Mutagenetix > Incidental Mutation

Incidental Mutation 'R0836:Stard9'

77880

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

039015-MU

Accession Numbers

Essential gene?

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

Stock #

R0836 (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: 99.6%
3x: 98.9%
10x: 96.9%
20x: 92.2%

Validation Efficiency

100% (102/102)

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110082I17Rik	A	G	5: 139,349,875 (GRCm39)	V58A	possibly damaging	Het
4932415M13Rik	A	T	17: 54,031,374 (GRCm39)		noncoding transcript	Het
A930003A15Rik	T	C	16: 19,702,622 (GRCm39)		noncoding transcript	Het
Abca8a	A	T	11: 109,931,390 (GRCm39)	D1253E	possibly damaging	Het
Acsm3	T	C	7: 119,376,323 (GRCm39)	I350T	possibly damaging	Het
Adcy9	T	C	16: 4,237,135 (GRCm39)	D92G	possibly damaging	Het
Aldh9a1	G	A	1: 167,177,824 (GRCm39)	G7D	probably benign	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
Asphd2	A	T	5: 112,539,635 (GRCm39)	L66H	probably damaging	Het
Astl	T	C	2: 127,184,339 (GRCm39)	F21L	probably benign	Het
Bptf	C	A	11: 107,001,638 (GRCm39)		probably null	Het
Cacna2d4	C	T	6: 119,284,247 (GRCm39)	R745W	probably damaging	Het
Cadps2	T	C	6: 23,328,775 (GRCm39)		probably benign	Het
Camk4	G	T	18: 33,072,507 (GRCm39)	S20I	unknown	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
Cd209e	G	T	8: 3,903,205 (GRCm39)	D62E	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
Cfap43	C	A	19: 47,804,285 (GRCm39)	V304L	probably benign	Het
Col26a1	A	G	5: 136,794,154 (GRCm39)		probably null	Het
Cpa5	T	C	6: 30,623,210 (GRCm39)	S124P	probably damaging	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
Dmxl1	T	C	18: 49,966,215 (GRCm39)	V20A	probably damaging	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
Fezf1	T	C	6: 23,246,998 (GRCm39)	H278R	probably benign	Het
Fhod3	T	A	18: 25,199,275 (GRCm39)	Y649N	probably damaging	Het
Ftdc2	G	A	16: 58,455,886 (GRCm39)	S129L	probably damaging	Het
Grap	T	A	11: 61,551,065 (GRCm39)	D32E	possibly damaging	Het
Hipk1	A	G	3: 103,661,612 (GRCm39)	S670P	probably damaging	Het
Iho1	A	T	9: 108,282,000 (GRCm39)	C563S	probably benign	Het
Ilrun	A	T	17: 28,005,112 (GRCm39)	S148R	probably damaging	Het
Itga2	A	G	13: 114,993,215 (GRCm39)	V800A	probably damaging	Het
Itgae	A	T	11: 73,020,032 (GRCm39)	M845L	probably benign	Het
Itgb5	A	G	16: 33,720,953 (GRCm39)	K339R	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
Kcnd2	T	A	6: 21,727,328 (GRCm39)	V627E	probably damaging	Het
Kcnd2	T	C	6: 21,726,238 (GRCm39)		probably benign	Het
Ktn1	A	G	14: 47,938,519 (GRCm39)		probably null	Het
Lamp1	T	A	8: 13,222,654 (GRCm39)	F279L	probably damaging	Het
Macf1	A	G	4: 123,388,675 (GRCm39)		probably null	Het
Mark2	A	G	19: 7,263,189 (GRCm39)	Y193H	probably damaging	Het
Mcrs1	T	C	15: 99,141,330 (GRCm39)		probably benign	Het
Mtnr1a	A	T	8: 45,540,974 (GRCm39)	I312F	probably benign	Het
Myom2	A	T	8: 15,182,924 (GRCm39)	K1454*	probably null	Het
Nfkbia	C	A	12: 55,537,561 (GRCm39)	A211S	probably damaging	Het
Or52ae9	T	C	7: 103,390,132 (GRCm39)	H105R	probably damaging	Het
Or56b1b	T	C	7: 108,164,205 (GRCm39)	T266A	possibly damaging	Het
Or8b1c	A	T	9: 38,384,081 (GRCm39)	I13F	probably benign	Het
Otog	C	T	7: 45,918,786 (GRCm39)	T954I	possibly damaging	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
Pmch	A	G	10: 87,927,086 (GRCm39)	I30V	probably benign	Het
Ppat	A	C	5: 77,070,348 (GRCm39)	Y157D	probably benign	Het
Ppp1r16a	C	T	15: 76,577,869 (GRCm39)	Q328*	probably null	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
Rbp3	T	G	14: 33,678,595 (GRCm39)	S848A	possibly damaging	Het
Rgs1	A	T	1: 144,123,671 (GRCm39)	S85T	probably damaging	Het
Rictor	A	G	15: 6,793,759 (GRCm39)		probably null	Het
Rims1	T	C	1: 22,497,709 (GRCm39)		probably null	Het
Shc1	A	G	3: 89,330,276 (GRCm39)	D70G	probably damaging	Het
Slc22a28	T	C	19: 8,094,197 (GRCm39)	Y245C	possibly damaging	Het
Slc25a1	T	A	16: 17,745,300 (GRCm39)	H78L	probably benign	Het
Slc30a7	T	A	3: 115,783,789 (GRCm39)		probably null	Het
Slc34a2	A	G	5: 53,225,049 (GRCm39)	T397A	probably benign	Het
Slc51a	T	A	16: 32,294,667 (GRCm39)	T306S	probably benign	Het
Sorcs3	G	A	19: 48,475,833 (GRCm39)	V231I	probably benign	Het
Sp100	A	T	1: 85,627,465 (GRCm39)	I86L	probably damaging	Het
Spata31e5	A	G	1: 28,816,902 (GRCm39)	S377P	possibly damaging	Het
Stxbp5	A	T	10: 9,740,843 (GRCm39)	S116R	probably damaging	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
Tax1bp1	C	T	6: 52,718,925 (GRCm39)		probably benign	Het
Tcof1	T	C	18: 60,978,904 (GRCm39)	D48G	probably damaging	Het
Tex24	A	T	8: 27,834,748 (GRCm39)	H92L	possibly damaging	Het
Tgm3	C	T	2: 129,868,602 (GRCm39)		probably benign	Het
Thbs4	T	G	13: 92,894,546 (GRCm39)	D659A	probably damaging	Het
Tmed11	A	T	5: 108,943,175 (GRCm39)	M1K	probably null	Het
Tmpo	A	T	10: 90,997,815 (GRCm39)	C657*	probably null	Het
Unc5a	C	A	13: 55,151,746 (GRCm39)	N56K	possibly damaging	Het
Urb1	T	C	16: 90,592,336 (GRCm39)	D308G	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
Vmn2r17	A	T	5: 109,575,822 (GRCm39)	H231L	possibly damaging	Het
Wrn	A	G	8: 33,785,034 (GRCm39)	I446T	possibly damaging	Het
Zfp266	G	A	9: 20,411,095 (GRCm39)	H361Y	probably damaging	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
R0833: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