Mutagenetix > Incidental Mutation

Incidental Mutation 'R6235:Stard9'

504851

Institutional Source

Beutler Lab

Gene Symbol

Stard9

Ensembl Gene

ENSMUSG00000033705

Gene Name

START domain containing 9

Synonyms

E230025N21Rik, Kif16a, 4831403C07Rik, N-3 kinesin

MMRRC Submission

044433-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.146) question?

Stock #

R6235 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

120629121-120731895 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 120713546 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 4442 (V4442M)

Ref Sequence

ENSEMBL: ENSMUSP00000136055 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110700] [ENSMUST00000110701] [ENSMUST00000140843] [ENSMUST00000154193] [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: ENSMUST00000110700

SMART Domains

Protein: ENSMUSP00000106328
Gene: ENSMUSG00000027284

Domain	Start	End	E-Value	Type
low complexity region	25	42	N/A	INTRINSIC
low complexity region	78	99	N/A	INTRINSIC
low complexity region	102	151	N/A	INTRINSIC
low complexity region	154	180	N/A	INTRINSIC
low complexity region	326	337	N/A	INTRINSIC
low complexity region	561	576	N/A	INTRINSIC
low complexity region	724	735	N/A	INTRINSIC
Pfam:Codanin-1_C	786	906	2.4e-48	PFAM
low complexity region	1157	1171	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000110701

SMART Domains

Protein: ENSMUSP00000106329
Gene: ENSMUSG00000027284

Domain	Start	End	E-Value	Type
low complexity region	77	98	N/A	INTRINSIC
low complexity region	101	150	N/A	INTRINSIC
low complexity region	153	179	N/A	INTRINSIC
low complexity region	326	337	N/A	INTRINSIC
low complexity region	561	576	N/A	INTRINSIC
low complexity region	724	735	N/A	INTRINSIC
Pfam:Codanin-1_C	789	904	2.4e-41	PFAM
low complexity region	1164	1178	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129384

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

noncoding transcript
Transcript: ENSMUST00000141917

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148285

Predicted Effect

probably damaging
Transcript: ENSMUST00000154193
AA Change: V666M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000116900
Gene: ENSMUSG00000033705
AA Change: V666M

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 damaging
Transcript: ENSMUST00000180041
AA Change: V4442M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: V4442M

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

0.1749

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.4%

Validation Efficiency

95% (73/77)

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam6b	T	C	12: 113,491,710 (GRCm38)	F716L	probably benign	Het
Akip1	A	G	7: 109,707,413 (GRCm38)	M106V	probably benign	Het
Aldh1l1	A	T	6: 90,564,457 (GRCm38)	I278F	probably benign	Het
Aplnr	A	G	2: 85,137,626 (GRCm38)	T332A	probably benign	Het
Aqp4	A	G	18: 15,398,113 (GRCm38)	V197A	probably damaging	Het
Arid4a	A	T	12: 71,069,772 (GRCm38)		probably null	Het
Baiap2	A	T	11: 119,981,408 (GRCm38)	N99Y	probably damaging	Het
Ceacam1	A	T	7: 25,471,792 (GRCm38)		probably null	Het
Cep78	T	C	19: 15,976,486 (GRCm38)		probably null	Het
Cldn3	T	C	5: 134,986,719 (GRCm38)	F92S	possibly damaging	Het
Clec16a	C	A	16: 10,694,635 (GRCm38)	P812Q	probably damaging	Het
Cnga4	T	G	7: 105,407,699 (GRCm38)	Y336*	probably null	Het
Copg2	A	G	6: 30,816,071 (GRCm38)	I443T	probably damaging	Het
Crhbp	C	A	13: 95,443,850 (GRCm38)	A81S	probably damaging	Het
Csad	A	T	15: 102,178,606 (GRCm38)	V410D	probably damaging	Het
Ctps	G	A	4: 120,558,806 (GRCm38)	L207F	probably benign	Het
Dab2ip	A	G	2: 35,723,087 (GRCm38)	E1003G	probably damaging	Het
Ddx31	C	G	2: 28,844,842 (GRCm38)	A5G	probably benign	Het
Dnah12	A	T	14: 26,854,804 (GRCm38)	I3004F	probably damaging	Het
Fbxo15	A	G	18: 84,980,904 (GRCm38)		probably benign	Het
Fbxw28	C	A	9: 109,326,190 (GRCm38)	W356C	probably damaging	Het
Gimap6	G	T	6: 48,702,457 (GRCm38)	T215K	probably benign	Het
Gm5346	T	G	8: 43,625,912 (GRCm38)	N425T	probably benign	Het
Hspa4	C	T	11: 53,262,939 (GRCm38)	E702K	probably benign	Het
Hunk	A	G	16: 90,432,706 (GRCm38)	I152V	probably damaging	Het
Itk	T	C	11: 46,336,428 (GRCm38)	E456G	probably benign	Het
Krt40	G	A	11: 99,543,094 (GRCm38)	A22V	possibly damaging	Het
Lars2	T	C	9: 123,411,880 (GRCm38)	V204A	probably damaging	Het
Lipo1	A	G	19: 33,783,563 (GRCm38)	Y140H	probably damaging	Het
Lrp1	G	A	10: 127,588,177 (GRCm38)	R809W	probably damaging	Het
Magi3	C	T	3: 104,016,068 (GRCm38)	G1111D	probably damaging	Het
Mis18bp1	A	T	12: 65,158,408 (GRCm38)	V47E	probably damaging	Het
Mpdz	T	C	4: 81,385,281 (GRCm38)	E140G	probably damaging	Het
Myo1d	T	C	11: 80,692,944 (GRCm38)	I81V	probably benign	Het
Nek10	T	A	14: 14,821,113 (GRCm38)	Y26*	probably null	Het
Ntng2	C	A	2: 29,227,979 (GRCm38)	E152D	probably damaging	Het
Olfr1036	T	C	2: 86,075,166 (GRCm38)	L142P	possibly damaging	Het
Olfr1490	C	A	19: 13,654,781 (GRCm38)	C117*	probably null	Het
Otud3	A	T	4: 138,901,901 (GRCm38)	V185D	probably damaging	Het
Parp6	C	T	9: 59,630,815 (GRCm38)	R248W	probably benign	Het
Pcdhga7	A	G	18: 37,716,430 (GRCm38)	T497A	probably benign	Het
Ppp1r18	A	G	17: 35,873,877 (GRCm38)	E140G	probably damaging	Het
Prl3b1	T	C	13: 27,247,945 (GRCm38)	L151P	probably damaging	Het
Pth1r	C	T	9: 110,722,316 (GRCm38)	E572K	possibly damaging	Het
Ptprq	T	A	10: 107,635,338 (GRCm38)	T1401S	possibly damaging	Het
Rad51ap2	A	G	12: 11,457,516 (GRCm38)	T480A	possibly damaging	Het
Rax	T	A	18: 65,935,161 (GRCm38)	Q291L	unknown	Het
Reck	T	C	4: 43,937,450 (GRCm38)	L734P	probably damaging	Het
Rgmb	A	G	17: 15,820,819 (GRCm38)	F169L	probably damaging	Het
Rhobtb3	T	C	13: 75,892,910 (GRCm38)	I426M	probably damaging	Het
Ring1	C	A	17: 34,023,306 (GRCm38)	A76S	probably damaging	Het
Robo3	T	G	9: 37,420,929 (GRCm38)	Y891S	probably damaging	Het
Rpusd2	A	G	2: 119,034,857 (GRCm38)	I12V	probably benign	Het
Rragd	T	C	4: 32,995,985 (GRCm38)	V165A	possibly damaging	Het
Rsf1	G	GACGGCGGCT	7: 97,579,909 (GRCm38)		probably benign	Homo
Ryr1	G	T	7: 29,116,181 (GRCm38)	Q95K	probably benign	Het
S1pr4	T	A	10: 81,498,882 (GRCm38)	N253Y	possibly damaging	Het
Scn3a	A	C	2: 65,461,335 (GRCm38)	V1689G	probably damaging	Het
Sdhb	A	G	4: 140,973,673 (GRCm38)	N147D	probably damaging	Het
Sdk1	A	T	5: 142,034,426 (GRCm38)	H913L	possibly damaging	Het
Serpina3i	T	A	12: 104,266,532 (GRCm38)	M232K	probably damaging	Het
Sipa1l2	A	T	8: 125,474,871 (GRCm38)	V646E	probably damaging	Het
Slc38a1	A	T	15: 96,578,792 (GRCm38)	I396N	probably benign	Het
Slc6a13	A	T	6: 121,302,794 (GRCm38)	E42D	probably benign	Het
Sumo3	T	A	10: 77,616,237 (GRCm38)		probably benign	Het
Syngap1	A	G	17: 26,958,130 (GRCm38)	I356V	probably benign	Het
Tcam1	C	T	11: 106,284,054 (GRCm38)	Q112*	probably null	Het
Tdp2	T	A	13: 24,840,395 (GRCm38)	L225*	probably null	Het
Tmprss7	A	G	16: 45,658,122 (GRCm38)	V747A	probably benign	Het
Ugt2b34	T	A	5: 86,906,364 (GRCm38)	Y186F	probably benign	Het
Usp37	G	T	1: 74,475,133 (GRCm38)	S293*	probably null	Het
Vmn1r36	A	G	6: 66,716,246 (GRCm38)	I109T	probably benign	Het
Vsig10l	T	A	7: 43,468,972 (GRCm38)	V798E	probably benign	Het
Zfp36l1	G	T	12: 80,112,822 (GRCm38)	C18*	probably null	Het
Zfp959	T	C	17: 55,897,427 (GRCm38)	Y152H	probably damaging	Het
Zfyve26	A	T	12: 79,249,599 (GRCm38)	C1949S	probably damaging	Het
Zswim9	T	A	7: 13,261,603 (GRCm38)	E209V	probably damaging	Het

Other mutations in Stard9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Stard9	APN	2	120,701,847 (GRCm38)	missense	possibly damaging	0.52
IGL01122:Stard9	APN	2	120,698,479 (GRCm38)	missense	possibly damaging	0.93
IGL01318:Stard9	APN	2	120,698,719 (GRCm38)	missense	possibly damaging	0.56
IGL01371:Stard9	APN	2	120,701,368 (GRCm38)	missense	probably benign	0.04
IGL01394:Stard9	APN	2	120,706,327 (GRCm38)	missense	possibly damaging	0.78
IGL01531:Stard9	APN	2	120,673,604 (GRCm38)	missense	possibly damaging	0.93
IGL01721:Stard9	APN	2	120,703,330 (GRCm38)	missense	probably damaging	1.00
IGL01810:Stard9	APN	2	120,699,084 (GRCm38)	missense	possibly damaging	0.95
IGL01829:Stard9	APN	2	120,706,446 (GRCm38)	missense	possibly damaging	0.59
IGL01916:Stard9	APN	2	120,668,016 (GRCm38)	missense	probably damaging	1.00
IGL02031:Stard9	APN	2	120,702,339 (GRCm38)	missense	probably benign	0.27
IGL02081:Stard9	APN	2	120,664,910 (GRCm38)	missense	probably damaging	0.98
IGL02558:Stard9	APN	2	120,696,907 (GRCm38)	missense	possibly damaging	0.95
IGL02646:Stard9	APN	2	120,698,992 (GRCm38)	missense	probably damaging	1.00
IGL02873:Stard9	APN	2	120,713,807 (GRCm38)	missense	probably damaging	1.00
IGL03195:Stard9	APN	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
IGL03204:Stard9	APN	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
FR4737:Stard9	UTSW	2	120,696,085 (GRCm38)	small insertion	probably benign
IGL03014:Stard9	UTSW	2	120,702,194 (GRCm38)	unclassified	probably benign
PIT4151001:Stard9	UTSW	2	120,702,756 (GRCm38)	nonsense	probably null
PIT4498001:Stard9	UTSW	2	120,697,435 (GRCm38)	missense	possibly damaging	0.86
R0027:Stard9	UTSW	2	120,703,501 (GRCm38)	missense	probably benign
R0027:Stard9	UTSW	2	120,703,501 (GRCm38)	missense	probably benign
R0038:Stard9	UTSW	2	120,695,832 (GRCm38)	missense	probably benign
R0049:Stard9	UTSW	2	120,699,819 (GRCm38)	missense	probably damaging	1.00
R0049:Stard9	UTSW	2	120,699,819 (GRCm38)	missense	probably damaging	1.00
R0116:Stard9	UTSW	2	120,634,255 (GRCm38)	missense	probably damaging	0.99
R0398:Stard9	UTSW	2	120,696,307 (GRCm38)	missense	probably benign	0.03
R0479:Stard9	UTSW	2	120,697,596 (GRCm38)	missense	probably damaging	1.00
R0556:Stard9	UTSW	2	120,698,923 (GRCm38)	missense	probably benign	0.09
R0589:Stard9	UTSW	2	120,698,547 (GRCm38)	missense	probably benign	0.00
R0609:Stard9	UTSW	2	120,706,306 (GRCm38)	missense	probably damaging	1.00
R0611:Stard9	UTSW	2	120,699,257 (GRCm38)	missense	probably benign	0.00
R0683:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R0751:Stard9	UTSW	2	120,697,485 (GRCm38)	missense	probably benign	0.04
R0833:Stard9	UTSW	2	120,696,999 (GRCm38)	missense	possibly damaging	0.86
R0836:Stard9	UTSW	2	120,696,999 (GRCm38)	missense	possibly damaging	0.86
R0838:Stard9	UTSW	2	120,700,842 (GRCm38)	missense	probably damaging	1.00
R0848:Stard9	UTSW	2	120,695,823 (GRCm38)	missense	probably damaging	1.00
R0849:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R0961:Stard9	UTSW	2	120,693,439 (GRCm38)	missense	probably benign	0.01
R0993:Stard9	UTSW	2	120,705,169 (GRCm38)	missense	probably damaging	1.00
R1005:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1006:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1115:Stard9	UTSW	2	120,692,850 (GRCm38)	missense	probably benign	0.05
R1163:Stard9	UTSW	2	120,696,213 (GRCm38)	missense	possibly damaging	0.86
R1199:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1200:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1331:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1332:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1333:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1334:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1335:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1336:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1338:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1346:Stard9	UTSW	2	120,713,448 (GRCm38)	missense	probably damaging	1.00
R1370:Stard9	UTSW	2	120,697,477 (GRCm38)	missense	probably benign	0.11
R1384:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1401:Stard9	UTSW	2	120,712,847 (GRCm38)	splice site	probably benign
R1416:Stard9	UTSW	2	120,700,972 (GRCm38)	missense	probably benign	0.00
R1453:Stard9	UTSW	2	120,666,376 (GRCm38)	missense	probably damaging	1.00
R1468:Stard9	UTSW	2	120,703,197 (GRCm38)	missense	possibly damaging	0.90
R1468:Stard9	UTSW	2	120,703,197 (GRCm38)	missense	possibly damaging	0.90
R1525:Stard9	UTSW	2	120,702,052 (GRCm38)	missense	probably benign	0.09
R1538:Stard9	UTSW	2	120,696,711 (GRCm38)	missense	probably benign	0.25
R1614:Stard9	UTSW	2	120,697,675 (GRCm38)	missense	possibly damaging	0.95
R1654:Stard9	UTSW	2	120,703,722 (GRCm38)	missense	probably benign	0.37
R1658:Stard9	UTSW	2	120,701,542 (GRCm38)	missense	probably benign	0.02
R1686:Stard9	UTSW	2	120,699,492 (GRCm38)	missense	probably benign	0.00
R1797:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1803:Stard9	UTSW	2	120,701,489 (GRCm38)	missense	probably benign	0.24
R1806:Stard9	UTSW	2	120,679,453 (GRCm38)	splice site	probably null
R1847:Stard9	UTSW	2	120,698,489 (GRCm38)	missense	possibly damaging	0.51
R1853:Stard9	UTSW	2	120,688,751 (GRCm38)	missense	probably damaging	1.00
R1892:Stard9	UTSW	2	120,693,708 (GRCm38)	missense	probably benign	0.01
R1906:Stard9	UTSW	2	120,696,427 (GRCm38)	missense	probably benign	0.00
R1907:Stard9	UTSW	2	120,713,812 (GRCm38)	missense	probably damaging	1.00
R1930:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R1933:Stard9	UTSW	2	120,698,656 (GRCm38)	missense	possibly damaging	0.55
R1989:Stard9	UTSW	2	120,701,406 (GRCm38)	missense	probably benign
R1999:Stard9	UTSW	2	120,692,868 (GRCm38)	missense	probably damaging	0.99
R2004:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,673,636 (GRCm38)	missense	probably damaging	1.00
R2005:Stard9	UTSW	2	120,664,945 (GRCm38)	missense	possibly damaging	0.90
R2021:Stard9	UTSW	2	120,704,235 (GRCm38)	missense	probably benign	0.05
R2025:Stard9	UTSW	2	120,702,398 (GRCm38)	missense	probably benign	0.20
R2190:Stard9	UTSW	2	120,714,120 (GRCm38)	missense	probably benign	0.22
R2204:Stard9	UTSW	2	120,698,531 (GRCm38)	frame shift	probably null
R2422:Stard9	UTSW	2	120,700,284 (GRCm38)	missense	probably benign	0.29
R3401:Stard9	UTSW	2	120,703,689 (GRCm38)	missense	probably damaging	0.98
R3618:Stard9	UTSW	2	120,699,019 (GRCm38)	missense	possibly damaging	0.49
R3619:Stard9	UTSW	2	120,699,019 (GRCm38)	missense	possibly damaging	0.49
R3900:Stard9	UTSW	2	120,713,549 (GRCm38)	missense	possibly damaging	0.93
R3943:Stard9	UTSW	2	120,698,229 (GRCm38)	missense	probably benign	0.11
R4022:Stard9	UTSW	2	120,704,155 (GRCm38)	missense	probably benign	0.05
R4223:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4224:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4225:Stard9	UTSW	2	120,664,991 (GRCm38)	missense	possibly damaging	0.95
R4345:Stard9	UTSW	2	120,701,946 (GRCm38)	missense	probably benign	0.43
R4382:Stard9	UTSW	2	120,634,222 (GRCm38)	missense	probably damaging	1.00
R4453:Stard9	UTSW	2	120,697,791 (GRCm38)	missense	probably benign
R4499:Stard9	UTSW	2	120,700,241 (GRCm38)	missense	probably benign	0.05
R4524:Stard9	UTSW	2	120,696,445 (GRCm38)	missense	probably damaging	1.00
R4671:Stard9	UTSW	2	120,698,640 (GRCm38)	missense	probably damaging	0.98
R4701:Stard9	UTSW	2	120,705,713 (GRCm38)	missense	possibly damaging	0.85
R4744:Stard9	UTSW	2	120,696,123 (GRCm38)	missense	probably benign	0.01
R4822:Stard9	UTSW	2	120,695,941 (GRCm38)	missense	possibly damaging	0.94
R4847:Stard9	UTSW	2	120,703,113 (GRCm38)	missense	probably benign	0.18
R4863:Stard9	UTSW	2	120,700,860 (GRCm38)	missense	probably benign	0.00
R4898:Stard9	UTSW	2	120,706,419 (GRCm38)	nonsense	probably null
R5033:Stard9	UTSW	2	120,693,399 (GRCm38)	missense	probably benign	0.00
R5087:Stard9	UTSW	2	120,697,019 (GRCm38)	nonsense	probably null
R5157:Stard9	UTSW	2	120,697,861 (GRCm38)	missense	probably benign
R5213:Stard9	UTSW	2	120,699,226 (GRCm38)	missense	probably damaging	1.00
R5237:Stard9	UTSW	2	120,699,358 (GRCm38)	missense	probably damaging	0.96
R5257:Stard9	UTSW	2	120,699,343 (GRCm38)	missense	probably damaging	0.99
R5258:Stard9	UTSW	2	120,699,343 (GRCm38)	missense	probably damaging	0.99
R5273:Stard9	UTSW	2	120,705,087 (GRCm38)	missense	possibly damaging	0.94
R5286:Stard9	UTSW	2	120,701,947 (GRCm38)	missense	probably benign	0.43
R5288:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5292:Stard9	UTSW	2	120,699,145 (GRCm38)	missense	probably benign	0.17
R5328:Stard9	UTSW	2	120,699,230 (GRCm38)	missense	probably damaging	1.00
R5385:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5386:Stard9	UTSW	2	120,700,630 (GRCm38)	missense	probably damaging	0.98
R5393:Stard9	UTSW	2	120,702,906 (GRCm38)	missense	possibly damaging	0.87
R5405:Stard9	UTSW	2	120,693,668 (GRCm38)	missense	probably benign	0.17
R5685:Stard9	UTSW	2	120,705,322 (GRCm38)	missense	probably damaging	1.00
R5749:Stard9	UTSW	2	120,703,786 (GRCm38)	missense	probably damaging	1.00
R5780:Stard9	UTSW	2	120,703,396 (GRCm38)	missense	probably benign	0.02
R5901:Stard9	UTSW	2	120,701,370 (GRCm38)	missense	probably damaging	1.00
R5941:Stard9	UTSW	2	120,713,558 (GRCm38)	missense	probably damaging	1.00
R5960:Stard9	UTSW	2	120,699,961 (GRCm38)	missense	probably benign	0.05
R5966:Stard9	UTSW	2	120,697,099 (GRCm38)	missense	probably damaging	1.00
R5967:Stard9	UTSW	2	120,706,894 (GRCm38)	missense	probably damaging	0.99
R6012:Stard9	UTSW	2	120,704,586 (GRCm38)	missense	probably damaging	1.00
R6019:Stard9	UTSW	2	120,693,715 (GRCm38)	frame shift	probably null
R6020:Stard9	UTSW	2	120,693,715 (GRCm38)	frame shift	probably null
R6036:Stard9	UTSW	2	120,700,075 (GRCm38)	missense	probably benign	0.09
R6036:Stard9	UTSW	2	120,700,075 (GRCm38)	missense	probably benign	0.09
R6090:Stard9	UTSW	2	120,693,654 (GRCm38)	missense	probably damaging	0.99
R6192:Stard9	UTSW	2	120,696,760 (GRCm38)	missense	probably damaging	0.99
R6228:Stard9	UTSW	2	120,713,750 (GRCm38)	missense	probably damaging	1.00
R6280:Stard9	UTSW	2	120,701,127 (GRCm38)	missense	probably benign
R6338:Stard9	UTSW	2	120,697,485 (GRCm38)	missense	probably benign
R6344:Stard9	UTSW	2	120,704,320 (GRCm38)	missense	probably benign	0.12
R6364:Stard9	UTSW	2	120,713,429 (GRCm38)	missense	probably damaging	1.00
R6383:Stard9	UTSW	2	120,666,407 (GRCm38)	critical splice donor site	probably null
R6644:Stard9	UTSW	2	120,695,772 (GRCm38)	missense	probably benign	0.11
R6747:Stard9	UTSW	2	120,698,383 (GRCm38)	missense	possibly damaging	0.62
R6833:Stard9	UTSW	2	120,701,259 (GRCm38)	missense	probably damaging	1.00
R6836:Stard9	UTSW	2	120,699,843 (GRCm38)	missense	probably benign	0.15
R6861:Stard9	UTSW	2	120,705,186 (GRCm38)	missense	probably benign	0.09
R6872:Stard9	UTSW	2	120,714,068 (GRCm38)	nonsense	probably null
R6875:Stard9	UTSW	2	120,697,436 (GRCm38)	missense	probably benign	0.04
R6915:Stard9	UTSW	2	120,702,630 (GRCm38)	missense	probably benign	0.00
R6934:Stard9	UTSW	2	120,697,695 (GRCm38)	missense	probably benign	0.00
R6943:Stard9	UTSW	2	120,702,196 (GRCm38)	missense	probably benign	0.29
R7009:Stard9	UTSW	2	120,697,191 (GRCm38)	missense	probably benign	0.37
R7031:Stard9	UTSW	2	120,700,450 (GRCm38)	missense	possibly damaging	0.61
R7132:Stard9	UTSW	2	120,679,378 (GRCm38)	nonsense	probably null
R7151:Stard9	UTSW	2	120,696,142 (GRCm38)	missense	probably benign
R7154:Stard9	UTSW	2	120,704,542 (GRCm38)	missense	probably benign	0.02
R7154:Stard9	UTSW	2	120,701,314 (GRCm38)	missense	probably benign	0.00
R7165:Stard9	UTSW	2	120,704,158 (GRCm38)	missense	probably damaging	1.00
R7260:Stard9	UTSW	2	120,706,938 (GRCm38)	missense	possibly damaging	0.90
R7270:Stard9	UTSW	2	120,634,274 (GRCm38)	nonsense	probably null
R7282:Stard9	UTSW	2	120,698,503 (GRCm38)	missense	probably benign	0.00
R7344:Stard9	UTSW	2	120,704,686 (GRCm38)	missense	possibly damaging	0.90
R7347:Stard9	UTSW	2	120,666,534 (GRCm38)	missense	probably benign
R7359:Stard9	UTSW	2	120,698,280 (GRCm38)	missense	probably damaging	1.00
R7375:Stard9	UTSW	2	120,665,002 (GRCm38)	splice site	probably null
R7410:Stard9	UTSW	2	120,701,497 (GRCm38)	missense	probably benign	0.41
R7422:Stard9	UTSW	2	120,702,152 (GRCm38)	missense	probably benign	0.21
R7475:Stard9	UTSW	2	120,688,110 (GRCm38)	missense	probably damaging	1.00
R7523:Stard9	UTSW	2	120,699,597 (GRCm38)	missense	probably benign
R7553:Stard9	UTSW	2	120,693,808 (GRCm38)	splice site	probably null
R7624:Stard9	UTSW	2	120,688,146 (GRCm38)	missense	probably benign	0.15
R7761:Stard9	UTSW	2	120,699,379 (GRCm38)	missense	probably benign	0.00
R7794:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R7819:Stard9	UTSW	2	120,700,984 (GRCm38)	missense	probably damaging	1.00
R7823:Stard9	UTSW	2	120,702,106 (GRCm38)	missense	probably damaging	0.96
R7837:Stard9	UTSW	2	120,703,665 (GRCm38)	missense	probably benign	0.06
R7889:Stard9	UTSW	2	120,704,461 (GRCm38)	missense	probably benign	0.11
R7905:Stard9	UTSW	2	120,696,081 (GRCm38)	missense	not run
R7956:Stard9	UTSW	2	120,705,371 (GRCm38)	nonsense	probably null
R8013:Stard9	UTSW	2	120,688,101 (GRCm38)	missense	probably damaging	1.00
R8113:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8114:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8116:Stard9	UTSW	2	120,664,939 (GRCm38)	nonsense	probably null
R8117:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8118:Stard9	UTSW	2	120,704,430 (GRCm38)	missense	probably benign	0.01
R8170:Stard9	UTSW	2	120,700,048 (GRCm38)	missense	possibly damaging	0.76
R8300:Stard9	UTSW	2	120,704,769 (GRCm38)	missense	possibly damaging	0.71
R8333:Stard9	UTSW	2	120,701,789 (GRCm38)	missense	probably benign	0.00
R8337:Stard9	UTSW	2	120,679,825 (GRCm38)	missense	probably damaging	1.00
R8536:Stard9	UTSW	2	120,714,659 (GRCm38)	missense	possibly damaging	0.93
R8682:Stard9	UTSW	2	120,703,315 (GRCm38)	missense	possibly damaging	0.65
R8696:Stard9	UTSW	2	120,701,114 (GRCm38)	missense	probably benign	0.02
R8708:Stard9	UTSW	2	120,703,578 (GRCm38)	missense	probably damaging	1.00
R8732:Stard9	UTSW	2	120,679,961 (GRCm38)	missense	probably damaging	1.00
R8798:Stard9	UTSW	2	120,704,731 (GRCm38)	missense	probably benign	0.09
R8807:Stard9	UTSW	2	120,705,451 (GRCm38)	missense	probably damaging	1.00
R8807:Stard9	UTSW	2	120,705,462 (GRCm38)	missense	probably damaging	1.00
R8862:Stard9	UTSW	2	120,703,618 (GRCm38)	missense	probably benign
R8920:Stard9	UTSW	2	120,702,607 (GRCm38)	missense	probably damaging	0.96
R9026:Stard9	UTSW	2	120,705,802 (GRCm38)	missense	probably damaging	1.00
R9048:Stard9	UTSW	2	120,677,934 (GRCm38)	missense	probably damaging	0.99
R9049:Stard9	UTSW	2	120,679,937 (GRCm38)	missense	probably benign	0.30
R9152:Stard9	UTSW	2	120,698,587 (GRCm38)	missense	probably damaging	0.99
R9189:Stard9	UTSW	2	120,703,019 (GRCm38)	missense	possibly damaging	0.95
R9238:Stard9	UTSW	2	120,697,966 (GRCm38)	missense	probably damaging	1.00
R9372:Stard9	UTSW	2	120,664,939 (GRCm38)	nonsense	probably null
R9393:Stard9	UTSW	2	120,688,175 (GRCm38)	missense	possibly damaging	0.88
R9444:Stard9	UTSW	2	120,664,933 (GRCm38)	missense	probably damaging	1.00
R9514:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9515:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9516:Stard9	UTSW	2	120,704,083 (GRCm38)	missense	probably damaging	1.00
R9570:Stard9	UTSW	2	120,704,233 (GRCm38)	missense	probably benign	0.02
R9649:Stard9	UTSW	2	120,696,154 (GRCm38)	missense	probably benign	0.20
R9789:Stard9	UTSW	2	120,679,936 (GRCm38)	missense	probably damaging	1.00
X0023:Stard9	UTSW	2	120,702,963 (GRCm38)	missense	possibly damaging	0.92
X0023:Stard9	UTSW	2	120,702,744 (GRCm38)	missense	probably benign	0.00
Z1176:Stard9	UTSW	2	120,698,322 (GRCm38)	missense	probably damaging	1.00
Z1176:Stard9	UTSW	2	120,696,612 (GRCm38)	missense	probably benign
Z1176:Stard9	UTSW	2	120,695,818 (GRCm38)	missense	probably benign	0.01
Z1177:Stard9	UTSW	2	120,673,676 (GRCm38)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- GGAGCAAGAGGTACAGCTTTAC -3'
(R):5'- TCGCAGTTGCTTCAGCTCAC -3'

Sequencing Primer
(F):5'- CAAGAGGTACAGCTTTACTACAAG -3'
(R):5'- ACAGTGTGGTATTGCACACC -3'

Posted On

2018-02-28