Incidental Mutation 'R8337:Stard9'
ID 644655
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 067800-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.146) question?
Stock # R8337 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 120629121-120731895 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 120679825 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Isoleucine at position 296 (F296I)
Ref Sequence ENSEMBL: ENSMUSP00000136055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000140843] [ENSMUST00000180041]
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000117178
Gene: ENSMUSG00000033705
AA Change: F296I

DomainStartEndE-ValueType
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 damaging
Transcript: ENSMUST00000180041
AA Change: F296I

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
AA Change: F296I

DomainStartEndE-ValueType
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: 99.5%
  • 20x: 98.2%
Validation Efficiency 100% (55/55)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310034C09Rik T C 16: 88,759,263 (GRCm38) Y122H probably damaging Het
Abhd14b T A 9: 106,450,041 (GRCm38) H7Q probably benign Het
Acod1 C T 14: 103,049,344 (GRCm38) R28W possibly damaging Het
Agap2 A G 10: 127,088,325 (GRCm38) T803A unknown Het
Angptl7 T C 4: 148,497,284 (GRCm38) E215G probably damaging Het
Ankrd34c T A 9: 89,729,898 (GRCm38) D130V probably damaging Het
BC028528 A G 3: 95,884,986 (GRCm38) V144A probably benign Het
Cab39l T C 14: 59,539,191 (GRCm38) F274L probably damaging Het
Cdsn T C 17: 35,555,518 (GRCm38) S315P possibly damaging Het
Celsr3 CGGGG CGGGGG 9: 108,841,272 (GRCm38) probably null Het
Cep97 A T 16: 55,915,031 (GRCm38) L540* probably null Het
Chrna2 G T 14: 66,149,568 (GRCm38) E388* probably null Het
Ckap4 A G 10: 84,528,596 (GRCm38) V201A probably damaging Het
Clec4b1 A G 6: 123,065,963 (GRCm38) K47R probably benign Het
Clvs2 A T 10: 33,528,488 (GRCm38) I244N possibly damaging Het
Cmtr1 G A 17: 29,674,177 (GRCm38) E57K probably benign Het
Cxxc1 T A 18: 74,220,839 (GRCm38) D565E possibly damaging Het
Dpcr1 T C 17: 35,637,594 (GRCm38) H371R possibly damaging Het
Dtx3l T A 16: 35,933,703 (GRCm38) M178L probably benign Het
Eml2 A G 7: 19,196,236 (GRCm38) D294G possibly damaging Het
Flt3 A G 5: 147,332,888 (GRCm38) probably null Het
Frs3 T A 17: 47,703,852 (GRCm38) L490Q probably damaging Het
Gm14085 C T 2: 122,525,136 (GRCm38) T603I probably benign Het
Gm35339 T C 15: 76,361,484 (GRCm38) V1307A Het
Gm6882 G A 7: 21,427,634 (GRCm38) T103I possibly damaging Het
Gsdmd C T 15: 75,864,421 (GRCm38) T133I probably benign Het
Hhipl2 C A 1: 183,428,632 (GRCm38) C331* probably null Het
Ifnar1 C A 16: 91,505,336 (GRCm38) D566E possibly damaging Het
Ighv1-34 A T 12: 114,851,319 (GRCm38) N74K probably benign Het
Itk T C 11: 46,342,395 (GRCm38) probably null Het
Kdm7a T C 6: 39,145,527 (GRCm38) D801G probably benign Het
March1 T C 8: 66,418,989 (GRCm38) L139P probably damaging Het
Metap1d T C 2: 71,515,638 (GRCm38) V181A probably damaging Het
Mfsd8 G A 3: 40,835,193 (GRCm38) R140C probably damaging Het
Mrps25 T C 6: 92,175,764 (GRCm38) T92A probably benign Het
Ntng2 C A 2: 29,248,038 (GRCm38) M1I probably null Het
Olfr635 A C 7: 103,979,374 (GRCm38) M61L probably damaging Het
Olfr64 C T 7: 103,893,049 (GRCm38) G229R probably benign Het
Olfr983 T C 9: 40,092,399 (GRCm38) K189R probably benign Het
Pla2g12a A G 3: 129,878,816 (GRCm38) D33G probably damaging Het
Prlhr A G 19: 60,467,846 (GRCm38) V94A possibly damaging Het
Ralgapb T A 2: 158,450,272 (GRCm38) S793T probably benign Het
Rapgef6 T A 11: 54,631,301 (GRCm38) L455* probably null Het
Sbf2 T C 7: 110,441,462 (GRCm38) H386R probably benign Het
Sec23ip C A 7: 128,764,025 (GRCm38) N539K probably damaging Het
Shisa4 A G 1: 135,373,169 (GRCm38) L121P probably damaging Het
Strn3 T C 12: 51,661,172 (GRCm38) K147E probably damaging Het
Taf5l T C 8: 123,998,102 (GRCm38) N326S probably benign Het
Tfb2m T A 1: 179,542,349 (GRCm38) I170L probably benign Het
Tfec T C 6: 16,845,423 (GRCm38) N79S possibly damaging Het
Tnn C T 1: 160,118,483 (GRCm38) G922R probably damaging Het
Tox3 T C 8: 90,347,879 (GRCm38) Y24C probably damaging Het
Vmn2r6 A T 3: 64,556,105 (GRCm38) L436* probably null Het
Vmn2r80 A G 10: 79,148,873 (GRCm38) I20V probably benign Het
Other mutations in Stard9
AlleleSourceChrCoordTypePredicted EffectPPH 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
R6235:Stard9 UTSW 2 120,713,546 (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
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'- GAGTGACCATCATTCCAGAATAATG -3'
(R):5'- ACTCCACTTACTGGCAACCATG -3'

Sequencing Primer
(F):5'- AAGGAGTATGGCACTCAG -3'
(R):5'- CCATGATGGTTTTGGAGTTGCCTC -3'
Posted On 2020-09-02