Incidental Mutation 'IGL01528:Gm2832'
ID89633
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm2832
Ensembl Gene ENSMUSG00000091110
Gene Namepredicted gene 2832
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01528
Quality Score
Status
Chromosome14
Chromosomal Location41278805-41288815 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 41281713 bp
ZygosityHeterozygous
Amino Acid Change Valine to Alanine at position 167 (V167A)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000172412
AA Change: V167A
SMART Domains Protein: ENSMUSP00000131087
Gene: ENSMUSG00000091110
AA Change: V167A

DomainStartEndE-ValueType
Pfam:Takusan 57 137 7.3e-26 PFAM
coiled coil region 156 185 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AB124611 T A 9: 21,539,894 probably benign Het
Cdc45 A G 16: 18,811,561 F2S probably damaging Het
Cdon A G 9: 35,470,107 R598G possibly damaging Het
Dusp22 C T 13: 30,705,628 T64I probably benign Het
Gfer T A 17: 24,695,929 T47S probably benign Het
Gfra2 T C 14: 70,966,298 S296P possibly damaging Het
Gjb2 G A 14: 57,100,668 L28F probably damaging Het
Gm17782 A G 17: 36,161,790 probably benign Het
Gpr155 A G 2: 73,362,423 probably null Het
Gpr45 A G 1: 43,033,223 H342R probably benign Het
Gsdmd A T 15: 75,863,505 T33S possibly damaging Het
Hal T A 10: 93,497,593 L341Q probably damaging Het
Igfbp7 T G 5: 77,351,332 D273A probably damaging Het
Kdm2a T C 19: 4,343,055 D424G probably benign Het
Kif13a C T 13: 46,864,837 probably benign Het
Krt35 A T 11: 100,094,594 L207Q probably damaging Het
Lrp1b A T 2: 40,919,182 D2572E probably damaging Het
Lrp2 A G 2: 69,492,460 V1848A probably damaging Het
Myo9a T C 9: 59,779,674 Y21H probably damaging Het
Ncan G T 8: 70,110,081 A509E probably benign Het
Olfr450 T C 6: 42,818,274 S268P probably damaging Het
Pde11a G A 2: 76,194,956 probably benign Het
Phf19 G T 2: 34,897,107 D448E probably damaging Het
Ptprj A T 2: 90,452,144 V799D probably damaging Het
Rpgrip1 T A 14: 52,112,177 Y7* probably null Het
Sema3c A G 5: 17,714,415 H483R probably benign Het
Slc4a11 A G 2: 130,685,408 probably benign Het
St3gal1 C A 15: 67,112,617 R103L probably benign Het
Tet2 A T 3: 133,480,298 V1126E possibly damaging Het
Tmem117 A T 15: 95,094,664 I402L probably benign Het
Tmem2 T C 19: 21,835,545 V1038A possibly damaging Het
Ttc28 T A 5: 111,101,960 probably benign Het
Ttn A T 2: 76,871,838 probably benign Het
Vmn1r7 T A 6: 57,024,547 M243L probably benign Het
Wnt1 G T 15: 98,791,833 W167L probably damaging Het
Zfp553 G T 7: 127,236,215 S314I probably damaging Het
Zranb2 T C 3: 157,544,965 probably benign Het
Other mutations in Gm2832
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1997:Gm2832 UTSW 14 41280986 critical splice donor site probably null
R4105:Gm2832 UTSW 14 41280899 missense unknown
R7024:Gm2832 UTSW 14 41279739 missense
R7526:Gm2832 UTSW 14 41280962 missense
Posted On2013-12-03