Mutagenetix > Incidental Mutation

Incidental Mutation 'R5121:Tex15'

393032

Institutional Source

Beutler Lab

Gene Symbol

Tex15

Ensembl Gene

ENSMUSG00000009628

Gene Name

testis expressed gene 15

Synonyms

2210014E14Rik

MMRRC Submission

042709-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.292) question?

Stock #

R5121 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

33516738-33585582 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 33571766 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Isoleucine at position 408 (K408I)

Ref Sequence

ENSEMBL: ENSMUSP00000009772 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000009772] [ENSMUST00000124496] [ENSMUST00000124501]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000009772
AA Change: K408I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000009772
Gene: ENSMUSG00000009628
AA Change: K408I

Domain	Start	End	E-Value	Type
low complexity region	262	274	N/A	INTRINSIC
low complexity region	302	313	N/A	INTRINSIC
low complexity region	524	536	N/A	INTRINSIC
low complexity region	665	674	N/A	INTRINSIC
low complexity region	713	725	N/A	INTRINSIC
low complexity region	946	961	N/A	INTRINSIC
low complexity region	1497	1508	N/A	INTRINSIC
Pfam:TEX15	1572	1788	1.3e-109	PFAM
Pfam:TEX15	1901	2119	1.1e-16	PFAM
low complexity region	2758	2770	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000124496
AA Change: K682I

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000120744
Gene: ENSMUSG00000009628
AA Change: K682I

Domain	Start	End	E-Value	Type
Pfam:DUF3715	89	251	1.6e-58	PFAM
low complexity region	536	548	N/A	INTRINSIC
low complexity region	576	587	N/A	INTRINSIC
low complexity region	798	810	N/A	INTRINSIC
low complexity region	939	948	N/A	INTRINSIC
low complexity region	987	999	N/A	INTRINSIC
low complexity region	1220	1235	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000124501

SMART Domains

Protein: ENSMUSP00000138070
Gene: ENSMUSG00000009628

Domain	Start	End	E-Value	Type
Pfam:DUF3715	96	251	2.4e-52	PFAM

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.1%
20x: 91.7%

Validation Efficiency

MGI Phenotype

Strain: 3526165
PHENOTYPE: Male mice are infertile due to arrest of meiosis stemming from failure to repair double-strand breaks. However, female mice are fertile. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted(3) Gene trapped(1)

Other mutations in this stock

Total: 101 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acvr1c	A	G	2: 58,281,650 (GRCm38)	I234T	probably damaging	Het
Adam24	A	G	8: 40,679,511 (GRCm38)	E6G	probably damaging	Het
Amz1	A	G	5: 140,744,164 (GRCm38)	D151G	probably benign	Het
Arhgap24	T	C	5: 102,841,335 (GRCm38)	L10P	probably damaging	Het
Arhgap25	T	G	6: 87,532,864 (GRCm38)	N8T	probably benign	Het
Arsi	T	G	18: 60,917,439 (GRCm38)	F465V	probably damaging	Het
Atp2c1	A	G	9: 105,448,825 (GRCm38)	V293A	probably damaging	Het
Bzw2	A	G	12: 36,104,351 (GRCm38)	L340P	probably damaging	Het
Camkmt	C	T	17: 85,096,581 (GRCm38)	T77I	probably benign	Het
Camsap1	G	T	2: 25,935,550 (GRCm38)	Q1375K	probably benign	Het
Catsper2	G	T	2: 121,397,123 (GRCm38)		probably null	Het
Cd163	T	C	6: 124,317,989 (GRCm38)	C671R	probably damaging	Het
Cdk7	T	C	13: 100,717,684 (GRCm38)		probably null	Het
Cfi	C	T	3: 129,873,077 (GRCm38)	P483L	probably damaging	Het
Chn2	C	T	6: 54,218,561 (GRCm38)	L72F	possibly damaging	Het
Cimip4	C	T	15: 78,386,173 (GRCm38)	E132K	probably benign	Het
Cntn2	C	A	1: 132,517,060 (GRCm38)	E363*	probably null	Het
Crebbp	T	C	16: 4,093,511 (GRCm38)	E999G	probably damaging	Het
Cspp1	T	A	1: 10,126,463 (GRCm38)	N900K	probably damaging	Het
Cts3	A	C	13: 61,567,595 (GRCm38)	I141M	probably benign	Het
Cwc27	A	T	13: 104,804,353 (GRCm38)	V166D	probably damaging	Het
Defb26	T	C	2: 152,508,165 (GRCm38)	E65G	possibly damaging	Het
Dnah8	A	G	17: 30,810,353 (GRCm38)	T4099A	probably benign	Het
Eml6	A	G	11: 29,744,606 (GRCm38)	F1953L	probably benign	Het
Etl4	T	A	2: 20,340,111 (GRCm38)		probably null	Het
Fbln1	A	G	15: 85,237,671 (GRCm38)	E331G	probably damaging	Het
Gabra4	G	A	5: 71,572,203 (GRCm38)	H76Y	probably benign	Het
Gcat	T	C	15: 79,035,282 (GRCm38)	V149A	probably damaging	Het
Glp2r	A	T	11: 67,722,100 (GRCm38)		probably null	Het
Gm572	T	C	4: 148,666,845 (GRCm38)		probably null	Het
Golgb1	T	C	16: 36,919,258 (GRCm38)	V2653A	probably damaging	Het
Grap2	G	A	15: 80,646,144 (GRCm38)	R155Q	possibly damaging	Het
Gspt1	T	A	16: 11,223,301 (GRCm38)	I533L	probably damaging	Het
Gypa	A	T	8: 80,496,348 (GRCm38)	Y27F	unknown	Het
Hipk4	G	A	7: 27,529,492 (GRCm38)	V456I	probably benign	Het
Homer2	A	T	7: 81,649,563 (GRCm38)	D51E	probably benign	Het
Hspa1b	A	T	17: 34,958,004 (GRCm38)	V335E	possibly damaging	Het
Ift122	A	G	6: 115,912,534 (GRCm38)	T827A	probably benign	Het
Igkv1-35	T	C	6: 70,011,135 (GRCm38)	N58S	probably benign	Het
Kat6b	A	T	14: 21,619,258 (GRCm38)	H297L	probably damaging	Het
Kirrel3	G	T	9: 35,013,305 (GRCm38)	G296W	probably damaging	Het
Klhl17	A	G	4: 156,230,625 (GRCm38)	V525A	probably benign	Het
Lrrn1	G	T	6: 107,569,207 (GRCm38)	R655S	possibly damaging	Het
Ltk	T	C	2: 119,753,227 (GRCm38)	N256D	probably damaging	Het
Mill2	G	A	7: 18,856,666 (GRCm38)	G209S	probably benign	Het
Mmp27	A	T	9: 7,581,368 (GRCm38)	H544L	probably benign	Het
Mphosph10	A	G	7: 64,389,596 (GRCm38)	S209P	probably damaging	Het
Mphosph8	A	T	14: 56,676,546 (GRCm38)	K415*	probably null	Het
Myb	T	A	10: 21,126,238 (GRCm38)	M616L	probably benign	Het
Myo15b	C	T	11: 115,886,054 (GRCm38)	R867W	probably damaging	Het
Myo18b	A	T	5: 112,874,480 (GRCm38)		probably benign	Het
Nip7	A	G	8: 107,056,957 (GRCm38)	E8G	possibly damaging	Het
Optn	T	A	2: 5,046,106 (GRCm38)	I155F	probably benign	Het
Or2f1b	T	A	6: 42,762,997 (GRCm38)	L315*	probably null	Het
Or4f62	A	T	2: 112,156,286 (GRCm38)	M112L	possibly damaging	Het
Or52e4	A	G	7: 105,056,482 (GRCm38)	T79A	possibly damaging	Het
Or5c1	T	G	2: 37,332,589 (GRCm38)	F281V	probably damaging	Het
Or6b6	T	C	7: 106,972,231 (GRCm38)	I38V	probably benign	Het
Papolb	A	T	5: 142,528,837 (GRCm38)	H350Q	probably benign	Het
Pappa2	T	A	1: 158,838,627 (GRCm38)	M1128L	probably benign	Het
Pcdhb5	T	A	18: 37,321,117 (GRCm38)	N183K	probably benign	Het
Pde12	G	T	14: 26,669,422 (GRCm38)	S44*	probably null	Het
Peg3	T	C	7: 6,710,289 (GRCm38)	K645E	probably benign	Het
Pkd1	C	T	17: 24,573,463 (GRCm38)	R1375C	probably benign	Het
Plekha5	G	A	6: 140,579,474 (GRCm38)	E21K	probably damaging	Het
Plk2	C	T	13: 110,399,424 (GRCm38)	P554L	probably benign	Het
Pnkp	C	T	7: 44,862,403 (GRCm38)	S113L	probably damaging	Het
Polg	A	T	7: 79,464,605 (GRCm38)	W203R	probably damaging	Het
Ppcdc	A	G	9: 57,421,163 (GRCm38)	V65A	possibly damaging	Het
Ppm1m	T	A	9: 106,195,805 (GRCm38)	Q353L	probably benign	Het
Ppp1r13l	G	C	7: 19,370,095 (GRCm38)	R167P	probably damaging	Het
Ppp1r9b	T	A	11: 94,996,653 (GRCm38)	V497E	probably damaging	Het
Prpf6	T	A	2: 181,636,043 (GRCm38)	H399Q	probably benign	Het
Psg25	T	A	7: 18,526,536 (GRCm38)	I146F	possibly damaging	Het
Rasgef1c	A	T	11: 49,960,429 (GRCm38)	Q116L	probably damaging	Het
Rbbp9	A	G	2: 144,550,756 (GRCm38)	V8A	possibly damaging	Het
Rfk	T	C	19: 17,399,566 (GRCm38)	F144S	probably damaging	Het
Rfwd3	A	C	8: 111,282,753 (GRCm38)		probably null	Het
Rhpn1	T	C	15: 75,709,260 (GRCm38)	I117T	probably damaging	Het
Sars2	A	T	7: 28,747,908 (GRCm38)	N244Y	probably damaging	Het
Scnn1b	A	T	7: 121,902,887 (GRCm38)	H256L	probably benign	Het
Sgcz	G	A	8: 37,539,667 (GRCm38)	T195I	probably damaging	Het
Sh3gl2	T	A	4: 85,379,257 (GRCm38)	H157Q	probably benign	Het
Spen	T	A	4: 141,476,099 (GRCm38)	Q1739L	probably benign	Het
Susd1	G	T	4: 59,379,657 (GRCm38)	S323R	possibly damaging	Het
Szt2	T	C	4: 118,385,444 (GRCm38)	E1482G	possibly damaging	Het
Trem1	T	A	17: 48,232,836 (GRCm38)	F14L	probably null	Het
Trim26	G	T	17: 36,851,066 (GRCm38)	E126*	probably null	Het
Trpv3	T	C	11: 73,277,834 (GRCm38)		probably null	Het
Ttn	T	A	2: 76,916,491 (GRCm38)		probably null	Het
Ubap1	C	T	4: 41,379,688 (GRCm38)	L301F	probably benign	Het
Uchl1	T	C	5: 66,676,437 (GRCm38)	M12T	probably benign	Het
Vill	C	T	9: 119,070,025 (GRCm38)	T253I	possibly damaging	Het
Vmn2r107	C	T	17: 20,355,753 (GRCm38)	T115I	probably benign	Het
Vmn2r98	T	C	17: 19,053,553 (GRCm38)	S21P	probably benign	Het
Wapl	A	G	14: 34,677,162 (GRCm38)	K63E	probably benign	Het
Wnt2	T	C	6: 18,023,126 (GRCm38)	K175E	possibly damaging	Het
Zfp592	T	C	7: 81,023,561 (GRCm38)	L91P	probably damaging	Het
Zfp74	T	C	7: 29,932,507 (GRCm38)		probably null	Het
Zglp1	A	T	9: 21,062,661 (GRCm38)	I243N	probably benign	Het
Zranb1	A	G	7: 132,950,187 (GRCm38)	E215G	probably benign	Het

Other mutations in Tex15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00639:Tex15	APN	8	33,575,311 (GRCm38)	missense	probably benign	0.18
IGL00705:Tex15	APN	8	33,581,592 (GRCm38)	missense	probably damaging	1.00
IGL00820:Tex15	APN	8	33,579,006 (GRCm38)	splice site	probably benign
IGL01288:Tex15	APN	8	33,571,384 (GRCm38)	missense	probably benign	0.02
IGL01328:Tex15	APN	8	33,571,396 (GRCm38)	nonsense	probably null
IGL01359:Tex15	APN	8	33,581,898 (GRCm38)	missense	probably damaging	0.99
IGL01603:Tex15	APN	8	33,573,547 (GRCm38)	missense	possibly damaging	0.93
IGL01861:Tex15	APN	8	33,570,689 (GRCm38)	missense	probably damaging	1.00
IGL02052:Tex15	APN	8	33,582,465 (GRCm38)	missense	probably benign	0.28
IGL02560:Tex15	APN	8	33,581,751 (GRCm38)	missense	probably benign	0.00
IGL02677:Tex15	APN	8	33,571,080 (GRCm38)	missense	probably benign	0.03
IGL02739:Tex15	APN	8	33,581,693 (GRCm38)	missense	possibly damaging	0.68
Big_gulp	UTSW	8	33,581,734 (GRCm38)	missense	probably damaging	1.00
P0005:Tex15	UTSW	8	33,570,868 (GRCm38)	missense	probably benign	0.00
P0037:Tex15	UTSW	8	33,581,580 (GRCm38)	missense	probably benign	0.00
PIT4377001:Tex15	UTSW	8	33,571,101 (GRCm38)	missense	probably damaging	1.00
R0056:Tex15	UTSW	8	33,582,027 (GRCm38)	missense	probably benign	0.00
R0056:Tex15	UTSW	8	33,582,027 (GRCm38)	missense	probably benign	0.00
R0058:Tex15	UTSW	8	33,581,502 (GRCm38)	splice site	probably benign
R0058:Tex15	UTSW	8	33,581,502 (GRCm38)	splice site	probably benign
R0595:Tex15	UTSW	8	33,572,617 (GRCm38)	missense	probably damaging	1.00
R0646:Tex15	UTSW	8	33,582,326 (GRCm38)	missense	possibly damaging	0.83
R0688:Tex15	UTSW	8	33,573,500 (GRCm38)	missense	probably damaging	1.00
R0842:Tex15	UTSW	8	33,571,547 (GRCm38)	missense	possibly damaging	0.95
R0987:Tex15	UTSW	8	33,576,847 (GRCm38)	missense	probably damaging	1.00
R1084:Tex15	UTSW	8	33,577,004 (GRCm38)	missense	probably benign	0.28
R1183:Tex15	UTSW	8	33,574,865 (GRCm38)	missense	probably benign	0.35
R1186:Tex15	UTSW	8	33,571,633 (GRCm38)	missense	probably benign	0.19
R1378:Tex15	UTSW	8	33,575,216 (GRCm38)	missense	probably damaging	0.99
R1500:Tex15	UTSW	8	33,575,092 (GRCm38)	missense	probably damaging	0.96
R1508:Tex15	UTSW	8	33,576,852 (GRCm38)	missense	probably damaging	1.00
R1597:Tex15	UTSW	8	33,571,483 (GRCm38)	missense	probably damaging	0.96
R1636:Tex15	UTSW	8	33,576,387 (GRCm38)	nonsense	probably null
R1639:Tex15	UTSW	8	33,570,817 (GRCm38)	missense	possibly damaging	0.94
R1809:Tex15	UTSW	8	33,574,234 (GRCm38)	missense	probably benign
R1843:Tex15	UTSW	8	33,576,654 (GRCm38)	missense	probably benign	0.27
R2029:Tex15	UTSW	8	33,571,274 (GRCm38)	missense	probably damaging	0.99
R2228:Tex15	UTSW	8	33,571,237 (GRCm38)	missense	probably benign	0.05
R2229:Tex15	UTSW	8	33,571,237 (GRCm38)	missense	probably benign	0.05
R2245:Tex15	UTSW	8	33,571,496 (GRCm38)	missense	possibly damaging	0.77
R2246:Tex15	UTSW	8	33,582,512 (GRCm38)	missense	possibly damaging	0.49
R2880:Tex15	UTSW	8	33,574,907 (GRCm38)	nonsense	probably null
R2881:Tex15	UTSW	8	33,574,907 (GRCm38)	nonsense	probably null
R2882:Tex15	UTSW	8	33,574,907 (GRCm38)	nonsense	probably null
R3001:Tex15	UTSW	8	33,574,528 (GRCm38)	missense	probably benign	0.15
R3002:Tex15	UTSW	8	33,574,528 (GRCm38)	missense	probably benign	0.15
R3020:Tex15	UTSW	8	33,576,670 (GRCm38)	missense	probably damaging	1.00
R3084:Tex15	UTSW	8	33,574,885 (GRCm38)	missense	probably benign	0.11
R3085:Tex15	UTSW	8	33,574,885 (GRCm38)	missense	probably benign	0.11
R3701:Tex15	UTSW	8	33,574,166 (GRCm38)	missense	probably benign	0.00
R3702:Tex15	UTSW	8	33,574,166 (GRCm38)	missense	probably benign	0.00
R3752:Tex15	UTSW	8	33,571,415 (GRCm38)	missense	probably benign
R4162:Tex15	UTSW	8	33,581,558 (GRCm38)	missense	probably damaging	1.00
R4231:Tex15	UTSW	8	33,572,137 (GRCm38)	missense	probably damaging	0.99
R4589:Tex15	UTSW	8	33,557,373 (GRCm38)	missense	probably damaging	1.00
R4707:Tex15	UTSW	8	33,582,497 (GRCm38)	missense	probably benign	0.00
R4773:Tex15	UTSW	8	33,582,732 (GRCm38)	missense	probably benign	0.42
R4967:Tex15	UTSW	8	33,574,470 (GRCm38)	missense	probably benign	0.34
R5063:Tex15	UTSW	8	33,582,610 (GRCm38)	missense	possibly damaging	0.59
R5147:Tex15	UTSW	8	33,572,312 (GRCm38)	nonsense	probably null
R5166:Tex15	UTSW	8	33,576,392 (GRCm38)	missense	probably benign	0.07
R5173:Tex15	UTSW	8	33,571,740 (GRCm38)	missense	possibly damaging	0.73
R5439:Tex15	UTSW	8	33,574,171 (GRCm38)	missense	possibly damaging	0.93
R5537:Tex15	UTSW	8	33,571,613 (GRCm38)	missense	probably damaging	1.00
R5580:Tex15	UTSW	8	33,572,429 (GRCm38)	missense	probably damaging	1.00
R5588:Tex15	UTSW	8	33,577,187 (GRCm38)	missense	probably damaging	1.00
R5696:Tex15	UTSW	8	33,573,192 (GRCm38)	missense	probably benign	0.01
R5734:Tex15	UTSW	8	33,546,336 (GRCm38)	missense	probably benign	0.01
R5756:Tex15	UTSW	8	33,575,833 (GRCm38)	missense	probably benign	0.17
R5823:Tex15	UTSW	8	33,570,934 (GRCm38)	missense	possibly damaging	0.67
R6126:Tex15	UTSW	8	33,573,563 (GRCm38)	missense	probably benign	0.19
R6129:Tex15	UTSW	8	33,574,130 (GRCm38)	missense	possibly damaging	0.90
R6276:Tex15	UTSW	8	33,577,189 (GRCm38)	missense	possibly damaging	0.93
R6374:Tex15	UTSW	8	33,575,912 (GRCm38)	missense	probably damaging	1.00
R6430:Tex15	UTSW	8	33,571,301 (GRCm38)	missense	probably benign	0.01
R6452:Tex15	UTSW	8	33,572,816 (GRCm38)	missense	probably damaging	1.00
R6471:Tex15	UTSW	8	33,581,734 (GRCm38)	missense	probably damaging	1.00
R6700:Tex15	UTSW	8	33,574,889 (GRCm38)	missense	possibly damaging	0.93
R6918:Tex15	UTSW	8	33,573,184 (GRCm38)	missense	probably benign	0.27
R6958:Tex15	UTSW	8	33,570,871 (GRCm38)	missense	probably benign	0.01
R6970:Tex15	UTSW	8	33,557,428 (GRCm38)	missense	probably benign	0.03
R7059:Tex15	UTSW	8	33,574,730 (GRCm38)	missense	possibly damaging	0.57
R7069:Tex15	UTSW	8	33,570,720 (GRCm38)	missense	probably benign
R7072:Tex15	UTSW	8	33,575,431 (GRCm38)	missense	possibly damaging	0.85
R7212:Tex15	UTSW	8	33,572,995 (GRCm38)	missense	probably damaging	1.00
R7212:Tex15	UTSW	8	33,570,826 (GRCm38)	nonsense	probably null
R7216:Tex15	UTSW	8	33,572,986 (GRCm38)	missense	possibly damaging	0.93
R7219:Tex15	UTSW	8	33,546,240 (GRCm38)	missense	probably benign	0.40
R7313:Tex15	UTSW	8	33,574,817 (GRCm38)	missense	possibly damaging	0.82
R7315:Tex15	UTSW	8	33,581,516 (GRCm38)	missense	probably benign	0.01
R7444:Tex15	UTSW	8	33,576,562 (GRCm38)	missense	possibly damaging	0.92
R7455:Tex15	UTSW	8	33,576,997 (GRCm38)	missense	possibly damaging	0.91
R7643:Tex15	UTSW	8	33,575,120 (GRCm38)	missense	probably damaging	1.00
R7644:Tex15	UTSW	8	33,574,417 (GRCm38)	missense	probably benign	0.01
R7724:Tex15	UTSW	8	33,546,263 (GRCm38)	missense	possibly damaging	0.60
R7779:Tex15	UTSW	8	33,575,281 (GRCm38)	missense	probably damaging	1.00
R7798:Tex15	UTSW	8	33,581,847 (GRCm38)	missense	possibly damaging	0.69
R7816:Tex15	UTSW	8	33,581,655 (GRCm38)	missense	probably benign	0.14
R7820:Tex15	UTSW	8	33,575,062 (GRCm38)	missense	probably damaging	0.98
R8041:Tex15	UTSW	8	33,575,846 (GRCm38)	missense	probably damaging	1.00
R8150:Tex15	UTSW	8	33,573,506 (GRCm38)	missense	probably benign	0.06
R8152:Tex15	UTSW	8	33,572,893 (GRCm38)	missense	possibly damaging	0.82
R8237:Tex15	UTSW	8	33,577,399 (GRCm38)	missense	possibly damaging	0.72
R8250:Tex15	UTSW	8	33,565,205 (GRCm38)	missense	probably null	0.27
R8264:Tex15	UTSW	8	33,582,362 (GRCm38)	missense	probably benign	0.18
R8279:Tex15	UTSW	8	33,571,737 (GRCm38)	missense	probably damaging	0.96
R8353:Tex15	UTSW	8	33,576,871 (GRCm38)	nonsense	probably null
R8388:Tex15	UTSW	8	33,575,209 (GRCm38)	missense	probably benign	0.00
R8432:Tex15	UTSW	8	33,576,544 (GRCm38)	missense	probably damaging	0.99
R8453:Tex15	UTSW	8	33,576,871 (GRCm38)	nonsense	probably null
R8489:Tex15	UTSW	8	33,577,546 (GRCm38)	missense	probably benign	0.02
R8670:Tex15	UTSW	8	33,574,718 (GRCm38)	missense	probably benign	0.19
R8703:Tex15	UTSW	8	33,572,696 (GRCm38)	missense	probably benign	0.00
R8871:Tex15	UTSW	8	33,576,964 (GRCm38)	missense	possibly damaging	0.62
R8945:Tex15	UTSW	8	33,574,696 (GRCm38)	missense	probably benign	0.00
R9104:Tex15	UTSW	8	33,570,922 (GRCm38)	missense	possibly damaging	0.86
R9132:Tex15	UTSW	8	33,577,526 (GRCm38)	missense	possibly damaging	0.84
R9207:Tex15	UTSW	8	33,575,756 (GRCm38)	missense	probably damaging	1.00
R9210:Tex15	UTSW	8	33,574,291 (GRCm38)	missense	possibly damaging	0.91
R9330:Tex15	UTSW	8	33,575,115 (GRCm38)	missense	probably benign	0.01
R9354:Tex15	UTSW	8	33,573,316 (GRCm38)	missense	possibly damaging	0.86
R9365:Tex15	UTSW	8	33,574,536 (GRCm38)	missense	possibly damaging	0.56
R9440:Tex15	UTSW	8	33,582,245 (GRCm38)	missense	possibly damaging	0.90
R9534:Tex15	UTSW	8	33,570,971 (GRCm38)	missense	probably benign	0.45
R9570:Tex15	UTSW	8	33,577,281 (GRCm38)	missense	probably damaging	0.96
R9574:Tex15	UTSW	8	33,574,481 (GRCm38)	missense	probably benign	0.09
R9618:Tex15	UTSW	8	33,572,369 (GRCm38)	missense	probably benign	0.35
R9655:Tex15	UTSW	8	33,576,756 (GRCm38)	nonsense	probably null
R9786:Tex15	UTSW	8	33,572,429 (GRCm38)	missense	probably damaging	1.00
R9798:Tex15	UTSW	8	33,572,693 (GRCm38)	missense	probably damaging	0.98
RF005:Tex15	UTSW	8	33,576,677 (GRCm38)	missense	probably benign	0.05
X0020:Tex15	UTSW	8	33,576,579 (GRCm38)	missense	probably benign	0.03
X0065:Tex15	UTSW	8	33,575,517 (GRCm38)	nonsense	probably null
Z1088:Tex15	UTSW	8	33,571,315 (GRCm38)	missense	possibly damaging	0.89
Z1088:Tex15	UTSW	8	33,574,870 (GRCm38)	missense	probably benign
Z1088:Tex15	UTSW	8	33,571,810 (GRCm38)	missense	possibly damaging	0.68
Z1176:Tex15	UTSW	8	33,574,726 (GRCm38)	missense	possibly damaging	0.84

Predicted Primers

PCR Primer
(F):5'- AGATGTCTACAGTCTTCCCAGCC -3'
(R):5'- TGCTCCAAAGAGTGTTGCG -3'

Sequencing Primer
(F):5'- AGTCTTCCCAGCCCAGAAG -3'
(R):5'- CTCCAAAGAGTGTTGCGGGTAC -3'

Posted On

2016-06-15