Incidental Mutation 'IGL01638:Fcmr'
| ID |
93144 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Fcmr
|
| Ensembl Gene |
ENSMUSG00000042474 |
| Gene Name |
Fc fragment of IgM receptor |
| Synonyms |
1810037B05Rik, FcmuR, Faim3 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01638
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
130793514-130808528 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 130802859 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Aspartic acid
at position 157
(E157D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000048303
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038829]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000038829
AA Change: E157D
PolyPhen 2
Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000048303
Gene: ENSMUSG00000042474
AA Change: E157D
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
|
Pfam:V-set
|
21 |
122 |
1.3e-10 |
PFAM |
|
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
|
transmembrane domain
|
264 |
283 |
N/A |
INTRINSIC |
|
low complexity region
|
285 |
311 |
N/A |
INTRINSIC |
|
low complexity region
|
344 |
363 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126821
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145446
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149355
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Fc receptors specifically bind to the Fc region of immunoglobulins (Igs) to mediate the unique functions of each Ig class. FAIM3 encodes an Fc receptor for IgM (see MIM 147020) (Kubagawa et al., 2009 [PubMed 19858324]; Shima et al., 2010 [PubMed 20042454]).[supplied by OMIM, Jul 2010]
PHENOTYPE: Mice homozygous for knock-out alleles exhibit a slight decrease in B cell numbers reduced sensitivity to Gal-induced liver damage, increased granulocyte production of ROS and increased sensitivity to infection by Listeria monocytogenes. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts9 |
T |
C |
6: 92,849,409 (GRCm39) |
T436A |
probably benign |
Het |
| Adgrb3 |
T |
A |
1: 25,598,832 (GRCm39) |
|
probably benign |
Het |
| Ajap1 |
A |
G |
4: 153,516,693 (GRCm39) |
V216A |
possibly damaging |
Het |
| Akap7 |
T |
A |
10: 25,143,323 (GRCm39) |
I124F |
probably damaging |
Het |
| Arfgef2 |
G |
A |
2: 166,715,865 (GRCm39) |
V1385M |
probably damaging |
Het |
| Arhgap30 |
A |
G |
1: 171,225,138 (GRCm39) |
K65E |
probably damaging |
Het |
| Bltp1 |
A |
G |
3: 37,028,460 (GRCm39) |
N2377D |
probably damaging |
Het |
| Cacna1a |
T |
C |
8: 85,298,456 (GRCm39) |
F1260S |
probably damaging |
Het |
| Cad |
T |
A |
5: 31,224,958 (GRCm39) |
C954S |
probably damaging |
Het |
| Gm4204 |
A |
T |
1: 135,160,873 (GRCm39) |
|
noncoding transcript |
Het |
| Gzmn |
A |
T |
14: 56,406,476 (GRCm39) |
D16E |
probably benign |
Het |
| Krt86 |
A |
C |
15: 101,373,353 (GRCm39) |
|
probably benign |
Het |
| Macc1 |
T |
C |
12: 119,410,246 (GRCm39) |
L338P |
probably benign |
Het |
| Ms4a6d |
A |
T |
19: 11,564,532 (GRCm39) |
L113Q |
probably damaging |
Het |
| Myh15 |
T |
C |
16: 48,889,843 (GRCm39) |
S145P |
probably damaging |
Het |
| Nav3 |
T |
C |
10: 109,688,724 (GRCm39) |
K518E |
probably damaging |
Het |
| Or8d6 |
T |
C |
9: 39,853,816 (GRCm39) |
S87P |
probably benign |
Het |
| Parp11 |
T |
A |
6: 127,468,492 (GRCm39) |
F181I |
probably benign |
Het |
| Ppil1 |
C |
A |
17: 29,480,766 (GRCm39) |
K52N |
probably benign |
Het |
| Prl5a1 |
T |
A |
13: 28,329,422 (GRCm39) |
C34S |
possibly damaging |
Het |
| Prss55 |
A |
G |
14: 64,314,636 (GRCm39) |
V178A |
probably benign |
Het |
| S100a7a |
A |
G |
3: 90,562,837 (GRCm39) |
D8G |
probably benign |
Het |
| Sh3glb2 |
A |
G |
2: 30,235,862 (GRCm39) |
V310A |
possibly damaging |
Het |
| Slc22a7 |
T |
C |
17: 46,748,920 (GRCm39) |
|
probably null |
Het |
| Slc27a6 |
A |
G |
18: 58,740,885 (GRCm39) |
D482G |
probably damaging |
Het |
| Smarcc2 |
T |
A |
10: 128,323,943 (GRCm39) |
|
probably benign |
Het |
| Specc1l |
T |
A |
10: 75,082,039 (GRCm39) |
Y478* |
probably null |
Het |
| Spryd3 |
A |
G |
15: 102,038,711 (GRCm39) |
|
probably null |
Het |
| Tcerg1l |
G |
A |
7: 137,881,805 (GRCm39) |
R295C |
probably damaging |
Het |
| Trpv1 |
T |
C |
11: 73,144,155 (GRCm39) |
I637T |
probably damaging |
Het |
| Ttc7 |
A |
C |
17: 87,666,540 (GRCm39) |
|
probably null |
Het |
| Vmn1r6 |
C |
T |
6: 56,980,177 (GRCm39) |
Q280* |
probably null |
Het |
|
| Other mutations in Fcmr |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01652:Fcmr
|
APN |
1 |
130,806,244 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02106:Fcmr
|
APN |
1 |
130,802,872 (GRCm39) |
missense |
probably benign |
|
|
IGL03270:Fcmr
|
APN |
1 |
130,803,779 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R1635:Fcmr
|
UTSW |
1 |
130,803,922 (GRCm39) |
splice site |
probably null |
|
|
R1651:Fcmr
|
UTSW |
1 |
130,805,988 (GRCm39) |
missense |
probably benign |
|
|
R1728:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1728:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1729:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1729:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1730:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1730:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1739:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1739:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1762:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1762:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1783:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1783:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1784:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1784:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R1785:Fcmr
|
UTSW |
1 |
130,806,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1785:Fcmr
|
UTSW |
1 |
130,803,711 (GRCm39) |
missense |
probably benign |
|
|
R2037:Fcmr
|
UTSW |
1 |
130,806,070 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R6111:Fcmr
|
UTSW |
1 |
130,805,566 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6217:Fcmr
|
UTSW |
1 |
130,806,060 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6538:Fcmr
|
UTSW |
1 |
130,802,762 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6712:Fcmr
|
UTSW |
1 |
130,805,588 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6965:Fcmr
|
UTSW |
1 |
130,803,724 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R7765:Fcmr
|
UTSW |
1 |
130,802,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8770:Fcmr
|
UTSW |
1 |
130,803,799 (GRCm39) |
missense |
probably benign |
|
|
R9343:Fcmr
|
UTSW |
1 |
130,802,072 (GRCm39) |
missense |
|
|
|
R9468:Fcmr
|
UTSW |
1 |
130,801,951 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
X0025:Fcmr
|
UTSW |
1 |
130,802,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-09 |
Incidental Mutation