Incidental Mutation 'R7236:Ikzf2'
| ID |
562799 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ikzf2
|
| Ensembl Gene |
ENSMUSG00000025997 |
| Gene Name |
IKAROS family zinc finger 2 |
| Synonyms |
A730095J18Rik, Helios, Zfpn1a2 |
| MMRRC Submission |
045306-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7236 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
69570373-69726404 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 69578240 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Isoleucine
at position 423
(N423I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027146
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027146]
[ENSMUST00000187184]
[ENSMUST00000188110]
[ENSMUST00000190771]
[ENSMUST00000190855]
[ENSMUST00000191262]
|
| AlphaFold |
P81183 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000027146
AA Change: N423I
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000027146
Gene: ENSMUSG00000025997
AA Change: N423I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
76 |
89 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
112 |
134 |
7.67e-2 |
SMART |
|
ZnF_C2H2
|
140 |
162 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
168 |
190 |
3.95e-4 |
SMART |
|
ZnF_C2H2
|
196 |
219 |
3.58e-2 |
SMART |
|
ZnF_C2H2
|
471 |
493 |
9.46e0 |
SMART |
|
ZnF_C2H2
|
499 |
523 |
6.13e-1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187184
AA Change: N397I
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000141075
Gene: ENSMUSG00000025997
AA Change: N397I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
76 |
89 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
114 |
136 |
1.72e-4 |
SMART |
|
ZnF_C2H2
|
142 |
164 |
3.95e-4 |
SMART |
|
ZnF_C2H2
|
170 |
193 |
3.58e-2 |
SMART |
|
ZnF_C2H2
|
445 |
467 |
9.46e0 |
SMART |
|
ZnF_C2H2
|
473 |
497 |
6.13e-1 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000188110
AA Change: N351I
PolyPhen 2
Score 0.674 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000140069
Gene: ENSMUSG00000025997
AA Change: N351I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
76 |
89 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
114 |
136 |
7.3e-7 |
SMART |
|
ZnF_C2H2
|
142 |
164 |
1.6e-6 |
SMART |
|
ZnF_C2H2
|
399 |
421 |
4e-2 |
SMART |
|
ZnF_C2H2
|
427 |
451 |
2.6e-3 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000190771
AA Change: N429I
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000139543
Gene: ENSMUSG00000025997
AA Change: N429I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
95 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
118 |
140 |
3.2e-4 |
SMART |
|
ZnF_C2H2
|
146 |
168 |
7.3e-7 |
SMART |
|
ZnF_C2H2
|
174 |
196 |
1.6e-6 |
SMART |
|
ZnF_C2H2
|
202 |
225 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
477 |
499 |
4e-2 |
SMART |
|
ZnF_C2H2
|
505 |
529 |
2.6e-3 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000190855
AA Change: N349I
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000140043
Gene: ENSMUSG00000025997
AA Change: N349I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
76 |
89 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
114 |
136 |
7.3e-7 |
SMART |
|
ZnF_C2H2
|
142 |
164 |
1.6e-6 |
SMART |
|
ZnF_C2H2
|
170 |
193 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
397 |
419 |
4e-2 |
SMART |
|
ZnF_C2H2
|
425 |
449 |
2.6e-3 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000191262
AA Change: N278I
PolyPhen 2
Score 0.175 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000139530
Gene: ENSMUSG00000025997
AA Change: N278I
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
51 |
74 |
1.5e-4 |
SMART |
|
ZnF_C2H2
|
326 |
348 |
4e-2 |
SMART |
|
ZnF_C2H2
|
354 |
378 |
2.6e-3 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
100% (66/66) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice exhibit postnatal lethality for unknown reasons. Survivors have decreased body weight. Postnatal lethality has complete penetrance on the C57BL/6 strain. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 66 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Actn3 |
C |
T |
19: 4,921,644 (GRCm39) |
V179I |
probably benign |
Het |
| Adra1b |
A |
G |
11: 43,667,151 (GRCm39) |
I362T |
possibly damaging |
Het |
| B3galnt1 |
T |
C |
3: 69,482,950 (GRCm39) |
K104E |
probably benign |
Het |
| Bnc2 |
T |
C |
4: 84,474,101 (GRCm39) |
Y15C |
probably benign |
Het |
| C2cd2l |
C |
A |
9: 44,228,960 (GRCm39) |
A124S |
possibly damaging |
Het |
| Camsap3 |
T |
A |
8: 3,654,116 (GRCm39) |
F595L |
probably damaging |
Het |
| Cct2 |
A |
T |
10: 116,897,464 (GRCm39) |
D93E |
probably benign |
Het |
| Cd200l2 |
A |
T |
16: 45,348,030 (GRCm39) |
I169N |
possibly damaging |
Het |
| Cemip |
A |
T |
7: 83,598,012 (GRCm39) |
|
probably null |
Het |
| Ciapin1 |
T |
C |
8: 95,550,338 (GRCm39) |
T34A |
|
Het |
| Dop1a |
G |
A |
9: 86,397,431 (GRCm39) |
V912I |
probably damaging |
Het |
| Efcab3 |
A |
T |
11: 104,790,093 (GRCm39) |
Q2832L |
probably benign |
Het |
| Eif3c |
T |
C |
7: 126,151,495 (GRCm39) |
T610A |
possibly damaging |
Het |
| Ephb3 |
A |
G |
16: 21,033,231 (GRCm39) |
R106G |
probably damaging |
Het |
| Ephx3 |
T |
A |
17: 32,404,328 (GRCm39) |
|
probably null |
Het |
| Etv2 |
A |
T |
7: 30,334,455 (GRCm39) |
S93T |
probably benign |
Het |
| Fbxo34 |
T |
A |
14: 47,767,841 (GRCm39) |
D451E |
probably benign |
Het |
| Fmo9 |
A |
G |
1: 166,504,140 (GRCm39) |
F141L |
probably damaging |
Het |
| Fryl |
T |
C |
5: 73,265,821 (GRCm39) |
K500R |
possibly damaging |
Het |
| Gfra3 |
T |
C |
18: 34,828,884 (GRCm39) |
D170G |
probably damaging |
Het |
| Gnptg |
T |
C |
17: 25,458,897 (GRCm39) |
N34S |
possibly damaging |
Het |
| Golga5 |
T |
A |
12: 102,441,034 (GRCm39) |
|
probably null |
Het |
| Herc2 |
G |
T |
7: 55,734,828 (GRCm39) |
L139F |
probably benign |
Het |
| Il31ra |
A |
T |
13: 112,660,439 (GRCm39) |
*717R |
probably null |
Het |
| Itga2 |
G |
T |
13: 115,014,227 (GRCm39) |
Q234K |
probably benign |
Het |
| Kcnt1 |
A |
T |
2: 25,799,951 (GRCm39) |
|
probably null |
Het |
| Kif19b |
G |
T |
5: 140,457,400 (GRCm39) |
A390S |
probably benign |
Het |
| Man2a2 |
T |
C |
7: 80,018,653 (GRCm39) |
S69G |
probably damaging |
Het |
| Mccc1 |
A |
G |
3: 36,037,944 (GRCm39) |
V294A |
probably benign |
Het |
| Mphosph8 |
T |
A |
14: 56,911,754 (GRCm39) |
I259K |
possibly damaging |
Het |
| Mrpl15 |
A |
T |
1: 4,846,711 (GRCm39) |
N288K |
probably benign |
Het |
| Msantd2 |
T |
C |
9: 37,400,965 (GRCm39) |
W116R |
probably damaging |
Het |
| Msantd5f9 |
G |
T |
4: 73,835,808 (GRCm39) |
L219M |
probably benign |
Het |
| Mtmr10 |
T |
C |
7: 63,963,932 (GRCm39) |
|
probably benign |
Het |
| Mylk |
A |
T |
16: 34,742,899 (GRCm39) |
D1137V |
probably damaging |
Het |
| Nhsl1 |
A |
G |
10: 18,401,512 (GRCm39) |
K879E |
probably damaging |
Het |
| Or8j3c |
A |
T |
2: 86,253,533 (GRCm39) |
C162* |
probably null |
Het |
| Pak6 |
A |
G |
2: 118,523,909 (GRCm39) |
T355A |
probably benign |
Het |
| Patj |
C |
T |
4: 98,299,294 (GRCm39) |
R139C |
probably damaging |
Het |
| Pcdhb3 |
C |
T |
18: 37,434,505 (GRCm39) |
A157V |
probably damaging |
Het |
| Phkg1 |
C |
A |
5: 129,895,802 (GRCm39) |
D150Y |
probably damaging |
Het |
| Ppp2r5c |
C |
T |
12: 110,432,323 (GRCm39) |
S45L |
probably benign |
Het |
| Prl4a1 |
A |
C |
13: 28,202,556 (GRCm39) |
T44P |
probably benign |
Het |
| Ptpro |
G |
A |
6: 137,345,335 (GRCm39) |
V114M |
probably damaging |
Het |
| Pwp1 |
A |
G |
10: 85,715,147 (GRCm39) |
N211S |
probably benign |
Het |
| Ralgapb |
A |
G |
2: 158,282,747 (GRCm39) |
D504G |
probably benign |
Het |
| Rock2 |
A |
T |
12: 16,979,003 (GRCm39) |
I98F |
probably damaging |
Het |
| Senp6 |
G |
T |
9: 80,040,247 (GRCm39) |
V785L |
probably damaging |
Het |
| Simc1 |
A |
G |
13: 54,672,609 (GRCm39) |
D319G |
probably benign |
Het |
| Tas2r105 |
A |
T |
6: 131,663,723 (GRCm39) |
I235N |
probably damaging |
Het |
| Tas2r110 |
A |
T |
6: 132,845,667 (GRCm39) |
M233L |
possibly damaging |
Het |
| Tmem260 |
C |
T |
14: 48,746,647 (GRCm39) |
|
probably null |
Het |
| Trank1 |
G |
T |
9: 111,202,142 (GRCm39) |
V1590L |
possibly damaging |
Het |
| Tsc2 |
A |
T |
17: 24,842,568 (GRCm39) |
M286K |
possibly damaging |
Het |
| Ttn |
T |
C |
2: 76,697,796 (GRCm39) |
T202A |
|
Het |
| Ttyh1 |
A |
G |
7: 4,136,663 (GRCm39) |
N424D |
probably benign |
Het |
| Usp24 |
T |
A |
4: 106,263,502 (GRCm39) |
|
probably null |
Het |
| Utp20 |
G |
T |
10: 88,585,204 (GRCm39) |
P2620Q |
probably benign |
Het |
| Vmn1r45 |
A |
G |
6: 89,910,133 (GRCm39) |
M279T |
probably benign |
Het |
| Vmn2r115 |
T |
A |
17: 23,578,576 (GRCm39) |
I683K |
probably benign |
Het |
| Vmn2r34 |
T |
C |
7: 7,684,750 (GRCm39) |
K481E |
probably damaging |
Het |
| Vmn2r54 |
T |
A |
7: 12,365,917 (GRCm39) |
H339L |
possibly damaging |
Het |
| Vmn2r94 |
T |
A |
17: 18,477,811 (GRCm39) |
N200I |
possibly damaging |
Het |
| Wdfy3 |
A |
G |
5: 101,984,074 (GRCm39) |
Y3493H |
probably damaging |
Het |
| Wdr5b |
A |
G |
16: 35,862,208 (GRCm39) |
D109G |
possibly damaging |
Het |
| Zfp286 |
A |
T |
11: 62,674,496 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Ikzf2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00885:Ikzf2
|
APN |
1 |
69,578,481 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
IGL01295:Ikzf2
|
APN |
1 |
69,617,146 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL01313:Ikzf2
|
APN |
1 |
69,578,589 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01390:Ikzf2
|
APN |
1 |
69,609,801 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01862:Ikzf2
|
APN |
1 |
69,578,057 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Freefall
|
UTSW |
1 |
69,578,256 (GRCm39) |
nonsense |
probably null |
|
|
Wigwam
|
UTSW |
1 |
69,616,955 (GRCm39) |
nonsense |
probably null |
|
|
R1079:Ikzf2
|
UTSW |
1 |
69,578,264 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R1368:Ikzf2
|
UTSW |
1 |
69,578,474 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1661:Ikzf2
|
UTSW |
1 |
69,577,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1665:Ikzf2
|
UTSW |
1 |
69,577,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1688:Ikzf2
|
UTSW |
1 |
69,581,439 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1726:Ikzf2
|
UTSW |
1 |
69,587,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1829:Ikzf2
|
UTSW |
1 |
69,581,446 (GRCm39) |
missense |
probably benign |
0.34 |
|
R1860:Ikzf2
|
UTSW |
1 |
69,609,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2507:Ikzf2
|
UTSW |
1 |
69,578,447 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4457:Ikzf2
|
UTSW |
1 |
69,723,347 (GRCm39) |
unclassified |
probably benign |
|
|
R5633:Ikzf2
|
UTSW |
1 |
69,578,256 (GRCm39) |
nonsense |
probably null |
|
|
R5666:Ikzf2
|
UTSW |
1 |
69,617,059 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5670:Ikzf2
|
UTSW |
1 |
69,617,059 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5836:Ikzf2
|
UTSW |
1 |
69,578,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5950:Ikzf2
|
UTSW |
1 |
69,722,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6492:Ikzf2
|
UTSW |
1 |
69,578,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6758:Ikzf2
|
UTSW |
1 |
69,578,059 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6809:Ikzf2
|
UTSW |
1 |
69,609,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6946:Ikzf2
|
UTSW |
1 |
69,616,955 (GRCm39) |
nonsense |
probably null |
|
|
R6959:Ikzf2
|
UTSW |
1 |
69,577,929 (GRCm39) |
makesense |
probably null |
|
|
R7044:Ikzf2
|
UTSW |
1 |
69,578,060 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7256:Ikzf2
|
UTSW |
1 |
69,617,212 (GRCm39) |
splice site |
probably null |
|
|
R7488:Ikzf2
|
UTSW |
1 |
69,578,544 (GRCm39) |
missense |
probably benign |
0.45 |
|
R7731:Ikzf2
|
UTSW |
1 |
69,578,302 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7863:Ikzf2
|
UTSW |
1 |
69,609,796 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R8401:Ikzf2
|
UTSW |
1 |
69,578,255 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8401:Ikzf2
|
UTSW |
1 |
69,578,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8471:Ikzf2
|
UTSW |
1 |
69,578,499 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8724:Ikzf2
|
UTSW |
1 |
69,617,100 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8870:Ikzf2
|
UTSW |
1 |
69,722,417 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9035:Ikzf2
|
UTSW |
1 |
69,578,637 (GRCm39) |
nonsense |
probably null |
|
|
R9108:Ikzf2
|
UTSW |
1 |
69,577,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9370:Ikzf2
|
UTSW |
1 |
69,578,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9524:Ikzf2
|
UTSW |
1 |
69,578,337 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9763:Ikzf2
|
UTSW |
1 |
69,587,835 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
X0027:Ikzf2
|
UTSW |
1 |
69,617,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGTTGCATTCCAGTGGGTC -3'
(R):5'- GACCCATTAGCAGGGAAACATC -3'
Sequencing Primer
(F):5'- CCCATGTGAATGGTGTACATGAC -3'
(R):5'- CATTAGCAGGGAAACATCTGATAGTC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation