Incidental Mutation 'IGL03027:Gm7145'
ID 408229
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7145
Ensembl Gene ENSMUSG00000100617
Gene Name predicted gene 7145
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.284) question?
Stock # IGL03027
Quality Score
Status
Chromosome 1
Chromosomal Location 117893669-117914614 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 117895417 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 27 (S27P)
Ref Sequence ENSEMBL: ENSMUSP00000140916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000185381]
AlphaFold A0A087WS64
Predicted Effect probably benign
Transcript: ENSMUST00000185381
AA Change: S27P

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000140916
Gene: ENSMUSG00000100617
AA Change: S27P

DomainStartEndE-ValueType
KRAB 8 68 4.4e-36 SMART
ZnF_C2H2 109 131 3.6e-6 SMART
ZnF_C2H2 137 159 3.4e-5 SMART
ZnF_C2H2 165 187 1.7e-6 SMART
ZnF_C2H2 193 215 1e-7 SMART
ZnF_C2H2 221 243 2e-5 SMART
ZnF_C2H2 249 271 2.1e-7 SMART
ZnF_C2H2 277 299 9.3e-5 SMART
ZnF_C2H2 305 327 3.4e-4 SMART
ZnF_C2H2 333 355 3.2e-7 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrf1 A T 17: 43,607,605 (GRCm39) Y108F probably damaging Het
Afap1 T C 5: 36,119,094 (GRCm39) I243T probably benign Het
Ano5 A G 7: 51,216,025 (GRCm39) D320G probably damaging Het
Arhgef1 T A 7: 24,623,157 (GRCm39) I423K probably damaging Het
Casp9 A G 4: 141,539,584 (GRCm39) E410G probably benign Het
Ccdc39 A C 3: 33,884,267 (GRCm39) H358Q probably benign Het
Ces5a A T 8: 94,249,742 (GRCm39) probably null Het
Clip1 A T 5: 123,759,919 (GRCm39) M935K probably benign Het
Col12a1 A G 9: 79,548,833 (GRCm39) Y2171H probably benign Het
Cyp2f2 A T 7: 26,831,996 (GRCm39) N417I possibly damaging Het
Dock3 G A 9: 106,870,677 (GRCm39) P579L probably damaging Het
Dock7 T C 4: 98,866,164 (GRCm39) M1209V probably benign Het
Dock7 T C 4: 98,958,450 (GRCm39) T334A possibly damaging Het
Dst A T 1: 34,225,106 (GRCm39) I1171F possibly damaging Het
Eya1 G T 1: 14,241,190 (GRCm39) H576N probably damaging Het
Fam117a A G 11: 95,268,399 (GRCm39) T267A probably benign Het
Fam43a C T 16: 30,419,922 (GRCm39) R169C probably damaging Het
Gabra6 T C 11: 42,205,980 (GRCm39) H291R probably damaging Het
Gpt C T 15: 76,582,289 (GRCm39) probably benign Het
Grip2 A G 6: 91,755,852 (GRCm39) I586T probably benign Het
Hif1a C T 12: 73,987,251 (GRCm39) P448L probably benign Het
Hmcn1 C T 1: 150,684,290 (GRCm39) V427I probably benign Het
Ipo8 C A 6: 148,678,737 (GRCm39) V954L probably benign Het
Kdm5a G T 6: 120,351,951 (GRCm39) probably null Het
Klhl36 T A 8: 120,603,229 (GRCm39) S495T probably benign Het
Lpar5 T A 6: 125,059,203 (GRCm39) L308Q probably damaging Het
Lrp2 T G 2: 69,367,897 (GRCm39) D205A probably benign Het
Lrriq1 A G 10: 103,063,057 (GRCm39) I83T probably benign Het
Mapk8ip2 A T 15: 89,342,310 (GRCm39) D507V probably damaging Het
Mical1 T C 10: 41,355,501 (GRCm39) probably benign Het
Myef2 T A 2: 124,930,954 (GRCm39) H539L possibly damaging Het
Myh7 T C 14: 55,221,007 (GRCm39) E972G probably damaging Het
Naip5 A G 13: 100,359,524 (GRCm39) Y571H probably benign Het
Nfasc T A 1: 132,538,207 (GRCm39) N478I probably damaging Het
Or6c1b A G 10: 129,272,780 (GRCm39) Y33C probably damaging Het
Pde2a A T 7: 101,130,627 (GRCm39) Q89L probably benign Het
Ppard C A 17: 28,518,765 (GRCm39) T422K possibly damaging Het
Ppp1r13b G T 12: 111,796,830 (GRCm39) Y904* probably null Het
Ptx4 T A 17: 25,344,022 (GRCm39) I424K possibly damaging Het
Rab19 A G 6: 39,360,927 (GRCm39) D25G probably damaging Het
Rbl2 T A 8: 91,805,534 (GRCm39) I197N possibly damaging Het
Rttn A G 18: 88,997,814 (GRCm39) D273G probably damaging Het
Sec16a G A 2: 26,313,601 (GRCm39) R1920C probably benign Het
Sec23b A T 2: 144,429,465 (GRCm39) N731I possibly damaging Het
Serpinb9d G A 13: 33,386,698 (GRCm39) W255* probably null Het
Sim2 G A 16: 93,910,351 (GRCm39) probably benign Het
Tbl3 T C 17: 24,920,167 (GRCm39) probably null Het
Tmem176b C T 6: 48,812,573 (GRCm39) A131T probably damaging Het
Tmem181a T A 17: 6,348,494 (GRCm39) V332D probably damaging Het
Trgc1 G T 13: 19,398,563 (GRCm39) G97* probably null Het
Tuba3b T A 6: 145,565,117 (GRCm39) L195Q probably damaging Het
Ubc A T 5: 125,464,565 (GRCm39) V254D probably damaging Het
Ube4b G T 4: 149,465,734 (GRCm39) P239T probably damaging Het
Vars1 G T 17: 35,232,663 (GRCm39) M862I probably damaging Het
Vmn2r66 T C 7: 84,644,777 (GRCm39) probably benign Het
Wdr59 G A 8: 112,188,824 (GRCm39) A720V probably damaging Het
Zfhx3 G A 8: 109,519,820 (GRCm39) R314Q probably damaging Het
Other mutations in Gm7145
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6133:Gm7145 UTSW 1 117,913,618 (GRCm39) missense probably damaging 1.00
R6244:Gm7145 UTSW 1 117,913,870 (GRCm39) missense probably damaging 1.00
R6381:Gm7145 UTSW 1 117,913,669 (GRCm39) nonsense probably null
R6578:Gm7145 UTSW 1 117,913,525 (GRCm39) missense probably damaging 0.98
R6853:Gm7145 UTSW 1 117,913,874 (GRCm39) missense possibly damaging 0.95
R6913:Gm7145 UTSW 1 117,913,711 (GRCm39) missense probably damaging 1.00
R7159:Gm7145 UTSW 1 117,913,561 (GRCm39) missense probably benign 0.01
R7196:Gm7145 UTSW 1 117,913,791 (GRCm39) missense possibly damaging 0.81
R7313:Gm7145 UTSW 1 117,913,932 (GRCm39) missense probably damaging 1.00
R7343:Gm7145 UTSW 1 117,913,842 (GRCm39) missense probably damaging 1.00
R7369:Gm7145 UTSW 1 117,913,838 (GRCm39) missense probably benign 0.01
R8034:Gm7145 UTSW 1 117,913,894 (GRCm39) missense probably benign 0.03
R9316:Gm7145 UTSW 1 117,896,174 (GRCm39) missense probably benign 0.01
R9726:Gm7145 UTSW 1 117,913,706 (GRCm39) missense possibly damaging 0.95
R9732:Gm7145 UTSW 1 117,913,839 (GRCm39) missense probably benign 0.03
Z1176:Gm7145 UTSW 1 117,914,081 (GRCm39) missense probably benign 0.03
Posted On 2016-08-02