Incidental Mutation 'R5383:Unc79'
ID 424860
Institutional Source Beutler Lab
Gene Symbol Unc79
Ensembl Gene ENSMUSG00000021198
Gene Name unc-79 homolog
Synonyms 9030205A07Rik, Mlca3
MMRRC Submission 042958-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5383 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 102915118-103150324 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 103070886 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 1081 (N1081S)
Ref Sequence ENSEMBL: ENSMUSP00000082156 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085079] [ENSMUST00000101099] [ENSMUST00000178076] [ENSMUST00000179002]
AlphaFold Q0KK59
Predicted Effect possibly damaging
Transcript: ENSMUST00000085079
AA Change: N1081S

PolyPhen 2 Score 0.528 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000082156
Gene: ENSMUSG00000021198
AA Change: N1081S

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: N1258S

PolyPhen 2 Score 0.148 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000098659
Gene: ENSMUSG00000021198
AA Change: N1258S

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 unknown
Transcript: ENSMUST00000177984
AA Change: N43S
Predicted Effect possibly damaging
Transcript: ENSMUST00000178076
AA Change: N1084S

PolyPhen 2 Score 0.456 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000136888
Gene: ENSMUSG00000021198
AA Change: N1084S

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: N1227S

PolyPhen 2 Score 0.320 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000136332
Gene: ENSMUSG00000021198
AA Change: N1227S

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 0.0844 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 96.0%
Validation Efficiency 97% (61/63)
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: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010I14Rik A T 17: 9,211,532 (GRCm39) Y227F possibly damaging Het
Aadac T C 3: 59,943,496 (GRCm39) probably benign Het
Abl2 G A 1: 156,469,802 (GRCm39) G918E possibly damaging Het
Acvr1c T C 2: 58,177,747 (GRCm39) T241A probably damaging Het
Adck1 T C 12: 88,422,373 (GRCm39) V328A probably benign Het
Ano6 A G 15: 95,813,918 (GRCm39) I279V probably benign Het
AW551984 T A 9: 39,501,994 (GRCm39) Y704F probably benign Het
C1s1 T C 6: 124,511,360 (GRCm39) D321G probably damaging Het
Cacna1d T A 14: 29,767,236 (GRCm39) D1910V possibly damaging Het
Cdh5 A G 8: 104,864,479 (GRCm39) Q480R probably benign Het
Cdhr1 C T 14: 36,810,964 (GRCm39) V266M possibly damaging Het
Cdk5rap1 A T 2: 154,192,755 (GRCm39) V414D possibly damaging Het
Ctdnep1 T A 11: 69,875,222 (GRCm39) probably benign Het
Cyfip2 T C 11: 46,168,918 (GRCm39) M212V possibly damaging Het
D130043K22Rik G A 13: 25,041,397 (GRCm39) S273N probably benign Het
Ddi2 A G 4: 141,412,163 (GRCm39) S250P probably damaging Het
Dennd1b A G 1: 139,095,409 (GRCm39) T486A probably benign Het
Disc1 A G 8: 125,862,196 (GRCm39) T523A probably damaging Het
Dmbx1 A G 4: 115,775,342 (GRCm39) S313P probably damaging Het
Dmpk C G 7: 18,821,944 (GRCm39) L301V probably benign Het
Dnah11 T C 12: 118,049,432 (GRCm39) E1664G probably damaging Het
Dpysl3 A T 18: 43,571,103 (GRCm39) V57E probably damaging Het
Fam98a C T 17: 75,845,576 (GRCm39) G390E unknown Het
Hook3 C A 8: 26,609,017 (GRCm39) R9L probably benign Het
Igkv4-80 A C 6: 68,993,649 (GRCm39) S81A probably benign Het
Impg2 A G 16: 56,063,989 (GRCm39) D298G probably benign Het
Inf2 T A 12: 112,566,579 (GRCm39) V48D probably damaging Het
Itprid1 T A 6: 55,955,275 (GRCm39) L961H probably benign Het
Kcnh1 G A 1: 192,187,999 (GRCm39) G820D probably benign Het
Lsm14a C T 7: 34,088,789 (GRCm39) A39T possibly damaging Het
Muc2 T C 7: 141,307,456 (GRCm39) C804R probably damaging Het
Nim1k C T 13: 120,189,335 (GRCm39) V25M probably benign Het
Or11g25 T A 14: 50,723,509 (GRCm39) L198* probably null Het
Or4a73 T C 2: 89,421,457 (GRCm39) M1V probably null Het
Or5b122 T A 19: 13,563,439 (GRCm39) M257K probably damaging Het
Or6c68 A G 10: 129,158,205 (GRCm39) T238A probably damaging Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Phf8-ps T C 17: 33,284,231 (GRCm39) D857G probably benign Het
Pitrm1 T A 13: 6,627,468 (GRCm39) H856Q probably damaging Het
Pkd1 T C 17: 24,793,349 (GRCm39) C1679R probably benign Het
Pkp4 T A 2: 59,140,617 (GRCm39) L441* probably null Het
Ppp4r4 T C 12: 103,550,427 (GRCm39) F284L probably benign Het
Ptprt T A 2: 161,539,969 (GRCm39) K769M probably damaging Het
Rbm12 G T 2: 155,945,285 (GRCm39) probably benign Het
Rpf1 T C 3: 146,225,146 (GRCm39) D94G possibly damaging Het
Scap G T 9: 110,203,597 (GRCm39) K310N probably damaging Het
Smpd2 C T 10: 41,364,698 (GRCm39) probably benign Het
Sp110 TC TCC 1: 85,519,290 (GRCm39) probably null Het
Specc1l T A 10: 75,082,539 (GRCm39) I662N possibly damaging Het
Sptan1 T A 2: 29,901,340 (GRCm39) V1496D probably damaging Het
Srrm4 T C 5: 116,609,319 (GRCm39) probably benign Het
Taf2 A G 15: 54,912,815 (GRCm39) I515T possibly damaging Het
Tdrd3 C T 14: 87,718,227 (GRCm39) Q203* probably null Het
Tfap2b A T 1: 19,296,722 (GRCm39) M222L probably benign Het
Tmem43 G A 6: 91,450,872 (GRCm39) A2T probably benign Het
Trav9-1 T A 14: 53,725,833 (GRCm39) I49N probably benign Het
Trim23 T G 13: 104,335,205 (GRCm39) N410K probably damaging Het
Ttbk1 T C 17: 46,778,342 (GRCm39) T567A probably damaging Het
Zfp451 A C 1: 33,852,887 (GRCm39) I9R probably damaging Het
Zfp563 T A 17: 33,323,681 (GRCm39) M92K probably benign Het
Zfp618 G A 4: 63,013,729 (GRCm39) G198D probably benign Het
Zfp637 G T 6: 117,820,270 (GRCm39) probably benign 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
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
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'- GCGTCTGTTCCAGGAATGAC -3'
(R):5'- GCTGGTCATAGCCAAGTAAAAC -3'

Sequencing Primer
(F):5'- TCCAGGAATGACACTTTGCTGAG -3'
(R):5'- GCCAAGTAAAACATAGAGGTGCCTC -3'
Posted On 2016-08-04