Incidental Mutation 'R4751:Shroom3'
ID 357575
Institutional Source Beutler Lab
Gene Symbol Shroom3
Ensembl Gene ENSMUSG00000029381
Gene Name shroom family member 3
Synonyms Shrm3, D5Ertd287e, Shrm
MMRRC Submission 041970-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4751 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 92831294-93113177 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 93090945 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Phenylalanine at position 1151 (V1151F)
Ref Sequence ENSEMBL: ENSMUSP00000153516 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113051] [ENSMUST00000113054] [ENSMUST00000113055] [ENSMUST00000168878] [ENSMUST00000172706] [ENSMUST00000225438]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000113051
AA Change: V1057F

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000108674
Gene: ENSMUSG00000029381
AA Change: V1057F

DomainStartEndE-ValueType
low complexity region 16 27 N/A INTRINSIC
low complexity region 83 93 N/A INTRINSIC
low complexity region 572 586 N/A INTRINSIC
low complexity region 621 639 N/A INTRINSIC
low complexity region 685 704 N/A INTRINSIC
Pfam:ASD1 706 885 2.3e-65 PFAM
low complexity region 939 952 N/A INTRINSIC
low complexity region 1132 1143 N/A INTRINSIC
low complexity region 1172 1184 N/A INTRINSIC
low complexity region 1274 1288 N/A INTRINSIC
low complexity region 1333 1345 N/A INTRINSIC
Pfam:ASD2 1478 1765 3.1e-107 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000113054
AA Change: V1057F

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000108677
Gene: ENSMUSG00000029381
AA Change: V1057F

DomainStartEndE-ValueType
low complexity region 16 27 N/A INTRINSIC
low complexity region 83 93 N/A INTRINSIC
low complexity region 572 586 N/A INTRINSIC
low complexity region 621 639 N/A INTRINSIC
low complexity region 685 704 N/A INTRINSIC
Pfam:ASD1 706 885 2.3e-65 PFAM
low complexity region 939 952 N/A INTRINSIC
low complexity region 1132 1143 N/A INTRINSIC
low complexity region 1172 1184 N/A INTRINSIC
low complexity region 1274 1288 N/A INTRINSIC
low complexity region 1333 1345 N/A INTRINSIC
Pfam:ASD2 1478 1765 3.1e-107 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000113055
AA Change: V1232F

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000108678
Gene: ENSMUSG00000029381
AA Change: V1232F

DomainStartEndE-ValueType
PDZ 35 109 5.81e-11 SMART
low complexity region 191 202 N/A INTRINSIC
low complexity region 258 268 N/A INTRINSIC
low complexity region 747 761 N/A INTRINSIC
low complexity region 796 814 N/A INTRINSIC
low complexity region 860 879 N/A INTRINSIC
Pfam:ASD1 882 1060 1e-57 PFAM
low complexity region 1114 1127 N/A INTRINSIC
low complexity region 1307 1318 N/A INTRINSIC
low complexity region 1347 1359 N/A INTRINSIC
low complexity region 1449 1463 N/A INTRINSIC
low complexity region 1508 1520 N/A INTRINSIC
Pfam:ASD2 1654 1940 9.9e-112 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000168878
AA Change: V1101F
SMART Domains Protein: ENSMUSP00000130419
Gene: ENSMUSG00000029381
AA Change: V1101F

DomainStartEndE-ValueType
PDZ 35 109 5.81e-11 SMART
low complexity region 191 202 N/A INTRINSIC
low complexity region 258 268 N/A INTRINSIC
low complexity region 747 761 N/A INTRINSIC
low complexity region 796 814 N/A INTRINSIC
low complexity region 860 879 N/A INTRINSIC
low complexity region 983 996 N/A INTRINSIC
low complexity region 1176 1187 N/A INTRINSIC
low complexity region 1216 1228 N/A INTRINSIC
low complexity region 1318 1332 N/A INTRINSIC
low complexity region 1377 1389 N/A INTRINSIC
Pfam:ASD2 1522 1809 8.9e-108 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172706
SMART Domains Protein: ENSMUSP00000133690
Gene: ENSMUSG00000029381

DomainStartEndE-ValueType
low complexity region 16 27 N/A INTRINSIC
low complexity region 83 93 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200869
Predicted Effect noncoding transcript
Transcript: ENSMUST00000201800
Predicted Effect probably damaging
Transcript: ENSMUST00000225438
AA Change: V1151F

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.4%
Validation Efficiency 95% (124/131)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a PDZ-domain-containing protein that belongs to a family of Shroom-related proteins. This protein may be involved in regulating cell shape in certain tissues. A similar protein in mice is required for proper neurulation. [provided by RefSeq, Jan 2011]
PHENOTYPE: Homozygous mutation of this locus results in failed neural tube closure leading to exencephaly, acrania, facial clefting, and spina bifida. Homozygotes develop to term but die either at birth or shortly thereafter. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 115 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130023H24Rik A T 7: 127,836,258 (GRCm39) C112S probably benign Het
Abca13 G A 11: 9,227,973 (GRCm39) probably null Het
Abca14 A G 7: 119,911,400 (GRCm39) E1328G probably benign Het
Abca9 T A 11: 110,021,396 (GRCm39) I1105F probably benign Het
Abr T C 11: 76,347,434 (GRCm39) N396D possibly damaging Het
Aftph A C 11: 20,677,074 (GRCm39) C178W probably damaging Het
Akr1c14 T C 13: 4,115,338 (GRCm39) F89S possibly damaging Het
Ank3 C T 10: 69,822,036 (GRCm39) A1518V probably benign Het
Arfgap2 T G 2: 91,097,713 (GRCm39) S143R probably benign Het
Aspdh T A 7: 44,116,629 (GRCm39) C107* probably null Het
Asphd2 C A 5: 112,539,612 (GRCm39) G74W probably damaging Het
AU040320 G A 4: 126,748,259 (GRCm39) probably null Het
B3glct T A 5: 149,648,867 (GRCm39) probably null Het
Bcl9l A G 9: 44,418,100 (GRCm39) K646R probably damaging Het
Brat1 T G 5: 140,704,051 (GRCm39) L768R probably damaging Het
Btbd18 T A 2: 84,498,265 (GRCm39) Y634* probably null Het
Bub1 T A 2: 127,665,858 (GRCm39) probably benign Het
Carns1 A T 19: 4,216,417 (GRCm39) D588E probably damaging Het
Cast T C 13: 74,894,166 (GRCm39) K141E probably damaging Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Chsy3 T C 18: 59,308,872 (GRCm39) S42P possibly damaging Het
Clca3a1 A T 3: 144,710,609 (GRCm39) F865I possibly damaging Het
Clec4f T A 6: 83,622,264 (GRCm39) M526L possibly damaging Het
Clnk T C 5: 38,878,256 (GRCm39) E301G probably benign Het
Colgalt2 T A 1: 152,365,627 (GRCm39) I309N probably benign Het
Cyp2e1 A T 7: 140,354,629 (GRCm39) K326* probably null Het
Dagla T A 19: 10,227,758 (GRCm39) T717S probably benign Het
Dnajc11 G A 4: 152,052,999 (GRCm39) R141H probably benign Het
Dst A G 1: 34,230,965 (GRCm39) K2853E probably benign Het
Eif4g1 A G 16: 20,505,265 (GRCm39) K1208E possibly damaging Het
Elane A G 10: 79,722,625 (GRCm39) R48G probably benign Het
Fbxo30 T A 10: 11,165,939 (GRCm39) N220K probably benign Het
Fbxo33 A T 12: 59,247,714 (GRCm39) probably benign Het
Fetub G A 16: 22,756,645 (GRCm39) V169I probably benign Het
Gpx6 A C 13: 21,501,234 (GRCm39) Q107H probably damaging Het
H2bc18 A T 3: 96,176,467 (GRCm39) probably benign Het
Homer3 A T 8: 70,738,084 (GRCm39) I19F probably damaging Het
Hspa4 C T 11: 53,175,026 (GRCm39) V144I probably benign Het
Icos C T 1: 61,032,876 (GRCm39) S25L probably benign Het
Ifna4 A G 4: 88,760,185 (GRCm39) T30A probably benign Het
Ino80b C T 6: 83,101,731 (GRCm39) G46D probably damaging Het
Kpna2 T G 11: 106,883,490 (GRCm39) I100L possibly damaging Het
Krt71 C T 15: 101,643,901 (GRCm39) G446R probably damaging Het
Krtap31-2 A G 11: 99,827,402 (GRCm39) N78S possibly damaging Het
Lman1 A G 18: 66,131,505 (GRCm39) S132P probably benign Het
Lmna T C 3: 88,393,840 (GRCm39) Q246R possibly damaging Het
Lrp10 T A 14: 54,706,049 (GRCm39) V413E probably damaging Het
Macf1 A C 4: 123,365,443 (GRCm39) I1541S probably benign Het
Med24 A G 11: 98,597,258 (GRCm39) L874P probably damaging Het
Mgll T A 6: 88,702,093 (GRCm39) probably benign Het
Mrpl37 A T 4: 106,914,672 (GRCm39) L364Q probably damaging Het
Mrpl47 C T 3: 32,782,590 (GRCm39) R209H probably benign Het
Muc5ac T C 7: 141,371,338 (GRCm39) F3285L probably benign Het
Mylk A G 16: 34,699,539 (GRCm39) R301G probably benign Het
Nacad A G 11: 6,555,726 (GRCm39) L8P unknown Het
Ncf1 T A 5: 134,258,399 (GRCm39) H8L probably damaging Het
Ncoa3 T A 2: 165,911,823 (GRCm39) M1383K possibly damaging Het
Necab2 C T 8: 120,194,337 (GRCm39) S271L probably benign Het
Nme8 A T 13: 19,859,808 (GRCm39) probably null Het
Nsrp1 T G 11: 76,967,545 (GRCm39) T16P possibly damaging Het
Obox3 A T 7: 15,359,617 (GRCm39) probably null Het
Or1l8 T C 2: 36,817,595 (GRCm39) H177R probably damaging Het
Or4c108 A G 2: 88,803,477 (GRCm39) C253R probably damaging Het
Or4c15 T A 2: 88,760,258 (GRCm39) I134F probably damaging Het
Or4d6 T A 19: 12,086,541 (GRCm39) Y123F probably damaging Het
Or52n2b A T 7: 104,565,617 (GRCm39) Y295* probably null Het
Or6b2 C A 1: 92,407,705 (GRCm39) A213S probably benign Het
Osbpl3 C G 6: 50,277,977 (GRCm39) E790Q possibly damaging Het
Osmr A T 15: 6,872,333 (GRCm39) W254R probably damaging Het
Otoa T C 7: 120,732,147 (GRCm39) probably benign Het
Pagr1a A T 7: 126,614,551 (GRCm39) L218H probably damaging Het
Pcdha11 G A 18: 37,139,997 (GRCm39) G542D probably damaging Het
Pck2 T A 14: 55,780,018 (GRCm39) I54N probably damaging Het
Ppif T C 14: 25,699,923 (GRCm39) V173A probably damaging Het
Ptgs2 T A 1: 149,979,771 (GRCm39) L292H probably damaging Het
Ptpru A G 4: 131,529,897 (GRCm39) S604P probably damaging Het
Qrfpr T C 3: 36,236,771 (GRCm39) H210R possibly damaging Het
Rasgrf1 A G 9: 89,792,171 (GRCm39) T41A probably damaging Het
Rasgrf1 A G 9: 89,894,919 (GRCm39) H1113R probably damaging Het
Rhoc T A 3: 104,699,963 (GRCm39) I80N probably damaging Het
Riok3 A G 18: 12,287,040 (GRCm39) N472S probably benign Het
Rnf213 A G 11: 119,336,571 (GRCm39) Y3314C probably benign Het
Shank2 C T 7: 143,963,205 (GRCm39) T264I probably damaging Het
Sipa1l1 A G 12: 82,387,968 (GRCm39) I65V probably benign Het
Slc22a19 T C 19: 7,668,510 (GRCm39) K291R possibly damaging Het
Slc22a20 T C 19: 6,030,488 (GRCm39) I315V probably benign Het
Slc44a1 A T 4: 53,560,973 (GRCm39) D563V probably damaging Het
Smchd1 A T 17: 71,698,463 (GRCm39) H1104Q probably benign Het
Spcs2 A T 7: 99,493,976 (GRCm39) probably null Het
Speer1e T A 5: 11,236,458 (GRCm39) Y138N probably damaging Het
Sptb T C 12: 76,673,884 (GRCm39) E301G probably benign Het
Stum T C 1: 180,270,234 (GRCm39) D86G probably damaging Het
Sufu A T 19: 46,472,088 (GRCm39) D449V probably benign Het
Sun5 T C 2: 153,707,936 (GRCm39) probably null Het
Tbc1d15 T A 10: 115,038,492 (GRCm39) I574F probably damaging Het
Tert G A 13: 73,776,182 (GRCm39) S311N possibly damaging Het
Tiparp T C 3: 65,460,225 (GRCm39) Y507H probably damaging Het
Tnk2 T C 16: 32,498,675 (GRCm39) C158R probably damaging Het
Tpgs1 T C 10: 79,511,454 (GRCm39) S199P possibly damaging Het
Trdmt1 G T 2: 13,549,464 (GRCm39) probably benign Het
Trp53bp1 T A 2: 121,058,290 (GRCm39) D944V probably damaging Het
Tsc1 T A 2: 28,569,093 (GRCm39) I720N probably damaging Het
Ttn T C 2: 76,539,949 (GRCm39) T34346A probably benign Het
Ttn T C 2: 76,727,925 (GRCm39) probably benign Het
Uba7 T A 9: 107,857,004 (GRCm39) C686S possibly damaging Het
Ush2a T A 1: 188,582,284 (GRCm39) F3782L probably damaging Het
Vars2 A T 17: 35,970,235 (GRCm39) H745Q possibly damaging Het
Vgf T A 5: 137,061,255 (GRCm39) D472E probably damaging Het
Vmn2r15 T C 5: 109,434,620 (GRCm39) M695V probably benign Het
Vps41 A T 13: 18,995,792 (GRCm39) D208V probably damaging Het
Vta1 C T 10: 14,531,560 (GRCm39) A272T probably benign Het
Wnk4 G A 11: 101,167,188 (GRCm39) probably benign Het
Zfp507 T C 7: 35,493,807 (GRCm39) K412R probably damaging Het
Zfp768 A G 7: 126,943,934 (GRCm39) F65L possibly damaging Het
Zfp956 T C 6: 47,940,510 (GRCm39) S290P probably benign Het
Other mutations in Shroom3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00850:Shroom3 APN 5 93,098,924 (GRCm39) missense probably damaging 1.00
IGL01086:Shroom3 APN 5 93,096,311 (GRCm39) missense probably benign 0.01
IGL01363:Shroom3 APN 5 93,088,852 (GRCm39) missense probably benign 0.01
IGL01468:Shroom3 APN 5 93,088,201 (GRCm39) missense probably damaging 1.00
IGL01675:Shroom3 APN 5 93,089,539 (GRCm39) missense probably damaging 0.99
IGL01862:Shroom3 APN 5 93,110,148 (GRCm39) missense probably damaging 1.00
IGL01987:Shroom3 APN 5 93,090,048 (GRCm39) missense probably damaging 0.99
IGL02104:Shroom3 APN 5 93,088,248 (GRCm39) missense probably benign 0.32
IGL03248:Shroom3 APN 5 93,100,399 (GRCm39) missense probably benign 0.00
IGL03386:Shroom3 APN 5 93,096,342 (GRCm39) splice site probably benign
R0167:Shroom3 UTSW 5 93,096,254 (GRCm39) splice site probably benign
R0388:Shroom3 UTSW 5 93,099,152 (GRCm39) missense probably benign 0.39
R0395:Shroom3 UTSW 5 92,928,762 (GRCm39) missense probably damaging 1.00
R0567:Shroom3 UTSW 5 93,112,312 (GRCm39) missense possibly damaging 0.53
R1496:Shroom3 UTSW 5 93,090,693 (GRCm39) missense possibly damaging 0.69
R1772:Shroom3 UTSW 5 93,088,515 (GRCm39) missense probably damaging 0.97
R1845:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R1921:Shroom3 UTSW 5 93,110,224 (GRCm39) critical splice donor site probably null
R2059:Shroom3 UTSW 5 92,831,643 (GRCm39) missense probably damaging 1.00
R2203:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2204:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2205:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2301:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2344:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2345:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2346:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2348:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2371:Shroom3 UTSW 5 92,928,729 (GRCm39) missense probably damaging 1.00
R2435:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2829:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2830:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2831:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2897:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R2898:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3079:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3080:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3433:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3729:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3730:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3735:Shroom3 UTSW 5 93,112,303 (GRCm39) missense possibly damaging 0.84
R3736:Shroom3 UTSW 5 93,112,303 (GRCm39) missense possibly damaging 0.84
R3851:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3852:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3943:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R3969:Shroom3 UTSW 5 93,088,738 (GRCm39) missense probably benign 0.05
R4008:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4009:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4012:Shroom3 UTSW 5 93,096,342 (GRCm39) splice site probably benign
R4154:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4157:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4172:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4173:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4201:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4202:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4204:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4205:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4206:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4284:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4285:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4364:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4384:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4456:Shroom3 UTSW 5 93,088,858 (GRCm39) missense probably benign 0.14
R4707:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4712:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4755:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4760:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4773:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4774:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4776:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4801:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4802:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4856:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4857:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4860:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4860:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4882:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R4883:Shroom3 UTSW 5 93,098,993 (GRCm39) missense probably benign 0.14
R4886:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R5262:Shroom3 UTSW 5 93,112,432 (GRCm39) missense probably damaging 1.00
R5271:Shroom3 UTSW 5 93,110,107 (GRCm39) missense probably damaging 1.00
R5719:Shroom3 UTSW 5 93,090,877 (GRCm39) missense probably benign 0.04
R5726:Shroom3 UTSW 5 93,090,864 (GRCm39) missense probably benign 0.00
R5993:Shroom3 UTSW 5 93,088,047 (GRCm39) missense probably damaging 1.00
R6078:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R6079:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R6138:Shroom3 UTSW 5 93,090,945 (GRCm39) missense probably damaging 1.00
R6153:Shroom3 UTSW 5 93,112,267 (GRCm39) missense probably damaging 0.99
R6493:Shroom3 UTSW 5 93,089,420 (GRCm39) missense probably benign 0.03
R6495:Shroom3 UTSW 5 93,089,928 (GRCm39) missense possibly damaging 0.66
R6693:Shroom3 UTSW 5 93,088,617 (GRCm39) missense possibly damaging 0.61
R6801:Shroom3 UTSW 5 93,088,795 (GRCm39) missense probably damaging 1.00
R6893:Shroom3 UTSW 5 93,090,063 (GRCm39) missense probably damaging 0.97
R6912:Shroom3 UTSW 5 93,090,876 (GRCm39) missense probably benign 0.02
R6924:Shroom3 UTSW 5 93,112,262 (GRCm39) missense probably damaging 1.00
R7083:Shroom3 UTSW 5 93,112,384 (GRCm39) missense probably damaging 1.00
R7197:Shroom3 UTSW 5 93,090,463 (GRCm39) missense probably damaging 1.00
R7366:Shroom3 UTSW 5 93,112,465 (GRCm39) nonsense probably null
R7712:Shroom3 UTSW 5 93,098,806 (GRCm39) missense probably benign 0.01
R7725:Shroom3 UTSW 5 93,089,512 (GRCm39) missense probably benign 0.19
R7728:Shroom3 UTSW 5 92,831,566 (GRCm39) missense possibly damaging 0.73
R7774:Shroom3 UTSW 5 93,098,348 (GRCm39) missense probably damaging 0.98
R7795:Shroom3 UTSW 5 93,067,508 (GRCm39) missense probably damaging 0.99
R7821:Shroom3 UTSW 5 93,088,705 (GRCm39) missense probably damaging 0.98
R7971:Shroom3 UTSW 5 93,098,933 (GRCm39) missense probably damaging 1.00
R8276:Shroom3 UTSW 5 93,088,339 (GRCm39) missense probably damaging 0.99
R8934:Shroom3 UTSW 5 93,089,584 (GRCm39) missense probably damaging 1.00
R8938:Shroom3 UTSW 5 93,090,930 (GRCm39) missense probably damaging 1.00
R9083:Shroom3 UTSW 5 93,098,533 (GRCm39) missense probably damaging 0.97
R9108:Shroom3 UTSW 5 93,087,975 (GRCm39) missense probably damaging 1.00
R9124:Shroom3 UTSW 5 93,112,401 (GRCm39) missense probably benign 0.19
R9295:Shroom3 UTSW 5 93,098,478 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AAGGAGCACACTCATCCGTC -3'
(R):5'- TGTCTTAACTGTCAGAACGGTAAC -3'

Sequencing Primer
(F):5'- GTGATCGCAGCAGCTCCTTC -3'
(R):5'- TTAACTGTCAGAACGGTAACCAACC -3'
Posted On 2015-11-11