Incidental Mutation 'IGL01718:Gm7102'
ID105011
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7102
Ensembl Gene ENSMUSG00000094649
Gene Namepredicted gene 7102
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.193) question?
Stock #IGL01718
Quality Score
Status
Chromosome19
Chromosomal Location61174686-61176309 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 61175761 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 79 (S79P)
Ref Sequence ENSEMBL: ENSMUSP00000137574 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000180168]
Predicted Effect probably damaging
Transcript: ENSMUST00000180168
AA Change: S79P

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000137574
Gene: ENSMUSG00000094649
AA Change: S79P

DomainStartEndE-ValueType
Pfam:MPLKIP 31 170 8.9e-27 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh1a3 A G 7: 66,400,205 F422L possibly damaging Het
Ap2m1 T C 16: 20,542,194 probably benign Het
Asic1 A G 15: 99,672,002 Y68C probably damaging Het
Ccdc18 A G 5: 108,201,348 D1002G possibly damaging Het
Cyp2c29 A T 19: 39,330,260 I434F possibly damaging Het
Diaph3 T A 14: 86,656,338 R78S unknown Het
Dnase1l2 T C 17: 24,441,716 D188G possibly damaging Het
Exosc9 T C 3: 36,553,929 probably benign Het
Fgf23 G A 6: 127,080,473 V251I probably benign Het
Fndc3c1 T C X: 106,445,928 T296A probably benign Het
Gm5592 A G 7: 41,289,193 E633G probably damaging Het
Gpr155 T C 2: 73,382,232 M16V probably benign Het
Jakmip3 T G 7: 138,989,392 S2A possibly damaging Het
Lrba T A 3: 86,351,248 N1347K probably damaging Het
Mars T C 10: 127,305,838 R266G possibly damaging Het
Mrgpra1 A T 7: 47,335,927 probably null Het
Olfr835 T A 9: 19,035,288 L55* probably null Het
Pdzk1ip1 T A 4: 115,092,914 probably benign Het
Ppid G T 3: 79,593,679 C52F probably damaging Het
Reln A G 5: 21,947,514 I2318T possibly damaging Het
Rhpn2 G A 7: 35,370,754 D146N probably benign Het
Tspoap1 G T 11: 87,780,255 R1670L possibly damaging Het
Ttc22 G A 4: 106,638,576 V376M probably damaging Het
Ttn T A 2: 76,730,402 L29218F probably damaging Het
Ttn A T 2: 76,730,404 L29218I probably damaging Het
Zfp609 G A 9: 65,702,400 Q1094* probably null Het
Zfp831 C T 2: 174,643,838 T102I possibly damaging Het
Zglp1 C T 9: 21,063,379 C171Y probably benign Het
Other mutations in Gm7102
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02958:Gm7102 APN 19 61175680 missense possibly damaging 0.83
R0427:Gm7102 UTSW 19 61175470 missense probably damaging 1.00
R1886:Gm7102 UTSW 19 61175698 missense probably damaging 0.97
R4576:Gm7102 UTSW 19 61175926 missense unknown
R4578:Gm7102 UTSW 19 61175926 missense unknown
R4615:Gm7102 UTSW 19 61175926 missense unknown
R4616:Gm7102 UTSW 19 61175926 missense unknown
R4617:Gm7102 UTSW 19 61175926 missense unknown
R4621:Gm7102 UTSW 19 61175926 missense unknown
R4622:Gm7102 UTSW 19 61175926 missense unknown
R4623:Gm7102 UTSW 19 61175926 missense unknown
R4826:Gm7102 UTSW 19 61175926 missense unknown
R4827:Gm7102 UTSW 19 61175926 missense unknown
R4829:Gm7102 UTSW 19 61175926 missense unknown
R4830:Gm7102 UTSW 19 61175926 missense unknown
R4870:Gm7102 UTSW 19 61175926 missense unknown
R4871:Gm7102 UTSW 19 61175926 missense unknown
R4951:Gm7102 UTSW 19 61175926 missense unknown
R5112:Gm7102 UTSW 19 61175926 missense unknown
R5301:Gm7102 UTSW 19 61175926 missense unknown
R5317:Gm7102 UTSW 19 61175926 missense unknown
R5335:Gm7102 UTSW 19 61175926 missense unknown
R5397:Gm7102 UTSW 19 61175926 missense unknown
R5399:Gm7102 UTSW 19 61175926 missense unknown
R5591:Gm7102 UTSW 19 61175926 missense unknown
R5592:Gm7102 UTSW 19 61175926 missense unknown
R5594:Gm7102 UTSW 19 61175926 missense unknown
R5616:Gm7102 UTSW 19 61175926 missense unknown
R5884:Gm7102 UTSW 19 61175926 missense unknown
R5919:Gm7102 UTSW 19 61175469 missense probably damaging 1.00
R7003:Gm7102 UTSW 19 61175881 missense possibly damaging 0.93
R7112:Gm7102 UTSW 19 61175559 missense probably damaging 1.00
R7266:Gm7102 UTSW 19 61175535 missense possibly damaging 0.84
Z1177:Gm7102 UTSW 19 61175750 frame shift probably null
Posted On2014-01-21