Incidental Mutation 'R1649:Gm1527'
ID 174076
Institutional Source Beutler Lab
Gene Symbol Gm1527
Ensembl Gene ENSMUSG00000074655
Gene Name predicted gene 1527
Synonyms LOC385263
MMRRC Submission 039685-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R1649 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 28946768-28980874 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 28952880 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 60 (I60T)
Ref Sequence ENSEMBL: ENSMUSP00000096773 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099170]
AlphaFold Q3V0P3
Predicted Effect probably damaging
Transcript: ENSMUST00000099170
AA Change: I60T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000096773
Gene: ENSMUSG00000074655
AA Change: I60T

DomainStartEndE-ValueType
PH 16 119 2.37e-6 SMART
Pfam:RA 125 214 1.7e-8 PFAM
RhoGAP 300 471 2.8e-29 SMART
transmembrane domain 623 645 N/A INTRINSIC
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.0%
  • 20x: 88.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1a1 T A 4: 116,495,217 (GRCm39) I261F probably damaging Het
Aldh1l1 T C 6: 90,541,371 (GRCm39) V255A probably benign Het
Ambn T A 5: 88,612,340 (GRCm39) M172K probably benign Het
Arhgef18 A G 8: 3,439,094 (GRCm39) probably benign Het
BC034090 T C 1: 155,101,319 (GRCm39) H315R possibly damaging Het
Btaf1 T A 19: 36,959,122 (GRCm39) D707E probably benign Het
C6 T C 15: 4,764,739 (GRCm39) L145P possibly damaging Het
Cav3 T A 6: 112,449,207 (GRCm39) L75Q probably damaging Het
Cavin2 T A 1: 51,339,939 (GRCm39) D205E probably benign Het
Cdadc1 T C 14: 59,811,242 (GRCm39) T423A probably damaging Het
Cep120 A T 18: 53,857,648 (GRCm39) H272Q probably damaging Het
Chd9 A T 8: 91,659,229 (GRCm39) Q63L possibly damaging Het
Clspn T C 4: 126,460,228 (GRCm39) probably benign Het
Cramp1 G T 17: 25,202,217 (GRCm39) H422N probably damaging Het
Csn1s2b A T 5: 87,966,943 (GRCm39) M71L probably benign Het
D630045J12Rik C A 6: 38,158,366 (GRCm39) A1104S probably damaging Het
D930048N14Rik A G 11: 51,545,663 (GRCm39) probably benign Het
Ern2 G A 7: 121,776,623 (GRCm39) P366S probably damaging Het
Gse1 T C 8: 121,305,254 (GRCm39) probably benign Het
Ildr1 T C 16: 36,528,681 (GRCm39) L42P probably damaging Het
Itih2 G A 2: 10,110,546 (GRCm39) T515I probably benign Het
Jcad C A 18: 4,673,309 (GRCm39) P357Q probably damaging Het
Kitl A G 10: 99,899,976 (GRCm39) T94A probably benign Het
Klri1 C T 6: 129,675,204 (GRCm39) M185I probably benign Het
Lsamp A T 16: 41,775,661 (GRCm39) M171L probably benign Het
Macf1 T G 4: 123,377,846 (GRCm39) I1460L probably damaging Het
Map1b C G 13: 99,652,986 (GRCm39) V4L probably benign Het
Mboat7 A T 7: 3,688,817 (GRCm39) V237D probably benign Het
Mctp2 A T 7: 71,811,006 (GRCm39) I656K probably damaging Het
Ms4a6b A G 19: 11,497,806 (GRCm39) D35G possibly damaging Het
Nipsnap2 T A 5: 129,830,301 (GRCm39) I205N probably damaging Het
Nsd2 T C 5: 34,011,984 (GRCm39) V264A probably damaging Het
Oacyl C T 18: 65,883,167 (GRCm39) T582I probably damaging Het
Olfm1 A T 2: 28,119,279 (GRCm39) T333S possibly damaging Het
Olfm4 G A 14: 80,249,422 (GRCm39) E180K probably damaging Het
Or14j6 T C 17: 38,215,060 (GRCm39) F208L probably benign Het
Or2ad1 A T 13: 21,326,912 (GRCm39) L105Q probably damaging Het
Or8g17 T G 9: 38,930,776 (GRCm39) Q20H probably benign Het
Parp4 T A 14: 56,827,885 (GRCm39) V212E possibly damaging Het
Pcdhb21 T A 18: 37,648,666 (GRCm39) N598K probably damaging Het
Piezo2 C A 18: 63,250,743 (GRCm39) W452L probably benign Het
Plec C A 15: 76,090,011 (GRCm39) A110S possibly damaging Het
Popdc3 T C 10: 45,191,320 (GRCm39) Y144H probably damaging Het
Ptgdr T C 14: 45,095,959 (GRCm39) H251R probably benign Het
Ptpro T A 6: 137,421,015 (GRCm39) Y246* probably null Het
Pyroxd2 T C 19: 42,726,573 (GRCm39) D247G probably damaging Het
Robo2 T C 16: 73,695,889 (GRCm39) E1418G probably benign Het
Rtp3 T C 9: 110,815,772 (GRCm39) T198A probably benign Het
Sec16a A T 2: 26,315,536 (GRCm39) V1767D probably damaging Het
Septin14 T C 5: 129,774,819 (GRCm39) N119D probably benign Het
Serpina5 A T 12: 104,071,484 (GRCm39) T364S possibly damaging Het
Setd2 A G 9: 110,378,932 (GRCm39) S632G probably benign Het
Sh3bp2 C T 5: 34,716,348 (GRCm39) A253V possibly damaging Het
Slc6a5 G T 7: 49,586,010 (GRCm39) G443C probably damaging Het
Spag9 T A 11: 93,999,278 (GRCm39) probably null Het
Sptbn1 T C 11: 30,087,301 (GRCm39) E1033G probably damaging Het
Timm17a T G 1: 135,237,540 (GRCm39) Q39P probably damaging Het
Tmem26 A T 10: 68,587,103 (GRCm39) T184S probably damaging Het
Tpi1 A T 6: 124,789,891 (GRCm39) probably null Het
Tssk5 T C 15: 76,258,003 (GRCm39) Y118C possibly damaging Het
Ttll4 T A 1: 74,736,629 (GRCm39) L1118Q possibly damaging Het
Ttll5 T A 12: 85,969,788 (GRCm39) L691Q probably damaging Het
Vmn1r49 A T 6: 90,049,623 (GRCm39) H126Q possibly damaging Het
Zfp518b A T 5: 38,829,224 (GRCm39) V927E probably damaging Het
Zfp618 T C 4: 63,013,774 (GRCm39) F213S probably damaging Het
Zfp759 T A 13: 67,287,668 (GRCm39) N406K probably benign Het
Other mutations in Gm1527
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01518:Gm1527 APN 3 28,949,737 (GRCm39) utr 5 prime probably benign
IGL02069:Gm1527 APN 3 28,980,763 (GRCm39) missense possibly damaging 0.53
IGL02794:Gm1527 APN 3 28,949,829 (GRCm39) missense unknown
IGL03285:Gm1527 APN 3 28,974,566 (GRCm39) missense probably damaging 1.00
PIT4403001:Gm1527 UTSW 3 28,972,134 (GRCm39) missense possibly damaging 0.82
R0316:Gm1527 UTSW 3 28,969,923 (GRCm39) missense probably damaging 1.00
R0487:Gm1527 UTSW 3 28,980,828 (GRCm39) missense probably benign 0.00
R1411:Gm1527 UTSW 3 28,968,632 (GRCm39) missense probably benign 0.04
R1458:Gm1527 UTSW 3 28,972,199 (GRCm39) missense possibly damaging 0.52
R1470:Gm1527 UTSW 3 28,969,417 (GRCm39) missense possibly damaging 0.82
R1470:Gm1527 UTSW 3 28,969,417 (GRCm39) missense possibly damaging 0.82
R1476:Gm1527 UTSW 3 28,980,705 (GRCm39) missense probably benign 0.19
R1523:Gm1527 UTSW 3 28,974,567 (GRCm39) missense probably damaging 1.00
R1613:Gm1527 UTSW 3 28,953,002 (GRCm39) critical splice donor site probably null
R1722:Gm1527 UTSW 3 28,975,783 (GRCm39) missense probably benign 0.10
R1760:Gm1527 UTSW 3 28,949,699 (GRCm39) splice site probably benign
R1857:Gm1527 UTSW 3 28,957,539 (GRCm39) missense probably damaging 0.99
R1981:Gm1527 UTSW 3 28,969,984 (GRCm39) critical splice donor site probably null
R2063:Gm1527 UTSW 3 28,980,796 (GRCm39) missense probably benign 0.04
R2080:Gm1527 UTSW 3 28,980,810 (GRCm39) missense probably benign 0.01
R2115:Gm1527 UTSW 3 28,972,098 (GRCm39) missense probably benign 0.00
R2440:Gm1527 UTSW 3 28,949,764 (GRCm39) missense probably damaging 0.98
R3799:Gm1527 UTSW 3 28,980,745 (GRCm39) missense possibly damaging 0.53
R4012:Gm1527 UTSW 3 28,952,969 (GRCm39) missense probably benign 0.04
R4132:Gm1527 UTSW 3 28,974,779 (GRCm39) missense probably benign 0.37
R4234:Gm1527 UTSW 3 28,968,515 (GRCm39) missense probably damaging 1.00
R4406:Gm1527 UTSW 3 28,949,874 (GRCm39) missense possibly damaging 0.81
R4528:Gm1527 UTSW 3 28,968,542 (GRCm39) missense probably damaging 0.99
R4567:Gm1527 UTSW 3 28,968,556 (GRCm39) missense probably damaging 0.99
R4795:Gm1527 UTSW 3 28,974,812 (GRCm39) missense possibly damaging 0.56
R4796:Gm1527 UTSW 3 28,974,812 (GRCm39) missense possibly damaging 0.56
R5127:Gm1527 UTSW 3 28,957,567 (GRCm39) missense probably damaging 1.00
R5774:Gm1527 UTSW 3 28,972,239 (GRCm39) missense probably benign 0.22
R5890:Gm1527 UTSW 3 28,969,544 (GRCm39) missense probably benign 0.03
R6024:Gm1527 UTSW 3 28,974,752 (GRCm39) missense probably benign 0.10
R7092:Gm1527 UTSW 3 28,968,696 (GRCm39) critical splice donor site probably null
R7128:Gm1527 UTSW 3 28,969,460 (GRCm39) missense possibly damaging 0.95
R7197:Gm1527 UTSW 3 28,980,690 (GRCm39) missense probably null 0.00
R7308:Gm1527 UTSW 3 28,956,429 (GRCm39) missense probably benign 0.02
R7360:Gm1527 UTSW 3 28,968,691 (GRCm39) nonsense probably null
R7380:Gm1527 UTSW 3 28,974,621 (GRCm39) missense probably benign 0.10
R7566:Gm1527 UTSW 3 28,974,767 (GRCm39) missense probably benign 0.02
R7864:Gm1527 UTSW 3 28,980,619 (GRCm39) missense probably benign 0.01
R7896:Gm1527 UTSW 3 28,975,742 (GRCm39) splice site probably null
R8261:Gm1527 UTSW 3 28,974,749 (GRCm39) missense probably damaging 1.00
R8300:Gm1527 UTSW 3 28,980,744 (GRCm39) missense possibly damaging 0.96
R9106:Gm1527 UTSW 3 28,956,440 (GRCm39) missense probably damaging 0.99
R9615:Gm1527 UTSW 3 28,969,475 (GRCm39) missense probably damaging 0.98
X0021:Gm1527 UTSW 3 28,974,617 (GRCm39) missense probably damaging 1.00
X0028:Gm1527 UTSW 3 28,968,649 (GRCm39) missense probably benign 0.04
Predicted Primers PCR Primer
(F):5'- CAGGCTACCTCTATTTGTGAGCACTG -3'
(R):5'- GCTCTCTTCCTGTGAATACAAGCCC -3'

Sequencing Primer
(F):5'- CCTCTATTTGTGAGCACTGAGAAG -3'
(R):5'- CAAACTGTAGGTCTTACCGAAAG -3'
Posted On 2014-04-24