Incidental Mutation 'R5635:Lrrc36'
ID501559
Institutional Source Beutler Lab
Gene Symbol Lrrc36
Ensembl Gene ENSMUSG00000054320
Gene Nameleucine rich repeat containing 36
Synonyms
MMRRC Submission 043286-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.249) question?
Stock #R5635 (G1)
Quality Score225
Status Validated
Chromosome8
Chromosomal Location105413571-105464086 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 105457573 bp
ZygosityHeterozygous
Amino Acid Change Valine to Methionine at position 480 (V480M)
Ref Sequence ENSEMBL: ENSMUSP00000066345 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067305] [ENSMUST00000109355] [ENSMUST00000213547] [ENSMUST00000216765]
Predicted Effect probably damaging
Transcript: ENSMUST00000067305
AA Change: V480M

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000066345
Gene: ENSMUSG00000054320
AA Change: V480M

DomainStartEndE-ValueType
low complexity region 377 389 N/A INTRINSIC
coiled coil region 478 550 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000109355
AA Change: V603M

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000104979
Gene: ENSMUSG00000054320
AA Change: V603M

DomainStartEndE-ValueType
Pfam:LRR_8 24 84 2.9e-8 PFAM
low complexity region 500 512 N/A INTRINSIC
coiled coil region 601 673 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000213547
AA Change: V601M

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Predicted Effect probably benign
Transcript: ENSMUST00000216457
Predicted Effect probably benign
Transcript: ENSMUST00000216765
AA Change: V601M

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 99% (90/91)
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9330159F19Rik T A 10: 29,218,277 M53K possibly damaging Het
Aldh3b3 C T 19: 3,968,512 T409I probably benign Het
Ankrd13a C A 5: 114,801,717 H468Q possibly damaging Het
Ap2a1 A C 7: 44,923,901 probably benign Het
Arfgef1 A T 1: 10,188,860 S671T possibly damaging Het
C1ra G A 6: 124,516,724 C145Y probably damaging Het
Catsperd G A 17: 56,632,335 V55M possibly damaging Het
Ccdc30 T C 4: 119,359,674 N123D possibly damaging Het
Cdc20 A T 4: 118,436,027 V232E possibly damaging Het
Cfap58 T A 19: 47,983,542 V637E possibly damaging Het
Coq4 T A 2: 29,788,355 V24E possibly damaging Het
Crim1 T A 17: 78,315,641 F423I probably damaging Het
Crls1 T C 2: 132,864,142 V262A possibly damaging Het
Crybb1 T C 5: 112,257,559 probably null Het
Cutc T A 19: 43,755,630 N23K probably benign Het
Cxcl10 T A 5: 92,347,839 I82F probably damaging Het
Cyp3a44 A T 5: 145,801,314 F60L possibly damaging Het
Dhx9 A G 1: 153,483,747 M35T probably benign Het
Dnah8 A G 17: 30,706,386 E1265G probably benign Het
Dzank1 C G 2: 144,483,407 D548H probably damaging Het
Eef2kmt A G 16: 5,249,029 V120A probably damaging Het
Elp4 A G 2: 105,814,264 probably null Het
Etl4 A T 2: 20,807,035 I1310F probably damaging Het
Exoc6b A T 6: 84,851,927 F492I probably damaging Het
F2rl2 A T 13: 95,700,782 I112F possibly damaging Het
Farp1 T A 14: 121,276,304 I837N possibly damaging Het
Fars2 A G 13: 36,410,146 E378G probably damaging Het
Fgg A G 3: 83,011,423 T248A probably benign Het
Flrt3 T A 2: 140,660,500 T403S probably damaging Het
Fndc3b C T 3: 27,541,931 E170K probably damaging Het
Gm17728 A G 17: 9,422,370 H104R probably benign Het
Hist2h2ab C A 3: 96,220,277 T121K possibly damaging Het
Hivep1 A G 13: 42,160,127 T1948A probably benign Het
Hspa4l T A 3: 40,745,745 I23N probably damaging Het
Ighv1-75 A G 12: 115,834,209 V31A probably benign Het
Kalrn T A 16: 34,014,084 N627I probably damaging Het
Lrp1b T G 2: 42,652,822 probably benign Het
Map4k3 A T 17: 80,613,495 N534K possibly damaging Het
Mybpc3 C T 2: 91,134,829 T1081I probably benign Het
Nfrkb T C 9: 31,399,298 S351P probably damaging Het
Nme4 A T 17: 26,094,231 V43E probably damaging Het
Notch1 C T 2: 26,476,161 E794K probably damaging Het
Nufip1 A T 14: 76,126,146 K270M probably damaging Het
Olfr1093 A G 2: 86,785,726 probably null Het
Olfr1330 G T 4: 118,893,635 G184V probably benign Het
Olfr390 G T 11: 73,787,634 R232L probably benign Het
Olfr65 G A 7: 103,906,638 M66I probably benign Het
Olfr919 A G 9: 38,698,159 I73T possibly damaging Het
Pcdhb15 T A 18: 37,473,770 Y18* probably null Het
Pcdhb21 A T 18: 37,513,917 Y33F probably benign Het
Pds5b T A 5: 150,778,221 H772Q possibly damaging Het
Pik3r4 C A 9: 105,667,825 H168N probably benign Het
Pitpnm3 A G 11: 72,067,160 S386P possibly damaging Het
Plg A G 17: 12,395,754 H307R probably damaging Het
Prdm9 A C 17: 15,562,440 D96E probably damaging Het
Prmt8 A G 6: 127,768,729 S7P probably damaging Het
Prune2 T C 19: 17,118,209 V359A probably benign Het
Pxn A T 5: 115,551,492 Q279L probably benign Het
Rarb A T 14: 16,443,788 C167S probably damaging Het
Rps6kb2 T A 19: 4,161,134 I131F probably damaging Het
Sec14l3 T A 11: 4,071,484 V219E probably damaging Het
Simc1 A G 13: 54,525,404 T522A probably benign Het
Slc1a6 T C 10: 78,789,091 V110A possibly damaging Het
Slc38a11 T G 2: 65,361,403 probably null Het
Snx13 T A 12: 35,140,171 D840E probably benign Het
Sp100 C A 1: 85,682,264 probably benign Het
Spc24 G T 9: 21,757,390 L104I probably damaging Het
Surf4 T C 2: 26,933,313 N4D probably benign Het
Tas2r131 A T 6: 132,957,608 D79E probably benign Het
Tbc1d20 T C 2: 152,311,461 S304P probably benign Het
Tbrg1 T C 9: 37,654,991 probably benign Het
Tmem214 A G 5: 30,871,517 N150S probably damaging Het
Trappc13 A T 13: 104,150,098 I217K probably benign Het
Ttc41 T A 10: 86,736,977 C738S probably benign Het
Ttn T C 2: 76,709,724 Q25979R probably benign Het
Tubb2b A T 13: 34,128,197 N204K probably damaging Het
Ube3a T A 7: 59,288,488 M713K probably damaging Het
Usp37 T C 1: 74,495,811 probably benign Het
Vegfb T A 19: 6,982,846 *189C probably null Het
Vmn2r82 A G 10: 79,378,818 N212D probably benign Het
Vta1 A T 10: 14,668,122 probably null Het
Wdr66 A T 5: 123,322,572 Q225L probably benign Het
Xdh T G 17: 73,913,875 I620L possibly damaging Het
Xpnpep3 A G 15: 81,436,769 Y283C probably benign Het
Zscan18 A G 7: 12,770,864 S609P probably benign Het
Other mutations in Lrrc36
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1509:Lrrc36 UTSW 8 105461129 missense probably damaging 1.00
R1638:Lrrc36 UTSW 8 105449641 missense possibly damaging 0.92
R1800:Lrrc36 UTSW 8 105449765 missense probably damaging 1.00
R2296:Lrrc36 UTSW 8 105461019 missense possibly damaging 0.81
R4030:Lrrc36 UTSW 8 105426807 missense probably damaging 1.00
R4059:Lrrc36 UTSW 8 105427796 missense probably damaging 1.00
R4613:Lrrc36 UTSW 8 105449614 missense possibly damaging 0.95
R4755:Lrrc36 UTSW 8 105452144 missense possibly damaging 0.83
R4786:Lrrc36 UTSW 8 105455278 missense probably benign 0.01
R4828:Lrrc36 UTSW 8 105455230 missense probably benign 0.45
R4911:Lrrc36 UTSW 8 105426935 missense probably benign 0.26
R5135:Lrrc36 UTSW 8 105463898 missense probably benign
R5221:Lrrc36 UTSW 8 105443856 missense probably damaging 0.99
R5354:Lrrc36 UTSW 8 105425364 missense probably damaging 0.99
R6793:Lrrc36 UTSW 8 105458433 missense probably damaging 1.00
R6950:Lrrc36 UTSW 8 105425389 splice site probably null
R6986:Lrrc36 UTSW 8 105458447 missense probably damaging 0.99
R7231:Lrrc36 UTSW 8 105461057 missense possibly damaging 0.46
R7326:Lrrc36 UTSW 8 105449769 missense possibly damaging 0.92
R7349:Lrrc36 UTSW 8 105452268 missense probably damaging 1.00
R7728:Lrrc36 UTSW 8 105449498 missense probably benign
R7751:Lrrc36 UTSW 8 105452035 missense possibly damaging 0.83
R7988:Lrrc36 UTSW 8 105452086 missense possibly damaging 0.81
R8145:Lrrc36 UTSW 8 105443764 missense probably damaging 0.96
R8195:Lrrc36 UTSW 8 105452085 missense possibly damaging 0.90
R8380:Lrrc36 UTSW 8 105426828 missense probably damaging 1.00
R8499:Lrrc36 UTSW 8 105449536 missense possibly damaging 0.66
U24488:Lrrc36 UTSW 8 105449752 missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- GCGGTCTTTAAGATTTTCCCACG -3'
(R):5'- AGTCATTCCCGAAGAGCCTG -3'

Sequencing Primer
(F):5'- TTAAGATTTTCCCACGTACCCAAC -3'
(R):5'- GCGTGTTCCCGTCCTAACAAG -3'
Posted On2017-12-01