Incidental Mutation 'R1565:Lmo7'
ID 175220
Institutional Source Beutler Lab
Gene Symbol Lmo7
Ensembl Gene ENSMUSG00000033060
Gene Name LIM domain only 7
Synonyms FBXO20, LOC380928
MMRRC Submission 039604-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.176) question?
Stock # R1565 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 101729957-101934710 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 101887521 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 472 (Q472L)
Ref Sequence ENSEMBL: ENSMUSP00000123706 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100337] [ENSMUST00000159026] [ENSMUST00000159258] [ENSMUST00000159314] [ENSMUST00000159597]
AlphaFold E9PYF4
Predicted Effect possibly damaging
Transcript: ENSMUST00000100337
AA Change: Q594L

PolyPhen 2 Score 0.853 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000097910
Gene: ENSMUSG00000033060
AA Change: Q594L

DomainStartEndE-ValueType
CH 14 124 2.57e-13 SMART
low complexity region 200 211 N/A INTRINSIC
Pfam:DUF4757 242 348 2.2e-14 PFAM
low complexity region 448 462 N/A INTRINSIC
Pfam:DUF4757 568 735 1.8e-46 PFAM
low complexity region 861 879 N/A INTRINSIC
low complexity region 979 991 N/A INTRINSIC
low complexity region 1003 1015 N/A INTRINSIC
PDZ 1047 1119 1.05e-8 SMART
coiled coil region 1222 1275 N/A INTRINSIC
coiled coil region 1319 1411 N/A INTRINSIC
low complexity region 1585 1596 N/A INTRINSIC
low complexity region 1599 1617 N/A INTRINSIC
LIM 1629 1687 6.54e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000159026
AA Change: Q361L

PolyPhen 2 Score 0.202 (Sensitivity: 0.92; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000124605
Gene: ENSMUSG00000033060
AA Change: Q361L

DomainStartEndE-ValueType
low complexity region 215 229 N/A INTRINSIC
coiled coil region 435 471 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000159258
AA Change: Q361L

PolyPhen 2 Score 0.280 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000125465
Gene: ENSMUSG00000033060
AA Change: Q361L

DomainStartEndE-ValueType
low complexity region 215 229 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000159314
AA Change: Q361L

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000124349
Gene: ENSMUSG00000033060
AA Change: Q361L

DomainStartEndE-ValueType
low complexity region 215 229 N/A INTRINSIC
coiled coil region 435 492 N/A INTRINSIC
low complexity region 628 646 N/A INTRINSIC
low complexity region 746 758 N/A INTRINSIC
low complexity region 770 782 N/A INTRINSIC
PDZ 814 886 1.05e-8 SMART
coiled coil region 989 1042 N/A INTRINSIC
coiled coil region 1086 1178 N/A INTRINSIC
low complexity region 1352 1363 N/A INTRINSIC
low complexity region 1366 1384 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000159597
AA Change: Q472L

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000123706
Gene: ENSMUSG00000033060
AA Change: Q472L

DomainStartEndE-ValueType
low complexity region 78 89 N/A INTRINSIC
internal_repeat_1 111 141 6.96e-5 PROSPERO
internal_repeat_1 218 248 6.96e-5 PROSPERO
low complexity region 326 340 N/A INTRINSIC
coiled coil region 546 603 N/A INTRINSIC
low complexity region 739 757 N/A INTRINSIC
low complexity region 857 869 N/A INTRINSIC
low complexity region 881 893 N/A INTRINSIC
PDZ 925 997 1.05e-8 SMART
coiled coil region 1127 1180 N/A INTRINSIC
coiled coil region 1224 1316 N/A INTRINSIC
low complexity region 1490 1501 N/A INTRINSIC
low complexity region 1504 1522 N/A INTRINSIC
LIM 1534 1592 6.54e-10 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159797
Predicted Effect probably benign
Transcript: ENSMUST00000159806
SMART Domains Protein: ENSMUSP00000124300
Gene: ENSMUSG00000033060

DomainStartEndE-ValueType
low complexity region 34 45 N/A INTRINSIC
Pfam:DUF4757 76 225 4.5e-53 PFAM
low complexity region 351 369 N/A INTRINSIC
low complexity region 469 481 N/A INTRINSIC
low complexity region 493 505 N/A INTRINSIC
PDZ 537 609 1.05e-8 SMART
internal_repeat_1 620 691 9.31e-5 PROSPERO
coiled coil region 711 764 N/A INTRINSIC
coiled coil region 808 900 N/A INTRINSIC
internal_repeat_1 921 976 9.31e-5 PROSPERO
low complexity region 1075 1086 N/A INTRINSIC
low complexity region 1089 1107 N/A INTRINSIC
LIM 1119 1177 6.54e-10 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159812
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159948
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160876
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161668
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162091
Meta Mutation Damage Score 0.1248 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 90.0%
Validation Efficiency 96% (82/85)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009]
PHENOTYPE: Targeted mutations in this gene result in postnatal lethality, growth defects, skeletal muscle abnormalities and retinal defects reflective of retinal degeneration. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik G A 11: 58,880,501 (GRCm38) G270S probably benign Het
Abtb1 T C 6: 88,836,554 (GRCm38) T401A probably benign Het
Adamts14 A T 10: 61,270,897 (GRCm38) M148K probably damaging Het
Adcy5 A G 16: 35,268,957 (GRCm38) E508G probably damaging Het
Ankfy1 T A 11: 72,757,318 (GRCm38) L875H probably damaging Het
Cacng3 A T 7: 122,768,401 (GRCm38) D168V probably damaging Het
Clpb G A 7: 101,785,461 (GRCm38) R488Q probably benign Het
Cpxm2 A T 7: 132,062,145 (GRCm38) Y350N probably damaging Het
D130040H23Rik T A 8: 69,303,160 (GRCm38) *406R probably null Het
Dnah10 T A 5: 124,829,614 (GRCm38) D4236E probably damaging Het
Dpf3 T A 12: 83,370,617 (GRCm38) Y27F probably damaging Het
Esp4 T C 17: 40,602,595 (GRCm38) *118Q probably null Het
Fam222b T C 11: 78,154,662 (GRCm38) S222P possibly damaging Het
Flnc T C 6: 29,455,171 (GRCm38) V1933A probably damaging Het
Gem T C 4: 11,713,709 (GRCm38) F282L possibly damaging Het
Gli2 T C 1: 118,841,930 (GRCm38) T631A possibly damaging Het
Gm13088 G A 4: 143,655,617 (GRCm38) Q170* probably null Het
Gpld1 T A 13: 24,956,068 (GRCm38) V116E probably damaging Het
Gpr176 A G 2: 118,280,214 (GRCm38) M188T probably benign Het
Grk5 T C 19: 61,089,972 (GRCm38) V489A probably damaging Het
H2-Ke6 C T 17: 34,027,495 (GRCm38) V105I possibly damaging Het
Hpdl T C 4: 116,820,883 (GRCm38) N127S probably damaging Het
Id4 G T 13: 48,262,294 (GRCm38) V151L possibly damaging Het
Kcnh8 G T 17: 52,956,881 (GRCm38) G802V probably benign Het
Lamc1 C A 1: 153,242,743 (GRCm38) S894I probably benign Het
Larp1b A G 3: 40,972,384 (GRCm38) N184S probably damaging Het
Lhx1 A T 11: 84,519,821 (GRCm38) S226T probably benign Het
Mog G C 17: 37,017,582 (GRCm38) N152K possibly damaging Het
Mttp A G 3: 138,116,405 (GRCm38) probably null Het
Mycbp2 A G 14: 103,252,509 (GRCm38) V953A possibly damaging Het
Myo3a A T 2: 22,340,280 (GRCm38) Y509F probably damaging Het
Myo9b A G 8: 71,315,192 (GRCm38) N303S possibly damaging Het
Nek3 T C 8: 22,132,201 (GRCm38) probably null Het
Nlrc4 A T 17: 74,441,931 (GRCm38) D771E probably benign Het
Nup160 A T 2: 90,722,061 (GRCm38) N1127I possibly damaging Het
Oas1h A T 5: 120,862,600 (GRCm38) N91I probably damaging Het
Olfr1225 A T 2: 89,170,627 (GRCm38) V195D probably benign Het
Olfr1226 G T 2: 89,193,883 (GRCm38) S50R probably damaging Het
Olfr1342 T A 4: 118,690,192 (GRCm38) N87Y probably damaging Het
Parp4 T C 14: 56,589,872 (GRCm38) probably benign Het
Pi4ka G A 16: 17,281,900 (GRCm38) C96Y probably null Het
Pira2 A T 7: 3,844,549 (GRCm38) F47Y probably damaging Het
Pkhd1 C A 1: 20,347,457 (GRCm38) G2490V probably damaging Het
Plekhg1 C T 10: 3,940,526 (GRCm38) T394I probably damaging Het
Psmd1 T C 1: 86,091,997 (GRCm38) probably benign Het
Rab3ip A T 10: 116,939,223 (GRCm38) C77S probably benign Het
Reln A T 5: 21,925,213 (GRCm38) M2700K probably benign Het
Rfx1 A G 8: 84,073,946 (GRCm38) T59A probably benign Het
Ric8b G T 10: 84,980,099 (GRCm38) V405L probably benign Het
Rufy3 G T 5: 88,640,632 (GRCm38) A479S probably damaging Het
Sardh A T 2: 27,242,719 (GRCm38) Y166N probably damaging Het
Slamf6 T G 1: 171,934,408 (GRCm38) V132G possibly damaging Het
Slc12a3 T G 8: 94,345,877 (GRCm38) H674Q possibly damaging Het
Sned1 G A 1: 93,281,654 (GRCm38) V830M possibly damaging Het
Srsf9 A G 5: 115,327,370 (GRCm38) N21S possibly damaging Het
Stkld1 A T 2: 26,950,090 (GRCm38) T391S probably benign Het
Sumf2 C A 5: 129,859,914 (GRCm38) N230K probably damaging Het
Tbc1d22a T C 15: 86,235,569 (GRCm38) V22A possibly damaging Het
Thsd7b T A 1: 129,596,041 (GRCm38) S194T possibly damaging Het
Tmem27 A G X: 164,118,234 (GRCm38) D184G possibly damaging Het
Tnn T A 1: 160,097,265 (GRCm38) Y1173F probably damaging Het
Top2a A G 11: 99,001,054 (GRCm38) F1122L probably damaging Het
Trappc9 G A 15: 73,025,967 (GRCm38) R377W probably damaging Het
Trim39 G A 17: 36,268,854 (GRCm38) R70W probably damaging Het
Ttn G A 2: 76,794,261 (GRCm38) T15289I probably damaging Het
Ugt2b38 A T 5: 87,411,914 (GRCm38) V373E probably damaging Het
Usp54 A G 14: 20,607,159 (GRCm38) S24P probably damaging Het
Vmn2r27 C T 6: 124,231,634 (GRCm38) G51S probably benign Het
Xylt2 C T 11: 94,667,594 (GRCm38) A579T probably benign Het
Zbtb21 A G 16: 97,952,427 (GRCm38) S247P probably benign Het
Zc3h7b C T 15: 81,777,088 (GRCm38) P376L probably benign Het
Zfp251 C T 15: 76,853,039 (GRCm38) R613K possibly damaging Het
Zfp251 T A 15: 76,853,038 (GRCm38) R613S probably damaging Het
Zfp91 T C 19: 12,779,075 (GRCm38) D135G probably benign Het
Other mutations in Lmo7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00569:Lmo7 APN 14 101,887,051 (GRCm38) missense probably damaging 0.99
IGL00733:Lmo7 APN 14 101,915,702 (GRCm38) missense probably damaging 1.00
IGL00778:Lmo7 APN 14 101,910,885 (GRCm38) splice site probably benign
IGL01014:Lmo7 APN 14 101,920,557 (GRCm38) splice site probably benign
IGL01401:Lmo7 APN 14 101,794,277 (GRCm38) nonsense probably null
IGL01550:Lmo7 APN 14 101,926,140 (GRCm38) utr 3 prime probably benign
IGL01570:Lmo7 APN 14 101,902,371 (GRCm38) critical splice donor site probably null
IGL01602:Lmo7 APN 14 101,910,756 (GRCm38) splice site probably benign
IGL01605:Lmo7 APN 14 101,910,756 (GRCm38) splice site probably benign
IGL02012:Lmo7 APN 14 101,888,716 (GRCm38) intron probably benign
IGL02145:Lmo7 APN 14 101,902,223 (GRCm38) missense probably benign 0.00
IGL02236:Lmo7 APN 14 101,926,088 (GRCm38) splice site probably benign
IGL02318:Lmo7 APN 14 101,900,066 (GRCm38) splice site probably benign
IGL02345:Lmo7 APN 14 101,887,473 (GRCm38) missense probably damaging 1.00
IGL02498:Lmo7 APN 14 101,807,482 (GRCm38) missense probably benign 0.01
IGL02583:Lmo7 APN 14 101,933,924 (GRCm38) utr 3 prime probably benign
IGL02670:Lmo7 APN 14 101,880,980 (GRCm38) missense probably damaging 1.00
IGL02694:Lmo7 APN 14 101,887,170 (GRCm38) missense probably damaging 1.00
IGL03026:Lmo7 APN 14 101,929,333 (GRCm38) utr 3 prime probably benign
IGL03062:Lmo7 APN 14 101,912,079 (GRCm38) missense possibly damaging 0.66
IGL03068:Lmo7 APN 14 101,875,492 (GRCm38) unclassified probably benign
IGL03178:Lmo7 APN 14 101,929,260 (GRCm38) nonsense probably null
IGL03279:Lmo7 APN 14 101,900,508 (GRCm38) missense probably benign 0.30
PIT4458001:Lmo7 UTSW 14 101,887,487 (GRCm38) nonsense probably null
R0029:Lmo7 UTSW 14 101,933,921 (GRCm38) utr 3 prime probably benign
R0112:Lmo7 UTSW 14 101,887,193 (GRCm38) nonsense probably null
R0345:Lmo7 UTSW 14 101,876,877 (GRCm38) missense probably damaging 1.00
R0372:Lmo7 UTSW 14 101,918,053 (GRCm38) splice site probably benign
R0393:Lmo7 UTSW 14 101,900,456 (GRCm38) missense probably benign
R0514:Lmo7 UTSW 14 101,896,559 (GRCm38) missense probably damaging 1.00
R0514:Lmo7 UTSW 14 101,887,173 (GRCm38) missense probably damaging 1.00
R0526:Lmo7 UTSW 14 101,900,560 (GRCm38) missense probably damaging 1.00
R0615:Lmo7 UTSW 14 101,876,859 (GRCm38) nonsense probably null
R0900:Lmo7 UTSW 14 101,887,188 (GRCm38) missense probably damaging 1.00
R0961:Lmo7 UTSW 14 101,794,269 (GRCm38) missense probably benign 0.00
R0964:Lmo7 UTSW 14 101,920,567 (GRCm38) splice site probably benign
R1078:Lmo7 UTSW 14 101,920,474 (GRCm38) splice site probably benign
R1252:Lmo7 UTSW 14 101,900,583 (GRCm38) missense probably damaging 1.00
R1527:Lmo7 UTSW 14 101,876,828 (GRCm38) missense probably damaging 1.00
R1537:Lmo7 UTSW 14 101,929,264 (GRCm38) utr 3 prime probably benign
R1637:Lmo7 UTSW 14 101,880,832 (GRCm38) missense probably damaging 1.00
R1943:Lmo7 UTSW 14 101,902,302 (GRCm38) missense probably damaging 1.00
R1967:Lmo7 UTSW 14 101,900,215 (GRCm38) missense probably benign 0.36
R2002:Lmo7 UTSW 14 101,887,061 (GRCm38) missense probably benign 0.13
R2057:Lmo7 UTSW 14 101,887,178 (GRCm38) missense probably damaging 1.00
R2131:Lmo7 UTSW 14 101,900,238 (GRCm38) missense probably damaging 0.99
R2153:Lmo7 UTSW 14 101,920,515 (GRCm38) utr 3 prime probably benign
R2257:Lmo7 UTSW 14 101,900,130 (GRCm38) missense probably damaging 1.00
R2355:Lmo7 UTSW 14 101,888,685 (GRCm38) missense probably damaging 1.00
R2356:Lmo7 UTSW 14 101,886,945 (GRCm38) missense probably damaging 1.00
R2898:Lmo7 UTSW 14 101,876,914 (GRCm38) missense possibly damaging 0.93
R3847:Lmo7 UTSW 14 101,922,095 (GRCm38) critical splice acceptor site probably null
R3848:Lmo7 UTSW 14 101,922,095 (GRCm38) critical splice acceptor site probably null
R3849:Lmo7 UTSW 14 101,922,095 (GRCm38) critical splice acceptor site probably null
R3916:Lmo7 UTSW 14 101,929,342 (GRCm38) utr 3 prime probably benign
R4050:Lmo7 UTSW 14 101,902,277 (GRCm38) nonsense probably null
R4326:Lmo7 UTSW 14 101,900,074 (GRCm38) missense possibly damaging 0.93
R4357:Lmo7 UTSW 14 101,887,655 (GRCm38) missense probably null 1.00
R4571:Lmo7 UTSW 14 101,887,594 (GRCm38) missense probably damaging 0.96
R4658:Lmo7 UTSW 14 101,886,957 (GRCm38) missense probably damaging 1.00
R4857:Lmo7 UTSW 14 101,887,348 (GRCm38) splice site probably null
R5006:Lmo7 UTSW 14 101,926,237 (GRCm38) utr 3 prime probably benign
R5528:Lmo7 UTSW 14 101,902,086 (GRCm38) missense probably damaging 1.00
R5588:Lmo7 UTSW 14 101,896,590 (GRCm38) splice site probably null
R5643:Lmo7 UTSW 14 101,929,336 (GRCm38) utr 3 prime probably benign
R5644:Lmo7 UTSW 14 101,929,336 (GRCm38) utr 3 prime probably benign
R5650:Lmo7 UTSW 14 101,898,674 (GRCm38) missense probably damaging 1.00
R5737:Lmo7 UTSW 14 101,887,236 (GRCm38) missense probably damaging 1.00
R5832:Lmo7 UTSW 14 101,884,213 (GRCm38) missense probably damaging 1.00
R5966:Lmo7 UTSW 14 101,900,502 (GRCm38) missense possibly damaging 0.92
R6026:Lmo7 UTSW 14 101,880,990 (GRCm38) missense probably benign 0.04
R6072:Lmo7 UTSW 14 101,929,336 (GRCm38) utr 3 prime probably benign
R6158:Lmo7 UTSW 14 101,900,137 (GRCm38) missense probably benign 0.03
R6246:Lmo7 UTSW 14 101,918,700 (GRCm38) missense probably damaging 1.00
R6335:Lmo7 UTSW 14 101,900,636 (GRCm38) missense probably damaging 1.00
R6620:Lmo7 UTSW 14 101,875,452 (GRCm38) missense probably benign 0.29
R6658:Lmo7 UTSW 14 101,910,845 (GRCm38) missense possibly damaging 0.84
R6917:Lmo7 UTSW 14 101,918,010 (GRCm38) missense probably damaging 1.00
R7064:Lmo7 UTSW 14 101,884,179 (GRCm38) missense probably damaging 1.00
R7072:Lmo7 UTSW 14 101,898,700 (GRCm38) critical splice donor site probably null
R7121:Lmo7 UTSW 14 101,887,035 (GRCm38) missense probably damaging 1.00
R7136:Lmo7 UTSW 14 101,920,539 (GRCm38) missense unknown
R7196:Lmo7 UTSW 14 101,896,500 (GRCm38) missense possibly damaging 0.75
R7228:Lmo7 UTSW 14 101,896,535 (GRCm38) missense probably damaging 0.99
R7337:Lmo7 UTSW 14 101,884,204 (GRCm38) missense probably damaging 0.98
R7341:Lmo7 UTSW 14 101,885,512 (GRCm38) missense probably benign 0.30
R7408:Lmo7 UTSW 14 101,880,953 (GRCm38) missense probably damaging 1.00
R7432:Lmo7 UTSW 14 101,902,115 (GRCm38) missense probably benign 0.42
R7470:Lmo7 UTSW 14 101,900,604 (GRCm38) missense possibly damaging 0.83
R7506:Lmo7 UTSW 14 101,919,609 (GRCm38) missense unknown
R7559:Lmo7 UTSW 14 101,887,226 (GRCm38) nonsense probably null
R7565:Lmo7 UTSW 14 101,885,301 (GRCm38) missense probably damaging 0.98
R7788:Lmo7 UTSW 14 101,898,576 (GRCm38) missense possibly damaging 0.64
R8095:Lmo7 UTSW 14 101,887,419 (GRCm38) missense possibly damaging 0.88
R8100:Lmo7 UTSW 14 101,900,463 (GRCm38) missense probably benign 0.33
R8121:Lmo7 UTSW 14 101,926,300 (GRCm38) missense unknown
R8308:Lmo7 UTSW 14 101,902,371 (GRCm38) critical splice donor site probably null
R8371:Lmo7 UTSW 14 101,887,008 (GRCm38) missense possibly damaging 0.95
R8403:Lmo7 UTSW 14 101,902,364 (GRCm38) missense probably benign 0.03
R8690:Lmo7 UTSW 14 101,931,208 (GRCm38) missense unknown
R8778:Lmo7 UTSW 14 101,919,219 (GRCm38) missense probably benign 0.24
R8778:Lmo7 UTSW 14 101,912,067 (GRCm38) missense probably damaging 0.98
R8822:Lmo7 UTSW 14 101,884,174 (GRCm38) missense probably damaging 1.00
R8849:Lmo7 UTSW 14 101,926,107 (GRCm38) missense unknown
R8923:Lmo7 UTSW 14 101,900,243 (GRCm38) missense probably benign 0.31
R9006:Lmo7 UTSW 14 101,917,636 (GRCm38) small deletion probably benign
R9135:Lmo7 UTSW 14 101,880,861 (GRCm38) missense probably damaging 1.00
R9154:Lmo7 UTSW 14 101,885,307 (GRCm38) missense probably damaging 0.99
R9178:Lmo7 UTSW 14 101,807,470 (GRCm38) nonsense probably null
R9375:Lmo7 UTSW 14 101,898,687 (GRCm38) missense probably damaging 0.99
R9428:Lmo7 UTSW 14 101,917,640 (GRCm38) missense probably damaging 0.99
R9488:Lmo7 UTSW 14 101,885,347 (GRCm38) missense possibly damaging 0.85
R9493:Lmo7 UTSW 14 101,900,471 (GRCm38) missense probably benign 0.01
R9594:Lmo7 UTSW 14 101,918,700 (GRCm38) missense probably null 0.98
R9674:Lmo7 UTSW 14 101,840,904 (GRCm38) missense probably damaging 1.00
R9736:Lmo7 UTSW 14 101,920,493 (GRCm38) missense unknown
X0066:Lmo7 UTSW 14 101,887,461 (GRCm38) missense probably damaging 1.00
X0067:Lmo7 UTSW 14 101,886,933 (GRCm38) splice site probably null
Z1176:Lmo7 UTSW 14 101,919,281 (GRCm38) missense probably benign 0.00
Z1176:Lmo7 UTSW 14 101,884,306 (GRCm38) missense probably damaging 0.99
Z1176:Lmo7 UTSW 14 101,929,228 (GRCm38) missense unknown
Z1176:Lmo7 UTSW 14 101,919,443 (GRCm38) missense unknown
Z1177:Lmo7 UTSW 14 101,898,557 (GRCm38) missense probably damaging 1.00
Z1177:Lmo7 UTSW 14 101,896,518 (GRCm38) missense possibly damaging 0.96
Predicted Primers PCR Primer
(F):5'- CGCAGGATTCCAGCTCAGAAGAAAG -3'
(R):5'- GGATGCTTCAAAACGGCACACAG -3'

Sequencing Primer
(F):5'- AAAGAAGTGCCCCTTTCTGG -3'
(R):5'- TTTCCCCAATAAGGAAAGTTACAC -3'
Posted On 2014-04-24