Incidental Mutation 'R2696:Zfp27'
| ID |
251061 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp27
|
| Ensembl Gene |
ENSMUSG00000062040 |
| Gene Name |
zinc finger protein 27 |
| Synonyms |
Zfp-27, mkr-4 |
| MMRRC Submission |
040434-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.602)
|
| Stock # |
R2696 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
29592758-29605997 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 29595792 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 58
(A58T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000127677
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053521]
[ENSMUST00000159920]
[ENSMUST00000161904]
[ENSMUST00000162592]
[ENSMUST00000172448]
|
| AlphaFold |
P10077 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000053521
AA Change: A58T
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000054012
Gene: ENSMUSG00000062040
AA Change: A58T
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
1 |
59 |
2.94e-12 |
SMART |
|
internal_repeat_2
|
108 |
195 |
4.1e-6 |
PROSPERO |
|
ZnF_C2H2
|
205 |
227 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
233 |
255 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
261 |
283 |
2.09e-3 |
SMART |
|
ZnF_C2H2
|
289 |
311 |
2.91e-2 |
SMART |
|
ZnF_C2H2
|
317 |
339 |
4.17e-3 |
SMART |
|
ZnF_C2H2
|
345 |
367 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
401 |
423 |
7.15e-2 |
SMART |
|
ZnF_C2H2
|
429 |
451 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
457 |
479 |
1.08e-1 |
SMART |
|
ZnF_C2H2
|
485 |
507 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
513 |
535 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
541 |
563 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
569 |
591 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
597 |
619 |
3.34e-2 |
SMART |
|
ZnF_C2H2
|
625 |
647 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
653 |
675 |
2.36e-2 |
SMART |
|
ZnF_C2H2
|
681 |
703 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
709 |
731 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
737 |
759 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
765 |
787 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
793 |
815 |
3.83e-2 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000159920
AA Change: A58T
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000125232
Gene: ENSMUSG00000062040
AA Change: A58T
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
1 |
59 |
2.94e-12 |
SMART |
|
internal_repeat_2
|
108 |
195 |
4.1e-6 |
PROSPERO |
|
ZnF_C2H2
|
205 |
227 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
233 |
255 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
261 |
283 |
2.09e-3 |
SMART |
|
ZnF_C2H2
|
289 |
311 |
2.91e-2 |
SMART |
|
ZnF_C2H2
|
317 |
339 |
4.17e-3 |
SMART |
|
ZnF_C2H2
|
345 |
367 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
401 |
423 |
7.15e-2 |
SMART |
|
ZnF_C2H2
|
429 |
451 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
457 |
479 |
1.08e-1 |
SMART |
|
ZnF_C2H2
|
485 |
507 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
513 |
535 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
541 |
563 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
569 |
591 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
597 |
619 |
3.34e-2 |
SMART |
|
ZnF_C2H2
|
625 |
647 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
653 |
675 |
2.36e-2 |
SMART |
|
ZnF_C2H2
|
681 |
703 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
709 |
731 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
737 |
759 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
765 |
787 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
793 |
815 |
3.83e-2 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160411
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000161904
AA Change: A58T
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000124684
Gene: ENSMUSG00000062040
AA Change: A58T
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
1 |
59 |
2.94e-12 |
SMART |
|
internal_repeat_2
|
108 |
195 |
4.1e-6 |
PROSPERO |
|
ZnF_C2H2
|
205 |
227 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
233 |
255 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
261 |
283 |
2.09e-3 |
SMART |
|
ZnF_C2H2
|
289 |
311 |
2.91e-2 |
SMART |
|
ZnF_C2H2
|
317 |
339 |
4.17e-3 |
SMART |
|
ZnF_C2H2
|
345 |
367 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
401 |
423 |
7.15e-2 |
SMART |
|
ZnF_C2H2
|
429 |
451 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
457 |
479 |
1.08e-1 |
SMART |
|
ZnF_C2H2
|
485 |
507 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
513 |
535 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
541 |
563 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
569 |
591 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
597 |
619 |
3.34e-2 |
SMART |
|
ZnF_C2H2
|
625 |
647 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
653 |
675 |
2.36e-2 |
SMART |
|
ZnF_C2H2
|
681 |
703 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
709 |
731 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
737 |
759 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
765 |
787 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
793 |
815 |
3.83e-2 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000162592
AA Change: A58T
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000123953
Gene: ENSMUSG00000062040
AA Change: A58T
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
1 |
59 |
2.94e-12 |
SMART |
|
internal_repeat_2
|
108 |
195 |
4.1e-6 |
PROSPERO |
|
ZnF_C2H2
|
205 |
227 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
233 |
255 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
261 |
283 |
2.09e-3 |
SMART |
|
ZnF_C2H2
|
289 |
311 |
2.91e-2 |
SMART |
|
ZnF_C2H2
|
317 |
339 |
4.17e-3 |
SMART |
|
ZnF_C2H2
|
345 |
367 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
401 |
423 |
7.15e-2 |
SMART |
|
ZnF_C2H2
|
429 |
451 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
457 |
479 |
1.08e-1 |
SMART |
|
ZnF_C2H2
|
485 |
507 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
513 |
535 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
541 |
563 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
569 |
591 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
597 |
619 |
3.34e-2 |
SMART |
|
ZnF_C2H2
|
625 |
647 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
653 |
675 |
2.36e-2 |
SMART |
|
ZnF_C2H2
|
681 |
703 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
709 |
731 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
737 |
759 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
765 |
787 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
793 |
815 |
3.83e-2 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000172448
AA Change: A58T
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000127677
Gene: ENSMUSG00000062040
AA Change: A58T
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
1 |
59 |
2.94e-12 |
SMART |
|
internal_repeat_2
|
108 |
195 |
4.1e-6 |
PROSPERO |
|
ZnF_C2H2
|
205 |
227 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
233 |
255 |
8.47e-4 |
SMART |
|
ZnF_C2H2
|
261 |
283 |
2.09e-3 |
SMART |
|
ZnF_C2H2
|
289 |
311 |
2.91e-2 |
SMART |
|
ZnF_C2H2
|
317 |
339 |
4.17e-3 |
SMART |
|
ZnF_C2H2
|
345 |
367 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
401 |
423 |
7.15e-2 |
SMART |
|
ZnF_C2H2
|
429 |
451 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
457 |
479 |
1.08e-1 |
SMART |
|
ZnF_C2H2
|
485 |
507 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
513 |
535 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
541 |
563 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
569 |
591 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
597 |
619 |
3.34e-2 |
SMART |
|
ZnF_C2H2
|
625 |
647 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
653 |
675 |
2.36e-2 |
SMART |
|
ZnF_C2H2
|
681 |
703 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
709 |
731 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
737 |
759 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
765 |
787 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
793 |
815 |
3.83e-2 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930562C15Rik |
A |
T |
16: 4,668,228 (GRCm39) |
T540S |
probably benign |
Het |
| Acp7 |
G |
T |
7: 28,314,001 (GRCm39) |
H369Q |
probably benign |
Het |
| Adgrg3 |
A |
G |
8: 95,747,702 (GRCm39) |
N65S |
probably benign |
Het |
| Anln |
A |
G |
9: 22,272,259 (GRCm39) |
V620A |
probably benign |
Het |
| Atp10a |
T |
A |
7: 58,463,366 (GRCm39) |
S966R |
probably benign |
Het |
| Atp8b3 |
T |
A |
10: 80,370,017 (GRCm39) |
Q132L |
possibly damaging |
Het |
| Col4a1 |
T |
A |
8: 11,285,092 (GRCm39) |
|
probably null |
Het |
| Ddx21 |
T |
C |
10: 62,429,871 (GRCm39) |
H291R |
possibly damaging |
Het |
| Dlgap3 |
A |
G |
4: 127,088,416 (GRCm39) |
Y4C |
probably damaging |
Het |
| Dnah5 |
A |
G |
15: 28,278,722 (GRCm39) |
N1106D |
probably benign |
Het |
| Esyt1 |
T |
C |
10: 128,352,914 (GRCm39) |
D662G |
probably damaging |
Het |
| F830016B08Rik |
T |
A |
18: 60,433,808 (GRCm39) |
V297E |
possibly damaging |
Het |
| Faf1 |
T |
A |
4: 109,698,525 (GRCm39) |
N328K |
possibly damaging |
Het |
| Gdf3 |
A |
C |
6: 122,583,859 (GRCm39) |
F169L |
probably benign |
Het |
| Ifi213 |
G |
A |
1: 173,417,590 (GRCm39) |
T274I |
probably benign |
Het |
| Igf2r |
T |
C |
17: 12,914,231 (GRCm39) |
D1746G |
possibly damaging |
Het |
| Ighv1-75 |
T |
C |
12: 115,797,826 (GRCm39) |
K32R |
probably benign |
Het |
| Ipo8 |
T |
A |
6: 148,698,239 (GRCm39) |
Q594L |
probably benign |
Het |
| Krt87 |
A |
T |
15: 101,384,890 (GRCm39) |
I402N |
probably benign |
Het |
| Med18 |
G |
A |
4: 132,187,281 (GRCm39) |
R118W |
probably damaging |
Het |
| Mmrn2 |
A |
G |
14: 34,120,372 (GRCm39) |
E414G |
probably damaging |
Het |
| Myo6 |
A |
G |
9: 80,168,176 (GRCm39) |
T447A |
probably benign |
Het |
| Ncoa6 |
T |
C |
2: 155,279,935 (GRCm39) |
E27G |
probably benign |
Het |
| Ngly1 |
T |
C |
14: 16,283,439 (GRCm38) |
L406S |
possibly damaging |
Het |
| Or14j1 |
T |
C |
17: 38,145,998 (GRCm39) |
I36T |
probably benign |
Het |
| Or51l4 |
A |
G |
7: 103,404,735 (GRCm39) |
I19T |
probably damaging |
Het |
| Phldb1 |
T |
C |
9: 44,629,585 (GRCm39) |
Y156C |
probably damaging |
Het |
| Pkd2l1 |
T |
A |
19: 44,145,708 (GRCm39) |
T172S |
probably benign |
Het |
| Pknox2 |
G |
A |
9: 36,820,987 (GRCm39) |
R292* |
probably null |
Het |
| Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
| Polr3e |
T |
C |
7: 120,532,600 (GRCm39) |
L212P |
probably damaging |
Het |
| Ppp4r4 |
A |
G |
12: 103,547,653 (GRCm39) |
I215M |
possibly damaging |
Het |
| Psmg2 |
T |
C |
18: 67,781,288 (GRCm39) |
Y127H |
possibly damaging |
Het |
| Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
| Ptp4a1 |
A |
T |
1: 30,985,213 (GRCm39) |
M4K |
probably benign |
Het |
| R3hcc1l |
A |
T |
19: 42,552,427 (GRCm39) |
I475L |
possibly damaging |
Het |
| Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
| Rsf1 |
GGC |
GGCGGCGGCGGC |
7: 97,229,140 (GRCm39) |
|
probably benign |
Het |
| Sec63 |
T |
A |
10: 42,659,522 (GRCm39) |
I70N |
probably benign |
Het |
| Slc2a5 |
A |
C |
4: 150,205,203 (GRCm39) |
K4T |
probably benign |
Het |
| Slc4a3 |
A |
G |
1: 75,532,119 (GRCm39) |
Y939C |
possibly damaging |
Het |
| Slc7a15 |
T |
C |
12: 8,579,345 (GRCm39) |
*229W |
probably null |
Het |
| Slco1a6 |
C |
A |
6: 142,058,662 (GRCm39) |
G206C |
probably damaging |
Het |
| Spata9 |
A |
G |
13: 76,125,895 (GRCm39) |
Q126R |
probably benign |
Het |
| Speg |
A |
T |
1: 75,383,570 (GRCm39) |
D1186V |
probably benign |
Het |
| Spink5 |
T |
G |
18: 44,115,359 (GRCm39) |
M197R |
probably damaging |
Het |
| Stab2 |
T |
C |
10: 86,697,363 (GRCm39) |
D1975G |
probably benign |
Het |
| Syngap1 |
T |
A |
17: 27,176,385 (GRCm39) |
C224* |
probably null |
Het |
| Ttn |
T |
C |
2: 76,698,807 (GRCm39) |
|
probably benign |
Het |
| Txnrd1 |
G |
A |
10: 82,721,116 (GRCm39) |
E397K |
probably benign |
Het |
| Ugt2b36 |
A |
T |
5: 87,237,344 (GRCm39) |
M313K |
probably damaging |
Het |
| Ulk3 |
A |
G |
9: 57,497,724 (GRCm39) |
I74V |
possibly damaging |
Het |
| Zcchc4 |
T |
C |
5: 52,953,573 (GRCm39) |
V194A |
probably damaging |
Het |
| Zfp398 |
T |
G |
6: 47,843,879 (GRCm39) |
*512E |
probably null |
Het |
|
| Other mutations in Zfp27 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00972:Zfp27
|
APN |
7 |
29,594,383 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02490:Zfp27
|
APN |
7 |
29,594,360 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL02899:Zfp27
|
APN |
7 |
29,595,680 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0179:Zfp27
|
UTSW |
7 |
29,595,850 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R0234:Zfp27
|
UTSW |
7 |
29,593,532 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0234:Zfp27
|
UTSW |
7 |
29,593,532 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0511:Zfp27
|
UTSW |
7 |
29,593,947 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1185:Zfp27
|
UTSW |
7 |
29,595,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1185:Zfp27
|
UTSW |
7 |
29,595,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1185:Zfp27
|
UTSW |
7 |
29,595,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1294:Zfp27
|
UTSW |
7 |
29,595,737 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1581:Zfp27
|
UTSW |
7 |
29,595,549 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1763:Zfp27
|
UTSW |
7 |
29,594,801 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R2083:Zfp27
|
UTSW |
7 |
29,594,208 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2217:Zfp27
|
UTSW |
7 |
29,595,536 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R4084:Zfp27
|
UTSW |
7 |
29,594,792 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4864:Zfp27
|
UTSW |
7 |
29,594,261 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6057:Zfp27
|
UTSW |
7 |
29,594,444 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R6063:Zfp27
|
UTSW |
7 |
29,593,727 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6553:Zfp27
|
UTSW |
7 |
29,595,818 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6585:Zfp27
|
UTSW |
7 |
29,595,818 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6800:Zfp27
|
UTSW |
7 |
29,593,860 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7051:Zfp27
|
UTSW |
7 |
29,594,446 (GRCm39) |
small deletion |
probably benign |
|
|
R7052:Zfp27
|
UTSW |
7 |
29,594,446 (GRCm39) |
small deletion |
probably benign |
|
|
R7066:Zfp27
|
UTSW |
7 |
29,594,446 (GRCm39) |
small deletion |
probably benign |
|
|
R7106:Zfp27
|
UTSW |
7 |
29,594,446 (GRCm39) |
small deletion |
probably benign |
|
|
R7432:Zfp27
|
UTSW |
7 |
29,594,784 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7473:Zfp27
|
UTSW |
7 |
29,595,324 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7670:Zfp27
|
UTSW |
7 |
29,594,221 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7739:Zfp27
|
UTSW |
7 |
29,593,699 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7817:Zfp27
|
UTSW |
7 |
29,595,815 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R8750:Zfp27
|
UTSW |
7 |
29,594,804 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8819:Zfp27
|
UTSW |
7 |
29,594,013 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8820:Zfp27
|
UTSW |
7 |
29,594,013 (GRCm39) |
missense |
probably benign |
0.15 |
|
R9189:Zfp27
|
UTSW |
7 |
29,595,359 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R9511:Zfp27
|
UTSW |
7 |
29,593,641 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9705:Zfp27
|
UTSW |
7 |
29,595,342 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
Z1177:Zfp27
|
UTSW |
7 |
29,595,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
Z1177:Zfp27
|
UTSW |
7 |
29,594,586 (GRCm39) |
missense |
probably benign |
0.33 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCCCATTACTTTCATCATGAGTCTG -3'
(R):5'- ACAGACACCTTGCTGTGCTG -3'
Sequencing Primer
(F):5'- GTAAATCTGAACTATGCTTCGGCTC -3'
(R):5'- AGGAACTTGGCTTTAGAGCTG -3'
|
| Posted On |
2014-12-04 |
Incidental Mutation