Incidental Mutation 'IGL01724:Brd2'
| ID |
105199 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Brd2
|
| Ensembl Gene |
ENSMUSG00000024335 |
| Gene Name |
bromodomain containing 2 |
| Synonyms |
Frg-1, D17H6S113E, Ring3, Rnf3, Fsrg1 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01724
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
34330993-34341581 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 34335975 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Histidine
at position 79
(Q79H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000128835
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025193]
[ENSMUST00000095347]
[ENSMUST00000114242]
[ENSMUST00000151986]
[ENSMUST00000154232]
|
| AlphaFold |
Q7JJ13 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000025193
AA Change: Q79H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000025193
Gene: ENSMUSG00000024335
AA Change: Q79H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
29 |
N/A |
INTRINSIC |
|
BROMO
|
71 |
181 |
2.13e-43 |
SMART |
|
low complexity region
|
256 |
276 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
290 |
N/A |
INTRINSIC |
|
low complexity region
|
294 |
304 |
N/A |
INTRINSIC |
|
BROMO
|
345 |
454 |
1.13e-47 |
SMART |
|
coiled coil region
|
486 |
537 |
N/A |
INTRINSIC |
|
low complexity region
|
542 |
560 |
N/A |
INTRINSIC |
|
low complexity region
|
583 |
593 |
N/A |
INTRINSIC |
|
PDB:2JNS|A
|
635 |
712 |
3e-37 |
PDB |
|
coiled coil region
|
721 |
750 |
N/A |
INTRINSIC |
|
low complexity region
|
772 |
797 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000095347
|
| SMART Domains |
Protein: ENSMUSP00000092990
Gene: ENSMUSG00000024335
| Domain | Start | End | E-Value | Type |
|---|
|
BROMO
|
25 |
135 |
1.3e-45 |
SMART |
|
low complexity region
|
210 |
230 |
N/A |
INTRINSIC |
|
low complexity region
|
238 |
244 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
258 |
N/A |
INTRINSIC |
|
BROMO
|
299 |
408 |
6.8e-50 |
SMART |
|
coiled coil region
|
440 |
491 |
N/A |
INTRINSIC |
|
low complexity region
|
496 |
514 |
N/A |
INTRINSIC |
|
low complexity region
|
537 |
547 |
N/A |
INTRINSIC |
|
PDB:2JNS|A
|
589 |
666 |
2e-37 |
PDB |
|
coiled coil region
|
675 |
704 |
N/A |
INTRINSIC |
|
low complexity region
|
726 |
751 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000114242
AA Change: Q79H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000109880
Gene: ENSMUSG00000024335
AA Change: Q79H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
29 |
N/A |
INTRINSIC |
|
BROMO
|
71 |
181 |
2.13e-43 |
SMART |
|
low complexity region
|
256 |
276 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
290 |
N/A |
INTRINSIC |
|
low complexity region
|
294 |
304 |
N/A |
INTRINSIC |
|
BROMO
|
345 |
454 |
1.13e-47 |
SMART |
|
coiled coil region
|
486 |
537 |
N/A |
INTRINSIC |
|
low complexity region
|
542 |
560 |
N/A |
INTRINSIC |
|
low complexity region
|
583 |
593 |
N/A |
INTRINSIC |
|
Pfam:BET
|
639 |
703 |
7.4e-35 |
PFAM |
|
coiled coil region
|
721 |
750 |
N/A |
INTRINSIC |
|
low complexity region
|
772 |
797 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142570
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148143
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000151986
AA Change: Q79H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000117359
Gene: ENSMUSG00000024335
AA Change: Q79H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
29 |
N/A |
INTRINSIC |
|
BROMO
|
71 |
181 |
2.13e-43 |
SMART |
|
low complexity region
|
256 |
276 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
290 |
N/A |
INTRINSIC |
|
low complexity region
|
294 |
304 |
N/A |
INTRINSIC |
|
BROMO
|
345 |
454 |
1.13e-47 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000154232
AA Change: Q79H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000128835
Gene: ENSMUSG00000024335
AA Change: Q79H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
29 |
N/A |
INTRINSIC |
|
low complexity region
|
50 |
71 |
N/A |
INTRINSIC |
|
Blast:BROMO
|
72 |
110 |
4e-21 |
BLAST |
|
PDB:3AQA|C
|
72 |
110 |
2e-22 |
PDB |
|
SCOP:d1f68a_
|
76 |
103 |
1e-7 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177828
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000179687
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000179722
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155286
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173032
|
| SMART Domains |
Protein: ENSMUSP00000134608
Gene: ENSMUSG00000024335
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Bromodomain
|
1 |
43 |
1.4e-6 |
PFAM |
|
coiled coil region
|
73 |
124 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173204
|
| 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 transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]
PHENOTYPE: Mice homozygous for a null mutation display embryonic lethality during organogenesis with decreased embryo size, decreased cell proliferation, a delay in the cell cycle, and increased cell death. Heterozygous mice also display decreased cell proliferation. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(16) : Targeted, other(2) Gene trapped(14) |
| Other mutations in this stock |
Total: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2200002D01Rik |
C |
T |
7: 28,947,321 (GRCm39) |
|
probably null |
Het |
| Abcc9 |
A |
G |
6: 142,610,259 (GRCm39) |
V635A |
probably benign |
Het |
| Adgre1 |
T |
A |
17: 57,751,064 (GRCm39) |
Y579* |
probably null |
Het |
| Adgrg3 |
T |
C |
8: 95,766,053 (GRCm39) |
F295L |
probably benign |
Het |
| Arhgap42 |
A |
T |
9: 8,998,254 (GRCm39) |
|
probably benign |
Het |
| Capn15 |
A |
G |
17: 26,181,037 (GRCm39) |
S705P |
probably damaging |
Het |
| Cebpz |
T |
A |
17: 79,243,342 (GRCm39) |
D104V |
probably benign |
Het |
| Chl1 |
T |
C |
6: 103,626,534 (GRCm39) |
I94T |
probably damaging |
Het |
| Csf2rb |
C |
T |
15: 78,220,614 (GRCm39) |
A52V |
probably damaging |
Het |
| Ddx27 |
T |
C |
2: 166,870,309 (GRCm39) |
L459P |
probably damaging |
Het |
| Dhtkd1 |
T |
C |
2: 5,919,651 (GRCm39) |
T577A |
probably benign |
Het |
| Dync2h1 |
G |
A |
9: 7,081,077 (GRCm39) |
T2873I |
probably benign |
Het |
| Emg1 |
A |
G |
6: 124,688,984 (GRCm39) |
F8S |
possibly damaging |
Het |
| Fermt3 |
A |
G |
19: 6,979,143 (GRCm39) |
I553T |
probably damaging |
Het |
| Gaa |
A |
G |
11: 119,165,947 (GRCm39) |
D419G |
possibly damaging |
Het |
| Hdac10 |
T |
C |
15: 89,008,912 (GRCm39) |
|
probably benign |
Het |
| Hsf1 |
T |
A |
15: 76,381,037 (GRCm39) |
V122E |
possibly damaging |
Het |
| Lig3 |
C |
A |
11: 82,681,448 (GRCm39) |
T480K |
possibly damaging |
Het |
| Magi1 |
T |
C |
6: 93,769,381 (GRCm39) |
|
probably null |
Het |
| Mcm2 |
G |
T |
6: 88,863,044 (GRCm39) |
H683N |
probably damaging |
Het |
| Ncapg2 |
G |
T |
12: 116,390,331 (GRCm39) |
A427S |
probably damaging |
Het |
| Nkd1 |
T |
C |
8: 89,248,923 (GRCm39) |
F23L |
probably damaging |
Het |
| Or9i2 |
G |
A |
19: 13,816,225 (GRCm39) |
T104M |
probably damaging |
Het |
| Pcdhb5 |
T |
G |
18: 37,454,075 (GRCm39) |
S152A |
probably benign |
Het |
| Pdx1 |
A |
T |
5: 147,211,217 (GRCm39) |
E146V |
probably damaging |
Het |
| Qrsl1 |
T |
C |
10: 43,750,604 (GRCm39) |
T485A |
probably benign |
Het |
| Slc17a4 |
A |
G |
13: 24,089,516 (GRCm39) |
Y134H |
probably benign |
Het |
| Slc24a4 |
A |
T |
12: 102,185,219 (GRCm39) |
M110L |
possibly damaging |
Het |
| Tent5a |
A |
G |
9: 85,207,103 (GRCm39) |
C232R |
probably damaging |
Het |
| Tnni3k |
T |
A |
3: 154,645,263 (GRCm39) |
I541F |
possibly damaging |
Het |
| Uhrf2 |
T |
C |
19: 30,052,652 (GRCm39) |
V382A |
probably benign |
Het |
| Vac14 |
T |
A |
8: 111,345,523 (GRCm39) |
M1K |
probably null |
Het |
| Virma |
A |
G |
4: 11,528,672 (GRCm39) |
E1303G |
probably damaging |
Het |
| Xirp2 |
T |
C |
2: 67,356,411 (GRCm39) |
V3724A |
probably benign |
Het |
|
| Other mutations in Brd2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00432:Brd2
|
APN |
17 |
34,333,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01589:Brd2
|
APN |
17 |
34,336,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01724:Brd2
|
APN |
17 |
34,335,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02043:Brd2
|
APN |
17 |
34,331,590 (GRCm39) |
unclassified |
probably benign |
|
|
crater
|
UTSW |
17 |
34,332,233 (GRCm39) |
missense |
probably damaging |
0.96 |
|
FR4449:Brd2
|
UTSW |
17 |
34,335,310 (GRCm39) |
unclassified |
probably benign |
|
|
FR4548:Brd2
|
UTSW |
17 |
34,335,310 (GRCm39) |
unclassified |
probably benign |
|
|
R0085:Brd2
|
UTSW |
17 |
34,332,233 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0497:Brd2
|
UTSW |
17 |
34,333,334 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0879:Brd2
|
UTSW |
17 |
34,332,420 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1150:Brd2
|
UTSW |
17 |
34,332,981 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R1152:Brd2
|
UTSW |
17 |
34,332,981 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R1280:Brd2
|
UTSW |
17 |
34,333,124 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1426:Brd2
|
UTSW |
17 |
34,332,981 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R2247:Brd2
|
UTSW |
17 |
34,333,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3737:Brd2
|
UTSW |
17 |
34,336,054 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5286:Brd2
|
UTSW |
17 |
34,334,205 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5673:Brd2
|
UTSW |
17 |
34,331,581 (GRCm39) |
unclassified |
probably benign |
|
|
R6134:Brd2
|
UTSW |
17 |
34,332,669 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6318:Brd2
|
UTSW |
17 |
34,331,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7257:Brd2
|
UTSW |
17 |
34,332,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7493:Brd2
|
UTSW |
17 |
34,341,231 (GRCm39) |
unclassified |
probably benign |
|
|
R7888:Brd2
|
UTSW |
17 |
34,335,995 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7975:Brd2
|
UTSW |
17 |
34,334,424 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8762:Brd2
|
UTSW |
17 |
34,335,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8912:Brd2
|
UTSW |
17 |
34,332,458 (GRCm39) |
unclassified |
probably benign |
|
|
R9197:Brd2
|
UTSW |
17 |
34,333,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9430:Brd2
|
UTSW |
17 |
34,331,610 (GRCm39) |
missense |
unknown |
|
|
R9670:Brd2
|
UTSW |
17 |
34,334,205 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Z1176:Brd2
|
UTSW |
17 |
34,332,662 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
Z1177:Brd2
|
UTSW |
17 |
34,335,882 (GRCm39) |
unclassified |
probably benign |
|
|
Z1177:Brd2
|
UTSW |
17 |
34,335,881 (GRCm39) |
critical splice donor site |
probably null |
|
|
| Posted On |
2014-01-21 |
Incidental Mutation