110,812,026	T1121A	probably damaging	Het
Sgk3	T	C	1: 9,872,309	V102A	probably benign	Het
Sh2b1	T	C	7: 126,469,182	T486A	probably damaging	Het
Slc22a5	C	T	11: 53,876,155	R169H	probably damaging	Het
Slc4a5	T	C	6: 83,289,241	V889A	possibly damaging	Het
Spast	C	A	17: 74,339,074	S13*	probably null	Het
Srek1	T	C	13: 103,753,146		probably null	Het
Sugp1	G	T	8: 70,056,570	E164D	probably benign	Het
Synpo2	T	C	3: 123,117,324	D224G	probably benign	Het
Tanc1	A	G	2: 59,800,088	D804G	probably damaging	Het
Tep1	C	T	14: 50,844,309	C1228Y	probably damaging	Het
Themis	T	C	10: 28,863,394	V620A	probably benign	Het
Trim17	T	C	11: 58,971,431	S430P	probably damaging	Het
Tubgcp5	T	C	7: 55,795,945	I65T	possibly damaging	Het
Unc13b	T	C	4: 43,171,955	S928P	unknown	Het
Vat1l	C	T	8: 114,289,432	A354V	probably damaging	Het
Vmn1r170	T	A	7: 23,606,838	S222T	probably benign	Het
Vmn2r112	A	T	17: 22,601,232	M29L	probably benign	Het
Vmn2r72	T	C	7: 85,751,203	I213V	probably benign	Het
Wdr89	T	A	12: 75,632,790	Q230L	possibly damaging	Het
Zfp386	A	G	12: 116,059,663	T334A	probably benign	Het
Zfp442	T	A	2: 150,409,367	H205L	probably benign	Het
Zfyve26	A	T	12: 79,276,302	I890N	possibly damaging	Het
Zic1	T	C	9: 91,364,320	E233G	probably damaging	Het

Other mutations in Tes

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01408:Tes	APN	6	17099879	missense	probably damaging	1.00
IGL02070:Tes	APN	6	17099780	missense	probably damaging	1.00
R0501:Tes	UTSW	6	17097558	missense	probably benign
R1591:Tes	UTSW	6	17097442	missense	probably damaging	0.98
R1777:Tes	UTSW	6	17104755	missense	probably benign	0.02
R2968:Tes	UTSW	6	17096234	missense	probably benign	0.00
R3983:Tes	UTSW	6	17099701	splice site	probably null
R4532:Tes	UTSW	6	17097408	missense	possibly damaging	0.95
R4893:Tes	UTSW	6	17104596	missense	probably damaging	1.00
R4949:Tes	UTSW	6	17100360	missense	probably benign
R5026:Tes	UTSW	6	17096340	missense	probably benign	0.41
R6220:Tes	UTSW	6	17086196	nonsense	probably null
R6810:Tes	UTSW	6	17104652	missense	probably benign	0.12
R6903:Tes	UTSW	6	17099863	missense	probably damaging	0.99
R6987:Tes	UTSW	6	17086155	missense	probably benign	0.09
R7210:Tes	UTSW	6	17104762	missense	probably damaging	1.00
R7391:Tes	UTSW	6	17096167	missense	probably damaging	1.00
R7549:Tes	UTSW	6	17099741	frame shift	probably null
R7818:Tes	UTSW	6	17099744	missense	probably damaging	0.99
R7978:Tes	UTSW	6	17096323	missense	probably benign	0.00
R7992:Tes	UTSW	6	17096243	missense	possibly damaging	0.80
R8052:Tes	UTSW	6	17097292	missense	probably benign	0.08
R8129:Tes	UTSW	6	17065243	start gained	probably benign
R8552:Tes	UTSW	6	17097328	missense	probably damaging	1.00
R8703:Tes	UTSW	6	17099789	missense	probably damaging	1.00
R9556:Tes	UTSW	6	17096234	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATTTTCAAATCTTAAGCGCCCC -3'
(R):5'- CACTCTTAGGTGATGCAAGGAG -3'

Sequencing Primer
(F):5'- CCAAAAGGCATCTGCTCTTGTAGG -3'
(R):5'- CTTAGGTGATGCAAGGAGAGGCC -3'

Posted On

2022-03-25