Incidental Mutation 'IGL01971:4930432E11Rik'
| ID |
182560 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
4930432E11Rik
|
| Ensembl Gene |
ENSMUSG00000046958 |
| Gene Name |
RIKEN cDNA 4930432E11 gene |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.082)
|
| Stock # |
IGL01971
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
29255998-29276204 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
C to T
at 29273987 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000053635
|
| SMART Domains |
Protein: ENSMUSP00000049518
Gene: ENSMUSG00000046958
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:WD40
|
43 |
79 |
3e-11 |
BLAST |
|
WD40
|
131 |
172 |
1.97e2 |
SMART |
|
WD40
|
175 |
214 |
2.24e-2 |
SMART |
|
Blast:WD40
|
257 |
296 |
4e-15 |
BLAST |
|
WD40
|
393 |
437 |
1.32e2 |
SMART |
|
WD40
|
494 |
533 |
2.15e-4 |
SMART |
|
low complexity region
|
598 |
617 |
N/A |
INTRINSIC |
|
low complexity region
|
1082 |
1094 |
N/A |
INTRINSIC |
|
low complexity region
|
1107 |
1148 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000063585
|
| SMART Domains |
Protein: ENSMUSP00000063695
Gene: ENSMUSG00000051976
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
28 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
35 |
67 |
3.29e-5 |
PROSPERO |
|
internal_repeat_1
|
73 |
102 |
3.29e-5 |
PROSPERO |
|
low complexity region
|
122 |
135 |
N/A |
INTRINSIC |
|
coiled coil region
|
161 |
182 |
N/A |
INTRINSIC |
|
low complexity region
|
216 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
239 |
249 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187265
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 20 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ankmy2 |
A |
T |
12: 36,243,792 (GRCm39) |
K336* |
probably null |
Het |
| Areg |
A |
G |
5: 91,288,870 (GRCm39) |
T59A |
probably benign |
Het |
| Atp8b4 |
T |
C |
2: 126,304,536 (GRCm39) |
I66V |
probably benign |
Het |
| Atrnl1 |
C |
T |
19: 57,741,715 (GRCm39) |
T1158M |
probably damaging |
Het |
| Ckmt1 |
T |
A |
2: 121,194,064 (GRCm39) |
I409N |
probably benign |
Het |
| Cnnm2 |
A |
G |
19: 46,860,115 (GRCm39) |
T730A |
probably benign |
Het |
| Fan1 |
T |
C |
7: 64,003,459 (GRCm39) |
R788G |
probably damaging |
Het |
| Fbf1 |
T |
C |
11: 116,034,208 (GRCm39) |
|
probably benign |
Het |
| Galnt2l |
G |
A |
8: 125,070,081 (GRCm39) |
V499M |
probably benign |
Het |
| Heca |
A |
G |
10: 17,791,162 (GRCm39) |
F298S |
probably damaging |
Het |
| Klhl6 |
A |
T |
16: 19,768,276 (GRCm39) |
V423E |
probably damaging |
Het |
| Notch3 |
T |
C |
17: 32,343,321 (GRCm39) |
N1951D |
probably damaging |
Het |
| Osbp |
T |
C |
19: 11,967,999 (GRCm39) |
V636A |
probably benign |
Het |
| Szt2 |
T |
C |
4: 118,244,152 (GRCm39) |
T1318A |
probably benign |
Het |
| Tnxb |
G |
A |
17: 34,891,271 (GRCm39) |
G538D |
probably damaging |
Het |
| Tpbpa |
A |
T |
13: 61,088,047 (GRCm39) |
F46L |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,554,123 (GRCm39) |
V30860A |
probably damaging |
Het |
| Usf3 |
A |
G |
16: 44,037,809 (GRCm39) |
|
probably null |
Het |
| Utp23 |
C |
A |
15: 51,745,671 (GRCm39) |
A57E |
probably benign |
Het |
| Vmn2r13 |
T |
C |
5: 109,321,981 (GRCm39) |
M239V |
probably benign |
Het |
|
| Other mutations in 4930432E11Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01121:4930432E11Rik
|
APN |
7 |
29,273,426 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL01955:4930432E11Rik
|
APN |
7 |
29,273,420 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02132:4930432E11Rik
|
APN |
7 |
29,262,704 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02484:4930432E11Rik
|
APN |
7 |
29,262,777 (GRCm39) |
unclassified |
noncoding transcript |
|
|
P0016:4930432E11Rik
|
UTSW |
7 |
29,262,537 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0051:4930432E11Rik
|
UTSW |
7 |
29,278,526 (GRCm39) |
exon |
noncoding transcript |
|
|
R0060:4930432E11Rik
|
UTSW |
7 |
29,273,595 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0094:4930432E11Rik
|
UTSW |
7 |
29,260,236 (GRCm39) |
exon |
noncoding transcript |
|
|
R0268:4930432E11Rik
|
UTSW |
7 |
29,274,027 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0423:4930432E11Rik
|
UTSW |
7 |
29,261,825 (GRCm39) |
exon |
noncoding transcript |
|
|
R0478:4930432E11Rik
|
UTSW |
7 |
29,262,014 (GRCm39) |
exon |
noncoding transcript |
|
|
R0646:4930432E11Rik
|
UTSW |
7 |
29,260,710 (GRCm39) |
exon |
noncoding transcript |
|
|
R1208:4930432E11Rik
|
UTSW |
7 |
29,260,708 (GRCm39) |
exon |
noncoding transcript |
|
|
R1778:4930432E11Rik
|
UTSW |
7 |
29,260,131 (GRCm39) |
exon |
noncoding transcript |
|
|
R1779:4930432E11Rik
|
UTSW |
7 |
29,278,591 (GRCm39) |
exon |
noncoding transcript |
|
|
R1918:4930432E11Rik
|
UTSW |
7 |
29,273,514 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R2360:4930432E11Rik
|
UTSW |
7 |
29,274,214 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R3736:4930432E11Rik
|
UTSW |
7 |
29,273,996 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R3780:4930432E11Rik
|
UTSW |
7 |
29,260,263 (GRCm39) |
exon |
noncoding transcript |
|
|
R4427:4930432E11Rik
|
UTSW |
7 |
29,278,678 (GRCm39) |
exon |
noncoding transcript |
|
|
R4835:4930432E11Rik
|
UTSW |
7 |
29,274,326 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R4929:4930432E11Rik
|
UTSW |
7 |
29,273,467 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5042:4930432E11Rik
|
UTSW |
7 |
29,273,927 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5129:4930432E11Rik
|
UTSW |
7 |
29,260,786 (GRCm39) |
exon |
noncoding transcript |
|
|
R5371:4930432E11Rik
|
UTSW |
7 |
29,261,918 (GRCm39) |
exon |
noncoding transcript |
|
|
R5381:4930432E11Rik
|
UTSW |
7 |
29,262,393 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5586:4930432E11Rik
|
UTSW |
7 |
29,277,153 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5874:4930432E11Rik
|
UTSW |
7 |
29,280,610 (GRCm39) |
exon |
noncoding transcript |
|
|
| Posted On |
2014-05-07 |
Incidental Mutation