Incidental Mutation 'IGL02421:Polb'
| ID |
292676 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Polb
|
| Ensembl Gene |
ENSMUSG00000031536 |
| Gene Name |
polymerase (DNA directed), beta |
| Synonyms |
A430088C08Rik, Pol beta |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02421
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
23118142-23143451 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 23130389 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Aspartic acid
at position 179
(G179D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000033938
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033938]
[ENSMUST00000210950]
|
| AlphaFold |
Q8K409 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000033938
AA Change: G179D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000033938
Gene: ENSMUSG00000031536
AA Change: G179D
| Domain | Start | End | E-Value | Type |
|---|
|
POLXc
|
10 |
334 |
4.58e-159 |
SMART |
|
HhH1
|
57 |
76 |
1.91e-1 |
SMART |
|
HhH1
|
98 |
117 |
1.14e1 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000181668
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000210950
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a DNA polymerase involved in base excision and repair, also called gap-filling DNA synthesis. The encoded protein, acting as a monomer, is normally found in the cytoplasm, but it translocates to the nucleus upon DNA damage. Several transcript variants of this gene exist, but the full-length nature of only one has been described to date. [provided by RefSeq, Sep 2011]
PHENOTYPE: Homozygotes for one knock-out allele die from E10.5 to birth and those for another one exhibit embryonic growth retardation, abnormal neurogenesis, and neonatal lethality due to respiratory failure. Hypomorphic allele mice develop systemic lupus erythematosus-like phentoypes. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| a |
T |
C |
2: 154,892,672 (GRCm39) |
F117S |
probably damaging |
Het |
| A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
| A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
| Acacb |
A |
G |
5: 114,361,939 (GRCm39) |
T1394A |
probably benign |
Het |
| Adam19 |
A |
G |
11: 46,028,380 (GRCm39) |
N671S |
probably damaging |
Het |
| Akap13 |
A |
T |
7: 75,367,554 (GRCm39) |
N1815I |
possibly damaging |
Het |
| Aloxe3 |
A |
G |
11: 69,020,872 (GRCm39) |
D199G |
possibly damaging |
Het |
| Ap1g2 |
G |
A |
14: 55,339,859 (GRCm39) |
A440V |
probably damaging |
Het |
| Bmt2 |
G |
T |
6: 13,628,841 (GRCm39) |
Q281K |
probably damaging |
Het |
| Celsr3 |
T |
C |
9: 108,717,662 (GRCm39) |
F2243L |
probably damaging |
Het |
| Cenpb |
G |
A |
2: 131,021,601 (GRCm39) |
R66C |
probably damaging |
Het |
| Chl1 |
A |
T |
6: 103,694,541 (GRCm39) |
H1121L |
probably damaging |
Het |
| Cpb1 |
T |
C |
3: 20,306,148 (GRCm39) |
Y344C |
probably damaging |
Het |
| Cspg5 |
T |
A |
9: 110,076,460 (GRCm39) |
|
probably benign |
Het |
| Dnah11 |
T |
C |
12: 118,150,637 (GRCm39) |
N374D |
probably damaging |
Het |
| Dnah3 |
A |
G |
7: 119,550,215 (GRCm39) |
V3368A |
possibly damaging |
Het |
| Eml4 |
T |
C |
17: 83,785,321 (GRCm39) |
S829P |
probably benign |
Het |
| Got2-ps1 |
T |
C |
5: 138,362,811 (GRCm39) |
|
noncoding transcript |
Het |
| Hal |
T |
C |
10: 93,339,335 (GRCm39) |
C475R |
probably damaging |
Het |
| Mapkbp1 |
C |
T |
2: 119,850,136 (GRCm39) |
P806S |
possibly damaging |
Het |
| Mmrn1 |
A |
T |
6: 60,921,806 (GRCm39) |
T88S |
probably benign |
Het |
| Napsa |
A |
G |
7: 44,234,479 (GRCm39) |
H237R |
probably damaging |
Het |
| Opn5 |
C |
T |
17: 42,907,446 (GRCm39) |
|
probably benign |
Het |
| Or1d2 |
T |
C |
11: 74,256,017 (GRCm39) |
I174T |
probably damaging |
Het |
| Or4c110 |
T |
C |
2: 88,831,688 (GRCm39) |
|
probably null |
Het |
| Or51f2 |
T |
C |
7: 102,526,966 (GRCm39) |
I213T |
probably damaging |
Het |
| Or56b2 |
A |
G |
7: 104,337,740 (GRCm39) |
N173D |
probably benign |
Het |
| Pira12 |
T |
C |
7: 3,899,994 (GRCm39) |
N203D |
possibly damaging |
Het |
| Primpol |
G |
T |
8: 47,060,830 (GRCm39) |
|
probably benign |
Het |
| Prom2 |
T |
A |
2: 127,373,802 (GRCm39) |
|
probably null |
Het |
| Psmb10 |
A |
G |
8: 106,664,124 (GRCm39) |
|
probably null |
Het |
| Ranbp2 |
T |
G |
10: 58,316,376 (GRCm39) |
S2365R |
probably damaging |
Het |
| Sgce |
G |
A |
6: 4,694,187 (GRCm39) |
|
probably benign |
Het |
| Slc25a34 |
A |
G |
4: 141,348,753 (GRCm39) |
V237A |
probably benign |
Het |
| Slc39a2 |
A |
T |
14: 52,131,329 (GRCm39) |
T25S |
probably benign |
Het |
| Smarca4 |
T |
C |
9: 21,550,535 (GRCm39) |
C423R |
probably damaging |
Het |
| Stt3b |
G |
A |
9: 115,080,920 (GRCm39) |
|
probably benign |
Het |
| Tbl1xr1 |
A |
T |
3: 22,257,327 (GRCm39) |
I397F |
probably damaging |
Het |
| Tie1 |
A |
G |
4: 118,343,591 (GRCm39) |
V117A |
probably damaging |
Het |
| Tmc3 |
T |
C |
7: 83,271,952 (GRCm39) |
F1035L |
probably benign |
Het |
| Trhde |
T |
A |
10: 114,248,366 (GRCm39) |
K944N |
probably damaging |
Het |
| Vmn1r54 |
G |
A |
6: 90,246,133 (GRCm39) |
A16T |
probably benign |
Het |
| Washc4 |
T |
A |
10: 83,415,414 (GRCm39) |
N801K |
probably damaging |
Het |
| Xylt2 |
A |
G |
11: 94,558,588 (GRCm39) |
Y523H |
possibly damaging |
Het |
| Znfx1 |
T |
C |
2: 166,902,000 (GRCm39) |
R5G |
probably damaging |
Het |
|
| Other mutations in Polb |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01455:Polb
|
APN |
8 |
23,143,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02618:Polb
|
APN |
8 |
23,127,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02850:Polb
|
APN |
8 |
23,138,277 (GRCm39) |
splice site |
probably benign |
|
|
IGL03143:Polb
|
APN |
8 |
23,130,367 (GRCm39) |
splice site |
probably benign |
|
|
IGL02796:Polb
|
UTSW |
8 |
23,121,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0280:Polb
|
UTSW |
8 |
23,130,408 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0383:Polb
|
UTSW |
8 |
23,130,011 (GRCm39) |
nonsense |
probably null |
|
|
R0788:Polb
|
UTSW |
8 |
23,132,354 (GRCm39) |
missense |
probably null |
|
|
R1374:Polb
|
UTSW |
8 |
23,143,073 (GRCm39) |
splice site |
probably benign |
|
|
R1564:Polb
|
UTSW |
8 |
23,120,357 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2194:Polb
|
UTSW |
8 |
23,137,483 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2295:Polb
|
UTSW |
8 |
23,143,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2314:Polb
|
UTSW |
8 |
23,130,018 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R4992:Polb
|
UTSW |
8 |
23,135,087 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5107:Polb
|
UTSW |
8 |
23,135,062 (GRCm39) |
splice site |
probably null |
|
|
R5474:Polb
|
UTSW |
8 |
23,120,386 (GRCm39) |
missense |
probably benign |
0.13 |
|
R5905:Polb
|
UTSW |
8 |
23,130,011 (GRCm39) |
nonsense |
probably null |
|
|
R5908:Polb
|
UTSW |
8 |
23,132,319 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6028:Polb
|
UTSW |
8 |
23,130,011 (GRCm39) |
nonsense |
probably null |
|
|
R6188:Polb
|
UTSW |
8 |
23,137,463 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7304:Polb
|
UTSW |
8 |
23,129,975 (GRCm39) |
missense |
probably benign |
|
|
R7644:Polb
|
UTSW |
8 |
23,130,443 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7766:Polb
|
UTSW |
8 |
23,143,107 (GRCm39) |
missense |
probably benign |
0.23 |
|
R8964:Polb
|
UTSW |
8 |
23,143,341 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9249:Polb
|
UTSW |
8 |
23,143,084 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9681:Polb
|
UTSW |
8 |
23,118,346 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Posted On |
2015-04-16 |
Incidental Mutation