Mutagenetix > Incidental Mutation

Incidental Mutation 'R4382:Stard9'

325357

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

041679-MU

Accession Numbers

Essential gene?

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

Stock #

R4382 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

120629121-120731895 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 120634222 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Glycine at position 56 (A56G)

Ref Sequence

ENSEMBL: ENSMUSP00000136055 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000140843] [ENSMUST00000150912] [ENSMUST00000180041]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000140843
AA Change: A56G

PolyPhen 2 Score 0.065 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000117178
Gene: ENSMUSG00000033705
AA Change: A56G

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 damaging
Transcript: ENSMUST00000150912
AA Change: A56G

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

SMART Domains

Protein: ENSMUSP00000121874
Gene: ENSMUSG00000033705
AA Change: A56G

Domain	Start	End	E-Value	Type
KISc	1	392	3.31e-143	SMART
low complexity region	398	409	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000180041
AA Change: A56G

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

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: A56G

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

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.0%
20x: 94.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp2	T	C	2: 91,208,109 (GRCm38)	S309P	possibly damaging	Het
Adam23	T	C	1: 63,566,628 (GRCm38)	Y624H	probably damaging	Het
B4galnt4	T	C	7: 141,070,536 (GRCm38)	V772A	probably damaging	Het
BC067074	T	C	13: 113,322,754 (GRCm38)	I1273T	probably benign	Het
Boc	A	T	16: 44,491,182 (GRCm38)	L726H	probably damaging	Het
Calr3	T	A	8: 72,428,164 (GRCm38)	D120V	probably damaging	Het
Ccdc92b	G	A	11: 74,630,016 (GRCm38)	S48N	probably damaging	Het
Ceacam12	C	T	7: 18,066,034 (GRCm38)		probably benign	Het
Clca3a1	T	A	3: 144,760,722 (GRCm38)	M1L	probably benign	Het
Cnot1	T	C	8: 95,769,779 (GRCm38)	T300A	probably damaging	Het
Col12a1	A	T	9: 79,630,741 (GRCm38)	Y2514*	probably null	Het
Col6a6	G	A	9: 105,783,690 (GRCm38)	R407W	probably damaging	Het
Csnk1g1	T	C	9: 66,019,908 (GRCm38)	V119A	probably damaging	Het
Ddx60	G	A	8: 61,948,978 (GRCm38)		probably null	Het
Dnajb12	A	T	10: 59,897,499 (GRCm38)	K372N	probably benign	Het
Fhl5	A	C	4: 25,200,118 (GRCm38)	C239G	probably benign	Het
Gad2	G	A	2: 22,685,410 (GRCm38)	V509I	probably benign	Het
Glrb	T	A	3: 80,879,639 (GRCm38)	R72S	probably damaging	Het
Gm13124	T	A	4: 144,555,026 (GRCm38)	T399S	possibly damaging	Het
Gm6811	T	C	17: 21,094,603 (GRCm38)		noncoding transcript	Het
Hecw1	C	T	13: 14,316,164 (GRCm38)	D748N	probably damaging	Het
Hk2	A	T	6: 82,735,341 (GRCm38)	L542Q	probably null	Het
Iglc1	A	T	16: 19,061,758 (GRCm38)	C104*	probably null	Het
Kel	T	A	6: 41,698,400 (GRCm38)	T306S	probably benign	Het
Lpo	T	C	11: 87,822,201 (GRCm38)	D25G	probably benign	Het
Mboat7	T	A	7: 3,688,546 (GRCm38)	Y109F	possibly damaging	Het
Myh15	T	G	16: 49,142,943 (GRCm38)	N1082K	probably benign	Het
Nagk	A	G	6: 83,798,011 (GRCm38)	E90G	probably benign	Het
Nagpa	A	T	16: 5,203,955 (GRCm38)	F10I	possibly damaging	Het
Olfr460	T	A	6: 40,572,064 (GRCm38)	L226H	probably damaging	Het
Otog	T	A	7: 46,289,698 (GRCm38)	C2051S	probably damaging	Het
Ptpn6	A	G	6: 124,727,398 (GRCm38)	V315A	possibly damaging	Het
Rbp3	G	C	14: 33,955,296 (GRCm38)	E400D	probably benign	Het
Rnf41	T	C	10: 128,436,523 (GRCm38)	S140P	probably benign	Het
Ros1	C	T	10: 52,120,959 (GRCm38)	V1206I	possibly damaging	Het
Scgb2b12	T	A	7: 32,325,445 (GRCm38)	E112D	probably benign	Het
Serpinb3b	T	A	1: 107,155,543 (GRCm38)	M210L	probably damaging	Het
Sipa1l1	A	G	12: 82,446,822 (GRCm38)	R1672G	possibly damaging	Het
Smc5	A	G	19: 23,268,846 (GRCm38)	S70P	probably benign	Het
Spen	C	T	4: 141,473,139 (GRCm38)	G2703S	possibly damaging	Het
Wtap	A	G	17: 12,975,420 (GRCm38)	S87P	probably damaging	Het
Zzef1	T	G	11: 72,875,112 (GRCm38)	S1488R	probably benign	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
R1686:Stard9	UTSW	2	120,699,492 (GRCm38)	missense	probably benign	0.00
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
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'- AGGCTTTCTCTGCTGAGCTG -3'
(R):5'- TCTGGAAAAGCAGTTTGCATGG -3'

Sequencing Primer
(F):5'- ACCAGATCCCATTACAGGTGGTTG -3'
(R):5'- GCAGTTTGCATGGAGATTTTCC -3'

Posted On

2015-07-06