Mutagenetix > Incidental Mutation

Incidental Mutation 'R0833:Stard9'

77606

Institutional Source

Beutler Lab

Gene Symbol

Stard9

Ensembl Gene

ENSMUSG00000033705

Gene Name

StAR related lipid transfer domain containing 9

Synonyms

4831403C07Rik, E230025N21Rik, Kif16a, N-3 kinesin

MMRRC Submission

039012-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.173) question?

Stock #

R0833 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

120459602-120562376 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 120527480 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Alanine at position 1246 (S1246A)

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

possibly damaging
Transcript: ENSMUST00000180041
AA Change: S1246A

PolyPhen 2 Score 0.855 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: S1246A

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

0.0700

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.3%
20x: 94.6%

Validation Efficiency

100% (97/97)

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	T	C	10: 87,000,931 (GRCm39)	L41P	probably damaging	Het
3110082I17Rik	A	G	5: 139,349,875 (GRCm39)	V58A	possibly damaging	Het
4932415M13Rik	A	T	17: 54,031,374 (GRCm39)		noncoding transcript	Het
Aldh1a7	C	T	19: 20,679,607 (GRCm39)	V390M	probably damaging	Het
Alg14	A	G	3: 121,092,259 (GRCm39)	H34R	probably damaging	Het
Ankrd27	A	G	7: 35,307,772 (GRCm39)	N337S	probably damaging	Het
Apoa2	T	A	1: 171,052,948 (GRCm39)		probably benign	Het
Arl2	T	G	19: 6,186,052 (GRCm39)	K126T	probably damaging	Het
Ascc3	T	C	10: 50,721,762 (GRCm39)	W2072R	probably benign	Het
Astl	T	C	2: 127,184,339 (GRCm39)	F21L	probably benign	Het
Asxl3	A	G	18: 22,649,097 (GRCm39)	D362G	probably damaging	Het
Bdp1	A	T	13: 100,172,333 (GRCm39)	H2094Q	probably benign	Het
Cacna2d4	C	T	6: 119,284,247 (GRCm39)	R745W	probably damaging	Het
Ccdc85a	T	A	11: 28,533,296 (GRCm39)	I83F	probably damaging	Het
Ccnt2	T	A	1: 127,730,131 (GRCm39)	M336K	probably benign	Het
Cd226	A	C	18: 89,225,144 (GRCm39)		probably benign	Het
Ceacam23	C	A	7: 17,638,906 (GRCm39)	A301E	possibly damaging	Het
Ces1f	A	T	8: 93,996,652 (GRCm39)	S214T	probably damaging	Het
Clip1	T	C	5: 123,768,784 (GRCm39)	D605G	probably benign	Het
Col26a1	A	G	5: 136,794,154 (GRCm39)		probably null	Het
Crtc1	A	G	8: 70,845,663 (GRCm39)	V306A	probably benign	Het
D130043K22Rik	G	A	13: 25,047,563 (GRCm39)		probably benign	Het
D17H6S53E	A	T	17: 35,346,385 (GRCm39)		probably null	Het
Dnah11	G	A	12: 118,160,397 (GRCm39)	A111V	probably benign	Het
Dyrk2	T	C	10: 118,697,027 (GRCm39)	H77R	probably benign	Het
Epha3	A	G	16: 63,423,882 (GRCm39)		probably benign	Het
Epn2	T	C	11: 61,410,317 (GRCm39)	N611S	probably benign	Het
Erich6	A	C	3: 58,526,365 (GRCm39)		probably benign	Het
Fam217b	T	C	2: 178,062,782 (GRCm39)	S249P	probably benign	Het
Fam219b	A	G	9: 57,445,299 (GRCm39)		probably benign	Het
Fryl	A	T	5: 73,246,424 (GRCm39)		probably benign	Het
Ftdc2	G	A	16: 58,455,886 (GRCm39)	S129L	probably damaging	Het
Gm14496	T	C	2: 181,638,059 (GRCm39)	W378R	probably damaging	Het
Gm57858	A	G	3: 36,074,362 (GRCm39)		probably benign	Het
Gm8674	A	T	13: 50,058,611 (GRCm39)		noncoding transcript	Het
Grap	T	A	11: 61,551,065 (GRCm39)	D32E	possibly damaging	Het
Grk2	C	A	19: 4,339,385 (GRCm39)	L428F	probably damaging	Het
Grm8	T	A	6: 27,363,178 (GRCm39)	E779V	probably damaging	Het
Hipk1	A	G	3: 103,661,612 (GRCm39)	S670P	probably damaging	Het
Ilrun	A	T	17: 28,005,112 (GRCm39)	S148R	probably damaging	Het
Itgae	A	T	11: 73,020,032 (GRCm39)	M845L	probably benign	Het
Itih1	A	T	14: 30,663,512 (GRCm39)	V164E	probably damaging	Het
Itpka	T	A	2: 119,581,312 (GRCm39)	N448K	probably damaging	Het
Jak3	A	C	8: 72,136,622 (GRCm39)	N643T	probably damaging	Het
Lrfn5	A	C	12: 61,886,454 (GRCm39)	T81P	probably damaging	Het
Lrrc45	T	A	11: 120,609,019 (GRCm39)		probably null	Het
Marchf6	T	C	15: 31,480,437 (GRCm39)	Y562C	probably benign	Het
Mcrs1	T	C	15: 99,141,330 (GRCm39)		probably benign	Het
Meis1	G	A	11: 18,831,767 (GRCm39)	H424Y	possibly damaging	Het
Mst1r	A	G	9: 107,791,975 (GRCm39)	N837S	probably benign	Het
Mst1r	G	A	9: 107,790,366 (GRCm39)	V660I	probably benign	Het
Mthfd2l	T	C	5: 91,094,801 (GRCm39)	V90A	probably damaging	Het
Mtnr1a	A	T	8: 45,540,974 (GRCm39)	I312F	probably benign	Het
Or10g3b	T	C	14: 52,586,835 (GRCm39)	I223V	probably benign	Het
Or51g1	C	A	7: 102,634,043 (GRCm39)	L109F	possibly damaging	Het
Or8b12b	T	C	9: 37,684,372 (GRCm39)	V139A	probably benign	Het
Otog	C	T	7: 45,918,786 (GRCm39)	T954I	possibly damaging	Het
Pdcd6	A	G	13: 74,464,443 (GRCm39)		probably benign	Het
Phlpp2	A	G	8: 110,663,738 (GRCm39)	T926A	probably damaging	Het
Plec	GGCAGCAG	GGCAGCAGCAG	15: 76,066,107 (GRCm39)		probably benign	Het
Plekha5	T	A	6: 140,535,360 (GRCm39)		probably benign	Het
Ppp1r16a	C	T	15: 76,577,869 (GRCm39)	Q328*	probably null	Het
Pramel18	G	A	4: 101,767,294 (GRCm39)	C181Y	probably damaging	Het
Pramel23	A	T	4: 143,425,056 (GRCm39)	M129K	probably benign	Het
Rab27b	T	C	18: 70,120,112 (GRCm39)		probably benign	Het
Rapsn	T	C	2: 90,867,153 (GRCm39)	Y152H	probably damaging	Het
Rasd1	A	T	11: 59,855,379 (GRCm39)	F85I	probably damaging	Het
Rgs1	A	T	1: 144,123,671 (GRCm39)	S85T	probably damaging	Het
Samd9l	T	C	6: 3,372,725 (GRCm39)	E1512G	possibly damaging	Het
Sgsm1	C	T	5: 113,427,050 (GRCm39)	A127T	probably benign	Het
Shc1	A	G	3: 89,330,276 (GRCm39)	D70G	probably damaging	Het
Slc26a1	T	A	5: 108,821,389 (GRCm39)	T167S	probably benign	Het
Slc26a7	A	T	4: 14,593,873 (GRCm39)	Y81N	probably damaging	Het
Slc2a12	T	C	10: 22,577,915 (GRCm39)		probably benign	Het
Slc30a7	T	A	3: 115,783,789 (GRCm39)		probably null	Het
Slc44a5	T	C	3: 153,971,111 (GRCm39)	S654P	probably damaging	Het
Stxbp5	A	T	10: 9,740,843 (GRCm39)	S116R	probably damaging	Het
Syvn1	C	T	19: 6,102,483 (GRCm39)	P517L	probably benign	Het
Tas2r105	T	C	6: 131,664,393 (GRCm39)	I12V	probably benign	Het
Tas2r121	A	G	6: 132,677,325 (GRCm39)	S216P	probably damaging	Het
Tcof1	T	C	18: 60,978,904 (GRCm39)	D48G	probably damaging	Het
Tgm3	C	T	2: 129,868,602 (GRCm39)		probably benign	Het
Tle2	T	C	10: 81,424,781 (GRCm39)	F667L	probably damaging	Het
Tnfaip3	C	A	10: 18,878,697 (GRCm39)	A704S	probably benign	Het
Trabd2b	A	G	4: 114,437,519 (GRCm39)	Q232R	probably benign	Het
Ttc28	T	A	5: 111,378,947 (GRCm39)	I1144N	probably damaging	Het
Ucp3	T	A	7: 100,128,748 (GRCm39)	C25*	probably null	Het
Ugt3a1	A	G	15: 9,370,236 (GRCm39)	D460G	probably damaging	Het
Urb1	T	C	16: 90,592,336 (GRCm39)	D308G	possibly damaging	Het
Ush1g	G	T	11: 115,209,694 (GRCm39)	R167S	possibly damaging	Het
Vav3	A	G	3: 109,554,995 (GRCm39)	N81S	possibly damaging	Het
Vmn2r108	A	T	17: 20,691,721 (GRCm39)	D267E	probably benign	Het
Zng1	A	G	19: 24,918,203 (GRCm39)		probably benign	Het

Other mutations in Stard9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Stard9	APN	2	120,532,328 (GRCm39)	missense	possibly damaging	0.52
IGL01122:Stard9	APN	2	120,528,960 (GRCm39)	missense	possibly damaging	0.93
IGL01318:Stard9	APN	2	120,529,200 (GRCm39)	missense	possibly damaging	0.56
IGL01371:Stard9	APN	2	120,531,849 (GRCm39)	missense	probably benign	0.04
IGL01394:Stard9	APN	2	120,536,808 (GRCm39)	missense	possibly damaging	0.78
IGL01531:Stard9	APN	2	120,504,085 (GRCm39)	missense	possibly damaging	0.93
IGL01721:Stard9	APN	2	120,533,811 (GRCm39)	missense	probably damaging	1.00
IGL01810:Stard9	APN	2	120,529,565 (GRCm39)	missense	possibly damaging	0.95
IGL01829:Stard9	APN	2	120,536,927 (GRCm39)	missense	possibly damaging	0.59
IGL01916:Stard9	APN	2	120,498,497 (GRCm39)	missense	probably damaging	1.00
IGL02031:Stard9	APN	2	120,532,820 (GRCm39)	missense	probably benign	0.27
IGL02081:Stard9	APN	2	120,495,391 (GRCm39)	missense	probably damaging	0.98
IGL02558:Stard9	APN	2	120,527,388 (GRCm39)	missense	possibly damaging	0.95
IGL02646:Stard9	APN	2	120,529,473 (GRCm39)	missense	probably damaging	1.00
IGL02873:Stard9	APN	2	120,544,288 (GRCm39)	missense	probably damaging	1.00
IGL03195:Stard9	APN	2	120,536,283 (GRCm39)	missense	probably damaging	1.00
IGL03204:Stard9	APN	2	120,536,283 (GRCm39)	missense	probably damaging	1.00
FR4737:Stard9	UTSW	2	120,526,566 (GRCm39)	small insertion	probably benign
IGL03014:Stard9	UTSW	2	120,532,675 (GRCm39)	unclassified	probably benign
PIT4151001:Stard9	UTSW	2	120,533,237 (GRCm39)	nonsense	probably null
PIT4498001:Stard9	UTSW	2	120,527,916 (GRCm39)	missense	possibly damaging	0.86
R0027:Stard9	UTSW	2	120,533,982 (GRCm39)	missense	probably benign
R0027:Stard9	UTSW	2	120,533,982 (GRCm39)	missense	probably benign
R0038:Stard9	UTSW	2	120,526,313 (GRCm39)	missense	probably benign
R0049:Stard9	UTSW	2	120,530,300 (GRCm39)	missense	probably damaging	1.00
R0049:Stard9	UTSW	2	120,530,300 (GRCm39)	missense	probably damaging	1.00
R0116:Stard9	UTSW	2	120,464,736 (GRCm39)	missense	probably damaging	0.99
R0398:Stard9	UTSW	2	120,526,788 (GRCm39)	missense	probably benign	0.03
R0479:Stard9	UTSW	2	120,528,077 (GRCm39)	missense	probably damaging	1.00
R0556:Stard9	UTSW	2	120,529,404 (GRCm39)	missense	probably benign	0.09
R0589:Stard9	UTSW	2	120,529,028 (GRCm39)	missense	probably benign	0.00
R0609:Stard9	UTSW	2	120,536,787 (GRCm39)	missense	probably damaging	1.00
R0611:Stard9	UTSW	2	120,529,738 (GRCm39)	missense	probably benign	0.00
R0683:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R0751:Stard9	UTSW	2	120,527,966 (GRCm39)	missense	probably benign	0.04
R0836:Stard9	UTSW	2	120,527,480 (GRCm39)	missense	possibly damaging	0.86
R0838:Stard9	UTSW	2	120,531,323 (GRCm39)	missense	probably damaging	1.00
R0848:Stard9	UTSW	2	120,526,304 (GRCm39)	missense	probably damaging	1.00
R0849:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R0961:Stard9	UTSW	2	120,523,920 (GRCm39)	missense	probably benign	0.01
R0993:Stard9	UTSW	2	120,535,650 (GRCm39)	missense	probably damaging	1.00
R1005:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1006:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1115:Stard9	UTSW	2	120,523,331 (GRCm39)	missense	probably benign	0.05
R1163:Stard9	UTSW	2	120,526,694 (GRCm39)	missense	possibly damaging	0.86
R1199:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1200:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1331:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1332:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1333:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1334:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1335:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1336:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1338:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1346:Stard9	UTSW	2	120,543,929 (GRCm39)	missense	probably damaging	1.00
R1370:Stard9	UTSW	2	120,527,958 (GRCm39)	missense	probably benign	0.11
R1384:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1401:Stard9	UTSW	2	120,543,328 (GRCm39)	splice site	probably benign
R1416:Stard9	UTSW	2	120,531,453 (GRCm39)	missense	probably benign	0.00
R1453:Stard9	UTSW	2	120,496,857 (GRCm39)	missense	probably damaging	1.00
R1468:Stard9	UTSW	2	120,533,678 (GRCm39)	missense	possibly damaging	0.90
R1468:Stard9	UTSW	2	120,533,678 (GRCm39)	missense	possibly damaging	0.90
R1525:Stard9	UTSW	2	120,532,533 (GRCm39)	missense	probably benign	0.09
R1538:Stard9	UTSW	2	120,527,192 (GRCm39)	missense	probably benign	0.25
R1614:Stard9	UTSW	2	120,528,156 (GRCm39)	missense	possibly damaging	0.95
R1654:Stard9	UTSW	2	120,534,203 (GRCm39)	missense	probably benign	0.37
R1658:Stard9	UTSW	2	120,532,023 (GRCm39)	missense	probably benign	0.02
R1686:Stard9	UTSW	2	120,529,973 (GRCm39)	missense	probably benign	0.00
R1797:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1803:Stard9	UTSW	2	120,531,970 (GRCm39)	missense	probably benign	0.24
R1806:Stard9	UTSW	2	120,509,934 (GRCm39)	splice site	probably null
R1847:Stard9	UTSW	2	120,528,970 (GRCm39)	missense	possibly damaging	0.51
R1853:Stard9	UTSW	2	120,519,232 (GRCm39)	missense	probably damaging	1.00
R1892:Stard9	UTSW	2	120,524,189 (GRCm39)	missense	probably benign	0.01
R1906:Stard9	UTSW	2	120,526,908 (GRCm39)	missense	probably benign	0.00
R1907:Stard9	UTSW	2	120,544,293 (GRCm39)	missense	probably damaging	1.00
R1930:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R1933:Stard9	UTSW	2	120,529,137 (GRCm39)	missense	possibly damaging	0.55
R1989:Stard9	UTSW	2	120,531,887 (GRCm39)	missense	probably benign
R1999:Stard9	UTSW	2	120,523,349 (GRCm39)	missense	probably damaging	0.99
R2004:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,504,117 (GRCm39)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,495,426 (GRCm39)	missense	possibly damaging	0.90
R2021:Stard9	UTSW	2	120,534,716 (GRCm39)	missense	probably benign	0.05
R2025:Stard9	UTSW	2	120,532,879 (GRCm39)	missense	probably benign	0.20
R2190:Stard9	UTSW	2	120,544,601 (GRCm39)	missense	probably benign	0.22
R2204:Stard9	UTSW	2	120,529,012 (GRCm39)	frame shift	probably null
R2422:Stard9	UTSW	2	120,530,765 (GRCm39)	missense	probably benign	0.29
R3401:Stard9	UTSW	2	120,534,170 (GRCm39)	missense	probably damaging	0.98
R3618:Stard9	UTSW	2	120,529,500 (GRCm39)	missense	possibly damaging	0.49
R3619:Stard9	UTSW	2	120,529,500 (GRCm39)	missense	possibly damaging	0.49
R3900:Stard9	UTSW	2	120,544,030 (GRCm39)	missense	possibly damaging	0.93
R3943:Stard9	UTSW	2	120,528,710 (GRCm39)	missense	probably benign	0.11
R4022:Stard9	UTSW	2	120,534,636 (GRCm39)	missense	probably benign	0.05
R4223:Stard9	UTSW	2	120,495,472 (GRCm39)	missense	possibly damaging	0.95
R4224:Stard9	UTSW	2	120,495,472 (GRCm39)	missense	possibly damaging	0.95
R4225:Stard9	UTSW	2	120,495,472 (GRCm39)	missense	possibly damaging	0.95
R4345:Stard9	UTSW	2	120,532,427 (GRCm39)	missense	probably benign	0.43
R4382:Stard9	UTSW	2	120,464,703 (GRCm39)	missense	probably damaging	1.00
R4453:Stard9	UTSW	2	120,528,272 (GRCm39)	missense	probably benign
R4499:Stard9	UTSW	2	120,530,722 (GRCm39)	missense	probably benign	0.05
R4524:Stard9	UTSW	2	120,526,926 (GRCm39)	missense	probably damaging	1.00
R4671:Stard9	UTSW	2	120,529,121 (GRCm39)	missense	probably damaging	0.98
R4701:Stard9	UTSW	2	120,536,194 (GRCm39)	missense	possibly damaging	0.85
R4744:Stard9	UTSW	2	120,526,604 (GRCm39)	missense	probably benign	0.01
R4822:Stard9	UTSW	2	120,526,422 (GRCm39)	missense	possibly damaging	0.94
R4847:Stard9	UTSW	2	120,533,594 (GRCm39)	missense	probably benign	0.18
R4863:Stard9	UTSW	2	120,531,341 (GRCm39)	missense	probably benign	0.00
R4898:Stard9	UTSW	2	120,536,900 (GRCm39)	nonsense	probably null
R5033:Stard9	UTSW	2	120,523,880 (GRCm39)	missense	probably benign	0.00
R5087:Stard9	UTSW	2	120,527,500 (GRCm39)	nonsense	probably null
R5157:Stard9	UTSW	2	120,528,342 (GRCm39)	missense	probably benign
R5213:Stard9	UTSW	2	120,529,707 (GRCm39)	missense	probably damaging	1.00
R5237:Stard9	UTSW	2	120,529,839 (GRCm39)	missense	probably damaging	0.96
R5257:Stard9	UTSW	2	120,529,824 (GRCm39)	missense	probably damaging	0.99
R5258:Stard9	UTSW	2	120,529,824 (GRCm39)	missense	probably damaging	0.99
R5273:Stard9	UTSW	2	120,535,568 (GRCm39)	missense	possibly damaging	0.94
R5286:Stard9	UTSW	2	120,532,428 (GRCm39)	missense	probably benign	0.43
R5288:Stard9	UTSW	2	120,531,111 (GRCm39)	missense	probably damaging	0.98
R5292:Stard9	UTSW	2	120,529,626 (GRCm39)	missense	probably benign	0.17
R5328:Stard9	UTSW	2	120,529,711 (GRCm39)	missense	probably damaging	1.00
R5385:Stard9	UTSW	2	120,531,111 (GRCm39)	missense	probably damaging	0.98
R5386:Stard9	UTSW	2	120,531,111 (GRCm39)	missense	probably damaging	0.98
R5393:Stard9	UTSW	2	120,533,387 (GRCm39)	missense	possibly damaging	0.87
R5405:Stard9	UTSW	2	120,524,149 (GRCm39)	missense	probably benign	0.17
R5685:Stard9	UTSW	2	120,535,803 (GRCm39)	missense	probably damaging	1.00
R5749:Stard9	UTSW	2	120,534,267 (GRCm39)	missense	probably damaging	1.00
R5780:Stard9	UTSW	2	120,533,877 (GRCm39)	missense	probably benign	0.02
R5901:Stard9	UTSW	2	120,531,851 (GRCm39)	missense	probably damaging	1.00
R5941:Stard9	UTSW	2	120,544,039 (GRCm39)	missense	probably damaging	1.00
R5960:Stard9	UTSW	2	120,530,442 (GRCm39)	missense	probably benign	0.05
R5966:Stard9	UTSW	2	120,527,580 (GRCm39)	missense	probably damaging	1.00
R5967:Stard9	UTSW	2	120,537,375 (GRCm39)	missense	probably damaging	0.99
R6012:Stard9	UTSW	2	120,535,067 (GRCm39)	missense	probably damaging	1.00
R6019:Stard9	UTSW	2	120,524,196 (GRCm39)	frame shift	probably null
R6020:Stard9	UTSW	2	120,524,196 (GRCm39)	frame shift	probably null
R6036:Stard9	UTSW	2	120,530,556 (GRCm39)	missense	probably benign	0.09
R6036:Stard9	UTSW	2	120,530,556 (GRCm39)	missense	probably benign	0.09
R6090:Stard9	UTSW	2	120,524,135 (GRCm39)	missense	probably damaging	0.99
R6192:Stard9	UTSW	2	120,527,241 (GRCm39)	missense	probably damaging	0.99
R6228:Stard9	UTSW	2	120,544,231 (GRCm39)	missense	probably damaging	1.00
R6235:Stard9	UTSW	2	120,544,027 (GRCm39)	missense	probably damaging	1.00
R6280:Stard9	UTSW	2	120,531,608 (GRCm39)	missense	probably benign
R6338:Stard9	UTSW	2	120,527,966 (GRCm39)	missense	probably benign
R6344:Stard9	UTSW	2	120,534,801 (GRCm39)	missense	probably benign	0.12
R6364:Stard9	UTSW	2	120,543,910 (GRCm39)	missense	probably damaging	1.00
R6383:Stard9	UTSW	2	120,496,888 (GRCm39)	critical splice donor site	probably null
R6644:Stard9	UTSW	2	120,526,253 (GRCm39)	missense	probably benign	0.11
R6747:Stard9	UTSW	2	120,528,864 (GRCm39)	missense	possibly damaging	0.62
R6833:Stard9	UTSW	2	120,531,740 (GRCm39)	missense	probably damaging	1.00
R6836:Stard9	UTSW	2	120,530,324 (GRCm39)	missense	probably benign	0.15
R6861:Stard9	UTSW	2	120,535,667 (GRCm39)	missense	probably benign	0.09
R6872:Stard9	UTSW	2	120,544,549 (GRCm39)	nonsense	probably null
R6875:Stard9	UTSW	2	120,527,917 (GRCm39)	missense	probably benign	0.04
R6915:Stard9	UTSW	2	120,533,111 (GRCm39)	missense	probably benign	0.00
R6934:Stard9	UTSW	2	120,528,176 (GRCm39)	missense	probably benign	0.00
R6943:Stard9	UTSW	2	120,532,677 (GRCm39)	missense	probably benign	0.29
R7009:Stard9	UTSW	2	120,527,672 (GRCm39)	missense	probably benign	0.37
R7031:Stard9	UTSW	2	120,530,931 (GRCm39)	missense	possibly damaging	0.61
R7132:Stard9	UTSW	2	120,509,859 (GRCm39)	nonsense	probably null
R7151:Stard9	UTSW	2	120,526,623 (GRCm39)	missense	probably benign
R7154:Stard9	UTSW	2	120,535,023 (GRCm39)	missense	probably benign	0.02
R7154:Stard9	UTSW	2	120,531,795 (GRCm39)	missense	probably benign	0.00
R7165:Stard9	UTSW	2	120,534,639 (GRCm39)	missense	probably damaging	1.00
R7260:Stard9	UTSW	2	120,537,419 (GRCm39)	missense	possibly damaging	0.90
R7270:Stard9	UTSW	2	120,464,755 (GRCm39)	nonsense	probably null
R7282:Stard9	UTSW	2	120,528,984 (GRCm39)	missense	probably benign	0.00
R7344:Stard9	UTSW	2	120,535,167 (GRCm39)	missense	possibly damaging	0.90
R7347:Stard9	UTSW	2	120,497,015 (GRCm39)	missense	probably benign
R7359:Stard9	UTSW	2	120,528,761 (GRCm39)	missense	probably damaging	1.00
R7375:Stard9	UTSW	2	120,495,483 (GRCm39)	splice site	probably null
R7410:Stard9	UTSW	2	120,531,978 (GRCm39)	missense	probably benign	0.41
R7422:Stard9	UTSW	2	120,532,633 (GRCm39)	missense	probably benign	0.21
R7475:Stard9	UTSW	2	120,518,591 (GRCm39)	missense	probably damaging	1.00
R7523:Stard9	UTSW	2	120,530,078 (GRCm39)	missense	probably benign
R7553:Stard9	UTSW	2	120,524,289 (GRCm39)	splice site	probably null
R7624:Stard9	UTSW	2	120,518,627 (GRCm39)	missense	probably benign	0.15
R7761:Stard9	UTSW	2	120,529,860 (GRCm39)	missense	probably benign	0.00
R7794:Stard9	UTSW	2	120,534,911 (GRCm39)	missense	probably benign	0.01
R7819:Stard9	UTSW	2	120,531,465 (GRCm39)	missense	probably damaging	1.00
R7823:Stard9	UTSW	2	120,532,587 (GRCm39)	missense	probably damaging	0.96
R7837:Stard9	UTSW	2	120,534,146 (GRCm39)	missense	probably benign	0.06
R7889:Stard9	UTSW	2	120,534,942 (GRCm39)	missense	probably benign	0.11
R7905:Stard9	UTSW	2	120,526,562 (GRCm39)	missense	not run
R7956:Stard9	UTSW	2	120,535,852 (GRCm39)	nonsense	probably null
R8013:Stard9	UTSW	2	120,518,582 (GRCm39)	missense	probably damaging	1.00
R8113:Stard9	UTSW	2	120,534,911 (GRCm39)	missense	probably benign	0.01
R8114:Stard9	UTSW	2	120,534,911 (GRCm39)	missense	probably benign	0.01
R8116:Stard9	UTSW	2	120,495,420 (GRCm39)	nonsense	probably null
R8117:Stard9	UTSW	2	120,534,911 (GRCm39)	missense	probably benign	0.01
R8118:Stard9	UTSW	2	120,534,911 (GRCm39)	missense	probably benign	0.01
R8170:Stard9	UTSW	2	120,530,529 (GRCm39)	missense	possibly damaging	0.76
R8300:Stard9	UTSW	2	120,535,250 (GRCm39)	missense	possibly damaging	0.71
R8333:Stard9	UTSW	2	120,532,270 (GRCm39)	missense	probably benign	0.00
R8337:Stard9	UTSW	2	120,510,306 (GRCm39)	missense	probably damaging	1.00
R8536:Stard9	UTSW	2	120,545,140 (GRCm39)	missense	possibly damaging	0.93
R8682:Stard9	UTSW	2	120,533,796 (GRCm39)	missense	possibly damaging	0.65
R8696:Stard9	UTSW	2	120,531,595 (GRCm39)	missense	probably benign	0.02
R8708:Stard9	UTSW	2	120,534,059 (GRCm39)	missense	probably damaging	1.00
R8732:Stard9	UTSW	2	120,510,442 (GRCm39)	missense	probably damaging	1.00
R8798:Stard9	UTSW	2	120,535,212 (GRCm39)	missense	probably benign	0.09
R8807:Stard9	UTSW	2	120,535,932 (GRCm39)	missense	probably damaging	1.00
R8807:Stard9	UTSW	2	120,535,943 (GRCm39)	missense	probably damaging	1.00
R8862:Stard9	UTSW	2	120,534,099 (GRCm39)	missense	probably benign
R8920:Stard9	UTSW	2	120,533,088 (GRCm39)	missense	probably damaging	0.96
R9026:Stard9	UTSW	2	120,536,283 (GRCm39)	missense	probably damaging	1.00
R9048:Stard9	UTSW	2	120,508,415 (GRCm39)	missense	probably damaging	0.99
R9049:Stard9	UTSW	2	120,510,418 (GRCm39)	missense	probably benign	0.30
R9152:Stard9	UTSW	2	120,529,068 (GRCm39)	missense	probably damaging	0.99
R9189:Stard9	UTSW	2	120,533,500 (GRCm39)	missense	possibly damaging	0.95
R9238:Stard9	UTSW	2	120,528,447 (GRCm39)	missense	probably damaging	1.00
R9372:Stard9	UTSW	2	120,495,420 (GRCm39)	nonsense	probably null
R9393:Stard9	UTSW	2	120,518,656 (GRCm39)	missense	possibly damaging	0.88
R9444:Stard9	UTSW	2	120,495,414 (GRCm39)	missense	probably damaging	1.00
R9514:Stard9	UTSW	2	120,534,564 (GRCm39)	missense	probably damaging	1.00
R9515:Stard9	UTSW	2	120,534,564 (GRCm39)	missense	probably damaging	1.00
R9516:Stard9	UTSW	2	120,534,564 (GRCm39)	missense	probably damaging	1.00
R9570:Stard9	UTSW	2	120,534,714 (GRCm39)	missense	probably benign	0.02
R9649:Stard9	UTSW	2	120,526,635 (GRCm39)	missense	probably benign	0.20
R9789:Stard9	UTSW	2	120,510,417 (GRCm39)	missense	probably damaging	1.00
X0023:Stard9	UTSW	2	120,533,444 (GRCm39)	missense	possibly damaging	0.92
X0023:Stard9	UTSW	2	120,533,225 (GRCm39)	missense	probably benign	0.00
Z1176:Stard9	UTSW	2	120,528,803 (GRCm39)	missense	probably damaging	1.00
Z1176:Stard9	UTSW	2	120,527,093 (GRCm39)	missense	probably benign
Z1176:Stard9	UTSW	2	120,526,299 (GRCm39)	missense	probably benign	0.01
Z1177:Stard9	UTSW	2	120,504,157 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- ATGGGCATTCAAGGGCCAGAAC -3'
(R):5'- AGAATGTATGTCCCCTGAGGGACTG -3'

Sequencing Primer
(F):5'- CTGCTGATGAGATGCCTACAG -3'
(R):5'- CTGCTGGGACTGACCTTAGAG -3'

Posted On

2013-10-16