Incidental Mutation 'R6932:Zgrf1'
ID |
540075 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zgrf1
|
Ensembl Gene |
ENSMUSG00000051278 |
Gene Name |
zinc finger, GRF-type containing 1 |
Synonyms |
4930422G04Rik |
MMRRC Submission |
045047-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.081)
|
Stock # |
R6932 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
127347138-127411672 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 127353281 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143761
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043108]
[ENSMUST00000195955]
[ENSMUST00000196141]
[ENSMUST00000199888]
[ENSMUST00000200490]
|
AlphaFold |
Q0VGT4 |
Predicted Effect |
probably null
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 null
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 null
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 |
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.2%
- 20x: 97.2%
|
Validation Efficiency |
98% (80/82) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acads |
A |
T |
5: 115,250,331 (GRCm39) |
F198I |
probably damaging |
Het |
Acy1 |
A |
G |
9: 106,314,826 (GRCm39) |
|
probably null |
Het |
Adk |
A |
G |
14: 21,126,376 (GRCm39) |
M1V |
probably null |
Het |
Ahi1 |
A |
G |
10: 20,839,590 (GRCm39) |
D167G |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,791,054 (GRCm39) |
V290A |
possibly damaging |
Het |
Arhgef5 |
T |
A |
6: 43,251,351 (GRCm39) |
S701T |
possibly damaging |
Het |
Atp13a5 |
C |
A |
16: 29,100,769 (GRCm39) |
M673I |
probably damaging |
Het |
BC005624 |
T |
C |
2: 30,868,940 (GRCm39) |
D78G |
possibly damaging |
Het |
Bcat2 |
C |
T |
7: 45,238,745 (GRCm39) |
H347Y |
probably damaging |
Het |
Bpifb4 |
A |
G |
2: 153,784,547 (GRCm39) |
Y85C |
possibly damaging |
Het |
Cdc42 |
T |
A |
4: 137,049,932 (GRCm39) |
|
probably null |
Het |
Cep170 |
G |
A |
1: 176,589,003 (GRCm39) |
L541F |
possibly damaging |
Het |
Cfap97d2 |
CA |
CAA |
8: 13,784,865 (GRCm39) |
|
probably null |
Het |
Cgrrf1 |
T |
A |
14: 47,091,179 (GRCm39) |
N234K |
probably benign |
Het |
Ctrc |
C |
T |
4: 141,568,879 (GRCm39) |
C108Y |
probably damaging |
Het |
Cyp2u1 |
C |
T |
3: 131,091,945 (GRCm39) |
V192M |
possibly damaging |
Het |
Dhx38 |
A |
T |
8: 110,279,307 (GRCm39) |
L1013Q |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,009,733 (GRCm39) |
N1945I |
probably damaging |
Het |
Dnah10 |
C |
G |
5: 124,898,514 (GRCm39) |
N3765K |
possibly damaging |
Het |
Dnah17 |
C |
A |
11: 117,950,905 (GRCm39) |
R2906L |
possibly damaging |
Het |
Dnajc10 |
C |
T |
2: 80,161,680 (GRCm39) |
T306I |
probably benign |
Het |
Efemp2 |
T |
A |
19: 5,530,273 (GRCm39) |
C287S |
probably damaging |
Het |
Efna1 |
T |
C |
3: 89,180,091 (GRCm39) |
R143G |
probably benign |
Het |
Emilin1 |
A |
C |
5: 31,074,421 (GRCm39) |
N221H |
probably damaging |
Het |
Epg5 |
A |
G |
18: 77,991,824 (GRCm39) |
T174A |
probably benign |
Het |
Fam184b |
T |
A |
5: 45,690,243 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
T |
A |
7: 100,926,621 (GRCm39) |
C570* |
probably null |
Het |
Gm4787 |
A |
T |
12: 81,425,974 (GRCm39) |
D61E |
probably benign |
Het |
Gm7356 |
C |
T |
17: 14,221,925 (GRCm39) |
G35R |
probably damaging |
Het |
Gm8220 |
A |
G |
14: 44,525,645 (GRCm39) |
T20A |
probably damaging |
Het |
Hivep2 |
C |
T |
10: 14,004,245 (GRCm39) |
T281M |
probably damaging |
Het |
Ighv2-9-1 |
A |
G |
12: 113,733,692 (GRCm39) |
V43A |
probably damaging |
Het |
Klhl33 |
A |
T |
14: 51,129,373 (GRCm39) |
C619S |
probably benign |
Het |
Kmt2a |
A |
T |
9: 44,740,558 (GRCm39) |
|
probably benign |
Het |
Lax1 |
A |
G |
1: 133,607,896 (GRCm39) |
C282R |
probably benign |
Het |
Lrrd1 |
A |
G |
5: 3,901,395 (GRCm39) |
K567E |
probably benign |
Het |
Luzp1 |
C |
T |
4: 136,268,124 (GRCm39) |
R116* |
probably null |
Het |
Lypd3 |
G |
C |
7: 24,337,858 (GRCm39) |
G75R |
probably damaging |
Het |
Macrod2 |
A |
T |
2: 140,261,833 (GRCm39) |
N38I |
probably damaging |
Het |
Map3k14 |
A |
T |
11: 103,132,958 (GRCm39) |
I80N |
probably damaging |
Het |
Mcm9 |
A |
G |
10: 53,496,299 (GRCm39) |
S368P |
probably benign |
Het |
Mfge8 |
T |
C |
7: 78,793,049 (GRCm39) |
D139G |
probably benign |
Het |
Mmp19 |
A |
T |
10: 128,627,523 (GRCm39) |
I54F |
probably benign |
Het |
Myo15a |
G |
T |
11: 60,390,320 (GRCm39) |
W2114L |
probably damaging |
Het |
Myo1a |
G |
T |
10: 127,546,327 (GRCm39) |
V277L |
probably benign |
Het |
Myoc |
A |
G |
1: 162,466,915 (GRCm39) |
D28G |
probably damaging |
Het |
Myrf |
G |
T |
19: 10,196,924 (GRCm39) |
N487K |
probably damaging |
Het |
Omd |
T |
A |
13: 49,743,710 (GRCm39) |
F253L |
probably damaging |
Het |
Or2ag19 |
G |
T |
7: 106,444,009 (GRCm39) |
G64* |
probably null |
Het |
Or5t5 |
C |
G |
2: 86,616,499 (GRCm39) |
L142V |
probably damaging |
Het |
Or6n1 |
G |
A |
1: 173,917,316 (GRCm39) |
A237T |
probably damaging |
Het |
Papss1 |
T |
G |
3: 131,305,732 (GRCm39) |
I238S |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,632,675 (GRCm39) |
F580Y |
probably benign |
Het |
Polk |
T |
A |
13: 96,653,189 (GRCm39) |
K70N |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,562,755 (GRCm39) |
D31E |
probably benign |
Het |
Ppp6r1 |
G |
T |
7: 4,636,291 (GRCm39) |
S766R |
possibly damaging |
Het |
Rab11fip5 |
T |
C |
6: 85,318,540 (GRCm39) |
D783G |
probably benign |
Het |
Reln |
T |
C |
5: 22,190,855 (GRCm39) |
I1511V |
probably benign |
Het |
Rnh1 |
T |
C |
7: 140,743,096 (GRCm39) |
N268S |
probably damaging |
Het |
Rpia |
A |
G |
6: 70,750,424 (GRCm39) |
V236A |
probably benign |
Het |
Rpl10a |
G |
T |
17: 28,548,424 (GRCm39) |
V80L |
probably benign |
Het |
Sap130 |
T |
G |
18: 31,799,407 (GRCm39) |
S295A |
possibly damaging |
Het |
Sgms1 |
C |
T |
19: 32,120,193 (GRCm39) |
V238I |
probably benign |
Het |
Sh3tc1 |
A |
G |
5: 35,864,778 (GRCm39) |
S470P |
probably benign |
Het |
Slc25a32 |
A |
G |
15: 38,960,984 (GRCm39) |
V233A |
possibly damaging |
Het |
Slc2a2 |
T |
C |
3: 28,771,668 (GRCm39) |
S158P |
probably benign |
Het |
Slc6a2 |
A |
G |
8: 93,722,653 (GRCm39) |
Y550C |
probably benign |
Het |
Slc7a9 |
C |
A |
7: 35,151,936 (GRCm39) |
T77K |
probably benign |
Het |
Snd1 |
A |
T |
6: 28,626,100 (GRCm39) |
D385V |
probably benign |
Het |
Ssh3 |
A |
T |
19: 4,314,448 (GRCm39) |
F369I |
probably damaging |
Het |
Syk |
A |
G |
13: 52,766,495 (GRCm39) |
|
probably null |
Het |
Tbc1d16 |
A |
G |
11: 119,099,742 (GRCm39) |
S211P |
probably damaging |
Het |
Ttc3 |
A |
G |
16: 94,244,312 (GRCm39) |
T1439A |
probably benign |
Het |
Usp18 |
A |
G |
6: 121,229,473 (GRCm39) |
M31V |
probably benign |
Het |
Vav1 |
G |
T |
17: 57,609,330 (GRCm39) |
E415D |
possibly damaging |
Het |
Vps13a |
A |
T |
19: 16,655,439 (GRCm39) |
V1863D |
probably benign |
Het |
Xdh |
T |
A |
17: 74,229,557 (GRCm39) |
I299F |
probably damaging |
Het |
Zc3h14 |
A |
G |
12: 98,737,336 (GRCm39) |
|
probably benign |
Het |
Zfp345 |
G |
A |
2: 150,315,331 (GRCm39) |
H69Y |
probably damaging |
Het |
Zfp652 |
G |
T |
11: 95,654,667 (GRCm39) |
V357L |
probably benign |
Het |
Zfp712 |
A |
T |
13: 67,188,891 (GRCm39) |
Y545* |
probably null |
Het |
|
Other mutations in Zgrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Zgrf1
|
APN |
3 |
127,381,790 (GRCm39) |
splice site |
probably benign |
|
IGL01153:Zgrf1
|
APN |
3 |
127,396,055 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Zgrf1
|
APN |
3 |
127,377,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01501:Zgrf1
|
APN |
3 |
127,396,211 (GRCm39) |
splice site |
probably null |
|
IGL01827:Zgrf1
|
APN |
3 |
127,409,930 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02600:Zgrf1
|
APN |
3 |
127,394,623 (GRCm39) |
splice site |
probably benign |
|
IGL03122:Zgrf1
|
APN |
3 |
127,381,782 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03365:Zgrf1
|
APN |
3 |
127,392,423 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0015_Zgrf1_014
|
UTSW |
3 |
127,349,046 (GRCm39) |
splice site |
probably benign |
|
R1298_Zgrf1_204
|
UTSW |
3 |
127,377,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7175_zgrf1_533
|
UTSW |
3 |
127,357,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Zgrf1
|
UTSW |
3 |
127,349,046 (GRCm39) |
splice site |
probably benign |
|
R0243:Zgrf1
|
UTSW |
3 |
127,409,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R0468:Zgrf1
|
UTSW |
3 |
127,355,690 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0497:Zgrf1
|
UTSW |
3 |
127,378,299 (GRCm39) |
splice site |
probably benign |
|
R0505:Zgrf1
|
UTSW |
3 |
127,366,887 (GRCm39) |
missense |
probably benign |
0.30 |
R0511:Zgrf1
|
UTSW |
3 |
127,378,309 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0539:Zgrf1
|
UTSW |
3 |
127,408,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Zgrf1
|
UTSW |
3 |
127,381,687 (GRCm39) |
missense |
probably benign |
0.39 |
R1298:Zgrf1
|
UTSW |
3 |
127,377,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1353:Zgrf1
|
UTSW |
3 |
127,405,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1593:Zgrf1
|
UTSW |
3 |
127,354,675 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1846:Zgrf1
|
UTSW |
3 |
127,409,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Zgrf1
|
UTSW |
3 |
127,356,786 (GRCm39) |
missense |
probably benign |
|
R2062:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Zgrf1
|
UTSW |
3 |
127,355,646 (GRCm39) |
missense |
probably benign |
0.18 |
R2321:Zgrf1
|
UTSW |
3 |
127,356,056 (GRCm39) |
nonsense |
probably null |
|
R2381:Zgrf1
|
UTSW |
3 |
127,349,863 (GRCm39) |
missense |
probably benign |
0.02 |
R2913:Zgrf1
|
UTSW |
3 |
127,392,356 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3147:Zgrf1
|
UTSW |
3 |
127,377,797 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3236:Zgrf1
|
UTSW |
3 |
127,407,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R3237:Zgrf1
|
UTSW |
3 |
127,407,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R4433:Zgrf1
|
UTSW |
3 |
127,355,727 (GRCm39) |
missense |
probably benign |
|
R4441:Zgrf1
|
UTSW |
3 |
127,379,786 (GRCm39) |
missense |
possibly damaging |
0.45 |
R4457:Zgrf1
|
UTSW |
3 |
127,389,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R4498:Zgrf1
|
UTSW |
3 |
127,379,749 (GRCm39) |
nonsense |
probably null |
|
R4598:Zgrf1
|
UTSW |
3 |
127,394,679 (GRCm39) |
missense |
probably benign |
0.14 |
R4701:Zgrf1
|
UTSW |
3 |
127,392,353 (GRCm39) |
missense |
probably benign |
0.03 |
R4898:Zgrf1
|
UTSW |
3 |
127,396,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4944:Zgrf1
|
UTSW |
3 |
127,355,517 (GRCm39) |
nonsense |
probably null |
|
R5256:Zgrf1
|
UTSW |
3 |
127,396,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R5294:Zgrf1
|
UTSW |
3 |
127,394,629 (GRCm39) |
missense |
probably benign |
0.14 |
R5358:Zgrf1
|
UTSW |
3 |
127,361,352 (GRCm39) |
critical splice donor site |
probably null |
|
R5359:Zgrf1
|
UTSW |
3 |
127,394,814 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5447:Zgrf1
|
UTSW |
3 |
127,356,768 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5569:Zgrf1
|
UTSW |
3 |
127,354,674 (GRCm39) |
missense |
probably benign |
0.33 |
R5887:Zgrf1
|
UTSW |
3 |
127,378,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Zgrf1
|
UTSW |
3 |
127,354,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R5925:Zgrf1
|
UTSW |
3 |
127,366,853 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5936:Zgrf1
|
UTSW |
3 |
127,355,902 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6087:Zgrf1
|
UTSW |
3 |
127,409,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Zgrf1
|
UTSW |
3 |
127,389,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Zgrf1
|
UTSW |
3 |
127,381,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Zgrf1
|
UTSW |
3 |
127,392,461 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6441:Zgrf1
|
UTSW |
3 |
127,381,683 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6659:Zgrf1
|
UTSW |
3 |
127,410,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R6857:Zgrf1
|
UTSW |
3 |
127,375,096 (GRCm39) |
missense |
probably damaging |
0.99 |
R7008:Zgrf1
|
UTSW |
3 |
127,355,421 (GRCm39) |
missense |
probably benign |
0.18 |
R7175:Zgrf1
|
UTSW |
3 |
127,357,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7264:Zgrf1
|
UTSW |
3 |
127,357,218 (GRCm39) |
missense |
probably benign |
0.00 |
R7272:Zgrf1
|
UTSW |
3 |
127,392,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R7298:Zgrf1
|
UTSW |
3 |
127,377,299 (GRCm39) |
nonsense |
probably null |
|
R7412:Zgrf1
|
UTSW |
3 |
127,356,720 (GRCm39) |
missense |
probably benign |
0.06 |
R7836:Zgrf1
|
UTSW |
3 |
127,357,080 (GRCm39) |
missense |
probably damaging |
0.96 |
R7945:Zgrf1
|
UTSW |
3 |
127,356,409 (GRCm39) |
missense |
probably benign |
0.37 |
R7996:Zgrf1
|
UTSW |
3 |
127,389,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8165:Zgrf1
|
UTSW |
3 |
127,357,032 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8198:Zgrf1
|
UTSW |
3 |
127,389,673 (GRCm39) |
critical splice donor site |
probably null |
|
R8296:Zgrf1
|
UTSW |
3 |
127,377,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R8298:Zgrf1
|
UTSW |
3 |
127,408,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R8341:Zgrf1
|
UTSW |
3 |
127,354,564 (GRCm39) |
nonsense |
probably null |
|
R8445:Zgrf1
|
UTSW |
3 |
127,379,854 (GRCm39) |
critical splice donor site |
probably null |
|
R9088:Zgrf1
|
UTSW |
3 |
127,377,326 (GRCm39) |
missense |
probably benign |
0.21 |
R9236:Zgrf1
|
UTSW |
3 |
127,378,312 (GRCm39) |
missense |
probably benign |
0.09 |
R9250:Zgrf1
|
UTSW |
3 |
127,379,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Zgrf1
|
UTSW |
3 |
127,392,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Zgrf1
|
UTSW |
3 |
127,377,741 (GRCm39) |
missense |
probably benign |
0.03 |
R9647:Zgrf1
|
UTSW |
3 |
127,355,251 (GRCm39) |
missense |
probably benign |
0.02 |
R9680:Zgrf1
|
UTSW |
3 |
127,409,216 (GRCm39) |
missense |
probably benign |
0.38 |
RF015:Zgrf1
|
UTSW |
3 |
127,356,882 (GRCm39) |
missense |
probably benign |
0.02 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCTGCTAAGTGTATGCAGTAGC -3'
(R):5'- CGCACTAAACCTTTCTGTGTTG -3'
Sequencing Primer
(F):5'- GCAGTAGCATTTGAAGTAGATGTAC -3'
(R):5'- CTGTGTTGTACTCCTGATGTAAAAAC -3'
|
Posted On |
2018-11-06 |