Incidental Mutation 'R0165:Gm7535'
ID 24136
Institutional Source Beutler Lab
Gene Symbol Gm7535
Ensembl Gene ENSMUSG00000090957
Gene Name predicted gene 7535
MMRRC Submission 038441-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.201) question?
Stock # R0165 (G1)
Quality Score 225
Status Validated (trace)
Chromosome 17
Chromosomal Location 17911039-17911947 bp(-) (GRCm38)
Type of Mutation intron
DNA Base Change (assembly) T to C at 17911175 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000093316 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054871] [ENSMUST00000164167]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000054871
SMART Domains Protein: ENSMUSP00000093316
Gene: ENSMUSG00000079700

Pfam:7tm_1 43 302 2.2e-43 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000164167
SMART Domains Protein: ENSMUSP00000125897
Gene: ENSMUSG00000090957

Pfam:CNDH2_C 15 292 6.7e-90 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231820
Meta Mutation Damage Score 0.7851 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.5%
  • 10x: 96.2%
  • 20x: 91.4%
Validation Efficiency 96% (81/84)
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik T C 12: 71,167,150 (GRCm38) I717T possibly damaging Het
6430571L13Rik A G 9: 107,346,184 (GRCm38) probably benign Het
Abca15 T A 7: 120,350,903 (GRCm38) probably benign Het
Abca6 A G 11: 110,219,604 (GRCm38) V573A possibly damaging Het
Adgrl2 A G 3: 148,852,863 (GRCm38) probably benign Het
Agap3 A G 5: 24,479,745 (GRCm38) T544A probably damaging Het
Ahrr G A 13: 74,283,024 (GRCm38) probably benign Het
Akr1c20 T C 13: 4,523,296 (GRCm38) T7A probably benign Het
Ankrd26 A G 6: 118,540,484 (GRCm38) S459P probably benign Het
Armh4 A G 14: 49,773,786 (GRCm38) S155P probably benign Het
Ascc3 T A 10: 50,842,127 (GRCm38) probably null Het
Brd1 T C 15: 88,729,777 (GRCm38) N305S probably damaging Het
Catip T A 1: 74,368,469 (GRCm38) L320Q possibly damaging Het
Cplane1 G A 15: 8,216,382 (GRCm38) V1413M probably damaging Het
Cttnbp2 G A 6: 18,435,410 (GRCm38) Q150* probably null Het
Cyp2d22 T G 15: 82,373,280 (GRCm38) N228T probably benign Het
Dapk1 T C 13: 60,761,593 (GRCm38) V1340A probably benign Het
Dcaf4 G A 12: 83,535,988 (GRCm38) probably benign Het
Ddhd1 G A 14: 45,595,592 (GRCm38) T849M probably damaging Het
Dnah6 A G 6: 73,021,323 (GRCm38) S3987P probably benign Het
Dst C A 1: 34,154,646 (GRCm38) probably benign Het
Epha2 T C 4: 141,321,892 (GRCm38) probably null Het
Ern2 T C 7: 122,179,779 (GRCm38) T281A probably benign Het
Extl1 A G 4: 134,357,703 (GRCm38) F652S probably damaging Het
Gckr A G 5: 31,326,948 (GRCm38) S541G possibly damaging Het
Gdap1l1 A G 2: 163,451,499 (GRCm38) probably null Het
Gmps T A 3: 63,993,954 (GRCm38) I398N probably damaging Het
Igf2r A G 17: 12,698,527 (GRCm38) V1556A probably benign Het
Il3ra T A 14: 14,350,967 (GRCm38) N283K probably benign Het
Ist1 A G 8: 109,675,366 (GRCm38) probably benign Het
Lama3 A T 18: 12,524,810 (GRCm38) I1934F probably damaging Het
Lars1 A T 18: 42,202,697 (GRCm38) M1118K possibly damaging Het
Lpin2 C T 17: 71,246,519 (GRCm38) S846L probably damaging Het
Lrrc4b C A 7: 44,462,315 (GRCm38) T537K probably damaging Het
Ltn1 G A 16: 87,405,519 (GRCm38) probably benign Het
Meiob A G 17: 24,835,161 (GRCm38) T401A probably benign Het
Mettl21e G A 1: 44,211,123 (GRCm38) T41M probably damaging Het
Miga1 C T 3: 152,290,843 (GRCm38) E323K probably damaging Het
Ndufs1 A T 1: 63,159,748 (GRCm38) probably null Het
Or5p62 T C 7: 108,172,675 (GRCm38) D23G probably benign Het
Otog G A 7: 46,304,231 (GRCm38) V2638M probably damaging Het
Parp6 T C 9: 59,632,925 (GRCm38) Y274H probably damaging Het
Prom2 A T 2: 127,539,514 (GRCm38) probably benign Het
Prune2 T A 19: 17,122,610 (GRCm38) M1826K probably benign Het
Qki T A 17: 10,238,963 (GRCm38) D159V probably damaging Het
Rab12 A T 17: 66,500,317 (GRCm38) I139N probably damaging Het
Rab25 T A 3: 88,548,055 (GRCm38) E7D probably benign Het
Rala A T 13: 17,888,589 (GRCm38) V139E probably benign Het
Ralgapa2 A G 2: 146,388,487 (GRCm38) probably benign Het
Rbl2 T A 8: 91,074,176 (GRCm38) Y89N probably damaging Het
Rho A T 6: 115,932,227 (GRCm38) I75F probably damaging Het
Slc38a4 C A 15: 97,008,949 (GRCm38) A303S probably benign Het
Slc6a15 A G 10: 103,409,809 (GRCm38) D551G probably null Het
Smyd3 T C 1: 179,043,872 (GRCm38) N314S probably benign Het
Speer4f1 T A 5: 17,479,514 (GRCm38) L180* probably null Het
Stat6 T C 10: 127,657,227 (GRCm38) V576A probably damaging Het
Strn T C 17: 78,677,374 (GRCm38) D127G possibly damaging Het
Syne1 T C 10: 5,033,096 (GRCm38) R8610G probably benign Het
Tbc1d7 A C 13: 43,153,202 (GRCm38) probably null Het
Tcf3 C T 10: 80,412,997 (GRCm38) R548Q probably damaging Het
Tlr9 C A 9: 106,226,087 (GRCm38) A859D probably benign Het
Tmem106c T A 15: 97,968,139 (GRCm38) probably benign Het
Tmprss11c A T 5: 86,231,927 (GRCm38) probably benign Het
Tnfsf18 A G 1: 161,494,731 (GRCm38) R7G probably benign Het
Tnrc6b T A 15: 80,858,670 (GRCm38) probably null Het
Trpm7 A T 2: 126,797,513 (GRCm38) F1684I probably damaging Het
Ttbk1 C A 17: 46,478,938 (GRCm38) R133L possibly damaging Het
Ttn A G 2: 76,721,342 (GRCm38) S22962P probably damaging Het
Ube2q1 T A 3: 89,776,153 (GRCm38) L135Q probably damaging Het
Vmn1r28 G A 6: 58,265,717 (GRCm38) A182T probably benign Het
Vwce T C 19: 10,659,973 (GRCm38) probably benign Het
Wdhd1 A G 14: 47,267,068 (GRCm38) S350P probably benign Het
Zbtb21 A G 16: 97,951,404 (GRCm38) S560P probably damaging Het
Other mutations in Gm7535
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00422:Gm7535 APN 17 17,911,888 (GRCm38) intron probably benign
IGL01663:Gm7535 APN 17 17,911,357 (GRCm38) intron probably benign
R0335:Gm7535 UTSW 17 17,911,112 (GRCm38) intron probably benign
R1985:Gm7535 UTSW 17 17,911,538 (GRCm38) intron probably benign
R2217:Gm7535 UTSW 17 17,911,674 (GRCm38) intron probably benign
R2218:Gm7535 UTSW 17 17,911,674 (GRCm38) intron probably benign
R4464:Gm7535 UTSW 17 17,911,662 (GRCm38) intron probably benign
R4581:Gm7535 UTSW 17 17,911,083 (GRCm38) intron probably benign
R4887:Gm7535 UTSW 17 17,911,071 (GRCm38) intron probably benign
R5225:Gm7535 UTSW 17 17,911,547 (GRCm38) intron probably benign
R5305:Gm7535 UTSW 17 17,911,799 (GRCm38) intron probably benign
R5641:Gm7535 UTSW 17 17,911,526 (GRCm38) intron probably benign
R5658:Gm7535 UTSW 17 17,911,320 (GRCm38) intron probably benign
R5760:Gm7535 UTSW 17 17,911,818 (GRCm38) intron probably benign
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2013-04-16