Incidental Mutation 'IGL03294:Zfp786'
| ID |
416008 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Zfp786
|
| Ensembl Gene |
ENSMUSG00000051499 |
| Gene Name |
zinc finger protein 786 |
| Synonyms |
A730012O14Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.068)
|
| Stock # |
IGL03294
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
47796200-47807801 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 47798258 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Stop codon
at position 227
(K227*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000057495
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058844]
|
| AlphaFold |
Q8BV42 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000058844
AA Change: K227*
|
| SMART Domains |
Protein: ENSMUSP00000057495
Gene: ENSMUSG00000051499
AA Change: K227*
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
9 |
69 |
2.6e-22 |
SMART |
|
low complexity region
|
156 |
164 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
240 |
262 |
5.34e-1 |
SMART |
|
ZnF_C2H2
|
268 |
295 |
1.41e2 |
SMART |
|
ZnF_C2H2
|
420 |
440 |
1.21e2 |
SMART |
|
ZnF_C2H2
|
448 |
470 |
3.52e-1 |
SMART |
|
ZnF_C2H2
|
476 |
498 |
1.89e-1 |
SMART |
|
ZnF_C2H2
|
504 |
526 |
1.69e-3 |
SMART |
|
ZnF_C2H2
|
532 |
554 |
5.59e-4 |
SMART |
|
ZnF_C2H2
|
560 |
582 |
4.79e-3 |
SMART |
|
ZnF_C2H2
|
588 |
610 |
3.69e-4 |
SMART |
|
ZnF_C2H2
|
616 |
638 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
644 |
665 |
5.92e0 |
SMART |
|
ZnF_C2H2
|
671 |
693 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
699 |
721 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
727 |
749 |
1.45e-2 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143979
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 6030498E09Rik |
A |
T |
X: 38,047,315 (GRCm39) |
M119L |
probably benign |
Het |
| Akap10 |
A |
T |
11: 61,768,179 (GRCm39) |
V646D |
probably damaging |
Het |
| Aldh3a1 |
A |
G |
11: 61,105,548 (GRCm39) |
Y218C |
probably damaging |
Het |
| Arfgef3 |
T |
A |
10: 18,540,660 (GRCm39) |
L174F |
probably damaging |
Het |
| Arhgef6 |
T |
C |
X: 56,382,338 (GRCm39) |
K99E |
possibly damaging |
Het |
| Atp9a |
T |
C |
2: 168,531,225 (GRCm39) |
K163E |
probably benign |
Het |
| Birc6 |
C |
T |
17: 74,956,881 (GRCm39) |
A3605V |
probably benign |
Het |
| C8b |
G |
A |
4: 104,637,888 (GRCm39) |
R120Q |
probably benign |
Het |
| Ccr1l1 |
A |
C |
9: 123,778,444 (GRCm39) |
M1R |
probably null |
Het |
| Clca3a2 |
A |
G |
3: 144,803,530 (GRCm39) |
S105P |
probably damaging |
Het |
| Cntnap1 |
A |
G |
11: 101,072,508 (GRCm39) |
T502A |
possibly damaging |
Het |
| Ddx10 |
C |
T |
9: 53,028,452 (GRCm39) |
|
probably null |
Het |
| Dnah5 |
G |
A |
15: 28,233,441 (GRCm39) |
|
probably null |
Het |
| Dock9 |
A |
T |
14: 121,879,035 (GRCm39) |
|
probably benign |
Het |
| Gli2 |
A |
G |
1: 118,765,166 (GRCm39) |
V995A |
probably benign |
Het |
| Gpr34 |
T |
C |
X: 13,505,788 (GRCm39) |
Y106H |
probably damaging |
Het |
| Kmt2a |
A |
T |
9: 44,731,862 (GRCm39) |
|
probably benign |
Het |
| Lamc1 |
C |
A |
1: 153,138,392 (GRCm39) |
R154L |
probably damaging |
Het |
| Mat1a |
T |
A |
14: 40,827,561 (GRCm39) |
V5E |
probably benign |
Het |
| Meioc |
A |
T |
11: 102,571,495 (GRCm39) |
E943V |
probably damaging |
Het |
| Mtcl1 |
G |
A |
17: 66,645,014 (GRCm39) |
P1478S |
probably damaging |
Het |
| Nav2 |
C |
T |
7: 49,141,205 (GRCm39) |
R917* |
probably null |
Het |
| Or4f47 |
T |
C |
2: 111,972,518 (GRCm39) |
I76T |
probably benign |
Het |
| Or7g32 |
T |
C |
9: 19,389,285 (GRCm39) |
N87S |
possibly damaging |
Het |
| Pcsk9 |
T |
A |
4: 106,303,967 (GRCm39) |
I506L |
probably benign |
Het |
| Phf14 |
T |
A |
6: 11,953,366 (GRCm39) |
D368E |
probably damaging |
Het |
| Phka1 |
C |
A |
X: 101,580,819 (GRCm39) |
S964I |
probably damaging |
Het |
| Pikfyve |
G |
A |
1: 65,286,226 (GRCm39) |
R1155Q |
probably damaging |
Het |
| Plin2 |
C |
T |
4: 86,580,315 (GRCm39) |
V60M |
probably damaging |
Het |
| Ptpn9 |
A |
G |
9: 56,934,671 (GRCm39) |
Q145R |
possibly damaging |
Het |
| Sap30 |
A |
G |
8: 57,940,335 (GRCm39) |
I89T |
probably damaging |
Het |
| Sec61a2 |
T |
C |
2: 5,881,276 (GRCm39) |
|
probably null |
Het |
| Slc34a2 |
A |
C |
5: 53,221,340 (GRCm39) |
D262A |
probably benign |
Het |
| Slc6a3 |
G |
A |
13: 73,705,300 (GRCm39) |
|
probably null |
Het |
| Slfn4 |
A |
T |
11: 83,077,400 (GRCm39) |
T63S |
probably benign |
Het |
| Tbx10 |
A |
T |
19: 4,048,571 (GRCm39) |
|
probably benign |
Het |
| Tie1 |
A |
T |
4: 118,337,420 (GRCm39) |
N501K |
probably damaging |
Het |
| Tmprss11f |
A |
T |
5: 86,685,966 (GRCm39) |
Y134N |
probably damaging |
Het |
| Uevld |
A |
T |
7: 46,580,778 (GRCm39) |
D361E |
possibly damaging |
Het |
| Ugt1a5 |
A |
C |
1: 88,094,537 (GRCm39) |
D255A |
probably damaging |
Het |
| Vmn2r11 |
A |
G |
5: 109,201,935 (GRCm39) |
F190L |
probably benign |
Het |
| Wfs1 |
G |
A |
5: 37,132,941 (GRCm39) |
R113C |
probably damaging |
Het |
| Yipf5 |
T |
G |
18: 40,339,449 (GRCm39) |
M206L |
probably benign |
Het |
| Zbtb10 |
A |
G |
3: 9,346,047 (GRCm39) |
D847G |
probably benign |
Het |
|
| Other mutations in Zfp786 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00593:Zfp786
|
APN |
6 |
47,796,605 (GRCm39) |
makesense |
probably null |
|
|
IGL02442:Zfp786
|
APN |
6 |
47,798,301 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02674:Zfp786
|
APN |
6 |
47,797,427 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL02814:Zfp786
|
APN |
6 |
47,796,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03072:Zfp786
|
APN |
6 |
47,798,177 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03393:Zfp786
|
APN |
6 |
47,798,458 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
3-1:Zfp786
|
UTSW |
6 |
47,797,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4581001:Zfp786
|
UTSW |
6 |
47,796,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1071:Zfp786
|
UTSW |
6 |
47,798,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1426:Zfp786
|
UTSW |
6 |
47,802,013 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1976:Zfp786
|
UTSW |
6 |
47,796,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2114:Zfp786
|
UTSW |
6 |
47,803,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2115:Zfp786
|
UTSW |
6 |
47,803,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2117:Zfp786
|
UTSW |
6 |
47,803,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2176:Zfp786
|
UTSW |
6 |
47,797,905 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R2304:Zfp786
|
UTSW |
6 |
47,797,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3110:Zfp786
|
UTSW |
6 |
47,797,160 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3112:Zfp786
|
UTSW |
6 |
47,797,160 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3623:Zfp786
|
UTSW |
6 |
47,798,357 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4654:Zfp786
|
UTSW |
6 |
47,797,868 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4741:Zfp786
|
UTSW |
6 |
47,797,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4927:Zfp786
|
UTSW |
6 |
47,797,087 (GRCm39) |
missense |
probably benign |
0.43 |
|
R4936:Zfp786
|
UTSW |
6 |
47,798,202 (GRCm39) |
nonsense |
probably null |
|
|
R5084:Zfp786
|
UTSW |
6 |
47,796,953 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5445:Zfp786
|
UTSW |
6 |
47,796,619 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6662:Zfp786
|
UTSW |
6 |
47,803,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7290:Zfp786
|
UTSW |
6 |
47,796,929 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7561:Zfp786
|
UTSW |
6 |
47,796,667 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8038:Zfp786
|
UTSW |
6 |
47,798,188 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8090:Zfp786
|
UTSW |
6 |
47,796,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8250:Zfp786
|
UTSW |
6 |
47,797,729 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8438:Zfp786
|
UTSW |
6 |
47,796,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8516:Zfp786
|
UTSW |
6 |
47,797,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8868:Zfp786
|
UTSW |
6 |
47,802,015 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9596:Zfp786
|
UTSW |
6 |
47,797,406 (GRCm39) |
nonsense |
probably null |
|
|
R9788:Zfp786
|
UTSW |
6 |
47,797,816 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation