Incidental Mutation 'R8348:Lef1'
| ID |
660420 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Lef1
|
| Ensembl Gene |
ENSMUSG00000027985 |
| Gene Name |
lymphoid enhancer binding factor 1 |
| Synonyms |
lymphoid enhancer factor 1, Lef-1 |
| MMRRC Submission |
067732-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8348 (G1)
|
| Quality Score |
209.009 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
130904120-131018005 bp(+) (GRCm39) |
| Type of Mutation |
start codon destroyed |
| DNA Base Change (assembly) |
A to T
at 130906461 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 1
(M1L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000096211
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029611]
[ENSMUST00000066849]
[ENSMUST00000098611]
[ENSMUST00000106341]
|
| AlphaFold |
P27782 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000029611
|
| SMART Domains |
Protein: ENSMUSP00000029611
Gene: ENSMUSG00000027985
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CTNNB1_binding
|
1 |
211 |
5e-88 |
PFAM |
|
low complexity region
|
245 |
259 |
N/A |
INTRINSIC |
|
HMG
|
296 |
366 |
7.68e-23 |
SMART |
|
low complexity region
|
372 |
380 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000066849
|
| SMART Domains |
Protein: ENSMUSP00000067808
Gene: ENSMUSG00000027985
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CTNNB1_binding
|
1 |
211 |
1e-75 |
PFAM |
|
low complexity region
|
217 |
231 |
N/A |
INTRINSIC |
|
HMG
|
268 |
338 |
7.68e-23 |
SMART |
|
low complexity region
|
344 |
352 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000098611
AA Change: M1L
PolyPhen 2
Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000096211
Gene: ENSMUSG00000027985
AA Change: M1L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CTNNB1_binding
|
1 |
145 |
2.8e-54 |
PFAM |
|
low complexity region
|
179 |
193 |
N/A |
INTRINSIC |
|
HMG
|
230 |
300 |
7.68e-23 |
SMART |
|
low complexity region
|
306 |
314 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106341
|
| SMART Domains |
Protein: ENSMUSP00000101948
Gene: ENSMUSG00000027985
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CTNNB1_binding
|
1 |
211 |
1.3e-75 |
PFAM |
|
low complexity region
|
217 |
231 |
N/A |
INTRINSIC |
|
HMG
|
268 |
338 |
7.68e-23 |
SMART |
|
low complexity region
|
344 |
352 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1087 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
| Validation Efficiency |
100% (59/59) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transcription factor belonging to a family of proteins that share homology with the high mobility group protein-1. The protein encoded by this gene can bind to a functionally important site in the T-cell receptor-alpha enhancer, thereby conferring maximal enhancer activity. This transcription factor is involved in the Wnt signaling pathway, and it may function in hair cell differentiation and follicle morphogenesis. Mutations in this gene have been found in somatic sebaceous tumors. This gene has also been linked to other cancers, including androgen-independent prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for a null allele are small and die postnatally showing lack of teeth, mammary and uterine glands, whiskers, body hair, dermal-associated fat, and a dentate gyrus, as well as defects in hippocampus morphology, hair follicle development, retinal vasculature, and vascular regression. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1600014C10Rik |
A |
G |
7: 37,894,384 (GRCm39) |
Y139C |
possibly damaging |
Het |
| A430033K04Rik |
A |
G |
5: 138,634,514 (GRCm39) |
D43G |
probably damaging |
Het |
| Actn3 |
C |
A |
19: 4,915,361 (GRCm39) |
V464L |
possibly damaging |
Het |
| Adamts15 |
C |
T |
9: 30,813,846 (GRCm39) |
R773Q |
probably benign |
Het |
| Angpt2 |
G |
A |
8: 18,791,135 (GRCm39) |
R54* |
probably null |
Het |
| Arhgef28 |
G |
T |
13: 98,190,375 (GRCm39) |
P195T |
possibly damaging |
Het |
| Axdnd1 |
A |
T |
1: 156,245,854 (GRCm39) |
D107E |
probably benign |
Het |
| Cdh23 |
C |
T |
10: 60,167,507 (GRCm39) |
V1828M |
probably benign |
Het |
| Cep95 |
A |
G |
11: 106,704,593 (GRCm39) |
T440A |
possibly damaging |
Het |
| Ctdp1 |
G |
A |
18: 80,493,325 (GRCm39) |
A390V |
probably benign |
Het |
| Desi2 |
T |
A |
1: 178,083,906 (GRCm39) |
|
probably benign |
Het |
| Dnah2 |
A |
T |
11: 69,320,273 (GRCm39) |
M3932K |
possibly damaging |
Het |
| Dnah8 |
A |
T |
17: 30,955,121 (GRCm39) |
Q2050L |
probably damaging |
Het |
| Etnppl |
T |
A |
3: 130,423,141 (GRCm39) |
M274K |
probably benign |
Het |
| Farp2 |
G |
T |
1: 93,504,614 (GRCm39) |
|
probably null |
Het |
| Fbxo46 |
G |
A |
7: 18,870,469 (GRCm39) |
G363R |
probably damaging |
Het |
| Fiz1 |
A |
G |
7: 5,015,909 (GRCm39) |
V27A |
probably benign |
Het |
| Fndc3b |
T |
A |
3: 27,494,144 (GRCm39) |
M994L |
probably benign |
Het |
| G3bp1 |
T |
G |
11: 55,389,457 (GRCm39) |
D384E |
possibly damaging |
Het |
| Galnt2 |
C |
T |
8: 125,061,025 (GRCm39) |
R306* |
probably null |
Het |
| Gle1 |
T |
C |
2: 29,832,556 (GRCm39) |
Y304H |
possibly damaging |
Het |
| Gm3415 |
G |
A |
5: 146,493,407 (GRCm39) |
R84H |
probably benign |
Het |
| Gm7694 |
A |
C |
1: 170,129,209 (GRCm39) |
S107A |
possibly damaging |
Het |
| Gpc6 |
A |
G |
14: 117,673,232 (GRCm39) |
D163G |
probably damaging |
Het |
| Gtpbp6 |
G |
A |
5: 110,251,892 (GRCm39) |
H514Y |
possibly damaging |
Het |
| Hdgfl2 |
A |
G |
17: 56,406,370 (GRCm39) |
E595G |
possibly damaging |
Het |
| Hoxc11 |
G |
A |
15: 102,863,186 (GRCm39) |
G76S |
possibly damaging |
Het |
| Hoxc4 |
T |
C |
15: 102,943,440 (GRCm39) |
C98R |
possibly damaging |
Het |
| Hydin |
A |
T |
8: 111,329,878 (GRCm39) |
I4871F |
possibly damaging |
Het |
| Ifnar1 |
A |
G |
16: 91,292,187 (GRCm39) |
D176G |
probably benign |
Het |
| Inafm1 |
A |
G |
7: 16,007,055 (GRCm39) |
I54T |
probably damaging |
Het |
| Inpp5b |
G |
A |
4: 124,678,967 (GRCm39) |
G458D |
probably damaging |
Het |
| Irs2 |
A |
T |
8: 11,054,974 (GRCm39) |
S1153T |
probably damaging |
Het |
| Kcnj15 |
A |
G |
16: 95,096,609 (GRCm39) |
Y77C |
probably damaging |
Het |
| Klhl35 |
C |
A |
7: 99,121,062 (GRCm39) |
D10E |
probably damaging |
Het |
| Lima1 |
T |
C |
15: 99,678,753 (GRCm39) |
T403A |
probably benign |
Het |
| Magi3 |
T |
A |
3: 103,958,531 (GRCm39) |
N518I |
probably damaging |
Het |
| Mcoln3 |
T |
C |
3: 145,836,974 (GRCm39) |
C269R |
probably damaging |
Het |
| Mis18a |
A |
T |
16: 90,523,919 (GRCm39) |
L81* |
probably null |
Het |
| Mug2 |
A |
T |
6: 122,049,192 (GRCm39) |
K903* |
probably null |
Het |
| Nhsl3 |
G |
A |
4: 129,117,699 (GRCm39) |
R322C |
probably damaging |
Het |
| Pex6 |
T |
C |
17: 47,034,039 (GRCm39) |
S656P |
probably benign |
Het |
| Pgr |
C |
A |
9: 8,922,602 (GRCm39) |
Q591K |
probably benign |
Het |
| Phactr3 |
T |
C |
2: 177,897,935 (GRCm39) |
S50P |
probably benign |
Het |
| Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
| Sipa1l1 |
T |
A |
12: 82,443,045 (GRCm39) |
N778K |
probably benign |
Het |
| Slc22a6 |
C |
G |
19: 8,599,169 (GRCm39) |
R267G |
probably damaging |
Het |
| Slc5a7 |
A |
G |
17: 54,583,655 (GRCm39) |
V545A |
possibly damaging |
Het |
| Snf8 |
A |
G |
11: 95,925,877 (GRCm39) |
K13R |
probably benign |
Het |
| St3gal1 |
G |
A |
15: 66,985,511 (GRCm39) |
R48C |
probably damaging |
Het |
| Tacc2 |
A |
C |
7: 130,225,019 (GRCm39) |
K568T |
possibly damaging |
Het |
| Tnxb |
C |
A |
17: 34,929,102 (GRCm39) |
T2715K |
possibly damaging |
Het |
| Vegfb |
T |
C |
19: 6,962,856 (GRCm39) |
I140V |
probably benign |
Het |
| Vmn2r89 |
A |
C |
14: 51,692,548 (GRCm39) |
D117A |
possibly damaging |
Het |
| Vps13c |
C |
T |
9: 67,786,385 (GRCm39) |
T284I |
possibly damaging |
Het |
| Wnk1 |
T |
C |
6: 119,906,960 (GRCm39) |
|
probably null |
Het |
| Wscd2 |
T |
A |
5: 113,710,371 (GRCm39) |
H298Q |
possibly damaging |
Het |
| Zfp69 |
A |
T |
4: 120,787,834 (GRCm39) |
C494S |
probably damaging |
Het |
| Zfp715 |
T |
C |
7: 42,949,361 (GRCm39) |
T200A |
possibly damaging |
Het |
|
| Other mutations in Lef1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00096:Lef1
|
APN |
3 |
130,907,499 (GRCm39) |
splice site |
probably benign |
|
|
IGL00515:Lef1
|
APN |
3 |
130,997,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00780:Lef1
|
APN |
3 |
130,986,779 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
IGL02057:Lef1
|
APN |
3 |
130,994,051 (GRCm39) |
nonsense |
probably null |
|
|
IGL02556:Lef1
|
APN |
3 |
130,988,442 (GRCm39) |
splice site |
probably null |
|
|
IGL02804:Lef1
|
APN |
3 |
130,988,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03143:Lef1
|
APN |
3 |
130,993,965 (GRCm39) |
nonsense |
probably null |
|
|
IGL03169:Lef1
|
APN |
3 |
130,988,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0470:Lef1
|
UTSW |
3 |
130,906,475 (GRCm39) |
intron |
probably benign |
|
|
R1354:Lef1
|
UTSW |
3 |
130,988,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1677:Lef1
|
UTSW |
3 |
130,993,938 (GRCm39) |
splice site |
probably benign |
|
|
R1860:Lef1
|
UTSW |
3 |
130,905,290 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2013:Lef1
|
UTSW |
3 |
130,905,236 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2015:Lef1
|
UTSW |
3 |
130,905,236 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3440:Lef1
|
UTSW |
3 |
130,978,407 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3736:Lef1
|
UTSW |
3 |
130,984,715 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R3918:Lef1
|
UTSW |
3 |
130,905,290 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4052:Lef1
|
UTSW |
3 |
130,988,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4346:Lef1
|
UTSW |
3 |
130,988,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4608:Lef1
|
UTSW |
3 |
130,978,382 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4764:Lef1
|
UTSW |
3 |
130,978,382 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4786:Lef1
|
UTSW |
3 |
130,905,173 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5298:Lef1
|
UTSW |
3 |
130,988,316 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5394:Lef1
|
UTSW |
3 |
130,988,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6827:Lef1
|
UTSW |
3 |
130,994,053 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6893:Lef1
|
UTSW |
3 |
130,909,149 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6974:Lef1
|
UTSW |
3 |
130,905,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7541:Lef1
|
UTSW |
3 |
130,984,748 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7544:Lef1
|
UTSW |
3 |
130,988,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7652:Lef1
|
UTSW |
3 |
130,994,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8074:Lef1
|
UTSW |
3 |
130,997,954 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8543:Lef1
|
UTSW |
3 |
130,909,138 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8762:Lef1
|
UTSW |
3 |
130,988,366 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Lef1
|
UTSW |
3 |
130,993,972 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Lef1
|
UTSW |
3 |
130,986,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCAAATGATGTGCCCAACG -3'
(R):5'- AGGCTACTCTACAGTCTGGTCAAG -3'
Sequencing Primer
(F):5'- CCTTCCAGAGAAACTTGG -3'
(R):5'- CCACCAGAGTTTAGATGGTATTTC -3'
|
| Posted On |
2021-01-18 |
Incidental Mutation