Incidental Mutation 'IGL02740:Antxr2'
| ID |
305884 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Antxr2
|
| Ensembl Gene |
ENSMUSG00000029338 |
| Gene Name |
anthrax toxin receptor 2 |
| Synonyms |
2310046B19Rik, CMG-2, cI-35, CMG2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.102)
|
| Stock # |
IGL02740
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
98032547-98178876 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 98178251 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142605
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031281]
[ENSMUST00000199088]
|
| AlphaFold |
Q6DFX2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000031281
|
| SMART Domains |
Protein: ENSMUSP00000031281
Gene: ENSMUSG00000029338
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
33 |
N/A |
INTRINSIC |
|
VWA
|
42 |
214 |
2.86e-18 |
SMART |
|
Pfam:Anth_Ig
|
215 |
317 |
4e-38 |
PFAM |
|
transmembrane domain
|
319 |
341 |
N/A |
INTRINSIC |
|
low complexity region
|
352 |
369 |
N/A |
INTRINSIC |
|
Pfam:Ant_C
|
394 |
485 |
7.4e-46 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195915
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199088
|
| SMART Domains |
Protein: ENSMUSP00000142605
Gene: ENSMUSG00000029338
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
31 |
N/A |
INTRINSIC |
|
VWA
|
42 |
214 |
1.7e-20 |
SMART |
|
transmembrane domain
|
319 |
341 |
N/A |
INTRINSIC |
|
low complexity region
|
352 |
369 |
N/A |
INTRINSIC |
|
Pfam:Ant_C
|
394 |
483 |
1.6e-41 |
PFAM |
|
| 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 receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
PHENOTYPE: Mice homozygous for null mutations display female infertility. Mice homozygous for one allele are highly resistant to Bacillus anthracis or anthrax toxin induced lethality. Young mice homozygous for a second allele display pregnancy-related premature death and failure of parturition. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 61 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Als2 |
C |
T |
1: 59,209,078 (GRCm39) |
E1494K |
probably benign |
Het |
| Arhgap23 |
A |
C |
11: 97,365,843 (GRCm39) |
K998Q |
probably damaging |
Het |
| Bap1 |
A |
G |
14: 30,978,729 (GRCm39) |
N47D |
possibly damaging |
Het |
| Carmil1 |
A |
G |
13: 24,278,501 (GRCm39) |
I156T |
probably damaging |
Het |
| Ccdc141 |
T |
C |
2: 76,884,953 (GRCm39) |
T563A |
probably benign |
Het |
| Cct7 |
T |
C |
6: 85,445,252 (GRCm39) |
F501S |
probably benign |
Het |
| Cd59b |
A |
G |
2: 103,909,242 (GRCm39) |
I8V |
probably benign |
Het |
| Cep135 |
T |
C |
5: 76,786,115 (GRCm39) |
|
probably null |
Het |
| Cep170 |
T |
G |
1: 176,621,166 (GRCm39) |
T4P |
probably damaging |
Het |
| Chaf1a |
G |
T |
17: 56,374,500 (GRCm39) |
G896W |
probably damaging |
Het |
| Cpt1b |
A |
T |
15: 89,308,535 (GRCm39) |
L131Q |
probably damaging |
Het |
| Dcaf13 |
C |
T |
15: 39,008,495 (GRCm39) |
R366* |
probably null |
Het |
| Ddr2 |
A |
T |
1: 169,812,514 (GRCm39) |
N659K |
probably damaging |
Het |
| Dmrt2 |
C |
A |
19: 25,655,837 (GRCm39) |
L479I |
possibly damaging |
Het |
| Dnah10 |
A |
G |
5: 124,903,927 (GRCm39) |
|
probably benign |
Het |
| Dsg3 |
C |
T |
18: 20,660,765 (GRCm39) |
T368M |
possibly damaging |
Het |
| Dspp |
C |
A |
5: 104,325,104 (GRCm39) |
S489* |
probably null |
Het |
| Eed |
A |
C |
7: 89,621,464 (GRCm39) |
V112G |
possibly damaging |
Het |
| Ehmt1 |
T |
A |
2: 24,705,851 (GRCm39) |
|
probably benign |
Het |
| Elavl3 |
T |
C |
9: 21,947,675 (GRCm39) |
D89G |
probably benign |
Het |
| Ercc5 |
T |
C |
1: 44,206,652 (GRCm39) |
S522P |
probably benign |
Het |
| Esrrg |
T |
C |
1: 187,930,938 (GRCm39) |
L320P |
probably benign |
Het |
| Gadl1 |
T |
A |
9: 115,835,629 (GRCm39) |
Y352* |
probably null |
Het |
| Gemin5 |
G |
A |
11: 58,042,390 (GRCm39) |
A477V |
probably damaging |
Het |
| Gm3086 |
A |
T |
12: 70,016,095 (GRCm39) |
|
probably benign |
Het |
| Gm8082 |
C |
T |
14: 42,846,570 (GRCm39) |
|
probably benign |
Het |
| Gpr180 |
T |
C |
14: 118,377,161 (GRCm39) |
L54P |
probably damaging |
Het |
| Gpsm1 |
G |
A |
2: 26,230,585 (GRCm39) |
V512M |
probably benign |
Het |
| Ighv5-4 |
A |
G |
12: 113,561,100 (GRCm39) |
S107P |
probably damaging |
Het |
| Irak4 |
T |
C |
15: 94,464,925 (GRCm39) |
*460Q |
probably null |
Het |
| Nfkbiz |
G |
T |
16: 55,638,317 (GRCm39) |
T381N |
probably benign |
Het |
| Or1e25 |
A |
T |
11: 73,493,657 (GRCm39) |
N84Y |
probably benign |
Het |
| Or5d39 |
T |
A |
2: 87,979,601 (GRCm39) |
H254L |
probably damaging |
Het |
| Or8b46 |
T |
C |
9: 38,450,226 (GRCm39) |
F12L |
probably damaging |
Het |
| Or8g23 |
T |
C |
9: 38,971,585 (GRCm39) |
I126V |
probably benign |
Het |
| Pou2f1 |
G |
A |
1: 165,710,685 (GRCm39) |
Q523* |
probably null |
Het |
| Ptcra |
A |
G |
17: 47,069,473 (GRCm39) |
S133P |
probably damaging |
Het |
| Ptgfrn |
A |
T |
3: 100,980,253 (GRCm39) |
D362E |
possibly damaging |
Het |
| Rbm33 |
A |
T |
5: 28,536,121 (GRCm39) |
D19V |
probably damaging |
Het |
| Rnf4 |
T |
A |
5: 34,506,898 (GRCm39) |
V74D |
possibly damaging |
Het |
| Rprd1b |
A |
G |
2: 157,889,899 (GRCm39) |
D7G |
probably damaging |
Het |
| Rrp1b |
A |
G |
17: 32,278,305 (GRCm39) |
T659A |
probably damaging |
Het |
| Scaf11 |
T |
C |
15: 96,316,883 (GRCm39) |
N894D |
probably benign |
Het |
| Scn1a |
G |
A |
2: 66,155,106 (GRCm39) |
R618C |
probably damaging |
Het |
| Scn1a |
A |
T |
2: 66,148,421 (GRCm39) |
D1041E |
probably benign |
Het |
| Slc43a1 |
G |
T |
2: 84,690,094 (GRCm39) |
A424S |
probably damaging |
Het |
| Sprtn |
T |
C |
8: 125,625,042 (GRCm39) |
L49P |
probably damaging |
Het |
| Sv2a |
G |
T |
3: 96,092,723 (GRCm39) |
R141L |
possibly damaging |
Het |
| Thsd7b |
C |
T |
1: 129,540,864 (GRCm39) |
S246F |
probably damaging |
Het |
| Tmem117 |
A |
T |
15: 94,612,863 (GRCm39) |
D133V |
probably benign |
Het |
| Tnn |
A |
T |
1: 159,968,347 (GRCm39) |
|
probably benign |
Het |
| Triobp |
G |
A |
15: 78,850,889 (GRCm39) |
V348I |
probably benign |
Het |
| Trps1 |
A |
T |
15: 50,709,935 (GRCm39) |
D134E |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,598,162 (GRCm39) |
I19584V |
probably benign |
Het |
| Uqcrfs1 |
T |
C |
13: 30,725,006 (GRCm39) |
H178R |
probably damaging |
Het |
| Ush2a |
A |
T |
1: 188,380,585 (GRCm39) |
Q2298L |
possibly damaging |
Het |
| Vmn2r67 |
A |
G |
7: 84,785,818 (GRCm39) |
I729T |
probably damaging |
Het |
| Vmn2r79 |
A |
T |
7: 86,653,366 (GRCm39) |
M544L |
probably benign |
Het |
| Vps41 |
T |
A |
13: 19,022,850 (GRCm39) |
L404Q |
probably damaging |
Het |
| Xrcc5 |
T |
G |
1: 72,379,240 (GRCm39) |
|
probably null |
Het |
| Zfp735 |
A |
G |
11: 73,601,412 (GRCm39) |
K119E |
possibly damaging |
Het |
|
| Other mutations in Antxr2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00566:Antxr2
|
APN |
5 |
98,034,466 (GRCm39) |
splice site |
probably benign |
|
|
IGL00661:Antxr2
|
APN |
5 |
98,152,155 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01105:Antxr2
|
APN |
5 |
98,152,802 (GRCm39) |
splice site |
probably benign |
|
|
IGL01472:Antxr2
|
APN |
5 |
98,175,358 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01719:Antxr2
|
APN |
5 |
98,096,132 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02184:Antxr2
|
APN |
5 |
98,125,454 (GRCm39) |
splice site |
probably null |
|
|
IGL02199:Antxr2
|
APN |
5 |
98,125,454 (GRCm39) |
splice site |
probably null |
|
|
IGL02250:Antxr2
|
APN |
5 |
98,125,454 (GRCm39) |
splice site |
probably null |
|
|
IGL02251:Antxr2
|
APN |
5 |
98,125,454 (GRCm39) |
splice site |
probably null |
|
|
IGL02368:Antxr2
|
APN |
5 |
98,097,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02447:Antxr2
|
APN |
5 |
98,178,267 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL02850:Antxr2
|
APN |
5 |
98,151,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02867:Antxr2
|
APN |
5 |
98,125,509 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02889:Antxr2
|
APN |
5 |
98,125,509 (GRCm39) |
missense |
probably benign |
0.00 |
|
G1Funyon:Antxr2
|
UTSW |
5 |
98,125,538 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0013:Antxr2
|
UTSW |
5 |
98,127,844 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0040:Antxr2
|
UTSW |
5 |
98,086,284 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0040:Antxr2
|
UTSW |
5 |
98,086,284 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0069:Antxr2
|
UTSW |
5 |
98,096,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0184:Antxr2
|
UTSW |
5 |
98,127,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0367:Antxr2
|
UTSW |
5 |
98,177,455 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0638:Antxr2
|
UTSW |
5 |
98,108,496 (GRCm39) |
nonsense |
probably null |
|
|
R0732:Antxr2
|
UTSW |
5 |
98,108,567 (GRCm39) |
splice site |
probably null |
|
|
R1255:Antxr2
|
UTSW |
5 |
98,123,231 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1471:Antxr2
|
UTSW |
5 |
98,123,199 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1520:Antxr2
|
UTSW |
5 |
98,108,551 (GRCm39) |
missense |
probably benign |
0.38 |
|
R1660:Antxr2
|
UTSW |
5 |
98,123,209 (GRCm39) |
nonsense |
probably null |
|
|
R1870:Antxr2
|
UTSW |
5 |
98,178,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2969:Antxr2
|
UTSW |
5 |
98,178,275 (GRCm39) |
nonsense |
probably null |
|
|
R3547:Antxr2
|
UTSW |
5 |
98,125,516 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4237:Antxr2
|
UTSW |
5 |
98,086,266 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4660:Antxr2
|
UTSW |
5 |
98,151,913 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4702:Antxr2
|
UTSW |
5 |
98,097,028 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4893:Antxr2
|
UTSW |
5 |
98,151,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4997:Antxr2
|
UTSW |
5 |
98,125,553 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5388:Antxr2
|
UTSW |
5 |
98,125,458 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5604:Antxr2
|
UTSW |
5 |
98,096,169 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6093:Antxr2
|
UTSW |
5 |
98,178,319 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6118:Antxr2
|
UTSW |
5 |
98,097,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6130:Antxr2
|
UTSW |
5 |
98,152,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6139:Antxr2
|
UTSW |
5 |
98,125,565 (GRCm39) |
splice site |
probably null |
|
|
R6992:Antxr2
|
UTSW |
5 |
98,108,564 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8127:Antxr2
|
UTSW |
5 |
98,127,876 (GRCm39) |
nonsense |
probably null |
|
|
R8267:Antxr2
|
UTSW |
5 |
98,113,621 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R8301:Antxr2
|
UTSW |
5 |
98,125,538 (GRCm39) |
missense |
probably benign |
0.20 |
|
R8324:Antxr2
|
UTSW |
5 |
98,086,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8840:Antxr2
|
UTSW |
5 |
98,152,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9125:Antxr2
|
UTSW |
5 |
98,151,973 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9340:Antxr2
|
UTSW |
5 |
98,086,306 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9722:Antxr2
|
UTSW |
5 |
98,096,186 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
| Posted On |
2015-04-16 |
Incidental Mutation