Mutagenetix > Incidental Mutation

Incidental Mutation 'R1538:Stard9'

169657

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

039577-MU

Accession Numbers

Essential gene?

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

Stock #

R1538 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

120459602-120562376 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 120527192 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Threonine at position 1150 (P1150T)

Ref Sequence

ENSEMBL: ENSMUSP00000136055 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000070420

SMART Domains

Protein: ENSMUSP00000070111
Gene: ENSMUSG00000033705

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

Predicted Effect

probably benign
Transcript: ENSMUST00000140843

SMART Domains

Protein: ENSMUSP00000117178
Gene: ENSMUSG00000033705

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

Predicted Effect

probably benign
Transcript: ENSMUST00000180041
AA Change: P1150T

PolyPhen 2 Score 0.254 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: P1150T

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: 99.0%
3x: 98.1%
10x: 95.5%
20x: 89.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	G	T	3: 137,771,162 (GRCm39)	R117L	probably benign	Het
4930447C04Rik	G	A	12: 72,928,120 (GRCm39)	A537V	possibly damaging	Het
4930579F01Rik	A	C	3: 137,889,517 (GRCm39)	D33E	probably damaging	Het
Acnat1	T	C	4: 49,447,835 (GRCm39)	K249E	possibly damaging	Het
Ankrd13a	T	C	5: 114,942,295 (GRCm39)	I526T	possibly damaging	Het
Aplp1	C	A	7: 30,135,452 (GRCm39)	E535D	probably benign	Het
Armc8	T	A	9: 99,387,343 (GRCm39)	H425L	probably damaging	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Asprv1	C	T	6: 86,605,618 (GRCm39)	Q155*	probably null	Het
Atl1	A	G	12: 69,972,962 (GRCm39)	Q94R	probably benign	Het
Atp2a2	A	G	5: 122,595,440 (GRCm39)	L970P	probably damaging	Het
Atp8a2	T	C	14: 60,097,719 (GRCm39)	K770E	probably benign	Het
Bod1l	A	G	5: 41,973,772 (GRCm39)	M2514T	probably benign	Het
Cacfd1	T	A	2: 26,908,951 (GRCm39)	D97E	probably benign	Het
Cacna1e	A	G	1: 154,437,504 (GRCm39)	L344P	probably damaging	Het
Cacna2d2	C	A	9: 107,394,615 (GRCm39)	R596S	probably damaging	Het
Catip	C	A	1: 74,403,811 (GRCm39)	S176*	probably null	Het
Cdcp1	G	A	9: 123,002,653 (GRCm39)	S806L	probably damaging	Het
Cdk6	A	T	5: 3,570,675 (GRCm39)	I289L	probably benign	Het
Cers3	C	T	7: 66,431,571 (GRCm39)	T182I	probably damaging	Het
Cfap46	T	A	7: 139,262,924 (GRCm39)	N43I	probably null	Het
Clec4n	A	T	6: 123,206,992 (GRCm39)	R5S	possibly damaging	Het
Cnr2	G	T	4: 135,644,012 (GRCm39)	S30I	probably benign	Het
Col18a1	C	T	10: 76,907,170 (GRCm39)	G870E	probably damaging	Het
Cpne6	T	C	14: 55,752,677 (GRCm39)	V289A	possibly damaging	Het
Crym	G	A	7: 119,796,938 (GRCm39)	L141F	probably benign	Het
Cxxc5	T	C	18: 35,991,622 (GRCm39)	S8P	unknown	Het
Dido1	A	C	2: 180,326,763 (GRCm39)	S453R	possibly damaging	Het
Dnah2	A	C	11: 69,368,028 (GRCm39)	S1770R	probably benign	Het
Dnah7a	A	G	1: 53,535,148 (GRCm39)	V2704A	possibly damaging	Het
Eml5	T	C	12: 98,760,535 (GRCm39)	N1738S	probably damaging	Het
Eri3	A	G	4: 117,439,836 (GRCm39)	T138A	possibly damaging	Het
Ext2	C	T	2: 93,537,632 (GRCm39)	E585K	probably damaging	Het
Fbxw19	T	A	9: 109,324,056 (GRCm39)	S38C	probably damaging	Het
Fcgbpl1	A	T	7: 27,854,917 (GRCm39)	I1848F	probably damaging	Het
Fmo6	G	A	1: 162,753,675 (GRCm39)	P156S	probably damaging	Het
Frem3	A	T	8: 81,339,764 (GRCm39)	I686F	probably benign	Het
Frem3	T	C	8: 81,339,339 (GRCm39)	L544P	probably damaging	Het
Gabra1	T	C	11: 42,031,177 (GRCm39)	Y251C	probably benign	Het
Gemin4	G	T	11: 76,101,987 (GRCm39)	Q925K	probably benign	Het
Gm18856	T	A	13: 14,139,274 (GRCm39)		probably benign	Het
Gnb1	A	T	4: 155,636,171 (GRCm39)	T164S	probably benign	Het
Gpx6	A	G	13: 21,497,822 (GRCm39)	D31G	possibly damaging	Het
Gzmd	A	C	14: 56,367,802 (GRCm39)	I157S	probably benign	Het
Il31ra	T	A	13: 112,684,000 (GRCm39)	N43I	possibly damaging	Het
Irak3	T	C	10: 120,001,035 (GRCm39)	T297A	probably benign	Het
Kank2	T	C	9: 21,685,927 (GRCm39)	D649G	probably damaging	Het
Kif3b	AGAGGAGGAGGAGGAGG	AGAGGAGGAGGAGG	2: 153,159,382 (GRCm39)		probably benign	Het
Kirrel1	C	T	3: 86,996,458 (GRCm39)	M380I	probably null	Het
Klhl18	A	G	9: 110,275,815 (GRCm39)	F111S	probably damaging	Het
Lratd2	A	G	15: 60,695,498 (GRCm39)	C83R	probably damaging	Het
Lrp5	A	G	19: 3,697,585 (GRCm39)	S319P	possibly damaging	Het
Mettl15	T	C	2: 108,962,010 (GRCm39)		probably null	Het
Mtarc1	T	C	1: 184,534,199 (GRCm39)	E223G	probably damaging	Het
Ncoa1	T	C	12: 4,320,748 (GRCm39)	Q1107R	possibly damaging	Het
Ncoa7	T	G	10: 30,570,207 (GRCm39)	M251L	probably damaging	Het
Nos2	A	T	11: 78,847,396 (GRCm39)	M1023L	probably benign	Het
Nup107	T	C	10: 117,626,399 (GRCm39)	K25E	probably damaging	Het
Or10q1b	A	T	19: 13,682,860 (GRCm39)	Y223F	probably damaging	Het
Or52s1b	A	G	7: 102,822,193 (GRCm39)	I217T	probably damaging	Het
Or5k14	T	A	16: 58,693,261 (GRCm39)	N84I	probably damaging	Het
Or5p58	T	A	7: 107,694,493 (GRCm39)	I95F	probably damaging	Het
Or6b6	A	T	7: 106,571,190 (GRCm39)	Y120*	probably null	Het
Or6c206	T	C	10: 129,097,082 (GRCm39)	I84T	probably damaging	Het
Parm1	G	A	5: 91,742,306 (GRCm39)	E225K	possibly damaging	Het
Pdzd2	A	C	15: 12,373,047 (GRCm39)	S2363A	probably damaging	Het
Piezo1	A	G	8: 123,218,142 (GRCm39)	L1199P	probably damaging	Het
Prpsap1	A	T	11: 116,370,534 (GRCm39)	M141K	probably benign	Het
Prss29	A	T	17: 25,539,257 (GRCm39)	M1L	possibly damaging	Het
Pter	T	A	2: 12,983,417 (GRCm39)	S141T	probably benign	Het
Ptpru	A	T	4: 131,501,662 (GRCm39)	D1181E	probably damaging	Het
Rab3ip	T	A	10: 116,775,159 (GRCm39)	Q66H	probably damaging	Het
Rgs12	A	T	5: 35,178,511 (GRCm39)	T779S	probably damaging	Het
Rgs22	A	G	15: 36,048,922 (GRCm39)	F786S	probably damaging	Het
Rnasel	A	T	1: 153,636,540 (GRCm39)	D640V	possibly damaging	Het
Rp1	T	C	1: 4,415,899 (GRCm39)	T1738A	probably damaging	Het
Sacs	T	C	14: 61,447,508 (GRCm39)	S3185P	probably damaging	Het
Scnn1a	T	A	6: 125,315,856 (GRCm39)	D321E	possibly damaging	Het
Sec31b	G	C	19: 44,507,025 (GRCm39)	L1014V	probably benign	Het
Serpinb10	A	G	1: 107,468,690 (GRCm39)	Y111C	probably damaging	Het
Shld2	C	G	14: 33,990,833 (GRCm39)	Q24H	probably damaging	Het
Siglecg	A	G	7: 43,067,313 (GRCm39)	K627E	possibly damaging	Het
Sigmar1	T	C	4: 41,740,845 (GRCm39)	I95V	probably benign	Het
Sirpb1b	T	A	3: 15,613,819 (GRCm39)	T88S	possibly damaging	Het
Spire2	T	G	8: 124,084,895 (GRCm39)	L245R	probably damaging	Het
Stat6	C	A	10: 127,489,125 (GRCm39)	T380N	probably damaging	Het
Sult3a1	G	A	10: 33,746,166 (GRCm39)	G162E	probably benign	Het
Surf4	T	C	2: 26,823,710 (GRCm39)		probably null	Het
Tacc2	T	C	7: 130,227,149 (GRCm39)	M1278T	probably benign	Het
Tacr2	T	A	10: 62,097,106 (GRCm39)		probably null	Het
Tcaf1	A	T	6: 42,655,923 (GRCm39)	V351E	probably damaging	Het
Tmcc2	A	G	1: 132,308,718 (GRCm39)	S59P	probably damaging	Het
Tmem17	G	A	11: 22,467,266 (GRCm39)	S60N	possibly damaging	Het
Tmem63b	C	G	17: 45,989,904 (GRCm39)	R88P	possibly damaging	Het
Tmprss7	A	T	16: 45,499,753 (GRCm39)	I307N	probably benign	Het
Treml2	A	T	17: 48,609,786 (GRCm39)	T73S	possibly damaging	Het
Trrap	A	G	5: 144,774,012 (GRCm39)	H2876R	possibly damaging	Het
Tyw3	A	G	3: 154,302,506 (GRCm39)	I53T	probably damaging	Het
Ugp2	A	G	11: 21,283,791 (GRCm39)	I92T	possibly damaging	Het
Vmn2r66	A	T	7: 84,644,166 (GRCm39)	M748K	possibly damaging	Het
Vmn2r82	T	C	10: 79,192,578 (GRCm39)	S52P	possibly damaging	Het
Wdr37	A	T	13: 8,886,828 (GRCm39)	S320T	probably benign	Het
Zbtb16	A	T	9: 48,743,583 (GRCm39)	M243K	probably benign	Het
Zfr	C	T	15: 12,150,329 (GRCm39)	T432I	possibly 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
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
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'- ACCATCTCCTTCAAGCAGGGCATC -3'
(R):5'- TTGCCTCCTGGTCTACTGAAGACG -3'

Sequencing Primer
(F):5'- AGCAGTTACTCAGTGGATTCTC -3'
(R):5'- CTACTGAAGACGGGGTGGC -3'

Posted On

2014-04-13