Incidental Mutation 'IGL02037:Brf1'
| ID |
184574 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Brf1
|
| Ensembl Gene |
ENSMUSG00000011158 |
| Gene Name |
BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit |
| Synonyms |
2510002F24Rik, TFIIIB90, GTF3B, TAF3C, TAFIII90 |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.967)
|
| Stock # |
IGL02037
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
12 |
| Chromosomal Location |
112923705-112964324 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to G
at 112956682 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000011302
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000011302]
[ENSMUST00000011302]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000011302
|
| SMART Domains |
Protein: ENSMUSP00000011302
Gene: ENSMUSG00000011158
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TF_Zn_Ribbon
|
4 |
46 |
4.3e-17 |
PFAM |
|
CYCLIN
|
91 |
172 |
1.93e-12 |
SMART |
|
CYCLIN
|
185 |
269 |
1.22e-9 |
SMART |
|
coiled coil region
|
298 |
334 |
N/A |
INTRINSIC |
|
low complexity region
|
362 |
374 |
N/A |
INTRINSIC |
|
low complexity region
|
431 |
444 |
N/A |
INTRINSIC |
|
Pfam:BRF1
|
452 |
545 |
3.3e-29 |
PFAM |
|
low complexity region
|
638 |
650 |
N/A |
INTRINSIC |
|
low complexity region
|
662 |
675 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000011302
|
| SMART Domains |
Protein: ENSMUSP00000011302
Gene: ENSMUSG00000011158
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TF_Zn_Ribbon
|
4 |
46 |
4.3e-17 |
PFAM |
|
CYCLIN
|
91 |
172 |
1.93e-12 |
SMART |
|
CYCLIN
|
185 |
269 |
1.22e-9 |
SMART |
|
coiled coil region
|
298 |
334 |
N/A |
INTRINSIC |
|
low complexity region
|
362 |
374 |
N/A |
INTRINSIC |
|
low complexity region
|
431 |
444 |
N/A |
INTRINSIC |
|
Pfam:BRF1
|
452 |
545 |
3.3e-29 |
PFAM |
|
low complexity region
|
638 |
650 |
N/A |
INTRINSIC |
|
low complexity region
|
662 |
675 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000222247
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223037
|
| 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 one of the three subunits of the RNA polymerase III transcription factor complex. This complex plays a central role in transcription initiation by RNA polymerase III on genes encoding tRNA, 5S rRNA, and other small structural RNAs. The gene product belongs to the TF2B family. Several alternatively spliced variants encoding different isoforms, that function at different promoters transcribed by RNA polymerase III, have been identified. [provided by RefSeq, Jun 2011]
|
| Allele List at MGI |
All alleles(3) : Gene trapped(3) |
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A730049H05Rik |
T |
A |
6: 92,804,997 (GRCm39) |
|
probably benign |
Het |
| Ace2 |
T |
A |
X: 162,946,996 (GRCm39) |
V293D |
probably damaging |
Het |
| Adgrg6 |
T |
C |
10: 14,317,185 (GRCm39) |
Y545C |
probably damaging |
Het |
| Arhgap40 |
A |
G |
2: 158,376,742 (GRCm39) |
T293A |
probably damaging |
Het |
| Arhgef19 |
A |
G |
4: 140,973,707 (GRCm39) |
T65A |
probably damaging |
Het |
| Cbfb |
T |
C |
8: 105,905,252 (GRCm39) |
S65P |
possibly damaging |
Het |
| Chsy1 |
T |
C |
7: 65,821,576 (GRCm39) |
S604P |
possibly damaging |
Het |
| Ckmt1 |
T |
C |
2: 121,191,643 (GRCm39) |
V271A |
probably damaging |
Het |
| Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
| Csmd2 |
T |
C |
4: 128,371,263 (GRCm39) |
|
probably benign |
Het |
| D430041D05Rik |
A |
G |
2: 104,038,559 (GRCm39) |
|
probably benign |
Het |
| Dsg1c |
A |
G |
18: 20,410,007 (GRCm39) |
T492A |
probably benign |
Het |
| Fam3a |
G |
A |
X: 73,430,241 (GRCm39) |
T156I |
probably damaging |
Het |
| Fbn2 |
A |
T |
18: 58,229,087 (GRCm39) |
C708S |
probably damaging |
Het |
| Fgf5 |
G |
A |
5: 98,409,831 (GRCm39) |
G127R |
probably damaging |
Het |
| Fhip1a |
T |
G |
3: 85,637,939 (GRCm39) |
K120T |
probably damaging |
Het |
| Fn3k |
A |
T |
11: 121,325,909 (GRCm39) |
Y32F |
probably benign |
Het |
| Frem3 |
T |
C |
8: 81,338,118 (GRCm39) |
I137T |
probably benign |
Het |
| Hc |
T |
C |
2: 34,903,531 (GRCm39) |
D1041G |
probably benign |
Het |
| Heatr6 |
T |
A |
11: 83,655,708 (GRCm39) |
|
probably benign |
Het |
| Hivep1 |
G |
A |
13: 42,309,553 (GRCm39) |
A598T |
probably benign |
Het |
| Ifngr1 |
T |
C |
10: 19,483,007 (GRCm39) |
S254P |
probably benign |
Het |
| Kel |
T |
C |
6: 41,674,408 (GRCm39) |
S341G |
probably benign |
Het |
| Klra6 |
A |
C |
6: 129,990,439 (GRCm39) |
M224R |
probably benign |
Het |
| Mis18bp1 |
A |
G |
12: 65,183,522 (GRCm39) |
|
probably null |
Het |
| Mpeg1 |
C |
T |
19: 12,440,660 (GRCm39) |
T706I |
probably benign |
Het |
| Mrpl41 |
T |
C |
2: 24,864,429 (GRCm39) |
D81G |
possibly damaging |
Het |
| Or5al7 |
G |
T |
2: 85,993,181 (GRCm39) |
F37L |
probably benign |
Het |
| Palld |
T |
C |
8: 61,978,148 (GRCm39) |
R881G |
probably damaging |
Het |
| Pdha2 |
A |
T |
3: 140,916,662 (GRCm39) |
V282E |
probably damaging |
Het |
| Pga5 |
C |
T |
19: 10,654,065 (GRCm39) |
R46Q |
probably benign |
Het |
| Plekhg2 |
T |
C |
7: 28,068,122 (GRCm39) |
Y189C |
probably damaging |
Het |
| Rnf43 |
A |
G |
11: 87,622,479 (GRCm39) |
T527A |
probably benign |
Het |
| Rplp0 |
G |
A |
5: 115,699,174 (GRCm39) |
R73Q |
probably benign |
Het |
| Smco3 |
A |
G |
6: 136,808,197 (GRCm39) |
*226R |
probably null |
Het |
| Sugp2 |
T |
C |
8: 70,712,324 (GRCm39) |
|
probably benign |
Het |
| Tsga10 |
T |
C |
1: 37,846,098 (GRCm39) |
I343V |
probably benign |
Het |
| Ube2q2 |
A |
G |
9: 55,075,502 (GRCm39) |
K104E |
probably damaging |
Het |
| Ube3a |
C |
T |
7: 58,925,506 (GRCm39) |
|
probably benign |
Het |
| Usp11 |
T |
C |
X: 20,585,381 (GRCm39) |
I785T |
probably damaging |
Het |
| Vmn2r22 |
A |
T |
6: 123,626,026 (GRCm39) |
C137S |
probably damaging |
Het |
| Zfp281 |
T |
C |
1: 136,555,185 (GRCm39) |
V721A |
possibly damaging |
Het |
| Zfp946 |
T |
C |
17: 22,672,469 (GRCm39) |
S23P |
probably damaging |
Het |
| Zfyve1 |
A |
G |
12: 83,594,694 (GRCm39) |
V766A |
probably damaging |
Het |
|
| Other mutations in Brf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00928:Brf1
|
APN |
12 |
112,927,220 (GRCm39) |
splice site |
probably benign |
|
|
IGL01609:Brf1
|
APN |
12 |
112,927,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01610:Brf1
|
APN |
12 |
112,951,703 (GRCm39) |
missense |
probably benign |
|
|
IGL01622:Brf1
|
APN |
12 |
112,924,795 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01623:Brf1
|
APN |
12 |
112,924,795 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01791:Brf1
|
APN |
12 |
112,926,095 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02227:Brf1
|
APN |
12 |
112,925,394 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0106:Brf1
|
UTSW |
12 |
112,937,083 (GRCm39) |
unclassified |
probably benign |
|
|
R0106:Brf1
|
UTSW |
12 |
112,937,083 (GRCm39) |
unclassified |
probably benign |
|
|
R0138:Brf1
|
UTSW |
12 |
112,924,759 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1345:Brf1
|
UTSW |
12 |
112,924,728 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1370:Brf1
|
UTSW |
12 |
112,924,728 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1927:Brf1
|
UTSW |
12 |
112,963,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2423:Brf1
|
UTSW |
12 |
112,963,819 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3608:Brf1
|
UTSW |
12 |
112,924,894 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3703:Brf1
|
UTSW |
12 |
112,932,991 (GRCm39) |
splice site |
probably null |
|
|
R4033:Brf1
|
UTSW |
12 |
112,943,352 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4817:Brf1
|
UTSW |
12 |
112,935,921 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4897:Brf1
|
UTSW |
12 |
112,929,507 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4985:Brf1
|
UTSW |
12 |
112,932,990 (GRCm39) |
splice site |
probably null |
|
|
R5092:Brf1
|
UTSW |
12 |
112,943,352 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7138:Brf1
|
UTSW |
12 |
112,933,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7187:Brf1
|
UTSW |
12 |
112,923,945 (GRCm39) |
missense |
unknown |
|
|
R7726:Brf1
|
UTSW |
12 |
112,927,865 (GRCm39) |
missense |
probably benign |
|
|
R7970:Brf1
|
UTSW |
12 |
112,927,820 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8719:Brf1
|
UTSW |
12 |
112,943,304 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R8897:Brf1
|
UTSW |
12 |
112,951,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8967:Brf1
|
UTSW |
12 |
112,937,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9109:Brf1
|
UTSW |
12 |
112,927,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2014-05-07 |
Incidental Mutation