Incidental Mutation 'IGL01446:Baiap2l1'
| ID |
84438 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Baiap2l1
|
| Ensembl Gene |
ENSMUSG00000038859 |
| Gene Name |
BAI1-associated protein 2-like 1 |
| Synonyms |
1300006M19Rik, IRTKS |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01446
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
144201336-144294922 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 144212723 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 431
(V431I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000053129
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055190]
[ENSMUST00000155491]
|
| AlphaFold |
Q9DBJ3 |
| PDB Structure |
Solution Structure of RSGI RUH-010, an SH3 Domain from Mouse cDNA [SOLUTION NMR]
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000055190
AA Change: V431I
PolyPhen 2
Score 0.096 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000053129
Gene: ENSMUSG00000038859
AA Change: V431I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:IMD
|
16 |
236 |
4.4e-65 |
PFAM |
|
SH3
|
343 |
402 |
1.42e-12 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000155491
|
| SMART Domains |
Protein: ENSMUSP00000122016
Gene: ENSMUSG00000047843
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2367
|
27 |
90 |
1.1e-24 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156467
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198873
|
| 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 encodes a member of the IMD (IRSp53/MIM homology domain) family. Members of this family can be subdivided in two groups, the IRSp53-like and MIM-like, based on the presence or absence of the SH3 (Src homology 3) domain. The protein encoded by this gene contains a conserved IMD, also known as F-actin bundling domain, at the N-terminus, and a canonical SH3 domain near the C-terminus, so it belongs to the IRSp53-like group. This protein is the substrate for insulin receptor tyrosine kinase and binds to the small GTPase Rac. It is involved in signal transduction pathways that link deformation of the plasma membrane and remodeling of the actin cytoskeleton. It also promotes actin assembly and membrane protrusions when overexpressed in mammalian cells, and is essential to the formation of a potent actin assembly complex during EHEC (Enterohemorrhagic Escherichia coli) pedestal formation. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased circulating glucose and insulin levels, impaired glucose tolerance and insulin resistance. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 41 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
A |
G |
11: 9,353,834 (GRCm39) |
T3719A |
probably damaging |
Het |
| Acaca |
A |
G |
11: 84,151,457 (GRCm39) |
K785R |
probably damaging |
Het |
| Acsm3 |
G |
A |
7: 119,377,677 (GRCm39) |
V401M |
probably damaging |
Het |
| Aff4 |
G |
T |
11: 53,306,296 (GRCm39) |
R1146L |
probably damaging |
Het |
| Alms1 |
C |
A |
6: 85,673,683 (GRCm39) |
P3562T |
probably damaging |
Het |
| Arsj |
A |
G |
3: 126,232,463 (GRCm39) |
E403G |
probably benign |
Het |
| Cecr2 |
T |
A |
6: 120,735,560 (GRCm39) |
M904K |
probably benign |
Het |
| Cenpe |
A |
T |
3: 134,943,300 (GRCm39) |
T775S |
probably benign |
Het |
| Dennd1b |
G |
A |
1: 138,950,848 (GRCm39) |
E30K |
possibly damaging |
Het |
| Dnah5 |
A |
G |
15: 28,326,815 (GRCm39) |
D2008G |
probably damaging |
Het |
| Dnm2 |
T |
C |
9: 21,392,672 (GRCm39) |
V460A |
probably damaging |
Het |
| Ell2 |
G |
T |
13: 75,910,110 (GRCm39) |
L285F |
probably benign |
Het |
| Erg |
A |
G |
16: 95,162,141 (GRCm39) |
S322P |
probably damaging |
Het |
| Extl3 |
A |
G |
14: 65,314,529 (GRCm39) |
F218L |
probably benign |
Het |
| Fzd9 |
T |
C |
5: 135,279,420 (GRCm39) |
E155G |
probably damaging |
Het |
| Ghr |
A |
G |
15: 3,362,837 (GRCm39) |
W212R |
probably damaging |
Het |
| Gulp1 |
A |
G |
1: 44,783,708 (GRCm39) |
|
probably benign |
Het |
| Hdgfl2 |
C |
T |
17: 56,404,281 (GRCm39) |
R332C |
possibly damaging |
Het |
| Lratd1 |
A |
T |
12: 14,199,929 (GRCm39) |
I266N |
probably damaging |
Het |
| Nsd2 |
T |
C |
5: 34,018,530 (GRCm39) |
|
probably benign |
Het |
| Or4c12 |
A |
G |
2: 89,774,282 (GRCm39) |
F59S |
probably damaging |
Het |
| Or5a3 |
T |
C |
19: 12,400,165 (GRCm39) |
I164T |
possibly damaging |
Het |
| Or5b121 |
C |
T |
19: 13,507,616 (GRCm39) |
T237I |
probably benign |
Het |
| Phf11b |
A |
C |
14: 59,578,740 (GRCm39) |
S9A |
probably benign |
Het |
| Psd4 |
T |
C |
2: 24,295,407 (GRCm39) |
S854P |
probably damaging |
Het |
| Reln |
C |
T |
5: 22,174,315 (GRCm39) |
D1963N |
probably damaging |
Het |
| Rpe65 |
T |
A |
3: 159,306,042 (GRCm39) |
|
probably benign |
Het |
| Sdccag8 |
T |
C |
1: 176,672,811 (GRCm39) |
S235P |
probably damaging |
Het |
| Sgip1 |
G |
T |
4: 102,786,110 (GRCm39) |
|
probably null |
Het |
| Skint5 |
G |
A |
4: 113,800,019 (GRCm39) |
P36L |
probably damaging |
Het |
| Slc26a3 |
G |
T |
12: 31,502,490 (GRCm39) |
|
probably benign |
Het |
| Snx13 |
T |
A |
12: 35,174,479 (GRCm39) |
C669* |
probably null |
Het |
| Svil |
A |
T |
18: 5,062,385 (GRCm39) |
T902S |
probably damaging |
Het |
| Syne2 |
T |
C |
12: 76,088,149 (GRCm39) |
S4989P |
probably damaging |
Het |
| Ttn |
G |
A |
2: 76,640,283 (GRCm39) |
T13775M |
probably damaging |
Het |
| Ubr4 |
T |
C |
4: 139,165,351 (GRCm39) |
|
probably benign |
Het |
| Ush1c |
C |
T |
7: 45,858,380 (GRCm39) |
R636H |
possibly damaging |
Het |
| Usp17lc |
A |
T |
7: 103,067,651 (GRCm39) |
R315S |
probably benign |
Het |
| Vmn1r236 |
T |
A |
17: 21,506,918 (GRCm39) |
V12D |
probably benign |
Het |
| Wsb2 |
T |
G |
5: 117,509,229 (GRCm39) |
I170S |
probably damaging |
Het |
| Zfp800 |
G |
A |
6: 28,242,983 (GRCm39) |
L661F |
possibly damaging |
Het |
|
| Other mutations in Baiap2l1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00789:Baiap2l1
|
APN |
5 |
144,222,879 (GRCm39) |
splice site |
probably null |
|
|
IGL00789:Baiap2l1
|
APN |
5 |
144,222,356 (GRCm39) |
nonsense |
probably null |
|
|
IGL00922:Baiap2l1
|
APN |
5 |
144,255,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01603:Baiap2l1
|
APN |
5 |
144,217,625 (GRCm39) |
intron |
probably benign |
|
|
IGL02748:Baiap2l1
|
APN |
5 |
144,203,415 (GRCm39) |
intron |
probably benign |
|
|
IGL03348:Baiap2l1
|
APN |
5 |
144,215,341 (GRCm39) |
missense |
probably benign |
0.08 |
|
PIT4382001:Baiap2l1
|
UTSW |
5 |
144,215,480 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R0066:Baiap2l1
|
UTSW |
5 |
144,221,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0066:Baiap2l1
|
UTSW |
5 |
144,221,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0110:Baiap2l1
|
UTSW |
5 |
144,212,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0197:Baiap2l1
|
UTSW |
5 |
144,202,820 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0469:Baiap2l1
|
UTSW |
5 |
144,212,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0744:Baiap2l1
|
UTSW |
5 |
144,203,451 (GRCm39) |
missense |
probably benign |
0.21 |
|
R0755:Baiap2l1
|
UTSW |
5 |
144,221,367 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0765:Baiap2l1
|
UTSW |
5 |
144,214,513 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1051:Baiap2l1
|
UTSW |
5 |
144,222,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1809:Baiap2l1
|
UTSW |
5 |
144,261,365 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3889:Baiap2l1
|
UTSW |
5 |
144,215,345 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4451:Baiap2l1
|
UTSW |
5 |
144,215,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5093:Baiap2l1
|
UTSW |
5 |
144,215,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5471:Baiap2l1
|
UTSW |
5 |
144,218,951 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5523:Baiap2l1
|
UTSW |
5 |
144,212,768 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5524:Baiap2l1
|
UTSW |
5 |
144,217,759 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5586:Baiap2l1
|
UTSW |
5 |
144,218,949 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5603:Baiap2l1
|
UTSW |
5 |
144,202,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5735:Baiap2l1
|
UTSW |
5 |
144,223,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6353:Baiap2l1
|
UTSW |
5 |
144,218,898 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6572:Baiap2l1
|
UTSW |
5 |
144,223,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6619:Baiap2l1
|
UTSW |
5 |
144,222,916 (GRCm39) |
missense |
probably benign |
0.22 |
|
R6981:Baiap2l1
|
UTSW |
5 |
144,222,389 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7218:Baiap2l1
|
UTSW |
5 |
144,212,687 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7352:Baiap2l1
|
UTSW |
5 |
144,261,436 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7662:Baiap2l1
|
UTSW |
5 |
144,294,700 (GRCm39) |
intron |
probably benign |
|
|
R7797:Baiap2l1
|
UTSW |
5 |
144,255,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7981:Baiap2l1
|
UTSW |
5 |
144,294,700 (GRCm39) |
intron |
probably benign |
|
|
R8170:Baiap2l1
|
UTSW |
5 |
144,214,502 (GRCm39) |
nonsense |
probably null |
|
|
R8308:Baiap2l1
|
UTSW |
5 |
144,214,487 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8333:Baiap2l1
|
UTSW |
5 |
144,217,691 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8673:Baiap2l1
|
UTSW |
5 |
144,212,852 (GRCm39) |
intron |
probably benign |
|
|
R8976:Baiap2l1
|
UTSW |
5 |
144,223,117 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9187:Baiap2l1
|
UTSW |
5 |
144,217,764 (GRCm39) |
missense |
probably benign |
0.01 |
|
X0022:Baiap2l1
|
UTSW |
5 |
144,215,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-11-11 |
Incidental Mutation