Incidental Mutation 'IGL02155:Dnajc22'
ID |
282185 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Dnajc22
|
Ensembl Gene |
ENSMUSG00000038009 |
Gene Name |
DnaJ heat shock protein family (Hsp40) member C22 |
Synonyms |
2810451A06Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.071)
|
Stock # |
IGL02155
|
Quality Score |
|
Status
|
|
Chromosome |
15 |
Chromosomal Location |
98991102-99002618 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 98998886 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Histidine
at position 24
(Y24H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000055482
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061295]
|
AlphaFold |
Q8CHS2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000061295
AA Change: Y24H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000055482 Gene: ENSMUSG00000038009 AA Change: Y24H
Domain | Start | End | E-Value | Type |
Pfam:TM2
|
1 |
50 |
1e-10 |
PFAM |
transmembrane domain
|
76 |
98 |
N/A |
INTRINSIC |
transmembrane domain
|
105 |
124 |
N/A |
INTRINSIC |
transmembrane domain
|
139 |
161 |
N/A |
INTRINSIC |
transmembrane domain
|
206 |
228 |
N/A |
INTRINSIC |
DnaJ
|
276 |
335 |
1.09e-19 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146173
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
A |
G |
5: 125,583,350 (GRCm39) |
H302R |
probably null |
Het |
Abi3bp |
A |
T |
16: 56,408,327 (GRCm39) |
H254L |
probably damaging |
Het |
Adcy3 |
G |
A |
12: 4,262,142 (GRCm39) |
W1064* |
probably null |
Het |
Arvcf |
C |
T |
16: 18,222,650 (GRCm39) |
P70S |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,896,906 (GRCm39) |
D624G |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,050,250 (GRCm39) |
|
probably benign |
Het |
Cyp2a5 |
T |
A |
7: 26,542,471 (GRCm39) |
F491Y |
probably benign |
Het |
Disp2 |
C |
T |
2: 118,622,285 (GRCm39) |
R1006C |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,153,245 (GRCm39) |
F3656L |
probably benign |
Het |
Fbxo31 |
A |
G |
8: 122,285,814 (GRCm39) |
F212S |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,828,696 (GRCm39) |
M6831T |
probably benign |
Het |
Gpi1 |
G |
T |
7: 33,929,614 (GRCm39) |
Q9K |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,439,349 (GRCm39) |
S5495C |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,567,488 (GRCm39) |
I394V |
probably benign |
Het |
Kcnh5 |
G |
A |
12: 75,223,312 (GRCm39) |
|
probably benign |
Het |
Lars2 |
A |
G |
9: 123,284,047 (GRCm39) |
D745G |
probably damaging |
Het |
Mitd1 |
T |
A |
1: 37,924,356 (GRCm39) |
I65F |
probably benign |
Het |
Mlxip |
T |
C |
5: 123,591,455 (GRCm39) |
M878T |
probably benign |
Het |
Mrgpra4 |
T |
C |
7: 47,631,292 (GRCm39) |
Y103C |
probably damaging |
Het |
Notch2 |
T |
C |
3: 98,045,806 (GRCm39) |
I1657T |
probably damaging |
Het |
Or5m11 |
T |
A |
2: 85,782,352 (GRCm39) |
M315K |
probably benign |
Het |
Orc1 |
T |
A |
4: 108,447,874 (GRCm39) |
D40E |
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,189,888 (GRCm39) |
|
probably benign |
Het |
Ro60 |
C |
T |
1: 143,637,007 (GRCm39) |
|
probably null |
Het |
Sema4d |
A |
G |
13: 51,857,303 (GRCm39) |
V643A |
probably benign |
Het |
Taf7 |
A |
T |
18: 37,776,564 (GRCm39) |
M1K |
probably null |
Het |
Tnfsf10 |
A |
T |
3: 27,389,380 (GRCm39) |
D147V |
possibly damaging |
Het |
Usp45 |
T |
A |
4: 21,798,743 (GRCm39) |
|
probably null |
Het |
Wdr62 |
T |
C |
7: 29,962,068 (GRCm39) |
D2G |
probably damaging |
Het |
Zp2 |
T |
A |
7: 119,743,340 (GRCm39) |
I50F |
probably benign |
Het |
|
Other mutations in Dnajc22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Dnajc22
|
APN |
15 |
98,999,059 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00922:Dnajc22
|
APN |
15 |
98,999,460 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02726:Dnajc22
|
APN |
15 |
98,998,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Dnajc22
|
APN |
15 |
98,999,403 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R1138:Dnajc22
|
UTSW |
15 |
99,002,308 (GRCm39) |
small deletion |
probably benign |
|
R1628:Dnajc22
|
UTSW |
15 |
98,998,817 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R2018:Dnajc22
|
UTSW |
15 |
98,999,114 (GRCm39) |
missense |
probably benign |
0.06 |
R2146:Dnajc22
|
UTSW |
15 |
99,002,264 (GRCm39) |
missense |
probably benign |
0.04 |
R4342:Dnajc22
|
UTSW |
15 |
99,002,345 (GRCm39) |
nonsense |
probably null |
|
R4950:Dnajc22
|
UTSW |
15 |
98,999,615 (GRCm39) |
missense |
probably benign |
0.29 |
R7123:Dnajc22
|
UTSW |
15 |
98,999,085 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7173:Dnajc22
|
UTSW |
15 |
98,999,187 (GRCm39) |
missense |
probably benign |
0.06 |
R7640:Dnajc22
|
UTSW |
15 |
98,998,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7997:Dnajc22
|
UTSW |
15 |
98,999,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Dnajc22
|
UTSW |
15 |
98,999,022 (GRCm39) |
missense |
probably benign |
0.00 |
R8745:Dnajc22
|
UTSW |
15 |
98,999,345 (GRCm39) |
missense |
probably benign |
0.01 |
V7580:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
V7581:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
V7582:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
V7583:Dnajc22
|
UTSW |
15 |
98,999,363 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2015-04-16 |