Incidental Mutation 'R6052:Ros1'
ID 484170
Institutional Source Beutler Lab
Gene Symbol Ros1
Ensembl Gene ENSMUSG00000019893
Gene Name Ros1 proto-oncogene
Synonyms Ros-1, c-ros
MMRRC Submission 044220-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # R6052 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 51921817-52071340 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 52039999 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 322 (I322L)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020045] [ENSMUST00000218452] [ENSMUST00000219173] [ENSMUST00000219692]
AlphaFold Q78DX7
Predicted Effect probably benign
Transcript: ENSMUST00000020045
AA Change: I331L

PolyPhen 2 Score 0.064 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000020045
Gene: ENSMUSG00000019893
AA Change: I331L

DomainStartEndE-ValueType
transmembrane domain 7 26 N/A INTRINSIC
FN3 109 187 1.05e-4 SMART
FN3 205 282 7.45e-10 SMART
LY 369 409 9.17e0 SMART
FN3 568 654 2.24e-4 SMART
LY 734 776 2.28e1 SMART
LY 777 815 4.61e0 SMART
FN3 944 1023 5.53e-4 SMART
FN3 1037 1133 1.07e1 SMART
FN3 1440 1532 1.19e1 SMART
FN3 1551 1637 2.11e0 SMART
FN3 1649 1731 6.8e-4 SMART
FN3 1746 1832 2.7e1 SMART
TyrKc 1938 2208 1.3e-145 SMART
low complexity region 2294 2307 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117992
AA Change: I331L

PolyPhen 2 Score 0.064 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000112873
Gene: ENSMUSG00000019893
AA Change: I331L

DomainStartEndE-ValueType
transmembrane domain 7 26 N/A INTRINSIC
FN3 109 187 1.05e-4 SMART
FN3 205 282 7.45e-10 SMART
LY 369 409 9.17e0 SMART
FN3 547 633 2.24e-4 SMART
LY 713 755 2.28e1 SMART
LY 756 794 4.61e0 SMART
FN3 923 1002 5.53e-4 SMART
FN3 1016 1112 1.07e1 SMART
FN3 1419 1511 1.19e1 SMART
FN3 1530 1616 2.11e0 SMART
FN3 1628 1710 6.8e-4 SMART
FN3 1725 1811 2.7e1 SMART
TyrKc 1917 2187 1.3e-145 SMART
low complexity region 2273 2286 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000175892
AA Change: I322L

PolyPhen 2 Score 0.387 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000135235
Gene: ENSMUSG00000019893
AA Change: I322L

DomainStartEndE-ValueType
transmembrane domain 7 26 N/A INTRINSIC
FN3 100 178 1.05e-4 SMART
FN3 196 273 7.45e-10 SMART
Blast:LY 360 400 1e-20 BLAST
Blast:LY 449 486 4e-15 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000177378
AA Change: I331L

PolyPhen 2 Score 0.083 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000134905
Gene: ENSMUSG00000019893
AA Change: I331L

DomainStartEndE-ValueType
transmembrane domain 7 26 N/A INTRINSIC
FN3 109 187 1.05e-4 SMART
FN3 205 282 7.45e-10 SMART
LY 369 409 9.17e0 SMART
FN3 547 633 2.24e-4 SMART
LY 713 755 2.28e1 SMART
LY 756 794 4.61e0 SMART
FN3 923 1002 5.53e-4 SMART
FN3 1016 1112 1.07e1 SMART
Blast:LY 1190 1236 2e-18 BLAST
FN3 1419 1511 1.19e1 SMART
FN3 1530 1616 2.11e0 SMART
FN3 1628 1710 6.8e-4 SMART
FN3 1725 1811 2.7e1 SMART
transmembrane domain 1832 1854 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000218452
AA Change: I331L

PolyPhen 2 Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)
Predicted Effect probably benign
Transcript: ENSMUST00000219173
AA Change: I331L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)
Predicted Effect probably benign
Transcript: ENSMUST00000219692
AA Change: I322L

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
Meta Mutation Damage Score 0.0909 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.7%
Validation Efficiency 96% (80/83)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This proto-oncogene, highly-expressed in a variety of tumor cell lines, belongs to the sevenless subfamily of tyrosine kinase insulin receptor genes. The protein encoded by this gene is a type I integral membrane protein with tyrosine kinase activity. The protein may function as a growth or differentiation factor receptor. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted null mutations exhibit male infertility due to impaired sperm maturation in the epididymis. Mutant sperm are capable of fertilization in vitro but not in vivo. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A G 17: 24,537,165 (GRCm39) F473L probably benign Het
Ankrd17 T C 5: 90,401,691 (GRCm39) I1449V probably benign Het
Aox4 T A 1: 58,293,477 (GRCm39) L943* probably null Het
Arap1 G A 7: 101,053,240 (GRCm39) V1257M probably damaging Het
B3gnt9 T C 8: 105,981,230 (GRCm39) S53G probably benign Het
Baiap3 A T 17: 25,467,444 (GRCm39) probably benign Het
Canx T C 11: 50,187,946 (GRCm39) D554G possibly damaging Het
Cbfa2t2 T C 2: 154,352,501 (GRCm39) V165A probably damaging Het
Ccdc17 C T 4: 116,457,145 (GRCm39) probably null Het
Cdcp1 A G 9: 123,014,396 (GRCm39) I126T probably benign Het
Cdk13 A T 13: 17,895,800 (GRCm39) D1036E probably damaging Het
Cfap157 A G 2: 32,669,863 (GRCm39) L240P probably damaging Het
Clec18a C A 8: 111,805,448 (GRCm39) E218* probably null Het
Col3a1 T C 1: 45,384,173 (GRCm39) probably benign Het
Dennd4a A G 9: 64,794,227 (GRCm39) E682G probably damaging Het
Dnah14 T C 1: 181,494,052 (GRCm39) V1736A possibly damaging Het
Dpep2 T A 8: 106,717,270 (GRCm39) D162V possibly damaging Het
Drd3 C A 16: 43,641,646 (GRCm39) P321T probably benign Het
Egfr A G 11: 16,861,554 (GRCm39) H1111R probably benign Het
Entpd1 T C 19: 40,708,928 (GRCm39) S58P probably damaging Het
Epha3 C A 16: 63,423,967 (GRCm39) V541L possibly damaging Het
Eri3 T A 4: 117,421,825 (GRCm39) D34E probably damaging Het
Eya1 T C 1: 14,353,374 (GRCm39) D58G probably damaging Het
Fat3 T A 9: 15,833,975 (GRCm39) S26C probably null Het
Fgl1 T C 8: 41,653,548 (GRCm39) D115G probably damaging Het
Fitm2 T C 2: 163,312,036 (GRCm39) Y59C probably damaging Het
Fras1 T A 5: 96,912,725 (GRCm39) I3343N probably damaging Het
Gba2 C A 4: 43,568,330 (GRCm39) C679F probably damaging Het
Glis2 G A 16: 4,431,603 (GRCm39) probably benign Het
Gm5150 T A 3: 16,044,917 (GRCm39) I103F probably damaging Het
Hhipl2 T C 1: 183,204,965 (GRCm39) S313P possibly damaging Het
Hmgcs1 A G 13: 120,166,995 (GRCm39) D474G probably benign Het
Homer3 C T 8: 70,744,076 (GRCm39) Q267* probably null Het
Hsd17b8 A G 17: 34,246,429 (GRCm39) L118P probably damaging Het
Igkv8-28 C T 6: 70,120,673 (GRCm39) G90D probably damaging Het
Kalrn T A 16: 34,181,255 (GRCm39) I128F probably damaging Het
Krt4 A G 15: 101,831,194 (GRCm39) probably null Het
Lamb2 T A 9: 108,364,811 (GRCm39) C1188* probably null Het
Lsr A T 7: 30,658,042 (GRCm39) M355K probably damaging Het
Map3k11 T G 19: 5,747,430 (GRCm39) D555E probably benign Het
Myocd A G 11: 65,087,082 (GRCm39) Y282H probably damaging Het
Nae1 T C 8: 105,261,176 (GRCm39) I7M probably benign Het
Nprl3 G T 11: 32,205,453 (GRCm39) H102N possibly damaging Het
Nup62 T A 7: 44,478,464 (GRCm39) F160I possibly damaging Het
Or10w1 C A 19: 13,631,871 (GRCm39) P26Q possibly damaging Het
Or2d3c A T 7: 106,525,896 (GRCm39) F257I probably benign Het
Or2r2 T A 6: 42,463,588 (GRCm39) T180S possibly damaging Het
Or5p76 A G 7: 108,122,945 (GRCm39) S71P probably benign Het
Or6c35 C A 10: 129,169,071 (GRCm39) T107K possibly damaging Het
Osbpl10 T C 9: 114,896,383 (GRCm39) probably null Het
Pcdh9 C T 14: 94,123,282 (GRCm39) V963I probably benign Het
Phf12 A G 11: 77,909,044 (GRCm39) R375G probably benign Het
Piezo1 G A 8: 123,233,008 (GRCm39) T108M probably damaging Het
Plxnc1 T A 10: 94,779,635 (GRCm39) Q269L probably benign Het
Pomgnt1 T A 4: 116,008,799 (GRCm39) N11K possibly damaging Het
Pramel22 T A 4: 143,382,222 (GRCm39) D158V probably damaging Het
Prkd1 A T 12: 50,413,083 (GRCm39) probably null Het
Prpf40a T C 2: 53,049,293 (GRCm39) T190A probably benign Het
Prrc2b A C 2: 32,102,297 (GRCm39) H790P possibly damaging Het
Rest T G 5: 77,429,027 (GRCm39) V482G probably benign Het
Rpl18 G A 7: 45,369,554 (GRCm39) probably benign Het
Rsad2 G A 12: 26,500,577 (GRCm39) H237Y probably benign Het
Sbf2 A G 7: 110,040,741 (GRCm39) L362S probably damaging Het
Sgsm3 A G 15: 80,893,464 (GRCm39) T409A probably benign Het
Slc16a14 T C 1: 84,890,430 (GRCm39) T292A possibly damaging Het
Spg11 T G 2: 121,927,837 (GRCm39) K649T probably damaging Het
Srprb T A 9: 103,067,415 (GRCm39) I268F possibly damaging Het
Tap2 G A 17: 34,433,683 (GRCm39) G566S probably damaging Het
Tecpr2 T C 12: 110,885,325 (GRCm39) V168A possibly damaging Het
Tln1 G C 4: 43,555,052 (GRCm39) F259L probably damaging Het
Tmem181a T A 17: 6,330,890 (GRCm39) L50H probably damaging Het
Tshz1 A G 18: 84,032,194 (GRCm39) I738T probably damaging Het
Tspan12 T C 6: 21,772,637 (GRCm39) E304G probably benign Het
Urb1 C T 16: 90,559,271 (GRCm39) G1671S probably damaging Het
Vmn2r2 T C 3: 64,024,782 (GRCm39) S600G possibly damaging Het
Wnt3 C A 11: 103,699,000 (GRCm39) Y35* probably null Het
Xpo7 T C 14: 70,921,159 (GRCm39) Y603C possibly damaging Het
Zfp457 G A 13: 67,442,015 (GRCm39) H91Y probably damaging Het
Zfp664 T A 5: 124,963,250 (GRCm39) C215S unknown Het
Zfp882 G A 8: 72,668,349 (GRCm39) G392D probably benign Het
Other mutations in Ros1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00236:Ros1 APN 10 52,070,986 (GRCm39) missense probably benign 0.01
IGL00338:Ros1 APN 10 52,001,907 (GRCm39) missense probably benign
IGL00419:Ros1 APN 10 51,967,150 (GRCm39) missense probably damaging 0.97
IGL00840:Ros1 APN 10 52,020,969 (GRCm39) missense possibly damaging 0.92
IGL00841:Ros1 APN 10 52,020,969 (GRCm39) missense possibly damaging 0.92
IGL00951:Ros1 APN 10 52,019,348 (GRCm39) missense probably damaging 0.99
IGL01123:Ros1 APN 10 51,996,905 (GRCm39) missense probably damaging 1.00
IGL01128:Ros1 APN 10 52,018,424 (GRCm39) nonsense probably null
IGL01300:Ros1 APN 10 51,977,809 (GRCm39) missense probably benign 0.01
IGL01316:Ros1 APN 10 51,963,975 (GRCm39) critical splice donor site probably null
IGL01349:Ros1 APN 10 51,927,122 (GRCm39) missense probably damaging 0.99
IGL01363:Ros1 APN 10 52,042,238 (GRCm39) missense probably damaging 1.00
IGL01457:Ros1 APN 10 51,922,426 (GRCm39) splice site probably benign
IGL01532:Ros1 APN 10 51,967,034 (GRCm39) splice site probably benign
IGL01585:Ros1 APN 10 52,031,198 (GRCm39) missense probably damaging 1.00
IGL01650:Ros1 APN 10 52,031,075 (GRCm39) missense probably damaging 0.99
IGL01672:Ros1 APN 10 51,977,899 (GRCm39) missense possibly damaging 0.92
IGL01904:Ros1 APN 10 51,954,007 (GRCm39) missense probably damaging 0.97
IGL02040:Ros1 APN 10 51,992,018 (GRCm39) missense probably damaging 0.99
IGL02053:Ros1 APN 10 52,038,816 (GRCm39) missense probably damaging 1.00
IGL02147:Ros1 APN 10 51,996,991 (GRCm39) missense probably damaging 1.00
IGL02169:Ros1 APN 10 51,958,053 (GRCm39) critical splice donor site probably null
IGL02247:Ros1 APN 10 52,005,677 (GRCm39) missense probably damaging 0.99
IGL02262:Ros1 APN 10 52,055,065 (GRCm39) missense probably damaging 0.96
IGL02307:Ros1 APN 10 52,004,534 (GRCm39) missense possibly damaging 0.53
IGL02398:Ros1 APN 10 52,020,980 (GRCm39) splice site probably benign
IGL02525:Ros1 APN 10 51,992,138 (GRCm39) missense possibly damaging 0.66
IGL02718:Ros1 APN 10 51,994,328 (GRCm39) missense probably damaging 1.00
IGL02721:Ros1 APN 10 52,048,927 (GRCm39) splice site probably benign
IGL02808:Ros1 APN 10 52,001,985 (GRCm39) missense probably damaging 1.00
IGL03009:Ros1 APN 10 52,022,003 (GRCm39) missense probably benign 0.00
IGL03035:Ros1 APN 10 51,952,080 (GRCm39) splice site probably benign
IGL03092:Ros1 APN 10 51,974,902 (GRCm39) missense probably damaging 0.99
IGL03309:Ros1 APN 10 51,994,357 (GRCm39) missense possibly damaging 0.83
IGL03333:Ros1 APN 10 52,031,267 (GRCm39) missense probably damaging 1.00
boss UTSW 10 51,967,091 (GRCm39) nonsense probably null
Chuckwagon UTSW 10 51,994,299 (GRCm39) missense probably damaging 1.00
R1005_Ros1_648 UTSW 10 52,004,501 (GRCm39) splice site probably benign
R1220_Ros1_012 UTSW 10 51,974,966 (GRCm39) missense probably damaging 0.97
R3423_Ros1_122 UTSW 10 52,004,512 (GRCm39) splice site probably null
trail UTSW 10 52,037,991 (GRCm39) nonsense probably null
R0049:Ros1 UTSW 10 51,977,857 (GRCm39) missense possibly damaging 0.66
R0049:Ros1 UTSW 10 51,977,857 (GRCm39) missense possibly damaging 0.66
R0050:Ros1 UTSW 10 51,977,899 (GRCm39) missense probably damaging 0.97
R0050:Ros1 UTSW 10 51,977,899 (GRCm39) missense probably damaging 0.97
R0057:Ros1 UTSW 10 52,056,287 (GRCm39) missense probably benign 0.00
R0057:Ros1 UTSW 10 52,056,287 (GRCm39) missense probably benign 0.00
R0106:Ros1 UTSW 10 52,018,363 (GRCm39) missense possibly damaging 0.85
R0106:Ros1 UTSW 10 52,018,363 (GRCm39) missense possibly damaging 0.85
R0125:Ros1 UTSW 10 52,001,885 (GRCm39) missense probably benign 0.38
R0403:Ros1 UTSW 10 52,019,534 (GRCm39) splice site probably benign
R0487:Ros1 UTSW 10 52,031,204 (GRCm39) missense possibly damaging 0.69
R0502:Ros1 UTSW 10 52,070,919 (GRCm39) splice site probably benign
R0557:Ros1 UTSW 10 51,961,359 (GRCm39) missense possibly damaging 0.82
R0599:Ros1 UTSW 10 51,999,396 (GRCm39) missense probably damaging 1.00
R0620:Ros1 UTSW 10 51,994,444 (GRCm39) missense probably damaging 1.00
R0679:Ros1 UTSW 10 51,942,391 (GRCm39) missense possibly damaging 0.95
R1005:Ros1 UTSW 10 52,004,501 (GRCm39) splice site probably benign
R1073:Ros1 UTSW 10 51,922,221 (GRCm39) missense probably damaging 1.00
R1220:Ros1 UTSW 10 51,974,966 (GRCm39) missense probably damaging 0.97
R1279:Ros1 UTSW 10 52,018,262 (GRCm39) missense possibly damaging 0.81
R1295:Ros1 UTSW 10 51,964,028 (GRCm39) missense possibly damaging 0.92
R1336:Ros1 UTSW 10 52,044,758 (GRCm39) missense probably damaging 1.00
R1371:Ros1 UTSW 10 51,964,041 (GRCm39) missense probably damaging 0.98
R1447:Ros1 UTSW 10 51,974,954 (GRCm39) missense possibly damaging 0.66
R1486:Ros1 UTSW 10 52,048,954 (GRCm39) missense probably damaging 1.00
R1499:Ros1 UTSW 10 51,974,773 (GRCm39) missense possibly damaging 0.92
R1669:Ros1 UTSW 10 52,037,907 (GRCm39) missense probably damaging 1.00
R1744:Ros1 UTSW 10 51,999,475 (GRCm39) missense probably damaging 0.99
R1759:Ros1 UTSW 10 51,996,922 (GRCm39) missense probably damaging 1.00
R1791:Ros1 UTSW 10 51,976,183 (GRCm39) missense probably benign 0.00
R1794:Ros1 UTSW 10 52,000,199 (GRCm39) nonsense probably null
R2031:Ros1 UTSW 10 51,943,164 (GRCm39) missense possibly damaging 0.88
R2115:Ros1 UTSW 10 52,004,651 (GRCm39) missense probably benign 0.00
R2219:Ros1 UTSW 10 52,042,175 (GRCm39) missense probably damaging 1.00
R2290:Ros1 UTSW 10 51,994,477 (GRCm39) missense probably damaging 0.96
R2329:Ros1 UTSW 10 52,038,983 (GRCm39) missense probably damaging 1.00
R2371:Ros1 UTSW 10 52,039,991 (GRCm39) missense possibly damaging 0.66
R2879:Ros1 UTSW 10 52,048,936 (GRCm39) critical splice donor site probably null
R3154:Ros1 UTSW 10 51,927,077 (GRCm39) missense probably benign
R3423:Ros1 UTSW 10 52,004,512 (GRCm39) splice site probably null
R3424:Ros1 UTSW 10 52,004,512 (GRCm39) splice site probably null
R3425:Ros1 UTSW 10 52,004,512 (GRCm39) splice site probably null
R3433:Ros1 UTSW 10 51,967,204 (GRCm39) missense probably benign 0.45
R3522:Ros1 UTSW 10 51,967,091 (GRCm39) nonsense probably null
R3686:Ros1 UTSW 10 52,021,912 (GRCm39) missense probably damaging 1.00
R3710:Ros1 UTSW 10 52,037,991 (GRCm39) nonsense probably null
R3771:Ros1 UTSW 10 52,005,087 (GRCm39) missense probably damaging 0.97
R3808:Ros1 UTSW 10 51,996,944 (GRCm39) missense probably benign 0.08
R3930:Ros1 UTSW 10 52,070,944 (GRCm39) missense possibly damaging 0.92
R3950:Ros1 UTSW 10 51,942,484 (GRCm39) missense probably damaging 1.00
R3981:Ros1 UTSW 10 51,996,974 (GRCm39) missense possibly damaging 0.46
R4007:Ros1 UTSW 10 51,994,328 (GRCm39) missense probably damaging 1.00
R4346:Ros1 UTSW 10 52,044,705 (GRCm39) missense possibly damaging 0.92
R4382:Ros1 UTSW 10 51,997,055 (GRCm39) missense possibly damaging 0.46
R4414:Ros1 UTSW 10 52,038,800 (GRCm39) critical splice donor site probably null
R4450:Ros1 UTSW 10 51,954,038 (GRCm39) missense probably damaging 0.98
R4468:Ros1 UTSW 10 51,994,452 (GRCm39) missense probably damaging 1.00
R4569:Ros1 UTSW 10 52,040,090 (GRCm39) missense probably damaging 0.99
R4649:Ros1 UTSW 10 52,005,764 (GRCm39) missense possibly damaging 0.66
R4684:Ros1 UTSW 10 52,005,192 (GRCm39) missense probably damaging 1.00
R4706:Ros1 UTSW 10 51,977,990 (GRCm39) missense possibly damaging 0.95
R4731:Ros1 UTSW 10 52,018,325 (GRCm39) missense probably damaging 1.00
R4748:Ros1 UTSW 10 51,992,093 (GRCm39) missense probably benign 0.00
R4806:Ros1 UTSW 10 51,972,271 (GRCm39) missense probably damaging 0.96
R4865:Ros1 UTSW 10 52,048,966 (GRCm39) missense probably damaging 0.99
R4973:Ros1 UTSW 10 52,031,087 (GRCm39) missense probably damaging 0.98
R5022:Ros1 UTSW 10 52,000,171 (GRCm39) missense possibly damaging 0.46
R5033:Ros1 UTSW 10 52,004,512 (GRCm39) critical splice donor site probably null
R5082:Ros1 UTSW 10 52,040,037 (GRCm39) missense possibly damaging 0.66
R5083:Ros1 UTSW 10 52,040,037 (GRCm39) missense possibly damaging 0.66
R5130:Ros1 UTSW 10 52,040,037 (GRCm39) missense possibly damaging 0.66
R5269:Ros1 UTSW 10 51,927,104 (GRCm39) missense probably damaging 1.00
R5399:Ros1 UTSW 10 51,967,040 (GRCm39) critical splice donor site probably null
R5414:Ros1 UTSW 10 52,031,189 (GRCm39) missense probably damaging 1.00
R5659:Ros1 UTSW 10 52,019,482 (GRCm39) missense possibly damaging 0.92
R5742:Ros1 UTSW 10 52,018,234 (GRCm39) critical splice donor site probably null
R5780:Ros1 UTSW 10 52,070,953 (GRCm39) missense probably damaging 1.00
R5805:Ros1 UTSW 10 51,999,385 (GRCm39) missense probably damaging 1.00
R5843:Ros1 UTSW 10 52,042,293 (GRCm39) missense possibly damaging 0.92
R5881:Ros1 UTSW 10 52,057,894 (GRCm39) missense probably benign 0.26
R6027:Ros1 UTSW 10 52,040,064 (GRCm39) missense possibly damaging 0.82
R6035:Ros1 UTSW 10 51,954,067 (GRCm39) missense probably benign
R6035:Ros1 UTSW 10 51,954,067 (GRCm39) missense probably benign
R6175:Ros1 UTSW 10 51,977,881 (GRCm39) missense probably benign 0.02
R6315:Ros1 UTSW 10 51,994,306 (GRCm39) missense probably benign
R6342:Ros1 UTSW 10 52,031,351 (GRCm39) missense probably damaging 1.00
R6470:Ros1 UTSW 10 52,042,140 (GRCm39) critical splice donor site probably null
R6527:Ros1 UTSW 10 52,019,473 (GRCm39) missense possibly damaging 0.66
R6568:Ros1 UTSW 10 52,038,908 (GRCm39) missense probably damaging 1.00
R6573:Ros1 UTSW 10 52,031,106 (GRCm39) missense possibly damaging 0.84
R6653:Ros1 UTSW 10 52,018,299 (GRCm39) missense probably damaging 1.00
R6959:Ros1 UTSW 10 52,040,090 (GRCm39) missense probably damaging 0.99
R7011:Ros1 UTSW 10 52,056,272 (GRCm39) missense probably damaging 1.00
R7111:Ros1 UTSW 10 52,057,906 (GRCm39) missense probably benign 0.02
R7243:Ros1 UTSW 10 51,999,477 (GRCm39) missense probably damaging 1.00
R7355:Ros1 UTSW 10 52,042,175 (GRCm39) missense probably damaging 1.00
R7385:Ros1 UTSW 10 52,031,222 (GRCm39) missense probably benign 0.00
R7460:Ros1 UTSW 10 51,994,299 (GRCm39) missense probably damaging 1.00
R7549:Ros1 UTSW 10 52,021,930 (GRCm39) missense probably damaging 0.96
R7573:Ros1 UTSW 10 52,046,072 (GRCm39) missense probably benign 0.03
R7650:Ros1 UTSW 10 51,922,305 (GRCm39) missense probably benign 0.00
R7667:Ros1 UTSW 10 52,040,067 (GRCm39) missense probably damaging 1.00
R7696:Ros1 UTSW 10 52,018,379 (GRCm39) missense probably damaging 1.00
R7785:Ros1 UTSW 10 52,038,944 (GRCm39) missense probably damaging 1.00
R7814:Ros1 UTSW 10 51,972,233 (GRCm39) missense probably benign 0.28
R7830:Ros1 UTSW 10 52,031,030 (GRCm39) missense probably damaging 0.99
R7832:Ros1 UTSW 10 52,020,957 (GRCm39) missense probably damaging 0.99
R7854:Ros1 UTSW 10 52,004,563 (GRCm39) missense probably damaging 1.00
R7912:Ros1 UTSW 10 52,044,791 (GRCm39) missense probably damaging 1.00
R7972:Ros1 UTSW 10 52,030,926 (GRCm39) nonsense probably null
R7993:Ros1 UTSW 10 51,999,443 (GRCm39) missense probably benign 0.34
R8036:Ros1 UTSW 10 52,041,439 (GRCm39) missense probably benign
R8137:Ros1 UTSW 10 52,001,933 (GRCm39) missense possibly damaging 0.87
R8169:Ros1 UTSW 10 51,940,768 (GRCm39) critical splice donor site probably null
R8199:Ros1 UTSW 10 51,977,813 (GRCm39) nonsense probably null
R8293:Ros1 UTSW 10 51,964,014 (GRCm39) missense probably damaging 1.00
R8368:Ros1 UTSW 10 51,940,833 (GRCm39) missense probably damaging 1.00
R8406:Ros1 UTSW 10 51,977,941 (GRCm39) missense possibly damaging 0.56
R8471:Ros1 UTSW 10 51,997,078 (GRCm39) missense probably benign 0.00
R8498:Ros1 UTSW 10 52,055,047 (GRCm39) missense probably damaging 0.99
R8532:Ros1 UTSW 10 51,974,852 (GRCm39) missense possibly damaging 0.92
R8678:Ros1 UTSW 10 51,963,998 (GRCm39) missense probably benign
R8726:Ros1 UTSW 10 51,954,769 (GRCm39) missense possibly damaging 0.46
R8789:Ros1 UTSW 10 51,999,328 (GRCm39) missense probably damaging 0.99
R8799:Ros1 UTSW 10 51,922,143 (GRCm39) missense probably benign 0.08
R8915:Ros1 UTSW 10 51,977,805 (GRCm39) splice site probably benign
R8958:Ros1 UTSW 10 51,972,190 (GRCm39) missense probably damaging 1.00
R8972:Ros1 UTSW 10 51,999,333 (GRCm39) missense probably benign 0.05
R9020:Ros1 UTSW 10 52,031,023 (GRCm39) missense probably benign 0.32
R9147:Ros1 UTSW 10 51,927,039 (GRCm39) missense probably benign
R9154:Ros1 UTSW 10 51,922,301 (GRCm39) missense possibly damaging 0.87
R9189:Ros1 UTSW 10 52,019,502 (GRCm39) missense probably damaging 0.99
R9341:Ros1 UTSW 10 51,972,116 (GRCm39) critical splice donor site probably null
R9343:Ros1 UTSW 10 51,972,116 (GRCm39) critical splice donor site probably null
R9407:Ros1 UTSW 10 51,994,491 (GRCm39) missense probably damaging 1.00
R9428:Ros1 UTSW 10 51,958,061 (GRCm39) missense probably benign 0.00
R9502:Ros1 UTSW 10 52,000,174 (GRCm39) missense probably benign 0.00
R9531:Ros1 UTSW 10 52,007,063 (GRCm39) missense probably damaging 1.00
R9546:Ros1 UTSW 10 51,994,215 (GRCm39) critical splice donor site probably null
R9562:Ros1 UTSW 10 51,943,170 (GRCm39) missense probably damaging 1.00
R9565:Ros1 UTSW 10 51,943,170 (GRCm39) missense probably damaging 1.00
R9604:Ros1 UTSW 10 51,994,249 (GRCm39) missense probably damaging 1.00
R9645:Ros1 UTSW 10 51,948,148 (GRCm39) critical splice donor site probably null
R9658:Ros1 UTSW 10 51,967,069 (GRCm39) missense probably damaging 0.99
R9664:Ros1 UTSW 10 51,996,931 (GRCm39) missense probably benign 0.18
RF018:Ros1 UTSW 10 52,031,217 (GRCm39) missense probably benign
Z1176:Ros1 UTSW 10 51,967,205 (GRCm39) missense possibly damaging 0.89
Z1177:Ros1 UTSW 10 52,044,767 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- TACCTAGCTCTGGGATCTAAGAG -3'
(R):5'- ATTTCCTACTGCCAGCCATG -3'

Sequencing Primer
(F):5'- GCTAGCCTTGAACTCAGAAATTTGCC -3'
(R):5'- GATTATGTCACAGATGCAATACCTC -3'
Posted On 2017-07-14