Mutagenetix > Incidental Mutation

Incidental Mutation 'R7401:Tsga10'

574138

Institutional Source

Beutler Lab

Gene Symbol

Tsga10

Ensembl Gene

ENSMUSG00000060771

Gene Name

testis specific 10

Synonyms

4933432N21Rik, Mtsga10

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.126) question?

Stock #

R7401 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

37754776-37866429 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 37834187 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 204 (R204G)

Ref Sequence

ENSEMBL: ENSMUSP00000048859 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041815] [ENSMUST00000088072] [ENSMUST00000114902] [ENSMUST00000123082] [ENSMUST00000151735] [ENSMUST00000155852] [ENSMUST00000193669]

AlphaFold

Q6NY15

Predicted Effect

probably null
Transcript: ENSMUST00000041815
AA Change: R204G

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000048859
Gene: ENSMUSG00000060771
AA Change: R204G

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	249	N/A	INTRINSIC
Blast:SPEC	294	391	5e-6	BLAST

Predicted Effect

probably null
Transcript: ENSMUST00000088072
AA Change: R204G

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000085391
Gene: ENSMUSG00000060771
AA Change: R204G

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	249	N/A	INTRINSIC
Blast:SPEC	294	391	5e-6	BLAST

Predicted Effect

probably null
Transcript: ENSMUST00000114902
AA Change: R204G

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000110552
Gene: ENSMUSG00000060771
AA Change: R204G

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	249	N/A	INTRINSIC
Blast:SPEC	294	391	5e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000123082

SMART Domains

Protein: ENSMUSP00000141261
Gene: ENSMUSG00000060771

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	157	N/A	INTRINSIC
low complexity region	159	170	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000151735
AA Change: R204G

PolyPhen 2 Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000120554
Gene: ENSMUSG00000060771
AA Change: R204G

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	229	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000155852

SMART Domains

Protein: ENSMUSP00000141630
Gene: ENSMUSG00000060771

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	157	N/A	INTRINSIC
low complexity region	159	170	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000193669

SMART Domains

Protein: ENSMUSP00000142218
Gene: ENSMUSG00000060771

Domain	Start	End	E-Value	Type
low complexity region	5	17	N/A	INTRINSIC
coiled coil region	24	85	N/A	INTRINSIC
coiled coil region	110	157	N/A	INTRINSIC
low complexity region	159	170	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610318N02Rik	A	T	16: 17,118,404	L152Q	probably benign	Het
Abcg3	A	T	5: 104,966,774	N292K	probably damaging	Het
Adamts3	T	A	5: 89,707,450		probably null	Het
Adgrg7	T	C	16: 56,742,418	N519D	probably benign	Het
Adsl	A	G	15: 80,962,782	H263R	probably damaging	Het
Ak9	A	T	10: 41,423,004	D1567V	unknown	Het
Bscl2	T	C	19: 8,846,550	F280L	possibly damaging	Het
Cacna1b	T	A	2: 24,679,294	T873S	probably benign	Het
Cacna1c	T	C	6: 119,052,708		probably null	Het
Cast	G	T	13: 74,808,458	A18E	unknown	Het
Ccdc114	A	C	7: 45,942,765	Q323P	probably damaging	Het
Cd207	A	C	6: 83,677,848		probably benign	Het
Cd79b	A	G	11: 106,312,852	S130P	probably benign	Het
Cfap52	A	T	11: 67,949,633	N157K	probably benign	Het
Cfap57	C	T	4: 118,614,931	V84I	probably benign	Het
Chaf1b	G	T	16: 93,884,380		probably benign	Het
Cntn1	A	G	15: 92,317,989	I968V	probably benign	Het
Cntn5	C	T	9: 9,833,461	V362I	probably benign	Het
Crem	A	G	18: 3,295,329	S80P	probably damaging	Het
Csnk1g3	C	T	18: 53,930,318	T267I	probably damaging	Het
Cyth1	A	T	11: 118,182,251	N274K	possibly damaging	Het
Dicer1	C	T	12: 104,712,278	G594S	probably benign	Het
Enpp1	C	T	10: 24,645,282	C849Y	probably damaging	Het
Fam193a	A	G	5: 34,465,635	E1189G	possibly damaging	Het
Fermt1	C	A	2: 132,917,559	V426L	probably benign	Het
Fes	A	G	7: 80,378,776		probably null	Het
Gm16486	T	C	8: 70,717,272	I1337T	probably benign	Het
Gmeb1	C	A	4: 132,225,774	L560F	probably damaging	Het
Hace1	T	C	10: 45,670,626	L452P	probably damaging	Het
Hecw2	T	A	1: 53,904,343	H975L	probably damaging	Het
Idh2	GGTCCCAG	GG	7: 80,098,329		probably benign	Het
Il1r2	T	A	1: 40,123,210	C338S	probably damaging	Het
Kcnb1	T	C	2: 167,188,284	S114G	probably damaging	Het
Lce1c	A	T	3: 92,680,316	T17S	unknown	Het
Lhfpl4	C	A	6: 113,176,666	L141F	possibly damaging	Het
Ms4a14	T	C	19: 11,302,230	E988G	possibly damaging	Het
Naip5	T	C	13: 100,219,696	Q1137R	probably benign	Het
Naip5	G	T	13: 100,219,697	Q1137K	not run	Het
Neurod1	T	A	2: 79,454,946	D31V	probably benign	Het
Neurod4	A	G	10: 130,271,058	C116R	probably damaging	Het
Nisch	A	G	14: 31,206,580	V28A	probably benign	Het
Olfr1174-ps	T	G	2: 88,311,428	M123L	probably benign	Het
Olfr1245	A	G	2: 89,575,105	V207A	probably benign	Het
Pabpc4l	A	T	3: 46,446,252	I319N	probably damaging	Het
Pabpc4l	T	A	3: 46,446,589	R207W	probably damaging	Het
Pcm1	G	A	8: 41,309,531	D1371N	probably damaging	Het
Peg10	G	GGTC	6: 4,756,452		probably benign	Het
Plxnc1	C	T	10: 94,871,005	A557T	probably benign	Het
Prkdc	T	A	16: 15,648,738	V58D	probably damaging	Het
Prpf40a	A	G	2: 53,156,947	V259A	probably benign	Het
Psmd3	A	T	11: 98,685,640	T123S	probably benign	Het
Ptgr2	G	T	12: 84,292,329		probably benign	Het
Ptprr	A	G	10: 116,048,236	H66R	probably benign	Het
Rftn2	A	G	1: 55,194,242		probably null	Het
Rsph14	T	A	10: 75,029,796	E70V	possibly damaging	Het
Slc24a5	G	A	2: 125,088,191	V471I	probably benign	Het
Sorbs1	G	C	19: 40,376,800	R180G	probably benign	Het
Spag9	A	T	11: 94,097,689	T862S	probably benign	Het
Ssbp2	T	A	13: 91,690,883	D291E	probably benign	Het
Supt5	T	C	7: 28,323,772	K329E	probably damaging	Het
Syne2	G	T	12: 75,967,381	K3115N	probably damaging	Het
Tars	A	T	15: 11,392,009	L239*	probably null	Het
Tbxa2r	T	C	10: 81,332,791	Y105H	probably benign	Het
Tesk1	T	A	4: 43,445,743	D265E	probably damaging	Het
Tril	T	C	6: 53,818,281	D652G	possibly damaging	Het
Twnk	A	G	19: 45,011,780	D645G	probably benign	Het
Umodl1	A	T	17: 30,998,148	D1118V	probably damaging	Het
Unc119	T	C	11: 78,347,245	I83T	probably benign	Het
Unc80	T	C	1: 66,646,415	W2233R	possibly damaging	Het
Vmn1r45	T	A	6: 89,933,434	T185S	possibly damaging	Het
Vmn2r111	G	T	17: 22,571,086	T313K	possibly damaging	Het
Wdr4	A	G	17: 31,509,832	L123S	probably damaging	Het
Zfpm2	A	G	15: 41,102,990	E957G	possibly damaging	Het

Other mutations in Tsga10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00573:Tsga10	APN	1	37807070	missense	probably damaging	0.99
IGL00579:Tsga10	APN	1	37835453	missense	probably damaging	1.00
IGL00837:Tsga10	APN	1	37801911	splice site	probably benign
IGL01577:Tsga10	APN	1	37835457	missense	possibly damaging	0.85
IGL01727:Tsga10	APN	1	37835274	missense	probably damaging	1.00
IGL02037:Tsga10	APN	1	37807017	missense	probably benign	0.05
IGL02510:Tsga10	APN	1	37760985	missense	possibly damaging	0.89
R0346:Tsga10	UTSW	1	37840519	missense	possibly damaging	0.65
R0789:Tsga10	UTSW	1	37801787	missense	possibly damaging	0.87
R0961:Tsga10	UTSW	1	37761428	critical splice donor site	probably null
R1370:Tsga10	UTSW	1	37835453	missense	probably damaging	1.00
R1440:Tsga10	UTSW	1	37819599	missense	probably damaging	1.00
R1827:Tsga10	UTSW	1	37835580	missense	probably damaging	1.00
R2504:Tsga10	UTSW	1	37815677	missense	probably damaging	1.00
R3104:Tsga10	UTSW	1	37801791	missense	probably damaging	1.00
R3105:Tsga10	UTSW	1	37801791	missense	probably damaging	1.00
R3106:Tsga10	UTSW	1	37801791	missense	probably damaging	1.00
R3824:Tsga10	UTSW	1	37834197	missense	possibly damaging	0.73
R3825:Tsga10	UTSW	1	37834197	missense	possibly damaging	0.73
R4560:Tsga10	UTSW	1	37807082	missense	probably benign	0.00
R4773:Tsga10	UTSW	1	37835525	missense	probably damaging	1.00
R4927:Tsga10	UTSW	1	37801850	missense	probably damaging	1.00
R5036:Tsga10	UTSW	1	37783968	missense	possibly damaging	0.65
R5326:Tsga10	UTSW	1	37761517	missense	probably damaging	1.00
R5345:Tsga10	UTSW	1	37763311	missense	probably damaging	1.00
R5503:Tsga10	UTSW	1	37760947	makesense	probably null
R5542:Tsga10	UTSW	1	37761517	missense	probably damaging	1.00
R5793:Tsga10	UTSW	1	37835459	missense	probably damaging	1.00
R6340:Tsga10	UTSW	1	37835185	intron	probably benign
R7096:Tsga10	UTSW	1	37840614	missense	probably damaging	0.98
R7130:Tsga10	UTSW	1	37783884	missense	probably damaging	1.00
R7609:Tsga10	UTSW	1	37804893	splice site	probably null
R7649:Tsga10	UTSW	1	37835148	missense	unknown
R7773:Tsga10	UTSW	1	37835242	missense	unknown
R8242:Tsga10	UTSW	1	37807101	missense	probably benign	0.28
R8379:Tsga10	UTSW	1	37801878	missense	probably benign	0.00
R9205:Tsga10	UTSW	1	37841278	start gained	probably benign
R9252:Tsga10	UTSW	1	37834283	missense	probably benign	0.35

Predicted Primers

PCR Primer
(F):5'- ATCTCAGTTTTCAGAGGGCTG -3'
(R):5'- AAGGCTGCACACTGATGGTAG -3'

Sequencing Primer
(F):5'- CAGTTTTCAGAGGGCTGTATAAAAAC -3'
(R):5'- CTGCACACTGATGGTAGCTAACTG -3'

Posted On

2019-09-13