Incidental Mutation 'R0015:Zgrf1'
| ID |
216014 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zgrf1
|
| Ensembl Gene |
ENSMUSG00000051278 |
| Gene Name |
zinc finger, GRF-type containing 1 |
| Synonyms |
4930422G04Rik |
| MMRRC Submission |
038310-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.066)
|
| Stock # |
R0015 (G1)
|
| Quality Score |
65 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
127553489-127618023 bp(+) (GRCm38) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
T to C
at 127555397 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000143585
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029588]
[ENSMUST00000043108]
[ENSMUST00000195955]
[ENSMUST00000196141]
[ENSMUST00000197668]
[ENSMUST00000199888]
[ENSMUST00000200490]
|
| AlphaFold |
Q0VGT4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000029588
|
| SMART Domains |
Protein: ENSMUSP00000029588
Gene: ENSMUSG00000027968
| Domain | Start | End | E-Value | Type |
|---|
|
LA
|
26 |
106 |
1.29e-30 |
SMART |
|
RRM
|
120 |
196 |
5.37e-15 |
SMART |
|
low complexity region
|
210 |
226 |
N/A |
INTRINSIC |
|
low complexity region
|
257 |
273 |
N/A |
INTRINSIC |
|
low complexity region
|
302 |
311 |
N/A |
INTRINSIC |
|
low complexity region
|
350 |
364 |
N/A |
INTRINSIC |
|
Pfam:RRM_3
|
442 |
540 |
1.3e-31 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043108
|
| SMART Domains |
Protein: ENSMUSP00000044432
Gene: ENSMUSG00000051278
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.7e-23 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
low complexity region
|
896 |
906 |
N/A |
INTRINSIC |
|
Pfam:zf-GRF
|
1109 |
1153 |
1.5e-17 |
PFAM |
|
low complexity region
|
1316 |
1328 |
N/A |
INTRINSIC |
|
Pfam:AAA_11
|
1501 |
1608 |
1.6e-21 |
PFAM |
|
Pfam:AAA_12
|
1616 |
1802 |
1.3e-51 |
PFAM |
|
coiled coil region
|
1833 |
1861 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195955
|
| SMART Domains |
Protein: ENSMUSP00000142886
Gene: ENSMUSG00000051278
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
82 |
1.6e-25 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000196141
|
| SMART Domains |
Protein: ENSMUSP00000143761
Gene: ENSMUSG00000051278
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.7e-23 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
low complexity region
|
896 |
906 |
N/A |
INTRINSIC |
|
Pfam:zf-GRF
|
1109 |
1153 |
1.5e-17 |
PFAM |
|
low complexity region
|
1316 |
1328 |
N/A |
INTRINSIC |
|
Pfam:AAA_11
|
1501 |
1608 |
1.6e-21 |
PFAM |
|
Pfam:AAA_12
|
1616 |
1802 |
1.3e-51 |
PFAM |
|
coiled coil region
|
1833 |
1861 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000196949
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000197668
|
| SMART Domains |
Protein: ENSMUSP00000143331
Gene: ENSMUSG00000027968
| Domain | Start | End | E-Value | Type |
|---|
|
LA
|
26 |
80 |
9.2e-10 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197698
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199888
|
| SMART Domains |
Protein: ENSMUSP00000142693
Gene: ENSMUSG00000051278
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
82 |
3.5e-22 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000200490
|
| SMART Domains |
Protein: ENSMUSP00000143585
Gene: ENSMUSG00000051278
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.4e-20 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.2%
|
| Validation Efficiency |
97% (71/73) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 65 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2410089E03Rik |
G |
A |
15: 8,186,184 (GRCm38) |
R408H |
probably damaging |
Het |
| A130050O07Rik |
A |
G |
1: 137,928,656 (GRCm38) |
Y23C |
unknown |
Het |
| Adcy3 |
G |
A |
12: 4,195,260 (GRCm38) |
|
probably null |
Het |
| Aldh6a1 |
G |
A |
12: 84,441,780 (GRCm38) |
L86F |
probably damaging |
Het |
| Arl10 |
G |
T |
13: 54,575,957 (GRCm38) |
|
probably benign |
Het |
| Armc3 |
A |
G |
2: 19,296,321 (GRCm38) |
|
probably null |
Het |
| Astn2 |
T |
G |
4: 66,266,382 (GRCm38) |
|
probably null |
Het |
| Cacna1d |
G |
A |
14: 30,114,971 (GRCm38) |
T804I |
probably benign |
Het |
| Ccny |
A |
C |
18: 9,316,682 (GRCm38) |
|
probably benign |
Het |
| Cdh5 |
C |
T |
8: 104,140,927 (GRCm38) |
T612I |
probably benign |
Het |
| Cfap58 |
A |
G |
19: 48,029,100 (GRCm38) |
M800V |
probably benign |
Het |
| Clrn1 |
A |
T |
3: 58,846,427 (GRCm38) |
I171K |
probably damaging |
Het |
| Cnp |
T |
A |
11: 100,578,908 (GRCm38) |
|
probably null |
Het |
| Col12a1 |
T |
C |
9: 79,651,385 (GRCm38) |
T1933A |
probably damaging |
Het |
| Cwf19l2 |
A |
G |
9: 3,454,666 (GRCm38) |
S660G |
probably benign |
Het |
| Dync1i2 |
C |
A |
2: 71,214,484 (GRCm38) |
R13S |
probably damaging |
Het |
| Eps8l1 |
A |
T |
7: 4,477,557 (GRCm38) |
|
probably benign |
Het |
| Espn |
T |
C |
4: 152,139,152 (GRCm38) |
T188A |
possibly damaging |
Het |
| F2 |
T |
C |
2: 91,630,607 (GRCm38) |
E260G |
probably benign |
Het |
| Fat4 |
T |
A |
3: 38,982,503 (GRCm38) |
S3435T |
probably damaging |
Het |
| Fchsd1 |
A |
G |
18: 37,962,959 (GRCm38) |
C533R |
probably benign |
Het |
| Fstl5 |
G |
A |
3: 76,322,191 (GRCm38) |
V100M |
probably damaging |
Het |
| Gls2 |
T |
G |
10: 128,209,350 (GRCm38) |
L572R |
probably damaging |
Het |
| Gm20939 |
A |
T |
17: 94,876,768 (GRCm38) |
E281D |
probably benign |
Het |
| Gpr35 |
T |
G |
1: 92,983,232 (GRCm38) |
L222W |
probably damaging |
Het |
| Hsf5 |
C |
A |
11: 87,657,335 (GRCm38) |
H615N |
probably benign |
Het |
| Id2 |
C |
T |
12: 25,095,803 (GRCm38) |
D70N |
probably damaging |
Het |
| Ints2 |
T |
C |
11: 86,249,287 (GRCm38) |
T240A |
probably damaging |
Het |
| Kcnn3 |
A |
C |
3: 89,662,773 (GRCm38) |
D631A |
probably damaging |
Het |
| Klhdc8a |
A |
G |
1: 132,303,005 (GRCm38) |
T203A |
probably damaging |
Het |
| Lama4 |
C |
T |
10: 39,075,436 (GRCm38) |
T1059M |
possibly damaging |
Het |
| Lgals8 |
A |
G |
13: 12,447,298 (GRCm38) |
L226P |
probably damaging |
Het |
| Lifr |
T |
A |
15: 7,188,186 (GRCm38) |
|
probably null |
Het |
| Lonp1 |
T |
A |
17: 56,618,406 (GRCm38) |
Q462L |
probably benign |
Het |
| Lypd1 |
A |
G |
1: 125,910,438 (GRCm38) |
V48A |
possibly damaging |
Het |
| Mapkapk2 |
A |
G |
1: 131,097,326 (GRCm38) |
I67T |
possibly damaging |
Het |
| Mbd3l1 |
A |
T |
9: 18,484,858 (GRCm38) |
D93V |
probably benign |
Het |
| Mdh1b |
T |
C |
1: 63,721,800 (GRCm38) |
|
probably benign |
Het |
| Myh7b |
C |
T |
2: 155,622,286 (GRCm38) |
P569L |
probably damaging |
Het |
| Ncapd3 |
C |
A |
9: 27,051,809 (GRCm38) |
A470E |
probably damaging |
Het |
| Ndrg2 |
A |
G |
14: 51,910,445 (GRCm38) |
|
probably benign |
Het |
| Nprl2 |
A |
T |
9: 107,544,419 (GRCm38) |
I209F |
probably damaging |
Het |
| Ntrk1 |
A |
G |
3: 87,791,750 (GRCm38) |
|
probably benign |
Het |
| Olfm2 |
T |
C |
9: 20,668,741 (GRCm38) |
E268G |
probably damaging |
Het |
| Olfr884 |
T |
A |
9: 38,047,667 (GRCm38) |
Y148* |
probably null |
Het |
| Pcf11 |
T |
A |
7: 92,658,317 (GRCm38) |
H881L |
probably benign |
Het |
| Pde10a |
A |
G |
17: 8,977,197 (GRCm38) |
D640G |
probably damaging |
Het |
| Pde9a |
G |
A |
17: 31,386,356 (GRCm38) |
|
probably null |
Het |
| Pianp |
G |
T |
6: 125,001,540 (GRCm38) |
G236V |
probably damaging |
Het |
| Polr2g |
A |
G |
19: 8,793,652 (GRCm38) |
I160T |
probably damaging |
Het |
| Ppp1r3a |
A |
G |
6: 14,717,661 (GRCm38) |
S1085P |
possibly damaging |
Het |
| Pter |
G |
A |
2: 13,001,000 (GRCm38) |
G328D |
probably damaging |
Het |
| Rad51 |
T |
A |
2: 119,116,327 (GRCm38) |
M5K |
probably benign |
Het |
| Rbm43 |
T |
A |
2: 51,925,667 (GRCm38) |
I181F |
probably benign |
Het |
| Rgs12 |
T |
C |
5: 35,022,776 (GRCm38) |
|
probably benign |
Het |
| Rnf213 |
A |
C |
11: 119,441,606 (GRCm38) |
D2547A |
possibly damaging |
Het |
| Slc20a2 |
C |
A |
8: 22,535,345 (GRCm38) |
A21E |
probably damaging |
Het |
| Stab2 |
A |
G |
10: 86,843,617 (GRCm38) |
S2503P |
probably benign |
Het |
| Sv2b |
A |
T |
7: 75,125,641 (GRCm38) |
F479L |
probably damaging |
Het |
| Sybu |
T |
C |
15: 44,673,500 (GRCm38) |
R349G |
probably damaging |
Het |
| Tead3 |
T |
C |
17: 28,341,351 (GRCm38) |
Y2C |
probably damaging |
Het |
| Tnrc6c |
T |
A |
11: 117,721,458 (GRCm38) |
N307K |
probably damaging |
Het |
| Ubxn11 |
C |
G |
4: 134,116,025 (GRCm38) |
|
probably null |
Het |
| Ust |
T |
C |
10: 8,330,065 (GRCm38) |
|
probably benign |
Het |
| Vmn2r116 |
T |
A |
17: 23,401,849 (GRCm38) |
N852K |
probably benign |
Het |
|
| Other mutations in Zgrf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01088:Zgrf1
|
APN |
3 |
127,588,141 (GRCm38) |
splice site |
probably benign |
|
|
IGL01153:Zgrf1
|
APN |
3 |
127,602,406 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01330:Zgrf1
|
APN |
3 |
127,584,007 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01501:Zgrf1
|
APN |
3 |
127,602,562 (GRCm38) |
splice site |
probably null |
|
|
IGL01827:Zgrf1
|
APN |
3 |
127,616,281 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02600:Zgrf1
|
APN |
3 |
127,600,974 (GRCm38) |
splice site |
probably benign |
|
|
IGL03122:Zgrf1
|
APN |
3 |
127,588,133 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
IGL03365:Zgrf1
|
APN |
3 |
127,598,774 (GRCm38) |
missense |
possibly damaging |
0.48 |
|
R0015_Zgrf1_014
|
UTSW |
3 |
127,555,397 (GRCm38) |
splice site |
probably benign |
|
|
R1298_Zgrf1_204
|
UTSW |
3 |
127,583,889 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R7175_zgrf1_533
|
UTSW |
3 |
127,563,590 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0243:Zgrf1
|
UTSW |
3 |
127,615,446 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0468:Zgrf1
|
UTSW |
3 |
127,562,041 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R0497:Zgrf1
|
UTSW |
3 |
127,584,650 (GRCm38) |
splice site |
probably benign |
|
|
R0505:Zgrf1
|
UTSW |
3 |
127,573,238 (GRCm38) |
missense |
probably benign |
0.30 |
|
R0511:Zgrf1
|
UTSW |
3 |
127,584,660 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R0539:Zgrf1
|
UTSW |
3 |
127,615,192 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0617:Zgrf1
|
UTSW |
3 |
127,588,038 (GRCm38) |
missense |
probably benign |
0.39 |
|
R1298:Zgrf1
|
UTSW |
3 |
127,583,889 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R1353:Zgrf1
|
UTSW |
3 |
127,611,803 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1593:Zgrf1
|
UTSW |
3 |
127,561,026 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R1846:Zgrf1
|
UTSW |
3 |
127,615,463 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1912:Zgrf1
|
UTSW |
3 |
127,563,137 (GRCm38) |
missense |
probably benign |
|
|
R2062:Zgrf1
|
UTSW |
3 |
127,613,350 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2064:Zgrf1
|
UTSW |
3 |
127,613,350 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2065:Zgrf1
|
UTSW |
3 |
127,613,350 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2066:Zgrf1
|
UTSW |
3 |
127,613,350 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2067:Zgrf1
|
UTSW |
3 |
127,613,350 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2256:Zgrf1
|
UTSW |
3 |
127,561,997 (GRCm38) |
missense |
probably benign |
0.18 |
|
R2321:Zgrf1
|
UTSW |
3 |
127,562,407 (GRCm38) |
nonsense |
probably null |
|
|
R2381:Zgrf1
|
UTSW |
3 |
127,556,214 (GRCm38) |
missense |
probably benign |
0.02 |
|
R2913:Zgrf1
|
UTSW |
3 |
127,598,707 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R3147:Zgrf1
|
UTSW |
3 |
127,584,148 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R3236:Zgrf1
|
UTSW |
3 |
127,613,375 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3237:Zgrf1
|
UTSW |
3 |
127,613,375 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4433:Zgrf1
|
UTSW |
3 |
127,562,078 (GRCm38) |
missense |
probably benign |
|
|
R4441:Zgrf1
|
UTSW |
3 |
127,586,137 (GRCm38) |
missense |
possibly damaging |
0.45 |
|
R4457:Zgrf1
|
UTSW |
3 |
127,595,929 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4498:Zgrf1
|
UTSW |
3 |
127,586,100 (GRCm38) |
nonsense |
probably null |
|
|
R4598:Zgrf1
|
UTSW |
3 |
127,601,030 (GRCm38) |
missense |
probably benign |
0.14 |
|
R4701:Zgrf1
|
UTSW |
3 |
127,598,704 (GRCm38) |
missense |
probably benign |
0.03 |
|
R4898:Zgrf1
|
UTSW |
3 |
127,602,436 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4944:Zgrf1
|
UTSW |
3 |
127,561,868 (GRCm38) |
nonsense |
probably null |
|
|
R5256:Zgrf1
|
UTSW |
3 |
127,602,445 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5294:Zgrf1
|
UTSW |
3 |
127,600,980 (GRCm38) |
missense |
probably benign |
0.14 |
|
R5358:Zgrf1
|
UTSW |
3 |
127,567,703 (GRCm38) |
critical splice donor site |
probably null |
|
|
R5359:Zgrf1
|
UTSW |
3 |
127,601,165 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R5447:Zgrf1
|
UTSW |
3 |
127,563,119 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R5569:Zgrf1
|
UTSW |
3 |
127,561,025 (GRCm38) |
missense |
probably benign |
0.33 |
|
R5887:Zgrf1
|
UTSW |
3 |
127,584,765 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5914:Zgrf1
|
UTSW |
3 |
127,561,023 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5925:Zgrf1
|
UTSW |
3 |
127,573,204 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R5936:Zgrf1
|
UTSW |
3 |
127,562,253 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R6087:Zgrf1
|
UTSW |
3 |
127,615,486 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6089:Zgrf1
|
UTSW |
3 |
127,595,993 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6181:Zgrf1
|
UTSW |
3 |
127,587,941 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6277:Zgrf1
|
UTSW |
3 |
127,598,812 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R6441:Zgrf1
|
UTSW |
3 |
127,588,034 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R6659:Zgrf1
|
UTSW |
3 |
127,616,506 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6857:Zgrf1
|
UTSW |
3 |
127,581,447 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6932:Zgrf1
|
UTSW |
3 |
127,559,632 (GRCm38) |
critical splice donor site |
probably null |
|
|
R7008:Zgrf1
|
UTSW |
3 |
127,561,772 (GRCm38) |
missense |
probably benign |
0.18 |
|
R7175:Zgrf1
|
UTSW |
3 |
127,563,590 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7264:Zgrf1
|
UTSW |
3 |
127,563,569 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7272:Zgrf1
|
UTSW |
3 |
127,598,760 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7298:Zgrf1
|
UTSW |
3 |
127,583,650 (GRCm38) |
nonsense |
probably null |
|
|
R7412:Zgrf1
|
UTSW |
3 |
127,563,071 (GRCm38) |
missense |
probably benign |
0.06 |
|
R7836:Zgrf1
|
UTSW |
3 |
127,563,431 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R7945:Zgrf1
|
UTSW |
3 |
127,562,760 (GRCm38) |
missense |
probably benign |
0.37 |
|
R7996:Zgrf1
|
UTSW |
3 |
127,595,924 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R8165:Zgrf1
|
UTSW |
3 |
127,563,383 (GRCm38) |
missense |
possibly damaging |
0.76 |
|
R8198:Zgrf1
|
UTSW |
3 |
127,596,024 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8296:Zgrf1
|
UTSW |
3 |
127,583,995 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8298:Zgrf1
|
UTSW |
3 |
127,615,229 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8341:Zgrf1
|
UTSW |
3 |
127,560,915 (GRCm38) |
nonsense |
probably null |
|
|
R8445:Zgrf1
|
UTSW |
3 |
127,586,205 (GRCm38) |
critical splice donor site |
probably null |
|
|
R9088:Zgrf1
|
UTSW |
3 |
127,583,677 (GRCm38) |
missense |
probably benign |
0.21 |
|
R9236:Zgrf1
|
UTSW |
3 |
127,584,663 (GRCm38) |
missense |
probably benign |
0.09 |
|
R9250:Zgrf1
|
UTSW |
3 |
127,586,148 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9253:Zgrf1
|
UTSW |
3 |
127,598,779 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9464:Zgrf1
|
UTSW |
3 |
127,584,092 (GRCm38) |
missense |
probably benign |
0.03 |
|
R9647:Zgrf1
|
UTSW |
3 |
127,561,602 (GRCm38) |
missense |
probably benign |
0.02 |
|
R9680:Zgrf1
|
UTSW |
3 |
127,615,567 (GRCm38) |
missense |
probably benign |
0.38 |
|
RF015:Zgrf1
|
UTSW |
3 |
127,563,233 (GRCm38) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGCAAGCCACTGGAGAGATGTTTAC -3'
(R):5'- CGTCAGAGGAAGAATGCAGTTCCC -3'
Sequencing Primer
(F):5'- GTCCTCCATGACAGATACAGTTTTG -3'
(R):5'- GCTGCATGTTACTACCTCAAATG -3'
|
| Posted On |
2014-07-17 |
Incidental Mutation