Incidental Mutation 'R0412:Gm9894'
ID36730
Institutional Source Beutler Lab
Gene Symbol Gm9894
Ensembl Gene ENSMUSG00000052909
Gene Namepredicted gene 9894
Synonyms
MMRRC Submission 038614-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.086) question?
Stock #R0412 (G1)
Quality Score225
Status Validated
Chromosome13
Chromosomal Location67764247-67765065 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to T at 67765026 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171257
SMART Domains Protein: ENSMUSP00000125787
Gene: ENSMUSG00000052909

DomainStartEndE-ValueType
KRAB 5 65 9.53e-30 SMART
ZnF_C2H2 109 132 7.15e-2 SMART
ZnF_C2H2 138 160 8.34e-3 SMART
ZnF_C2H2 166 188 5.4e1 SMART
ZnF_C2H2 194 216 9.96e-1 SMART
ZnF_C2H2 222 244 1.18e-2 SMART
ZnF_C2H2 278 300 2.57e-3 SMART
ZnF_C2H2 306 328 5.26e1 SMART
Meta Mutation Damage Score 0.4547 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.8%
  • 20x: 90.2%
Validation Efficiency 94% (67/71)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932431P20Rik C G 7: 29,530,570 noncoding transcript Het
Arap1 C A 7: 101,390,222 A563D probably damaging Het
Arhgap28 G A 17: 67,896,258 L67F probably damaging Het
Atp7b G T 8: 21,995,659 probably null Het
Auts2 A G 5: 131,446,831 F485L probably benign Het
Ccdc68 A G 18: 69,960,439 E239G probably damaging Het
Cdc42bpg T G 19: 6,313,457 L449R probably damaging Het
Colgalt2 G T 1: 152,508,561 A551S possibly damaging Het
Ddx41 G T 13: 55,530,608 S630Y probably damaging Het
Dntt T C 19: 41,042,933 L274P probably damaging Het
Fhl4 G T 10: 85,098,816 H34N possibly damaging Het
Filip1 A T 9: 79,820,289 N349K possibly damaging Het
Gpr179 A G 11: 97,338,807 S841P probably damaging Het
Gpr35 G T 1: 92,982,784 V73L probably benign Het
Grik5 A G 7: 25,013,674 V809A possibly damaging Het
H2-Bl T A 17: 36,081,521 probably benign Het
Heatr5b T C 17: 78,820,854 T451A probably benign Het
Hmcn2 G A 2: 31,388,247 V1654M probably damaging Het
Htra3 G T 5: 35,671,065 A157E probably damaging Het
Igf2r A T 17: 12,683,948 V2405D probably damaging Het
Irs3 C A 5: 137,643,877 R433L probably benign Het
Kcmf1 G A 6: 72,848,241 Q239* probably null Het
Kcnk9 A G 15: 72,513,056 probably benign Het
Kif28 A G 1: 179,702,526 V622A probably benign Het
Klrb1f A T 6: 129,054,331 I164F probably benign Het
Lama2 A G 10: 27,190,625 S1087P possibly damaging Het
Mchr1 A T 15: 81,235,747 probably benign Het
Mcidas A G 13: 112,999,143 T367A probably damaging Het
Mphosph8 A C 14: 56,674,413 K298Q probably damaging Het
Mroh2a G T 1: 88,235,216 Q360H probably benign Het
Mst1 A C 9: 108,083,594 D461A probably benign Het
Nckap1l A T 15: 103,464,652 S311C probably benign Het
Olfr1036 C T 2: 86,075,091 A117V probably benign Het
Olfr1233 T A 2: 89,340,078 M75L probably benign Het
Olfr1385 T A 11: 49,494,767 V78E probably damaging Het
Olfr251 A C 9: 38,378,794 K298N probably damaging Het
Pde3a T G 6: 141,498,684 C1073G probably damaging Het
Pkhd1 T C 1: 20,117,788 D3432G probably damaging Het
Ppargc1b G T 18: 61,315,861 P130Q probably damaging Het
Ppp6r1 A G 7: 4,642,214 I228T probably damaging Het
Pram1 A G 17: 33,641,506 N349S probably benign Het
Ranbp6 C T 19: 29,812,083 V290I possibly damaging Het
Rcan3 A T 4: 135,416,603 probably null Het
Scn8a G C 15: 101,008,306 probably benign Het
Slc12a5 C T 2: 164,994,062 T900M probably benign Het
Srsf10 A G 4: 135,858,403 Y55C probably damaging Het
Syt7 G T 19: 10,444,080 E450* probably null Het
Tbrg4 T C 11: 6,623,832 K130R probably benign Het
Tgm7 C A 2: 121,101,065 V206F probably damaging Het
Tmem131l T C 3: 84,031,648 D67G probably damaging Het
Ttc7 A G 17: 87,330,044 K409R probably benign Het
Unc80 A T 1: 66,550,937 probably benign Het
Vmn1r171 C T 7: 23,632,655 L102F possibly damaging Het
Vmn2r59 A C 7: 42,046,492 probably benign Het
Vsig2 A G 9: 37,542,690 R191G probably damaging Het
Wdr86 T A 5: 24,718,234 Q153H probably benign Het
Xxylt1 T A 16: 31,007,798 N233I probably damaging Het
Zfp160 A T 17: 21,026,877 E563V probably damaging Het
Zfp345 T A 2: 150,473,403 E71D probably benign Het
Zfp541 A G 7: 16,082,174 D862G possibly damaging Het
Zfp639 A C 3: 32,517,110 Q47P possibly damaging Het
Other mutations in Gm9894
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00473:Gm9894 APN 13 67765117 exon noncoding transcript
IGL02474:Gm9894 APN 13 67765094 exon noncoding transcript
R1170:Gm9894 UTSW 13 67764701 exon noncoding transcript
R1604:Gm9894 UTSW 13 67764889 exon noncoding transcript
R1617:Gm9894 UTSW 13 67772726 critical splice donor site noncoding transcript
R1961:Gm9894 UTSW 13 67763915 exon noncoding transcript
R3879:Gm9894 UTSW 13 67764797 exon noncoding transcript
R4450:Gm9894 UTSW 13 67765080 exon noncoding transcript
R4666:Gm9894 UTSW 13 67765094 exon noncoding transcript
R6020:Gm9894 UTSW 13 67763835 exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GCCACACACTTCACACTTGCATGTT -3'
(R):5'- GGCCTATAGTACCAGCCCATCACTT -3'

Sequencing Primer
(F):5'- aaccttttcccaccataccc -3'
(R):5'- AGCCCATCACTTTTTatacaccag -3'
Posted On2013-05-09