Incidental Mutation 'R9658:Dnajc13'
ID |
735549 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dnajc13
|
Ensembl Gene |
ENSMUSG00000032560 |
Gene Name |
DnaJ heat shock protein family (Hsp40) member C13 |
Synonyms |
Rme8, D030002L11Rik, LOC382100 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.940)
|
Stock # |
R9658 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
104028481-104140129 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 104115728 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 27
(V27A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139804
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035170]
[ENSMUST00000186788]
|
AlphaFold |
D4AFX7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000035170
AA Change: V27A
PolyPhen 2
Score 0.213 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000035170 Gene: ENSMUSG00000032560 AA Change: V27A
Domain | Start | End | E-Value | Type |
low complexity region
|
706 |
719 |
N/A |
INTRINSIC |
low complexity region
|
832 |
843 |
N/A |
INTRINSIC |
low complexity region
|
913 |
926 |
N/A |
INTRINSIC |
Blast:ARM
|
927 |
963 |
6e-12 |
BLAST |
Pfam:DUF4339
|
976 |
1020 |
1.5e-18 |
PFAM |
Blast:ARM
|
1071 |
1110 |
5e-12 |
BLAST |
DnaJ
|
1300 |
1358 |
5.69e-18 |
SMART |
low complexity region
|
1417 |
1426 |
N/A |
INTRINSIC |
low complexity region
|
1813 |
1829 |
N/A |
INTRINSIC |
Blast:ARM
|
1843 |
1884 |
6e-8 |
BLAST |
low complexity region
|
1968 |
1984 |
N/A |
INTRINSIC |
low complexity region
|
2006 |
2016 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000186788
AA Change: V27A
PolyPhen 2
Score 0.113 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000139804 Gene: ENSMUSG00000032560 AA Change: V27A
Domain | Start | End | E-Value | Type |
low complexity region
|
706 |
719 |
N/A |
INTRINSIC |
low complexity region
|
837 |
848 |
N/A |
INTRINSIC |
low complexity region
|
918 |
931 |
N/A |
INTRINSIC |
Blast:ARM
|
932 |
968 |
6e-12 |
BLAST |
Pfam:DUF4339
|
980 |
1025 |
8.1e-14 |
PFAM |
Blast:ARM
|
1076 |
1115 |
5e-12 |
BLAST |
DnaJ
|
1305 |
1363 |
5.69e-18 |
SMART |
low complexity region
|
1422 |
1431 |
N/A |
INTRINSIC |
low complexity region
|
1818 |
1834 |
N/A |
INTRINSIC |
Blast:ARM
|
1848 |
1889 |
6e-8 |
BLAST |
low complexity region
|
1973 |
1989 |
N/A |
INTRINSIC |
low complexity region
|
2011 |
2021 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 99.4%
- 20x: 98.7%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Dnaj protein family whose members act as co-chaperones of a partner heat-shock protein by binding to the latter and stimulating ATP hydrolysis. The encoded protein associates with the heat-shock protein Hsc70 and plays a role in clathrin-mediated endocytosis. It may also be involved in post-endocytic transport mechanisms via its associations with other proteins, including the sorting nexin SNX1. Mutations in this gene are associated with Parkinson's disease. [provided by RefSeq, Jun 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
C |
T |
18: 70,600,401 (GRCm39) |
|
probably null |
Het |
Abca12 |
T |
C |
1: 71,325,634 (GRCm39) |
I1521M |
probably damaging |
Het |
Abcc3 |
A |
G |
11: 94,263,703 (GRCm39) |
S268P |
possibly damaging |
Het |
Adamts20 |
G |
C |
15: 94,249,626 (GRCm39) |
P464A |
probably damaging |
Het |
Apoa1 |
C |
A |
9: 46,141,280 (GRCm39) |
D125E |
probably benign |
Het |
Atp6v0a1 |
C |
A |
11: 100,909,414 (GRCm39) |
Q48K |
probably benign |
Het |
Bptf |
T |
C |
11: 107,002,170 (GRCm39) |
N314S |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 109,988,785 (GRCm39) |
V229A |
probably damaging |
Het |
Cfap46 |
G |
A |
7: 139,246,229 (GRCm39) |
T378M |
|
Het |
Clca3b |
T |
A |
3: 144,543,575 (GRCm39) |
D418V |
probably damaging |
Het |
Dennd4c |
T |
A |
4: 86,754,625 (GRCm39) |
L1545* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,611,120 (GRCm39) |
K321E |
probably benign |
Het |
Eif2ak2 |
A |
T |
17: 79,183,632 (GRCm39) |
D72E |
probably benign |
Het |
Eif2ak4 |
T |
C |
2: 118,269,511 (GRCm39) |
I862T |
probably damaging |
Het |
Eif4g1 |
T |
C |
16: 20,502,863 (GRCm39) |
I1022T |
probably benign |
Het |
Enpp3 |
A |
T |
10: 24,649,802 (GRCm39) |
*875R |
probably null |
Het |
F11 |
T |
C |
8: 45,698,671 (GRCm39) |
Y491C |
probably damaging |
Het |
Fam98c |
A |
C |
7: 28,852,206 (GRCm39) |
W118G |
probably damaging |
Het |
Fbxo43 |
A |
T |
15: 36,152,282 (GRCm39) |
L509Q |
probably damaging |
Het |
Fbxw5 |
A |
G |
2: 25,393,870 (GRCm39) |
H366R |
probably damaging |
Het |
Flt1 |
G |
T |
5: 147,525,377 (GRCm39) |
N920K |
probably damaging |
Het |
Git1 |
T |
A |
11: 77,390,581 (GRCm39) |
F106I |
probably damaging |
Het |
Glipr1l2 |
A |
G |
10: 111,942,868 (GRCm39) |
E241G |
probably damaging |
Het |
Gm2381 |
A |
C |
7: 42,469,729 (GRCm39) |
C132G |
probably damaging |
Het |
Gm49383 |
A |
G |
12: 69,239,628 (GRCm39) |
I237T |
|
Het |
Gm7324 |
T |
A |
14: 43,952,282 (GRCm39) |
D308E |
probably benign |
Het |
Gpr17 |
A |
G |
18: 32,080,421 (GRCm39) |
L214P |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,306,734 (GRCm39) |
L39Q |
probably damaging |
Het |
H2-Q6 |
C |
T |
17: 35,644,185 (GRCm39) |
R56C |
probably damaging |
Het |
Hcar2 |
T |
C |
5: 124,002,532 (GRCm39) |
T324A |
possibly damaging |
Het |
Ksr2 |
T |
C |
5: 117,885,425 (GRCm39) |
S750P |
probably damaging |
Het |
Lipi |
C |
A |
16: 75,357,689 (GRCm39) |
R292L |
probably benign |
Het |
Map4k3 |
C |
A |
17: 80,961,306 (GRCm39) |
M133I |
probably benign |
Het |
Marf1 |
A |
T |
16: 13,958,087 (GRCm39) |
L805Q |
probably damaging |
Het |
Mccc2 |
T |
A |
13: 100,090,754 (GRCm39) |
R460W |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,721,311 (GRCm39) |
D312G |
possibly damaging |
Het |
Nadk2 |
A |
T |
15: 9,103,449 (GRCm39) |
K360* |
probably null |
Het |
Nalf1 |
T |
C |
8: 9,820,114 (GRCm39) |
D302G |
probably benign |
Het |
Nars2 |
A |
G |
7: 96,689,178 (GRCm39) |
I367V |
probably benign |
Het |
Nppb |
T |
C |
4: 148,070,951 (GRCm39) |
S109P |
possibly damaging |
Het |
Odf2 |
G |
A |
2: 29,779,813 (GRCm39) |
R15Q |
probably benign |
Het |
Or4f59 |
C |
A |
2: 111,872,823 (GRCm39) |
A185S |
probably damaging |
Het |
Or51l4 |
C |
T |
7: 103,404,028 (GRCm39) |
V255M |
probably damaging |
Het |
Or5ac25 |
A |
T |
16: 59,182,106 (GRCm39) |
H158Q |
probably damaging |
Het |
Osbpl1a |
A |
T |
18: 12,889,269 (GRCm39) |
I949N |
probably benign |
Het |
Pan3 |
T |
C |
5: 147,479,881 (GRCm39) |
F55L |
probably benign |
Het |
Patj |
A |
G |
4: 98,353,377 (GRCm39) |
D640G |
probably null |
Het |
Pdxk |
T |
C |
10: 78,287,403 (GRCm39) |
K53E |
probably benign |
Het |
Pja2 |
A |
G |
17: 64,599,868 (GRCm39) |
S539P |
probably damaging |
Het |
Plscr1 |
T |
A |
9: 92,148,535 (GRCm39) |
C158* |
probably null |
Het |
Prdm14 |
T |
C |
1: 13,189,145 (GRCm39) |
T400A |
probably benign |
Het |
Rag1 |
C |
T |
2: 101,473,229 (GRCm39) |
V638M |
possibly damaging |
Het |
Ros1 |
A |
G |
10: 51,967,069 (GRCm39) |
S1734P |
probably damaging |
Het |
S100a9 |
T |
C |
3: 90,600,081 (GRCm39) |
H105R |
unknown |
Het |
Shisa9 |
A |
T |
16: 12,062,520 (GRCm39) |
Q247L |
possibly damaging |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc27a4 |
G |
A |
2: 29,701,301 (GRCm39) |
R364Q |
probably damaging |
Het |
Spag17 |
C |
T |
3: 99,934,932 (GRCm39) |
P713S |
possibly damaging |
Het |
Tbc1d4 |
T |
A |
14: 101,845,856 (GRCm39) |
H14L |
probably damaging |
Het |
Tmem144 |
T |
A |
3: 79,729,991 (GRCm39) |
Y253F |
probably damaging |
Het |
Tmem204 |
C |
T |
17: 25,299,322 (GRCm39) |
G66R |
possibly damaging |
Het |
Tnfrsf1b |
A |
T |
4: 144,942,424 (GRCm39) |
V453E |
probably damaging |
Het |
Tns1 |
G |
C |
1: 73,981,182 (GRCm39) |
Q1061E |
probably benign |
Het |
Tns1 |
G |
T |
1: 73,981,183 (GRCm39) |
N1060K |
probably benign |
Het |
Trav5-1 |
A |
G |
14: 52,860,428 (GRCm39) |
K78E |
probably benign |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Usp17lc |
G |
A |
7: 103,067,389 (GRCm39) |
G228D |
possibly damaging |
Het |
Uvssa |
T |
C |
5: 33,568,333 (GRCm39) |
C574R |
probably damaging |
Het |
Veph1 |
G |
A |
3: 66,171,434 (GRCm39) |
Q3* |
probably null |
Het |
Vps13b |
T |
A |
15: 35,623,774 (GRCm39) |
D1230E |
probably benign |
Het |
Xkr9 |
T |
A |
1: 13,771,318 (GRCm39) |
I278N |
probably damaging |
Het |
Zbed4 |
C |
A |
15: 88,664,742 (GRCm39) |
A270E |
probably benign |
Het |
Zfp366 |
A |
T |
13: 99,365,435 (GRCm39) |
T199S |
probably benign |
Het |
|
Other mutations in Dnajc13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Dnajc13
|
APN |
9 |
104,039,979 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00754:Dnajc13
|
APN |
9 |
104,051,697 (GRCm39) |
nonsense |
probably null |
|
IGL00914:Dnajc13
|
APN |
9 |
104,090,081 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01014:Dnajc13
|
APN |
9 |
104,080,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01077:Dnajc13
|
APN |
9 |
104,108,220 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01137:Dnajc13
|
APN |
9 |
104,037,689 (GRCm39) |
missense |
probably benign |
|
IGL01305:Dnajc13
|
APN |
9 |
104,107,836 (GRCm39) |
splice site |
probably null |
|
IGL01707:Dnajc13
|
APN |
9 |
104,106,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01868:Dnajc13
|
APN |
9 |
104,039,944 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01950:Dnajc13
|
APN |
9 |
104,067,631 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02102:Dnajc13
|
APN |
9 |
104,106,208 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02350:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02357:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02470:Dnajc13
|
APN |
9 |
104,052,946 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02888:Dnajc13
|
APN |
9 |
104,057,261 (GRCm39) |
splice site |
probably benign |
|
IGL03079:Dnajc13
|
APN |
9 |
104,090,068 (GRCm39) |
nonsense |
probably null |
|
IGL03179:Dnajc13
|
APN |
9 |
104,044,634 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03293:Dnajc13
|
APN |
9 |
104,051,625 (GRCm39) |
missense |
possibly damaging |
0.64 |
impressario
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
Kaiser
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
BB018:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4142001:Dnajc13
|
UTSW |
9 |
104,115,672 (GRCm39) |
missense |
probably damaging |
0.96 |
R0323:Dnajc13
|
UTSW |
9 |
104,034,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Dnajc13
|
UTSW |
9 |
104,044,258 (GRCm39) |
missense |
probably benign |
0.18 |
R0480:Dnajc13
|
UTSW |
9 |
104,077,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R0558:Dnajc13
|
UTSW |
9 |
104,079,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0707:Dnajc13
|
UTSW |
9 |
104,049,781 (GRCm39) |
missense |
probably benign |
0.12 |
R0831:Dnajc13
|
UTSW |
9 |
104,049,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1234:Dnajc13
|
UTSW |
9 |
104,091,356 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1433:Dnajc13
|
UTSW |
9 |
104,057,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Dnajc13
|
UTSW |
9 |
104,056,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1489:Dnajc13
|
UTSW |
9 |
104,108,234 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1575:Dnajc13
|
UTSW |
9 |
104,034,037 (GRCm39) |
missense |
probably benign |
0.29 |
R1750:Dnajc13
|
UTSW |
9 |
104,098,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R1903:Dnajc13
|
UTSW |
9 |
104,106,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R2066:Dnajc13
|
UTSW |
9 |
104,098,640 (GRCm39) |
missense |
probably benign |
0.01 |
R2206:Dnajc13
|
UTSW |
9 |
104,080,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3162:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4158:Dnajc13
|
UTSW |
9 |
104,067,641 (GRCm39) |
missense |
probably damaging |
0.96 |
R4460:Dnajc13
|
UTSW |
9 |
104,058,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R4537:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4538:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4631:Dnajc13
|
UTSW |
9 |
104,067,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Dnajc13
|
UTSW |
9 |
104,084,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dnajc13
|
UTSW |
9 |
104,091,017 (GRCm39) |
missense |
probably benign |
|
R4731:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4732:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4758:Dnajc13
|
UTSW |
9 |
104,049,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4802:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4928:Dnajc13
|
UTSW |
9 |
104,110,837 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4944:Dnajc13
|
UTSW |
9 |
104,044,586 (GRCm39) |
unclassified |
probably benign |
|
R4979:Dnajc13
|
UTSW |
9 |
104,063,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Dnajc13
|
UTSW |
9 |
104,108,185 (GRCm39) |
missense |
probably benign |
0.39 |
R5190:Dnajc13
|
UTSW |
9 |
104,051,724 (GRCm39) |
missense |
probably benign |
0.00 |
R5256:Dnajc13
|
UTSW |
9 |
104,080,528 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5452:Dnajc13
|
UTSW |
9 |
104,069,313 (GRCm39) |
missense |
probably benign |
0.01 |
R5657:Dnajc13
|
UTSW |
9 |
104,105,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Dnajc13
|
UTSW |
9 |
104,069,973 (GRCm39) |
splice site |
probably null |
|
R5789:Dnajc13
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Dnajc13
|
UTSW |
9 |
104,053,865 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5846:Dnajc13
|
UTSW |
9 |
104,067,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Dnajc13
|
UTSW |
9 |
104,061,814 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6189:Dnajc13
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
R6355:Dnajc13
|
UTSW |
9 |
104,080,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R6483:Dnajc13
|
UTSW |
9 |
104,085,003 (GRCm39) |
missense |
probably damaging |
0.96 |
R6613:Dnajc13
|
UTSW |
9 |
104,091,076 (GRCm39) |
missense |
probably benign |
0.07 |
R6962:Dnajc13
|
UTSW |
9 |
104,058,208 (GRCm39) |
missense |
probably benign |
0.02 |
R7048:Dnajc13
|
UTSW |
9 |
104,080,613 (GRCm39) |
critical splice donor site |
probably null |
|
R7101:Dnajc13
|
UTSW |
9 |
104,042,221 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7304:Dnajc13
|
UTSW |
9 |
104,115,713 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Dnajc13
|
UTSW |
9 |
104,107,230 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7366:Dnajc13
|
UTSW |
9 |
104,061,905 (GRCm39) |
missense |
probably benign |
0.43 |
R7528:Dnajc13
|
UTSW |
9 |
104,056,164 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7635:Dnajc13
|
UTSW |
9 |
104,039,566 (GRCm39) |
missense |
probably benign |
|
R7673:Dnajc13
|
UTSW |
9 |
104,110,891 (GRCm39) |
missense |
probably benign |
0.09 |
R7856:Dnajc13
|
UTSW |
9 |
104,044,684 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7931:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
R7995:Dnajc13
|
UTSW |
9 |
104,051,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Dnajc13
|
UTSW |
9 |
104,067,590 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Dnajc13
|
UTSW |
9 |
104,094,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Dnajc13
|
UTSW |
9 |
104,057,338 (GRCm39) |
missense |
probably benign |
|
R8686:Dnajc13
|
UTSW |
9 |
104,048,004 (GRCm39) |
missense |
probably benign |
0.00 |
R8707:Dnajc13
|
UTSW |
9 |
104,069,847 (GRCm39) |
missense |
probably damaging |
0.96 |
R8847:Dnajc13
|
UTSW |
9 |
104,057,360 (GRCm39) |
nonsense |
probably null |
|
R8868:Dnajc13
|
UTSW |
9 |
104,042,987 (GRCm39) |
missense |
probably benign |
0.13 |
R8986:Dnajc13
|
UTSW |
9 |
104,057,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Dnajc13
|
UTSW |
9 |
104,085,039 (GRCm39) |
missense |
probably benign |
0.02 |
R9334:Dnajc13
|
UTSW |
9 |
104,051,659 (GRCm39) |
missense |
probably benign |
0.00 |
R9353:Dnajc13
|
UTSW |
9 |
104,067,571 (GRCm39) |
missense |
probably benign |
0.31 |
R9470:Dnajc13
|
UTSW |
9 |
104,107,919 (GRCm39) |
missense |
probably benign |
0.01 |
R9528:Dnajc13
|
UTSW |
9 |
104,114,904 (GRCm39) |
missense |
probably benign |
|
R9578:Dnajc13
|
UTSW |
9 |
104,115,726 (GRCm39) |
missense |
probably benign |
0.04 |
R9691:Dnajc13
|
UTSW |
9 |
104,042,211 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Dnajc13
|
UTSW |
9 |
104,115,677 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0028:Dnajc13
|
UTSW |
9 |
104,042,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGCTGACATTTCTCTTCTGAAC -3'
(R):5'- CATGTTTGTCCAGAGGTCGGTC -3'
Sequencing Primer
(F):5'- TCTTCTGAACTGCTGACTTCAG -3'
(R):5'- GATCCCCTGGAATTGGAGTTACAC -3'
|
Posted On |
2022-11-14 |