Incidental Mutation 'IGL02048:Brinp1'
| ID |
184997 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Brinp1
|
| Ensembl Gene |
ENSMUSG00000028351 |
| Gene Name |
bone morphogenic protein/retinoic acid inducible neural specific 1 |
| Synonyms |
Fam5a, Dbc1, Dbccr1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.109)
|
| Stock # |
IGL02048
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
68679751-68872634 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 68681379 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 384
(I384V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030036
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030036]
|
| AlphaFold |
Q920P3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030036
AA Change: I384V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000030036
Gene: ENSMUSG00000028351
AA Change: I384V
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
MACPF
|
72 |
251 |
2.35e-46 |
SMART |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is located within a chromosomal region that shows loss of heterozygosity in some bladder cancers. It contains a 5' CpG island that may be a frequent target of hypermethylation, and it may undergo hypermethylation-based silencing in some bladder cancers. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice show increased adult neurogenesis in the subgranular zone of the dentate gyrus, altered neuronal differentiation in the hippocampus, and behavioral anomalies such as hyperactivity, reduced anxiety-like behaviors, poor social interaction, and a slight deficit in working memory. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca1 |
C |
T |
4: 53,069,831 (GRCm39) |
D1288N |
probably damaging |
Het |
| Abcc1 |
T |
C |
16: 14,229,383 (GRCm39) |
F372L |
probably damaging |
Het |
| Adcy2 |
G |
T |
13: 69,036,186 (GRCm39) |
N158K |
possibly damaging |
Het |
| Apba1 |
A |
G |
19: 23,915,000 (GRCm39) |
|
probably null |
Het |
| Arap3 |
T |
C |
18: 38,130,032 (GRCm39) |
E43G |
possibly damaging |
Het |
| Bet1 |
A |
T |
6: 4,082,456 (GRCm39) |
|
probably null |
Het |
| Blm |
A |
G |
7: 80,152,709 (GRCm39) |
|
probably benign |
Het |
| Cyp3a13 |
T |
C |
5: 137,917,257 (GRCm39) |
|
probably benign |
Het |
| Dlg5 |
A |
T |
14: 24,222,271 (GRCm39) |
I480N |
possibly damaging |
Het |
| Exoc3l4 |
A |
G |
12: 111,394,917 (GRCm39) |
K538R |
probably benign |
Het |
| Flna |
G |
T |
X: 73,272,106 (GRCm39) |
T2008K |
probably benign |
Het |
| Hc |
T |
A |
2: 34,886,039 (GRCm39) |
Q1388L |
probably benign |
Het |
| Ifitm1 |
T |
C |
7: 140,548,205 (GRCm39) |
S13P |
probably benign |
Het |
| Il1rapl2 |
A |
G |
X: 137,690,398 (GRCm39) |
I288V |
probably benign |
Het |
| Il31 |
C |
T |
5: 123,618,553 (GRCm39) |
V157M |
possibly damaging |
Het |
| N4bp2l1 |
A |
G |
5: 150,500,103 (GRCm39) |
|
probably null |
Het |
| Nell1 |
T |
C |
7: 49,869,355 (GRCm39) |
I210T |
probably damaging |
Het |
| Or52b3 |
T |
C |
7: 102,204,090 (GRCm39) |
Y200H |
probably damaging |
Het |
| Or7e176 |
T |
A |
9: 20,171,784 (GRCm39) |
I216N |
possibly damaging |
Het |
| Phf1 |
A |
G |
17: 27,153,515 (GRCm39) |
|
probably benign |
Het |
| Phf10 |
G |
A |
17: 15,165,411 (GRCm39) |
P482S |
probably benign |
Het |
| Ppp6r3 |
T |
G |
19: 3,523,848 (GRCm39) |
M522L |
possibly damaging |
Het |
| Qtrt1 |
T |
C |
9: 21,328,651 (GRCm39) |
L205P |
probably damaging |
Het |
| Vmn2r11 |
T |
C |
5: 109,202,658 (GRCm39) |
I140V |
probably benign |
Het |
| Xylt2 |
C |
T |
11: 94,557,171 (GRCm39) |
E107K |
possibly damaging |
Het |
| Zfp512b |
A |
T |
2: 181,231,715 (GRCm39) |
F155Y |
possibly damaging |
Het |
| Zfyve27 |
A |
G |
19: 42,174,296 (GRCm39) |
D314G |
probably damaging |
Het |
|
| Other mutations in Brinp1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00818:Brinp1
|
APN |
4 |
68,681,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01024:Brinp1
|
APN |
4 |
68,680,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02115:Brinp1
|
APN |
4 |
68,680,635 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02332:Brinp1
|
APN |
4 |
68,823,121 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03115:Brinp1
|
APN |
4 |
68,822,973 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02796:Brinp1
|
UTSW |
4 |
68,680,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0382:Brinp1
|
UTSW |
4 |
68,680,545 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0468:Brinp1
|
UTSW |
4 |
68,681,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1141:Brinp1
|
UTSW |
4 |
68,711,215 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1164:Brinp1
|
UTSW |
4 |
68,716,928 (GRCm39) |
missense |
probably benign |
|
|
R1178:Brinp1
|
UTSW |
4 |
68,680,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1545:Brinp1
|
UTSW |
4 |
68,681,192 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R1672:Brinp1
|
UTSW |
4 |
68,747,520 (GRCm39) |
splice site |
probably null |
|
|
R1998:Brinp1
|
UTSW |
4 |
68,680,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2218:Brinp1
|
UTSW |
4 |
68,680,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2262:Brinp1
|
UTSW |
4 |
68,747,591 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2370:Brinp1
|
UTSW |
4 |
68,681,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4542:Brinp1
|
UTSW |
4 |
68,680,329 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4617:Brinp1
|
UTSW |
4 |
68,681,198 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4864:Brinp1
|
UTSW |
4 |
68,717,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5287:Brinp1
|
UTSW |
4 |
68,711,201 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5403:Brinp1
|
UTSW |
4 |
68,711,201 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5932:Brinp1
|
UTSW |
4 |
68,711,178 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7106:Brinp1
|
UTSW |
4 |
68,747,615 (GRCm39) |
missense |
probably benign |
0.36 |
|
R7127:Brinp1
|
UTSW |
4 |
68,711,260 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7398:Brinp1
|
UTSW |
4 |
68,759,591 (GRCm39) |
missense |
probably benign |
|
|
R7917:Brinp1
|
UTSW |
4 |
68,823,190 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
|
R8164:Brinp1
|
UTSW |
4 |
68,681,158 (GRCm39) |
nonsense |
probably null |
|
|
R8369:Brinp1
|
UTSW |
4 |
68,716,936 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8487:Brinp1
|
UTSW |
4 |
68,747,692 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9124:Brinp1
|
UTSW |
4 |
68,747,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9253:Brinp1
|
UTSW |
4 |
68,711,083 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
Z1176:Brinp1
|
UTSW |
4 |
68,716,988 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2014-05-07 |
Incidental Mutation