Incidental Mutation 'R1196:Zfp791'
ID |
101123 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp791
|
Ensembl Gene |
ENSMUSG00000074194 |
Gene Name |
zinc finger protein 791 |
Synonyms |
EG244556 |
MMRRC Submission |
039268-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1196 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
85835182-85849724 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 85837583 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 94
(K94*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000147335
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098550]
[ENSMUST00000211109]
|
AlphaFold |
Q497V9 |
Predicted Effect |
probably null
Transcript: ENSMUST00000098550
AA Change: K94*
|
SMART Domains |
Protein: ENSMUSP00000096150 Gene: ENSMUSG00000074194 AA Change: K94*
Domain | Start | End | E-Value | Type |
KRAB
|
4 |
64 |
4.26e-18 |
SMART |
ZnF_C2H2
|
102 |
124 |
2.53e-2 |
SMART |
ZnF_C2H2
|
139 |
161 |
7.78e-3 |
SMART |
ZnF_C2H2
|
167 |
189 |
3.34e-2 |
SMART |
ZnF_C2H2
|
195 |
217 |
2.79e-4 |
SMART |
ZnF_C2H2
|
223 |
245 |
6.78e-3 |
SMART |
ZnF_C2H2
|
251 |
273 |
2.12e-4 |
SMART |
ZnF_C2H2
|
281 |
303 |
2.02e-1 |
SMART |
ZnF_C2H2
|
309 |
331 |
7.78e-3 |
SMART |
ZnF_C2H2
|
337 |
359 |
6.42e-4 |
SMART |
ZnF_C2H2
|
365 |
387 |
2.29e0 |
SMART |
ZnF_C2H2
|
393 |
415 |
1.13e-4 |
SMART |
ZnF_C2H2
|
421 |
443 |
2.75e-3 |
SMART |
ZnF_C2H2
|
449 |
471 |
2.05e-2 |
SMART |
ZnF_C2H2
|
477 |
499 |
3.95e-4 |
SMART |
ZnF_C2H2
|
505 |
527 |
2.71e-2 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158588
|
Predicted Effect |
probably null
Transcript: ENSMUST00000211109
AA Change: K94*
|
Meta Mutation Damage Score |
0.9639 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.3%
- 10x: 94.9%
- 20x: 86.8%
|
Validation Efficiency |
97% (38/39) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
C |
5: 114,383,153 (GRCm39) |
I2112T |
probably benign |
Het |
Agtpbp1 |
C |
A |
13: 59,598,132 (GRCm39) |
|
probably benign |
Het |
Ash1l |
T |
C |
3: 88,890,623 (GRCm39) |
M834T |
probably damaging |
Het |
Aspg |
A |
G |
12: 112,082,958 (GRCm39) |
T213A |
possibly damaging |
Het |
Chpf2 |
T |
C |
5: 24,794,646 (GRCm39) |
V272A |
possibly damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Ddah2 |
G |
T |
17: 35,280,503 (GRCm39) |
D215Y |
probably damaging |
Het |
Dna2 |
C |
T |
10: 62,784,966 (GRCm39) |
R28W |
probably benign |
Het |
Fbrsl1 |
T |
A |
5: 110,522,385 (GRCm39) |
M150L |
probably benign |
Het |
Hmces |
T |
A |
6: 87,913,164 (GRCm39) |
D306E |
probably benign |
Het |
Itga2 |
C |
T |
13: 115,002,691 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
T |
C |
10: 67,075,015 (GRCm39) |
|
probably benign |
Het |
Krr1 |
T |
A |
10: 111,811,562 (GRCm39) |
H85Q |
probably benign |
Het |
Krt87 |
C |
T |
15: 101,389,314 (GRCm39) |
R6Q |
probably benign |
Het |
Krtap24-1 |
T |
C |
16: 88,408,530 (GRCm39) |
M199V |
probably benign |
Het |
Krtap5-2 |
A |
T |
7: 141,728,620 (GRCm39) |
C353* |
probably null |
Het |
Myo7a |
T |
G |
7: 97,746,880 (GRCm39) |
I178L |
possibly damaging |
Het |
Myof |
G |
A |
19: 37,899,408 (GRCm39) |
T1043I |
probably damaging |
Het |
Noc4l |
C |
T |
5: 110,798,450 (GRCm39) |
E247K |
probably damaging |
Het |
Notch4 |
T |
C |
17: 34,787,837 (GRCm39) |
C437R |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Or4p19 |
A |
T |
2: 88,242,890 (GRCm39) |
N37K |
probably damaging |
Het |
Or7e168 |
A |
G |
9: 19,719,928 (GRCm39) |
I105V |
probably benign |
Het |
Pank4 |
T |
C |
4: 155,062,630 (GRCm39) |
F584L |
probably damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,312,875 (GRCm39) |
F1198L |
probably damaging |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Tent5c |
T |
C |
3: 100,380,316 (GRCm39) |
T147A |
possibly damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Unc13a |
A |
G |
8: 72,107,630 (GRCm39) |
I554T |
probably damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,247,866 (GRCm39) |
D1023G |
probably damaging |
Het |
|
Other mutations in Zfp791 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01512:Zfp791
|
APN |
8 |
85,840,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Zfp791
|
UTSW |
8 |
85,837,495 (GRCm39) |
missense |
probably benign |
0.01 |
R0085:Zfp791
|
UTSW |
8 |
85,838,862 (GRCm39) |
nonsense |
probably null |
|
R0496:Zfp791
|
UTSW |
8 |
85,836,609 (GRCm39) |
missense |
probably benign |
0.03 |
R1927:Zfp791
|
UTSW |
8 |
85,837,312 (GRCm39) |
missense |
probably benign |
0.17 |
R4240:Zfp791
|
UTSW |
8 |
85,836,295 (GRCm39) |
missense |
probably null |
1.00 |
R4370:Zfp791
|
UTSW |
8 |
85,840,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R4637:Zfp791
|
UTSW |
8 |
85,836,514 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4684:Zfp791
|
UTSW |
8 |
85,837,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4713:Zfp791
|
UTSW |
8 |
85,837,597 (GRCm39) |
missense |
probably damaging |
0.98 |
R4822:Zfp791
|
UTSW |
8 |
85,837,035 (GRCm39) |
missense |
probably benign |
0.01 |
R4914:Zfp791
|
UTSW |
8 |
85,837,580 (GRCm39) |
missense |
probably benign |
0.06 |
R4915:Zfp791
|
UTSW |
8 |
85,837,580 (GRCm39) |
missense |
probably benign |
0.06 |
R4916:Zfp791
|
UTSW |
8 |
85,837,580 (GRCm39) |
missense |
probably benign |
0.06 |
R4918:Zfp791
|
UTSW |
8 |
85,837,580 (GRCm39) |
missense |
probably benign |
0.06 |
R5106:Zfp791
|
UTSW |
8 |
85,837,259 (GRCm39) |
nonsense |
probably null |
|
R5549:Zfp791
|
UTSW |
8 |
85,836,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R6093:Zfp791
|
UTSW |
8 |
85,840,135 (GRCm39) |
critical splice donor site |
probably null |
|
R6362:Zfp791
|
UTSW |
8 |
85,846,279 (GRCm39) |
start gained |
probably benign |
|
R7737:Zfp791
|
UTSW |
8 |
85,838,844 (GRCm39) |
missense |
probably benign |
0.02 |
R8986:Zfp791
|
UTSW |
8 |
85,837,327 (GRCm39) |
missense |
probably benign |
0.00 |
R9050:Zfp791
|
UTSW |
8 |
85,837,334 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
Predicted Primers |
|
Posted On |
2014-01-15 |