Incidental Mutation 'IGL01721:Ing3'
| ID |
105128 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ing3
|
| Ensembl Gene |
ENSMUSG00000029670 |
| Gene Name |
inhibitor of growth family, member 3 |
| Synonyms |
P47ING3, 1300013A07Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.965)
|
| Stock # |
IGL01721
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
21949570-21976037 bp(+) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
T to A
at 21968879 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000138244
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031680]
[ENSMUST00000115389]
[ENSMUST00000136200]
[ENSMUST00000149728]
[ENSMUST00000151473]
[ENSMUST00000152877]
|
| AlphaFold |
Q8VEK6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000031680
|
| SMART Domains |
Protein: ENSMUSP00000031680
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
3 |
104 |
2.7e-31 |
PFAM |
|
low complexity region
|
214 |
239 |
N/A |
INTRINSIC |
|
low complexity region
|
308 |
345 |
N/A |
INTRINSIC |
|
PHD
|
365 |
410 |
4e-14 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115389
|
| SMART Domains |
Protein: ENSMUSP00000111047
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
2 |
104 |
1.5e-33 |
PFAM |
|
low complexity region
|
203 |
228 |
N/A |
INTRINSIC |
|
low complexity region
|
297 |
334 |
N/A |
INTRINSIC |
|
PHD
|
354 |
399 |
6.39e-12 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136200
|
| SMART Domains |
Protein: ENSMUSP00000138656
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
2 |
41 |
1.5e-12 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144534
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000149728
|
| SMART Domains |
Protein: ENSMUSP00000145391
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
1 |
89 |
6.8e-25 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000151473
|
| SMART Domains |
Protein: ENSMUSP00000120651
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
2 |
80 |
1.9e-19 |
PFAM |
|
low complexity region
|
190 |
215 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000152877
|
| SMART Domains |
Protein: ENSMUSP00000138244
Gene: ENSMUSG00000029670
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ING
|
2 |
89 |
1.5e-27 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is similar to ING1, a tumor suppressor protein that can interact with TP53, inhibit cell growth, and induce apoptosis. This protein contains a PHD-finger, which is a common motif in proteins involved in chromatin remodeling. This gene can activate p53 trans-activated promoters, including promoters of p21/waf1 and bax. Overexpression of this gene has been shown to inhibit cell growth and induce apoptosis. Allelic loss and reduced expression of this gene were detected in head and neck cancers. Two alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700088E04Rik |
T |
C |
15: 79,023,453 (GRCm39) |
M51V |
possibly damaging |
Het |
| Acad8 |
A |
G |
9: 26,903,563 (GRCm39) |
|
probably benign |
Het |
| Atp2a2 |
A |
G |
5: 122,638,855 (GRCm39) |
V53A |
possibly damaging |
Het |
| Bicra |
T |
C |
7: 15,722,624 (GRCm39) |
T298A |
probably benign |
Het |
| Ccdc185 |
C |
T |
1: 182,576,543 (GRCm39) |
E49K |
possibly damaging |
Het |
| Cfhr2 |
A |
G |
1: 139,741,352 (GRCm39) |
S208P |
probably benign |
Het |
| Chd1 |
T |
C |
17: 15,990,430 (GRCm39) |
Y1661H |
probably damaging |
Het |
| Cntnap5a |
A |
G |
1: 116,085,367 (GRCm39) |
H435R |
probably benign |
Het |
| Cog8 |
A |
G |
8: 107,780,697 (GRCm39) |
V187A |
probably benign |
Het |
| Col24a1 |
A |
G |
3: 145,244,322 (GRCm39) |
H1532R |
probably benign |
Het |
| Dpp6 |
A |
G |
5: 27,836,518 (GRCm39) |
Y336C |
probably damaging |
Het |
| Drosha |
T |
A |
15: 12,846,198 (GRCm39) |
Y444* |
probably null |
Het |
| Egf |
A |
T |
3: 129,491,371 (GRCm39) |
C374* |
probably null |
Het |
| Eif2b3 |
C |
T |
4: 116,916,001 (GRCm39) |
H203Y |
probably damaging |
Het |
| Erbb4 |
A |
G |
1: 68,293,722 (GRCm39) |
V723A |
possibly damaging |
Het |
| Fbxo21 |
T |
C |
5: 118,126,855 (GRCm39) |
I202T |
probably benign |
Het |
| Gbp6 |
T |
C |
5: 105,422,073 (GRCm39) |
M544V |
probably benign |
Het |
| Gm10750 |
T |
C |
2: 148,857,964 (GRCm39) |
T96A |
unknown |
Het |
| Gm8232 |
A |
T |
14: 44,674,640 (GRCm39) |
|
probably null |
Het |
| Gpi-ps |
A |
T |
8: 5,689,896 (GRCm39) |
|
noncoding transcript |
Het |
| Gsdma3 |
T |
C |
11: 98,528,782 (GRCm39) |
V412A |
possibly damaging |
Het |
| Hs6st1 |
A |
T |
1: 36,108,016 (GRCm39) |
H93L |
probably damaging |
Het |
| Hsf2 |
G |
A |
10: 57,372,277 (GRCm39) |
E77K |
probably benign |
Het |
| Ints6 |
T |
C |
14: 62,951,188 (GRCm39) |
I280M |
probably damaging |
Het |
| Kazn |
C |
A |
4: 141,886,354 (GRCm39) |
|
probably null |
Het |
| Klhl20 |
T |
C |
1: 160,923,157 (GRCm39) |
Y13C |
probably damaging |
Het |
| Krtap26-1 |
G |
A |
16: 88,444,060 (GRCm39) |
P187L |
probably damaging |
Het |
| Mga |
T |
A |
2: 119,765,720 (GRCm39) |
I1329K |
probably damaging |
Het |
| Mindy4 |
A |
G |
6: 55,200,984 (GRCm39) |
D223G |
probably damaging |
Het |
| Ncor2 |
T |
C |
5: 125,128,001 (GRCm39) |
E124G |
probably damaging |
Het |
| Nfat5 |
G |
A |
8: 108,071,611 (GRCm39) |
|
probably null |
Het |
| Nkain1 |
A |
G |
4: 130,532,134 (GRCm38) |
F184L |
probably benign |
Het |
| Or8k25 |
T |
C |
2: 86,243,677 (GRCm39) |
T240A |
probably damaging |
Het |
| Rars1 |
A |
T |
11: 35,719,491 (GRCm39) |
F110L |
probably damaging |
Het |
| Rfx6 |
A |
C |
10: 51,599,173 (GRCm39) |
K509N |
probably damaging |
Het |
| Serpinb2 |
T |
C |
1: 107,443,333 (GRCm39) |
L44P |
probably damaging |
Het |
| Sin3a |
G |
A |
9: 57,002,609 (GRCm39) |
R167Q |
probably damaging |
Het |
| Sos2 |
T |
A |
12: 69,650,641 (GRCm39) |
T809S |
probably damaging |
Het |
| Stard9 |
A |
G |
2: 120,533,811 (GRCm39) |
E3356G |
probably damaging |
Het |
| Vmn1r52 |
A |
G |
6: 90,155,905 (GRCm39) |
T70A |
probably benign |
Het |
|
| Other mutations in Ing3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02330:Ing3
|
APN |
6 |
21,952,120 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02668:Ing3
|
APN |
6 |
21,950,058 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02897:Ing3
|
APN |
6 |
21,969,325 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL03065:Ing3
|
APN |
6 |
21,971,221 (GRCm39) |
missense |
probably benign |
|
|
R0076:Ing3
|
UTSW |
6 |
21,952,170 (GRCm39) |
missense |
probably benign |
|
|
R0513:Ing3
|
UTSW |
6 |
21,970,034 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0711:Ing3
|
UTSW |
6 |
21,971,236 (GRCm39) |
nonsense |
probably null |
|
|
R2369:Ing3
|
UTSW |
6 |
21,950,090 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4660:Ing3
|
UTSW |
6 |
21,973,710 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4672:Ing3
|
UTSW |
6 |
21,965,729 (GRCm39) |
splice site |
probably null |
|
|
R5557:Ing3
|
UTSW |
6 |
21,968,908 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5682:Ing3
|
UTSW |
6 |
21,968,949 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5773:Ing3
|
UTSW |
6 |
21,971,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5774:Ing3
|
UTSW |
6 |
21,967,688 (GRCm39) |
missense |
probably benign |
|
|
R5914:Ing3
|
UTSW |
6 |
21,968,904 (GRCm39) |
missense |
probably benign |
0.18 |
|
R5976:Ing3
|
UTSW |
6 |
21,971,173 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6265:Ing3
|
UTSW |
6 |
21,953,813 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7239:Ing3
|
UTSW |
6 |
21,952,193 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7526:Ing3
|
UTSW |
6 |
21,953,798 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8112:Ing3
|
UTSW |
6 |
21,952,181 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2014-01-21 |
Incidental Mutation