Incidental Mutation 'R8747:Kat7'
| ID |
663617 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Kat7
|
| Ensembl Gene |
ENSMUSG00000038909 |
| Gene Name |
K(lysine) acetyltransferase 7 |
| Synonyms |
Hboa, Hbo1, Myst2 |
| MMRRC Submission |
068618-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8747 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
95165085-95201072 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to C
at 95185392 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tryptophan
at position 161
(C161W)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000099448
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072621]
[ENSMUST00000092766]
[ENSMUST00000103159]
[ENSMUST00000107733]
[ENSMUST00000107734]
|
| AlphaFold |
Q5SVQ0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000072621
AA Change: C222W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000072416
Gene: ENSMUSG00000038909
AA Change: C222W
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
37 |
59 |
N/A |
INTRINSIC |
|
low complexity region
|
136 |
147 |
N/A |
INTRINSIC |
|
Pfam:zf-C2HC
|
184 |
214 |
3.2e-17 |
PFAM |
|
ZnF_C2H2
|
338 |
364 |
1.86e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000092766
AA Change: C222W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000090441
Gene: ENSMUSG00000038909
AA Change: C222W
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
37 |
59 |
N/A |
INTRINSIC |
|
low complexity region
|
136 |
147 |
N/A |
INTRINSIC |
|
Pfam:zf-C2HC
|
186 |
214 |
1.2e-16 |
PFAM |
|
ZnF_C2H2
|
368 |
394 |
1.86e1 |
SMART |
|
Pfam:MOZ_SAS
|
395 |
573 |
7.9e-89 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000103159
AA Change: C161W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000099448
Gene: ENSMUSG00000038909
AA Change: C161W
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
35 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
75 |
86 |
N/A |
INTRINSIC |
|
Pfam:zf-C2HC
|
123 |
153 |
2.8e-17 |
PFAM |
|
ZnF_C2H2
|
277 |
303 |
1.86e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000107733
AA Change: C220W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000103361
Gene: ENSMUSG00000038909
AA Change: C220W
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
35 |
57 |
N/A |
INTRINSIC |
|
low complexity region
|
134 |
145 |
N/A |
INTRINSIC |
|
Pfam:zf-C2HC
|
182 |
212 |
2.3e-17 |
PFAM |
|
ZnF_C2H2
|
336 |
362 |
1.86e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000107734
AA Change: C220W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000103362
Gene: ENSMUSG00000038909
AA Change: C220W
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
35 |
57 |
N/A |
INTRINSIC |
|
low complexity region
|
134 |
145 |
N/A |
INTRINSIC |
|
Pfam:zf-C2HC
|
182 |
212 |
2.5e-17 |
PFAM |
|
ZnF_C2H2
|
366 |
392 |
1.86e1 |
SMART |
|
| Meta Mutation Damage Score |
0.7293 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
| Validation Efficiency |
100% (52/52) |
| 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 part of the multimeric HBO1 complex, which possesses histone H4-specific acetyltransferase activity. This activity is required for functional replication origins and is involved in transcriptional activation of some genes. In both cases, the acetylation of histone H4 helps unfold chromatin so that the DNA can be accessed and replicated or transcribed. [provided by RefSeq, Oct 2016]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic growth arrest, incomplete embryo turning, disorganized yolk sac vascular plexus, and increased apoptosis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700109H08Rik |
A |
G |
5: 3,632,240 (GRCm39) |
D190G |
probably benign |
Het |
| Abhd11 |
A |
G |
5: 135,040,760 (GRCm39) |
I271V |
possibly damaging |
Het |
| Akap6 |
T |
G |
12: 53,188,999 (GRCm39) |
S2138A |
probably benign |
Het |
| Amn |
C |
A |
12: 111,241,440 (GRCm39) |
P235H |
probably damaging |
Het |
| Arf2 |
A |
T |
11: 103,859,975 (GRCm39) |
M18L |
probably benign |
Het |
| Asic2 |
A |
T |
11: 81,043,233 (GRCm39) |
F20Y |
possibly damaging |
Het |
| Bok |
T |
C |
1: 93,622,664 (GRCm39) |
|
probably null |
Het |
| Cachd1 |
T |
A |
4: 100,860,045 (GRCm39) |
|
probably benign |
Het |
| Casp8 |
A |
G |
1: 58,883,617 (GRCm39) |
N308S |
probably benign |
Het |
| Cavin3 |
G |
T |
7: 105,131,154 (GRCm39) |
H71Q |
possibly damaging |
Het |
| Ccdc87 |
A |
G |
19: 4,891,646 (GRCm39) |
I713V |
probably benign |
Het |
| Clcn6 |
A |
T |
4: 148,093,354 (GRCm39) |
|
probably null |
Het |
| Cmas |
T |
C |
6: 142,716,927 (GRCm39) |
I273T |
possibly damaging |
Het |
| Ctxn3 |
A |
T |
18: 57,610,378 (GRCm39) |
D65V |
probably damaging |
Het |
| D130040H23Rik |
C |
A |
8: 69,755,705 (GRCm39) |
N387K |
probably benign |
Het |
| Depp1 |
T |
A |
6: 116,629,122 (GRCm39) |
L155Q |
possibly damaging |
Het |
| Dnah9 |
T |
C |
11: 65,818,816 (GRCm39) |
K3174R |
possibly damaging |
Het |
| Ecpas |
C |
T |
4: 58,828,632 (GRCm39) |
V934I |
probably damaging |
Het |
| Efcab14 |
A |
G |
4: 115,603,793 (GRCm39) |
N157S |
probably damaging |
Het |
| Ets1 |
G |
A |
9: 32,641,474 (GRCm39) |
G109D |
probably damaging |
Het |
| Fbln5 |
G |
A |
12: 101,734,754 (GRCm39) |
R173C |
probably damaging |
Het |
| Fchsd1 |
G |
A |
18: 38,096,035 (GRCm39) |
P525L |
probably benign |
Het |
| Gmppa |
G |
A |
1: 75,416,025 (GRCm39) |
V156I |
probably damaging |
Het |
| Gtpbp1 |
A |
G |
15: 79,603,482 (GRCm39) |
D182G |
|
Het |
| Ift140 |
T |
A |
17: 25,254,809 (GRCm39) |
S430T |
probably benign |
Het |
| Lipk |
T |
A |
19: 33,996,184 (GRCm39) |
M32K |
probably damaging |
Het |
| Lum |
A |
T |
10: 97,404,351 (GRCm39) |
D82V |
possibly damaging |
Het |
| Macf1 |
C |
A |
4: 123,248,944 (GRCm39) |
A7196S |
probably damaging |
Het |
| Mroh2b |
T |
A |
15: 4,964,782 (GRCm39) |
S926T |
probably damaging |
Het |
| Nbn |
G |
T |
4: 15,981,555 (GRCm39) |
R549I |
probably damaging |
Het |
| Nfu1 |
T |
C |
6: 86,996,400 (GRCm39) |
I117T |
probably damaging |
Het |
| Or51f1 |
T |
C |
7: 102,506,139 (GRCm39) |
T117A |
probably benign |
Het |
| Or7a39 |
A |
G |
10: 78,715,155 (GRCm39) |
T50A |
probably benign |
Het |
| Parp1 |
T |
C |
1: 180,422,275 (GRCm39) |
L778P |
probably damaging |
Het |
| Pbld2 |
G |
T |
10: 62,888,069 (GRCm39) |
V125F |
probably benign |
Het |
| Prkag2 |
A |
G |
5: 25,085,680 (GRCm39) |
|
probably null |
Het |
| Prss54 |
A |
G |
8: 96,286,351 (GRCm39) |
F241L |
probably benign |
Het |
| Rnf121 |
T |
C |
7: 101,678,316 (GRCm39) |
D177G |
probably damaging |
Het |
| Slc12a7 |
G |
A |
13: 73,933,241 (GRCm39) |
V100I |
probably benign |
Het |
| Slc28a1 |
C |
T |
7: 80,774,719 (GRCm39) |
L189F |
possibly damaging |
Het |
| Slc35a3 |
T |
C |
3: 116,488,219 (GRCm39) |
Q16R |
probably damaging |
Het |
| Snap91 |
A |
G |
9: 86,686,577 (GRCm39) |
F354L |
probably damaging |
Het |
| Steap2 |
A |
G |
5: 5,723,539 (GRCm39) |
I447T |
probably benign |
Het |
| Tagap |
T |
A |
17: 8,147,602 (GRCm39) |
I104N |
probably damaging |
Het |
| Tas1r2 |
A |
G |
4: 139,387,318 (GRCm39) |
D259G |
probably benign |
Het |
| Tgm3 |
T |
C |
2: 129,886,452 (GRCm39) |
S558P |
probably benign |
Het |
| Tuba3a |
A |
G |
6: 125,258,018 (GRCm39) |
V324A |
probably damaging |
Het |
| Vmn1r238 |
T |
G |
18: 3,123,232 (GRCm39) |
I61L |
possibly damaging |
Het |
| Vmn1r52 |
A |
G |
6: 90,156,451 (GRCm39) |
T252A |
probably benign |
Het |
| Vmp1 |
A |
G |
11: 86,492,885 (GRCm39) |
V308A |
probably damaging |
Het |
| Wdfy4 |
A |
C |
14: 32,874,611 (GRCm39) |
V159G |
|
Het |
| Zfp180 |
A |
G |
7: 23,804,687 (GRCm39) |
T369A |
possibly damaging |
Het |
| Zfp827 |
A |
G |
8: 79,755,316 (GRCm39) |
M1V |
probably null |
Het |
| Zmym4 |
A |
G |
4: 126,787,198 (GRCm39) |
I1031T |
probably damaging |
Het |
|
| Other mutations in Kat7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01886:Kat7
|
APN |
11 |
95,196,959 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03287:Kat7
|
APN |
11 |
95,190,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0047:Kat7
|
UTSW |
11 |
95,191,034 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0578:Kat7
|
UTSW |
11 |
95,182,350 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1739:Kat7
|
UTSW |
11 |
95,167,373 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R2038:Kat7
|
UTSW |
11 |
95,190,928 (GRCm39) |
missense |
probably benign |
0.14 |
|
R2115:Kat7
|
UTSW |
11 |
95,194,120 (GRCm39) |
missense |
probably benign |
0.10 |
|
R2214:Kat7
|
UTSW |
11 |
95,166,631 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2355:Kat7
|
UTSW |
11 |
95,182,407 (GRCm39) |
missense |
probably benign |
|
|
R3425:Kat7
|
UTSW |
11 |
95,193,991 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3775:Kat7
|
UTSW |
11 |
95,182,357 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3811:Kat7
|
UTSW |
11 |
95,182,441 (GRCm39) |
splice site |
probably benign |
|
|
R4066:Kat7
|
UTSW |
11 |
95,174,967 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4169:Kat7
|
UTSW |
11 |
95,171,298 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4657:Kat7
|
UTSW |
11 |
95,168,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4814:Kat7
|
UTSW |
11 |
95,193,949 (GRCm39) |
splice site |
probably benign |
|
|
R5186:Kat7
|
UTSW |
11 |
95,177,242 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6015:Kat7
|
UTSW |
11 |
95,174,860 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6820:Kat7
|
UTSW |
11 |
95,174,965 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6894:Kat7
|
UTSW |
11 |
95,174,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7192:Kat7
|
UTSW |
11 |
95,166,656 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7217:Kat7
|
UTSW |
11 |
95,182,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7728:Kat7
|
UTSW |
11 |
95,190,907 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7999:Kat7
|
UTSW |
11 |
95,174,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8230:Kat7
|
UTSW |
11 |
95,168,415 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8929:Kat7
|
UTSW |
11 |
95,196,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9166:Kat7
|
UTSW |
11 |
95,190,928 (GRCm39) |
missense |
probably benign |
|
|
R9239:Kat7
|
UTSW |
11 |
95,197,020 (GRCm39) |
missense |
probably benign |
0.20 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTACCAAGGAAATGAATGCGGC -3'
(R):5'- CTTCACGGCAGCTCCATTTG -3'
Sequencing Primer
(F):5'- ACAATCCTTTTATTTGTTCGTGGAG -3'
(R):5'- CAGCTCCATTTGGAAGCATTTG -3'
|
| Posted On |
2021-03-08 |
Incidental Mutation