Incidental Mutation 'IGL02277:Fcrl6'
ID |
287381 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Fcrl6
|
Ensembl Gene |
ENSMUSG00000070504 |
Gene Name |
Fc receptor-like 6 |
Synonyms |
FcRH6, moFcRH6, mIFGP6, ENSMUSG00000070504 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL02277
|
Quality Score |
|
Status
|
|
Chromosome |
1 |
Chromosomal Location |
172424209-172430118 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 172426686 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Arginine
at position 87
(C87R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000091861
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094303]
|
AlphaFold |
A1YIY0 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000094303
AA Change: C87R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000091861 Gene: ENSMUSG00000070504 AA Change: C87R
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
Pfam:Ig_3
|
19 |
91 |
1.2e-4 |
PFAM |
Pfam:Ig_2
|
20 |
106 |
8e-9 |
PFAM |
Pfam:Ig_3
|
113 |
187 |
1.9e-9 |
PFAM |
transmembrane domain
|
215 |
237 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193431
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193566
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
C |
T |
9: 57,165,708 (GRCm39) |
G222D |
probably benign |
Het |
Abcc6 |
T |
C |
7: 45,650,485 (GRCm39) |
D625G |
probably benign |
Het |
Akr1c12 |
C |
T |
13: 4,322,268 (GRCm39) |
R258Q |
probably damaging |
Het |
Akr1c20 |
T |
A |
13: 4,564,404 (GRCm39) |
E36D |
probably benign |
Het |
Csn2 |
A |
G |
5: 87,845,881 (GRCm39) |
|
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,497,176 (GRCm39) |
I1084V |
possibly damaging |
Het |
Dlg1 |
A |
G |
16: 31,609,082 (GRCm39) |
I259V |
probably damaging |
Het |
Dpysl5 |
A |
G |
5: 30,946,125 (GRCm39) |
I344V |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,735,977 (GRCm39) |
E524G |
probably benign |
Het |
Gabpb2 |
A |
G |
3: 95,096,595 (GRCm39) |
V270A |
probably benign |
Het |
Gm5591 |
T |
A |
7: 38,218,462 (GRCm39) |
I804F |
possibly damaging |
Het |
Gm5591 |
T |
C |
7: 38,219,856 (GRCm39) |
D339G |
probably damaging |
Het |
Ighv2-5 |
T |
A |
12: 113,649,127 (GRCm39) |
T109S |
possibly damaging |
Het |
Ints4 |
T |
A |
7: 97,136,665 (GRCm39) |
L119Q |
probably damaging |
Het |
Kansl3 |
A |
T |
1: 36,388,028 (GRCm39) |
D386E |
possibly damaging |
Het |
Kdm3b |
A |
T |
18: 34,956,717 (GRCm39) |
H1224L |
probably damaging |
Het |
Macf1 |
C |
A |
4: 123,380,497 (GRCm39) |
R1523L |
probably damaging |
Het |
Myo1f |
A |
G |
17: 33,798,835 (GRCm39) |
|
probably null |
Het |
Nup188 |
A |
G |
2: 30,216,523 (GRCm39) |
T776A |
possibly damaging |
Het |
Or1q1 |
G |
A |
2: 36,887,196 (GRCm39) |
|
probably null |
Het |
Or2y8 |
T |
A |
11: 52,036,189 (GRCm39) |
H56L |
probably damaging |
Het |
Or4f56 |
T |
A |
2: 111,703,925 (GRCm39) |
I92F |
possibly damaging |
Het |
Plxnb1 |
T |
A |
9: 108,941,201 (GRCm39) |
L1660Q |
probably damaging |
Het |
Ppp1r17 |
A |
G |
6: 56,003,123 (GRCm39) |
D71G |
probably damaging |
Het |
Ptprt |
T |
C |
2: 161,389,301 (GRCm39) |
Q1264R |
probably damaging |
Het |
Rgl3 |
C |
T |
9: 21,885,405 (GRCm39) |
V642M |
probably damaging |
Het |
Slc26a2 |
T |
C |
18: 61,332,052 (GRCm39) |
T460A |
probably damaging |
Het |
Smtnl2 |
T |
A |
11: 72,282,199 (GRCm39) |
M395L |
probably damaging |
Het |
St3gal5 |
A |
T |
6: 72,119,184 (GRCm39) |
T99S |
possibly damaging |
Het |
Unc5b |
T |
C |
10: 60,610,521 (GRCm39) |
N421S |
probably benign |
Het |
Zcchc17 |
G |
A |
4: 130,221,014 (GRCm39) |
T179M |
probably benign |
Het |
Zfp369 |
T |
C |
13: 65,432,746 (GRCm39) |
S79P |
probably damaging |
Het |
|
Other mutations in Fcrl6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00903:Fcrl6
|
APN |
1 |
172,426,674 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01074:Fcrl6
|
APN |
1 |
172,426,680 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02146:Fcrl6
|
APN |
1 |
172,426,264 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03162:Fcrl6
|
APN |
1 |
172,425,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Fcrl6
|
APN |
1 |
172,425,255 (GRCm39) |
missense |
probably damaging |
0.99 |
K3955:Fcrl6
|
UTSW |
1 |
172,425,251 (GRCm39) |
missense |
probably benign |
0.00 |
R0051:Fcrl6
|
UTSW |
1 |
172,426,320 (GRCm39) |
missense |
probably benign |
0.24 |
R0051:Fcrl6
|
UTSW |
1 |
172,426,320 (GRCm39) |
missense |
probably benign |
0.24 |
R1336:Fcrl6
|
UTSW |
1 |
172,426,791 (GRCm39) |
nonsense |
probably null |
|
R2125:Fcrl6
|
UTSW |
1 |
172,426,815 (GRCm39) |
missense |
probably benign |
0.41 |
R2126:Fcrl6
|
UTSW |
1 |
172,426,815 (GRCm39) |
missense |
probably benign |
0.41 |
R5376:Fcrl6
|
UTSW |
1 |
172,426,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Fcrl6
|
UTSW |
1 |
172,426,287 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6314:Fcrl6
|
UTSW |
1 |
172,426,186 (GRCm39) |
splice site |
probably null |
|
R7525:Fcrl6
|
UTSW |
1 |
172,425,239 (GRCm39) |
missense |
probably benign |
0.25 |
R7690:Fcrl6
|
UTSW |
1 |
172,426,223 (GRCm39) |
missense |
probably damaging |
0.97 |
R8033:Fcrl6
|
UTSW |
1 |
172,426,748 (GRCm39) |
missense |
probably benign |
0.03 |
R8894:Fcrl6
|
UTSW |
1 |
172,426,856 (GRCm39) |
missense |
probably benign |
0.05 |
U24488:Fcrl6
|
UTSW |
1 |
172,426,437 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2015-04-16 |