Incidental Mutation 'IGL03373:Nob1'
| ID |
420401 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nob1
|
| Ensembl Gene |
ENSMUSG00000003848 |
| Gene Name |
NIN1/RPN12 binding protein 1 homolog |
| Synonyms |
1700021I09Rik, ART-4, Nob1p, Psmd8bp1 |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.963)
|
| Stock # |
IGL03373
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
108139121-108151670 bp(-) (GRCm39) |
| Type of Mutation |
intron |
| DNA Base Change (assembly) |
C to T
at 108144678 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000126868
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000003946]
[ENSMUST00000169311]
|
| AlphaFold |
Q8BW10 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000003946
|
| SMART Domains |
Protein: ENSMUSP00000003946
Gene: ENSMUSG00000003848
| Domain | Start | End | E-Value | Type |
|---|
|
PINc
|
5 |
108 |
2.28e-6 |
SMART |
|
Pfam:AF1Q
|
135 |
211 |
1.8e-30 |
PFAM |
|
Pfam:NOB1_Zn_bind
|
251 |
323 |
1e-34 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000076585
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000109273
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000163757
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000163973
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000165266
|
| SMART Domains |
Protein: ENSMUSP00000129298
Gene: ENSMUSG00000003848
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:PINc
|
5 |
61 |
9e-34 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000169311
|
| SMART Domains |
Protein: ENSMUSP00000126868
Gene: ENSMUSG00000003848
| Domain | Start | End | E-Value | Type |
|---|
|
PINc
|
5 |
108 |
2.28e-6 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170796
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] In yeast, over 200 protein and RNA cofactors are required for ribosome assembly, and these are generally conserved in eukaryotes. These factors orchestrate modification and cleavage of the initial 35S precursor rRNA transcript into the mature 18S, 5.8S, and 25S rRNAs, folding of the rRNA, and binding of ribosomal proteins and 5S RNA. Nob1 is involved in pre-rRNA processing. In a late cytoplasmic processing step, Nob1 cleaves a 20S rRNA intermediate at cleavage site D to produce the mature 18S rRNA (Lamanna and Karbstein, 2009 [PubMed 19706509]).[supplied by OMIM, Nov 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 30 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam6a |
A |
T |
12: 113,509,172 (GRCm39) |
Y515F |
possibly damaging |
Het |
| Adgrv1 |
A |
G |
13: 81,711,751 (GRCm39) |
V1075A |
probably damaging |
Het |
| Alox8 |
T |
C |
11: 69,077,443 (GRCm39) |
T436A |
probably benign |
Het |
| Cdc7 |
T |
A |
5: 107,120,785 (GRCm39) |
|
probably benign |
Het |
| Cdhr1 |
T |
A |
14: 36,818,257 (GRCm39) |
D65V |
possibly damaging |
Het |
| Dnase1 |
A |
G |
16: 3,857,707 (GRCm39) |
E278G |
probably damaging |
Het |
| Eif3g |
A |
T |
9: 20,805,722 (GRCm39) |
|
probably benign |
Het |
| Flnb |
G |
A |
14: 7,890,867 (GRCm38) |
|
probably null |
Het |
| Hars2 |
G |
T |
18: 36,918,998 (GRCm39) |
R86L |
probably damaging |
Het |
| Lmod1 |
C |
T |
1: 135,292,264 (GRCm39) |
A373V |
possibly damaging |
Het |
| Mdga2 |
A |
G |
12: 66,763,496 (GRCm39) |
I200T |
probably damaging |
Het |
| Mup1 |
T |
G |
4: 60,457,849 (GRCm39) |
|
probably benign |
Het |
| Nat8f5 |
A |
C |
6: 85,794,529 (GRCm39) |
S144A |
probably benign |
Het |
| Ndnf |
A |
C |
6: 65,681,272 (GRCm39) |
Y517S |
possibly damaging |
Het |
| Nedd4l |
G |
A |
18: 65,314,391 (GRCm39) |
|
probably benign |
Het |
| Nlrp4g |
A |
T |
9: 124,349,853 (GRCm38) |
|
noncoding transcript |
Het |
| Nploc4 |
G |
A |
11: 120,300,455 (GRCm39) |
R326* |
probably null |
Het |
| Obox3 |
A |
T |
7: 15,359,715 (GRCm39) |
V318D |
probably benign |
Het |
| Or10a3m |
G |
A |
7: 108,313,339 (GRCm39) |
V248I |
probably damaging |
Het |
| Or10ag57 |
T |
C |
2: 87,218,577 (GRCm39) |
F176S |
probably damaging |
Het |
| Pgm1 |
T |
C |
4: 99,818,741 (GRCm39) |
I130T |
probably damaging |
Het |
| Ptprk |
A |
T |
10: 28,442,533 (GRCm39) |
D845V |
probably damaging |
Het |
| Ptx4 |
T |
A |
17: 25,339,873 (GRCm39) |
S17T |
probably benign |
Het |
| Rasgrf1 |
T |
C |
9: 89,899,084 (GRCm39) |
|
probably benign |
Het |
| Rfx6 |
A |
G |
10: 51,596,096 (GRCm39) |
T426A |
probably damaging |
Het |
| Sfpq |
C |
A |
4: 126,920,578 (GRCm39) |
R564S |
possibly damaging |
Het |
| Spint2 |
A |
G |
7: 28,957,634 (GRCm39) |
|
probably benign |
Het |
| Vmn1r27 |
A |
G |
6: 58,192,689 (GRCm39) |
I105T |
probably damaging |
Het |
| Vmn1r78 |
T |
C |
7: 11,887,270 (GRCm39) |
S294P |
possibly damaging |
Het |
| Vmn2r40 |
T |
C |
7: 8,923,092 (GRCm39) |
D423G |
probably benign |
Het |
|
| Other mutations in Nob1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01434:Nob1
|
APN |
8 |
108,151,360 (GRCm39) |
splice site |
probably benign |
|
|
IGL01661:Nob1
|
APN |
8 |
108,139,814 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02110:Nob1
|
APN |
8 |
108,142,804 (GRCm39) |
makesense |
probably null |
|
|
PIT4531001:Nob1
|
UTSW |
8 |
108,145,049 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0627:Nob1
|
UTSW |
8 |
108,142,856 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1181:Nob1
|
UTSW |
8 |
108,148,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1264:Nob1
|
UTSW |
8 |
108,148,136 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2257:Nob1
|
UTSW |
8 |
108,143,729 (GRCm39) |
intron |
probably benign |
|
|
R4402:Nob1
|
UTSW |
8 |
108,145,120 (GRCm39) |
intron |
probably benign |
|
|
R5330:Nob1
|
UTSW |
8 |
108,142,881 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6907:Nob1
|
UTSW |
8 |
108,142,860 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7702:Nob1
|
UTSW |
8 |
108,139,737 (GRCm39) |
nonsense |
probably null |
|
|
R8412:Nob1
|
UTSW |
8 |
108,148,230 (GRCm39) |
nonsense |
probably null |
|
|
R9119:Nob1
|
UTSW |
8 |
108,142,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0017:Nob1
|
UTSW |
8 |
108,151,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation