Incidental Mutation 'IGL01670:Gm12666'
ID103474
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm12666
Ensembl Gene ENSMUSG00000066107
Gene Namepredicted gene 12666
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.154) question?
Stock #IGL01670
Quality Score
Status
Chromosome4
Chromosomal Location92190744-92191749 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 92191500 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000122212 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000123179]
Predicted Effect probably null
Transcript: ENSMUST00000123179
SMART Domains Protein: ENSMUSP00000122212
Gene: ENSMUSG00000066107

DomainStartEndE-ValueType
RRM 3 73 9.8e-9 SMART
low complexity region 87 103 N/A INTRINSIC
low complexity region 134 153 N/A INTRINSIC
low complexity region 179 188 N/A INTRINSIC
low complexity region 228 246 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acy1 A C 9: 106,436,807 probably benign Het
Add1 C A 5: 34,620,063 Q57K probably damaging Het
Alms1 A G 6: 85,678,150 E3226G probably benign Het
Arl1 G T 10: 88,742,022 R151L probably damaging Het
Cabs1 T A 5: 87,980,010 D173E possibly damaging Het
Cdc34b T C 11: 94,742,019 L15P probably benign Het
Cdyl2 A G 8: 116,624,353 V13A probably damaging Het
Chd7 G T 4: 8,827,033 R1026L probably damaging Het
Cldn34b4 T C X: 76,397,589 S151P probably damaging Het
Col14a1 T A 15: 55,329,266 I25N unknown Het
Crisp4 T A 1: 18,128,677 T178S probably benign Het
Csmd2 C T 4: 128,513,371 probably benign Het
Csmd3 T G 15: 47,611,829 N2454H probably damaging Het
Cytip A T 2: 58,133,773 I345N probably damaging Het
Frem2 A T 3: 53,656,937 S50T possibly damaging Het
Gm9747 C T 1: 82,234,149 probably benign Het
Gpr37 A G 6: 25,669,834 F337S probably damaging Het
Herc1 A G 9: 66,487,060 E4182G probably damaging Het
Isyna1 C T 8: 70,597,056 P511L probably benign Het
Kdm4a T C 4: 118,160,501 Y456C probably damaging Het
Kera A T 10: 97,609,077 R99S possibly damaging Het
Mcm2 A G 6: 88,887,632 probably benign Het
Myl12a T C 17: 70,996,853 T10A probably benign Het
Nav3 A G 10: 109,714,241 V1876A possibly damaging Het
Nkx6-1 T A 5: 101,661,940 Q247L probably benign Het
Nol8 A C 13: 49,661,308 K297N possibly damaging Het
Olfr1143 A G 2: 87,802,880 T164A probably benign Het
Olfr1224-ps1 T A 2: 89,156,917 Y86F probably benign Het
Olfr558 A T 7: 102,709,565 Q102L probably damaging Het
Pard3b A T 1: 62,211,648 N579Y probably damaging Het
Pdcd11 T A 19: 47,106,304 L509H probably damaging Het
Prss29 T C 17: 25,322,463 S266P probably benign Het
Rapgef3 G T 15: 97,749,662 H766N probably benign Het
Rasa1 A T 13: 85,225,490 S818T probably damaging Het
Rtn4ip1 A G 10: 43,928,326 M1V probably null Het
Sall1 A T 8: 89,031,571 V635D probably benign Het
Slc35b4 C T 6: 34,170,549 V35I probably benign Het
Slc5a11 G A 7: 123,269,949 A587T probably benign Het
Slc6a21 T C 7: 45,288,133 V616A possibly damaging Het
Sorl1 A G 9: 42,001,492 S1398P possibly damaging Het
Srcap A G 7: 127,528,432 K390E probably damaging Het
Sycp2 C T 2: 178,378,050 E558K probably benign Het
Tcf20 T C 15: 82,855,363 N629S possibly damaging Het
Tmem154 A G 3: 84,684,230 Y29C probably damaging Het
Tmtc3 A G 10: 100,447,125 I856T probably benign Het
Zswim6 A G 13: 107,728,566 noncoding transcript Het
Other mutations in Gm12666
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01373:Gm12666 APN 4 92191625 missense probably damaging 0.98
IGL02690:Gm12666 APN 4 92191011 missense probably damaging 0.98
IGL03052:Gm12666 UTSW 4 92191050 missense probably benign 0.01
R2094:Gm12666 UTSW 4 92191656 missense probably damaging 1.00
R2567:Gm12666 UTSW 4 92191323 missense probably benign 0.10
R3438:Gm12666 UTSW 4 92191682 missense possibly damaging 0.94
R3439:Gm12666 UTSW 4 92191682 missense possibly damaging 0.94
R4388:Gm12666 UTSW 4 92191114 missense probably benign 0.00
R4710:Gm12666 UTSW 4 92190975 missense possibly damaging 0.94
R5810:Gm12666 UTSW 4 92191583 critical splice donor site probably null
R6969:Gm12666 UTSW 4 92191589 missense probably damaging 1.00
X0067:Gm12666 UTSW 4 92191334 splice site probably null
Posted On2014-01-21