Incidental Mutation 'R1078:Unc79'
ID 85745
Institutional Source Beutler Lab
Gene Symbol Unc79
Ensembl Gene ENSMUSG00000021198
Gene Name unc-79 homolog
Synonyms 9030205A07Rik, Mlca3
MMRRC Submission 039164-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1078 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 102915118-103150324 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 103041112 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Arginine at position 715 (M715R)
Ref Sequence ENSEMBL: ENSMUSP00000136332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085079] [ENSMUST00000101099] [ENSMUST00000178076] [ENSMUST00000179002]
AlphaFold Q0KK59
Predicted Effect probably benign
Transcript: ENSMUST00000085079
AA Change: M591R

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000082156
Gene: ENSMUSG00000021198
AA Change: M591R

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 benign
Transcript: ENSMUST00000101099
AA Change: M768R

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000098659
Gene: ENSMUSG00000021198
AA Change: M768R

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: M572R

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000136888
Gene: ENSMUSG00000021198
AA Change: M572R

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 noncoding transcript
Transcript: ENSMUST00000178846
Predicted Effect probably benign
Transcript: ENSMUST00000179002
AA Change: M715R

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000136332
Gene: ENSMUSG00000021198
AA Change: M715R

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
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.7%
  • 3x: 99.1%
  • 10x: 97.4%
  • 20x: 94.4%
Validation Efficiency 96% (53/55)
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: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130230L23Rik T C 5: 66,145,698 (GRCm39) T138A unknown Het
Abi3bp T C 16: 56,474,444 (GRCm39) probably null Het
Alpk3 A T 7: 80,728,348 (GRCm39) M493L probably benign Het
Bace2 C T 16: 97,158,060 (GRCm39) A20V unknown Het
Bms1 T C 6: 118,382,182 (GRCm39) D452G probably benign Het
Ccdc187 T C 2: 26,184,389 (GRCm39) T3A probably damaging Het
Ctu2 T C 8: 123,208,238 (GRCm39) V95A possibly damaging Het
Cyp2a5 A G 7: 26,534,966 (GRCm39) K60E probably benign Het
Cyp4f13 T C 17: 33,144,542 (GRCm39) H318R probably damaging Het
Dlgap5 G A 14: 47,637,023 (GRCm39) T485M probably damaging Het
Dsp C T 13: 38,367,082 (GRCm39) probably benign Het
Ell2 T C 13: 75,894,538 (GRCm39) probably benign Het
Eml2 A T 7: 18,913,687 (GRCm39) Y168F probably benign Het
Entrep1 T A 19: 23,950,939 (GRCm39) R547S probably benign Het
Ep400 C T 5: 110,883,388 (GRCm39) probably benign Het
Ercc4 C A 16: 12,948,061 (GRCm39) A336D probably benign Het
Fat4 T C 3: 39,037,235 (GRCm39) L3629S probably benign Het
Gabbr2 C T 4: 46,664,833 (GRCm39) R925H probably damaging Het
Gfi1b A T 2: 28,503,877 (GRCm39) W108R probably damaging Het
Gtse1 C T 15: 85,746,508 (GRCm39) P108L probably damaging Het
Hfm1 A T 5: 107,026,696 (GRCm39) F140I probably damaging Het
Hyal2 T A 9: 107,449,445 (GRCm39) H400Q probably benign Het
Igfn1 A G 1: 135,902,585 (GRCm39) Y371H probably damaging Het
Il22b T G 10: 118,126,056 (GRCm39) *180C probably null Het
Kdm2b T C 5: 123,099,604 (GRCm39) T118A possibly damaging Het
Lama5 A T 2: 179,821,557 (GRCm39) probably benign Het
Lgr6 C T 1: 134,921,748 (GRCm39) A199T probably damaging Het
Lmo7 C T 14: 102,157,910 (GRCm39) probably benign Het
Lrrc37a G T 11: 103,388,457 (GRCm39) P2323T unknown Het
Lrrc38 A G 4: 143,077,088 (GRCm39) Y117C probably benign Het
Myo1e T C 9: 70,291,281 (GRCm39) V1024A probably benign Het
Myrfl T C 10: 116,612,637 (GRCm39) N904S possibly damaging Het
Or12d13 T A 17: 37,647,917 (GRCm39) I69F probably damaging Het
Or4k47 T C 2: 111,451,690 (GRCm39) H243R probably damaging Het
Or9g4b T C 2: 85,616,437 (GRCm39) V194A possibly damaging Het
Pld4 A T 12: 112,729,876 (GRCm39) I53F probably benign Het
Plekhg4 T A 8: 106,108,309 (GRCm39) C1117* probably null Het
Prss39 G A 1: 34,541,167 (GRCm39) E224K probably benign Het
Psme1 G T 14: 55,818,107 (GRCm39) G149V probably damaging Het
Sanbr A C 11: 23,561,762 (GRCm39) I358S probably benign Het
Soat2 T A 15: 102,061,573 (GRCm39) probably null Het
Stab2 C T 10: 86,742,997 (GRCm39) probably null Het
Tcf7l2 A G 19: 55,731,627 (GRCm39) T127A probably benign Het
Tcp1 T C 17: 13,142,091 (GRCm39) probably benign Het
Thbs4 G A 13: 92,899,434 (GRCm39) probably benign Het
Tmf1 T C 6: 97,150,261 (GRCm39) D482G probably damaging Het
Trim66 G T 7: 109,071,526 (GRCm39) P591H probably damaging Het
Umodl1 T C 17: 31,178,347 (GRCm39) S108P probably benign Het
Usp34 C A 11: 23,383,175 (GRCm39) probably benign Het
Utrn T G 10: 12,331,310 (GRCm39) probably null Het
Zfp830 T C 11: 82,656,165 (GRCm39) probably null 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
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
R4898:Unc79 UTSW 12 103,128,079 (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'- TTTCCAGACCGCTCAGAGGAAAAC -3'
(R):5'- GGAATCTCATGCTTCCACTACCTGC -3'

Sequencing Primer
(F):5'- GGGTTCTCAGATACCTCAGATAG -3'
(R):5'- CACTACCTGCTTTAGGAGAAGGTC -3'
Posted On 2013-11-18