Incidental Mutation 'IGL00164:Zfp607a'
ID |
1518 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp607a
|
Ensembl Gene |
ENSMUSG00000020420 |
Gene Name |
zinc finger protein 607A |
Synonyms |
Zfp607, 4732475C15Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.058)
|
Stock # |
IGL00164
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
27556952-27580250 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 27577214 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Lysine
at position 95
(E95K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146006
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053722]
[ENSMUST00000205534]
[ENSMUST00000205715]
|
AlphaFold |
Q3TQG9 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000053722
AA Change: E95K
PolyPhen 2
Score 0.553 (Sensitivity: 0.88; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000051496 Gene: ENSMUSG00000020420 AA Change: E95K
Domain | Start | End | E-Value | Type |
KRAB
|
14 |
75 |
8.48e-36 |
SMART |
ZnF_C2H2
|
173 |
195 |
2.91e-2 |
SMART |
ZnF_C2H2
|
201 |
223 |
3.44e-4 |
SMART |
ZnF_C2H2
|
229 |
251 |
3.83e-2 |
SMART |
ZnF_C2H2
|
257 |
279 |
4.87e-4 |
SMART |
ZnF_C2H2
|
285 |
307 |
1.38e-3 |
SMART |
ZnF_C2H2
|
313 |
335 |
4.17e-3 |
SMART |
ZnF_C2H2
|
341 |
363 |
2.86e-1 |
SMART |
ZnF_C2H2
|
369 |
391 |
5.14e-3 |
SMART |
ZnF_C2H2
|
397 |
419 |
1.2e-3 |
SMART |
ZnF_C2H2
|
425 |
447 |
4.47e-3 |
SMART |
ZnF_C2H2
|
453 |
475 |
1.1e-2 |
SMART |
ZnF_C2H2
|
481 |
503 |
1.45e-2 |
SMART |
ZnF_C2H2
|
509 |
531 |
1.12e-3 |
SMART |
ZnF_C2H2
|
537 |
559 |
1.5e-4 |
SMART |
ZnF_C2H2
|
565 |
587 |
8.34e-3 |
SMART |
ZnF_C2H2
|
593 |
615 |
1.12e-3 |
SMART |
ZnF_C2H2
|
621 |
643 |
6.42e-4 |
SMART |
ZnF_C2H2
|
649 |
671 |
6.23e-2 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000205534
AA Change: E95K
PolyPhen 2
Score 0.553 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000205715
AA Change: E95K
PolyPhen 2
Score 0.553 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206136
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
A |
13: 77,471,477 (GRCm39) |
|
probably benign |
Het |
Abcg4 |
A |
G |
9: 44,186,439 (GRCm39) |
|
probably benign |
Het |
Actr2 |
A |
G |
11: 20,030,015 (GRCm39) |
|
probably benign |
Het |
Adgrb3 |
A |
G |
1: 25,267,581 (GRCm39) |
L843P |
probably benign |
Het |
Cdk19 |
G |
A |
10: 40,312,161 (GRCm39) |
D137N |
probably benign |
Het |
Cuedc2 |
T |
A |
19: 46,320,359 (GRCm39) |
I71F |
probably damaging |
Het |
Dag1 |
A |
G |
9: 108,086,487 (GRCm39) |
V218A |
probably damaging |
Het |
Dlg5 |
A |
C |
14: 24,208,532 (GRCm39) |
S868R |
possibly damaging |
Het |
Ecsit |
C |
T |
9: 21,984,310 (GRCm39) |
G340D |
probably benign |
Het |
Fkbp8 |
A |
G |
8: 70,987,211 (GRCm39) |
M358V |
probably damaging |
Het |
Gckr |
G |
A |
5: 31,456,920 (GRCm39) |
V79M |
probably damaging |
Het |
Gpd1 |
C |
A |
15: 99,618,532 (GRCm39) |
D172E |
probably benign |
Het |
Josd2 |
T |
C |
7: 44,120,740 (GRCm39) |
|
probably benign |
Het |
Kcna2 |
T |
C |
3: 107,011,946 (GRCm39) |
S176P |
probably damaging |
Het |
Kcnq4 |
G |
A |
4: 120,555,213 (GRCm39) |
Q657* |
probably null |
Het |
Kif14 |
G |
A |
1: 136,396,756 (GRCm39) |
S354N |
probably benign |
Het |
Notch1 |
G |
A |
2: 26,350,058 (GRCm39) |
R2361W |
probably damaging |
Het |
Or5w1 |
T |
C |
2: 87,486,582 (GRCm39) |
M228V |
probably benign |
Het |
Palb2 |
A |
C |
7: 121,720,271 (GRCm39) |
|
probably benign |
Het |
Pan2 |
C |
T |
10: 128,148,795 (GRCm39) |
Q452* |
probably null |
Het |
Pcnx1 |
T |
C |
12: 81,941,875 (GRCm39) |
V91A |
probably damaging |
Het |
Rgs22 |
T |
A |
15: 36,100,077 (GRCm39) |
I213F |
possibly damaging |
Het |
Serpina3b |
G |
T |
12: 104,105,046 (GRCm39) |
W407C |
probably benign |
Het |
Sf3b2 |
T |
C |
19: 5,329,615 (GRCm39) |
D687G |
probably benign |
Het |
Slc8a3 |
T |
C |
12: 81,361,343 (GRCm39) |
E492G |
probably benign |
Het |
Sox4 |
C |
A |
13: 29,136,956 (GRCm39) |
G17W |
probably damaging |
Het |
Sp2 |
C |
T |
11: 96,845,387 (GRCm39) |
R578H |
probably damaging |
Het |
Surf1 |
C |
T |
2: 26,803,584 (GRCm39) |
|
probably null |
Het |
Tmem190 |
T |
C |
7: 4,785,998 (GRCm39) |
|
probably benign |
Het |
Zfhx2 |
A |
G |
14: 55,302,483 (GRCm39) |
S1834P |
possibly damaging |
Het |
|
Other mutations in Zfp607a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Zfp607a
|
APN |
7 |
27,578,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01412:Zfp607a
|
APN |
7 |
27,578,109 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03206:Zfp607a
|
APN |
7 |
27,577,248 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0071:Zfp607a
|
UTSW |
7 |
27,577,694 (GRCm39) |
missense |
probably damaging |
0.96 |
R0304:Zfp607a
|
UTSW |
7 |
27,578,637 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0685:Zfp607a
|
UTSW |
7 |
27,577,901 (GRCm39) |
missense |
probably damaging |
0.97 |
R0726:Zfp607a
|
UTSW |
7 |
27,578,574 (GRCm39) |
missense |
probably benign |
0.00 |
R1201:Zfp607a
|
UTSW |
7 |
27,578,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1304:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1648:Zfp607a
|
UTSW |
7 |
27,578,493 (GRCm39) |
missense |
probably benign |
0.02 |
R1732:Zfp607a
|
UTSW |
7 |
27,577,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R2194:Zfp607a
|
UTSW |
7 |
27,578,805 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3793:Zfp607a
|
UTSW |
7 |
27,578,331 (GRCm39) |
missense |
probably benign |
0.01 |
R3808:Zfp607a
|
UTSW |
7 |
27,578,826 (GRCm39) |
missense |
probably benign |
0.01 |
R4296:Zfp607a
|
UTSW |
7 |
27,565,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Zfp607a
|
UTSW |
7 |
27,578,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Zfp607a
|
UTSW |
7 |
27,578,078 (GRCm39) |
missense |
probably benign |
0.23 |
R4915:Zfp607a
|
UTSW |
7 |
27,577,985 (GRCm39) |
missense |
probably benign |
0.00 |
R4950:Zfp607a
|
UTSW |
7 |
27,578,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Zfp607a
|
UTSW |
7 |
27,578,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Zfp607a
|
UTSW |
7 |
27,577,269 (GRCm39) |
missense |
probably damaging |
0.97 |
R5270:Zfp607a
|
UTSW |
7 |
27,577,730 (GRCm39) |
nonsense |
probably null |
|
R5403:Zfp607a
|
UTSW |
7 |
27,578,744 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6010:Zfp607a
|
UTSW |
7 |
27,577,254 (GRCm39) |
nonsense |
probably null |
|
R6224:Zfp607a
|
UTSW |
7 |
27,578,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Zfp607a
|
UTSW |
7 |
27,578,473 (GRCm39) |
nonsense |
probably null |
|
R6953:Zfp607a
|
UTSW |
7 |
27,577,790 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7082:Zfp607a
|
UTSW |
7 |
27,578,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Zfp607a
|
UTSW |
7 |
27,565,000 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7909:Zfp607a
|
UTSW |
7 |
27,578,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Zfp607a
|
UTSW |
7 |
27,578,868 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8224:Zfp607a
|
UTSW |
7 |
27,577,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Zfp607a
|
UTSW |
7 |
27,577,944 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8962:Zfp607a
|
UTSW |
7 |
27,578,786 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9178:Zfp607a
|
UTSW |
7 |
27,577,382 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Zfp607a
|
UTSW |
7 |
27,578,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2011-07-12 |