Incidental Mutation 'R6405:Unc79'
ID 516265
Institutional Source Beutler Lab
Gene Symbol Unc79
Ensembl Gene ENSMUSG00000021198
Gene Name unc-79 homolog
Synonyms 9030205A07Rik, Mlca3
MMRRC Submission 044550-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6405 (G1)
Quality Score 225.009
Status Not validated
Chromosome 12
Chromosomal Location 102915118-103150324 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 103134595 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 2189 (V2189A)
Ref Sequence ENSEMBL: ENSMUSP00000136888 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085079] [ENSMUST00000101099] [ENSMUST00000178076] [ENSMUST00000179002]
AlphaFold Q0KK59
Predicted Effect possibly damaging
Transcript: ENSMUST00000085079
AA Change: V2186A

PolyPhen 2 Score 0.678 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000082156
Gene: ENSMUSG00000021198
AA Change: V2186A

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 possibly damaging
Transcript: ENSMUST00000101099
AA Change: V2324A

PolyPhen 2 Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000098659
Gene: ENSMUSG00000021198
AA Change: V2324A

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 damaging
Transcript: ENSMUST00000178076
AA Change: V2189A

PolyPhen 2 Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136888
Gene: ENSMUSG00000021198
AA Change: V2189A

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: V2382A

PolyPhen 2 Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000136332
Gene: ENSMUSG00000021198
AA Change: V2382A

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: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.2%
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik T C 16: 4,669,742 (GRCm39) V769A probably damaging Het
Abca4 A G 3: 121,967,311 (GRCm39) probably null Het
Ahnak2 A T 12: 112,739,771 (GRCm39) S628T probably damaging Het
Ano8 T C 8: 71,935,674 (GRCm39) T315A probably damaging Het
Arhgap32 T A 9: 32,159,784 (GRCm39) V267E probably benign Het
Asnsd1 A T 1: 53,387,154 (GRCm39) S158T probably damaging Het
Asxl2 T A 12: 3,543,758 (GRCm39) V309E probably damaging Het
Bhlhe40 TG TGG 6: 108,641,818 (GRCm39) 254 probably null Het
Ccdc110 T A 8: 46,394,734 (GRCm39) Y208* probably null Het
Cfap157 G T 2: 32,671,408 (GRCm39) Q133K probably damaging Het
Cfap53 A G 18: 74,492,677 (GRCm39) E467G probably damaging Het
Csmd3 T C 15: 47,683,767 (GRCm39) I1688M probably damaging Het
Cyp3a11 A T 5: 145,799,230 (GRCm39) L319Q probably damaging Het
Dchs2 A G 3: 83,261,570 (GRCm39) I2613V probably benign Het
Dhx35 T A 2: 158,636,839 (GRCm39) W11R probably damaging Het
Dscam C T 16: 96,479,625 (GRCm39) G1174D probably damaging Het
Fan1 T A 7: 64,022,234 (GRCm39) N340Y probably damaging Het
Fsip2 A G 2: 82,820,430 (GRCm39) T5388A possibly damaging Het
Gm10549 C A 18: 33,597,358 (GRCm39) probably benign Het
Greb1l T A 18: 10,501,076 (GRCm39) I402K probably benign Het
Hectd3 A T 4: 116,857,821 (GRCm39) M585L probably benign Het
Inpp5k T C 11: 75,524,004 (GRCm39) probably null Het
Lalba T G 15: 98,378,632 (GRCm39) probably null Het
Lgals9 C A 11: 78,862,211 (GRCm39) V125L probably benign Het
Ncbp2 CGTCTGGATG CG 16: 31,775,161 (GRCm39) probably null Het
Or2g25 A G 17: 37,971,014 (GRCm39) I70T possibly damaging Het
Peg10 C CTCG 6: 4,756,453 (GRCm39) probably benign Het
Rab4b T A 7: 26,872,379 (GRCm39) D94V probably damaging Het
Rhpn2 A G 7: 35,071,864 (GRCm39) E243G probably benign Het
Rp1 T C 1: 4,415,994 (GRCm39) D1706G probably damaging Het
Slc29a3 A T 10: 60,551,805 (GRCm39) I413N probably damaging Het
Slc7a9 T C 7: 35,154,064 (GRCm39) L229P probably damaging Het
Tenm2 T C 11: 36,755,686 (GRCm39) H104R probably benign Het
Tmem87a A G 2: 120,210,231 (GRCm39) Y241H probably damaging Het
Trpv5 G T 6: 41,651,602 (GRCm39) T192K probably damaging Het
Vmn2r106 A C 17: 20,499,361 (GRCm39) S183R probably benign Het
Vmn2r112 G T 17: 22,837,216 (GRCm39) C559F probably damaging Het
Wdhd1 T C 14: 47,481,324 (GRCm39) D1031G possibly damaging Het
Wnt5b T C 6: 119,410,457 (GRCm39) S328G probably benign Het
Zcchc7 T C 4: 44,926,032 (GRCm39) Y344H 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
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
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'- CAAGATGCTAAGCAGGTTGTG -3'
(R):5'- AGATGCTAGGCACCTAGTCC -3'

Sequencing Primer
(F):5'- TGGGAACAATCTGACCGTTC -3'
(R):5'- AGGCACCTAGTCCCCCTC -3'
Posted On 2018-05-04