Incidental Mutation 'R8698:Zfp106'
| ID |
668818 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp106
|
| Ensembl Gene |
ENSMUSG00000027288 |
| Gene Name |
zinc finger protein 106 |
| Synonyms |
Cd-1, H3a, Sh3bp3, sirm |
| MMRRC Submission |
068552-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8698 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
120337301-120394324 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to G
at 120354600 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000132902
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055241]
[ENSMUST00000152347]
[ENSMUST00000171215]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
silent
Transcript: ENSMUST00000055241
|
| SMART Domains |
Protein: ENSMUSP00000055602
Gene: ENSMUSG00000027288
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
5 |
29 |
1.51e0 |
SMART |
|
ZnF_C2H2
|
43 |
67 |
7.18e1 |
SMART |
|
low complexity region
|
75 |
92 |
N/A |
INTRINSIC |
|
low complexity region
|
141 |
152 |
N/A |
INTRINSIC |
|
low complexity region
|
199 |
212 |
N/A |
INTRINSIC |
|
low complexity region
|
466 |
480 |
N/A |
INTRINSIC |
|
coiled coil region
|
800 |
823 |
N/A |
INTRINSIC |
|
low complexity region
|
842 |
856 |
N/A |
INTRINSIC |
|
low complexity region
|
1049 |
1062 |
N/A |
INTRINSIC |
|
low complexity region
|
1312 |
1321 |
N/A |
INTRINSIC |
|
low complexity region
|
1361 |
1373 |
N/A |
INTRINSIC |
|
low complexity region
|
1389 |
1409 |
N/A |
INTRINSIC |
|
WD40
|
1525 |
1562 |
9.24e-4 |
SMART |
|
WD40
|
1565 |
1607 |
1.83e-7 |
SMART |
|
PQQ
|
1587 |
1618 |
3.42e2 |
SMART |
|
WD40
|
1651 |
1691 |
3.45e-1 |
SMART |
|
PQQ
|
1671 |
1702 |
9.14e1 |
SMART |
|
WD40
|
1694 |
1731 |
2.12e-3 |
SMART |
|
PQQ
|
1711 |
1742 |
6.42e0 |
SMART |
|
WD40
|
1734 |
1771 |
6e-3 |
SMART |
|
PQQ
|
1751 |
1782 |
5.7e2 |
SMART |
|
WD40
|
1774 |
1811 |
3.58e-1 |
SMART |
|
ZnF_C2H2
|
1818 |
1843 |
5.34e-1 |
SMART |
|
ZnF_C2H2
|
1851 |
1879 |
1.31e2 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000152347
|
| SMART Domains |
Protein: ENSMUSP00000132902
Gene: ENSMUSG00000027288
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
|
low complexity region
|
115 |
127 |
N/A |
INTRINSIC |
|
low complexity region
|
143 |
163 |
N/A |
INTRINSIC |
|
Pfam:WD40
|
234 |
265 |
1.3e-5 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163384
|
| Predicted Effect |
silent
Transcript: ENSMUST00000171215
|
| SMART Domains |
Protein: ENSMUSP00000128995
Gene: ENSMUSG00000027288
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
20 |
44 |
7.18e1 |
SMART |
|
low complexity region
|
52 |
69 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
129 |
N/A |
INTRINSIC |
|
low complexity region
|
176 |
189 |
N/A |
INTRINSIC |
|
low complexity region
|
443 |
457 |
N/A |
INTRINSIC |
|
coiled coil region
|
777 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
819 |
833 |
N/A |
INTRINSIC |
|
low complexity region
|
1026 |
1039 |
N/A |
INTRINSIC |
|
low complexity region
|
1289 |
1298 |
N/A |
INTRINSIC |
|
low complexity region
|
1338 |
1350 |
N/A |
INTRINSIC |
|
low complexity region
|
1366 |
1386 |
N/A |
INTRINSIC |
|
WD40
|
1502 |
1539 |
9.24e-4 |
SMART |
|
WD40
|
1542 |
1584 |
1.83e-7 |
SMART |
|
PQQ
|
1564 |
1595 |
3.42e2 |
SMART |
|
WD40
|
1628 |
1668 |
3.45e-1 |
SMART |
|
PQQ
|
1648 |
1679 |
9.14e1 |
SMART |
|
WD40
|
1671 |
1708 |
2.12e-3 |
SMART |
|
PQQ
|
1688 |
1719 |
6.42e0 |
SMART |
|
WD40
|
1711 |
1748 |
6e-3 |
SMART |
|
PQQ
|
1728 |
1759 |
5.7e2 |
SMART |
|
WD40
|
1751 |
1788 |
3.58e-1 |
SMART |
|
ZnF_C2H2
|
1795 |
1820 |
5.34e-1 |
SMART |
|
ZnF_C2H2
|
1828 |
1856 |
1.31e2 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.3%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a null allele exhibit an abnormal gait, progressive motor deficits, kyphosis, weight loss, severe adult-onset degenerative sensory-motor axonopathy, mitochondrial dysfunction, and premature death. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aaas |
A |
G |
15: 102,247,250 (GRCm39) |
|
probably benign |
Het |
| Adamtsl1 |
A |
G |
4: 86,306,714 (GRCm39) |
N1384S |
probably benign |
Het |
| Adgre1 |
T |
C |
17: 57,709,003 (GRCm39) |
S65P |
probably benign |
Het |
| Adgrl4 |
G |
T |
3: 151,203,512 (GRCm39) |
C124F |
probably damaging |
Het |
| Aldh1b1 |
G |
A |
4: 45,802,942 (GRCm39) |
G160D |
probably damaging |
Het |
| Alpi |
T |
G |
1: 87,028,208 (GRCm39) |
D205A |
probably damaging |
Het |
| AW146154 |
C |
A |
7: 41,129,934 (GRCm39) |
R394L |
probably benign |
Het |
| Bcl10 |
G |
A |
3: 145,639,022 (GRCm39) |
M221I |
probably benign |
Het |
| Brpf3 |
G |
A |
17: 29,037,436 (GRCm39) |
R768H |
probably damaging |
Het |
| Cad |
G |
T |
5: 31,234,819 (GRCm39) |
R2116L |
probably benign |
Het |
| Cand2 |
G |
T |
6: 115,763,852 (GRCm39) |
R258L |
probably damaging |
Het |
| Car4 |
A |
T |
11: 84,855,009 (GRCm39) |
N119I |
probably benign |
Het |
| Carmil1 |
C |
T |
13: 24,220,229 (GRCm39) |
G1165D |
probably damaging |
Het |
| Ccdc66 |
T |
C |
14: 27,212,647 (GRCm39) |
T403A |
probably benign |
Het |
| Cdon |
T |
G |
9: 35,398,269 (GRCm39) |
|
probably null |
Het |
| Cemip |
T |
C |
7: 83,607,790 (GRCm39) |
I739V |
probably damaging |
Het |
| Cep85l |
A |
G |
10: 53,234,201 (GRCm39) |
I59T |
probably damaging |
Het |
| Clec4f |
A |
T |
6: 83,630,267 (GRCm39) |
V97D |
probably benign |
Het |
| Cnot6l |
A |
G |
5: 96,225,149 (GRCm39) |
C515R |
probably damaging |
Het |
| Cntnap2 |
G |
A |
6: 47,026,156 (GRCm39) |
G935D |
probably damaging |
Het |
| Cntrl |
A |
G |
2: 35,023,974 (GRCm39) |
H553R |
probably damaging |
Het |
| Cops3 |
A |
G |
11: 59,708,886 (GRCm39) |
S423P |
probably damaging |
Het |
| Cox15 |
C |
T |
19: 43,739,948 (GRCm39) |
R39H |
probably benign |
Het |
| Ctnna2 |
A |
G |
6: 77,630,100 (GRCm39) |
V131A |
probably benign |
Het |
| Dcst2 |
T |
A |
3: 89,276,044 (GRCm39) |
F392I |
probably benign |
Het |
| Decr1 |
A |
G |
4: 15,922,483 (GRCm39) |
|
probably null |
Het |
| Dennd3 |
A |
C |
15: 73,394,154 (GRCm39) |
T60P |
possibly damaging |
Het |
| Dipk1a |
A |
T |
5: 108,057,776 (GRCm39) |
F261I |
probably damaging |
Het |
| Dmxl2 |
T |
C |
9: 54,281,953 (GRCm39) |
N2859S |
probably benign |
Het |
| Dnah12 |
A |
T |
14: 26,428,418 (GRCm39) |
I280F |
probably benign |
Het |
| Dnah8 |
A |
C |
17: 31,094,009 (GRCm39) |
D4701A |
probably damaging |
Het |
| Dyrk1a |
C |
A |
16: 94,487,414 (GRCm39) |
H541Q |
possibly damaging |
Het |
| Eml4 |
T |
C |
17: 83,785,345 (GRCm39) |
S906P |
probably benign |
Het |
| Fam169a |
G |
T |
13: 97,243,578 (GRCm39) |
V203F |
probably damaging |
Het |
| Fmn1 |
C |
T |
2: 113,260,152 (GRCm39) |
L682F |
unknown |
Het |
| Gli2 |
T |
C |
1: 118,769,887 (GRCm39) |
Y555C |
probably damaging |
Het |
| Gm3278 |
A |
G |
14: 16,081,505 (GRCm39) |
Y130C |
possibly damaging |
Het |
| Gm8237 |
T |
A |
14: 5,863,554 (GRCm38) |
Y37F |
probably damaging |
Het |
| Golga4 |
T |
G |
9: 118,385,029 (GRCm39) |
L717R |
probably damaging |
Het |
| Gtpbp4 |
C |
T |
13: 9,024,249 (GRCm39) |
R568H |
probably benign |
Het |
| Il1f10 |
A |
G |
2: 24,183,197 (GRCm39) |
N47S |
probably damaging |
Het |
| Itga6 |
A |
G |
2: 71,673,618 (GRCm39) |
H884R |
probably benign |
Het |
| Kdm1a |
T |
C |
4: 136,286,518 (GRCm39) |
K482R |
probably benign |
Het |
| Klk12 |
T |
C |
7: 43,419,113 (GRCm39) |
V26A |
probably benign |
Het |
| Lrp2 |
T |
A |
2: 69,278,583 (GRCm39) |
R3923S |
probably benign |
Het |
| Lrp2 |
C |
T |
2: 69,288,767 (GRCm39) |
V3700M |
probably benign |
Het |
| Lrrk2 |
A |
G |
15: 91,636,400 (GRCm39) |
D1458G |
probably benign |
Het |
| Mapre2 |
T |
A |
18: 24,011,090 (GRCm39) |
S233T |
probably benign |
Het |
| Mki67 |
T |
C |
7: 135,296,937 (GRCm39) |
D2699G |
possibly damaging |
Het |
| Mthfr |
T |
A |
4: 148,128,947 (GRCm39) |
Y214* |
probably null |
Het |
| Ncoa6 |
A |
T |
2: 155,257,041 (GRCm39) |
M834K |
possibly damaging |
Het |
| Neurl2 |
C |
T |
2: 164,675,054 (GRCm39) |
D103N |
probably benign |
Het |
| Niban3 |
T |
A |
8: 72,060,159 (GRCm39) |
I93N |
unknown |
Het |
| Or1j15 |
T |
C |
2: 36,458,915 (GRCm39) |
Y102H |
possibly damaging |
Het |
| Or2ag16 |
A |
T |
7: 106,352,571 (GRCm39) |
V8E |
probably benign |
Het |
| Or2b7 |
G |
A |
13: 21,739,890 (GRCm39) |
L101F |
probably damaging |
Het |
| P2ry14 |
A |
G |
3: 59,022,596 (GRCm39) |
V288A |
possibly damaging |
Het |
| Pde6b |
G |
T |
5: 108,576,105 (GRCm39) |
S730I |
possibly damaging |
Het |
| Pdpk1 |
A |
T |
17: 24,298,542 (GRCm39) |
V496D |
probably damaging |
Het |
| Plekho2 |
A |
T |
9: 65,463,554 (GRCm39) |
L432M |
probably damaging |
Het |
| Ppa2 |
T |
C |
3: 133,082,362 (GRCm39) |
L151P |
unknown |
Het |
| Ppp2r3c |
G |
A |
12: 55,328,499 (GRCm39) |
T422I |
probably benign |
Het |
| Prelid3a |
T |
C |
18: 67,610,122 (GRCm39) |
S151P |
probably damaging |
Het |
| Rad21l |
G |
A |
2: 151,487,373 (GRCm39) |
P537L |
probably damaging |
Het |
| Sacs |
T |
A |
14: 61,450,802 (GRCm39) |
S4283T |
probably benign |
Het |
| Samd9l |
A |
T |
6: 3,373,843 (GRCm39) |
D1139E |
probably benign |
Het |
| Scn9a |
G |
T |
2: 66,366,628 (GRCm39) |
H718Q |
probably benign |
Het |
| Slc1a3 |
A |
T |
15: 8,668,636 (GRCm39) |
I443N |
probably damaging |
Het |
| Slc22a6 |
A |
G |
19: 8,600,889 (GRCm39) |
M361V |
probably benign |
Het |
| Slc8a2 |
A |
G |
7: 15,891,132 (GRCm39) |
Y724C |
probably damaging |
Het |
| Slf1 |
A |
T |
13: 77,197,284 (GRCm39) |
S777T |
possibly damaging |
Het |
| Sltm |
T |
C |
9: 70,494,352 (GRCm39) |
S901P |
probably benign |
Het |
| Smc1b |
A |
T |
15: 84,997,047 (GRCm39) |
H524Q |
probably benign |
Het |
| Spast |
T |
C |
17: 74,666,341 (GRCm39) |
S225P |
probably benign |
Het |
| Srsf12 |
C |
T |
4: 33,231,246 (GRCm39) |
R252W |
probably damaging |
Het |
| Syne1 |
A |
G |
10: 5,179,229 (GRCm39) |
L4415P |
probably damaging |
Het |
| Tmem117 |
A |
T |
15: 94,535,990 (GRCm39) |
Y8F |
probably benign |
Het |
| Tmem241 |
T |
C |
18: 12,197,288 (GRCm39) |
D180G |
possibly damaging |
Het |
| Tomm40 |
C |
T |
7: 19,444,890 (GRCm39) |
V164I |
probably benign |
Het |
| Ttc41 |
T |
C |
10: 86,548,841 (GRCm39) |
Y12H |
probably benign |
Het |
| Twnk |
T |
C |
19: 44,996,299 (GRCm39) |
V244A |
probably benign |
Het |
| Ugt1a8 |
T |
C |
1: 88,015,952 (GRCm39) |
S122P |
probably damaging |
Het |
| Vmn1r78 |
A |
G |
7: 11,886,539 (GRCm39) |
K50R |
probably benign |
Het |
| Vmn2r10 |
A |
G |
5: 109,151,390 (GRCm39) |
F75L |
probably benign |
Het |
| Wbp4 |
G |
T |
14: 79,707,573 (GRCm39) |
Y179* |
probably null |
Het |
| Zfp974 |
A |
T |
7: 27,610,361 (GRCm39) |
C455S |
possibly damaging |
Het |
|
| Other mutations in Zfp106 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00330:Zfp106
|
APN |
2 |
120,369,978 (GRCm39) |
missense |
probably benign |
0.45 |
|
IGL00816:Zfp106
|
APN |
2 |
120,357,329 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL00822:Zfp106
|
APN |
2 |
120,344,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00848:Zfp106
|
APN |
2 |
120,343,208 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01293:Zfp106
|
APN |
2 |
120,365,516 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL01323:Zfp106
|
APN |
2 |
120,354,945 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
IGL01662:Zfp106
|
APN |
2 |
120,354,034 (GRCm39) |
missense |
probably benign |
0.17 |
|
IGL01683:Zfp106
|
APN |
2 |
120,355,036 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01809:Zfp106
|
APN |
2 |
120,364,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01958:Zfp106
|
APN |
2 |
120,365,288 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01960:Zfp106
|
APN |
2 |
120,369,803 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL01960:Zfp106
|
APN |
2 |
120,354,524 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02168:Zfp106
|
APN |
2 |
120,364,712 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02623:Zfp106
|
APN |
2 |
120,376,395 (GRCm39) |
splice site |
probably null |
|
|
IGL02798:Zfp106
|
APN |
2 |
120,340,991 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02828:Zfp106
|
APN |
2 |
120,362,178 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03022:Zfp106
|
APN |
2 |
120,359,120 (GRCm39) |
splice site |
probably benign |
|
|
IGL03308:Zfp106
|
APN |
2 |
120,354,505 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03324:Zfp106
|
APN |
2 |
120,365,868 (GRCm39) |
missense |
probably benign |
0.01 |
|
lepton
|
UTSW |
2 |
120,362,585 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Proton
|
UTSW |
2 |
120,341,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
quark
|
UTSW |
2 |
120,365,541 (GRCm39) |
nonsense |
probably null |
|
|
R0040_zfp106_031
|
UTSW |
2 |
120,362,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
string
|
UTSW |
2 |
120,364,075 (GRCm39) |
missense |
probably damaging |
0.96 |
|
theory
|
UTSW |
2 |
120,364,158 (GRCm39) |
nonsense |
probably null |
|
|
R0040:Zfp106
|
UTSW |
2 |
120,362,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Zfp106
|
UTSW |
2 |
120,362,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0135:Zfp106
|
UTSW |
2 |
120,350,968 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0180:Zfp106
|
UTSW |
2 |
120,364,356 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0387:Zfp106
|
UTSW |
2 |
120,358,953 (GRCm39) |
splice site |
probably null |
|
|
R0558:Zfp106
|
UTSW |
2 |
120,362,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0680:Zfp106
|
UTSW |
2 |
120,357,497 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0729:Zfp106
|
UTSW |
2 |
120,385,729 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0828:Zfp106
|
UTSW |
2 |
120,366,084 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1124:Zfp106
|
UTSW |
2 |
120,365,195 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1147:Zfp106
|
UTSW |
2 |
120,351,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1147:Zfp106
|
UTSW |
2 |
120,351,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1226:Zfp106
|
UTSW |
2 |
120,354,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1239:Zfp106
|
UTSW |
2 |
120,364,075 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1634:Zfp106
|
UTSW |
2 |
120,364,158 (GRCm39) |
nonsense |
probably null |
|
|
R1754:Zfp106
|
UTSW |
2 |
120,364,245 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1754:Zfp106
|
UTSW |
2 |
120,364,244 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1755:Zfp106
|
UTSW |
2 |
120,365,656 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1763:Zfp106
|
UTSW |
2 |
120,350,909 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1875:Zfp106
|
UTSW |
2 |
120,344,096 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1903:Zfp106
|
UTSW |
2 |
120,357,329 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1932:Zfp106
|
UTSW |
2 |
120,362,162 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R2070:Zfp106
|
UTSW |
2 |
120,354,010 (GRCm39) |
missense |
probably benign |
0.11 |
|
R2301:Zfp106
|
UTSW |
2 |
120,366,131 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3429:Zfp106
|
UTSW |
2 |
120,357,544 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3720:Zfp106
|
UTSW |
2 |
120,365,080 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3875:Zfp106
|
UTSW |
2 |
120,365,094 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3881:Zfp106
|
UTSW |
2 |
120,362,630 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3921:Zfp106
|
UTSW |
2 |
120,364,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3923:Zfp106
|
UTSW |
2 |
120,365,337 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4087:Zfp106
|
UTSW |
2 |
120,357,380 (GRCm39) |
splice site |
probably null |
|
|
R4678:Zfp106
|
UTSW |
2 |
120,364,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4965:Zfp106
|
UTSW |
2 |
120,364,400 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5011:Zfp106
|
UTSW |
2 |
120,341,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5013:Zfp106
|
UTSW |
2 |
120,341,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5151:Zfp106
|
UTSW |
2 |
120,365,208 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5227:Zfp106
|
UTSW |
2 |
120,354,449 (GRCm39) |
missense |
probably benign |
0.11 |
|
R5328:Zfp106
|
UTSW |
2 |
120,350,898 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5403:Zfp106
|
UTSW |
2 |
120,365,262 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5624:Zfp106
|
UTSW |
2 |
120,362,438 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5686:Zfp106
|
UTSW |
2 |
120,363,988 (GRCm39) |
splice site |
probably null |
|
|
R5691:Zfp106
|
UTSW |
2 |
120,354,952 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5852:Zfp106
|
UTSW |
2 |
120,346,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6032:Zfp106
|
UTSW |
2 |
120,365,874 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6032:Zfp106
|
UTSW |
2 |
120,365,874 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6298:Zfp106
|
UTSW |
2 |
120,353,185 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6409:Zfp106
|
UTSW |
2 |
120,362,585 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6505:Zfp106
|
UTSW |
2 |
120,364,983 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6598:Zfp106
|
UTSW |
2 |
120,365,541 (GRCm39) |
nonsense |
probably null |
|
|
R6765:Zfp106
|
UTSW |
2 |
120,369,935 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7013:Zfp106
|
UTSW |
2 |
120,362,113 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7453:Zfp106
|
UTSW |
2 |
120,376,400 (GRCm39) |
splice site |
probably null |
|
|
R7453:Zfp106
|
UTSW |
2 |
120,341,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7643:Zfp106
|
UTSW |
2 |
120,343,215 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7829:Zfp106
|
UTSW |
2 |
120,354,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7897:Zfp106
|
UTSW |
2 |
120,366,096 (GRCm39) |
nonsense |
probably null |
|
|
R7909:Zfp106
|
UTSW |
2 |
120,344,700 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8054:Zfp106
|
UTSW |
2 |
120,355,000 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8124:Zfp106
|
UTSW |
2 |
120,354,812 (GRCm39) |
missense |
probably benign |
0.44 |
|
R8203:Zfp106
|
UTSW |
2 |
120,349,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8350:Zfp106
|
UTSW |
2 |
120,366,099 (GRCm39) |
missense |
|
|
|
R8450:Zfp106
|
UTSW |
2 |
120,366,099 (GRCm39) |
missense |
|
|
|
R8985:Zfp106
|
UTSW |
2 |
120,366,077 (GRCm39) |
missense |
|
|
|
R9015:Zfp106
|
UTSW |
2 |
120,364,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9036:Zfp106
|
UTSW |
2 |
120,369,906 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9142:Zfp106
|
UTSW |
2 |
120,350,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9154:Zfp106
|
UTSW |
2 |
120,364,812 (GRCm39) |
nonsense |
probably null |
|
|
R9175:Zfp106
|
UTSW |
2 |
120,353,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9529:Zfp106
|
UTSW |
2 |
120,351,007 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9572:Zfp106
|
UTSW |
2 |
120,349,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9581:Zfp106
|
UTSW |
2 |
120,365,807 (GRCm39) |
missense |
|
|
|
RF008:Zfp106
|
UTSW |
2 |
120,355,026 (GRCm39) |
small deletion |
probably benign |
|
|
RF025:Zfp106
|
UTSW |
2 |
120,355,026 (GRCm39) |
small deletion |
probably benign |
|
|
X0025:Zfp106
|
UTSW |
2 |
120,365,297 (GRCm39) |
missense |
probably benign |
|
|
Z1088:Zfp106
|
UTSW |
2 |
120,360,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCTGTTCTGCAGCGATCCAG -3'
(R):5'- GGAAACTCAGTCTCCAGCTGAC -3'
Sequencing Primer
(F):5'- TCTGCAGCGATCCAGGCATC -3'
(R):5'- ACTGGCATCAGCTGAAACTAG -3'
|
| Posted On |
2021-04-30 |
Incidental Mutation