Incidental Mutation 'R9154:Ros1'
ID 695257
Institutional Source Beutler Lab
Gene Symbol Ros1
Ensembl Gene ENSMUSG00000019893
Gene Name Ros1 proto-oncogene
Synonyms Ros-1, c-ros
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # R9154 (G1)
Quality Score 225.009
Status Not validated
Chromosome 10
Chromosomal Location 51921817-52071340 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 51922301 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Aspartic acid at position 2278 (E2278D)
Ref Sequence ENSEMBL: ENSMUSP00000020045 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020045] [ENSMUST00000218452] [ENSMUST00000219173] [ENSMUST00000219692]
AlphaFold Q78DX7
Predicted Effect possibly damaging
Transcript: ENSMUST00000020045
AA Change: E2278D

PolyPhen 2 Score 0.873 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000020045
Gene: ENSMUSG00000019893
AA Change: E2278D

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 possibly damaging
Transcript: ENSMUST00000218452
AA Change: E2257D

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
Predicted Effect probably benign
Transcript: ENSMUST00000219173
Predicted Effect probably benign
Transcript: ENSMUST00000219692
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
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: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930590J08Rik T C 6: 91,926,926 (GRCm39) V862A probably benign Het
A2m A T 6: 121,645,512 (GRCm39) K1019M probably damaging Het
Acot6 G T 12: 84,147,789 (GRCm39) W15L possibly damaging Het
Adam32 CCAGCAGCAGCAGCAGCAG CCAGCAGCAGCAGCAG 8: 25,438,769 (GRCm39) probably benign Het
Adnp C A 2: 168,026,580 (GRCm39) Q238H possibly damaging Het
Akap7 T C 10: 25,047,053 (GRCm39) Y281C probably damaging Het
Ank1 A G 8: 23,605,387 (GRCm39) E1085G probably damaging Het
Arhgef38 A T 3: 132,837,924 (GRCm39) S669T unknown Het
Atp8b2 A T 3: 89,865,927 (GRCm39) S50R possibly damaging Het
Atp8b5 T C 4: 43,372,630 (GRCm39) I1090T probably benign Het
Ccdc198 A T 14: 49,473,367 (GRCm39) H129Q probably benign Het
Chrna4 G A 2: 180,670,602 (GRCm39) R385C probably damaging Het
Col4a1 T A 8: 11,267,446 (GRCm39) I1105F probably damaging Het
Crybg2 G A 4: 133,792,620 (GRCm39) R85Q probably benign Het
Cspg4 T A 9: 56,798,287 (GRCm39) L1434Q Het
Cyp3a13 T C 5: 137,919,758 (GRCm39) N6S probably benign Het
Dnase2b A T 3: 146,299,326 (GRCm39) Y42* probably null Het
F11r A G 1: 171,289,376 (GRCm39) E233G probably damaging Het
Fip1l1 T C 5: 74,747,703 (GRCm39) I390T possibly damaging Het
Fiz1 G A 7: 5,011,280 (GRCm39) R413C probably damaging Het
Fus G A 7: 127,580,440 (GRCm39) G450E unknown Het
Gm11569 C A 11: 99,689,267 (GRCm39) C144F unknown Het
Gm7298 A T 6: 121,756,436 (GRCm39) Y1027F probably damaging Het
Grik5 C A 7: 24,758,403 (GRCm39) W340L probably damaging Het
H1f2 A G 13: 23,923,373 (GRCm39) K181R unknown Het
Hectd4 G A 5: 121,391,967 (GRCm39) R77H Het
Ift81 C A 5: 122,689,122 (GRCm39) V665L probably benign Het
Ints2 A G 11: 86,125,524 (GRCm39) F559L probably damaging Het
Kdm8 G A 7: 125,054,296 (GRCm39) V176I probably benign Het
Keap1 A T 9: 21,142,121 (GRCm39) Y584* probably null Het
Klra1 T C 6: 130,357,607 (GRCm39) T7A Het
Lmo7 T A 14: 102,122,743 (GRCm39) W311R probably damaging Het
Lrp6 A G 6: 134,518,855 (GRCm39) V70A probably damaging Het
Luc7l3 A T 11: 94,190,793 (GRCm39) S174T unknown Het
Madd T C 2: 90,998,162 (GRCm39) T653A probably damaging Het
Mlph G T 1: 90,855,716 (GRCm39) G41V probably damaging Het
Mov10l1 A G 15: 88,896,118 (GRCm39) E654G possibly damaging Het
Mpp3 T C 11: 101,911,328 (GRCm39) I165V Het
Mrgpra2a T G 7: 47,076,394 (GRCm39) Y288S probably damaging Het
Mroh9 T A 1: 162,890,030 (GRCm39) M236L Het
Muc5b A C 7: 141,417,974 (GRCm39) K3640T probably damaging Het
Myh13 A G 11: 67,253,318 (GRCm39) I1485V probably benign Het
Nf2 A T 11: 4,744,873 (GRCm39) F285L probably damaging Het
Nfx1 T A 4: 40,990,845 (GRCm39) C471S probably damaging Het
Nsd1 C T 13: 55,361,253 (GRCm39) R74W probably damaging Het
Nudt16l1 A T 16: 4,758,281 (GRCm39) *212C probably null Het
Oaf T C 9: 43,133,992 (GRCm39) Y243C probably damaging Het
Or51e1 T C 7: 102,358,541 (GRCm39) V25A probably benign Het
Or6c3 T C 10: 129,308,690 (GRCm39) I43T probably benign Het
Or7g30 T A 9: 19,352,531 (GRCm39) F107L probably benign Het
Or7h8 A G 9: 20,124,173 (GRCm39) H176R possibly damaging Het
Or8b36 T A 9: 37,937,690 (GRCm39) L196* probably null Het
Parp9 T C 16: 35,768,543 (GRCm39) I241T probably damaging Het
Phlpp2 G T 8: 110,666,590 (GRCm39) A1040S possibly damaging Het
Pon2 A T 6: 5,265,391 (GRCm39) V332E possibly damaging Het
Ptprc A G 1: 138,016,302 (GRCm39) V544A probably damaging Het
Rfx6 A G 10: 51,597,600 (GRCm39) S446G probably benign Het
Rnf103 T A 6: 71,487,099 (GRCm39) C577S probably benign Het
Rpl37 A G 15: 5,147,109 (GRCm39) S50G probably benign Het
Rrad C T 8: 105,355,343 (GRCm39) V222M possibly damaging Het
Ryr1 T C 7: 28,769,283 (GRCm39) T2770A probably benign Het
Secisbp2l G A 2: 125,617,623 (GRCm39) P18L probably damaging Het
Septin2 T A 1: 93,429,310 (GRCm39) W260R probably damaging Het
Slc35c2 A G 2: 165,122,797 (GRCm39) M117T probably benign Het
Slc44a5 A G 3: 153,953,373 (GRCm39) T252A probably benign Het
Speer4f2 T A 5: 17,581,610 (GRCm39) L184Q Het
Sphkap C G 1: 83,234,982 (GRCm39) V1615L probably damaging Het
Sult2a3 C T 7: 13,806,981 (GRCm39) V234I probably benign Het
Tanc1 T C 2: 59,630,132 (GRCm39) L704P probably damaging Het
Tas2r126 T C 6: 42,412,174 (GRCm39) S236P probably benign Het
Tnik A G 3: 28,704,235 (GRCm39) I1020V probably damaging Het
Tomm5 T C 4: 45,106,724 (GRCm39) Q64R unknown Het
Ttll13 A G 7: 79,897,182 (GRCm39) E16G probably benign Het
Vmn1r21 C A 6: 57,821,348 (GRCm39) C32F probably benign Het
Vmn2r51 T A 7: 9,839,480 (GRCm39) D36V probably damaging Het
Vmn2r63 C T 7: 42,576,413 (GRCm39) D467N probably damaging Het
Vwce A G 19: 10,625,850 (GRCm39) N454S possibly damaging Het
Wfdc1 A C 8: 120,406,116 (GRCm39) D77A Het
Yme1l1 T A 2: 23,077,815 (GRCm39) I419N probably damaging Het
Zfp106 G A 2: 120,364,812 (GRCm39) Q555* probably null Het
Zfp773 A C 7: 7,138,302 (GRCm39) M111R probably damaging Het
Zmat3 G A 3: 32,397,767 (GRCm39) A165V possibly damaging 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
R6052:Ros1 UTSW 10 52,039,999 (GRCm39) missense probably benign 0.39
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
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'- TCACTGTGAGCAAGACAGGC -3'
(R):5'- GCCATTCACATAAGATACTGTCAAGC -3'

Sequencing Primer
(F):5'- GCATAATTCAGGCCTTCAGACAGG -3'
(R):5'- CTCTCACAGGTGAAGATGA -3'
Posted On 2022-01-20