Incidental Mutation 'IGL02670:Lmo7'
| ID |
302896 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Lmo7
|
| Ensembl Gene |
ENSMUSG00000033060 |
| Gene Name |
LIM domain only 7 |
| Synonyms |
FBXO20, LOC380928 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.195)
|
| Stock # |
IGL02670
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
101729957-101934710 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 101880980 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 214
(T214S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097910
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100337]
[ENSMUST00000159026]
[ENSMUST00000159258]
[ENSMUST00000159314]
[ENSMUST00000159597]
|
| AlphaFold |
E9PYF4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000100337
AA Change: T214S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000097910
Gene: ENSMUSG00000033060
AA Change: T214S
| Domain | Start | End | E-Value | Type |
|---|
|
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
|
| SMART Domains |
Protein: ENSMUSP00000124605
Gene: ENSMUSG00000033060
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
215 |
229 |
N/A |
INTRINSIC |
|
coiled coil region
|
435 |
471 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000159258
|
| SMART Domains |
Protein: ENSMUSP00000125465
Gene: ENSMUSG00000033060
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
215 |
229 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000159314
|
| SMART Domains |
Protein: ENSMUSP00000124349
Gene: ENSMUSG00000033060
| Domain | Start | End | E-Value | Type |
|---|
|
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 |
possibly damaging
Transcript: ENSMUST00000159597
AA Change: T92S
PolyPhen 2
Score 0.925 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000123706
Gene: ENSMUSG00000033060
AA Change: T92S
| Domain | Start | End | E-Value | Type |
|---|
|
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: ENSMUST00000159769
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159797
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000159806
AA Change: T47S
|
| SMART Domains |
Protein: ENSMUSP00000124300
Gene: ENSMUSG00000033060
AA Change: T47S
| Domain | Start | End | E-Value | Type |
|---|
|
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
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932438A13Rik |
C |
T |
3: 36,967,305 |
Q2193* |
probably null |
Het |
| Asb1 |
T |
C |
1: 91,546,918 |
|
probably benign |
Het |
| Cnot6 |
G |
A |
11: 49,685,114 |
Q178* |
probably null |
Het |
| Col5a1 |
C |
T |
2: 27,974,715 |
A737V |
unknown |
Het |
| Cyp27b1 |
T |
C |
10: 127,050,358 |
S303P |
probably benign |
Het |
| Dnah5 |
T |
C |
15: 28,409,296 |
L3620P |
probably damaging |
Het |
| Dock7 |
A |
T |
4: 98,966,286 |
|
probably null |
Het |
| Fam161b |
T |
C |
12: 84,357,594 |
D104G |
probably benign |
Het |
| Fam8a1 |
A |
G |
13: 46,673,604 |
M284V |
possibly damaging |
Het |
| Fkbp3 |
T |
A |
12: 65,069,103 |
K65* |
probably null |
Het |
| Gatb |
A |
G |
3: 85,613,551 |
|
probably null |
Het |
| Gm572 |
A |
T |
4: 148,651,228 |
H38L |
probably benign |
Het |
| Gm6576 |
A |
C |
15: 27,025,512 |
|
noncoding transcript |
Het |
| L2hgdh |
G |
A |
12: 69,692,480 |
R406W |
possibly damaging |
Het |
| Map3k12 |
T |
C |
15: 102,503,546 |
H361R |
probably benign |
Het |
| Mios |
T |
C |
6: 8,235,378 |
|
probably benign |
Het |
| Mta1 |
T |
C |
12: 113,130,121 |
L315P |
probably damaging |
Het |
| Pask |
A |
C |
1: 93,310,818 |
V1315G |
probably damaging |
Het |
| Pias4 |
A |
T |
10: 81,164,070 |
C50S |
probably damaging |
Het |
| Rgs11 |
G |
A |
17: 26,207,631 |
V279I |
probably benign |
Het |
| Sgk1 |
T |
A |
10: 21,928,546 |
C92S |
probably benign |
Het |
| Slc2a13 |
C |
T |
15: 91,497,509 |
G259E |
probably damaging |
Het |
| Slc5a4b |
A |
G |
10: 76,075,100 |
C301R |
probably damaging |
Het |
| Sstr4 |
G |
T |
2: 148,396,533 |
G355* |
probably null |
Het |
| Tnrc6a |
T |
A |
7: 123,171,312 |
L775Q |
possibly damaging |
Het |
| Vmn1r218 |
A |
G |
13: 23,137,004 |
I94V |
probably benign |
Het |
| Xpa |
A |
G |
4: 46,185,682 |
F99L |
probably benign |
Het |
|
| Other mutations in Lmo7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00569:Lmo7
|
APN |
14 |
101887051 |
missense |
probably damaging |
0.99 |
|
IGL00733:Lmo7
|
APN |
14 |
101915702 |
missense |
probably damaging |
1.00 |
|
IGL00778:Lmo7
|
APN |
14 |
101910885 |
splice site |
probably benign |
|
|
IGL01014:Lmo7
|
APN |
14 |
101920557 |
splice site |
probably benign |
|
|
IGL01401:Lmo7
|
APN |
14 |
101794277 |
nonsense |
probably null |
|
|
IGL01550:Lmo7
|
APN |
14 |
101926140 |
utr 3 prime |
probably benign |
|
|
IGL01570:Lmo7
|
APN |
14 |
101902371 |
critical splice donor site |
probably null |
|
|
IGL01602:Lmo7
|
APN |
14 |
101910756 |
splice site |
probably benign |
|
|
IGL01605:Lmo7
|
APN |
14 |
101910756 |
splice site |
probably benign |
|
|
IGL02012:Lmo7
|
APN |
14 |
101888716 |
intron |
probably benign |
|
|
IGL02145:Lmo7
|
APN |
14 |
101902223 |
missense |
probably benign |
0.00 |
|
IGL02236:Lmo7
|
APN |
14 |
101926088 |
splice site |
probably benign |
|
|
IGL02318:Lmo7
|
APN |
14 |
101900066 |
splice site |
probably benign |
|
|
IGL02345:Lmo7
|
APN |
14 |
101887473 |
missense |
probably damaging |
1.00 |
|
IGL02498:Lmo7
|
APN |
14 |
101807482 |
missense |
probably benign |
0.01 |
|
IGL02583:Lmo7
|
APN |
14 |
101933924 |
utr 3 prime |
probably benign |
|
|
IGL02694:Lmo7
|
APN |
14 |
101887170 |
missense |
probably damaging |
1.00 |
|
IGL03026:Lmo7
|
APN |
14 |
101929333 |
utr 3 prime |
probably benign |
|
|
IGL03062:Lmo7
|
APN |
14 |
101912079 |
missense |
possibly damaging |
0.66 |
|
IGL03068:Lmo7
|
APN |
14 |
101875492 |
unclassified |
probably benign |
|
|
IGL03178:Lmo7
|
APN |
14 |
101929260 |
nonsense |
probably null |
|
|
IGL03279:Lmo7
|
APN |
14 |
101900508 |
missense |
probably benign |
0.30 |
|
PIT4458001:Lmo7
|
UTSW |
14 |
101887487 |
nonsense |
probably null |
|
|
R0029:Lmo7
|
UTSW |
14 |
101933921 |
utr 3 prime |
probably benign |
|
|
R0112:Lmo7
|
UTSW |
14 |
101887193 |
nonsense |
probably null |
|
|
R0345:Lmo7
|
UTSW |
14 |
101876877 |
missense |
probably damaging |
1.00 |
|
R0372:Lmo7
|
UTSW |
14 |
101918053 |
splice site |
probably benign |
|
|
R0393:Lmo7
|
UTSW |
14 |
101900456 |
missense |
probably benign |
|
|
R0514:Lmo7
|
UTSW |
14 |
101887173 |
missense |
probably damaging |
1.00 |
|
R0514:Lmo7
|
UTSW |
14 |
101896559 |
missense |
probably damaging |
1.00 |
|
R0526:Lmo7
|
UTSW |
14 |
101900560 |
missense |
probably damaging |
1.00 |
|
R0615:Lmo7
|
UTSW |
14 |
101876859 |
nonsense |
probably null |
|
|
R0900:Lmo7
|
UTSW |
14 |
101887188 |
missense |
probably damaging |
1.00 |
|
R0961:Lmo7
|
UTSW |
14 |
101794269 |
missense |
probably benign |
0.00 |
|
R0964:Lmo7
|
UTSW |
14 |
101920567 |
splice site |
probably benign |
|
|
R1078:Lmo7
|
UTSW |
14 |
101920474 |
splice site |
probably benign |
|
|
R1252:Lmo7
|
UTSW |
14 |
101900583 |
missense |
probably damaging |
1.00 |
|
R1527:Lmo7
|
UTSW |
14 |
101876828 |
missense |
probably damaging |
1.00 |
|
R1537:Lmo7
|
UTSW |
14 |
101929264 |
utr 3 prime |
probably benign |
|
|
R1565:Lmo7
|
UTSW |
14 |
101887521 |
missense |
probably damaging |
0.99 |
|
R1637:Lmo7
|
UTSW |
14 |
101880832 |
missense |
probably damaging |
1.00 |
|
R1943:Lmo7
|
UTSW |
14 |
101902302 |
missense |
probably damaging |
1.00 |
|
R1967:Lmo7
|
UTSW |
14 |
101900215 |
missense |
probably benign |
0.36 |
|
R2002:Lmo7
|
UTSW |
14 |
101887061 |
missense |
probably benign |
0.13 |
|
R2057:Lmo7
|
UTSW |
14 |
101887178 |
missense |
probably damaging |
1.00 |
|
R2131:Lmo7
|
UTSW |
14 |
101900238 |
missense |
probably damaging |
0.99 |
|
R2153:Lmo7
|
UTSW |
14 |
101920515 |
utr 3 prime |
probably benign |
|
|
R2257:Lmo7
|
UTSW |
14 |
101900130 |
missense |
probably damaging |
1.00 |
|
R2355:Lmo7
|
UTSW |
14 |
101888685 |
missense |
probably damaging |
1.00 |
|
R2356:Lmo7
|
UTSW |
14 |
101886945 |
missense |
probably damaging |
1.00 |
|
R2898:Lmo7
|
UTSW |
14 |
101876914 |
missense |
possibly damaging |
0.93 |
|
R3847:Lmo7
|
UTSW |
14 |
101922095 |
critical splice acceptor site |
probably null |
|
|
R3848:Lmo7
|
UTSW |
14 |
101922095 |
critical splice acceptor site |
probably null |
|
|
R3849:Lmo7
|
UTSW |
14 |
101922095 |
critical splice acceptor site |
probably null |
|
|
R3916:Lmo7
|
UTSW |
14 |
101929342 |
utr 3 prime |
probably benign |
|
|
R4050:Lmo7
|
UTSW |
14 |
101902277 |
nonsense |
probably null |
|
|
R4326:Lmo7
|
UTSW |
14 |
101900074 |
missense |
possibly damaging |
0.93 |
|
R4357:Lmo7
|
UTSW |
14 |
101887655 |
missense |
probably null |
1.00 |
|
R4571:Lmo7
|
UTSW |
14 |
101887594 |
missense |
probably damaging |
0.96 |
|
R4658:Lmo7
|
UTSW |
14 |
101886957 |
missense |
probably damaging |
1.00 |
|
R4857:Lmo7
|
UTSW |
14 |
101887348 |
splice site |
probably null |
|
|
R5006:Lmo7
|
UTSW |
14 |
101926237 |
utr 3 prime |
probably benign |
|
|
R5528:Lmo7
|
UTSW |
14 |
101902086 |
missense |
probably damaging |
1.00 |
|
R5588:Lmo7
|
UTSW |
14 |
101896590 |
splice site |
probably null |
|
|
R5643:Lmo7
|
UTSW |
14 |
101929336 |
utr 3 prime |
probably benign |
|
|
R5644:Lmo7
|
UTSW |
14 |
101929336 |
utr 3 prime |
probably benign |
|
|
R5650:Lmo7
|
UTSW |
14 |
101898674 |
missense |
probably damaging |
1.00 |
|
R5737:Lmo7
|
UTSW |
14 |
101887236 |
missense |
probably damaging |
1.00 |
|
R5832:Lmo7
|
UTSW |
14 |
101884213 |
missense |
probably damaging |
1.00 |
|
R5966:Lmo7
|
UTSW |
14 |
101900502 |
missense |
possibly damaging |
0.92 |
|
R6026:Lmo7
|
UTSW |
14 |
101880990 |
missense |
probably benign |
0.04 |
|
R6072:Lmo7
|
UTSW |
14 |
101929336 |
utr 3 prime |
probably benign |
|
|
R6158:Lmo7
|
UTSW |
14 |
101900137 |
missense |
probably benign |
0.03 |
|
R6246:Lmo7
|
UTSW |
14 |
101918700 |
missense |
probably damaging |
1.00 |
|
R6335:Lmo7
|
UTSW |
14 |
101900636 |
missense |
probably damaging |
1.00 |
|
R6620:Lmo7
|
UTSW |
14 |
101875452 |
missense |
probably benign |
0.29 |
|
R6658:Lmo7
|
UTSW |
14 |
101910845 |
missense |
possibly damaging |
0.84 |
|
R6917:Lmo7
|
UTSW |
14 |
101918010 |
missense |
probably damaging |
1.00 |
|
R7064:Lmo7
|
UTSW |
14 |
101884179 |
missense |
probably damaging |
1.00 |
|
R7072:Lmo7
|
UTSW |
14 |
101898700 |
critical splice donor site |
probably null |
|
|
R7121:Lmo7
|
UTSW |
14 |
101887035 |
missense |
probably damaging |
1.00 |
|
R7136:Lmo7
|
UTSW |
14 |
101920539 |
missense |
unknown |
|
|
R7196:Lmo7
|
UTSW |
14 |
101896500 |
missense |
possibly damaging |
0.75 |
|
R7228:Lmo7
|
UTSW |
14 |
101896535 |
missense |
probably damaging |
0.99 |
|
R7337:Lmo7
|
UTSW |
14 |
101884204 |
missense |
probably damaging |
0.98 |
|
R7341:Lmo7
|
UTSW |
14 |
101885512 |
missense |
probably benign |
0.30 |
|
R7408:Lmo7
|
UTSW |
14 |
101880953 |
missense |
probably damaging |
1.00 |
|
R7432:Lmo7
|
UTSW |
14 |
101902115 |
missense |
probably benign |
0.42 |
|
R7470:Lmo7
|
UTSW |
14 |
101900604 |
missense |
possibly damaging |
0.83 |
|
R7506:Lmo7
|
UTSW |
14 |
101919609 |
missense |
unknown |
|
|
R7559:Lmo7
|
UTSW |
14 |
101887226 |
nonsense |
probably null |
|
|
R7565:Lmo7
|
UTSW |
14 |
101885301 |
missense |
probably damaging |
0.98 |
|
R7788:Lmo7
|
UTSW |
14 |
101898576 |
missense |
possibly damaging |
0.64 |
|
R8095:Lmo7
|
UTSW |
14 |
101887419 |
missense |
possibly damaging |
0.88 |
|
R8100:Lmo7
|
UTSW |
14 |
101900463 |
missense |
probably benign |
0.33 |
|
R8121:Lmo7
|
UTSW |
14 |
101926300 |
missense |
unknown |
|
|
R8308:Lmo7
|
UTSW |
14 |
101902371 |
critical splice donor site |
probably null |
|
|
R8371:Lmo7
|
UTSW |
14 |
101887008 |
missense |
possibly damaging |
0.95 |
|
R8403:Lmo7
|
UTSW |
14 |
101902364 |
missense |
probably benign |
0.03 |
|
R8690:Lmo7
|
UTSW |
14 |
101931208 |
missense |
unknown |
|
|
R8778:Lmo7
|
UTSW |
14 |
101912067 |
missense |
probably damaging |
0.98 |
|
R8778:Lmo7
|
UTSW |
14 |
101919219 |
missense |
probably benign |
0.24 |
|
R8822:Lmo7
|
UTSW |
14 |
101884174 |
missense |
probably damaging |
1.00 |
|
R8849:Lmo7
|
UTSW |
14 |
101926107 |
missense |
unknown |
|
|
R8923:Lmo7
|
UTSW |
14 |
101900243 |
missense |
probably benign |
0.31 |
|
R9006:Lmo7
|
UTSW |
14 |
101917636 |
small deletion |
probably benign |
|
|
R9135:Lmo7
|
UTSW |
14 |
101880861 |
missense |
probably damaging |
1.00 |
|
R9154:Lmo7
|
UTSW |
14 |
101885307 |
missense |
probably damaging |
0.99 |
|
R9178:Lmo7
|
UTSW |
14 |
101807470 |
nonsense |
probably null |
|
|
R9375:Lmo7
|
UTSW |
14 |
101898687 |
missense |
probably damaging |
0.99 |
|
R9428:Lmo7
|
UTSW |
14 |
101917640 |
missense |
probably damaging |
0.99 |
|
R9488:Lmo7
|
UTSW |
14 |
101885347 |
missense |
possibly damaging |
0.85 |
|
R9493:Lmo7
|
UTSW |
14 |
101900471 |
missense |
probably benign |
0.01 |
|
R9594:Lmo7
|
UTSW |
14 |
101918700 |
missense |
probably null |
0.98 |
|
R9674:Lmo7
|
UTSW |
14 |
101840904 |
missense |
probably damaging |
1.00 |
|
R9736:Lmo7
|
UTSW |
14 |
101920493 |
missense |
unknown |
|
|
X0066:Lmo7
|
UTSW |
14 |
101887461 |
missense |
probably damaging |
1.00 |
|
X0067:Lmo7
|
UTSW |
14 |
101886933 |
splice site |
probably null |
|
|
Z1176:Lmo7
|
UTSW |
14 |
101884306 |
missense |
probably damaging |
0.99 |
|
Z1176:Lmo7
|
UTSW |
14 |
101919281 |
missense |
probably benign |
0.00 |
|
Z1176:Lmo7
|
UTSW |
14 |
101919443 |
missense |
unknown |
|
|
Z1176:Lmo7
|
UTSW |
14 |
101929228 |
missense |
unknown |
|
|
Z1177:Lmo7
|
UTSW |
14 |
101896518 |
missense |
possibly damaging |
0.96 |
|
Z1177:Lmo7
|
UTSW |
14 |
101898557 |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation