Incidental Mutation 'R4097:Nrf1'
| ID |
317166 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Nrf1
|
| Ensembl Gene |
ENSMUSG00000058440 |
| Gene Name |
nuclear respiratory factor 1 |
| Synonyms |
D6Ertd415e |
| MMRRC Submission |
040984-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4097 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
30047987-30153457 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 30151671 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 503
(Q503*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000130108
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000115208]
[ENSMUST00000115209]
[ENSMUST00000115211]
[ENSMUST00000115212]
[ENSMUST00000167972]
|
| AlphaFold |
Q9WU00 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115208
|
| SMART Domains |
Protein: ENSMUSP00000110863
Gene: ENSMUSG00000058440
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
39 |
57 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_DNA-bind
|
75 |
285 |
1.6e-132 |
PFAM |
|
low complexity region
|
377 |
394 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
423 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115209
AA Change: Q503*
|
| SMART Domains |
Protein: ENSMUSP00000110864
Gene: ENSMUSG00000058440
AA Change: Q503*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
39 |
57 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_DNA-bind
|
75 |
285 |
2.9e-132 |
PFAM |
|
low complexity region
|
377 |
394 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
423 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_activ_bdg
|
449 |
503 |
1.2e-9 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115211
AA Change: Q503*
|
| SMART Domains |
Protein: ENSMUSP00000110866
Gene: ENSMUSG00000058440
AA Change: Q503*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
39 |
57 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_DNA-bind
|
75 |
285 |
2.9e-132 |
PFAM |
|
low complexity region
|
377 |
394 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
423 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_activ_bdg
|
449 |
503 |
1.2e-9 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115212
AA Change: Q503*
|
| SMART Domains |
Protein: ENSMUSP00000110867
Gene: ENSMUSG00000058440
AA Change: Q503*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
39 |
57 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_DNA-bind
|
75 |
285 |
2.9e-132 |
PFAM |
|
low complexity region
|
377 |
394 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
423 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_activ_bdg
|
449 |
503 |
1.2e-9 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000167972
AA Change: Q503*
|
| SMART Domains |
Protein: ENSMUSP00000130108
Gene: ENSMUSG00000058440
AA Change: Q503*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
39 |
57 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_DNA-bind
|
75 |
285 |
2.9e-132 |
PFAM |
|
low complexity region
|
377 |
394 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
423 |
N/A |
INTRINSIC |
|
Pfam:Nrf1_activ_bdg
|
449 |
503 |
1.2e-9 |
PFAM |
|
| Meta Mutation Damage Score |
0.9754 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.5%
- 20x: 96.1%
|
| Validation Efficiency |
100% (48/48) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that homodimerizes and functions as a transcription factor which activates the expression of some key metabolic genes regulating cellular growth and nuclear genes required for respiration, heme biosynthesis, and mitochondrial DNA transcription and replication. The protein has also been associated with the regulation of neurite outgrowth. Alternative splicing results in multiple transcript variants. Confusion has occurred in bibliographic databases due to the shared symbol of NRF1 for this gene and for "nuclear factor (erythroid-derived 2)-like 1" which has an official symbol of NFE2L1. [provided by RefSeq, May 2014]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit early embryonic lethality between E3.5 and E6.5 associated with decreased cellular proliferation and mitochondrial DNA content. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aldh1l2 |
A |
G |
10: 83,348,228 (GRCm39) |
F292L |
probably damaging |
Het |
| Ankrd36 |
A |
G |
11: 5,578,703 (GRCm39) |
D664G |
possibly damaging |
Het |
| Bbs1 |
T |
A |
19: 4,947,345 (GRCm39) |
Y358F |
probably damaging |
Het |
| Becn1 |
C |
T |
11: 101,185,092 (GRCm39) |
|
probably benign |
Het |
| Cenpp |
A |
T |
13: 49,647,265 (GRCm39) |
N47I |
possibly damaging |
Het |
| Clec4n |
A |
T |
6: 123,207,700 (GRCm39) |
H55L |
possibly damaging |
Het |
| Cntnap4 |
A |
G |
8: 113,478,939 (GRCm39) |
I222V |
probably benign |
Het |
| Cttnbp2 |
T |
C |
6: 18,420,871 (GRCm39) |
E370G |
probably benign |
Het |
| Cyp4a10 |
T |
A |
4: 115,386,480 (GRCm39) |
V413E |
probably damaging |
Het |
| Dctn2 |
C |
T |
10: 127,113,362 (GRCm39) |
L249F |
probably damaging |
Het |
| Dnah9 |
T |
C |
11: 65,881,285 (GRCm39) |
S146G |
probably damaging |
Het |
| Dzip3 |
A |
T |
16: 48,778,852 (GRCm39) |
L315* |
probably null |
Het |
| Evpl |
T |
C |
11: 116,114,003 (GRCm39) |
E1229G |
possibly damaging |
Het |
| Ice2 |
T |
C |
9: 69,328,953 (GRCm39) |
V775A |
possibly damaging |
Het |
| Jmjd1c |
A |
G |
10: 67,054,787 (GRCm39) |
E69G |
probably benign |
Het |
| Lrrc66 |
T |
A |
5: 73,765,047 (GRCm39) |
R665S |
possibly damaging |
Het |
| Mpdz |
T |
A |
4: 81,253,937 (GRCm39) |
H1065L |
probably damaging |
Het |
| Nt5dc3 |
G |
A |
10: 86,669,820 (GRCm39) |
A472T |
probably benign |
Het |
| Oprk1 |
T |
A |
1: 5,673,034 (GRCm39) |
|
probably benign |
Het |
| Or7g17 |
T |
C |
9: 18,767,933 (GRCm39) |
I4T |
probably benign |
Het |
| Or9g3 |
T |
C |
2: 85,590,040 (GRCm39) |
I227V |
possibly damaging |
Het |
| Pramel6 |
T |
G |
2: 87,339,697 (GRCm39) |
F154V |
probably benign |
Het |
| Ralb |
T |
C |
1: 119,411,228 (GRCm39) |
D37G |
probably benign |
Het |
| Ranbp9 |
A |
T |
13: 43,574,733 (GRCm39) |
Y412N |
probably damaging |
Het |
| Scg2 |
T |
A |
1: 79,413,538 (GRCm39) |
D395V |
probably damaging |
Het |
| Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
| Serpine3 |
T |
A |
14: 62,908,395 (GRCm39) |
L141Q |
probably damaging |
Het |
| Sgpl1 |
C |
T |
10: 60,939,017 (GRCm39) |
G394D |
probably damaging |
Het |
| Sh3pxd2a |
T |
C |
19: 47,412,951 (GRCm39) |
Y44C |
probably damaging |
Het |
| Slc6a20b |
A |
G |
9: 123,441,822 (GRCm39) |
|
probably benign |
Het |
| Snapc5 |
T |
C |
9: 64,087,809 (GRCm39) |
I40T |
probably damaging |
Het |
| Spopl |
T |
C |
2: 23,401,413 (GRCm39) |
H365R |
probably benign |
Het |
| Stil |
T |
A |
4: 114,880,797 (GRCm39) |
I447N |
probably benign |
Het |
| Taf3 |
C |
A |
2: 9,957,178 (GRCm39) |
V330F |
possibly damaging |
Het |
| Tgoln1 |
T |
C |
6: 72,592,784 (GRCm39) |
E232G |
probably damaging |
Het |
| Thrap3 |
A |
G |
4: 126,065,595 (GRCm39) |
L729P |
probably damaging |
Het |
| Tmem269 |
A |
T |
4: 119,062,977 (GRCm39) |
F220Y |
probably damaging |
Het |
| Tnrc18 |
ATCTTCC |
A |
5: 142,759,561 (GRCm39) |
|
probably benign |
Het |
| Ubxn6 |
T |
C |
17: 56,376,712 (GRCm39) |
T227A |
probably benign |
Het |
| Wdr17 |
C |
A |
8: 55,088,504 (GRCm39) |
R1182I |
probably damaging |
Het |
| Wdr26 |
T |
C |
1: 181,010,352 (GRCm39) |
I550V |
probably benign |
Het |
| Wdr43 |
A |
G |
17: 71,964,532 (GRCm39) |
N637S |
probably benign |
Het |
| Zfp516 |
A |
G |
18: 83,005,381 (GRCm39) |
T762A |
possibly damaging |
Het |
|
| Other mutations in Nrf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00906:Nrf1
|
APN |
6 |
30,098,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00909:Nrf1
|
APN |
6 |
30,098,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01556:Nrf1
|
APN |
6 |
30,126,366 (GRCm39) |
intron |
probably benign |
|
|
IGL02371:Nrf1
|
APN |
6 |
30,118,990 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL03345:Nrf1
|
APN |
6 |
30,089,947 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1892:Nrf1
|
UTSW |
6 |
30,144,787 (GRCm39) |
missense |
probably null |
|
|
R5347:Nrf1
|
UTSW |
6 |
30,118,967 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5607:Nrf1
|
UTSW |
6 |
30,126,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5654:Nrf1
|
UTSW |
6 |
30,117,061 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5851:Nrf1
|
UTSW |
6 |
30,089,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6470:Nrf1
|
UTSW |
6 |
30,102,199 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7106:Nrf1
|
UTSW |
6 |
30,102,183 (GRCm39) |
missense |
probably benign |
|
|
R7334:Nrf1
|
UTSW |
6 |
30,118,970 (GRCm39) |
missense |
probably benign |
0.30 |
|
R7476:Nrf1
|
UTSW |
6 |
30,116,271 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7510:Nrf1
|
UTSW |
6 |
30,151,633 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7625:Nrf1
|
UTSW |
6 |
30,116,230 (GRCm39) |
missense |
probably benign |
0.20 |
|
R7882:Nrf1
|
UTSW |
6 |
30,090,299 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8101:Nrf1
|
UTSW |
6 |
30,098,449 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R8338:Nrf1
|
UTSW |
6 |
30,140,247 (GRCm39) |
missense |
|
|
|
R8506:Nrf1
|
UTSW |
6 |
30,126,256 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9446:Nrf1
|
UTSW |
6 |
30,090,019 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACCAACGGTCTTGCTTTGTC -3'
(R):5'- GTGAAATCGGTGGCGTTCATTC -3'
Sequencing Primer
(F):5'- GGTCTTGCTTTGTCTCTCCAGG -3'
(R):5'- TTCCACCAGATCCCAGAGTGG -3'
|
| Posted On |
2015-05-15 |
Incidental Mutation