Incidental Mutation 'IGL02986:L3mbtl1'
| ID |
406711 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
L3mbtl1
|
| Ensembl Gene |
ENSMUSG00000035576 |
| Gene Name |
L3MBTL1 histone methyl-lysine binding protein |
| Synonyms |
L3MBTL1 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02986
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
162785392-162816442 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 162812225 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Arginine
at position 757
(W757R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000044038
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035751]
|
| AlphaFold |
A2A5N8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000035751
AA Change: W757R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000044038
Gene: ENSMUSG00000035576
AA Change: W757R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
234 |
242 |
N/A |
INTRINSIC |
|
MBT
|
280 |
380 |
5.34e-53 |
SMART |
|
MBT
|
388 |
487 |
2.17e-53 |
SMART |
|
MBT
|
496 |
591 |
1.49e-51 |
SMART |
|
Pfam:zf-C2HC
|
627 |
655 |
1.7e-17 |
PFAM |
|
SAM
|
754 |
821 |
3.49e-8 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153416
|
| 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 represents a polycomb group gene. The encoded protein functions to regulate gene activity, likely via chromatin modification. The encoded protein may also be necessary for mitosis. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal nervous system phenotype, hematopoietic system phenotype, immune system phenotype, cellular phenotype, and lifespan. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agrn |
A |
G |
4: 156,263,311 (GRCm39) |
V264A |
possibly damaging |
Het |
| Akr1c6 |
G |
T |
13: 4,486,414 (GRCm39) |
V74L |
probably benign |
Het |
| Atp10a |
T |
G |
7: 58,478,469 (GRCm39) |
V1504G |
probably benign |
Het |
| Ccng1 |
A |
G |
11: 40,641,690 (GRCm39) |
|
probably benign |
Het |
| Celsr3 |
A |
T |
9: 108,718,454 (GRCm39) |
|
probably null |
Het |
| Coro1b |
T |
C |
19: 4,199,470 (GRCm39) |
V43A |
possibly damaging |
Het |
| Dab1 |
A |
G |
4: 104,336,418 (GRCm39) |
T5A |
probably benign |
Het |
| Dennd5a |
C |
T |
7: 109,534,731 (GRCm39) |
A47T |
probably benign |
Het |
| Dgkb |
A |
G |
12: 38,150,399 (GRCm39) |
T69A |
possibly damaging |
Het |
| Dhx37 |
G |
A |
5: 125,496,379 (GRCm39) |
P721L |
probably damaging |
Het |
| Efr3b |
T |
C |
12: 4,016,495 (GRCm39) |
N641D |
probably benign |
Het |
| Espnl |
A |
T |
1: 91,272,572 (GRCm39) |
Q600L |
probably benign |
Het |
| Esyt1 |
A |
G |
10: 128,352,626 (GRCm39) |
V693A |
probably damaging |
Het |
| Fscn2 |
A |
G |
11: 120,258,176 (GRCm39) |
D366G |
possibly damaging |
Het |
| Gcsam |
C |
A |
16: 45,440,366 (GRCm39) |
F136L |
probably benign |
Het |
| Gm10643 |
A |
T |
8: 84,790,887 (GRCm39) |
|
probably benign |
Het |
| Habp2 |
A |
T |
19: 56,299,624 (GRCm39) |
D174V |
probably benign |
Het |
| Hgfac |
T |
C |
5: 35,201,207 (GRCm39) |
V210A |
probably benign |
Het |
| Hipk3 |
T |
C |
2: 104,264,086 (GRCm39) |
D804G |
probably damaging |
Het |
| Lrrfip2 |
A |
G |
9: 110,990,461 (GRCm39) |
|
probably null |
Het |
| Ly75 |
T |
C |
2: 60,138,535 (GRCm39) |
D1444G |
probably damaging |
Het |
| Mars1 |
A |
G |
10: 127,133,438 (GRCm39) |
V765A |
probably benign |
Het |
| Med1 |
A |
G |
11: 98,047,086 (GRCm39) |
|
probably benign |
Het |
| Msln |
G |
A |
17: 25,971,907 (GRCm39) |
|
probably benign |
Het |
| Nup188 |
T |
A |
2: 30,197,645 (GRCm39) |
|
probably null |
Het |
| Or1p1c |
T |
G |
11: 74,160,928 (GRCm39) |
F238V |
possibly damaging |
Het |
| Or7e173 |
A |
T |
9: 19,939,007 (GRCm39) |
F76I |
probably benign |
Het |
| Otop2 |
T |
A |
11: 115,220,393 (GRCm39) |
M411K |
probably benign |
Het |
| Picalm |
A |
G |
7: 89,856,793 (GRCm39) |
I649M |
probably benign |
Het |
| Plekha8 |
T |
C |
6: 54,606,851 (GRCm39) |
L382P |
probably damaging |
Het |
| Pspn |
A |
G |
17: 57,306,853 (GRCm39) |
|
probably benign |
Het |
| Rnf215 |
A |
G |
11: 4,089,793 (GRCm39) |
T269A |
probably damaging |
Het |
| Rps6kc1 |
A |
T |
1: 190,566,258 (GRCm39) |
L329Q |
probably damaging |
Het |
| Srms |
T |
A |
2: 180,854,290 (GRCm39) |
R92S |
possibly damaging |
Het |
| Ssxb10 |
C |
A |
X: 8,201,845 (GRCm39) |
S157* |
probably null |
Het |
| Tfap2c |
T |
C |
2: 172,399,171 (GRCm39) |
S448P |
probably damaging |
Het |
| Thsd7b |
A |
G |
1: 129,843,352 (GRCm39) |
N855D |
probably benign |
Het |
| Timeless |
A |
C |
10: 128,085,629 (GRCm39) |
D887A |
possibly damaging |
Het |
| Tyms |
T |
C |
5: 30,266,997 (GRCm39) |
Y169C |
probably damaging |
Het |
| Unc45b |
T |
A |
11: 82,808,005 (GRCm39) |
C207S |
probably damaging |
Het |
| Utp20 |
A |
G |
10: 88,611,147 (GRCm39) |
F1390S |
probably damaging |
Het |
| Vmn2r53 |
A |
T |
7: 12,315,393 (GRCm39) |
|
probably benign |
Het |
| Zfp369 |
A |
T |
13: 65,428,095 (GRCm39) |
D18V |
probably damaging |
Het |
|
| Other mutations in L3mbtl1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00236:L3mbtl1
|
APN |
2 |
162,808,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01090:L3mbtl1
|
APN |
2 |
162,807,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01291:L3mbtl1
|
APN |
2 |
162,812,100 (GRCm39) |
missense |
probably benign |
0.30 |
|
IGL02897:L3mbtl1
|
APN |
2 |
162,807,692 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02974:L3mbtl1
|
APN |
2 |
162,812,103 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
IGL03057:L3mbtl1
|
APN |
2 |
162,809,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03372:L3mbtl1
|
APN |
2 |
162,813,077 (GRCm39) |
splice site |
probably benign |
|
|
ANU05:L3mbtl1
|
UTSW |
2 |
162,812,100 (GRCm39) |
missense |
probably benign |
0.30 |
|
R0006:L3mbtl1
|
UTSW |
2 |
162,806,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0006:L3mbtl1
|
UTSW |
2 |
162,806,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0067:L3mbtl1
|
UTSW |
2 |
162,790,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0067:L3mbtl1
|
UTSW |
2 |
162,790,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0078:L3mbtl1
|
UTSW |
2 |
162,789,146 (GRCm39) |
missense |
probably benign |
0.12 |
|
R0505:L3mbtl1
|
UTSW |
2 |
162,789,255 (GRCm39) |
splice site |
probably benign |
|
|
R0748:L3mbtl1
|
UTSW |
2 |
162,813,084 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0748:L3mbtl1
|
UTSW |
2 |
162,813,083 (GRCm39) |
splice site |
probably benign |
|
|
R0761:L3mbtl1
|
UTSW |
2 |
162,807,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1789:L3mbtl1
|
UTSW |
2 |
162,816,422 (GRCm39) |
missense |
probably benign |
|
|
R1970:L3mbtl1
|
UTSW |
2 |
162,801,492 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2114:L3mbtl1
|
UTSW |
2 |
162,801,990 (GRCm39) |
splice site |
probably null |
|
|
R2115:L3mbtl1
|
UTSW |
2 |
162,801,990 (GRCm39) |
splice site |
probably null |
|
|
R2116:L3mbtl1
|
UTSW |
2 |
162,801,990 (GRCm39) |
splice site |
probably null |
|
|
R2117:L3mbtl1
|
UTSW |
2 |
162,801,990 (GRCm39) |
splice site |
probably null |
|
|
R2513:L3mbtl1
|
UTSW |
2 |
162,809,505 (GRCm39) |
missense |
probably benign |
|
|
R3848:L3mbtl1
|
UTSW |
2 |
162,790,121 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4877:L3mbtl1
|
UTSW |
2 |
162,790,488 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4930:L3mbtl1
|
UTSW |
2 |
162,807,692 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5930:L3mbtl1
|
UTSW |
2 |
162,809,256 (GRCm39) |
small deletion |
probably benign |
|
|
R5932:L3mbtl1
|
UTSW |
2 |
162,809,256 (GRCm39) |
small deletion |
probably benign |
|
|
R6562:L3mbtl1
|
UTSW |
2 |
162,812,124 (GRCm39) |
missense |
probably benign |
0.28 |
|
R6601:L3mbtl1
|
UTSW |
2 |
162,790,095 (GRCm39) |
start gained |
probably benign |
|
|
R6995:L3mbtl1
|
UTSW |
2 |
162,803,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7188:L3mbtl1
|
UTSW |
2 |
162,791,460 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7346:L3mbtl1
|
UTSW |
2 |
162,808,926 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7379:L3mbtl1
|
UTSW |
2 |
162,802,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7474:L3mbtl1
|
UTSW |
2 |
162,808,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7553:L3mbtl1
|
UTSW |
2 |
162,790,151 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7599:L3mbtl1
|
UTSW |
2 |
162,806,434 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8745:L3mbtl1
|
UTSW |
2 |
162,812,137 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8910:L3mbtl1
|
UTSW |
2 |
162,812,213 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9039:L3mbtl1
|
UTSW |
2 |
162,807,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9216:L3mbtl1
|
UTSW |
2 |
162,806,972 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9253:L3mbtl1
|
UTSW |
2 |
162,789,632 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9483:L3mbtl1
|
UTSW |
2 |
162,790,734 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9509:L3mbtl1
|
UTSW |
2 |
162,809,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9683:L3mbtl1
|
UTSW |
2 |
162,812,228 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9688:L3mbtl1
|
UTSW |
2 |
162,790,697 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
| Posted On |
2016-08-02 |
Incidental Mutation