Incidental Mutation 'IGL00899:Bpifb9a'
| ID |
26823 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Bpifb9a
|
| Ensembl Gene |
ENSMUSG00000067998 |
| Gene Name |
BPI fold containing family B, member 9A |
| Synonyms |
4833413D08Rik, vomeromodulin |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00899
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
154099799-154113165 bp(+) (GRCm39) |
| Type of Mutation |
splice site (6 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 154106647 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000086314
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088924]
|
| AlphaFold |
Q80XI7 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000088924
|
| SMART Domains |
Protein: ENSMUSP00000086314
Gene: ENSMUSG00000067998
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
60 |
77 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
157 |
N/A |
INTRINSIC |
|
low complexity region
|
167 |
181 |
N/A |
INTRINSIC |
|
low complexity region
|
184 |
203 |
N/A |
INTRINSIC |
|
Pfam:LBP_BPI_CETP
|
216 |
377 |
1.1e-11 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126084
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000147299
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| AU018091 |
A |
G |
7: 3,208,603 (GRCm39) |
I442T |
probably benign |
Het |
| Ccp110 |
T |
A |
7: 118,321,907 (GRCm39) |
C521S |
probably benign |
Het |
| Chd6 |
A |
G |
2: 160,871,218 (GRCm39) |
|
probably benign |
Het |
| Cndp2 |
A |
T |
18: 84,695,501 (GRCm39) |
D133E |
probably damaging |
Het |
| Crygs |
T |
C |
16: 22,625,312 (GRCm39) |
E43G |
possibly damaging |
Het |
| Ednra |
C |
T |
8: 78,401,700 (GRCm39) |
G197R |
probably damaging |
Het |
| Esyt1 |
A |
G |
10: 128,352,932 (GRCm39) |
L656P |
probably damaging |
Het |
| Ets1 |
C |
T |
9: 32,664,104 (GRCm39) |
P118L |
probably damaging |
Het |
| Fam98c |
A |
G |
7: 28,852,278 (GRCm39) |
|
probably benign |
Het |
| Foxi1 |
G |
A |
11: 34,155,772 (GRCm39) |
T286I |
probably benign |
Het |
| Gimap5 |
G |
A |
6: 48,730,107 (GRCm39) |
A226T |
possibly damaging |
Het |
| Heatr1 |
C |
T |
13: 12,450,057 (GRCm39) |
A2017V |
probably benign |
Het |
| Ikbkb |
T |
C |
8: 23,150,463 (GRCm39) |
S740G |
possibly damaging |
Het |
| Inppl1 |
A |
T |
7: 101,478,365 (GRCm39) |
I617N |
probably damaging |
Het |
| Itpkb |
T |
C |
1: 180,160,558 (GRCm39) |
L228P |
probably benign |
Het |
| Kcnc4 |
T |
A |
3: 107,365,779 (GRCm39) |
D143V |
possibly damaging |
Het |
| Krtdap |
T |
A |
7: 30,489,387 (GRCm39) |
|
probably null |
Het |
| Lilra6 |
T |
A |
7: 3,916,056 (GRCm39) |
T268S |
probably damaging |
Het |
| M6pr |
A |
G |
6: 122,292,354 (GRCm39) |
E183G |
possibly damaging |
Het |
| Muc5ac |
T |
A |
7: 141,366,440 (GRCm39) |
V2168D |
possibly damaging |
Het |
| Nbea |
A |
G |
3: 55,550,266 (GRCm39) |
S2721P |
probably benign |
Het |
| Or1j20 |
A |
T |
2: 36,760,222 (GRCm39) |
I215L |
probably benign |
Het |
| Pqbp1 |
T |
C |
X: 7,762,243 (GRCm39) |
N94S |
probably benign |
Het |
| Prl3d2 |
T |
C |
13: 27,306,332 (GRCm39) |
S20P |
probably damaging |
Het |
| Psmb2 |
T |
C |
4: 126,601,350 (GRCm39) |
I151T |
probably benign |
Het |
| Rapgef6 |
G |
T |
11: 54,510,844 (GRCm39) |
E107* |
probably null |
Het |
| Slc2a13 |
T |
C |
15: 91,381,602 (GRCm39) |
T296A |
probably benign |
Het |
| Tcl1b4 |
A |
G |
12: 105,170,916 (GRCm39) |
T55A |
probably damaging |
Het |
| Tg |
T |
C |
15: 66,545,922 (GRCm39) |
|
probably null |
Het |
| Trim80 |
T |
G |
11: 115,338,491 (GRCm39) |
N440K |
probably benign |
Het |
| Ttc13 |
C |
T |
8: 125,415,586 (GRCm39) |
|
probably benign |
Het |
| Ttc38 |
T |
A |
15: 85,728,663 (GRCm39) |
I205N |
possibly damaging |
Het |
| Ufl1 |
T |
C |
4: 25,262,238 (GRCm39) |
D336G |
probably damaging |
Het |
| Vmn2r74 |
A |
T |
7: 85,606,338 (GRCm39) |
I336K |
probably benign |
Het |
| Zbtb26 |
G |
T |
2: 37,326,270 (GRCm39) |
Y255* |
probably null |
Het |
| Zfp462 |
T |
A |
4: 55,007,732 (GRCm39) |
V57E |
probably damaging |
Het |
|
| Other mutations in Bpifb9a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00833:Bpifb9a
|
APN |
2 |
154,106,195 (GRCm39) |
nonsense |
probably null |
|
|
IGL01998:Bpifb9a
|
APN |
2 |
154,110,120 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02158:Bpifb9a
|
APN |
2 |
154,108,733 (GRCm39) |
splice site |
probably benign |
|
|
IGL02331:Bpifb9a
|
APN |
2 |
154,104,307 (GRCm39) |
missense |
possibly damaging |
0.45 |
|
R0066:Bpifb9a
|
UTSW |
2 |
154,108,761 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0480:Bpifb9a
|
UTSW |
2 |
154,106,608 (GRCm39) |
missense |
probably benign |
0.33 |
|
R0545:Bpifb9a
|
UTSW |
2 |
154,103,870 (GRCm39) |
nonsense |
probably null |
|
|
R0904:Bpifb9a
|
UTSW |
2 |
154,106,145 (GRCm39) |
splice site |
probably benign |
|
|
R1028:Bpifb9a
|
UTSW |
2 |
154,104,327 (GRCm39) |
missense |
possibly damaging |
0.45 |
|
R1158:Bpifb9a
|
UTSW |
2 |
154,104,184 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1465:Bpifb9a
|
UTSW |
2 |
154,112,941 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1465:Bpifb9a
|
UTSW |
2 |
154,112,941 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1902:Bpifb9a
|
UTSW |
2 |
154,103,911 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2015:Bpifb9a
|
UTSW |
2 |
154,110,120 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2152:Bpifb9a
|
UTSW |
2 |
154,102,055 (GRCm39) |
missense |
probably benign |
0.28 |
|
R2206:Bpifb9a
|
UTSW |
2 |
154,106,161 (GRCm39) |
splice site |
probably null |
|
|
R5410:Bpifb9a
|
UTSW |
2 |
154,112,155 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5731:Bpifb9a
|
UTSW |
2 |
154,104,163 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5818:Bpifb9a
|
UTSW |
2 |
154,104,215 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5865:Bpifb9a
|
UTSW |
2 |
154,108,756 (GRCm39) |
missense |
probably benign |
0.26 |
|
R6564:Bpifb9a
|
UTSW |
2 |
154,102,098 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7291:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7294:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7295:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7453:Bpifb9a
|
UTSW |
2 |
154,106,615 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7570:Bpifb9a
|
UTSW |
2 |
154,104,183 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8187:Bpifb9a
|
UTSW |
2 |
154,111,377 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8245:Bpifb9a
|
UTSW |
2 |
154,104,646 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8459:Bpifb9a
|
UTSW |
2 |
154,102,153 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8481:Bpifb9a
|
UTSW |
2 |
154,111,399 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-04-17 |
Incidental Mutation