Mutagenetix > Incidental Mutation

Incidental Mutation 'R1686:Stard9'

189312

Institutional Source

Beutler Lab

Gene Symbol

Stard9

Ensembl Gene

ENSMUSG00000033705

Gene Name

START domain containing 9

Synonyms

E230025N21Rik, Kif16a, 4831403C07Rik, N-3 kinesin

MMRRC Submission

039719-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.146) question?

Stock #

R1686 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

120629121-120731895 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 120699492 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 2077 (T2077S)

Ref Sequence

ENSEMBL: ENSMUSP00000136055 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000140843] [ENSMUST00000180041]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000070420

SMART Domains

Protein: ENSMUSP00000070111
Gene: ENSMUSG00000033705

Domain	Start	End	E-Value	Type
coiled coil region	97	138	N/A	INTRINSIC
low complexity region	142	151	N/A	INTRINSIC
low complexity region	157	174	N/A	INTRINSIC
low complexity region	234	255	N/A	INTRINSIC
Pfam:START	274	469	3.2e-7	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000140843

SMART Domains

Protein: ENSMUSP00000117178
Gene: ENSMUSG00000033705

Domain	Start	End	E-Value	Type
FHA	63	115	2.8e-4	SMART
coiled coil region	334	354	N/A	INTRINSIC
low complexity region	573	584	N/A	INTRINSIC
low complexity region	866	871	N/A	INTRINSIC
low complexity region	1023	1035	N/A	INTRINSIC
low complexity region	1234	1248	N/A	INTRINSIC
low complexity region	1765	1775	N/A	INTRINSIC
low complexity region	2546	2559	N/A	INTRINSIC
low complexity region	2953	2963	N/A	INTRINSIC
low complexity region	3269	3281	N/A	INTRINSIC
low complexity region	3421	3435	N/A	INTRINSIC
coiled coil region	3767	3808	N/A	INTRINSIC
low complexity region	3812	3821	N/A	INTRINSIC
low complexity region	3827	3844	N/A	INTRINSIC
low complexity region	3904	3925	N/A	INTRINSIC
SCOP:d1jssa_	3946	4142	1e-28	SMART
Blast:START	3947	4143	1e-10	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000180041
AA Change: T2077S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: T2077S

Domain	Start	End	E-Value	Type
KISc	1	392	3.31e-143	SMART
low complexity region	398	409	N/A	INTRINSIC
FHA	481	533	2.8e-4	SMART
coiled coil region	752	772	N/A	INTRINSIC
low complexity region	991	1002	N/A	INTRINSIC
low complexity region	1284	1289	N/A	INTRINSIC
low complexity region	1441	1453	N/A	INTRINSIC
low complexity region	1652	1666	N/A	INTRINSIC
low complexity region	2183	2193	N/A	INTRINSIC
low complexity region	2964	2977	N/A	INTRINSIC
low complexity region	3371	3381	N/A	INTRINSIC
low complexity region	3687	3699	N/A	INTRINSIC
low complexity region	3839	3853	N/A	INTRINSIC
coiled coil region	4185	4226	N/A	INTRINSIC
low complexity region	4230	4239	N/A	INTRINSIC
low complexity region	4245	4262	N/A	INTRINSIC
low complexity region	4322	4343	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.9%

Validation Efficiency

100% (85/85)

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017N19Rik	G	A	10: 100,612,860 (GRCm38)	V400I	probably damaging	Het
Abcb1b	A	G	5: 8,798,782 (GRCm38)	N14S	probably damaging	Het
Adamts14	A	G	10: 61,198,660 (GRCm38)	Y1150H	probably benign	Het
Adgrg3	A	G	8: 95,033,369 (GRCm38)	N72S	probably benign	Het
Akain1	T	A	17: 69,439,532 (GRCm38)	F3I	possibly damaging	Het
Akr1c21	T	C	13: 4,577,453 (GRCm38)	L182P	probably damaging	Het
Arhgap21	A	T	2: 20,881,848 (GRCm38)	Y12N	probably damaging	Het
Aup1	A	T	6: 83,055,245 (GRCm38)	H131L	probably damaging	Het
Bag6	A	G	17: 35,144,952 (GRCm38)	T812A	possibly damaging	Het
BC005561	T	A	5: 104,519,923 (GRCm38)	Y770*	probably null	Het
Bmp2k	A	G	5: 97,063,533 (GRCm38)	Y520C	unknown	Het
Calm4	T	G	13: 3,838,302 (GRCm38)	V136G	probably damaging	Het
Catsper2	A	G	2: 121,400,042 (GRCm38)		probably null	Het
Cc2d2a	A	G	5: 43,739,371 (GRCm38)	T1537A	possibly damaging	Het
Cntn2	A	T	1: 132,526,311 (GRCm38)	V319D	possibly damaging	Het
Cux1	G	A	5: 136,275,381 (GRCm38)	R1314*	probably null	Het
Cxcl12	A	G	6: 117,173,547 (GRCm38)	I79V	probably damaging	Het
Cyp2j6	T	C	4: 96,523,777 (GRCm38)	D418G	probably benign	Het
Ddx28	G	C	8: 106,010,558 (GRCm38)	D289E	probably damaging	Het
Fabp3	C	T	4: 130,312,387 (GRCm38)	T57I	probably benign	Het
Fam135a	A	C	1: 24,029,806 (GRCm38)	S448A	probably benign	Het
Fbxo33	G	T	12: 59,204,840 (GRCm38)	N30K	possibly damaging	Het
Fgf12	A	C	16: 28,398,341 (GRCm38)	Y21D	probably damaging	Het
Galntl5	C	T	5: 25,210,434 (GRCm38)	S288L	probably benign	Het
Gart	G	T	16: 91,625,349 (GRCm38)	A760D	probably damaging	Het
Gba2	A	T	4: 43,573,869 (GRCm38)		probably benign	Het
Gm10518	C	A	1: 179,803,792 (GRCm38)	S139*	probably null	Het
Gm4781	A	T	10: 100,396,975 (GRCm38)		noncoding transcript	Het
Gm9790	A	G	3: 85,915,849 (GRCm38)		noncoding transcript	Het
Gmps	G	A	3: 63,985,654 (GRCm38)	G127R	probably damaging	Het
Golim4	A	T	3: 75,895,136 (GRCm38)	V283E	probably benign	Het
Gprc5a	A	T	6: 135,078,920 (GRCm38)	I122F	possibly damaging	Het
Gzmc	T	C	14: 56,233,884 (GRCm38)	K67E	probably benign	Het
Hapln3	C	A	7: 79,121,890 (GRCm38)	V84L	probably benign	Het
Hif3a	T	A	7: 17,044,864 (GRCm38)	N377Y	possibly damaging	Het
Ifi211	G	A	1: 173,899,403 (GRCm38)	H392Y	probably damaging	Het
Iqgap3	T	A	3: 88,108,356 (GRCm38)		probably benign	Het
Itga10	T	A	3: 96,651,825 (GRCm38)	F410Y	probably damaging	Het
Jup	T	C	11: 100,372,434 (GRCm38)	Y705C	probably damaging	Het
Khsrp	C	T	17: 57,025,597 (GRCm38)	A228T	probably benign	Het
Lmntd2	C	T	7: 141,211,085 (GRCm38)	G445D	probably damaging	Het
Lyst	T	C	13: 13,634,705 (GRCm38)	V320A	possibly damaging	Het
Magel2	T	A	7: 62,378,240 (GRCm38)	H297Q	possibly damaging	Het
Mbd6	T	C	10: 127,287,417 (GRCm38)	E33G	probably damaging	Het
Mob3b	A	G	4: 34,985,910 (GRCm38)		probably benign	Het
Mroh2a	T	C	1: 88,234,612 (GRCm38)		probably null	Het
Mroh2a	C	T	1: 88,230,680 (GRCm38)	R150*	probably null	Het
Mymk	A	T	2: 27,062,334 (GRCm38)	W174R	probably damaging	Het
Nckap1	C	T	2: 80,517,942 (GRCm38)	S889N	probably benign	Het
Nipal3	T	C	4: 135,447,288 (GRCm38)	Y384C	possibly damaging	Het
Nt5c3b	A	G	11: 100,440,094 (GRCm38)		probably benign	Het
Obox6	T	A	7: 15,833,825 (GRCm38)	L232F	probably damaging	Het
Obscn	A	C	11: 59,106,287 (GRCm38)		probably benign	Het
Olfr834	T	C	9: 18,988,543 (GRCm38)	L185P	probably damaging	Het
Phkb	A	G	8: 86,021,649 (GRCm38)	I706V	probably benign	Het
Plcb2	A	G	2: 118,715,687 (GRCm38)		probably benign	Het
Plek2	T	C	12: 78,894,410 (GRCm38)	D216G	probably damaging	Het
Plxnb2	T	C	15: 89,162,462 (GRCm38)	Y855C	probably damaging	Het
Prkcz	T	C	4: 155,271,256 (GRCm38)	T227A	probably damaging	Het
Psma7	A	T	2: 180,037,422 (GRCm38)	D184E	probably benign	Het
Rai14	T	A	15: 10,592,196 (GRCm38)	L204F	probably damaging	Het
Ralgapa2	A	G	2: 146,358,000 (GRCm38)	V1208A	probably benign	Het
Rapgef6	A	G	11: 54,691,632 (GRCm38)	R67G	possibly damaging	Het
Ryr2	C	T	13: 11,603,779 (GRCm38)		probably benign	Het
Satb1	T	C	17: 51,739,999 (GRCm38)	S763G	probably benign	Het
Sdk1	A	T	5: 142,034,537 (GRCm38)	H690L	probably benign	Het
Sfrp5	A	C	19: 42,201,704 (GRCm38)	V103G	possibly damaging	Het
Six6	A	G	12: 72,941,677 (GRCm38)	E208G	probably benign	Het
Sspo	A	T	6: 48,460,400 (GRCm38)	H1364L	probably benign	Het
Tacr3	T	C	3: 134,829,493 (GRCm38)	L74P	probably damaging	Het
Tep1	T	C	14: 50,836,788 (GRCm38)	E1880G	probably benign	Het
Tgfb3	A	T	12: 86,069,743 (GRCm38)		probably benign	Het
Thap7	G	A	16: 17,528,712 (GRCm38)	P136S	probably damaging	Het
Tmc2	T	C	2: 130,256,116 (GRCm38)	V717A	possibly damaging	Het
Usp43	T	A	11: 67,887,767 (GRCm38)	S446C	probably damaging	Het
Vwa3a	C	T	7: 120,780,148 (GRCm38)	S492L	probably damaging	Het
Wdhd1	T	A	14: 47,256,215 (GRCm38)	N16I	probably damaging	Het
Wdr95	A	T	5: 149,593,101 (GRCm38)	D327V	probably damaging	Het
Zfp128	T	G	7: 12,890,636 (GRCm38)	Y310*	probably null	Het

Other mutations in Stard9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Stard9	APN	2	120,701,847 (GRCm38)	missense	possibly damaging	0.52
IGL01122:Stard9	APN	2	120,698,479 (GRCm38)	missense	possibly damaging	0.93
IGL01318:Stard9	APN	2	120,698,719 (GRCm38)	missense	possibly damaging	0.56
IGL01371:Stard9	APN	2	120,701,368 (GRCm38)	missense	probably benign	0.04
IGL01394:Stard9	APN	2	120,706,327 (GRCm38)	missense	possibly damaging	0.78
IGL01531:Stard9	APN	2	120,673,604 (GRCm38)	missense	possibly damaging	0.93
IGL01721:Stard9	APN	2	120,703,330 (GRCm38)	missense	probably damaging	1.00
IGL01810:Stard9	APN	2	120,699,084 (GRCm38)	missense	possibly damaging	0.95
IGL01829:Stard9	APN	2	120,706,446 (GRCm38)	missense	possibly damaging	0.59
IGL01916:Stard9	APN	2	120,668,016 (GRCm38)	missense	probably damaging	1.00
IGL02031:Stard9	APN	2	120,702,339 (GRCm38)	missense	probably benign	0.27
IGL02081:Stard9	APN	2	120,664,910 (GRCm38)	missense	probably damaging	0.98
IGL02558:Stard9	APN	2	120,696,907 (GRCm38)	missense	possibly damaging	0.95
IGL02646:Stard9	APN	2	120,698,992 (GRCm38)	missense	probably damaging	1.00
IGL02873:Stard9	APN	2	120,713,807 (GRCm38)	missense	probably damaging	1.00
IGL03195:Stard9	APN	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
IGL03204:Stard9	APN	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
FR4737:Stard9	UTSW	2	120,696,085 (GRCm38)	small insertion	probably benign
IGL03014:Stard9	UTSW	2	120,702,194 (GRCm38)	unclassified	probably benign
PIT4151001:Stard9	UTSW	2	120,702,756 (GRCm38)	nonsense	probably null
PIT4498001:Stard9	UTSW	2	120,697,435 (GRCm38)	missense	possibly damaging	0.86
R0027:Stard9	UTSW	2	120,703,501 (GRCm38)	missense	probably benign
R0027:Stard9	UTSW	2	120,703,501 (GRCm38)	missense	probably benign
R0038:Stard9	UTSW	2	120,695,832 (GRCm38)	missense	probably benign
R0049:Stard9	UTSW	2	120,699,819 (GRCm38)	missense	probably damaging	1.00
R0049:Stard9	UTSW	2	120,699,819 (GRCm38)	missense	probably damaging	1.00
R0116:Stard9	UTSW	2	120,634,255 (GRCm38)	missense	probably damaging	0.99
R0398:Stard9	UTSW	2	120,696,307 (GRCm38)	missense	probably benign	0.03
R0479:Stard9	UTSW	2	120,697,596 (GRCm38)	missense	probably damaging	1.00
R0556:Stard9	UTSW	2	120,698,923 (GRCm38)	missense	probably benign	0.09
R0589:Stard9	UTSW	2	120,698,547 (GRCm38)	missense	probably benign	0.00
R0609:Stard9	UTSW	2	120,706,306 (GRCm38)	missense	probably damaging	1.00
R0611:Stard9	UTSW	2	120,699,257 (GRCm38)	missense	probably benign	0.00
R0683:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R0751:Stard9	UTSW	2	120,697,485 (GRCm38)	missense	probably benign	0.04
R0833:Stard9	UTSW	2	120,696,999 (GRCm38)	missense	possibly damaging	0.86
R0836:Stard9	UTSW	2	120,696,999 (GRCm38)	missense	possibly damaging	0.86
R0838:Stard9	UTSW	2	120,700,842 (GRCm38)	missense	probably damaging	1.00
R0848:Stard9	UTSW	2	120,695,823 (GRCm38)	missense	probably damaging	1.00
R0849:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R0961:Stard9	UTSW	2	120,693,439 (GRCm38)	missense	probably benign	0.01
R0993:Stard9	UTSW	2	120,705,169 (GRCm38)	missense	probably damaging	1.00
R1005:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1006:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1115:Stard9	UTSW	2	120,692,850 (GRCm38)	missense	probably benign	0.05
R1163:Stard9	UTSW	2	120,696,213 (GRCm38)	missense	possibly damaging	0.86
R1199:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1200:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1331:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1332:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1333:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1334:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1335:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1336:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1338:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1346:Stard9	UTSW	2	120,713,448 (GRCm38)	missense	probably damaging	1.00
R1370:Stard9	UTSW	2	120,697,477 (GRCm38)	missense	probably benign	0.11
R1384:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1401:Stard9	UTSW	2	120,712,847 (GRCm38)	splice site	probably benign
R1416:Stard9	UTSW	2	120,700,972 (GRCm38)	missense	probably benign	0.00
R1453:Stard9	UTSW	2	120,666,376 (GRCm38)	missense	probably damaging	1.00
R1468:Stard9	UTSW	2	120,703,197 (GRCm38)	missense	possibly damaging	0.90
R1468:Stard9	UTSW	2	120,703,197 (GRCm38)	missense	possibly damaging	0.90
R1525:Stard9	UTSW	2	120,702,052 (GRCm38)	missense	probably benign	0.09
R1538:Stard9	UTSW	2	120,696,711 (GRCm38)	missense	probably benign	0.25
R1614:Stard9	UTSW	2	120,697,675 (GRCm38)	missense	possibly damaging	0.95
R1654:Stard9	UTSW	2	120,703,722 (GRCm38)	missense	probably benign	0.37
R1658:Stard9	UTSW	2	120,701,542 (GRCm38)	missense	probably benign	0.02
R1797:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1803:Stard9	UTSW	2	120,701,489 (GRCm38)	missense	probably benign	0.24
R1806:Stard9	UTSW	2	120,679,453 (GRCm38)	splice site	probably null
R1847:Stard9	UTSW	2	120,698,489 (GRCm38)	missense	possibly damaging	0.51
R1853:Stard9	UTSW	2	120,688,751 (GRCm38)	missense	probably damaging	1.00
R1892:Stard9	UTSW	2	120,693,708 (GRCm38)	missense	probably benign	0.01
R1906:Stard9	UTSW	2	120,696,427 (GRCm38)	missense	probably benign	0.00
R1907:Stard9	UTSW	2	120,713,812 (GRCm38)	missense	probably damaging	1.00
R1930:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1933:Stard9	UTSW	2	120,698,656 (GRCm38)	missense	possibly damaging	0.55
R1989:Stard9	UTSW	2	120,701,406 (GRCm38)	missense	probably benign
R1999:Stard9	UTSW	2	120,692,868 (GRCm38)	missense	probably damaging	0.99
R2004:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,664,945 (GRCm38)	missense	possibly damaging	0.90
R2021:Stard9	UTSW	2	120,704,235 (GRCm38)	missense	probably benign	0.05
R2025:Stard9	UTSW	2	120,702,398 (GRCm38)	missense	probably benign	0.20
R2190:Stard9	UTSW	2	120,714,120 (GRCm38)	missense	probably benign	0.22
R2204:Stard9	UTSW	2	120,698,531 (GRCm38)	frame shift	probably null
R2422:Stard9	UTSW	2	120,700,284 (GRCm38)	missense	probably benign	0.29
R3401:Stard9	UTSW	2	120,703,689 (GRCm38)	missense	probably damaging	0.98
R3618:Stard9	UTSW	2	120,699,019 (GRCm38)	missense	possibly damaging	0.49
R3619:Stard9	UTSW	2	120,699,019 (GRCm38)	missense	possibly damaging	0.49
R3900:Stard9	UTSW	2	120,713,549 (GRCm38)	missense	possibly damaging	0.93
R3943:Stard9	UTSW	2	120,698,229 (GRCm38)	missense	probably benign	0.11
R4022:Stard9	UTSW	2	120,704,155 (GRCm38)	missense	probably benign	0.05
R4223:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4224:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4225:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4345:Stard9	UTSW	2	120,701,946 (GRCm38)	missense	probably benign	0.43
R4382:Stard9	UTSW	2	120,634,222 (GRCm38)	missense	probably damaging	1.00
R4453:Stard9	UTSW	2	120,697,791 (GRCm38)	missense	probably benign
R4499:Stard9	UTSW	2	120,700,241 (GRCm38)	missense	probably benign	0.05
R4524:Stard9	UTSW	2	120,696,445 (GRCm38)	missense	probably damaging	1.00
R4671:Stard9	UTSW	2	120,698,640 (GRCm38)	missense	probably damaging	0.98
R4701:Stard9	UTSW	2	120,705,713 (GRCm38)	missense	possibly damaging	0.85
R4744:Stard9	UTSW	2	120,696,123 (GRCm38)	missense	probably benign	0.01
R4822:Stard9	UTSW	2	120,695,941 (GRCm38)	missense	possibly damaging	0.94
R4847:Stard9	UTSW	2	120,703,113 (GRCm38)	missense	probably benign	0.18
R4863:Stard9	UTSW	2	120,700,860 (GRCm38)	missense	probably benign	0.00
R4898:Stard9	UTSW	2	120,706,419 (GRCm38)	nonsense	probably null
R5033:Stard9	UTSW	2	120,693,399 (GRCm38)	missense	probably benign	0.00
R5087:Stard9	UTSW	2	120,697,019 (GRCm38)	nonsense	probably null
R5157:Stard9	UTSW	2	120,697,861 (GRCm38)	missense	probably benign
R5213:Stard9	UTSW	2	120,699,226 (GRCm38)	missense	probably damaging	1.00
R5237:Stard9	UTSW	2	120,699,358 (GRCm38)	missense	probably damaging	0.96
R5257:Stard9	UTSW	2	120,699,343 (GRCm38)	missense	probably damaging	0.99
R5258:Stard9	UTSW	2	120,699,343 (GRCm38)	missense	probably damaging	0.99
R5273:Stard9	UTSW	2	120,705,087 (GRCm38)	missense	possibly damaging	0.94
R5286:Stard9	UTSW	2	120,701,947 (GRCm38)	missense	probably benign	0.43
R5288:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5292:Stard9	UTSW	2	120,699,145 (GRCm38)	missense	probably benign	0.17
R5328:Stard9	UTSW	2	120,699,230 (GRCm38)	missense	probably damaging	1.00
R5385:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5386:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5393:Stard9	UTSW	2	120,702,906 (GRCm38)	missense	possibly damaging	0.87
R5405:Stard9	UTSW	2	120,693,668 (GRCm38)	missense	probably benign	0.17
R5685:Stard9	UTSW	2	120,705,322 (GRCm38)	missense	probably damaging	1.00
R5749:Stard9	UTSW	2	120,703,786 (GRCm38)	missense	probably damaging	1.00
R5780:Stard9	UTSW	2	120,703,396 (GRCm38)	missense	probably benign	0.02
R5901:Stard9	UTSW	2	120,701,370 (GRCm38)	missense	probably damaging	1.00
R5941:Stard9	UTSW	2	120,713,558 (GRCm38)	missense	probably damaging	1.00
R5960:Stard9	UTSW	2	120,699,961 (GRCm38)	missense	probably benign	0.05
R5966:Stard9	UTSW	2	120,697,099 (GRCm38)	missense	probably damaging	1.00
R5967:Stard9	UTSW	2	120,706,894 (GRCm38)	missense	probably damaging	0.99
R6012:Stard9	UTSW	2	120,704,586 (GRCm38)	missense	probably damaging	1.00
R6019:Stard9	UTSW	2	120,693,715 (GRCm38)	frame shift	probably null
R6020:Stard9	UTSW	2	120,693,715 (GRCm38)	frame shift	probably null
R6036:Stard9	UTSW	2	120,700,075 (GRCm38)	missense	probably benign	0.09
R6036:Stard9	UTSW	2	120,700,075 (GRCm38)	missense	probably benign	0.09
R6090:Stard9	UTSW	2	120,693,654 (GRCm38)	missense	probably damaging	0.99
R6192:Stard9	UTSW	2	120,696,760 (GRCm38)	missense	probably damaging	0.99
R6228:Stard9	UTSW	2	120,713,750 (GRCm38)	missense	probably damaging	1.00
R6235:Stard9	UTSW	2	120,713,546 (GRCm38)	missense	probably damaging	1.00
R6280:Stard9	UTSW	2	120,701,127 (GRCm38)	missense	probably benign
R6338:Stard9	UTSW	2	120,697,485 (GRCm38)	missense	probably benign
R6344:Stard9	UTSW	2	120,704,320 (GRCm38)	missense	probably benign	0.12
R6364:Stard9	UTSW	2	120,713,429 (GRCm38)	missense	probably damaging	1.00
R6383:Stard9	UTSW	2	120,666,407 (GRCm38)	critical splice donor site	probably null
R6644:Stard9	UTSW	2	120,695,772 (GRCm38)	missense	probably benign	0.11
R6747:Stard9	UTSW	2	120,698,383 (GRCm38)	missense	possibly damaging	0.62
R6833:Stard9	UTSW	2	120,701,259 (GRCm38)	missense	probably damaging	1.00
R6836:Stard9	UTSW	2	120,699,843 (GRCm38)	missense	probably benign	0.15
R6861:Stard9	UTSW	2	120,705,186 (GRCm38)	missense	probably benign	0.09
R6872:Stard9	UTSW	2	120,714,068 (GRCm38)	nonsense	probably null
R6875:Stard9	UTSW	2	120,697,436 (GRCm38)	missense	probably benign	0.04
R6915:Stard9	UTSW	2	120,702,630 (GRCm38)	missense	probably benign	0.00
R6934:Stard9	UTSW	2	120,697,695 (GRCm38)	missense	probably benign	0.00
R6943:Stard9	UTSW	2	120,702,196 (GRCm38)	missense	probably benign	0.29
R7009:Stard9	UTSW	2	120,697,191 (GRCm38)	missense	probably benign	0.37
R7031:Stard9	UTSW	2	120,700,450 (GRCm38)	missense	possibly damaging	0.61
R7132:Stard9	UTSW	2	120,679,378 (GRCm38)	nonsense	probably null
R7151:Stard9	UTSW	2	120,696,142 (GRCm38)	missense	probably benign
R7154:Stard9	UTSW	2	120,704,542 (GRCm38)	missense	probably benign	0.02
R7154:Stard9	UTSW	2	120,701,314 (GRCm38)	missense	probably benign	0.00
R7165:Stard9	UTSW	2	120,704,158 (GRCm38)	missense	probably damaging	1.00
R7260:Stard9	UTSW	2	120,706,938 (GRCm38)	missense	possibly damaging	0.90
R7270:Stard9	UTSW	2	120,634,274 (GRCm38)	nonsense	probably null
R7282:Stard9	UTSW	2	120,698,503 (GRCm38)	missense	probably benign	0.00
R7344:Stard9	UTSW	2	120,704,686 (GRCm38)	missense	possibly damaging	0.90
R7347:Stard9	UTSW	2	120,666,534 (GRCm38)	missense	probably benign
R7359:Stard9	UTSW	2	120,698,280 (GRCm38)	missense	probably damaging	1.00
R7375:Stard9	UTSW	2	120,665,002 (GRCm38)	splice site	probably null
R7410:Stard9	UTSW	2	120,701,497 (GRCm38)	missense	probably benign	0.41
R7422:Stard9	UTSW	2	120,702,152 (GRCm38)	missense	probably benign	0.21
R7475:Stard9	UTSW	2	120,688,110 (GRCm38)	missense	probably damaging	1.00
R7523:Stard9	UTSW	2	120,699,597 (GRCm38)	missense	probably benign
R7553:Stard9	UTSW	2	120,693,808 (GRCm38)	splice site	probably null
R7624:Stard9	UTSW	2	120,688,146 (GRCm38)	missense	probably benign	0.15
R7761:Stard9	UTSW	2	120,699,379 (GRCm38)	missense	probably benign	0.00
R7794:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R7819:Stard9	UTSW	2	120,700,984 (GRCm38)	missense	probably damaging	1.00
R7823:Stard9	UTSW	2	120,702,106 (GRCm38)	missense	probably damaging	0.96
R7837:Stard9	UTSW	2	120,703,665 (GRCm38)	missense	probably benign	0.06
R7889:Stard9	UTSW	2	120,704,461 (GRCm38)	missense	probably benign	0.11
R7905:Stard9	UTSW	2	120,696,081 (GRCm38)	missense	not run
R7956:Stard9	UTSW	2	120,705,371 (GRCm38)	nonsense	probably null
R8013:Stard9	UTSW	2	120,688,101 (GRCm38)	missense	probably damaging	1.00
R8113:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8114:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8116:Stard9	UTSW	2	120,664,939 (GRCm38)	nonsense	probably null
R8117:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8118:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8170:Stard9	UTSW	2	120,700,048 (GRCm38)	missense	possibly damaging	0.76
R8300:Stard9	UTSW	2	120,704,769 (GRCm38)	missense	possibly damaging	0.71
R8333:Stard9	UTSW	2	120,701,789 (GRCm38)	missense	probably benign	0.00
R8337:Stard9	UTSW	2	120,679,825 (GRCm38)	missense	probably damaging	1.00
R8536:Stard9	UTSW	2	120,714,659 (GRCm38)	missense	possibly damaging	0.93
R8682:Stard9	UTSW	2	120,703,315 (GRCm38)	missense	possibly damaging	0.65
R8696:Stard9	UTSW	2	120,701,114 (GRCm38)	missense	probably benign	0.02
R8708:Stard9	UTSW	2	120,703,578 (GRCm38)	missense	probably damaging	1.00
R8732:Stard9	UTSW	2	120,679,961 (GRCm38)	missense	probably damaging	1.00
R8798:Stard9	UTSW	2	120,704,731 (GRCm38)	missense	probably benign	0.09
R8807:Stard9	UTSW	2	120,705,451 (GRCm38)	missense	probably damaging	1.00
R8807:Stard9	UTSW	2	120,705,462 (GRCm38)	missense	probably damaging	1.00
R8862:Stard9	UTSW	2	120,703,618 (GRCm38)	missense	probably benign
R8920:Stard9	UTSW	2	120,702,607 (GRCm38)	missense	probably damaging	0.96
R9026:Stard9	UTSW	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
R9048:Stard9	UTSW	2	120,677,934 (GRCm38)	missense	probably damaging	0.99
R9049:Stard9	UTSW	2	120,679,937 (GRCm38)	missense	probably benign	0.30
R9152:Stard9	UTSW	2	120,698,587 (GRCm38)	missense	probably damaging	0.99
R9189:Stard9	UTSW	2	120,703,019 (GRCm38)	missense	possibly damaging	0.95
R9238:Stard9	UTSW	2	120,697,966 (GRCm38)	missense	probably damaging	1.00
R9372:Stard9	UTSW	2	120,664,939 (GRCm38)	nonsense	probably null
R9393:Stard9	UTSW	2	120,688,175 (GRCm38)	missense	possibly damaging	0.88
R9444:Stard9	UTSW	2	120,664,933 (GRCm38)	missense	probably damaging	1.00
R9514:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9515:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9516:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9570:Stard9	UTSW	2	120,704,233 (GRCm38)	missense	probably benign	0.02
R9649:Stard9	UTSW	2	120,696,154 (GRCm38)	missense	probably benign	0.20
R9789:Stard9	UTSW	2	120,679,936 (GRCm38)	missense	probably damaging	1.00
X0023:Stard9	UTSW	2	120,702,963 (GRCm38)	missense	possibly damaging	0.92
X0023:Stard9	UTSW	2	120,702,744 (GRCm38)	missense	probably benign	0.00
Z1176:Stard9	UTSW	2	120,698,322 (GRCm38)	missense	probably damaging	1.00
Z1176:Stard9	UTSW	2	120,696,612 (GRCm38)	missense	probably benign
Z1176:Stard9	UTSW	2	120,695,818 (GRCm38)	missense	probably benign	0.01
Z1177:Stard9	UTSW	2	120,673,676 (GRCm38)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TCGACGAAATGGCTAGGCTGATG -3'
(R):5'- AGCTGTGCCTTTCCCCAAAGAATC -3'

Sequencing Primer
(F):5'- CGGGCATCTTAGAAATTGAATCC -3'
(R):5'- AGAATCGCATGTGTCCCTAG -3'

Posted On

2014-05-14