Incidental Mutation 'R1257:Dnajc9'
ID |
262740 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dnajc9
|
Ensembl Gene |
ENSMUSG00000021811 |
Gene Name |
DnaJ heat shock protein family (Hsp40) member C9 |
Synonyms |
5330419I01Rik |
MMRRC Submission |
039324-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1257 (G1)
|
Quality Score |
172 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
20434706-20438978 bp(-) (GRCm39) |
Type of Mutation |
splice site (607 bp from exon) |
DNA Base Change (assembly) |
G to A
at 20438765 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000055619
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022345]
[ENSMUST00000061444]
|
AlphaFold |
Q91WN1 |
Predicted Effect |
probably null
Transcript: ENSMUST00000022345
|
SMART Domains |
Protein: ENSMUSP00000022345 Gene: ENSMUSG00000021811
Domain | Start | End | E-Value | Type |
DnaJ
|
14 |
74 |
2.76e-16 |
SMART |
coiled coil region
|
176 |
212 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000061444
|
SMART Domains |
Protein: ENSMUSP00000055619 Gene: ENSMUSG00000049960
Domain | Start | End | E-Value | Type |
Pfam:Ribosomal_S16
|
24 |
84 |
9.9e-25 |
PFAM |
low complexity region
|
107 |
135 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223844
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223889
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223950
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000224286
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.2%
- 10x: 95.9%
- 20x: 91.7%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acoxl |
A |
T |
2: 127,886,286 (GRCm39) |
T174S |
probably benign |
Het |
Ank3 |
C |
T |
10: 69,710,665 (GRCm39) |
R408* |
probably null |
Het |
Ceacam15 |
A |
G |
7: 16,405,949 (GRCm39) |
S201P |
possibly damaging |
Het |
Ceacam20 |
A |
G |
7: 19,708,117 (GRCm39) |
I241V |
probably benign |
Het |
Cfap46 |
A |
T |
7: 139,234,545 (GRCm39) |
L237* |
probably null |
Het |
Col4a3 |
T |
A |
1: 82,694,086 (GRCm39) |
C133S |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,343,360 (GRCm39) |
V1568D |
probably damaging |
Het |
Gli3 |
C |
T |
13: 15,900,581 (GRCm39) |
Q1323* |
probably null |
Het |
Grhpr |
A |
G |
4: 44,989,045 (GRCm39) |
N287S |
probably damaging |
Het |
H2bl1 |
A |
T |
13: 99,121,023 (GRCm39) |
M1K |
probably null |
Het |
Hectd4 |
G |
A |
5: 121,456,687 (GRCm39) |
W684* |
probably null |
Het |
Kifc3 |
A |
G |
8: 95,832,400 (GRCm39) |
V474A |
probably damaging |
Het |
Lrrc37 |
A |
G |
11: 103,425,467 (GRCm39) |
V1462A |
unknown |
Het |
Mdn1 |
A |
T |
4: 32,667,089 (GRCm39) |
|
probably null |
Het |
Med7 |
C |
G |
11: 46,331,460 (GRCm39) |
I18M |
probably damaging |
Het |
Nid1 |
T |
C |
13: 13,658,375 (GRCm39) |
Y707H |
probably benign |
Het |
Nol4 |
A |
T |
18: 22,903,738 (GRCm39) |
N339K |
probably damaging |
Het |
Or6c209 |
A |
T |
10: 129,483,413 (GRCm39) |
K139* |
probably null |
Het |
Rbm34 |
C |
T |
8: 127,697,643 (GRCm39) |
G23S |
possibly damaging |
Het |
Rps19bp1 |
CCTTCTTCTTCTTCTTCTTCTT |
CCTTCTTCTTCTTCTTCTT |
15: 80,145,250 (GRCm39) |
|
probably benign |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Snap25 |
A |
T |
2: 136,600,268 (GRCm39) |
E37V |
probably damaging |
Het |
Taf1a |
A |
G |
1: 183,179,175 (GRCm39) |
T118A |
possibly damaging |
Het |
Tasor2 |
T |
C |
13: 3,625,049 (GRCm39) |
T1634A |
probably benign |
Het |
Thrb |
T |
A |
14: 18,008,642 (GRCm38) |
I122K |
probably damaging |
Het |
Xkr4 |
T |
G |
1: 3,287,036 (GRCm39) |
I385L |
probably benign |
Het |
Zeb1 |
G |
T |
18: 5,772,699 (GRCm39) |
R996L |
possibly damaging |
Het |
|
Other mutations in Dnajc9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00923:Dnajc9
|
APN |
14 |
20,435,515 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01631:Dnajc9
|
APN |
14 |
20,438,176 (GRCm39) |
missense |
probably benign |
0.02 |
R1258:Dnajc9
|
UTSW |
14 |
20,438,765 (GRCm39) |
splice site |
probably null |
|
R1261:Dnajc9
|
UTSW |
14 |
20,438,765 (GRCm39) |
splice site |
probably null |
|
R1765:Dnajc9
|
UTSW |
14 |
20,438,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1835:Dnajc9
|
UTSW |
14 |
20,438,402 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7218:Dnajc9
|
UTSW |
14 |
20,438,507 (GRCm39) |
missense |
probably benign |
0.02 |
R7570:Dnajc9
|
UTSW |
14 |
20,438,712 (GRCm39) |
missense |
probably benign |
0.01 |
R7600:Dnajc9
|
UTSW |
14 |
20,438,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Dnajc9
|
UTSW |
14 |
20,438,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9631:Dnajc9
|
UTSW |
14 |
20,438,670 (GRCm39) |
critical splice donor site |
probably null |
|
R9722:Dnajc9
|
UTSW |
14 |
20,438,279 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
|
Posted On |
2015-02-04 |