Incidental Mutation 'R4512:Parg'
| ID |
331281 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Parg
|
| Ensembl Gene |
ENSMUSG00000021911 |
| Gene Name |
poly (ADP-ribose) glycohydrolase |
| Synonyms |
|
| MMRRC Submission |
041587-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4512 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
31923906-32019507 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 31984693 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 241
(V241A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000132454
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022470]
[ENSMUST00000163350]
[ENSMUST00000170129]
[ENSMUST00000170840]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000022470
AA Change: V746A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000022470
Gene: ENSMUSG00000021911
AA Change: V746A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
190 |
204 |
N/A |
INTRINSIC |
|
low complexity region
|
286 |
298 |
N/A |
INTRINSIC |
|
Pfam:PARG_cat
|
574 |
902 |
2.5e-135 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000163350
AA Change: V746A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000131566
Gene: ENSMUSG00000021911
AA Change: V746A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
190 |
204 |
N/A |
INTRINSIC |
|
low complexity region
|
286 |
298 |
N/A |
INTRINSIC |
|
Pfam:PARG_cat
|
570 |
905 |
5.1e-134 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000163957
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000165950
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170129
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000170840
AA Change: V241A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000132454
Gene: ENSMUSG00000021911
AA Change: V241A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PARG_cat
|
117 |
452 |
9.7e-135 |
PFAM |
|
| Meta Mutation Damage Score |
0.5899 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.4%
|
| Validation Efficiency |
99% (67/68) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Poly(ADP-ribose) glycohydrolase (PARG) is the major enzyme responsible for the catabolism of poly(ADP-ribose), a reversible covalent-modifier of chromosomal proteins. The protein is found in many tissues and may be subject to proteolysis generating smaller, active products. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
PHENOTYPE: Mice homozygous for one allele of this gene are hypersensitive to alkylating agents and ionizing radiation and susceptible to streptozotocin induced diabetes and endotoxic shock. Mice homozygous for a second allele display embryonic lethality and fail tohatch from the zona pellucida. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 57 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb4 |
A |
T |
5: 8,978,573 (GRCm39) |
D573V |
probably damaging |
Het |
| Adgrg5 |
T |
C |
8: 95,660,652 (GRCm39) |
V93A |
possibly damaging |
Het |
| Akr1c20 |
A |
C |
13: 4,557,843 (GRCm39) |
V201G |
probably damaging |
Het |
| Alpk1 |
T |
C |
3: 127,478,120 (GRCm39) |
|
probably benign |
Het |
| Aopep |
A |
T |
13: 63,304,481 (GRCm39) |
T497S |
probably damaging |
Het |
| Atp6v1h |
T |
C |
1: 5,168,358 (GRCm39) |
|
probably null |
Het |
| Aup1 |
C |
T |
6: 83,033,368 (GRCm39) |
R248* |
probably null |
Het |
| BC016579 |
C |
A |
16: 45,453,363 (GRCm39) |
A151S |
possibly damaging |
Het |
| Cenpn |
A |
G |
8: 117,660,135 (GRCm39) |
Y68C |
probably damaging |
Het |
| Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
| Chsy3 |
A |
G |
18: 59,543,259 (GRCm39) |
D799G |
probably damaging |
Het |
| Dnah6 |
G |
A |
6: 73,155,399 (GRCm39) |
R739W |
probably damaging |
Het |
| Dync2h1 |
A |
T |
9: 7,085,009 (GRCm39) |
C553* |
probably null |
Het |
| Fhl4 |
A |
G |
10: 84,934,578 (GRCm39) |
S68P |
possibly damaging |
Het |
| Gcc1 |
T |
C |
6: 28,419,208 (GRCm39) |
E375G |
probably benign |
Het |
| Gm10110 |
A |
G |
14: 90,135,151 (GRCm39) |
|
noncoding transcript |
Het |
| Hspbap1 |
C |
T |
16: 35,607,611 (GRCm39) |
S39F |
probably damaging |
Het |
| Lmln |
G |
A |
16: 32,908,507 (GRCm39) |
R311Q |
probably benign |
Het |
| Ly6e |
T |
A |
15: 74,829,682 (GRCm39) |
V24D |
probably damaging |
Het |
| Magi3 |
T |
C |
3: 103,996,871 (GRCm39) |
T225A |
probably damaging |
Het |
| Mark1 |
C |
A |
1: 184,639,286 (GRCm39) |
R577L |
probably benign |
Het |
| Mlxip |
G |
T |
5: 123,533,128 (GRCm39) |
V46L |
probably benign |
Het |
| Mrpl40 |
T |
C |
16: 18,691,308 (GRCm39) |
D134G |
probably benign |
Het |
| Naip6 |
C |
T |
13: 100,437,108 (GRCm39) |
A472T |
probably benign |
Het |
| Nalcn |
T |
C |
14: 123,532,860 (GRCm39) |
Y1300C |
probably damaging |
Het |
| Nav3 |
T |
C |
10: 109,529,943 (GRCm39) |
I2133V |
possibly damaging |
Het |
| Ndst3 |
T |
C |
3: 123,465,315 (GRCm39) |
D219G |
probably damaging |
Het |
| Nfkbie |
C |
T |
17: 45,867,165 (GRCm39) |
S100L |
probably benign |
Het |
| Oard1 |
A |
G |
17: 48,723,788 (GRCm39) |
I145V |
probably benign |
Het |
| Odf2 |
C |
T |
2: 29,816,109 (GRCm39) |
|
probably null |
Het |
| Oplah |
A |
G |
15: 76,182,155 (GRCm39) |
L1035P |
probably damaging |
Het |
| Or4n4b |
C |
A |
14: 50,536,453 (GRCm39) |
L104F |
probably damaging |
Het |
| Or51t4 |
T |
C |
7: 102,597,945 (GRCm39) |
L81P |
probably damaging |
Het |
| Or5m3b |
T |
C |
2: 85,871,913 (GRCm39) |
S85P |
probably damaging |
Het |
| Otud7a |
T |
C |
7: 63,379,625 (GRCm39) |
F284L |
probably benign |
Het |
| Pla2g4a |
T |
A |
1: 149,736,802 (GRCm39) |
|
probably null |
Het |
| Psd4 |
C |
T |
2: 24,292,901 (GRCm39) |
R684C |
probably damaging |
Het |
| Pttg1ip |
T |
C |
10: 77,432,902 (GRCm39) |
|
probably benign |
Het |
| R3hcc1 |
A |
G |
14: 69,936,060 (GRCm39) |
S250P |
probably damaging |
Het |
| Rere |
T |
A |
4: 150,561,909 (GRCm39) |
Y272N |
unknown |
Het |
| Selplg |
A |
G |
5: 113,957,124 (GRCm39) |
V394A |
probably benign |
Het |
| Senp7 |
T |
G |
16: 55,986,246 (GRCm39) |
F559V |
probably damaging |
Het |
| Slc16a7 |
T |
G |
10: 125,069,308 (GRCm39) |
|
probably null |
Het |
| Smim3 |
A |
T |
18: 60,608,556 (GRCm39) |
V32D |
probably damaging |
Het |
| Spsb3 |
A |
G |
17: 25,109,270 (GRCm39) |
D47G |
probably damaging |
Het |
| St6gal2 |
A |
T |
17: 55,790,018 (GRCm39) |
N351Y |
probably benign |
Het |
| Stk11 |
T |
C |
10: 79,962,211 (GRCm39) |
|
probably benign |
Het |
| Susd1 |
A |
T |
4: 59,329,491 (GRCm39) |
L646Q |
possibly damaging |
Het |
| Tmprss11a |
A |
G |
5: 86,576,437 (GRCm39) |
V138A |
probably benign |
Het |
| Ttn |
C |
A |
2: 76,728,969 (GRCm39) |
|
probably benign |
Het |
| Ttn |
T |
C |
2: 76,580,814 (GRCm39) |
K15033E |
probably damaging |
Het |
| Tyrp1 |
G |
T |
4: 80,755,749 (GRCm39) |
D173Y |
probably damaging |
Het |
| Uncx |
A |
G |
5: 139,532,522 (GRCm39) |
I196V |
possibly damaging |
Het |
| Vamp4 |
A |
T |
1: 162,405,457 (GRCm39) |
D28V |
possibly damaging |
Het |
| Vmn2r78 |
C |
T |
7: 86,569,452 (GRCm39) |
S115F |
probably benign |
Het |
| Zeb1 |
G |
A |
18: 5,759,007 (GRCm39) |
C138Y |
probably damaging |
Het |
| Zfp985 |
G |
A |
4: 147,668,020 (GRCm39) |
C296Y |
probably damaging |
Het |
|
| Other mutations in Parg |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01324:Parg
|
APN |
14 |
32,018,142 (GRCm39) |
splice site |
probably benign |
|
|
IGL01879:Parg
|
APN |
14 |
31,993,579 (GRCm39) |
splice site |
probably benign |
|
|
IGL02391:Parg
|
APN |
14 |
31,984,638 (GRCm39) |
splice site |
probably null |
|
|
IGL02451:Parg
|
APN |
14 |
31,964,186 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02598:Parg
|
APN |
14 |
31,936,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02899:Parg
|
APN |
14 |
31,960,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0112:Parg
|
UTSW |
14 |
31,924,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0167:Parg
|
UTSW |
14 |
31,939,693 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0514:Parg
|
UTSW |
14 |
31,976,517 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0834:Parg
|
UTSW |
14 |
31,936,511 (GRCm39) |
splice site |
probably benign |
|
|
R1140:Parg
|
UTSW |
14 |
32,018,200 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1480:Parg
|
UTSW |
14 |
31,931,585 (GRCm39) |
nonsense |
probably null |
|
|
R1611:Parg
|
UTSW |
14 |
31,960,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1912:Parg
|
UTSW |
14 |
31,932,497 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1916:Parg
|
UTSW |
14 |
31,930,184 (GRCm39) |
splice site |
probably benign |
|
|
R1983:Parg
|
UTSW |
14 |
31,939,653 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2007:Parg
|
UTSW |
14 |
31,932,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R2275:Parg
|
UTSW |
14 |
32,017,195 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2942:Parg
|
UTSW |
14 |
31,931,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4206:Parg
|
UTSW |
14 |
31,976,493 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4482:Parg
|
UTSW |
14 |
31,984,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4519:Parg
|
UTSW |
14 |
31,931,592 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4611:Parg
|
UTSW |
14 |
31,996,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4831:Parg
|
UTSW |
14 |
31,924,408 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4876:Parg
|
UTSW |
14 |
31,993,625 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5298:Parg
|
UTSW |
14 |
31,924,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5606:Parg
|
UTSW |
14 |
31,984,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5782:Parg
|
UTSW |
14 |
31,996,862 (GRCm39) |
nonsense |
probably null |
|
|
R5878:Parg
|
UTSW |
14 |
31,939,619 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6373:Parg
|
UTSW |
14 |
31,931,454 (GRCm39) |
splice site |
probably null |
|
|
R6436:Parg
|
UTSW |
14 |
31,993,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6530:Parg
|
UTSW |
14 |
31,931,156 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7285:Parg
|
UTSW |
14 |
31,932,465 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7348:Parg
|
UTSW |
14 |
31,972,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7455:Parg
|
UTSW |
14 |
31,931,432 (GRCm39) |
missense |
probably benign |
|
|
R7780:Parg
|
UTSW |
14 |
31,930,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7887:Parg
|
UTSW |
14 |
31,939,619 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7968:Parg
|
UTSW |
14 |
31,936,327 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R8153:Parg
|
UTSW |
14 |
31,984,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8494:Parg
|
UTSW |
14 |
31,930,978 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8717:Parg
|
UTSW |
14 |
31,932,492 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8781:Parg
|
UTSW |
14 |
31,936,400 (GRCm39) |
missense |
probably benign |
0.33 |
|
R8826:Parg
|
UTSW |
14 |
31,931,175 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R9357:Parg
|
UTSW |
14 |
31,996,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9423:Parg
|
UTSW |
14 |
31,939,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9617:Parg
|
UTSW |
14 |
31,960,569 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9662:Parg
|
UTSW |
14 |
31,971,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9666:Parg
|
UTSW |
14 |
31,964,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAGCAACTGTGGTCACTCCTTAG -3'
(R):5'- AGGGTCTAATGCCCATTGAAG -3'
Sequencing Primer
(F):5'- GTCACTCCTTAGGAAAATTTGGGAGC -3'
(R):5'- AAACACCTTGTCTGGGCAG -3'
|
| Posted On |
2015-07-21 |
Incidental Mutation