Incidental Mutation 'IGL01448:Ints5'
| ID |
84493 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ints5
|
| Ensembl Gene |
ENSMUSG00000116347 |
| Gene Name |
integrator complex subunit 5 |
| Synonyms |
1110055N21Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.511)
|
| Stock # |
IGL01448
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
8870369-8875252 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 8872851 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Leucine
at position 270
(P270L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000093968
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096246]
[ENSMUST00000096249]
[ENSMUST00000096251]
[ENSMUST00000185488]
[ENSMUST00000187504]
[ENSMUST00000191089]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000096246
|
| SMART Domains |
Protein: ENSMUSP00000093965
Gene: ENSMUSG00000071650
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
32 |
N/A |
INTRINSIC |
|
low complexity region
|
157 |
169 |
N/A |
INTRINSIC |
|
Pfam:Gal_mutarotas_2
|
275 |
346 |
3.9e-24 |
PFAM |
|
Pfam:Glyco_hydro_31
|
387 |
832 |
8.7e-136 |
PFAM |
|
low complexity region
|
888 |
898 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000096249
AA Change: P270L
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000093968
Gene: ENSMUSG00000071652
AA Change: P270L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
7 |
25 |
N/A |
INTRINSIC |
|
Pfam:INTS5_N
|
29 |
252 |
1e-82 |
PFAM |
|
low complexity region
|
254 |
267 |
N/A |
INTRINSIC |
|
Pfam:INTS5_C
|
289 |
998 |
2.2e-249 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000096251
|
| SMART Domains |
Protein: ENSMUSP00000093970
Gene: ENSMUSG00000071653
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
37 |
N/A |
INTRINSIC |
|
low complexity region
|
99 |
112 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000185488
|
| SMART Domains |
Protein: ENSMUSP00000140221
Gene: ENSMUSG00000071653
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
37 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186647
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187504
|
| SMART Domains |
Protein: ENSMUSP00000139692
Gene: ENSMUSG00000096740
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Lbh
|
1 |
101 |
2.5e-20 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000188635
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190843
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190530
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000191089
|
| SMART Domains |
Protein: ENSMUSP00000140564
Gene: ENSMUSG00000116347
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
37 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The Integrator complex is a complex that associates with the C-terminal domain of RNA polymerase II large subunit. This complex is brought to U1 and U2 small nuclear RNA genes, where it is involved in the transcription and processing of their transcripts. The protein encoded by this gene represents a subunit of the Integrator complex. [provided by RefSeq, Aug 2016]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700020A23Rik |
A |
T |
2: 130,247,767 (GRCm39) |
E75D |
possibly damaging |
Het |
| 1700084J12Rik |
A |
G |
15: 33,405,779 (GRCm39) |
|
probably benign |
Het |
| 2610303G11Rik |
T |
A |
9: 98,068,762 (GRCm39) |
|
noncoding transcript |
Het |
| 4931414P19Rik |
T |
C |
14: 54,823,417 (GRCm39) |
D320G |
possibly damaging |
Het |
| Adamts6 |
G |
A |
13: 104,433,672 (GRCm39) |
E34K |
probably damaging |
Het |
| Alms1 |
T |
A |
6: 85,654,881 (GRCm39) |
N3142K |
possibly damaging |
Het |
| Anapc7 |
G |
A |
5: 122,566,276 (GRCm39) |
A62T |
probably damaging |
Het |
| Atp8b3 |
G |
A |
10: 80,356,256 (GRCm39) |
P1152L |
probably benign |
Het |
| Cc2d2a |
C |
T |
5: 43,841,527 (GRCm39) |
T181I |
possibly damaging |
Het |
| Celsr2 |
A |
G |
3: 108,300,555 (GRCm39) |
L2835P |
probably damaging |
Het |
| Ctns |
A |
T |
11: 73,079,548 (GRCm39) |
V99D |
possibly damaging |
Het |
| Dchs1 |
T |
C |
7: 105,421,134 (GRCm39) |
R429G |
probably damaging |
Het |
| Ddx11 |
T |
C |
17: 66,441,132 (GRCm39) |
V218A |
probably damaging |
Het |
| Eftud2 |
G |
A |
11: 102,756,389 (GRCm39) |
|
probably benign |
Het |
| Erich1 |
G |
T |
8: 14,128,853 (GRCm39) |
T29N |
possibly damaging |
Het |
| Exosc8 |
T |
C |
3: 54,636,686 (GRCm39) |
E215G |
probably damaging |
Het |
| Fam184a |
G |
T |
10: 53,575,045 (GRCm39) |
A188E |
probably benign |
Het |
| Fign |
A |
G |
2: 63,810,032 (GRCm39) |
S413P |
probably damaging |
Het |
| Fkbp6 |
A |
G |
5: 135,378,550 (GRCm39) |
S33P |
probably damaging |
Het |
| Glb1 |
A |
G |
9: 114,279,745 (GRCm39) |
|
probably benign |
Het |
| H2-Q1 |
T |
C |
17: 35,542,437 (GRCm39) |
|
probably benign |
Het |
| Helz2 |
T |
C |
2: 180,875,770 (GRCm39) |
T1575A |
probably damaging |
Het |
| Il18r1 |
A |
G |
1: 40,513,890 (GRCm39) |
E32G |
probably damaging |
Het |
| Itga7 |
G |
T |
10: 128,785,337 (GRCm39) |
E847* |
probably null |
Het |
| Kcns3 |
A |
C |
12: 11,141,644 (GRCm39) |
S352A |
possibly damaging |
Het |
| Kiz |
A |
G |
2: 146,705,721 (GRCm39) |
K94E |
probably benign |
Het |
| Lin7b |
C |
T |
7: 45,018,624 (GRCm39) |
V12M |
probably damaging |
Het |
| Myo18b |
A |
T |
5: 112,959,570 (GRCm39) |
I1409N |
probably damaging |
Het |
| Myo5b |
A |
G |
18: 74,777,161 (GRCm39) |
H407R |
probably damaging |
Het |
| Nelfa |
T |
C |
5: 34,056,146 (GRCm39) |
T506A |
probably damaging |
Het |
| Or10p21 |
A |
G |
10: 128,847,729 (GRCm39) |
T192A |
probably damaging |
Het |
| Or4d5 |
A |
T |
9: 40,012,378 (GRCm39) |
M136K |
probably damaging |
Het |
| Or5p72 |
T |
A |
7: 108,022,235 (GRCm39) |
Y152* |
probably null |
Het |
| Or6c69 |
A |
G |
10: 129,748,114 (GRCm39) |
I11T |
possibly damaging |
Het |
| Pclo |
A |
C |
5: 14,726,408 (GRCm39) |
|
probably benign |
Het |
| Pes1 |
G |
A |
11: 3,927,979 (GRCm39) |
E544K |
possibly damaging |
Het |
| Rabgap1l |
A |
G |
1: 160,568,315 (GRCm39) |
|
probably benign |
Het |
| Rapgef2 |
T |
C |
3: 78,976,244 (GRCm39) |
M1521V |
probably benign |
Het |
| Rapgef2 |
C |
T |
3: 79,011,269 (GRCm39) |
|
probably null |
Het |
| Reln |
A |
G |
5: 22,245,403 (GRCm39) |
V735A |
probably benign |
Het |
| Slc2a4 |
A |
G |
11: 69,835,902 (GRCm39) |
S316P |
possibly damaging |
Het |
| Smarce1 |
C |
T |
11: 99,101,013 (GRCm39) |
G373E |
possibly damaging |
Het |
| Spata31d1a |
T |
A |
13: 59,849,373 (GRCm39) |
R918S |
probably benign |
Het |
| St3gal4 |
T |
C |
9: 34,963,627 (GRCm39) |
K227R |
probably benign |
Het |
| Stra6l |
T |
A |
4: 45,864,864 (GRCm39) |
|
probably null |
Het |
| Stxbp5l |
T |
C |
16: 37,036,341 (GRCm39) |
I425V |
probably damaging |
Het |
| Tcaf2 |
T |
C |
6: 42,607,262 (GRCm39) |
T231A |
probably benign |
Het |
| Tiparp |
G |
T |
3: 65,460,030 (GRCm39) |
G442* |
probably null |
Het |
| Tnks |
A |
G |
8: 35,307,136 (GRCm39) |
Y1138H |
probably damaging |
Het |
| Vezt |
T |
A |
10: 93,832,719 (GRCm39) |
I231F |
probably damaging |
Het |
| Vmn2r4 |
A |
T |
3: 64,313,816 (GRCm39) |
N388K |
probably damaging |
Het |
| Zbed3 |
A |
G |
13: 95,473,142 (GRCm39) |
K189E |
possibly damaging |
Het |
| Zfp512b |
T |
C |
2: 181,229,578 (GRCm39) |
T625A |
possibly damaging |
Het |
| Zfp827 |
A |
T |
8: 79,787,362 (GRCm39) |
Q176L |
possibly damaging |
Het |
|
| Other mutations in Ints5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01915:Ints5
|
APN |
19 |
8,874,357 (GRCm39) |
missense |
probably benign |
|
|
IGL01993:Ints5
|
APN |
19 |
8,872,829 (GRCm39) |
missense |
probably benign |
|
|
IGL02264:Ints5
|
APN |
19 |
8,873,076 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02367:Ints5
|
APN |
19 |
8,872,959 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02955:Ints5
|
APN |
19 |
8,875,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4449:Ints5
|
UTSW |
19 |
8,874,594 (GRCm39) |
missense |
probably benign |
0.10 |
|
R0348:Ints5
|
UTSW |
19 |
8,873,114 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0379:Ints5
|
UTSW |
19 |
8,874,497 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0617:Ints5
|
UTSW |
19 |
8,873,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1954:Ints5
|
UTSW |
19 |
8,872,260 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2172:Ints5
|
UTSW |
19 |
8,873,646 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R2370:Ints5
|
UTSW |
19 |
8,874,143 (GRCm39) |
missense |
probably benign |
|
|
R3116:Ints5
|
UTSW |
19 |
8,872,136 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R4395:Ints5
|
UTSW |
19 |
8,873,808 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5390:Ints5
|
UTSW |
19 |
8,873,931 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6868:Ints5
|
UTSW |
19 |
8,874,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7133:Ints5
|
UTSW |
19 |
8,872,923 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7685:Ints5
|
UTSW |
19 |
8,874,168 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7999:Ints5
|
UTSW |
19 |
8,874,407 (GRCm39) |
missense |
probably benign |
|
|
R8024:Ints5
|
UTSW |
19 |
8,873,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8296:Ints5
|
UTSW |
19 |
8,872,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8672:Ints5
|
UTSW |
19 |
8,873,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9027:Ints5
|
UTSW |
19 |
8,873,322 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9493:Ints5
|
UTSW |
19 |
8,872,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0066:Ints5
|
UTSW |
19 |
8,873,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Ints5
|
UTSW |
19 |
8,872,337 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Ints5
|
UTSW |
19 |
8,872,299 (GRCm39) |
missense |
probably benign |
0.31 |
|
| Posted On |
2013-11-11 |
Incidental Mutation