Incidental Mutation 'R4898:Unc79'
ID 375954
Institutional Source Beutler Lab
Gene Symbol Unc79
Ensembl Gene ENSMUSG00000021198
Gene Name unc-79 homolog
Synonyms 9030205A07Rik, Mlca3
MMRRC Submission 042502-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4898 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 102915118-103150324 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 103128079 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Phenylalanine at position 2250 (C2250F)
Ref Sequence ENSEMBL: ENSMUSP00000098659 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085079] [ENSMUST00000101099] [ENSMUST00000178076] [ENSMUST00000179002]
AlphaFold Q0KK59
Predicted Effect possibly damaging
Transcript: ENSMUST00000085079
AA Change: C2112F

PolyPhen 2 Score 0.752 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000082156
Gene: ENSMUSG00000021198
AA Change: C2112F

DomainStartEndE-ValueType
Pfam:UNC-79 1 469 3.1e-223 PFAM
low complexity region 732 737 N/A INTRINSIC
low complexity region 846 862 N/A INTRINSIC
low complexity region 968 977 N/A INTRINSIC
low complexity region 1114 1125 N/A INTRINSIC
low complexity region 1313 1325 N/A INTRINSIC
low complexity region 1428 1440 N/A INTRINSIC
low complexity region 1471 1476 N/A INTRINSIC
low complexity region 1477 1489 N/A INTRINSIC
low complexity region 1490 1504 N/A INTRINSIC
low complexity region 1541 1556 N/A INTRINSIC
low complexity region 1861 1870 N/A INTRINSIC
low complexity region 2237 2246 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000101099
AA Change: C2250F

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000098659
Gene: ENSMUSG00000021198
AA Change: C2250F

DomainStartEndE-ValueType
Pfam:UNC-79 113 646 1.2e-226 PFAM
low complexity region 909 914 N/A INTRINSIC
low complexity region 1023 1039 N/A INTRINSIC
low complexity region 1145 1154 N/A INTRINSIC
low complexity region 1291 1302 N/A INTRINSIC
low complexity region 1490 1502 N/A INTRINSIC
low complexity region 1605 1617 N/A INTRINSIC
low complexity region 1648 1653 N/A INTRINSIC
low complexity region 1654 1666 N/A INTRINSIC
low complexity region 1667 1681 N/A INTRINSIC
low complexity region 1718 1733 N/A INTRINSIC
low complexity region 1999 2008 N/A INTRINSIC
low complexity region 2375 2384 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000178076
AA Change: C2115F

PolyPhen 2 Score 0.172 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000136888
Gene: ENSMUSG00000021198
AA Change: C2115F

DomainStartEndE-ValueType
Pfam:UNC-79 1 450 4.2e-213 PFAM
low complexity region 713 718 N/A INTRINSIC
low complexity region 827 843 N/A INTRINSIC
low complexity region 949 958 N/A INTRINSIC
low complexity region 1117 1128 N/A INTRINSIC
low complexity region 1316 1328 N/A INTRINSIC
low complexity region 1431 1443 N/A INTRINSIC
low complexity region 1474 1479 N/A INTRINSIC
low complexity region 1480 1492 N/A INTRINSIC
low complexity region 1493 1507 N/A INTRINSIC
low complexity region 1544 1559 N/A INTRINSIC
low complexity region 1864 1873 N/A INTRINSIC
low complexity region 2240 2249 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000179002
AA Change: C2308F

PolyPhen 2 Score 0.163 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000136332
Gene: ENSMUSG00000021198
AA Change: C2308F

DomainStartEndE-ValueType
Pfam:UNC-79 60 593 1.3e-226 PFAM
low complexity region 856 861 N/A INTRINSIC
low complexity region 970 986 N/A INTRINSIC
low complexity region 1092 1101 N/A INTRINSIC
low complexity region 1260 1271 N/A INTRINSIC
low complexity region 1509 1521 N/A INTRINSIC
low complexity region 1624 1636 N/A INTRINSIC
low complexity region 1667 1672 N/A INTRINSIC
low complexity region 1673 1685 N/A INTRINSIC
low complexity region 1686 1700 N/A INTRINSIC
low complexity region 1737 1752 N/A INTRINSIC
low complexity region 2057 2066 N/A INTRINSIC
low complexity region 2433 2442 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 93.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The NALCN channel is responsible for Na(+) leak currents. The protein encoded by this gene, along with UNC80, is an accessory subunit of the NALCN channel that contributes to the Ca(2+) sensitivity of the channel. [provided by RefSeq, Sep 2016]
PHENOTYPE: Homozygous mutation results in lethality within the first week after birth, mostly at P0 or P1. Pups fail to nurse and have no milk in stomachs resulting in weakness, inactivity and no weight gain. [provided by MGI curators]
Allele List at MGI

 All alleles(2) : Targeted, knock-out(1) Chemically induced(1)

Other mutations in this stock
Total: 116 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc6 T C 7: 45,639,111 (GRCm39) Y944C probably damaging Het
Acacb T C 5: 114,370,999 (GRCm39) V1747A probably benign Het
Acad8 C T 9: 26,889,698 (GRCm39) R332H probably damaging Het
Acrbp A C 6: 125,027,501 (GRCm39) T50P probably damaging Het
Ahctf1 G T 1: 179,583,077 (GRCm39) N1500K probably benign Het
Aoc1l3 A G 6: 48,964,651 (GRCm39) T220A possibly damaging Het
Arfgef1 A G 1: 10,229,798 (GRCm39) I1301T possibly damaging Het
Arhgef15 T C 11: 68,842,171 (GRCm39) S478G probably benign Het
Armh1 T C 4: 117,094,977 (GRCm39) D21G probably damaging Het
Atp13a4 A T 16: 29,227,779 (GRCm39) L1045* probably null Het
Atp2a3 T A 11: 72,873,506 (GRCm39) L793H probably damaging Het
B4galnt4 C A 7: 140,648,173 (GRCm39) P563Q probably benign Het
Bcl2a1b A T 9: 89,081,713 (GRCm39) K94* probably null Het
Bod1 T A 11: 31,616,853 (GRCm39) Q136L possibly damaging Het
C2cd3 A G 7: 100,055,166 (GRCm39) K443R probably damaging Het
Cadps A G 14: 12,411,588 (GRCm38) V1250A possibly damaging Het
Car12 T A 9: 66,671,600 (GRCm39) Y332* probably null Het
Ccdc186 A T 19: 56,790,432 (GRCm39) probably null Het
Cdh6 T C 15: 13,034,774 (GRCm39) T629A probably damaging Het
Cep112 T A 11: 108,397,471 (GRCm39) D353E probably damaging Het
Cep152 T C 2: 125,428,301 (GRCm39) S777G probably benign Het
Clec4b2 A C 6: 123,181,163 (GRCm39) K183Q probably benign Het
Cngb3 T C 4: 19,395,926 (GRCm39) Y323H probably benign Het
Cnp G T 11: 100,467,202 (GRCm39) E48D probably benign Het
Ctrb1 T A 8: 112,413,783 (GRCm39) I194F probably benign Het
Cyp2d11 T A 15: 82,275,224 (GRCm39) D241V probably benign Het
D5Ertd579e T A 5: 36,772,285 (GRCm39) E703D probably damaging Het
Dlg1 T C 16: 31,676,764 (GRCm39) V731A probably damaging Het
Dlgap5 T C 14: 47,651,276 (GRCm39) S86G probably benign Het
Dock3 A G 9: 106,807,266 (GRCm39) F1354L probably damaging Het
Dock3 C A 9: 106,870,171 (GRCm39) V638F possibly damaging Het
Eif3c A T 7: 126,156,626 (GRCm39) M407K probably benign Het
Eif4a3l1 A T 6: 136,305,737 (GRCm39) Q66L possibly damaging Het
Epha4 T A 1: 77,366,712 (GRCm39) K578* probably null Het
Erc2 C T 14: 27,375,285 (GRCm39) L168F probably damaging Het
Esyt2 A G 12: 116,305,708 (GRCm39) I313V probably benign Het
Far1 T A 7: 113,167,432 (GRCm39) Y506N probably damaging Het
Fbxw26 T A 9: 109,547,037 (GRCm39) N463Y possibly damaging Het
Fgg A G 3: 82,915,847 (GRCm39) D96G probably benign Het
Gfer A G 17: 24,914,274 (GRCm39) S130P probably damaging Het
Hdac10 A T 15: 89,012,650 (GRCm39) M1K probably null Het
Hsd3b1 A T 3: 98,760,642 (GRCm39) S110R probably benign Het
Ints15 A G 5: 143,287,592 (GRCm39) S438P probably benign Het
Itga6 T C 2: 71,668,717 (GRCm39) L552P possibly damaging Het
Klk14 G A 7: 43,341,501 (GRCm39) C51Y probably damaging Het
Lama2 TTTGCGCATT TTT 10: 26,919,639 (GRCm39) probably null Het
Llgl1 C T 11: 60,600,394 (GRCm39) P581L probably benign Het
Lrrc8a A G 2: 30,147,214 (GRCm39) K676R probably benign Het
Lrrc8b A T 5: 105,628,080 (GRCm39) Y142F probably benign Het
Lyz2 T A 10: 117,114,614 (GRCm39) D105V possibly damaging Het
Mamdc4 T C 2: 25,460,035 (GRCm39) D76G probably damaging Het
Map7d1 T C 4: 126,127,018 (GRCm39) K731E unknown Het
Mgam A C 6: 40,619,988 (GRCm39) I26L probably benign Het
Mmp13 A T 9: 7,272,953 (GRCm39) E104D probably benign Het
Morc2a C T 11: 3,626,664 (GRCm39) R241* probably null Het
Mtfmt C A 9: 65,359,386 (GRCm39) H354N probably benign Het
Myh3 T C 11: 66,990,233 (GRCm39) I1626T probably benign Het
Ndst1 A T 18: 60,825,059 (GRCm39) V753D probably benign Het
Neurl4 A G 11: 69,793,997 (GRCm39) D151G probably damaging Het
Nlrx1 T C 9: 44,168,194 (GRCm39) S568G probably benign Het
Or10g3b G C 14: 52,586,999 (GRCm39) P168R probably damaging Het
Or2t45 T C 11: 58,669,132 (GRCm39) Y60H possibly damaging Het
Or2t46 T G 11: 58,472,546 (GRCm39) L292R probably damaging Het
Or4c52 T C 2: 89,845,762 (GRCm39) F163L probably damaging Het
Or52s1 A G 7: 102,861,747 (GRCm39) I216V probably damaging Het
Or6c66 A T 10: 129,461,468 (GRCm39) I154N probably benign Het
Or8b42 A T 9: 38,342,111 (GRCm39) M178L probably benign Het
Osbpl7 A G 11: 96,950,976 (GRCm39) I608V probably damaging Het
Pard3b T C 1: 61,807,159 (GRCm39) I58T probably damaging Het
Pcare A G 17: 72,058,066 (GRCm39) M537T probably damaging Het
Pcdhga1 A C 18: 37,795,407 (GRCm39) E137A possibly damaging Het
Pde6c G A 19: 38,139,072 (GRCm39) V301I possibly damaging Het
Pdia5 G C 16: 35,230,786 (GRCm39) N338K possibly damaging Het
Pex11g T C 8: 3,514,042 (GRCm39) Y40C probably damaging Het
Plekhg3 A G 12: 76,610,899 (GRCm39) Y183C probably damaging Het
Pole A C 5: 110,438,090 (GRCm39) probably null Het
Ppfia1 A G 7: 144,045,313 (GRCm39) L948P probably damaging Het
Prdm2 A T 4: 142,860,761 (GRCm39) V843E probably damaging Het
Prss56 C A 1: 87,115,708 (GRCm39) F527L probably damaging Het
Psmd11 T C 11: 80,329,146 (GRCm39) L88P probably damaging Het
Ptx3 G C 3: 66,132,412 (GRCm39) G311A probably damaging Het
Rars1 A T 11: 35,699,385 (GRCm39) L636H probably damaging Het
Rnft2 A G 5: 118,375,507 (GRCm39) S81P probably benign Het
Rufy4 T C 1: 74,186,822 (GRCm39) C537R probably damaging Het
Rxra T A 2: 27,631,195 (GRCm39) I142N probably damaging Het
Scin T C 12: 40,154,931 (GRCm39) M221V probably benign Het
Sfmbt2 G A 2: 10,584,069 (GRCm39) V809I possibly damaging Het
Sirt1 T A 10: 63,157,783 (GRCm39) I505F probably benign Het
Six5 T C 7: 18,829,096 (GRCm39) Y179H probably damaging Het
Slc12a4 A C 8: 106,671,241 (GRCm39) M982R probably damaging Het
Slco4c1 T A 1: 96,765,237 (GRCm39) L404F probably damaging Het
Smn1 T C 13: 100,268,931 (GRCm39) L259P probably damaging Het
Sorl1 T G 9: 41,952,935 (GRCm39) D702A probably damaging Het
Spta1 A G 1: 174,065,400 (GRCm39) E1983G possibly damaging Het
Srsf1 T A 11: 87,940,788 (GRCm39) probably null Het
Stard9 C T 2: 120,536,900 (GRCm39) R4224* probably null Het
Sybu T G 15: 44,538,895 (GRCm39) M383L probably benign Het
Tbx15 A C 3: 99,259,583 (GRCm39) N485H possibly damaging Het
Tcerg1l A T 7: 137,819,786 (GRCm39) F485I probably damaging Het
Tdrd7 C A 4: 46,005,616 (GRCm39) T474N possibly damaging Het
Thada A T 17: 84,755,470 (GRCm39) probably null Het
Tnik A T 3: 28,704,235 (GRCm39) I1020F probably damaging Het
Tnxb A G 17: 34,914,566 (GRCm39) D1884G possibly damaging Het
Tprn T C 2: 25,158,845 (GRCm39) M623T probably damaging Het
Trdn T A 10: 33,350,413 (GRCm39) Y661N probably damaging Het
Ttc41 T C 10: 86,612,056 (GRCm39) S1110P possibly damaging Het
Ttc6 A C 12: 57,707,026 (GRCm39) R644S probably benign Het
Ttyh1 A T 7: 4,136,735 (GRCm39) M448L probably benign Het
Ush2a A G 1: 188,358,805 (GRCm39) I2110M probably benign Het
Uvssa G T 5: 33,571,257 (GRCm39) E634* probably null Het
Vac14 A C 8: 111,372,440 (GRCm39) T384P probably benign Het
Wdr11 A G 7: 129,235,445 (GRCm39) E1169G probably benign Het
Zfp36l1 T A 12: 80,157,298 (GRCm39) T28S probably benign Het
Zfp715 A T 7: 42,949,106 (GRCm39) Y285N possibly damaging Het
Zfp91 A T 19: 12,747,424 (GRCm39) D566E probably damaging Het
Zgrf1 G A 3: 127,396,085 (GRCm39) V544M probably damaging Het
Other mutations in Unc79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00718:Unc79 APN 12 103,135,906 (GRCm39) missense possibly damaging 0.68
IGL00835:Unc79 APN 12 103,108,149 (GRCm39) splice site probably benign
IGL00917:Unc79 APN 12 103,054,766 (GRCm39) missense possibly damaging 0.53
IGL01012:Unc79 APN 12 103,078,714 (GRCm39) missense probably damaging 1.00
IGL01121:Unc79 APN 12 103,131,890 (GRCm39) missense probably damaging 0.99
IGL01303:Unc79 APN 12 103,128,126 (GRCm39) missense possibly damaging 0.94
IGL01305:Unc79 APN 12 102,968,130 (GRCm39) missense probably damaging 0.99
IGL01315:Unc79 APN 12 103,054,780 (GRCm39) missense possibly damaging 0.66
IGL01388:Unc79 APN 12 103,136,018 (GRCm39) splice site probably benign
IGL01415:Unc79 APN 12 103,074,944 (GRCm39) missense probably damaging 1.00
IGL01447:Unc79 APN 12 103,045,177 (GRCm39) missense probably damaging 1.00
IGL01655:Unc79 APN 12 103,134,546 (GRCm39) missense probably benign 0.00
IGL01662:Unc79 APN 12 103,115,279 (GRCm39) missense possibly damaging 0.92
IGL01728:Unc79 APN 12 103,131,943 (GRCm39) missense probably damaging 0.98
IGL01767:Unc79 APN 12 103,108,256 (GRCm39) missense probably damaging 1.00
IGL02080:Unc79 APN 12 102,968,234 (GRCm39) missense probably damaging 1.00
IGL02115:Unc79 APN 12 102,964,933 (GRCm39) missense probably damaging 1.00
IGL02176:Unc79 APN 12 102,965,006 (GRCm39) splice site probably null
IGL02186:Unc79 APN 12 102,977,542 (GRCm39) missense probably benign 0.04
IGL02205:Unc79 APN 12 103,045,260 (GRCm39) missense probably damaging 1.00
IGL02337:Unc79 APN 12 103,122,705 (GRCm39) splice site probably benign
IGL02498:Unc79 APN 12 103,137,837 (GRCm39) missense probably damaging 0.99
IGL02508:Unc79 APN 12 103,078,535 (GRCm39) missense probably damaging 0.97
IGL02508:Unc79 APN 12 103,078,277 (GRCm39) splice site probably benign
IGL02557:Unc79 APN 12 103,148,418 (GRCm39) splice site probably benign
IGL02589:Unc79 APN 12 103,139,755 (GRCm39) missense probably damaging 1.00
IGL02611:Unc79 APN 12 103,131,967 (GRCm39) missense probably damaging 0.97
IGL02728:Unc79 APN 12 103,088,688 (GRCm39) missense possibly damaging 0.53
IGL02827:Unc79 APN 12 103,041,105 (GRCm39) missense possibly damaging 0.88
IGL03028:Unc79 APN 12 103,139,785 (GRCm39) missense possibly damaging 0.83
IGL03144:Unc79 APN 12 103,008,401 (GRCm39) missense probably damaging 1.00
IGL03229:Unc79 APN 12 103,100,798 (GRCm39) missense probably damaging 0.99
IGL03269:Unc79 APN 12 103,054,936 (GRCm39) missense probably damaging 1.00
IGL03325:Unc79 APN 12 103,135,869 (GRCm39) missense probably damaging 0.98
pencil-thin UTSW 12 103,075,040 (GRCm39) splice site probably null
sweetpea UTSW 12 103,025,777 (GRCm39) missense probably damaging 1.00
3-1:Unc79 UTSW 12 103,039,009 (GRCm39) nonsense probably null
ANU22:Unc79 UTSW 12 102,968,130 (GRCm39) missense probably damaging 0.99
R0046:Unc79 UTSW 12 103,091,940 (GRCm39) missense probably damaging 0.99
R0046:Unc79 UTSW 12 103,091,940 (GRCm39) missense probably damaging 0.99
R0067:Unc79 UTSW 12 103,025,777 (GRCm39) missense probably damaging 1.00
R0067:Unc79 UTSW 12 103,025,777 (GRCm39) missense probably damaging 1.00
R0107:Unc79 UTSW 12 103,100,784 (GRCm39) missense possibly damaging 0.70
R0110:Unc79 UTSW 12 103,045,329 (GRCm39) critical splice donor site probably null
R0128:Unc79 UTSW 12 103,054,693 (GRCm39) splice site probably benign
R0166:Unc79 UTSW 12 103,122,812 (GRCm39) missense probably damaging 1.00
R0208:Unc79 UTSW 12 103,058,286 (GRCm39) missense probably benign 0.00
R0211:Unc79 UTSW 12 103,039,051 (GRCm39) missense probably benign 0.01
R0211:Unc79 UTSW 12 103,039,051 (GRCm39) missense probably benign 0.01
R0218:Unc79 UTSW 12 103,075,040 (GRCm39) splice site probably null
R0244:Unc79 UTSW 12 103,079,150 (GRCm39) missense probably damaging 1.00
R0305:Unc79 UTSW 12 103,079,459 (GRCm39) missense probably benign 0.18
R0310:Unc79 UTSW 12 103,027,666 (GRCm39) missense probably damaging 1.00
R0325:Unc79 UTSW 12 103,137,903 (GRCm39) missense probably damaging 0.98
R0369:Unc79 UTSW 12 103,055,031 (GRCm39) critical splice donor site probably null
R0450:Unc79 UTSW 12 103,045,329 (GRCm39) critical splice donor site probably null
R0503:Unc79 UTSW 12 103,045,127 (GRCm39) missense probably benign 0.01
R0542:Unc79 UTSW 12 103,060,437 (GRCm39) splice site probably benign
R0845:Unc79 UTSW 12 103,139,703 (GRCm39) splice site probably benign
R0893:Unc79 UTSW 12 102,957,687 (GRCm39) missense probably damaging 1.00
R1078:Unc79 UTSW 12 103,041,112 (GRCm39) missense probably benign 0.03
R1148:Unc79 UTSW 12 103,078,926 (GRCm39) missense probably damaging 1.00
R1148:Unc79 UTSW 12 103,078,926 (GRCm39) missense probably damaging 1.00
R1159:Unc79 UTSW 12 103,013,311 (GRCm39) splice site probably benign
R1191:Unc79 UTSW 12 103,013,271 (GRCm39) nonsense probably null
R1307:Unc79 UTSW 12 103,036,335 (GRCm39) missense probably damaging 1.00
R1368:Unc79 UTSW 12 103,122,772 (GRCm39) missense probably damaging 1.00
R1476:Unc79 UTSW 12 103,149,784 (GRCm39) missense probably damaging 1.00
R1650:Unc79 UTSW 12 103,079,052 (GRCm39) missense possibly damaging 0.85
R1777:Unc79 UTSW 12 103,078,714 (GRCm39) missense probably damaging 1.00
R1796:Unc79 UTSW 12 103,109,005 (GRCm39) missense probably damaging 0.99
R1824:Unc79 UTSW 12 103,025,579 (GRCm39) missense probably damaging 1.00
R1830:Unc79 UTSW 12 103,100,737 (GRCm39) missense probably damaging 1.00
R1927:Unc79 UTSW 12 103,135,951 (GRCm39) missense probably damaging 1.00
R1958:Unc79 UTSW 12 103,041,178 (GRCm39) missense probably benign 0.19
R1958:Unc79 UTSW 12 102,957,621 (GRCm39) missense probably damaging 1.00
R1980:Unc79 UTSW 12 102,977,538 (GRCm39) nonsense probably null
R2019:Unc79 UTSW 12 103,137,830 (GRCm39) critical splice acceptor site probably null
R2290:Unc79 UTSW 12 103,112,625 (GRCm39) missense probably damaging 1.00
R2939:Unc79 UTSW 12 102,957,684 (GRCm39) missense probably damaging 1.00
R2962:Unc79 UTSW 12 103,061,378 (GRCm39) missense possibly damaging 0.72
R3176:Unc79 UTSW 12 103,079,476 (GRCm39) missense probably damaging 1.00
R3276:Unc79 UTSW 12 103,079,476 (GRCm39) missense probably damaging 1.00
R3683:Unc79 UTSW 12 103,041,062 (GRCm39) missense probably benign 0.00
R3684:Unc79 UTSW 12 103,041,062 (GRCm39) missense probably benign 0.00
R3686:Unc79 UTSW 12 103,054,920 (GRCm39) missense probably damaging 1.00
R3760:Unc79 UTSW 12 103,058,964 (GRCm39) missense probably damaging 1.00
R4031:Unc79 UTSW 12 103,039,018 (GRCm39) missense possibly damaging 0.46
R4039:Unc79 UTSW 12 103,041,208 (GRCm39) missense possibly damaging 0.88
R4110:Unc79 UTSW 12 103,025,629 (GRCm39) missense probably damaging 1.00
R4113:Unc79 UTSW 12 103,025,629 (GRCm39) missense probably damaging 1.00
R4159:Unc79 UTSW 12 103,036,512 (GRCm39) intron probably benign
R4273:Unc79 UTSW 12 103,088,612 (GRCm39) missense probably damaging 0.99
R4292:Unc79 UTSW 12 103,149,703 (GRCm39) missense probably damaging 0.99
R4334:Unc79 UTSW 12 103,045,233 (GRCm39) missense probably benign
R4513:Unc79 UTSW 12 102,988,019 (GRCm39) missense probably damaging 1.00
R4562:Unc79 UTSW 12 102,957,720 (GRCm39) missense probably damaging 1.00
R4576:Unc79 UTSW 12 102,968,062 (GRCm39) splice site probably benign
R4645:Unc79 UTSW 12 103,079,081 (GRCm39) missense probably benign
R4758:Unc79 UTSW 12 103,128,080 (GRCm39) nonsense probably null
R4787:Unc79 UTSW 12 103,013,257 (GRCm39) missense probably damaging 1.00
R4852:Unc79 UTSW 12 103,139,725 (GRCm39) missense probably damaging 0.98
R4883:Unc79 UTSW 12 103,060,592 (GRCm39) missense probably damaging 0.99
R4979:Unc79 UTSW 12 103,078,691 (GRCm39) missense probably benign
R5044:Unc79 UTSW 12 103,078,962 (GRCm39) missense probably benign 0.32
R5053:Unc79 UTSW 12 103,071,007 (GRCm39) missense probably damaging 1.00
R5061:Unc79 UTSW 12 103,134,700 (GRCm39) missense possibly damaging 0.94
R5075:Unc79 UTSW 12 103,041,213 (GRCm39) missense possibly damaging 0.63
R5101:Unc79 UTSW 12 103,078,769 (GRCm39) missense probably damaging 1.00
R5236:Unc79 UTSW 12 103,060,654 (GRCm39) critical splice donor site probably null
R5240:Unc79 UTSW 12 103,037,010 (GRCm39) missense probably damaging 0.99
R5383:Unc79 UTSW 12 103,070,886 (GRCm39) missense possibly damaging 0.53
R5461:Unc79 UTSW 12 103,078,397 (GRCm39) missense probably damaging 1.00
R5535:Unc79 UTSW 12 103,135,962 (GRCm39) missense possibly damaging 0.84
R5609:Unc79 UTSW 12 103,094,527 (GRCm39) missense probably benign
R5639:Unc79 UTSW 12 103,137,831 (GRCm39) missense probably damaging 1.00
R5704:Unc79 UTSW 12 102,968,202 (GRCm39) missense probably damaging 1.00
R5923:Unc79 UTSW 12 103,078,727 (GRCm39) missense probably damaging 1.00
R5925:Unc79 UTSW 12 103,091,989 (GRCm39) splice site probably null
R5975:Unc79 UTSW 12 103,091,885 (GRCm39) missense possibly damaging 0.53
R6047:Unc79 UTSW 12 103,027,717 (GRCm39) missense probably damaging 1.00
R6156:Unc79 UTSW 12 103,027,717 (GRCm39) missense probably damaging 1.00
R6175:Unc79 UTSW 12 103,149,708 (GRCm39) missense probably damaging 0.98
R6292:Unc79 UTSW 12 103,108,991 (GRCm39) missense possibly damaging 0.88
R6313:Unc79 UTSW 12 103,078,878 (GRCm39) missense probably damaging 1.00
R6391:Unc79 UTSW 12 102,987,269 (GRCm39) missense probably damaging 1.00
R6405:Unc79 UTSW 12 103,134,595 (GRCm39) missense probably damaging 0.97
R6416:Unc79 UTSW 12 103,097,905 (GRCm39) missense possibly damaging 0.86
R6467:Unc79 UTSW 12 103,139,771 (GRCm39) missense probably damaging 1.00
R6573:Unc79 UTSW 12 103,027,647 (GRCm39) missense probably damaging 1.00
R6614:Unc79 UTSW 12 102,957,689 (GRCm39) missense probably damaging 1.00
R6654:Unc79 UTSW 12 103,045,308 (GRCm39) missense probably damaging 1.00
R6654:Unc79 UTSW 12 103,045,307 (GRCm39) missense probably damaging 0.99
R6700:Unc79 UTSW 12 103,091,962 (GRCm39) missense possibly damaging 0.92
R6724:Unc79 UTSW 12 103,071,120 (GRCm39) missense probably damaging 1.00
R6819:Unc79 UTSW 12 103,108,267 (GRCm39) missense probably benign 0.12
R6869:Unc79 UTSW 12 103,079,331 (GRCm39) missense probably benign 0.33
R6879:Unc79 UTSW 12 103,115,046 (GRCm39) splice site probably null
R6942:Unc79 UTSW 12 103,088,704 (GRCm39) critical splice donor site probably null
R6961:Unc79 UTSW 12 103,079,174 (GRCm39) missense probably damaging 1.00
R6973:Unc79 UTSW 12 102,964,699 (GRCm39) missense possibly damaging 0.86
R6980:Unc79 UTSW 12 103,025,759 (GRCm39) missense probably damaging 1.00
R7124:Unc79 UTSW 12 103,027,652 (GRCm39) missense probably damaging 0.99
R7144:Unc79 UTSW 12 103,108,885 (GRCm39) missense probably benign 0.06
R7197:Unc79 UTSW 12 103,078,765 (GRCm39) missense probably benign
R7209:Unc79 UTSW 12 103,091,883 (GRCm39) missense probably benign
R7232:Unc79 UTSW 12 103,100,734 (GRCm39) missense possibly damaging 0.49
R7304:Unc79 UTSW 12 103,029,449 (GRCm39) missense probably damaging 1.00
R7354:Unc79 UTSW 12 103,108,961 (GRCm39) missense possibly damaging 0.79
R7384:Unc79 UTSW 12 103,137,837 (GRCm39) missense probably benign 0.11
R7400:Unc79 UTSW 12 103,070,889 (GRCm39) missense probably damaging 1.00
R7417:Unc79 UTSW 12 103,055,017 (GRCm39) missense possibly damaging 0.85
R7470:Unc79 UTSW 12 103,061,235 (GRCm39) missense probably damaging 1.00
R7842:Unc79 UTSW 12 103,058,313 (GRCm39) missense probably damaging 1.00
R8037:Unc79 UTSW 12 103,016,178 (GRCm39) missense probably damaging 1.00
R8041:Unc79 UTSW 12 103,054,726 (GRCm39) missense probably benign 0.06
R8146:Unc79 UTSW 12 103,036,416 (GRCm39) missense probably damaging 0.98
R8276:Unc79 UTSW 12 102,968,122 (GRCm39) missense possibly damaging 0.94
R8427:Unc79 UTSW 12 103,045,297 (GRCm39) missense probably benign 0.24
R8501:Unc79 UTSW 12 103,058,897 (GRCm39) missense probably damaging 1.00
R8510:Unc79 UTSW 12 103,070,898 (GRCm39) missense probably damaging 1.00
R8531:Unc79 UTSW 12 103,013,922 (GRCm39) missense probably damaging 1.00
R8531:Unc79 UTSW 12 103,049,855 (GRCm39) missense probably benign 0.13
R8795:Unc79 UTSW 12 103,074,513 (GRCm39) missense probably damaging 1.00
R9017:Unc79 UTSW 12 103,074,874 (GRCm39) critical splice acceptor site probably null
R9121:Unc79 UTSW 12 102,968,095 (GRCm39) missense probably damaging 1.00
R9196:Unc79 UTSW 12 103,078,613 (GRCm39) missense probably benign
R9443:Unc79 UTSW 12 103,037,035 (GRCm39) missense probably damaging 1.00
R9548:Unc79 UTSW 12 102,977,495 (GRCm39) missense probably damaging 1.00
R9600:Unc79 UTSW 12 103,135,972 (GRCm39) missense probably benign 0.07
R9767:Unc79 UTSW 12 103,079,234 (GRCm39) missense probably benign
R9787:Unc79 UTSW 12 103,112,620 (GRCm39) missense probably benign 0.00
RF010:Unc79 UTSW 12 103,079,046 (GRCm39) missense probably benign 0.17
X0017:Unc79 UTSW 12 103,074,520 (GRCm39) missense probably damaging 0.99
X0028:Unc79 UTSW 12 102,957,662 (GRCm39) missense probably damaging 1.00
Z1088:Unc79 UTSW 12 102,987,271 (GRCm39) missense probably damaging 1.00
Z1176:Unc79 UTSW 12 103,108,312 (GRCm39) missense probably benign 0.03
Z1176:Unc79 UTSW 12 103,054,937 (GRCm39) missense probably damaging 1.00
Z1177:Unc79 UTSW 12 103,131,948 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CTGATAGGGACGAACCACCATG -3'
(R):5'- GCTGTTTCTCAACATGGACG -3'

Sequencing Primer
(F):5'- ACCACCATGATGAGCAGGTCTG -3'
(R):5'- CTGTTTCTCAACATGGACGACAAGG -3'
Posted On 2016-03-17