Incidental Mutation 'R1415:Zfp787'
ID |
262758 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp787
|
Ensembl Gene |
ENSMUSG00000046792 |
Gene Name |
zinc finger protein 787 |
Synonyms |
2210018M03Rik |
MMRRC Submission |
039471-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.087)
|
Stock # |
R1415 (G1)
|
Quality Score |
91 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
6134490-6158996 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 6135694 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Cysteine
at position 186
(G186C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000092468
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094870]
[ENSMUST00000207315]
|
AlphaFold |
Q8BIF9 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000094870
AA Change: G186C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000092468 Gene: ENSMUSG00000046792 AA Change: G186C
Domain | Start | End | E-Value | Type |
low complexity region
|
41 |
65 |
N/A |
INTRINSIC |
ZnF_C2H2
|
66 |
88 |
5.67e-5 |
SMART |
ZnF_C2H2
|
94 |
116 |
9.58e-3 |
SMART |
ZnF_C2H2
|
122 |
144 |
1.84e-4 |
SMART |
ZnF_C2H2
|
150 |
172 |
1.3e-4 |
SMART |
ZnF_C2H2
|
178 |
200 |
6.88e-4 |
SMART |
low complexity region
|
245 |
277 |
N/A |
INTRINSIC |
ZnF_C2H2
|
280 |
303 |
2.36e-2 |
SMART |
ZnF_C2H2
|
317 |
339 |
4.72e-2 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000207315
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208973
|
Coding Region Coverage |
- 1x: 98.9%
- 3x: 98.0%
- 10x: 95.3%
- 20x: 89.6%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
C |
5: 114,303,982 (GRCm39) |
V135A |
probably benign |
Het |
Adam21 |
C |
T |
12: 81,606,321 (GRCm39) |
W480* |
probably null |
Het |
Ccdc71 |
T |
A |
9: 108,340,407 (GRCm39) |
Y73* |
probably null |
Het |
Cfap44 |
T |
A |
16: 44,301,752 (GRCm39) |
I1830N |
probably damaging |
Het |
Dnajb11 |
T |
C |
16: 22,689,371 (GRCm39) |
V264A |
probably benign |
Het |
Fam135b |
T |
C |
15: 71,328,777 (GRCm39) |
E1174G |
probably damaging |
Het |
Fam83e |
G |
A |
7: 45,376,135 (GRCm39) |
E283K |
probably damaging |
Het |
Gigyf1 |
A |
G |
5: 137,517,478 (GRCm39) |
|
probably null |
Het |
Letm1 |
A |
T |
5: 33,926,906 (GRCm39) |
N130K |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,519,676 (GRCm39) |
Y137C |
probably damaging |
Het |
Map3k2 |
A |
G |
18: 32,361,330 (GRCm39) |
I597V |
possibly damaging |
Het |
Nek1 |
A |
G |
8: 61,542,720 (GRCm39) |
E770G |
probably benign |
Het |
Or4d2b |
A |
C |
11: 87,780,473 (GRCm39) |
V83G |
possibly damaging |
Het |
Or52n2b |
A |
G |
7: 104,565,543 (GRCm39) |
I320T |
probably benign |
Het |
Pank2 |
T |
A |
2: 131,124,638 (GRCm39) |
Y68* |
probably null |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Secisbp2l |
C |
A |
2: 125,582,285 (GRCm39) |
G1057V |
probably benign |
Het |
Slc30a2 |
C |
T |
4: 134,076,660 (GRCm39) |
T265M |
probably damaging |
Het |
Smarca2 |
A |
G |
19: 26,688,084 (GRCm39) |
E1239G |
probably null |
Het |
Snx30 |
C |
T |
4: 59,879,261 (GRCm39) |
R167C |
probably damaging |
Het |
Tmem26 |
T |
C |
10: 68,614,491 (GRCm39) |
F302S |
possibly damaging |
Het |
Tpgs2 |
A |
G |
18: 25,301,610 (GRCm39) |
L19S |
probably damaging |
Het |
Trp53bp1 |
T |
G |
2: 121,066,665 (GRCm39) |
E687A |
probably damaging |
Het |
Ttc27 |
C |
T |
17: 75,046,667 (GRCm39) |
H243Y |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,763,137 (GRCm39) |
V2318D |
possibly damaging |
Het |
Wdr59 |
G |
A |
8: 112,225,228 (GRCm39) |
P141S |
probably damaging |
Het |
Zbed6 |
C |
T |
1: 133,585,556 (GRCm39) |
V594M |
possibly damaging |
Het |
|
Other mutations in Zfp787 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02546:Zfp787
|
APN |
7 |
6,135,297 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02721:Zfp787
|
APN |
7 |
6,135,463 (GRCm39) |
splice site |
probably null |
|
cheater
|
UTSW |
7 |
6,136,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0063:Zfp787
|
UTSW |
7 |
6,135,322 (GRCm39) |
splice site |
probably null |
|
R1434:Zfp787
|
UTSW |
7 |
6,135,234 (GRCm39) |
missense |
probably damaging |
0.98 |
R2042:Zfp787
|
UTSW |
7 |
6,135,763 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5657:Zfp787
|
UTSW |
7 |
6,136,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R5919:Zfp787
|
UTSW |
7 |
6,135,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R6306:Zfp787
|
UTSW |
7 |
6,135,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Zfp787
|
UTSW |
7 |
6,136,039 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7316:Zfp787
|
UTSW |
7 |
6,158,523 (GRCm39) |
unclassified |
probably benign |
|
R7396:Zfp787
|
UTSW |
7 |
6,135,106 (GRCm39) |
makesense |
probably null |
|
R7880:Zfp787
|
UTSW |
7 |
6,135,190 (GRCm39) |
missense |
probably benign |
0.00 |
R7979:Zfp787
|
UTSW |
7 |
6,146,094 (GRCm39) |
missense |
probably damaging |
0.97 |
R9412:Zfp787
|
UTSW |
7 |
6,135,946 (GRCm39) |
missense |
probably damaging |
0.98 |
R9527:Zfp787
|
UTSW |
7 |
6,136,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R9713:Zfp787
|
UTSW |
7 |
6,146,059 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Zfp787
|
UTSW |
7 |
6,135,123 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
|
Posted On |
2015-02-04 |