Incidental Mutation 'R0513:Zfp39'
ID |
48030 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp39
|
Ensembl Gene |
ENSMUSG00000037001 |
Gene Name |
zinc finger protein 39 |
Synonyms |
Zfp-39, CTfin33 |
MMRRC Submission |
038707-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.153)
|
Stock # |
R0513 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
58778979-58795051 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 58780813 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Isoleucine
at position 650
(V650I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099764
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102703]
|
AlphaFold |
Q02525 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000102703
AA Change: V650I
PolyPhen 2
Score 0.085 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000099764 Gene: ENSMUSG00000037001 AA Change: V650I
Domain | Start | End | E-Value | Type |
KRAB
|
59 |
119 |
8.23e-34 |
SMART |
low complexity region
|
171 |
180 |
N/A |
INTRINSIC |
ZnF_C2H2
|
298 |
320 |
9.58e-3 |
SMART |
ZnF_C2H2
|
326 |
347 |
2.2e2 |
SMART |
ZnF_C2H2
|
353 |
373 |
1.18e2 |
SMART |
ZnF_C2H2
|
409 |
431 |
8.34e-3 |
SMART |
ZnF_C2H2
|
437 |
459 |
7.26e-3 |
SMART |
ZnF_C2H2
|
465 |
487 |
1.53e-1 |
SMART |
ZnF_C2H2
|
493 |
515 |
9.08e-4 |
SMART |
ZnF_C2H2
|
521 |
543 |
2.61e-4 |
SMART |
ZnF_C2H2
|
549 |
571 |
1.12e-3 |
SMART |
ZnF_C2H2
|
577 |
599 |
4.94e-5 |
SMART |
ZnF_C2H2
|
605 |
627 |
5.14e-3 |
SMART |
ZnF_C2H2
|
633 |
655 |
1.38e-3 |
SMART |
ZnF_C2H2
|
661 |
683 |
6.78e-3 |
SMART |
ZnF_C2H2
|
689 |
711 |
5.14e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132394
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.5%
- 3x: 98.7%
- 10x: 96.6%
- 20x: 92.9%
|
Validation Efficiency |
99% (122/123) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a Kruppel-associated box (KRAB) zinc-finger protein, which belongs to a large group of transcriptional regulators in mammals. These proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation and apoptosis, and in regulating viral replication and transcription. A pseudogene of this gene was identified on chromosome 1. [provided by RefSeq, May 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
A |
G |
13: 119,606,195 (GRCm39) |
T146A |
probably benign |
Het |
Abcg4 |
A |
G |
9: 44,192,984 (GRCm39) |
S121P |
possibly damaging |
Het |
Actr2 |
T |
C |
11: 20,030,124 (GRCm39) |
T212A |
probably damaging |
Het |
Adcy10 |
T |
A |
1: 165,347,088 (GRCm39) |
D368E |
probably benign |
Het |
Albfm1 |
A |
T |
5: 90,725,786 (GRCm39) |
T333S |
probably benign |
Het |
Anapc15 |
T |
C |
7: 101,547,747 (GRCm39) |
|
probably benign |
Het |
Aox4 |
A |
G |
1: 58,256,678 (GRCm39) |
R67G |
probably benign |
Het |
Aox4 |
A |
G |
1: 58,286,459 (GRCm39) |
D697G |
probably damaging |
Het |
Arhgap42 |
A |
T |
9: 9,005,766 (GRCm39) |
S755T |
probably benign |
Het |
Atm |
A |
G |
9: 53,415,248 (GRCm39) |
V881A |
probably benign |
Het |
Cdkal1 |
C |
T |
13: 29,809,948 (GRCm39) |
|
probably benign |
Het |
Cfap20dc |
A |
C |
14: 8,536,609 (GRCm38) |
D199E |
probably damaging |
Het |
Cfap61 |
C |
A |
2: 145,877,215 (GRCm39) |
N491K |
possibly damaging |
Het |
Chgb |
T |
C |
2: 132,627,897 (GRCm39) |
|
probably benign |
Het |
Chrna1 |
C |
A |
2: 73,398,426 (GRCm39) |
|
probably benign |
Het |
Chst10 |
A |
G |
1: 38,904,844 (GRCm39) |
L283P |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,466,323 (GRCm39) |
|
probably null |
Het |
Crppa |
A |
T |
12: 36,440,467 (GRCm39) |
H125L |
probably damaging |
Het |
Cryzl1 |
G |
T |
16: 91,496,175 (GRCm39) |
A1E |
possibly damaging |
Het |
Csnk1a1 |
T |
C |
18: 61,709,618 (GRCm39) |
Y213H |
probably damaging |
Het |
Cspg4 |
A |
G |
9: 56,805,375 (GRCm39) |
Q2062R |
probably benign |
Het |
Ctnnal1 |
A |
G |
4: 56,835,348 (GRCm39) |
C310R |
probably benign |
Het |
D630003M21Rik |
T |
C |
2: 158,042,228 (GRCm39) |
E906G |
probably benign |
Het |
D930048N14Rik |
T |
C |
11: 51,545,755 (GRCm39) |
|
probably benign |
Het |
Dag1 |
G |
A |
9: 108,085,684 (GRCm39) |
P486S |
possibly damaging |
Het |
Dgkq |
A |
G |
5: 108,804,361 (GRCm39) |
L33P |
probably benign |
Het |
Dlc1 |
C |
T |
8: 37,051,164 (GRCm39) |
G856R |
probably damaging |
Het |
Dst |
T |
A |
1: 34,258,612 (GRCm39) |
|
probably benign |
Het |
Dtl |
A |
T |
1: 191,301,819 (GRCm39) |
Y79* |
probably null |
Het |
Egfr |
T |
G |
11: 16,822,855 (GRCm39) |
L406R |
probably damaging |
Het |
Elp3 |
A |
T |
14: 65,800,695 (GRCm39) |
|
probably null |
Het |
Fbxw19 |
C |
A |
9: 109,310,621 (GRCm39) |
|
probably null |
Het |
Frs2 |
T |
C |
10: 116,910,570 (GRCm39) |
E264G |
possibly damaging |
Het |
Fscn2 |
G |
T |
11: 120,252,706 (GRCm39) |
V58L |
probably damaging |
Het |
Gm17324 |
G |
A |
9: 78,356,007 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
A |
T |
12: 81,425,086 (GRCm39) |
N357K |
probably benign |
Het |
Gm9956 |
G |
T |
10: 56,621,291 (GRCm39) |
|
|
Het |
Gsg1l |
C |
T |
7: 125,619,795 (GRCm39) |
|
probably null |
Het |
Herc1 |
G |
A |
9: 66,352,927 (GRCm39) |
V2138M |
possibly damaging |
Het |
Htr2a |
T |
C |
14: 74,943,764 (GRCm39) |
L448P |
probably benign |
Het |
Ing3 |
C |
T |
6: 21,970,034 (GRCm39) |
S255L |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,859,384 (GRCm39) |
D271G |
probably damaging |
Het |
Lmbrd2 |
T |
A |
15: 9,194,816 (GRCm39) |
L606H |
probably damaging |
Het |
Lmod1 |
T |
A |
1: 135,252,906 (GRCm39) |
N53K |
probably damaging |
Het |
Lsr |
G |
C |
7: 30,657,763 (GRCm39) |
A467G |
probably benign |
Het |
Mbtd1 |
T |
A |
11: 93,823,038 (GRCm39) |
|
probably null |
Het |
Mill1 |
T |
A |
7: 17,998,802 (GRCm39) |
Y337* |
probably null |
Het |
Mlxipl |
A |
T |
5: 135,166,117 (GRCm39) |
Q833L |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,874,515 (GRCm39) |
V278M |
probably damaging |
Het |
Mxra8 |
A |
C |
4: 155,926,190 (GRCm39) |
M180L |
probably benign |
Het |
Myo18a |
A |
T |
11: 77,702,420 (GRCm39) |
|
probably benign |
Het |
Myo1c |
T |
G |
11: 75,556,657 (GRCm39) |
|
probably null |
Het |
Myo1g |
T |
C |
11: 6,460,203 (GRCm39) |
T782A |
probably benign |
Het |
Ncapd3 |
A |
G |
9: 26,975,401 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,198,699 (GRCm39) |
D414G |
probably damaging |
Het |
Nedd4l |
T |
A |
18: 65,328,256 (GRCm39) |
|
probably benign |
Het |
Nf2 |
T |
C |
11: 4,741,185 (GRCm39) |
K343R |
possibly damaging |
Het |
Nfasc |
A |
T |
1: 132,531,584 (GRCm39) |
D733E |
possibly damaging |
Het |
Nolc1 |
G |
A |
19: 46,072,598 (GRCm39) |
D699N |
probably damaging |
Het |
Nrbp2 |
C |
T |
15: 75,960,825 (GRCm39) |
A45T |
probably benign |
Het |
Obscn |
A |
G |
11: 58,952,348 (GRCm39) |
V3907A |
possibly damaging |
Het |
Or2b6 |
A |
T |
13: 21,823,119 (GRCm39) |
D191E |
probably benign |
Het |
Or2y6 |
T |
C |
11: 52,104,576 (GRCm39) |
Q80R |
possibly damaging |
Het |
Or8b8 |
A |
T |
9: 37,809,351 (GRCm39) |
Y217F |
probably damaging |
Het |
Pank2 |
C |
T |
2: 131,124,526 (GRCm39) |
T290I |
probably damaging |
Het |
Pbx4 |
T |
C |
8: 70,317,529 (GRCm39) |
V171A |
probably benign |
Het |
Pcgf1 |
G |
T |
6: 83,057,555 (GRCm39) |
V75F |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,515,660 (GRCm39) |
S778P |
probably damaging |
Het |
Pld6 |
T |
C |
11: 59,676,047 (GRCm39) |
I141M |
probably damaging |
Het |
Polq |
T |
A |
16: 36,914,864 (GRCm39) |
V2508E |
probably damaging |
Het |
Prkca |
C |
G |
11: 107,905,202 (GRCm39) |
D179H |
possibly damaging |
Het |
Pspn |
T |
C |
17: 57,306,720 (GRCm39) |
S70G |
probably damaging |
Het |
Ptchd4 |
C |
T |
17: 42,814,637 (GRCm39) |
T846I |
probably benign |
Het |
Reg3g |
A |
C |
6: 78,444,827 (GRCm39) |
Y50* |
probably null |
Het |
Rev3l |
C |
T |
10: 39,704,139 (GRCm39) |
H2062Y |
probably benign |
Het |
Rsph4a |
C |
T |
10: 33,788,987 (GRCm39) |
Q611* |
probably null |
Het |
Scart1 |
C |
A |
7: 139,804,873 (GRCm39) |
C625* |
probably null |
Het |
Scgb1b20 |
G |
A |
7: 33,072,739 (GRCm39) |
|
probably null |
Het |
Sfxn5 |
T |
C |
6: 85,246,955 (GRCm39) |
|
probably benign |
Het |
Sh3tc1 |
T |
A |
5: 35,857,651 (GRCm39) |
Q1179L |
possibly damaging |
Het |
Skint11 |
A |
G |
4: 114,051,762 (GRCm39) |
I37V |
probably benign |
Het |
Slc35f5 |
T |
C |
1: 125,503,906 (GRCm39) |
|
probably benign |
Het |
Slc8a2 |
A |
C |
7: 15,891,264 (GRCm39) |
D768A |
probably damaging |
Het |
Slco6b1 |
A |
G |
1: 96,924,909 (GRCm39) |
|
noncoding transcript |
Het |
Smurf2 |
T |
A |
11: 106,726,931 (GRCm39) |
T453S |
probably benign |
Het |
Spag16 |
A |
G |
1: 70,532,927 (GRCm39) |
|
probably benign |
Het |
Spindoc |
G |
A |
19: 7,351,509 (GRCm39) |
T205I |
probably benign |
Het |
Stab1 |
T |
C |
14: 30,870,902 (GRCm39) |
I1316V |
probably benign |
Het |
Stox2 |
T |
C |
8: 47,646,900 (GRCm39) |
R187G |
probably damaging |
Het |
Tcea2 |
A |
C |
2: 181,326,274 (GRCm39) |
T93P |
probably benign |
Het |
Tenm4 |
T |
C |
7: 96,544,830 (GRCm39) |
M2311T |
probably benign |
Het |
Tmem63a |
A |
G |
1: 180,788,026 (GRCm39) |
Q260R |
probably benign |
Het |
Tnpo2 |
A |
T |
8: 85,780,158 (GRCm39) |
H698L |
probably benign |
Het |
Trim33 |
A |
G |
3: 103,217,700 (GRCm39) |
D215G |
probably damaging |
Het |
Ttc3 |
T |
A |
16: 94,227,071 (GRCm39) |
I727N |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,773,669 (GRCm39) |
K2271N |
probably damaging |
Het |
Ubr2 |
T |
A |
17: 47,297,705 (GRCm39) |
K223* |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,144,186 (GRCm39) |
M1410V |
possibly damaging |
Het |
Ugt2b35 |
T |
C |
5: 87,151,271 (GRCm39) |
|
probably benign |
Het |
Ulk4 |
T |
A |
9: 120,981,391 (GRCm39) |
H880L |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,661,633 (GRCm39) |
C1686Y |
possibly damaging |
Het |
Upf2 |
T |
A |
2: 5,962,478 (GRCm39) |
L60Q |
unknown |
Het |
Usf2 |
A |
T |
7: 30,654,161 (GRCm39) |
|
probably benign |
Het |
Usp21 |
T |
A |
1: 171,110,586 (GRCm39) |
|
probably benign |
Het |
Usp21 |
T |
A |
1: 171,110,588 (GRCm39) |
|
probably benign |
Het |
Vmn2r118 |
T |
A |
17: 55,917,970 (GRCm39) |
K181* |
probably null |
Het |
Vmn2r124 |
T |
A |
17: 18,293,991 (GRCm39) |
S693T |
possibly damaging |
Het |
Vmn2r76 |
C |
A |
7: 85,877,987 (GRCm39) |
G470V |
probably benign |
Het |
Vps13c |
A |
C |
9: 67,838,017 (GRCm39) |
I1856L |
probably benign |
Het |
Vps50 |
C |
T |
6: 3,520,210 (GRCm39) |
L119F |
probably damaging |
Het |
Wdfy3 |
T |
A |
5: 102,038,655 (GRCm39) |
S2012C |
probably damaging |
Het |
Zfp1008 |
A |
C |
13: 62,753,029 (GRCm39) |
V99G |
possibly damaging |
Het |
Zfp142 |
A |
G |
1: 74,610,714 (GRCm39) |
V924A |
probably damaging |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
Zfp235 |
T |
C |
7: 23,841,644 (GRCm39) |
S688P |
probably damaging |
Het |
Zfp82 |
A |
T |
7: 29,756,265 (GRCm39) |
N272K |
probably damaging |
Het |
Zfyve21 |
A |
C |
12: 111,789,698 (GRCm39) |
D54A |
possibly damaging |
Het |
Zfyve26 |
C |
T |
12: 79,291,258 (GRCm39) |
D2116N |
probably damaging |
Het |
|
Other mutations in Zfp39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Zfp39
|
APN |
11 |
58,783,885 (GRCm39) |
splice site |
probably benign |
|
IGL01597:Zfp39
|
APN |
11 |
58,782,369 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02055:Zfp39
|
APN |
11 |
58,782,156 (GRCm39) |
missense |
probably benign |
|
IGL02456:Zfp39
|
APN |
11 |
58,793,626 (GRCm39) |
nonsense |
probably null |
|
IGL02873:Zfp39
|
APN |
11 |
58,781,848 (GRCm39) |
missense |
probably benign |
0.12 |
H8562:Zfp39
|
UTSW |
11 |
58,791,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R0462:Zfp39
|
UTSW |
11 |
58,781,232 (GRCm39) |
missense |
probably benign |
0.03 |
R1185:Zfp39
|
UTSW |
11 |
58,793,670 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1185:Zfp39
|
UTSW |
11 |
58,793,670 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1185:Zfp39
|
UTSW |
11 |
58,793,670 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1401:Zfp39
|
UTSW |
11 |
58,781,149 (GRCm39) |
missense |
probably benign |
0.01 |
R1797:Zfp39
|
UTSW |
11 |
58,791,486 (GRCm39) |
missense |
probably damaging |
0.96 |
R2146:Zfp39
|
UTSW |
11 |
58,781,158 (GRCm39) |
missense |
probably benign |
0.05 |
R3903:Zfp39
|
UTSW |
11 |
58,781,001 (GRCm39) |
missense |
probably benign |
0.44 |
R4303:Zfp39
|
UTSW |
11 |
58,780,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4706:Zfp39
|
UTSW |
11 |
58,793,633 (GRCm39) |
missense |
probably benign |
0.41 |
R4957:Zfp39
|
UTSW |
11 |
58,782,057 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5092:Zfp39
|
UTSW |
11 |
58,782,028 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5158:Zfp39
|
UTSW |
11 |
58,780,671 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5292:Zfp39
|
UTSW |
11 |
58,791,415 (GRCm39) |
missense |
probably damaging |
0.97 |
R5697:Zfp39
|
UTSW |
11 |
58,780,661 (GRCm39) |
missense |
probably benign |
0.08 |
R5906:Zfp39
|
UTSW |
11 |
58,793,717 (GRCm39) |
missense |
probably benign |
|
R5925:Zfp39
|
UTSW |
11 |
58,782,099 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6174:Zfp39
|
UTSW |
11 |
58,782,213 (GRCm39) |
missense |
probably benign |
0.01 |
R6177:Zfp39
|
UTSW |
11 |
58,781,887 (GRCm39) |
missense |
probably benign |
0.27 |
R6968:Zfp39
|
UTSW |
11 |
58,782,306 (GRCm39) |
missense |
probably benign |
0.00 |
R7045:Zfp39
|
UTSW |
11 |
58,781,269 (GRCm39) |
missense |
unknown |
|
R7139:Zfp39
|
UTSW |
11 |
58,781,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7421:Zfp39
|
UTSW |
11 |
58,780,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Zfp39
|
UTSW |
11 |
58,781,869 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7689:Zfp39
|
UTSW |
11 |
58,781,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Zfp39
|
UTSW |
11 |
58,793,573 (GRCm39) |
missense |
probably benign |
|
R8136:Zfp39
|
UTSW |
11 |
58,782,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R8955:Zfp39
|
UTSW |
11 |
58,780,946 (GRCm39) |
nonsense |
probably null |
|
Z1186:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1186:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1186:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1186:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1186:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1187:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1187:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1187:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1187:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,712 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Zfp39
|
UTSW |
11 |
58,781,702 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,712 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,702 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1188:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1188:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1188:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1188:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1189:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1189:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1189:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1189:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1189:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1189:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1189:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1189:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,702 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1190:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1190:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1190:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1190:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1191:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1191:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1191:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1191:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,712 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Zfp39
|
UTSW |
11 |
58,781,702 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,605 (GRCm39) |
missense |
probably benign |
0.09 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,597 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,526 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,274 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,273 (GRCm39) |
missense |
probably benign |
0.16 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1192:Zfp39
|
UTSW |
11 |
58,780,873 (GRCm39) |
missense |
probably benign |
0.01 |
Z1192:Zfp39
|
UTSW |
11 |
58,780,871 (GRCm39) |
nonsense |
probably null |
|
Z1192:Zfp39
|
UTSW |
11 |
58,791,409 (GRCm39) |
missense |
probably benign |
0.01 |
Z1192:Zfp39
|
UTSW |
11 |
58,791,407 (GRCm39) |
missense |
probably benign |
0.01 |
Z1192:Zfp39
|
UTSW |
11 |
58,782,142 (GRCm39) |
missense |
probably benign |
|
Z1192:Zfp39
|
UTSW |
11 |
58,782,123 (GRCm39) |
missense |
probably benign |
|
Z1192:Zfp39
|
UTSW |
11 |
58,781,967 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,751 (GRCm39) |
missense |
probably benign |
0.29 |
Z1192:Zfp39
|
UTSW |
11 |
58,781,724 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTTCCCACATCAGACGCACAG -3'
(R):5'- GGCATTTTACCGCAAGTCACACC -3'
Sequencing Primer
(F):5'- CCCTCAGGTGGATTCTCTGATG -3'
(R):5'- gaaaacacatacaggggagaaac -3'
|
Posted On |
2013-06-12 |