Incidental Mutation 'IGL02355:Rora'
| ID |
289642 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Rora
|
| Ensembl Gene |
ENSMUSG00000032238 |
| Gene Name |
RAR-related orphan receptor alpha |
| Synonyms |
tmgc26, Nr1f1, 9530021D13Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.911)
|
| Stock # |
IGL02355
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
68561068-69295528 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 69281374 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 329
(Y329H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000109254
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034766]
[ENSMUST00000113624]
|
| AlphaFold |
P51448 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000034766
AA Change: Y385H
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000034766
Gene: ENSMUSG00000032238
AA Change: Y385H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
26 |
N/A |
INTRINSIC |
|
ZnF_C4
|
70 |
141 |
4.71e-41 |
SMART |
|
low complexity region
|
161 |
175 |
N/A |
INTRINSIC |
|
HOLI
|
325 |
481 |
8.8e-32 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000113624
AA Change: Y329H
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000109254
Gene: ENSMUSG00000032238
AA Change: Y329H
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C4
|
14 |
85 |
4.71e-41 |
SMART |
|
low complexity region
|
105 |
119 |
N/A |
INTRINSIC |
|
HOLI
|
269 |
425 |
8.8e-32 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: The protein encoded by this gene is a member of the NR1 subfamily of nuclear hormone receptors. It can bind as a monomer or as a homodimer to hormone response elements upstream of several genes to enhance the expression of those genes. The encoded protein has been shown to interact with NM23-2, a nucleoside diphosphate kinase involved in organogenesis and differentiation, as well as with NM23-1, the product of a tumor metastasis suppressor candidate gene. Also, it has been shown to aid in the transcriptional regulation of some genes involved in circadian rhythm. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]
PHENOTYPE: Homozygotes for null mutations exhibit ataxia, cerebellar dysgenesis, impaired Purkinje and granule cell development, olfactory defects, hypoalphalipoproteinemia, and death around 4 weeks. Heterozygotes show slow Purkinje cell dedritic atrophy and loss. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam3 |
C |
A |
8: 25,187,207 (GRCm39) |
C428F |
probably damaging |
Het |
| Alas1 |
T |
C |
9: 106,113,838 (GRCm39) |
Y469C |
probably damaging |
Het |
| Asxl1 |
C |
T |
2: 153,243,706 (GRCm39) |
L1419F |
probably benign |
Het |
| Bcan |
C |
T |
3: 87,901,449 (GRCm39) |
D418N |
possibly damaging |
Het |
| Cdc42bpg |
A |
G |
19: 6,360,839 (GRCm39) |
D199G |
possibly damaging |
Het |
| Chst15 |
T |
C |
7: 131,868,401 (GRCm39) |
N340D |
probably benign |
Het |
| Col12a1 |
T |
G |
9: 79,537,993 (GRCm39) |
|
probably benign |
Het |
| Cyp2c67 |
T |
A |
19: 39,631,849 (GRCm39) |
H116L |
probably benign |
Het |
| Cyp2c67 |
G |
A |
19: 39,605,826 (GRCm39) |
R357* |
probably null |
Het |
| Ears2 |
T |
C |
7: 121,643,773 (GRCm39) |
D395G |
probably benign |
Het |
| Fam227a |
A |
T |
15: 79,528,139 (GRCm39) |
|
probably benign |
Het |
| Fap |
A |
G |
2: 62,403,842 (GRCm39) |
V11A |
probably benign |
Het |
| Ganc |
A |
G |
2: 120,264,238 (GRCm39) |
D397G |
probably damaging |
Het |
| Gjb6 |
C |
A |
14: 57,361,752 (GRCm39) |
G170C |
possibly damaging |
Het |
| Gria2 |
A |
T |
3: 80,614,244 (GRCm39) |
W599R |
probably damaging |
Het |
| Gvin-ps5 |
T |
C |
7: 105,929,480 (GRCm39) |
|
noncoding transcript |
Het |
| Ighv1-64 |
A |
G |
12: 115,471,236 (GRCm39) |
S94P |
probably benign |
Het |
| Kifc3 |
C |
T |
8: 95,836,507 (GRCm39) |
A85T |
probably damaging |
Het |
| Lifr |
G |
A |
15: 7,194,174 (GRCm39) |
|
probably null |
Het |
| Lonp2 |
T |
G |
8: 87,350,874 (GRCm39) |
S21R |
probably benign |
Het |
| Nxpe3 |
A |
G |
16: 55,710,949 (GRCm39) |
V30A |
probably benign |
Het |
| Olfml1 |
T |
C |
7: 107,167,010 (GRCm39) |
V13A |
probably benign |
Het |
| Or10w1 |
T |
C |
19: 13,632,597 (GRCm39) |
V268A |
probably benign |
Het |
| Or1af1 |
A |
G |
2: 37,109,681 (GRCm39) |
Y60C |
probably damaging |
Het |
| Pcnt |
G |
A |
10: 76,210,996 (GRCm39) |
Q2376* |
probably null |
Het |
| Pglyrp2 |
A |
G |
17: 32,635,996 (GRCm39) |
L380P |
probably damaging |
Het |
| Plin3 |
A |
G |
17: 56,593,636 (GRCm39) |
V26A |
probably benign |
Het |
| Potefam1 |
T |
C |
2: 111,041,996 (GRCm39) |
|
probably benign |
Het |
| Pramel25 |
A |
G |
4: 143,519,580 (GRCm39) |
S114G |
probably damaging |
Het |
| Rims1 |
A |
G |
1: 22,522,288 (GRCm39) |
I470T |
probably damaging |
Het |
| Scnn1b |
G |
A |
7: 121,516,770 (GRCm39) |
R503H |
probably damaging |
Het |
| Sec14l1 |
A |
G |
11: 117,035,675 (GRCm39) |
D237G |
possibly damaging |
Het |
| Selplg |
A |
G |
5: 113,957,467 (GRCm39) |
S280P |
probably benign |
Het |
| Serpina12 |
A |
G |
12: 104,004,140 (GRCm39) |
L164P |
probably benign |
Het |
| Sik2 |
C |
T |
9: 50,828,903 (GRCm39) |
W176* |
probably null |
Het |
| Slc2a1 |
T |
C |
4: 118,993,612 (GRCm39) |
F483S |
possibly damaging |
Het |
| Speg |
A |
G |
1: 75,400,559 (GRCm39) |
D2573G |
possibly damaging |
Het |
| Stil |
C |
T |
4: 114,867,308 (GRCm39) |
S239L |
probably damaging |
Het |
| Tmem94 |
C |
A |
11: 115,685,571 (GRCm39) |
S941R |
probably damaging |
Het |
| Tnfrsf11b |
T |
A |
15: 54,115,778 (GRCm39) |
D273V |
probably damaging |
Het |
| Tns2 |
A |
G |
15: 102,020,725 (GRCm39) |
T864A |
probably benign |
Het |
| Zfpm2 |
A |
G |
15: 40,962,890 (GRCm39) |
H184R |
probably damaging |
Het |
|
| Other mutations in Rora |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00811:Rora
|
APN |
9 |
69,278,572 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL02362:Rora
|
APN |
9 |
69,281,374 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4696001:Rora
|
UTSW |
9 |
69,271,841 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0091:Rora
|
UTSW |
9 |
69,281,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0555:Rora
|
UTSW |
9 |
69,269,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0609:Rora
|
UTSW |
9 |
69,269,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1483:Rora
|
UTSW |
9 |
69,271,667 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1712:Rora
|
UTSW |
9 |
69,282,771 (GRCm39) |
missense |
probably benign |
0.23 |
|
R1785:Rora
|
UTSW |
9 |
69,284,119 (GRCm39) |
missense |
probably benign |
0.30 |
|
R2883:Rora
|
UTSW |
9 |
69,282,717 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4173:Rora
|
UTSW |
9 |
68,561,192 (GRCm39) |
missense |
probably benign |
0.41 |
|
R5226:Rora
|
UTSW |
9 |
69,271,423 (GRCm39) |
intron |
probably benign |
|
|
R5660:Rora
|
UTSW |
9 |
68,561,203 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6029:Rora
|
UTSW |
9 |
69,271,734 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6054:Rora
|
UTSW |
9 |
69,286,084 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6114:Rora
|
UTSW |
9 |
69,278,605 (GRCm39) |
missense |
probably benign |
|
|
R6329:Rora
|
UTSW |
9 |
69,280,468 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7028:Rora
|
UTSW |
9 |
69,103,365 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7170:Rora
|
UTSW |
9 |
69,280,472 (GRCm39) |
nonsense |
probably null |
|
|
R7233:Rora
|
UTSW |
9 |
69,104,804 (GRCm39) |
nonsense |
probably null |
|
|
R7512:Rora
|
UTSW |
9 |
69,281,367 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9647:Rora
|
UTSW |
9 |
69,255,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Rora
|
UTSW |
9 |
69,271,654 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2015-04-16 |
Incidental Mutation