Incidental Mutation 'IGL00272:4932431P20Rik'
ID88882
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4932431P20Rik
Ensembl Gene ENSMUSG00000074224
Gene NameRIKEN cDNA 4932431P20 gene
Synonyms
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL00272
Quality Score
Status
Chromosome7
Chromosomal Location29519205-29538057 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) G to T at 29537622 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000098602
SMART Domains Protein: ENSMUSP00000096202
Gene: ENSMUSG00000074224

DomainStartEndE-ValueType
low complexity region 233 239 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141713
SMART Domains Protein: ENSMUSP00000120285
Gene: ENSMUSG00000074224

DomainStartEndE-ValueType
Blast:WD40 94 134 1e-9 BLAST
WD40 139 176 1.59e1 SMART
WD40 228 269 9.51e1 SMART
WD40 272 311 3.33e-1 SMART
Blast:WD40 354 393 4e-15 BLAST
Blast:WD40 445 490 2e-22 BLAST
Blast:WD40 493 538 8e-15 BLAST
WD40 595 634 1.68e-6 SMART
low complexity region 701 710 N/A INTRINSIC
low complexity region 915 926 N/A INTRINSIC
coiled coil region 1135 1168 N/A INTRINSIC
low complexity region 1211 1230 N/A INTRINSIC
low complexity region 1239 1273 N/A INTRINSIC
coiled coil region 1347 1375 N/A INTRINSIC
coiled coil region 1399 1433 N/A INTRINSIC
low complexity region 1435 1453 N/A INTRINSIC
low complexity region 1497 1519 N/A INTRINSIC
coiled coil region 1612 1707 N/A INTRINSIC
coiled coil region 1731 1989 N/A INTRINSIC
coiled coil region 2034 2072 N/A INTRINSIC
coiled coil region 2127 2154 N/A INTRINSIC
coiled coil region 2220 2302 N/A INTRINSIC
coiled coil region 2357 2561 N/A INTRINSIC
low complexity region 2993 2999 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030J22Rik A G 8: 116,973,540 V41A probably damaging Het
AI481877 A G 4: 59,086,961 F284L probably benign Het
Ankrd12 C T 17: 65,986,174 V755I probably benign Het
Arrdc3 T C 13: 80,890,572 S218P probably damaging Het
Bzw1 T C 1: 58,402,942 V292A possibly damaging Het
Cers2 T C 3: 95,321,900 Y228H probably damaging Het
Egf C T 3: 129,711,449 M625I probably benign Het
Fbxw8 A T 5: 118,068,097 H595Q probably benign Het
Fshr T A 17: 88,985,271 I660F probably benign Het
Gapdh C T 6: 125,162,507 V267M probably damaging Het
Ginm1 T C 10: 7,792,696 probably benign Het
Gja1 A G 10: 56,388,322 D259G probably benign Het
Gm21814 T A 6: 149,582,004 noncoding transcript Het
Gm26870 T C 9: 3,002,340 probably benign Het
Habp2 G A 19: 56,317,832 C482Y probably damaging Het
Knl1 A C 2: 119,064,083 N79T probably damaging Het
Lama3 G A 18: 12,491,548 C1450Y probably damaging Het
Lats2 T C 14: 57,691,569 T950A probably benign Het
Map2k2 T A 10: 81,121,073 M95K probably damaging Het
Med12l T A 3: 59,042,336 I160N probably damaging Het
Olfr1158 A T 2: 87,990,438 D109V probably damaging Het
Olfr1160 A G 2: 88,006,644 S45P probably damaging Het
Pes1 T C 11: 3,976,803 S362P probably damaging Het
Pih1h3b A G X: 140,105,962 I197V probably benign Het
Ppp6r2 G T 15: 89,285,813 A844S probably benign Het
Rnf130 A G 11: 50,093,796 I308V probably damaging Het
Scn11a T C 9: 119,816,603 N95S probably damaging Het
Skint2 A G 4: 112,624,212 T91A probably damaging Het
Smg1 A G 7: 118,198,271 probably benign Het
Snapc1 A G 12: 73,968,374 probably null Het
Stard10 A T 7: 101,321,966 Y47F probably damaging Het
Tenm3 C T 8: 48,417,060 V233I probably damaging Het
Tex14 G A 11: 87,535,643 S1165N probably damaging Het
Unc5a A G 13: 54,995,820 I106V probably benign Het
Vps54 T A 11: 21,277,909 Y275N possibly damaging Het
Other mutations in 4932431P20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00505:4932431P20Rik APN 7 29534183 exon noncoding transcript
IGL00557:4932431P20Rik APN 7 29535802 exon noncoding transcript
IGL00569:4932431P20Rik APN 7 29534140 exon noncoding transcript
IGL00966:4932431P20Rik APN 7 29537463 exon noncoding transcript
IGL01668:4932431P20Rik APN 7 29537430 exon noncoding transcript
K7371:4932431P20Rik UTSW 7 29530992 exon noncoding transcript
P0037:4932431P20Rik UTSW 7 29533614 exon noncoding transcript
R0179:4932431P20Rik UTSW 7 29535940 exon noncoding transcript
R0357:4932431P20Rik UTSW 7 29535582 exon noncoding transcript
R0358:4932431P20Rik UTSW 7 29532211 exon noncoding transcript
R0412:4932431P20Rik UTSW 7 29530570 exon noncoding transcript
R0530:4932431P20Rik UTSW 7 29530120 exon noncoding transcript
R0600:4932431P20Rik UTSW 7 29533265 exon noncoding transcript
R0675:4932431P20Rik UTSW 7 29532517 exon noncoding transcript
R1118:4932431P20Rik UTSW 7 29534244 exon noncoding transcript
R1395:4932431P20Rik UTSW 7 29531387 exon noncoding transcript
R1444:4932431P20Rik UTSW 7 29529955 exon noncoding transcript
R1476:4932431P20Rik UTSW 7 29534890 exon noncoding transcript
R1534:4932431P20Rik UTSW 7 29530429 exon noncoding transcript
R1535:4932431P20Rik UTSW 7 29529579 exon noncoding transcript
R2023:4932431P20Rik UTSW 7 29531534 exon noncoding transcript
R2127:4932431P20Rik UTSW 7 29537140 exon noncoding transcript
R2141:4932431P20Rik UTSW 7 29531510 exon noncoding transcript
R2198:4932431P20Rik UTSW 7 29527272 exon noncoding transcript
R2201:4932431P20Rik UTSW 7 29536525 exon noncoding transcript
R2262:4932431P20Rik UTSW 7 29532562 exon noncoding transcript
R2263:4932431P20Rik UTSW 7 29532562 exon noncoding transcript
R4874:4932431P20Rik UTSW 7 29536183 exon noncoding transcript
R5064:4932431P20Rik UTSW 7 29535655 exon noncoding transcript
R5130:4932431P20Rik UTSW 7 29529274 exon noncoding transcript
R5366:4932431P20Rik UTSW 7 29533539 exon noncoding transcript
Posted On2013-12-03