Incidental Mutation 'R1474:Trpm6'
ID 163970
Institutional Source Beutler Lab
Gene Symbol Trpm6
Ensembl Gene ENSMUSG00000024727
Gene Name transient receptor potential cation channel, subfamily M, member 6
Synonyms CHAK2
MMRRC Submission 039527-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1474 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 18727347-18869875 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 18773859 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Threonine at position 412 (M412T)
Ref Sequence ENSEMBL: ENSMUSP00000037443 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040489]
AlphaFold Q8CIR4
Predicted Effect probably benign
Transcript: ENSMUST00000040489
AA Change: M412T

PolyPhen 2 Score 0.280 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000037443
Gene: ENSMUSG00000024727
AA Change: M412T

DomainStartEndE-ValueType
Blast:ANK 430 459 4e-8 BLAST
low complexity region 580 604 N/A INTRINSIC
transmembrane domain 749 766 N/A INTRINSIC
Pfam:Ion_trans 847 1087 2.8e-13 PFAM
low complexity region 1113 1126 N/A INTRINSIC
low complexity region 1136 1154 N/A INTRINSIC
Pfam:TRPM_tetra 1176 1231 7.5e-27 PFAM
low complexity region 1320 1331 N/A INTRINSIC
low complexity region 1578 1596 N/A INTRINSIC
Blast:Alpha_kinase 1618 1673 9e-11 BLAST
low complexity region 1682 1695 N/A INTRINSIC
Alpha_kinase 1761 1978 1e-84 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency 95% (104/110)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is predominantly expressed in the kidney and colon, and encodes a protein containing an ion channel domain and a protein kinase domain. It is crucial for magnesium homeostasis, and plays an essential role in epithelial magnesium transport and in the active magnesium absorption in the gut and kidney. Mutations in this gene are associated with hypomagnesemia with secondary hypocalcemia. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Apr 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic and postnatal lethality with exencephaly, spina bifida occulta, and abnormal brain and facial development. Mice heterozygous for a knock-out allele exhibit some premature death and decreased serummagnesium. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a C A 11: 109,960,635 (GRCm39) A628S probably damaging Het
Abca9 T C 11: 110,036,405 (GRCm39) N568S probably damaging Het
Ada C T 2: 163,574,814 (GRCm39) A108T possibly damaging Het
Adam6a T A 12: 113,508,069 (GRCm39) D147E possibly damaging Het
Ampd1 A T 3: 103,006,154 (GRCm39) T655S probably damaging Het
Ankk1 A G 9: 49,327,139 (GRCm39) F680S probably damaging Het
Asap1 G A 15: 63,991,869 (GRCm39) T783I probably benign Het
Astn1 T A 1: 158,329,923 (GRCm39) N259K probably damaging Het
Birc6 T C 17: 74,886,673 (GRCm39) V667A probably damaging Het
Brat1 G A 5: 140,698,382 (GRCm39) V185I probably benign Het
Btnl6 T C 17: 34,732,620 (GRCm39) Y318C probably damaging Het
Caskin2 G A 11: 115,694,522 (GRCm39) P360S probably benign Het
Ccdc121rt3 T C 5: 112,503,642 (GRCm39) T21A probably benign Het
Cd68 T A 11: 69,555,754 (GRCm39) probably benign Het
Cdca2 T C 14: 67,952,355 (GRCm39) probably benign Het
Cdk6 G A 5: 3,523,217 (GRCm39) M212I probably benign Het
Ceacam5 T A 7: 17,481,159 (GRCm39) F302Y probably damaging Het
Celsr2 T C 3: 108,301,055 (GRCm39) E2746G possibly damaging Het
Clec4a4 G A 6: 122,989,703 (GRCm39) V115I probably benign Het
Clip3 C A 7: 29,998,307 (GRCm39) A251E possibly damaging Het
Cmah T C 13: 24,623,180 (GRCm39) L350P probably damaging Het
Cntnap5a C T 1: 116,370,103 (GRCm39) R907* probably null Het
Cntnap5b T C 1: 99,999,814 (GRCm39) Y191H probably benign Het
Col4a4 A T 1: 82,458,207 (GRCm39) C1122* probably null Het
Coq5 A G 5: 115,433,842 (GRCm39) probably benign Het
Cpxcr1 A G X: 115,387,136 (GRCm39) K16E possibly damaging Het
Dclk3 T C 9: 111,298,304 (GRCm39) I616T probably benign Het
Dhrs3 A T 4: 144,646,057 (GRCm39) T122S probably damaging Het
Dnm1 T C 2: 32,210,596 (GRCm39) I502V probably benign Het
Dscaml1 G T 9: 45,596,519 (GRCm39) G788W probably damaging Het
Dusp10 C T 1: 183,769,645 (GRCm39) probably null Het
Ehbp1l1 C A 19: 5,769,112 (GRCm39) L730F possibly damaging Het
Eif2ak1 C T 5: 143,808,785 (GRCm39) H75Y probably damaging Het
Evi2a T C 11: 79,418,398 (GRCm39) T71A probably benign Het
Fam184a A T 10: 53,511,461 (GRCm39) S1073T probably damaging Het
Fam227a T C 15: 79,499,582 (GRCm39) Y591C probably damaging Het
Fam83a C T 15: 57,873,272 (GRCm39) T367M probably benign Het
Fam83g A G 11: 61,593,819 (GRCm39) D451G probably damaging Het
Fbn1 A G 2: 125,203,185 (GRCm39) F1213L possibly damaging Het
Fcgbp G A 7: 27,791,273 (GRCm39) V845I probably benign Het
Fermt1 C T 2: 132,766,942 (GRCm39) E342K probably benign Het
Foxn1 T A 11: 78,251,933 (GRCm39) M433L probably benign Het
Gm6632 T G 5: 59,211,679 (GRCm39) noncoding transcript Het
Gnl3 A T 14: 30,738,418 (GRCm39) probably benign Het
Hhipl1 C T 12: 108,277,996 (GRCm39) T108I probably damaging Het
Hs2st1 A T 3: 144,141,256 (GRCm39) F271I possibly damaging Het
Ido1 T C 8: 25,074,462 (GRCm39) S303G probably damaging Het
Ints2 C T 11: 86,117,607 (GRCm39) R705H probably damaging Het
Kcnc2 A G 10: 112,292,305 (GRCm39) K49E probably damaging Het
Kif3b T A 2: 153,162,235 (GRCm39) V482E probably damaging Het
Ldlrad2 G A 4: 137,299,525 (GRCm39) P100S probably benign Het
Lrba G T 3: 86,687,573 (GRCm39) probably benign Het
Lsm11 A T 11: 45,824,730 (GRCm39) W266R probably benign Het
Mob3a A T 10: 80,522,988 (GRCm39) M215K probably benign Het
Mterf1b T G 5: 4,247,163 (GRCm39) L268R probably damaging Het
Mvk T C 5: 114,598,157 (GRCm39) F365L probably damaging Het
Myo16 T A 8: 10,552,796 (GRCm39) F945I probably damaging Het
Myo1f G T 17: 33,813,001 (GRCm39) K602N possibly damaging Het
Nr2c2ap A T 8: 70,585,765 (GRCm39) M108L probably benign Het
Ofcc1 C T 13: 40,362,305 (GRCm39) G206R probably benign Het
Ogfrl1 A G 1: 23,414,890 (GRCm39) F206L probably damaging Het
Ola1 A T 2: 72,987,188 (GRCm39) I148N probably damaging Het
Or14c46 G T 7: 85,918,270 (GRCm39) H242Q probably damaging Het
Or4d10b T A 19: 12,036,844 (GRCm39) T91S probably benign Het
Or51f1d A G 7: 102,701,288 (GRCm39) Y261C probably damaging Het
Or6c2 A T 10: 129,362,824 (GRCm39) M243L probably benign Het
Or9m2 A G 2: 87,821,334 (GRCm39) N293S probably damaging Het
Otof A G 5: 30,536,876 (GRCm39) probably null Het
Pah G T 10: 87,414,175 (GRCm39) K341N probably damaging Het
Pfdn5 T A 15: 102,236,946 (GRCm39) probably null Het
Piezo2 A G 18: 63,216,202 (GRCm39) C960R probably damaging Het
Pitx2 T C 3: 129,012,488 (GRCm39) V306A probably damaging Het
Pkd1l2 C A 8: 117,792,236 (GRCm39) probably benign Het
Plekho1 T C 3: 95,896,878 (GRCm39) E197G probably damaging Het
Polr2i A G 7: 29,932,227 (GRCm39) N34S probably damaging Het
Psph A T 5: 129,848,614 (GRCm39) D22E probably damaging Het
Ptprs C A 17: 56,731,128 (GRCm39) A687S probably damaging Het
Ralgapa1 T C 12: 55,788,265 (GRCm39) K606R probably benign Het
Rigi A G 4: 40,208,868 (GRCm39) V703A possibly damaging Het
Rims1 A G 1: 22,577,362 (GRCm39) probably benign Het
Rnf213 C T 11: 119,328,576 (GRCm39) P2002L probably damaging Het
Ryr3 A T 2: 112,740,307 (GRCm39) C555S probably damaging Het
Sftpd C A 14: 40,894,384 (GRCm39) G345V probably damaging Het
Slc41a1 T A 1: 131,774,319 (GRCm39) M462K probably damaging Het
Slc44a2 A G 9: 21,264,990 (GRCm39) E676G probably damaging Het
Sox6 T A 7: 115,300,926 (GRCm39) probably benign Het
Spdye4b G A 5: 143,181,472 (GRCm39) R109Q probably damaging Het
Spef1l C A 7: 139,556,555 (GRCm39) R144L probably benign Het
Spink8 A T 9: 109,649,706 (GRCm39) I63L probably damaging Het
St3gal3 A G 4: 117,871,983 (GRCm39) L73P probably damaging Het
Stab1 A G 14: 30,871,818 (GRCm39) L1247P probably benign Het
Tat A G 8: 110,718,195 (GRCm39) R27G probably benign Het
Tcerg1l C T 7: 137,881,804 (GRCm39) R295H probably damaging Het
Tfrc T C 16: 32,445,467 (GRCm39) V596A probably damaging Het
Tgfb3 C T 12: 86,116,120 (GRCm39) probably null Het
Tmed5 A T 5: 108,280,248 (GRCm39) S15T probably benign Het
Tph1 A T 7: 46,303,286 (GRCm39) S231T probably benign Het
Trim30d G A 7: 104,121,701 (GRCm39) S198L probably damaging Het
Ttn G T 2: 76,612,589 (GRCm39) D15417E probably benign Het
U2surp A G 9: 95,375,251 (GRCm39) I157T possibly damaging Het
Ubr4 A G 4: 139,156,890 (GRCm39) D2305G probably damaging Het
Uvssa A G 5: 33,546,165 (GRCm39) K179E probably benign Het
Vps35l T C 7: 118,359,436 (GRCm39) F230S probably damaging Het
Xirp2 A G 2: 67,355,411 (GRCm39) K3391E probably benign Het
Xpo7 T A 14: 70,936,473 (GRCm39) H170L probably benign Het
Zrsr2-ps1 T C 11: 22,924,404 (GRCm39) W393R probably benign Het
Other mutations in Trpm6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00540:Trpm6 APN 19 18,761,272 (GRCm39) splice site probably benign
IGL00862:Trpm6 APN 19 18,804,892 (GRCm39) missense probably damaging 1.00
IGL01348:Trpm6 APN 19 18,855,015 (GRCm39) missense probably damaging 1.00
IGL01400:Trpm6 APN 19 18,803,158 (GRCm39) nonsense probably null
IGL01451:Trpm6 APN 19 18,786,933 (GRCm39) missense probably damaging 1.00
IGL01508:Trpm6 APN 19 18,773,894 (GRCm39) nonsense probably null
IGL01995:Trpm6 APN 19 18,807,691 (GRCm39) splice site probably benign
IGL02092:Trpm6 APN 19 18,749,695 (GRCm39) missense possibly damaging 0.59
IGL02152:Trpm6 APN 19 18,809,903 (GRCm39) missense possibly damaging 0.93
IGL02294:Trpm6 APN 19 18,831,427 (GRCm39) missense probably benign
IGL02329:Trpm6 APN 19 18,831,581 (GRCm39) missense probably benign 0.17
IGL02366:Trpm6 APN 19 18,755,874 (GRCm39) splice site probably benign
IGL02402:Trpm6 APN 19 18,764,120 (GRCm39) missense probably benign 0.18
IGL02457:Trpm6 APN 19 18,804,762 (GRCm39) nonsense probably null
IGL02457:Trpm6 APN 19 18,803,155 (GRCm39) missense probably damaging 1.00
IGL02684:Trpm6 APN 19 18,779,571 (GRCm39) splice site probably benign
IGL02705:Trpm6 APN 19 18,754,097 (GRCm39) critical splice donor site probably null
IGL02728:Trpm6 APN 19 18,787,016 (GRCm39) missense possibly damaging 0.71
IGL02742:Trpm6 APN 19 18,807,376 (GRCm39) splice site probably benign
IGL02818:Trpm6 APN 19 18,843,621 (GRCm39) missense probably benign 0.04
IGL02836:Trpm6 APN 19 18,790,846 (GRCm39) missense probably damaging 1.00
IGL03119:Trpm6 APN 19 18,815,381 (GRCm39) nonsense probably null
IGL03193:Trpm6 APN 19 18,803,236 (GRCm39) missense possibly damaging 0.94
IGL03227:Trpm6 APN 19 18,764,143 (GRCm39) missense probably benign 0.12
IGL03227:Trpm6 APN 19 18,796,483 (GRCm39) missense probably benign 0.01
IGL03231:Trpm6 APN 19 18,796,545 (GRCm39) missense probably benign
IGL03245:Trpm6 APN 19 18,855,065 (GRCm39) missense probably damaging 1.00
IGL03328:Trpm6 APN 19 18,815,446 (GRCm39) missense possibly damaging 0.94
IGL03341:Trpm6 APN 19 18,790,850 (GRCm39) missense probably benign
P0043:Trpm6 UTSW 19 18,855,129 (GRCm39) missense probably damaging 1.00
PIT4260001:Trpm6 UTSW 19 18,803,166 (GRCm39) missense possibly damaging 0.48
R0057:Trpm6 UTSW 19 18,764,119 (GRCm39) missense probably benign 0.05
R0115:Trpm6 UTSW 19 18,807,316 (GRCm39) missense probably damaging 0.98
R0119:Trpm6 UTSW 19 18,809,957 (GRCm39) missense probably benign 0.05
R0140:Trpm6 UTSW 19 18,796,558 (GRCm39) splice site probably null
R0267:Trpm6 UTSW 19 18,800,742 (GRCm39) missense probably benign
R0350:Trpm6 UTSW 19 18,861,321 (GRCm39) splice site probably null
R0373:Trpm6 UTSW 19 18,830,951 (GRCm39) missense probably benign 0.15
R0393:Trpm6 UTSW 19 18,756,008 (GRCm39) missense probably damaging 0.99
R0416:Trpm6 UTSW 19 18,760,389 (GRCm39) splice site probably benign
R0505:Trpm6 UTSW 19 18,851,266 (GRCm39) splice site probably benign
R0526:Trpm6 UTSW 19 18,770,240 (GRCm39) missense probably damaging 0.97
R0607:Trpm6 UTSW 19 18,849,585 (GRCm39) missense probably benign 0.00
R0609:Trpm6 UTSW 19 18,803,226 (GRCm39) missense probably damaging 0.97
R0714:Trpm6 UTSW 19 18,815,451 (GRCm39) missense possibly damaging 0.90
R1215:Trpm6 UTSW 19 18,773,862 (GRCm39) missense probably damaging 1.00
R1512:Trpm6 UTSW 19 18,853,295 (GRCm39) missense probably benign
R1558:Trpm6 UTSW 19 18,764,192 (GRCm39) missense probably benign 0.04
R1597:Trpm6 UTSW 19 18,804,888 (GRCm39) missense probably damaging 0.98
R1618:Trpm6 UTSW 19 18,854,995 (GRCm39) missense possibly damaging 0.88
R1779:Trpm6 UTSW 19 18,833,581 (GRCm39) missense probably damaging 1.00
R1796:Trpm6 UTSW 19 18,804,931 (GRCm39) missense possibly damaging 0.90
R1799:Trpm6 UTSW 19 18,869,363 (GRCm39) splice site probably null
R1840:Trpm6 UTSW 19 18,843,631 (GRCm39) missense probably benign 0.21
R1991:Trpm6 UTSW 19 18,773,648 (GRCm39) missense probably benign 0.00
R2030:Trpm6 UTSW 19 18,831,629 (GRCm39) missense probably benign
R2073:Trpm6 UTSW 19 18,853,406 (GRCm39) missense probably damaging 1.00
R2074:Trpm6 UTSW 19 18,855,103 (GRCm39) missense probably damaging 1.00
R2096:Trpm6 UTSW 19 18,803,116 (GRCm39) missense probably damaging 0.97
R2103:Trpm6 UTSW 19 18,773,648 (GRCm39) missense probably benign 0.00
R2106:Trpm6 UTSW 19 18,790,714 (GRCm39) missense possibly damaging 0.95
R2117:Trpm6 UTSW 19 18,807,316 (GRCm39) missense probably damaging 0.98
R2850:Trpm6 UTSW 19 18,769,454 (GRCm39) missense possibly damaging 0.68
R3125:Trpm6 UTSW 19 18,831,795 (GRCm39) missense probably benign 0.05
R3719:Trpm6 UTSW 19 18,749,757 (GRCm39) nonsense probably null
R3779:Trpm6 UTSW 19 18,853,403 (GRCm39) missense possibly damaging 0.80
R4115:Trpm6 UTSW 19 18,809,921 (GRCm39) missense probably damaging 1.00
R4367:Trpm6 UTSW 19 18,804,889 (GRCm39) missense probably damaging 0.99
R4523:Trpm6 UTSW 19 18,773,864 (GRCm39) missense probably damaging 1.00
R4546:Trpm6 UTSW 19 18,809,841 (GRCm39) missense probably damaging 1.00
R4564:Trpm6 UTSW 19 18,809,961 (GRCm39) missense possibly damaging 0.95
R4565:Trpm6 UTSW 19 18,803,236 (GRCm39) missense probably damaging 1.00
R4697:Trpm6 UTSW 19 18,831,155 (GRCm39) missense probably benign 0.01
R4714:Trpm6 UTSW 19 18,831,564 (GRCm39) missense possibly damaging 0.93
R4750:Trpm6 UTSW 19 18,853,428 (GRCm39) missense probably damaging 0.99
R4771:Trpm6 UTSW 19 18,790,857 (GRCm39) missense probably damaging 0.97
R4791:Trpm6 UTSW 19 18,845,345 (GRCm39) missense probably benign 0.00
R4814:Trpm6 UTSW 19 18,839,576 (GRCm39) missense probably benign 0.11
R5028:Trpm6 UTSW 19 18,764,124 (GRCm39) missense probably damaging 1.00
R5237:Trpm6 UTSW 19 18,790,828 (GRCm39) missense probably damaging 1.00
R5615:Trpm6 UTSW 19 18,807,297 (GRCm39) missense probably damaging 0.96
R5642:Trpm6 UTSW 19 18,807,571 (GRCm39) missense probably damaging 1.00
R5645:Trpm6 UTSW 19 18,830,968 (GRCm39) missense probably damaging 1.00
R5726:Trpm6 UTSW 19 18,830,981 (GRCm39) missense probably damaging 1.00
R5832:Trpm6 UTSW 19 18,764,183 (GRCm39) missense possibly damaging 0.66
R5843:Trpm6 UTSW 19 18,833,539 (GRCm39) missense probably benign 0.04
R5955:Trpm6 UTSW 19 18,869,383 (GRCm39) missense possibly damaging 0.75
R6101:Trpm6 UTSW 19 18,831,112 (GRCm39) nonsense probably null
R6105:Trpm6 UTSW 19 18,831,112 (GRCm39) nonsense probably null
R6211:Trpm6 UTSW 19 18,760,492 (GRCm39) missense probably damaging 1.00
R6228:Trpm6 UTSW 19 18,831,655 (GRCm39) missense probably damaging 1.00
R6263:Trpm6 UTSW 19 18,831,472 (GRCm39) missense possibly damaging 0.94
R6453:Trpm6 UTSW 19 18,807,354 (GRCm39) missense probably damaging 1.00
R6562:Trpm6 UTSW 19 18,815,406 (GRCm39) missense probably damaging 1.00
R6624:Trpm6 UTSW 19 18,866,384 (GRCm39) missense probably damaging 1.00
R6624:Trpm6 UTSW 19 18,773,803 (GRCm39) critical splice acceptor site probably null
R6729:Trpm6 UTSW 19 18,807,661 (GRCm39) missense probably damaging 1.00
R6765:Trpm6 UTSW 19 18,855,129 (GRCm39) missense probably damaging 1.00
R6976:Trpm6 UTSW 19 18,760,527 (GRCm39) missense probably benign
R7103:Trpm6 UTSW 19 18,790,911 (GRCm39) missense possibly damaging 0.87
R7126:Trpm6 UTSW 19 18,831,397 (GRCm39) nonsense probably null
R7128:Trpm6 UTSW 19 18,789,137 (GRCm39) missense possibly damaging 0.92
R7157:Trpm6 UTSW 19 18,815,462 (GRCm39) missense possibly damaging 0.91
R7212:Trpm6 UTSW 19 18,831,155 (GRCm39) missense probably benign 0.01
R7263:Trpm6 UTSW 19 18,854,150 (GRCm39) missense probably damaging 1.00
R7268:Trpm6 UTSW 19 18,755,949 (GRCm39) missense probably benign 0.13
R7305:Trpm6 UTSW 19 18,853,455 (GRCm39) missense probably benign 0.30
R7498:Trpm6 UTSW 19 18,853,484 (GRCm39) missense probably damaging 1.00
R7558:Trpm6 UTSW 19 18,756,029 (GRCm39) missense probably damaging 0.96
R7590:Trpm6 UTSW 19 18,809,945 (GRCm39) missense probably benign 0.31
R7646:Trpm6 UTSW 19 18,845,325 (GRCm39) missense probably benign 0.10
R7650:Trpm6 UTSW 19 18,853,377 (GRCm39) missense possibly damaging 0.70
R7727:Trpm6 UTSW 19 18,831,613 (GRCm39) missense probably damaging 0.97
R7743:Trpm6 UTSW 19 18,804,772 (GRCm39) missense probably benign 0.03
R7747:Trpm6 UTSW 19 18,727,409 (GRCm39) splice site probably null
R7807:Trpm6 UTSW 19 18,807,220 (GRCm39) missense probably benign 0.11
R7870:Trpm6 UTSW 19 18,792,605 (GRCm39) missense probably benign 0.01
R7891:Trpm6 UTSW 19 18,754,074 (GRCm39) missense probably benign 0.01
R7955:Trpm6 UTSW 19 18,831,654 (GRCm39) missense probably benign 0.01
R7965:Trpm6 UTSW 19 18,853,474 (GRCm39) missense probably damaging 1.00
R7967:Trpm6 UTSW 19 18,756,023 (GRCm39) missense probably damaging 0.99
R7992:Trpm6 UTSW 19 18,792,714 (GRCm39) missense probably damaging 1.00
R8035:Trpm6 UTSW 19 18,770,226 (GRCm39) missense probably damaging 0.97
R8108:Trpm6 UTSW 19 18,789,154 (GRCm39) missense probably damaging 1.00
R8268:Trpm6 UTSW 19 18,851,225 (GRCm39) missense possibly damaging 0.85
R8411:Trpm6 UTSW 19 18,831,332 (GRCm39) missense probably benign 0.39
R8413:Trpm6 UTSW 19 18,809,849 (GRCm39) missense probably benign 0.00
R8534:Trpm6 UTSW 19 18,869,459 (GRCm39) missense probably benign 0.00
R8932:Trpm6 UTSW 19 18,815,366 (GRCm39) missense possibly damaging 0.87
R8990:Trpm6 UTSW 19 18,792,799 (GRCm39) missense probably damaging 1.00
R9403:Trpm6 UTSW 19 18,810,016 (GRCm39) missense possibly damaging 0.84
R9446:Trpm6 UTSW 19 18,815,462 (GRCm39) missense possibly damaging 0.91
R9463:Trpm6 UTSW 19 18,761,264 (GRCm39) critical splice donor site probably null
R9485:Trpm6 UTSW 19 18,755,978 (GRCm39) missense probably benign 0.06
R9536:Trpm6 UTSW 19 18,764,123 (GRCm39) missense probably damaging 1.00
R9549:Trpm6 UTSW 19 18,853,394 (GRCm39) nonsense probably null
R9564:Trpm6 UTSW 19 18,851,240 (GRCm39) missense possibly damaging 0.92
R9626:Trpm6 UTSW 19 18,790,846 (GRCm39) missense probably damaging 1.00
R9655:Trpm6 UTSW 19 18,869,466 (GRCm39) missense probably benign
R9721:Trpm6 UTSW 19 18,807,336 (GRCm39) missense probably benign 0.12
R9742:Trpm6 UTSW 19 18,800,766 (GRCm39) missense probably benign 0.09
Predicted Primers PCR Primer
(F):5'- TGATGCTGATTCTGAAGAGCACCAAG -3'
(R):5'- AAGAGCCATGCCTTTGCTTCCC -3'

Sequencing Primer
(F):5'- CTCTACTGAAGGGTGAGTGACC -3'
(R):5'- TTTGCTTCCCTGGGTGC -3'
Posted On 2014-03-28