Mutagenetix > Incidental Mutation

Incidental Mutation 'R9393:Stard9'

710649

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

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.185) question?

Stock #

R9393 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

120629121-120731895 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 120688175 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 527 (T527A)

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: 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

possibly damaging
Transcript: ENSMUST00000180041
AA Change: T527A

PolyPhen 2 Score 0.884 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: T527A

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: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	A	G	6: 121,639,311 (GRCm38)	S133G	possibly damaging	Het
Agps	A	G	2: 75,904,912 (GRCm38)	E567G	possibly damaging	Het
Ak9	T	C	10: 41,409,072 (GRCm38)	I1381T	unknown	Het
Apcdd1	C	T	18: 62,922,660 (GRCm38)		probably benign	Het
Arrb1	T	A	7: 99,589,684 (GRCm38)	C150S	probably damaging	Het
Asz1	T	C	6: 18,051,331 (GRCm38)	I450V	probably benign	Het
Atp10b	A	G	11: 43,172,781 (GRCm38)	N181S	probably damaging	Het
Bptf	A	C	11: 107,074,308 (GRCm38)	D1353E	probably benign	Het
Cacna2d1	T	C	5: 15,935,015 (GRCm38)	M1T	probably null	Het
Ccdc106	T	A	7: 5,056,201 (GRCm38)	I6N	possibly damaging	Het
Celf6	A	T	9: 59,603,242 (GRCm38)	Q252L	probably benign	Het
Colgalt2	A	T	1: 152,484,847 (GRCm38)	K212*	probably null	Het
Cryba4	T	C	5: 112,246,766 (GRCm38)	S166G	probably benign	Het
Cyp2w1	A	G	5: 139,356,280 (GRCm38)	E123G	probably benign	Het
Cyp4a10	G	C	4: 115,525,369 (GRCm38)	K285N	probably damaging	Het
Cyth1	G	T	11: 118,183,884 (GRCm38)	T197K	probably benign	Het
Ddhd1	A	G	14: 45,657,228 (GRCm38)	W262R	probably damaging	Het
Dnah8	T	A	17: 30,653,387 (GRCm38)	V450D	possibly damaging	Het
Eml5	C	T	12: 98,876,174 (GRCm38)	V222I	probably benign	Het
Fbxw19	A	G	9: 109,495,805 (GRCm38)	S15P	probably damaging	Het
Fhip2b	G	A	14: 70,594,023 (GRCm38)	Q24*	probably null	Het
Fignl2	C	A	15: 101,053,585 (GRCm38)	R272L	unknown	Het
Gm10842	A	T	11: 105,147,059 (GRCm38)	D56V	unknown	Het
Gmps	T	A	3: 63,993,219 (GRCm38)	N305K	probably benign	Het
Gnai1	A	T	5: 18,360,057 (GRCm38)	L38Q		Het
Golim4	A	T	3: 75,878,157 (GRCm38)	D642E	probably benign	Het
Gp1ba	A	T	11: 70,640,467 (GRCm38)	Q353L	unknown	Het
Gpnmb	T	C	6: 49,048,062 (GRCm38)	S343P	possibly damaging	Het
Hexb	G	A	13: 97,176,828 (GRCm38)	R507*	probably null	Het
Ifitm10	A	T	7: 142,370,967 (GRCm38)	V45D	probably damaging	Het
Khsrp	T	C	17: 57,023,350 (GRCm38)	Y585C	probably damaging	Het
Kif21a	A	T	15: 90,969,778 (GRCm38)	D795E	probably benign	Het
Klkb1	A	T	8: 45,276,355 (GRCm38)	V309E	probably benign	Het
Krtap9-1	C	A	11: 99,873,838 (GRCm38)	C133*	probably null	Het
Krtcap2	T	C	3: 89,246,271 (GRCm38)		probably benign	Het
Lilra5	T	C	7: 4,237,759 (GRCm38)	M1T	probably null	Het
Magi1	G	A	6: 93,682,909 (GRCm38)	T1019I	probably benign	Het
Mdn1	T	A	4: 32,713,825 (GRCm38)	H1967Q		Het
Mgat4f	A	G	1: 134,390,858 (GRCm38)	D456G	probably benign	Het
Mroh2b	A	T	15: 4,951,184 (GRCm38)	T1412S	probably benign	Het
Myh13	A	T	11: 67,352,068 (GRCm38)	M936L	probably benign	Het
Nalf2	C	T	X: 99,845,491 (GRCm38)	R321W	probably damaging	Het
Ncapd3	A	G	9: 27,051,386 (GRCm38)	T373A	possibly damaging	Het
Noc2l	T	C	4: 156,236,327 (GRCm38)		probably null	Het
Nrg4	C	T	9: 55,242,136 (GRCm38)	S59N	probably benign	Het
Nrip1	A	G	16: 76,294,465 (GRCm38)	V68A	probably benign	Het
Or11g24	T	C	14: 50,424,798 (GRCm38)	V93A	probably benign	Het
Or9k2	T	C	10: 130,163,147 (GRCm38)	T60A	probably benign	Het
Pcdhga6	G	T	18: 37,707,159 (GRCm38)		probably benign	Het
Phf20l1	A	G	15: 66,604,106 (GRCm38)	N196S	probably damaging	Het
Ppp4r4	T	A	12: 103,605,037 (GRCm38)	Y787*	probably null	Het
Psma8	G	A	18: 14,706,241 (GRCm38)	R4Q	probably null	Het
Reg4	A	G	3: 98,229,852 (GRCm38)	K46E	probably benign	Het
Rnf14	T	A	18: 38,309,627 (GRCm38)	M327K	possibly damaging	Het
Rtn1	A	T	12: 72,216,812 (GRCm38)	Y753*	probably null	Het
Slc26a11	A	G	11: 119,368,801 (GRCm38)	R275G	probably benign	Het
Stk26	C	T	X: 50,841,741 (GRCm38)		probably benign	Het
Tas1r1	C	T	4: 152,031,956 (GRCm38)	C407Y	probably damaging	Het
Tcstv1b	A	T	13: 120,173,422 (GRCm38)	Y80F	probably benign	Het
Tenm3	A	G	8: 48,674,524 (GRCm38)	S40P	probably damaging	Het
Tespa1	T	A	10: 130,347,197 (GRCm38)	S4T	probably damaging	Het
Tlr11	A	G	14: 50,362,090 (GRCm38)	N511S	probably benign	Het
Tmprss15	A	G	16: 78,957,323 (GRCm38)	I1014T	probably benign	Het
Tpte	T	A	8: 22,284,974 (GRCm38)	M20K	probably benign	Het
Ttn	A	G	2: 76,782,046 (GRCm38)	V17199A	possibly damaging	Het
Tubgcp3	A	G	8: 12,653,411 (GRCm38)	Y305H	probably damaging	Het
Ubr4	T	A	4: 139,485,302 (GRCm38)	V5081E	unknown	Het
Unkl	T	C	17: 25,229,418 (GRCm38)	S322P	probably damaging	Het
Uqcc6	A	G	10: 82,622,641 (GRCm38)	S59P	unknown	Het
Vav3	T	A	3: 109,578,366 (GRCm38)		probably null	Het
Vmn1r76	A	G	7: 11,930,838 (GRCm38)	S150P	probably benign	Het
Xpot	A	G	10: 121,609,695 (GRCm38)		probably null	Het
Xylt1	A	G	7: 117,643,679 (GRCm38)	I650V	probably benign	Het
Zan	C	A	5: 137,405,420 (GRCm38)	A3955S	unknown	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
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	120,705,462 (GRCm38)	missense	probably damaging	1.00
R8807:Stard9	UTSW	2	120,705,451 (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
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'- TCACCTCTTGATGGTTTCAGG -3'
(R):5'- TCTTGGGTCCTAGAATGAGGAG -3'

Sequencing Primer
(F):5'- TTTGTTGGGCTGGGAAATAATC -3'
(R):5'- CTGGCTGAGTAACACATG -3'

Posted On

2022-04-18