Incidental Mutation 'R1466:Zzef1'
ID |
201211 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zzef1
|
Ensembl Gene |
ENSMUSG00000055670 |
Gene Name |
zinc finger, ZZ-type with EF hand domain 1 |
Synonyms |
8430405D05Rik, C130099L13Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1466 (G1)
|
Quality Score |
198 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
72687052-72817946 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 72815505 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Serine
at position 2942
(P2942S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000147028
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069395]
[ENSMUST00000172220]
[ENSMUST00000207107]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000069395
AA Change: P2880S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000068790 Gene: ENSMUSG00000055670 AA Change: P2880S
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
20 |
N/A |
INTRINSIC |
low complexity region
|
28 |
68 |
N/A |
INTRINSIC |
low complexity region
|
78 |
93 |
N/A |
INTRINSIC |
APC10
|
246 |
397 |
2.65e-48 |
SMART |
internal_repeat_1
|
1122 |
1192 |
1.25e-7 |
PROSPERO |
low complexity region
|
1472 |
1485 |
N/A |
INTRINSIC |
low complexity region
|
1512 |
1525 |
N/A |
INTRINSIC |
ZnF_ZZ
|
1775 |
1823 |
2.54e-7 |
SMART |
ZnF_ZZ
|
1824 |
1868 |
1.2e-8 |
SMART |
low complexity region
|
1947 |
1963 |
N/A |
INTRINSIC |
low complexity region
|
2127 |
2140 |
N/A |
INTRINSIC |
low complexity region
|
2249 |
2263 |
N/A |
INTRINSIC |
internal_repeat_1
|
2657 |
2726 |
1.25e-7 |
PROSPERO |
low complexity region
|
2840 |
2853 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125122
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152481
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000172220
AA Change: P2913S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000130515 Gene: ENSMUSG00000055670 AA Change: P2913S
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
20 |
N/A |
INTRINSIC |
low complexity region
|
28 |
68 |
N/A |
INTRINSIC |
low complexity region
|
78 |
93 |
N/A |
INTRINSIC |
APC10
|
246 |
397 |
2.65e-48 |
SMART |
internal_repeat_1
|
1006 |
1192 |
1.57e-16 |
PROSPERO |
low complexity region
|
1472 |
1485 |
N/A |
INTRINSIC |
low complexity region
|
1512 |
1525 |
N/A |
INTRINSIC |
ZnF_ZZ
|
1775 |
1823 |
2.54e-7 |
SMART |
ZnF_ZZ
|
1824 |
1868 |
1.2e-8 |
SMART |
low complexity region
|
1947 |
1963 |
N/A |
INTRINSIC |
low complexity region
|
2127 |
2140 |
N/A |
INTRINSIC |
low complexity region
|
2249 |
2263 |
N/A |
INTRINSIC |
internal_repeat_1
|
2583 |
2759 |
1.57e-16 |
PROSPERO |
low complexity region
|
2873 |
2886 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000207107
AA Change: P2942S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Meta Mutation Damage Score |
0.1243 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.7%
- 10x: 94.7%
- 20x: 90.4%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 134 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,520,536 (GRCm39) |
|
probably benign |
Het |
Abcg8 |
G |
C |
17: 84,994,155 (GRCm39) |
|
probably benign |
Het |
Abhd15 |
C |
T |
11: 77,406,236 (GRCm39) |
A71V |
probably damaging |
Het |
AC167973.1 |
A |
T |
9: 43,176,649 (GRCm39) |
|
noncoding transcript |
Het |
Adamts12 |
T |
C |
15: 11,311,445 (GRCm39) |
F1234S |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,993,239 (GRCm39) |
D4841G |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,378,797 (GRCm39) |
S2095P |
possibly damaging |
Het |
Ampd2 |
T |
C |
3: 107,987,653 (GRCm39) |
|
probably null |
Het |
Arhgef17 |
G |
T |
7: 100,578,866 (GRCm39) |
P694Q |
possibly damaging |
Het |
Arrdc1 |
T |
C |
2: 24,815,807 (GRCm39) |
I398V |
probably benign |
Het |
Ash1l |
T |
C |
3: 88,959,372 (GRCm39) |
Y2250H |
probably damaging |
Het |
Aspg |
A |
G |
12: 112,088,286 (GRCm39) |
N385D |
probably benign |
Het |
Atxn3 |
G |
A |
12: 101,892,758 (GRCm39) |
R319C |
possibly damaging |
Het |
Brca2 |
G |
A |
5: 150,475,723 (GRCm39) |
A2478T |
probably damaging |
Het |
Btrc |
T |
A |
19: 45,501,821 (GRCm39) |
|
probably benign |
Het |
C1s1 |
C |
T |
6: 124,508,090 (GRCm39) |
C633Y |
probably damaging |
Het |
C8g |
C |
T |
2: 25,390,228 (GRCm39) |
A6T |
probably benign |
Het |
Capza2 |
T |
C |
6: 17,657,158 (GRCm39) |
|
probably benign |
Het |
Cbl |
A |
T |
9: 44,065,541 (GRCm39) |
V706E |
probably benign |
Het |
Ccdc121rt3 |
C |
T |
5: 112,502,630 (GRCm39) |
G358D |
probably benign |
Het |
Cenatac |
A |
T |
9: 44,324,977 (GRCm39) |
|
probably benign |
Het |
Cfhr1 |
C |
T |
1: 139,485,312 (GRCm39) |
E45K |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,840,561 (GRCm39) |
|
probably null |
Het |
Chek1 |
G |
T |
9: 36,637,153 (GRCm39) |
A2E |
probably damaging |
Het |
Clcn2 |
G |
A |
16: 20,531,302 (GRCm39) |
|
probably benign |
Het |
Cndp2 |
G |
A |
18: 84,695,440 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
C |
A |
11: 101,071,186 (GRCm39) |
F366L |
probably damaging |
Het |
Col5a1 |
G |
T |
2: 27,893,858 (GRCm39) |
|
probably benign |
Het |
Corin |
C |
T |
5: 72,460,133 (GRCm39) |
|
probably null |
Het |
Crb2 |
T |
C |
2: 37,673,400 (GRCm39) |
Y99H |
probably damaging |
Het |
Csf3r |
T |
A |
4: 125,925,725 (GRCm39) |
|
probably benign |
Het |
Ctdspl2 |
G |
A |
2: 121,834,410 (GRCm39) |
R332K |
probably benign |
Het |
Ctnnbl1 |
C |
T |
2: 157,641,337 (GRCm39) |
|
probably benign |
Het |
Cym |
G |
A |
3: 107,120,774 (GRCm39) |
T277I |
probably damaging |
Het |
Cyp2d11 |
C |
T |
15: 82,275,936 (GRCm39) |
C215Y |
probably benign |
Het |
Dido1 |
G |
A |
2: 180,304,121 (GRCm39) |
P1261L |
probably damaging |
Het |
Dnah10 |
T |
A |
5: 124,840,160 (GRCm39) |
Y1265N |
probably benign |
Het |
Dtx3l |
G |
A |
16: 35,753,098 (GRCm39) |
L503F |
probably damaging |
Het |
Eda |
T |
A |
X: 99,435,998 (GRCm39) |
|
probably benign |
Homo |
Efhb |
A |
G |
17: 53,744,206 (GRCm39) |
F462L |
probably damaging |
Het |
Enpep |
T |
A |
3: 129,113,097 (GRCm39) |
T203S |
probably damaging |
Het |
Exd1 |
G |
A |
2: 119,351,215 (GRCm39) |
|
probably benign |
Het |
Fam184b |
G |
A |
5: 45,737,851 (GRCm39) |
|
probably benign |
Het |
Fam20b |
T |
C |
1: 156,513,758 (GRCm39) |
|
probably benign |
Het |
Fat3 |
A |
C |
9: 16,286,778 (GRCm39) |
V915G |
probably damaging |
Het |
Fbln7 |
A |
G |
2: 128,719,349 (GRCm39) |
T49A |
probably benign |
Het |
Fcho1 |
C |
T |
8: 72,165,204 (GRCm39) |
A418T |
probably benign |
Het |
Fgf14 |
T |
A |
14: 124,913,951 (GRCm39) |
K60M |
probably benign |
Het |
Galnt4 |
A |
G |
10: 98,944,571 (GRCm39) |
R99G |
probably benign |
Het |
Gimap4 |
C |
A |
6: 48,668,216 (GRCm39) |
Q196K |
probably benign |
Het |
Glcci1 |
C |
T |
6: 8,537,964 (GRCm39) |
T6I |
probably damaging |
Het |
Gm10110 |
A |
T |
14: 90,135,511 (GRCm39) |
|
noncoding transcript |
Het |
Gm4884 |
A |
G |
7: 40,692,552 (GRCm39) |
K174E |
probably damaging |
Het |
Grip2 |
A |
T |
6: 91,765,424 (GRCm39) |
D19E |
probably damaging |
Het |
Grk4 |
T |
C |
5: 34,852,094 (GRCm39) |
S113P |
probably benign |
Het |
Hectd3 |
G |
A |
4: 116,853,763 (GRCm39) |
E220K |
probably damaging |
Het |
Helz2 |
G |
A |
2: 180,878,090 (GRCm39) |
P903S |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,259,585 (GRCm39) |
V2519E |
possibly damaging |
Het |
Igf2r |
A |
T |
17: 12,936,156 (GRCm39) |
|
probably benign |
Het |
Ints11 |
G |
A |
4: 155,972,567 (GRCm39) |
|
probably null |
Het |
Kif1a |
A |
G |
1: 92,982,651 (GRCm39) |
W718R |
possibly damaging |
Het |
Kif1b |
A |
T |
4: 149,307,709 (GRCm39) |
Y839N |
probably damaging |
Het |
Kif20b |
T |
A |
19: 34,927,999 (GRCm39) |
V1047D |
probably benign |
Het |
Klhl23 |
T |
C |
2: 69,664,232 (GRCm39) |
I527T |
probably damaging |
Het |
Klra10 |
T |
A |
6: 130,256,278 (GRCm39) |
R125S |
probably damaging |
Het |
Klra10 |
T |
C |
6: 130,256,394 (GRCm39) |
N87D |
probably damaging |
Het |
Lars1 |
G |
A |
18: 42,343,115 (GRCm39) |
R1101C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,558,588 (GRCm39) |
P166L |
probably damaging |
Het |
Letmd1 |
T |
A |
15: 100,370,423 (GRCm39) |
|
probably null |
Het |
Lrrc27 |
A |
G |
7: 138,810,224 (GRCm39) |
|
probably benign |
Het |
Map4k2 |
G |
T |
19: 6,391,947 (GRCm39) |
W87L |
probably damaging |
Het |
Mccc1 |
A |
G |
3: 36,028,435 (GRCm39) |
V457A |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,730,788 (GRCm39) |
S2886T |
probably benign |
Het |
Mgat4a |
A |
T |
1: 37,503,487 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,384,779 (GRCm39) |
|
probably benign |
Het |
Mroh2b |
G |
T |
15: 4,955,166 (GRCm39) |
D720Y |
probably damaging |
Het |
Mrpl24 |
T |
A |
3: 87,829,235 (GRCm39) |
Y21* |
probably null |
Het |
Mrps35 |
C |
T |
6: 146,957,482 (GRCm39) |
T169M |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,687,430 (GRCm39) |
D492V |
probably damaging |
Het |
Muc2 |
A |
G |
7: 141,302,711 (GRCm39) |
Y457C |
probably damaging |
Het |
Muc4 |
G |
A |
16: 32,574,886 (GRCm39) |
G1157D |
probably benign |
Het |
Myg1 |
T |
A |
15: 102,245,825 (GRCm39) |
L275Q |
probably damaging |
Het |
Naga |
T |
A |
15: 82,218,989 (GRCm39) |
M237L |
probably null |
Het |
Nek1 |
C |
T |
8: 61,578,170 (GRCm39) |
|
probably benign |
Het |
Oc90 |
T |
A |
15: 65,769,569 (GRCm39) |
Y96F |
probably damaging |
Het |
Or12d13 |
A |
T |
17: 37,647,847 (GRCm39) |
L92H |
probably benign |
Het |
Or13a18 |
A |
G |
7: 140,190,882 (GRCm39) |
I268V |
probably benign |
Het |
Or4a80 |
C |
T |
2: 89,582,611 (GRCm39) |
C187Y |
probably damaging |
Het |
Or5m11b |
T |
A |
2: 85,806,339 (GRCm39) |
F251I |
probably damaging |
Het |
Or6ae1 |
A |
G |
7: 139,742,116 (GRCm39) |
V249A |
probably damaging |
Het |
Orc4 |
A |
T |
2: 48,799,506 (GRCm39) |
C324S |
possibly damaging |
Het |
Pald1 |
T |
C |
10: 61,184,304 (GRCm39) |
|
probably benign |
Het |
Paox |
A |
G |
7: 139,709,194 (GRCm39) |
|
probably benign |
Het |
Pcdh10 |
T |
G |
3: 45,334,409 (GRCm39) |
L241R |
probably damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,668,418 (GRCm39) |
S857P |
probably benign |
Het |
Plec |
C |
T |
15: 76,070,108 (GRCm39) |
E1000K |
possibly damaging |
Het |
Plvap |
A |
T |
8: 71,961,125 (GRCm39) |
V149D |
probably benign |
Het |
Ppef1 |
C |
A |
X: 159,408,670 (GRCm39) |
|
probably null |
Homo |
Prkaa1 |
C |
A |
15: 5,208,279 (GRCm39) |
P507T |
probably benign |
Het |
Psmd2 |
A |
G |
16: 20,476,715 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
A |
G |
13: 63,672,783 (GRCm39) |
Y804H |
probably benign |
Het |
R3hdm2 |
A |
G |
10: 127,312,559 (GRCm39) |
I434V |
probably benign |
Het |
Rbm28 |
G |
A |
6: 29,155,016 (GRCm39) |
|
probably benign |
Het |
Rfx5 |
T |
A |
3: 94,863,614 (GRCm39) |
Y88N |
probably damaging |
Het |
Rnase2b |
A |
T |
14: 51,400,296 (GRCm39) |
K126* |
probably null |
Het |
Rpl3l |
A |
G |
17: 24,949,845 (GRCm39) |
I15V |
probably benign |
Het |
Saal1 |
G |
T |
7: 46,351,969 (GRCm39) |
|
probably null |
Het |
Sbpl |
A |
C |
17: 24,172,228 (GRCm39) |
D230E |
unknown |
Het |
Scn10a |
T |
C |
9: 119,495,556 (GRCm39) |
Y322C |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,321,169 (GRCm39) |
Y1308N |
probably damaging |
Het |
Sis |
A |
T |
3: 72,839,393 (GRCm39) |
D824E |
possibly damaging |
Het |
Slc25a36 |
A |
G |
9: 96,962,408 (GRCm39) |
F194L |
probably damaging |
Het |
Slc27a4 |
T |
A |
2: 29,701,202 (GRCm39) |
V331E |
probably damaging |
Het |
Slc7a11 |
G |
T |
3: 50,335,522 (GRCm39) |
|
probably null |
Het |
Slco4c1 |
A |
T |
1: 96,768,897 (GRCm39) |
S322T |
probably damaging |
Het |
Smarcc2 |
A |
T |
10: 128,310,114 (GRCm39) |
T376S |
probably damaging |
Het |
Srebf1 |
C |
T |
11: 60,091,528 (GRCm39) |
R999H |
probably benign |
Het |
St3gal3 |
A |
C |
4: 117,964,859 (GRCm39) |
M1R |
probably null |
Het |
Syp |
A |
T |
X: 7,514,944 (GRCm39) |
|
probably benign |
Homo |
Tas1r2 |
A |
G |
4: 139,396,722 (GRCm39) |
D687G |
probably damaging |
Het |
Tekt4 |
A |
T |
17: 25,691,048 (GRCm39) |
Q118L |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,666,123 (GRCm39) |
I215N |
probably damaging |
Het |
Tph2 |
T |
C |
10: 114,915,600 (GRCm39) |
N480S |
probably benign |
Het |
Tsc2 |
A |
T |
17: 24,827,947 (GRCm39) |
M839K |
probably damaging |
Het |
Ttc22 |
T |
C |
4: 106,479,977 (GRCm39) |
F77S |
probably damaging |
Het |
Uaca |
C |
T |
9: 60,761,603 (GRCm39) |
A205V |
possibly damaging |
Het |
Ubp1 |
T |
G |
9: 113,773,903 (GRCm39) |
|
probably benign |
Het |
Uhmk1 |
A |
T |
1: 170,036,222 (GRCm39) |
|
probably null |
Het |
Usp17lc |
A |
G |
7: 103,068,148 (GRCm39) |
H481R |
possibly damaging |
Het |
Vwa3a |
A |
G |
7: 120,367,388 (GRCm39) |
Y181C |
probably damaging |
Het |
Wdr26 |
C |
T |
1: 181,013,499 (GRCm39) |
|
probably benign |
Het |
Wfikkn2 |
G |
A |
11: 94,129,721 (GRCm39) |
T140I |
probably damaging |
Het |
Zfp704 |
G |
T |
3: 9,512,408 (GRCm39) |
T288N |
possibly damaging |
Het |
Zfp93 |
T |
C |
7: 23,975,521 (GRCm39) |
V502A |
probably damaging |
Het |
|
Other mutations in Zzef1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Zzef1
|
APN |
11 |
72,765,952 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00898:Zzef1
|
APN |
11 |
72,765,999 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00970:Zzef1
|
APN |
11 |
72,806,071 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01062:Zzef1
|
APN |
11 |
72,765,795 (GRCm39) |
missense |
probably benign |
|
IGL01832:Zzef1
|
APN |
11 |
72,765,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02005:Zzef1
|
APN |
11 |
72,779,125 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02026:Zzef1
|
APN |
11 |
72,772,164 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02110:Zzef1
|
APN |
11 |
72,803,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02305:Zzef1
|
APN |
11 |
72,757,423 (GRCm39) |
splice site |
probably benign |
|
IGL02308:Zzef1
|
APN |
11 |
72,777,573 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02315:Zzef1
|
APN |
11 |
72,766,083 (GRCm39) |
nonsense |
probably null |
|
IGL02332:Zzef1
|
APN |
11 |
72,807,335 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02389:Zzef1
|
APN |
11 |
72,782,043 (GRCm39) |
missense |
probably benign |
|
IGL02389:Zzef1
|
APN |
11 |
72,790,364 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02451:Zzef1
|
APN |
11 |
72,792,214 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02541:Zzef1
|
APN |
11 |
72,763,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02950:Zzef1
|
APN |
11 |
72,808,525 (GRCm39) |
splice site |
probably benign |
|
IGL02953:Zzef1
|
APN |
11 |
72,746,224 (GRCm39) |
missense |
probably benign |
|
IGL03053:Zzef1
|
APN |
11 |
72,722,365 (GRCm39) |
splice site |
probably benign |
|
IGL03085:Zzef1
|
APN |
11 |
72,746,350 (GRCm39) |
splice site |
probably benign |
|
IGL03152:Zzef1
|
APN |
11 |
72,814,008 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03329:Zzef1
|
APN |
11 |
72,808,099 (GRCm39) |
splice site |
probably benign |
|
IGL03376:Zzef1
|
APN |
11 |
72,767,377 (GRCm39) |
splice site |
probably benign |
|
IGL03394:Zzef1
|
APN |
11 |
72,777,601 (GRCm39) |
splice site |
probably null |
|
Dreidel
|
UTSW |
11 |
72,799,295 (GRCm39) |
nonsense |
probably null |
|
Hanukkah
|
UTSW |
11 |
72,784,158 (GRCm39) |
missense |
probably benign |
0.00 |
Mezuzah
|
UTSW |
11 |
72,739,559 (GRCm39) |
nonsense |
probably null |
|
BB005:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
BB015:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4508001:Zzef1
|
UTSW |
11 |
72,786,002 (GRCm39) |
missense |
probably benign |
|
PIT4581001:Zzef1
|
UTSW |
11 |
72,790,498 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4810001:Zzef1
|
UTSW |
11 |
72,741,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Zzef1
|
UTSW |
11 |
72,708,791 (GRCm39) |
missense |
probably benign |
0.01 |
R0119:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0136:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0140:Zzef1
|
UTSW |
11 |
72,790,377 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0212:Zzef1
|
UTSW |
11 |
72,764,736 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0217:Zzef1
|
UTSW |
11 |
72,779,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R0220:Zzef1
|
UTSW |
11 |
72,756,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Zzef1
|
UTSW |
11 |
72,771,450 (GRCm39) |
missense |
probably benign |
0.10 |
R0400:Zzef1
|
UTSW |
11 |
72,786,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Zzef1
|
UTSW |
11 |
72,756,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0471:Zzef1
|
UTSW |
11 |
72,813,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Zzef1
|
UTSW |
11 |
72,808,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Zzef1
|
UTSW |
11 |
72,742,726 (GRCm39) |
missense |
probably benign |
0.00 |
R0599:Zzef1
|
UTSW |
11 |
72,804,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R0603:Zzef1
|
UTSW |
11 |
72,708,895 (GRCm39) |
missense |
probably benign |
0.00 |
R0657:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0987:Zzef1
|
UTSW |
11 |
72,792,159 (GRCm39) |
small deletion |
probably benign |
|
R1246:Zzef1
|
UTSW |
11 |
72,765,735 (GRCm39) |
missense |
probably benign |
0.00 |
R1327:Zzef1
|
UTSW |
11 |
72,784,240 (GRCm39) |
critical splice donor site |
probably null |
|
R1438:Zzef1
|
UTSW |
11 |
72,803,771 (GRCm39) |
missense |
probably damaging |
0.96 |
R1466:Zzef1
|
UTSW |
11 |
72,815,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Zzef1
|
UTSW |
11 |
72,791,635 (GRCm39) |
splice site |
probably null |
|
R1556:Zzef1
|
UTSW |
11 |
72,806,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Zzef1
|
UTSW |
11 |
72,739,559 (GRCm39) |
nonsense |
probably null |
|
R1584:Zzef1
|
UTSW |
11 |
72,815,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1643:Zzef1
|
UTSW |
11 |
72,717,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Zzef1
|
UTSW |
11 |
72,754,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1764:Zzef1
|
UTSW |
11 |
72,784,158 (GRCm39) |
missense |
probably benign |
0.00 |
R1777:Zzef1
|
UTSW |
11 |
72,801,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Zzef1
|
UTSW |
11 |
72,777,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Zzef1
|
UTSW |
11 |
72,739,540 (GRCm39) |
missense |
probably damaging |
0.99 |
R2096:Zzef1
|
UTSW |
11 |
72,763,465 (GRCm39) |
missense |
probably benign |
0.02 |
R2134:Zzef1
|
UTSW |
11 |
72,771,450 (GRCm39) |
missense |
probably benign |
0.02 |
R2157:Zzef1
|
UTSW |
11 |
72,739,460 (GRCm39) |
splice site |
probably benign |
|
R2183:Zzef1
|
UTSW |
11 |
72,777,544 (GRCm39) |
nonsense |
probably null |
|
R2192:Zzef1
|
UTSW |
11 |
72,800,982 (GRCm39) |
splice site |
probably null |
|
R2230:Zzef1
|
UTSW |
11 |
72,775,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Zzef1
|
UTSW |
11 |
72,791,459 (GRCm39) |
nonsense |
probably null |
|
R2384:Zzef1
|
UTSW |
11 |
72,749,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R2426:Zzef1
|
UTSW |
11 |
72,806,091 (GRCm39) |
missense |
probably benign |
0.01 |
R2915:Zzef1
|
UTSW |
11 |
72,801,152 (GRCm39) |
splice site |
probably null |
|
R3700:Zzef1
|
UTSW |
11 |
72,777,598 (GRCm39) |
missense |
probably null |
1.00 |
R3875:Zzef1
|
UTSW |
11 |
72,779,866 (GRCm39) |
missense |
probably benign |
0.22 |
R3902:Zzef1
|
UTSW |
11 |
72,799,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R3927:Zzef1
|
UTSW |
11 |
72,749,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R4086:Zzef1
|
UTSW |
11 |
72,765,879 (GRCm39) |
missense |
probably benign |
0.02 |
R4301:Zzef1
|
UTSW |
11 |
72,779,861 (GRCm39) |
missense |
probably damaging |
0.96 |
R4359:Zzef1
|
UTSW |
11 |
72,714,334 (GRCm39) |
missense |
probably damaging |
0.98 |
R4382:Zzef1
|
UTSW |
11 |
72,765,938 (GRCm39) |
missense |
probably benign |
0.00 |
R4453:Zzef1
|
UTSW |
11 |
72,763,465 (GRCm39) |
missense |
probably benign |
0.02 |
R4466:Zzef1
|
UTSW |
11 |
72,815,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Zzef1
|
UTSW |
11 |
72,804,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Zzef1
|
UTSW |
11 |
72,778,996 (GRCm39) |
missense |
probably benign |
0.32 |
R4511:Zzef1
|
UTSW |
11 |
72,778,996 (GRCm39) |
missense |
probably benign |
0.32 |
R4714:Zzef1
|
UTSW |
11 |
72,728,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Zzef1
|
UTSW |
11 |
72,750,449 (GRCm39) |
missense |
probably benign |
0.12 |
R4906:Zzef1
|
UTSW |
11 |
72,792,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zzef1
|
UTSW |
11 |
72,749,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R5357:Zzef1
|
UTSW |
11 |
72,734,159 (GRCm39) |
nonsense |
probably null |
|
R5579:Zzef1
|
UTSW |
11 |
72,791,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R5598:Zzef1
|
UTSW |
11 |
72,807,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Zzef1
|
UTSW |
11 |
72,746,308 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5765:Zzef1
|
UTSW |
11 |
72,712,763 (GRCm39) |
nonsense |
probably null |
|
R5928:Zzef1
|
UTSW |
11 |
72,803,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R6003:Zzef1
|
UTSW |
11 |
72,714,891 (GRCm39) |
splice site |
probably null |
|
R6047:Zzef1
|
UTSW |
11 |
72,756,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R6224:Zzef1
|
UTSW |
11 |
72,746,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R6225:Zzef1
|
UTSW |
11 |
72,760,631 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6287:Zzef1
|
UTSW |
11 |
72,813,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Zzef1
|
UTSW |
11 |
72,775,175 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6451:Zzef1
|
UTSW |
11 |
72,813,982 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6467:Zzef1
|
UTSW |
11 |
72,802,090 (GRCm39) |
critical splice donor site |
probably null |
|
R6484:Zzef1
|
UTSW |
11 |
72,786,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6493:Zzef1
|
UTSW |
11 |
72,804,129 (GRCm39) |
missense |
probably benign |
0.06 |
R6520:Zzef1
|
UTSW |
11 |
72,716,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:Zzef1
|
UTSW |
11 |
72,765,816 (GRCm39) |
missense |
probably benign |
0.00 |
R6540:Zzef1
|
UTSW |
11 |
72,804,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Zzef1
|
UTSW |
11 |
72,803,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Zzef1
|
UTSW |
11 |
72,741,485 (GRCm39) |
missense |
probably benign |
0.00 |
R6927:Zzef1
|
UTSW |
11 |
72,803,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Zzef1
|
UTSW |
11 |
72,746,340 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7048:Zzef1
|
UTSW |
11 |
72,757,525 (GRCm39) |
nonsense |
probably null |
|
R7076:Zzef1
|
UTSW |
11 |
72,790,385 (GRCm39) |
missense |
probably benign |
0.00 |
R7099:Zzef1
|
UTSW |
11 |
72,763,475 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7132:Zzef1
|
UTSW |
11 |
72,808,697 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Zzef1
|
UTSW |
11 |
72,742,727 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7284:Zzef1
|
UTSW |
11 |
72,777,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R7300:Zzef1
|
UTSW |
11 |
72,765,830 (GRCm39) |
missense |
probably benign |
0.02 |
R7486:Zzef1
|
UTSW |
11 |
72,755,612 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7503:Zzef1
|
UTSW |
11 |
72,716,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Zzef1
|
UTSW |
11 |
72,784,104 (GRCm39) |
missense |
probably benign |
|
R7874:Zzef1
|
UTSW |
11 |
72,750,479 (GRCm39) |
missense |
probably benign |
0.01 |
R7898:Zzef1
|
UTSW |
11 |
72,687,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7928:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R8021:Zzef1
|
UTSW |
11 |
72,714,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R8145:Zzef1
|
UTSW |
11 |
72,799,295 (GRCm39) |
nonsense |
probably null |
|
R8255:Zzef1
|
UTSW |
11 |
72,765,955 (GRCm39) |
missense |
probably benign |
0.00 |
R8303:Zzef1
|
UTSW |
11 |
72,808,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Zzef1
|
UTSW |
11 |
72,777,572 (GRCm39) |
missense |
probably damaging |
0.97 |
R8492:Zzef1
|
UTSW |
11 |
72,763,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8498:Zzef1
|
UTSW |
11 |
72,744,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Zzef1
|
UTSW |
11 |
72,735,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8874:Zzef1
|
UTSW |
11 |
72,754,815 (GRCm39) |
missense |
probably benign |
0.00 |
R8885:Zzef1
|
UTSW |
11 |
72,687,402 (GRCm39) |
missense |
probably benign |
0.00 |
R8972:Zzef1
|
UTSW |
11 |
72,791,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Zzef1
|
UTSW |
11 |
72,766,003 (GRCm39) |
missense |
probably benign |
0.00 |
R9053:Zzef1
|
UTSW |
11 |
72,813,302 (GRCm39) |
missense |
probably benign |
|
R9108:Zzef1
|
UTSW |
11 |
72,790,604 (GRCm39) |
missense |
probably benign |
0.11 |
R9121:Zzef1
|
UTSW |
11 |
72,756,946 (GRCm39) |
nonsense |
probably null |
|
R9253:Zzef1
|
UTSW |
11 |
72,739,463 (GRCm39) |
splice site |
probably benign |
|
R9370:Zzef1
|
UTSW |
11 |
72,744,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Zzef1
|
UTSW |
11 |
72,755,653 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9467:Zzef1
|
UTSW |
11 |
72,807,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Zzef1
|
UTSW |
11 |
72,814,009 (GRCm39) |
critical splice donor site |
probably null |
|
R9563:Zzef1
|
UTSW |
11 |
72,765,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9647:Zzef1
|
UTSW |
11 |
72,760,651 (GRCm39) |
missense |
probably benign |
0.01 |
R9667:Zzef1
|
UTSW |
11 |
72,758,786 (GRCm39) |
missense |
probably benign |
|
R9742:Zzef1
|
UTSW |
11 |
72,749,179 (GRCm39) |
missense |
probably benign |
|
X0028:Zzef1
|
UTSW |
11 |
72,797,805 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Zzef1
|
UTSW |
11 |
72,687,354 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zzef1
|
UTSW |
11 |
72,791,457 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Zzef1
|
UTSW |
11 |
72,717,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zzef1
|
UTSW |
11 |
72,687,138 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Zzef1
|
UTSW |
11 |
72,806,146 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1187:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1188:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1189:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1190:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1191:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1192:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GCTTCAGCAACTAGACTGCTACCAC -3'
(R):5'- CAGAATCCTTTCAGAGACGGCTTCC -3'
Sequencing Primer
(F):5'- CATGGTTGTTTTATTACTTACCCAGG -3'
(R):5'- GAGCCACTCTACACTGCTGTG -3'
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Posted On |
2014-05-23 |