Mutagenetix > Incidental Mutation

Incidental Mutation 'R8862:Stard9'

675695

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

068741-MU

Accession Numbers

Essential gene?

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

Stock #

R8862 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

120459602-120562376 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 120534099 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 3452 (D3452G)

Ref Sequence

ENSEMBL: ENSMUSP00000136055 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000140843] [ENSMUST00000154193] [ENSMUST00000180041]

AlphaFold

no structure available at present

Predicted Effect

SMART Domains

Protein: ENSMUSP00000070111
Gene: ENSMUSG00000033705
AA Change: D759G

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: ENSMUST00000154193

SMART Domains

Protein: ENSMUSP00000116900
Gene: ENSMUSG00000033705

Domain	Start	End	E-Value	Type
low complexity region	63	77	N/A	INTRINSIC
coiled coil region	409	450	N/A	INTRINSIC
low complexity region	454	463	N/A	INTRINSIC
low complexity region	469	486	N/A	INTRINSIC
low complexity region	546	567	N/A	INTRINSIC
SCOP:d1jssa_	588	784	4e-29	SMART
Blast:START	589	785	6e-12	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000180041
AA Change: D3452G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: D3452G

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: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (61/61)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acin1	C	T	14: 54,901,172 (GRCm39)	G685R	probably benign	Het
Ahdc1	T	C	4: 132,791,129 (GRCm39)	F790S	possibly damaging	Het
Alg10b	T	C	15: 90,109,893 (GRCm39)	Y69H	probably damaging	Het
Amer3	A	T	1: 34,626,465 (GRCm39)	S235C	probably damaging	Het
Ankfy1	G	T	11: 72,644,469 (GRCm39)	S722I	probably benign	Het
Baz1a	T	C	12: 55,032,624 (GRCm39)		probably benign	Het
Ccdc177	A	G	12: 80,804,208 (GRCm39)	S689P	unknown	Het
Cdh24	C	A	14: 54,869,874 (GRCm39)	R681L	probably damaging	Het
Cdk14	T	G	5: 5,060,862 (GRCm39)	I338L	probably benign	Het
Clec2m	T	C	6: 129,308,494 (GRCm39)	T12A	probably benign	Het
Col18a1	G	T	10: 76,949,044 (GRCm39)	S156*	probably null	Het
Col6a6	T	C	9: 105,663,348 (GRCm39)	Y63C	probably damaging	Het
Cytip	G	A	2: 58,037,887 (GRCm39)	T159M	probably benign	Het
Dnah5	T	C	15: 28,459,502 (GRCm39)		probably benign	Het
Dock3	T	C	9: 106,855,927 (GRCm39)	Y744C	probably damaging	Het
Dop1a	T	C	9: 86,406,404 (GRCm39)		probably null	Het
Dse	A	T	10: 34,029,934 (GRCm39)	D385E	probably damaging	Het
Efhc1	A	C	1: 21,037,573 (GRCm39)	D250A		Het
Epha3	T	A	16: 63,431,348 (GRCm39)	T519S	probably benign	Het
Gas2l3	A	G	10: 89,250,282 (GRCm39)	Y279H	probably damaging	Het
Gatd3a	A	G	10: 78,005,461 (GRCm39)	S35P	probably damaging	Het
Gemin6	G	A	17: 80,535,432 (GRCm39)	V131I	probably damaging	Het
Gm40460	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	7: 141,794,554 (GRCm39)		probably benign	Het
Gnai2	C	A	9: 107,512,326 (GRCm39)	A31S		Het
Greb1l	A	G	18: 10,555,042 (GRCm39)	D1696G	possibly damaging	Het
Itfg2	T	C	6: 128,394,668 (GRCm39)	E35G	probably damaging	Het
Kctd10	A	G	5: 114,503,921 (GRCm39)	F244L	probably damaging	Het
Kif19b	C	A	5: 140,472,534 (GRCm39)	P686Q	probably damaging	Het
Krtap5-1	ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG	ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG	7: 141,850,333 (GRCm39)		probably benign	Het
Lgals9	G	T	11: 78,860,716 (GRCm39)		probably benign	Het
Lrriq4	A	T	3: 30,705,088 (GRCm39)	N372I	probably damaging	Het
Mical2	A	G	7: 111,910,574 (GRCm39)	N248S	probably damaging	Het
Mipep	T	A	14: 61,080,689 (GRCm39)	C560*	probably null	Het
Myo1a	G	A	10: 127,548,653 (GRCm39)	V396M	probably benign	Het
Myod1	A	G	7: 46,026,487 (GRCm39)	T131A	probably damaging	Het
Nalcn	T	A	14: 123,647,199 (GRCm39)	D558V	possibly damaging	Het
Odf2l	T	A	3: 144,833,758 (GRCm39)		probably benign	Het
Or6d13	G	A	6: 116,518,186 (GRCm39)	M257I	probably benign	Het
Plbd2	A	T	5: 120,624,728 (GRCm39)	M480K	probably damaging	Het
Ppargc1a	A	G	5: 51,631,235 (GRCm39)	F465L	possibly damaging	Het
Ppp1r15b	A	T	1: 133,064,506 (GRCm39)	I659F	probably damaging	Het
Prune2	C	T	19: 17,097,510 (GRCm39)	L1005F	probably benign	Het
Pter	T	C	2: 12,985,341 (GRCm39)	S224P	probably damaging	Het
Ralgapa2	A	G	2: 146,266,731 (GRCm39)	I615T	probably benign	Het
Ror1	T	C	4: 100,191,715 (GRCm39)		probably null	Het
Rps2	A	G	17: 24,940,662 (GRCm39)	T259A	probably benign	Het
Rsf1	GCG	GCGACGGCGCCG	7: 97,229,114 (GRCm39)		probably benign	Het
S1pr4	G	A	10: 81,334,533 (GRCm39)	R314C	probably damaging	Het
Sema4f	A	T	6: 82,891,081 (GRCm39)	H575Q	probably benign	Het
Son	A	G	16: 91,453,734 (GRCm39)	D827G	probably damaging	Het
Sox8	A	T	17: 25,787,045 (GRCm39)	H219Q	possibly damaging	Het
Spink2	C	T	5: 77,357,615 (GRCm39)	D24N	probably benign	Het
Syngr2	G	T	11: 117,703,507 (GRCm39)	D108Y	probably damaging	Het
Tardbp	G	A	4: 148,702,755 (GRCm39)	S403L	possibly damaging	Het
Tomm70a	T	C	16: 56,942,546 (GRCm39)	S108P	probably benign	Het
Ttc12	T	C	9: 49,351,515 (GRCm39)	T661A	probably benign	Het
Tubgcp6	A	G	15: 89,006,824 (GRCm39)	V66A	probably benign	Het
Unc13b	T	A	4: 43,235,207 (GRCm39)	L477Q	probably damaging	Het
Vmn1r77	T	A	7: 11,776,060 (GRCm39)	C279S	probably benign	Het
Vmn2r79	T	C	7: 86,645,712 (GRCm39)	S14P	probably benign	Het
Zan	T	C	5: 137,472,674 (GRCm39)	T72A	probably benign	Het
Zcchc2	A	G	1: 105,958,998 (GRCm39)	*1156W	probably null	Het
Zfp354c	A	T	11: 50,708,718 (GRCm39)	D26E	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
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
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	120,535,943 (GRCm39)	missense	probably damaging	1.00
R8807:Stard9	UTSW	2	120,535,932 (GRCm39)	missense	probably damaging	1.00
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'- CACAGGGACTTGTGCATATTGG -3'
(R):5'- TGACATTGTCCTGGCTTCAG -3'

Sequencing Primer
(F):5'- TGGAAGCAATATGTATTTGGAAGTGC -3'
(R):5'- TCAGTGCAACACCAGTGG -3'

Posted On

2021-07-15