Mutagenetix > Incidental Mutation

Incidental Mutation 'R7553:Stard9'

585993

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

045622-MU

Accession Numbers

Essential gene?

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

Stock #

R7553 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

120459602-120562376 bp(+) (GRCm39)

Type of Mutation

splice site (3 bp from exon)

DNA Base Change (assembly)

A to T at 120524289 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

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

probably null
Transcript: ENSMUST00000180041

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705

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: 99.7%
20x: 99.1%

Validation Efficiency

98% (62/63)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc6	A	G	7: 45,648,545 (GRCm39)	L649P	probably damaging	Het
Acad10	T	C	5: 121,777,318 (GRCm39)	Y371C	probably damaging	Het
Avp	A	G	2: 130,423,098 (GRCm39)	V71A	probably damaging	Het
Bhmt	C	T	13: 93,756,589 (GRCm39)		probably null	Het
Capn15	T	C	17: 26,179,738 (GRCm39)	E874G	probably damaging	Het
Capn5	A	G	7: 97,773,231 (GRCm39)	F591S	probably damaging	Het
Ccne2	A	T	4: 11,201,348 (GRCm39)	Q292L	probably benign	Het
Cd96	T	G	16: 45,872,384 (GRCm39)	T406P	probably damaging	Het
Csnk1e	G	A	15: 79,310,566 (GRCm39)	A153V	probably damaging	Het
Dlk1	G	A	12: 109,420,889 (GRCm39)	V15I	unknown	Het
Dmbt1	A	G	7: 130,706,597 (GRCm39)	N1372S	unknown	Het
Dntt	A	T	19: 41,017,926 (GRCm39)	R17W	probably damaging	Het
Erich3	G	T	3: 154,439,137 (GRCm39)	A260S	probably benign	Het
Foxp2	C	T	6: 15,437,881 (GRCm39)	S669L	unknown	Het
Gm40460	ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	7: 141,794,450 (GRCm39)		probably benign	Het
Grid2	A	G	6: 64,053,925 (GRCm39)	K375E	possibly damaging	Het
Grin2b	C	T	6: 135,749,394 (GRCm39)	G603S	possibly damaging	Het
Hexb	C	T	13: 97,334,681 (GRCm39)	R30Q	probably benign	Het
Homer3	A	T	8: 70,742,774 (GRCm39)	T162S	probably benign	Het
L3mbtl1	A	G	2: 162,790,151 (GRCm39)	E15G	probably benign	Het
Manea	A	T	4: 26,327,986 (GRCm39)	F352I	probably damaging	Het
Mcf2l	T	A	8: 13,047,268 (GRCm39)	M210K	probably benign	Het
Morc3	T	C	16: 93,667,824 (GRCm39)	L734P	probably damaging	Het
Mybpc2	A	G	7: 44,155,571 (GRCm39)	V894A	possibly damaging	Het
Myh4	T	A	11: 67,147,221 (GRCm39)	M1622K	probably damaging	Het
Myrf	A	G	19: 10,206,240 (GRCm39)	F59L	probably benign	Het
Ndst3	G	T	3: 123,350,709 (GRCm39)		probably null	Het
Nln	TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC	TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC	13: 104,186,924 (GRCm39)		probably null	Het
Nos3	A	T	5: 24,586,715 (GRCm39)	D986V	possibly damaging	Het
Nrp1	G	A	8: 129,158,468 (GRCm39)	A252T	probably damaging	Het
Nup205	G	T	6: 35,178,934 (GRCm39)	R668L	probably damaging	Het
Or51aa2	T	C	7: 103,188,363 (GRCm39)	Y26C	probably damaging	Het
Or5af2	T	A	11: 58,707,886 (GRCm39)	D17E	probably benign	Het
Or5p56	G	A	7: 107,589,682 (GRCm39)	V37I	probably benign	Het
Pcdhga1	T	A	18: 37,882,735 (GRCm39)		probably null	Het
Pck1	A	G	2: 172,998,860 (GRCm39)	I373V	probably benign	Het
Pde8b	T	C	13: 95,223,258 (GRCm39)	N227S	probably benign	Het
Pianp	T	G	6: 124,976,214 (GRCm39)	S8A	unknown	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 110,350,827 (GRCm39)		probably benign	Het
Pla2r1	A	T	2: 60,353,243 (GRCm39)	N239K	possibly damaging	Het
Pls1	T	A	9: 95,669,140 (GRCm39)	N27I	probably damaging	Het
Prep	T	C	10: 45,034,620 (GRCm39)	*711Q	probably null	Het
Prkag3	A	G	1: 74,783,894 (GRCm39)	F330L	probably damaging	Het
Prss56	A	G	1: 87,111,261 (GRCm39)	D16G	probably benign	Het
Rad17	A	T	13: 100,769,794 (GRCm39)	F255Y	probably damaging	Het
Rap1gap2	T	C	11: 74,326,548 (GRCm39)	E173G	probably damaging	Het
Retreg3	C	T	11: 100,997,216 (GRCm39)	R88H	possibly damaging	Het
Rhag	G	A	17: 41,139,286 (GRCm39)	G74R	probably damaging	Het
Rybp	A	G	6: 100,209,220 (GRCm39)	S201P	possibly damaging	Het
S100a10	G	A	3: 93,471,602 (GRCm39)	C62Y	probably benign	Het
Scgb2b3	T	A	7: 31,059,673 (GRCm39)	S34C	possibly damaging	Het
Serpind1	A	G	16: 17,154,539 (GRCm39)	D122G	probably benign	Het
Setdb1	A	G	3: 95,254,076 (GRCm39)	L242P	probably damaging	Het
Slc14a2	T	A	18: 78,198,803 (GRCm39)	I776F	probably damaging	Het
Slc9a1	A	G	4: 133,139,580 (GRCm39)	E266G	probably damaging	Het
Stpg2	A	G	3: 138,924,098 (GRCm39)	Y167C	probably damaging	Het
Tex264	T	C	9: 106,536,335 (GRCm39)	E274G	probably damaging	Het
Tigd2	G	A	6: 59,188,564 (GRCm39)	S477N	probably benign	Het
Urb1	A	G	16: 90,589,752 (GRCm39)	L343P	probably damaging	Het
Vars2	A	T	17: 35,975,680 (GRCm39)	C246S	possibly damaging	Het
Vil1	G	A	1: 74,465,891 (GRCm39)		probably null	Het
Vmn2r61	C	G	7: 41,916,205 (GRCm39)	L273V	not run	Het
Vmn2r-ps158	T	G	7: 42,697,447 (GRCm39)	C835G	probably damaging	Het
Zfp37	C	A	4: 62,110,236 (GRCm39)	G317V	probably damaging	Het
Zfp760	A	G	17: 21,941,872 (GRCm39)	K349R	possibly damaging	Het
Zyx	A	T	6: 42,327,408 (GRCm39)	E69V	probably null	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
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
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'- AGCAGCTCAGTACCTTCTTCTG -3'
(R):5'- TGAGTGAGTGGGACCAACC -3'

Sequencing Primer
(F):5'- CTTCTGGATCCAGGACGATG -3'
(R):5'- TCACAGACCAAGCAGCAGG -3'

Posted On

2019-10-18