Incidental Mutation 'R7042:Pax6'
| ID |
547098 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pax6
|
| Ensembl Gene |
ENSMUSG00000027168 |
| Gene Name |
paired box 6 |
| Synonyms |
Pax-6, Dickie's small eye, Gsfaey11, 1500038E17Rik, Dey, AEY11 |
| MMRRC Submission |
045141-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7042 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
105499245-105527709 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 105526718 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Leucine
at position 208
(H208L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000106717
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090391]
[ENSMUST00000090397]
[ENSMUST00000111082]
[ENSMUST00000111083]
[ENSMUST00000111085]
[ENSMUST00000111086]
[ENSMUST00000111087]
[ENSMUST00000111088]
[ENSMUST00000122965]
[ENSMUST00000167211]
|
| AlphaFold |
P63015 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090391
|
| SMART Domains |
Protein: ENSMUSP00000087870
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
142 |
7.36e-86 |
SMART |
|
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
|
HOX
|
224 |
286 |
4.93e-26 |
SMART |
|
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
|
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
|
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090397
|
| SMART Domains |
Protein: ENSMUSP00000087878
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
128 |
6.11e-92 |
SMART |
|
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
|
HOX
|
210 |
272 |
4.93e-26 |
SMART |
|
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
|
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111082
|
| SMART Domains |
Protein: ENSMUSP00000106711
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
128 |
6.11e-92 |
SMART |
|
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
|
HOX
|
210 |
272 |
4.93e-26 |
SMART |
|
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
|
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111083
|
| SMART Domains |
Protein: ENSMUSP00000106712
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
128 |
6.11e-92 |
SMART |
|
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
|
HOX
|
210 |
272 |
4.93e-26 |
SMART |
|
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
|
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111085
|
| SMART Domains |
Protein: ENSMUSP00000106714
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
142 |
7.36e-86 |
SMART |
|
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
|
HOX
|
224 |
286 |
4.93e-26 |
SMART |
|
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
|
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
|
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111086
|
| SMART Domains |
Protein: ENSMUSP00000106715
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
142 |
7.36e-86 |
SMART |
|
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
|
HOX
|
224 |
286 |
4.93e-26 |
SMART |
|
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
|
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
|
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111087
|
| SMART Domains |
Protein: ENSMUSP00000106716
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
128 |
6.11e-92 |
SMART |
|
low complexity region
|
174 |
185 |
N/A |
INTRINSIC |
|
HOX
|
210 |
272 |
4.93e-26 |
SMART |
|
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
|
low complexity region
|
387 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
398 |
412 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111088
AA Change: H208L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000106717
Gene: ENSMUSG00000027168
AA Change: H208L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
17 |
N/A |
INTRINSIC |
|
HOX
|
39 |
101 |
4.93e-26 |
SMART |
|
low complexity region
|
110 |
123 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122965
|
| SMART Domains |
Protein: ENSMUSP00000116575
Gene: ENSMUSG00000027167
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PAXNEB
|
28 |
422 |
4e-123 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000167211
|
| SMART Domains |
Protein: ENSMUSP00000129344
Gene: ENSMUSG00000027168
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
142 |
7.36e-86 |
SMART |
|
low complexity region
|
188 |
199 |
N/A |
INTRINSIC |
|
HOX
|
224 |
286 |
4.93e-26 |
SMART |
|
low complexity region
|
295 |
308 |
N/A |
INTRINSIC |
|
low complexity region
|
401 |
409 |
N/A |
INTRINSIC |
|
low complexity region
|
412 |
426 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
100% (54/54) |
| MGI Phenotype |
FUNCTION: This gene encodes a homeobox-containing protein that functions as a regulator of transcription. It plays a key role in the development of neural tissues, particularly the eye. Activity of this protein is also required for expression of glucagon in the pancreas. This gene is regulated by multiple enhancers located up to tens or hundreds of kilobases upstream and downstream of the transcription start sites. Mutations in this gene or deletion of these regulatory elements results in severe defects in eye development. Alternative splicing and the use of alternative promoters results in multiple transcript variants, some of which encode proteins that lack the N-terminal paired domain. [provided by RefSeq, Jul 2015]
PHENOTYPE: Null and hypomorphic mutants show a range of phenotypes from viable with small eyes and lens/cornea fusion to microphthalmia and cataract to embryonic or perinatal lethality with anophthalmia and severe craniofacial and forebrain defects. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 55 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acsbg3 |
A |
G |
17: 57,192,098 (GRCm39) |
S554G |
possibly damaging |
Het |
| Adcy7 |
G |
T |
8: 89,042,378 (GRCm39) |
R415L |
probably damaging |
Het |
| Aox1 |
A |
T |
1: 58,141,759 (GRCm39) |
I1182F |
probably damaging |
Het |
| Ccdc7b |
T |
A |
8: 129,811,730 (GRCm39) |
Y147N |
probably benign |
Het |
| Clcnka |
A |
G |
4: 141,118,691 (GRCm39) |
I398T |
probably damaging |
Het |
| Cst8 |
T |
A |
2: 148,641,796 (GRCm39) |
|
probably null |
Het |
| Dcxr |
T |
C |
11: 120,617,841 (GRCm39) |
D45G |
possibly damaging |
Het |
| Dhx38 |
A |
T |
8: 110,283,617 (GRCm39) |
M510K |
possibly damaging |
Het |
| Dync2i1 |
T |
C |
12: 116,218,061 (GRCm39) |
I182M |
probably benign |
Het |
| Ebf1 |
T |
A |
11: 44,882,338 (GRCm39) |
H431Q |
probably damaging |
Het |
| Eml4 |
T |
C |
17: 83,768,999 (GRCm39) |
I681T |
probably damaging |
Het |
| Etf1 |
T |
C |
18: 35,043,219 (GRCm39) |
N164S |
probably benign |
Het |
| Fmo2 |
A |
G |
1: 162,708,226 (GRCm39) |
V303A |
probably damaging |
Het |
| Foxl2 |
T |
A |
9: 98,837,715 (GRCm39) |
M1K |
probably null |
Het |
| Gm3404 |
A |
T |
5: 146,462,969 (GRCm39) |
E50D |
probably benign |
Het |
| Gpr61 |
G |
A |
3: 108,058,647 (GRCm39) |
P5S |
possibly damaging |
Het |
| Hcrtr1 |
A |
G |
4: 130,024,653 (GRCm39) |
|
probably benign |
Het |
| Ier3ip1 |
T |
A |
18: 77,017,828 (GRCm39) |
F3I |
possibly damaging |
Het |
| Ifi206 |
G |
A |
1: 173,308,808 (GRCm39) |
P396L |
|
Het |
| Ifi209 |
G |
A |
1: 173,470,236 (GRCm39) |
V275I |
probably benign |
Het |
| Ighv1-69 |
T |
C |
12: 115,586,909 (GRCm39) |
S75G |
probably benign |
Het |
| Kcnj3 |
A |
T |
2: 55,484,877 (GRCm39) |
H325L |
possibly damaging |
Het |
| Klrk1 |
A |
T |
6: 129,593,734 (GRCm39) |
S50T |
possibly damaging |
Het |
| Mfsd4b4 |
T |
A |
10: 39,768,514 (GRCm39) |
Y193F |
probably damaging |
Het |
| Nlrp5 |
A |
G |
7: 23,116,905 (GRCm39) |
I210V |
possibly damaging |
Het |
| Or4p20 |
T |
A |
2: 88,253,746 (GRCm39) |
I208F |
possibly damaging |
Het |
| Or5w12 |
A |
T |
2: 87,501,935 (GRCm39) |
Y259N |
possibly damaging |
Het |
| Or8b3 |
G |
T |
9: 38,314,196 (GRCm39) |
G6C |
probably damaging |
Het |
| Or8d23 |
A |
G |
9: 38,841,622 (GRCm39) |
S52G |
possibly damaging |
Het |
| Pgc |
C |
A |
17: 48,044,745 (GRCm39) |
Q331K |
probably benign |
Het |
| Phldb1 |
A |
G |
9: 44,605,721 (GRCm39) |
S370P |
probably damaging |
Het |
| Pi4k2a |
T |
C |
19: 42,093,337 (GRCm39) |
I226T |
probably benign |
Het |
| Pick1 |
T |
C |
15: 79,132,965 (GRCm39) |
S342P |
probably damaging |
Het |
| Plscr1 |
A |
G |
9: 92,153,588 (GRCm39) |
M312V |
probably damaging |
Het |
| Ppp3cc |
T |
G |
14: 70,462,468 (GRCm39) |
K399Q |
probably benign |
Het |
| Qpctl |
T |
C |
7: 18,880,943 (GRCm39) |
H163R |
probably benign |
Het |
| Rab11fip5 |
A |
G |
6: 85,351,110 (GRCm39) |
V134A |
possibly damaging |
Het |
| Rasal1 |
T |
A |
5: 120,802,025 (GRCm39) |
|
probably null |
Het |
| Rem2 |
T |
A |
14: 54,715,548 (GRCm39) |
I171N |
probably damaging |
Het |
| Sec22a |
T |
A |
16: 35,149,885 (GRCm39) |
I214L |
probably benign |
Het |
| Setbp1 |
T |
C |
18: 79,130,070 (GRCm39) |
D54G |
probably damaging |
Het |
| Slc27a2 |
C |
T |
2: 126,409,700 (GRCm39) |
A294V |
probably damaging |
Het |
| Slfn14 |
T |
A |
11: 83,167,430 (GRCm39) |
D695V |
probably damaging |
Het |
| Smc6 |
T |
A |
12: 11,359,301 (GRCm39) |
I975K |
probably damaging |
Het |
| Spice1 |
T |
C |
16: 44,206,043 (GRCm39) |
F835L |
probably benign |
Het |
| Tars2 |
A |
T |
3: 95,658,057 (GRCm39) |
H222Q |
probably benign |
Het |
| Tmtc2 |
A |
T |
10: 105,206,477 (GRCm39) |
F273I |
probably damaging |
Het |
| Ttc39d |
C |
A |
17: 80,523,891 (GRCm39) |
D183E |
probably benign |
Het |
| Vasp |
A |
G |
7: 18,995,946 (GRCm39) |
S128P |
probably benign |
Het |
| Vcpip1 |
A |
G |
1: 9,818,378 (GRCm39) |
S2P |
unknown |
Het |
| Vmn2r98 |
T |
C |
17: 19,301,184 (GRCm39) |
Y729H |
probably benign |
Het |
| Wdr18 |
A |
T |
10: 79,801,944 (GRCm39) |
D243V |
probably benign |
Het |
| Xirp2 |
T |
C |
2: 67,343,633 (GRCm39) |
V1958A |
probably benign |
Het |
| Zfp451 |
A |
T |
1: 33,816,474 (GRCm39) |
M492K |
probably damaging |
Het |
| Zfp804b |
A |
G |
5: 6,820,042 (GRCm39) |
I1007T |
probably benign |
Het |
|
| Other mutations in Pax6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02008:Pax6
|
APN |
2 |
105,522,623 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02256:Pax6
|
APN |
2 |
105,515,115 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL02500:Pax6
|
APN |
2 |
105,523,115 (GRCm39) |
missense |
probably benign |
0.13 |
|
beady
|
UTSW |
2 |
105,522,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|
red_hots
|
UTSW |
2 |
105,525,705 (GRCm39) |
missense |
probably benign |
0.00 |
|
G1citation:Pax6
|
UTSW |
2 |
105,516,268 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1067:Pax6
|
UTSW |
2 |
105,510,646 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1213:Pax6
|
UTSW |
2 |
105,516,258 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1494:Pax6
|
UTSW |
2 |
105,521,955 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1633:Pax6
|
UTSW |
2 |
105,522,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2291:Pax6
|
UTSW |
2 |
105,516,228 (GRCm39) |
missense |
probably benign |
0.09 |
|
R3834:Pax6
|
UTSW |
2 |
105,526,795 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3835:Pax6
|
UTSW |
2 |
105,526,795 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4665:Pax6
|
UTSW |
2 |
105,514,343 (GRCm39) |
intron |
probably benign |
|
|
R4714:Pax6
|
UTSW |
2 |
105,525,745 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R4747:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
|
R4764:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
|
R4767:Pax6
|
UTSW |
2 |
105,525,705 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4771:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
|
R4772:Pax6
|
UTSW |
2 |
105,526,847 (GRCm39) |
missense |
probably benign |
|
|
R4816:Pax6
|
UTSW |
2 |
105,514,129 (GRCm39) |
intron |
probably benign |
|
|
R4819:Pax6
|
UTSW |
2 |
105,522,622 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5418:Pax6
|
UTSW |
2 |
105,521,910 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5683:Pax6
|
UTSW |
2 |
105,516,252 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6041:Pax6
|
UTSW |
2 |
105,514,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6263:Pax6
|
UTSW |
2 |
105,523,199 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6651:Pax6
|
UTSW |
2 |
105,516,175 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6822:Pax6
|
UTSW |
2 |
105,516,268 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7088:Pax6
|
UTSW |
2 |
105,526,753 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7102:Pax6
|
UTSW |
2 |
105,522,604 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7294:Pax6
|
UTSW |
2 |
105,515,246 (GRCm39) |
nonsense |
probably null |
|
|
R7761:Pax6
|
UTSW |
2 |
105,522,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7948:Pax6
|
UTSW |
2 |
105,516,222 (GRCm39) |
missense |
probably benign |
|
|
R8882:Pax6
|
UTSW |
2 |
105,521,963 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R9151:Pax6
|
UTSW |
2 |
105,523,097 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9796:Pax6
|
UTSW |
2 |
105,522,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Pax6
|
UTSW |
2 |
105,516,161 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTAGAATCTACCTATGCGGATGG -3'
(R):5'- TTGTTCCAACTGATACCGTGC -3'
Sequencing Primer
(F):5'- AATTTTAGAAAGTCTGTGTGTTCGC -3'
(R):5'- TGCCTTCTGTACGCAAAGG -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation