Incidental Mutation 'R1928:Chd6'
ID |
215016 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Chd6
|
Ensembl Gene |
ENSMUSG00000057133 |
Gene Name |
chromodomain helicase DNA binding protein 6 |
Synonyms |
5430439G14Rik, 6330406J24Rik |
MMRRC Submission |
039946-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.745)
|
Stock # |
R1928 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
160788898-160950995 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 160809920 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042291
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039782]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000039782
|
SMART Domains |
Protein: ENSMUSP00000042291 Gene: ENSMUSG00000057133
Domain | Start | End | E-Value | Type |
low complexity region
|
86 |
106 |
N/A |
INTRINSIC |
low complexity region
|
113 |
143 |
N/A |
INTRINSIC |
low complexity region
|
214 |
229 |
N/A |
INTRINSIC |
CHROMO
|
289 |
355 |
1.35e-4 |
SMART |
CHROMO
|
372 |
430 |
3.48e-7 |
SMART |
DEXDc
|
456 |
658 |
1.73e-39 |
SMART |
HELICc
|
812 |
896 |
3.84e-23 |
SMART |
low complexity region
|
1080 |
1094 |
N/A |
INTRINSIC |
Blast:DEXDc
|
1108 |
1153 |
4e-23 |
BLAST |
SANT
|
1445 |
1504 |
1.51e0 |
SMART |
low complexity region
|
1866 |
1875 |
N/A |
INTRINSIC |
low complexity region
|
2048 |
2057 |
N/A |
INTRINSIC |
low complexity region
|
2130 |
2140 |
N/A |
INTRINSIC |
low complexity region
|
2277 |
2290 |
N/A |
INTRINSIC |
low complexity region
|
2333 |
2349 |
N/A |
INTRINSIC |
low complexity region
|
2437 |
2446 |
N/A |
INTRINSIC |
low complexity region
|
2539 |
2563 |
N/A |
INTRINSIC |
low complexity region
|
2652 |
2659 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137152
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.4%
- 20x: 92.6%
|
Validation Efficiency |
98% (120/123) |
MGI Phenotype |
FUNCTION: This gene encodes a member of the chromodomain/helicase/DNA-binding domain family of chromatin remodeling enzymes. This protein has been found to be specifically involved in transcription initiation and elongation. Homozygous knockout mice exhibit impaired motor coordination. A pseudogene has been identified on chromosome 8. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014] PHENOTYPE: Homozygous null mice display impaired coordination that is not due to muscle weakness or bradykinesia. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630073D07Rik |
T |
G |
6: 132,603,564 (GRCm39) |
Q64P |
unknown |
Het |
Adgrv1 |
A |
T |
13: 81,668,905 (GRCm39) |
F1830L |
probably benign |
Het |
Anks3 |
C |
T |
16: 4,763,918 (GRCm39) |
|
probably null |
Het |
Aqp12 |
G |
A |
1: 92,934,332 (GRCm39) |
D70N |
probably damaging |
Het |
B4galnt4 |
C |
T |
7: 140,648,061 (GRCm39) |
R526* |
probably null |
Het |
Best2 |
A |
G |
8: 85,737,882 (GRCm39) |
F171S |
probably benign |
Het |
C2cd5 |
A |
T |
6: 142,958,956 (GRCm39) |
V965D |
probably damaging |
Het |
Cd33 |
T |
C |
7: 43,179,303 (GRCm39) |
E282G |
probably benign |
Het |
Cep95 |
C |
T |
11: 106,681,554 (GRCm39) |
|
probably benign |
Het |
Clec4d |
A |
T |
6: 123,244,120 (GRCm39) |
|
probably null |
Het |
Cntd1 |
C |
T |
11: 101,174,678 (GRCm39) |
S128L |
probably damaging |
Het |
Col19a1 |
T |
C |
1: 24,490,835 (GRCm39) |
|
probably benign |
Het |
Ctrb1 |
C |
A |
8: 112,415,324 (GRCm39) |
V117L |
probably benign |
Het |
Dclk1 |
T |
C |
3: 55,154,942 (GRCm39) |
V124A |
possibly damaging |
Het |
Dcp2 |
T |
C |
18: 44,538,638 (GRCm39) |
|
probably null |
Het |
Dctn1 |
C |
A |
6: 83,176,166 (GRCm39) |
|
probably benign |
Het |
Dennd11 |
A |
G |
6: 40,388,648 (GRCm39) |
F238L |
probably benign |
Het |
Ephb3 |
T |
A |
16: 21,041,045 (GRCm39) |
M701K |
possibly damaging |
Het |
Ero1b |
A |
G |
13: 12,616,648 (GRCm39) |
E359G |
probably damaging |
Het |
Exosc8 |
G |
T |
3: 54,636,266 (GRCm39) |
A255E |
probably damaging |
Het |
Fhip1a |
G |
A |
3: 85,595,838 (GRCm39) |
P349L |
probably damaging |
Het |
Fndc3c1 |
C |
T |
X: 105,477,128 (GRCm39) |
A824T |
probably benign |
Het |
Gja10 |
G |
A |
4: 32,601,812 (GRCm39) |
Q191* |
probably null |
Het |
Gm1587 |
C |
T |
14: 78,036,288 (GRCm39) |
R6Q |
unknown |
Het |
Gm3409 |
A |
G |
5: 146,476,418 (GRCm39) |
I190V |
probably benign |
Het |
Gm4952 |
G |
T |
19: 12,600,973 (GRCm39) |
M64I |
probably damaging |
Het |
Gramd1b |
C |
T |
9: 40,217,765 (GRCm39) |
M595I |
possibly damaging |
Het |
Grik1 |
C |
T |
16: 87,848,241 (GRCm39) |
V176M |
probably damaging |
Het |
Grin2b |
A |
G |
6: 136,021,044 (GRCm39) |
C86R |
probably damaging |
Het |
Gtse1 |
C |
T |
15: 85,746,264 (GRCm39) |
|
probably benign |
Het |
Hectd2 |
T |
C |
19: 36,589,719 (GRCm39) |
Y615H |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,229,579 (GRCm39) |
F1552S |
possibly damaging |
Het |
Ifi207 |
A |
G |
1: 173,557,211 (GRCm39) |
V516A |
possibly damaging |
Het |
Igfbp5 |
G |
T |
1: 72,913,184 (GRCm39) |
P39T |
probably damaging |
Het |
Il23r |
T |
A |
6: 67,400,719 (GRCm39) |
D537V |
possibly damaging |
Het |
Invs |
A |
G |
4: 48,390,095 (GRCm39) |
Y251C |
probably damaging |
Het |
Isl1 |
G |
T |
13: 116,444,953 (GRCm39) |
H25Q |
probably damaging |
Het |
Kif13a |
A |
G |
13: 46,966,221 (GRCm39) |
L399P |
probably damaging |
Het |
Klhl1 |
A |
G |
14: 96,584,225 (GRCm39) |
V335A |
probably benign |
Het |
Klhl14 |
C |
A |
18: 21,784,843 (GRCm39) |
A195S |
probably damaging |
Het |
Lepr |
A |
G |
4: 101,639,927 (GRCm39) |
|
probably benign |
Het |
Map1b |
A |
C |
13: 99,567,454 (GRCm39) |
S1756A |
unknown |
Het |
Med23 |
C |
T |
10: 24,785,710 (GRCm39) |
A877V |
probably benign |
Het |
Mfsd4b2 |
T |
C |
10: 39,797,458 (GRCm39) |
Y299C |
probably damaging |
Het |
Mipol1 |
T |
A |
12: 57,379,205 (GRCm39) |
M221K |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,569,350 (GRCm39) |
S137C |
probably damaging |
Het |
Mutyh |
T |
C |
4: 116,673,855 (GRCm39) |
Y189H |
probably damaging |
Het |
Nabp2 |
T |
C |
10: 128,245,182 (GRCm39) |
T21A |
possibly damaging |
Het |
Nalf1 |
T |
C |
8: 9,820,217 (GRCm39) |
T268A |
probably benign |
Het |
Nell1 |
T |
A |
7: 50,350,943 (GRCm39) |
V530E |
possibly damaging |
Het |
Npc1 |
G |
C |
18: 12,346,435 (GRCm39) |
P254A |
possibly damaging |
Het |
Nup153 |
A |
G |
13: 46,854,502 (GRCm39) |
V530A |
probably damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Or10j5 |
T |
C |
1: 172,784,881 (GRCm39) |
V173A |
probably damaging |
Het |
Or11h4b |
A |
G |
14: 50,918,872 (GRCm39) |
V73A |
probably benign |
Het |
Or7e177 |
T |
C |
9: 20,212,354 (GRCm39) |
V287A |
probably benign |
Het |
Pabpc1l |
T |
A |
2: 163,874,174 (GRCm39) |
I193N |
possibly damaging |
Het |
Pabpc4l |
A |
G |
3: 46,401,066 (GRCm39) |
Y193H |
probably damaging |
Het |
Pank1 |
T |
C |
19: 34,856,281 (GRCm39) |
S66G |
probably benign |
Het |
Pcdhb1 |
A |
T |
18: 37,399,233 (GRCm39) |
K395* |
probably null |
Het |
Pcna |
A |
G |
2: 132,093,817 (GRCm39) |
|
probably benign |
Het |
Pgr |
T |
A |
9: 8,903,630 (GRCm39) |
Y550* |
probably null |
Het |
Phf11a |
A |
G |
14: 59,519,316 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,151,524 (GRCm39) |
|
probably benign |
Het |
Pofut2 |
T |
A |
10: 77,096,642 (GRCm39) |
Y122* |
probably null |
Het |
Pole |
A |
G |
5: 110,475,644 (GRCm39) |
M1818V |
probably benign |
Het |
Rapgef3 |
A |
G |
15: 97,647,914 (GRCm39) |
L696P |
probably damaging |
Het |
Rasal3 |
T |
C |
17: 32,616,327 (GRCm39) |
D310G |
probably damaging |
Het |
Rhoq |
A |
G |
17: 87,302,486 (GRCm39) |
K141E |
probably benign |
Het |
Rilpl1 |
A |
G |
5: 124,652,813 (GRCm39) |
|
probably benign |
Het |
Rnaseh1 |
T |
C |
12: 28,703,088 (GRCm39) |
S91P |
probably benign |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Saa1 |
C |
A |
7: 46,391,856 (GRCm39) |
G31W |
probably null |
Het |
Saxo5 |
T |
A |
8: 3,536,947 (GRCm39) |
I431K |
possibly damaging |
Het |
Scaf8 |
A |
G |
17: 3,218,352 (GRCm39) |
T241A |
unknown |
Het |
Scarb2 |
C |
T |
5: 92,592,125 (GRCm39) |
A473T |
possibly damaging |
Het |
Scnn1b |
T |
C |
7: 121,509,670 (GRCm39) |
F273S |
probably damaging |
Het |
Sdccag8 |
T |
C |
1: 176,656,536 (GRCm39) |
V136A |
probably damaging |
Het |
Sdr16c6 |
A |
T |
4: 4,069,926 (GRCm39) |
V138E |
probably damaging |
Het |
Sf3a3 |
G |
A |
4: 124,615,886 (GRCm39) |
A180T |
possibly damaging |
Het |
Slc16a5 |
T |
A |
11: 115,360,842 (GRCm39) |
S342T |
probably damaging |
Het |
Slc18a1 |
A |
G |
8: 69,526,464 (GRCm39) |
S75P |
probably benign |
Het |
Slc7a6 |
T |
A |
8: 106,920,120 (GRCm39) |
|
probably benign |
Het |
Smco3 |
G |
A |
6: 136,808,845 (GRCm39) |
Q10* |
probably null |
Het |
Spem2 |
T |
C |
11: 69,708,290 (GRCm39) |
Q225R |
probably benign |
Het |
Ssb |
G |
T |
2: 69,697,901 (GRCm39) |
|
probably null |
Het |
Stx8 |
T |
C |
11: 68,000,106 (GRCm39) |
I182T |
probably damaging |
Het |
Synj2 |
T |
A |
17: 6,040,542 (GRCm39) |
I121N |
probably damaging |
Het |
Tbc1d1 |
T |
C |
5: 64,502,643 (GRCm39) |
Y1055H |
probably damaging |
Het |
Thbs3 |
G |
T |
3: 89,125,067 (GRCm39) |
R52L |
probably damaging |
Het |
Tmem101 |
C |
T |
11: 102,044,222 (GRCm39) |
V222I |
probably benign |
Het |
Tnks2 |
C |
T |
19: 36,823,068 (GRCm39) |
Q112* |
probably null |
Het |
Tnrc6b |
T |
A |
15: 80,764,924 (GRCm39) |
W809R |
probably damaging |
Het |
Trib2 |
T |
A |
12: 15,865,454 (GRCm39) |
R16S |
probably damaging |
Het |
Trim12a |
T |
C |
7: 103,956,331 (GRCm39) |
N70D |
probably damaging |
Het |
Trim55 |
T |
A |
3: 19,716,046 (GRCm39) |
|
probably null |
Het |
Tspyl5 |
T |
A |
15: 33,687,153 (GRCm39) |
D264V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,555,388 (GRCm39) |
V30539A |
probably damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,713,988 (GRCm39) |
F43S |
possibly damaging |
Het |
Tut7 |
A |
G |
13: 59,964,548 (GRCm39) |
L209P |
probably damaging |
Het |
Ube3d |
A |
G |
9: 86,305,056 (GRCm39) |
L262P |
probably damaging |
Het |
Ugt1a7c |
T |
C |
1: 88,023,651 (GRCm39) |
V270A |
probably benign |
Het |
Vav3 |
T |
A |
3: 109,413,738 (GRCm39) |
F225L |
possibly damaging |
Het |
Vmn1r21 |
G |
T |
6: 57,821,077 (GRCm39) |
Y122* |
probably null |
Het |
Vmn1r225 |
C |
A |
17: 20,723,071 (GRCm39) |
Q171K |
probably benign |
Het |
Vmn2r103 |
T |
C |
17: 20,032,029 (GRCm39) |
V601A |
possibly damaging |
Het |
Vmn2r19 |
T |
A |
6: 123,308,589 (GRCm39) |
N555K |
probably damaging |
Het |
Vps33a |
G |
A |
5: 123,696,684 (GRCm39) |
A323V |
probably benign |
Het |
Wdr77 |
C |
T |
3: 105,874,618 (GRCm39) |
P337S |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,929,884 (GRCm39) |
I93N |
probably damaging |
Het |
Zbtb9 |
T |
A |
17: 27,193,612 (GRCm39) |
I339N |
probably damaging |
Het |
Zfp202 |
T |
A |
9: 40,121,083 (GRCm39) |
D241E |
probably damaging |
Het |
Zfp235 |
T |
A |
7: 23,840,563 (GRCm39) |
Y327* |
probably null |
Het |
Zfp820 |
A |
C |
17: 22,038,316 (GRCm39) |
D337E |
probably benign |
Het |
Zfp944 |
T |
C |
17: 22,560,065 (GRCm39) |
T14A |
probably damaging |
Het |
Zfy1 |
A |
G |
Y: 729,733 (GRCm39) |
V303A |
unknown |
Het |
Zfyve26 |
C |
T |
12: 79,286,744 (GRCm39) |
W2281* |
probably null |
Het |
|
Other mutations in Chd6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00837:Chd6
|
APN |
2 |
160,883,999 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00899:Chd6
|
APN |
2 |
160,871,218 (GRCm39) |
splice site |
probably benign |
|
IGL01104:Chd6
|
APN |
2 |
160,803,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01295:Chd6
|
APN |
2 |
160,830,290 (GRCm39) |
splice site |
probably benign |
|
IGL01717:Chd6
|
APN |
2 |
160,807,179 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01795:Chd6
|
APN |
2 |
160,803,294 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01814:Chd6
|
APN |
2 |
160,901,849 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02016:Chd6
|
APN |
2 |
160,825,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02104:Chd6
|
APN |
2 |
160,819,432 (GRCm39) |
missense |
probably benign |
|
IGL02158:Chd6
|
APN |
2 |
160,868,212 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02313:Chd6
|
APN |
2 |
160,807,595 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:Chd6
|
APN |
2 |
160,826,372 (GRCm39) |
splice site |
probably benign |
|
IGL02522:Chd6
|
APN |
2 |
160,807,716 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02626:Chd6
|
APN |
2 |
160,881,270 (GRCm39) |
splice site |
probably benign |
|
IGL02727:Chd6
|
APN |
2 |
160,811,383 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02738:Chd6
|
APN |
2 |
160,807,618 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02743:Chd6
|
APN |
2 |
160,802,183 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02800:Chd6
|
APN |
2 |
160,826,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02811:Chd6
|
APN |
2 |
160,832,221 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02850:Chd6
|
APN |
2 |
160,861,536 (GRCm39) |
nonsense |
probably null |
|
IGL02979:Chd6
|
APN |
2 |
160,808,090 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02993:Chd6
|
APN |
2 |
160,894,304 (GRCm39) |
splice site |
probably benign |
|
IGL03277:Chd6
|
APN |
2 |
160,824,981 (GRCm39) |
missense |
probably null |
1.00 |
IGL03346:Chd6
|
APN |
2 |
160,802,282 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03357:Chd6
|
APN |
2 |
160,859,936 (GRCm39) |
splice site |
probably benign |
|
IGL03134:Chd6
|
UTSW |
2 |
160,807,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0106:Chd6
|
UTSW |
2 |
160,809,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0106:Chd6
|
UTSW |
2 |
160,809,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Chd6
|
UTSW |
2 |
160,894,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R0363:Chd6
|
UTSW |
2 |
160,856,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Chd6
|
UTSW |
2 |
160,894,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Chd6
|
UTSW |
2 |
160,834,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R0771:Chd6
|
UTSW |
2 |
160,861,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Chd6
|
UTSW |
2 |
160,832,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Chd6
|
UTSW |
2 |
160,832,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Chd6
|
UTSW |
2 |
160,872,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R1277:Chd6
|
UTSW |
2 |
160,809,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1396:Chd6
|
UTSW |
2 |
160,825,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Chd6
|
UTSW |
2 |
160,883,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Chd6
|
UTSW |
2 |
160,883,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Chd6
|
UTSW |
2 |
160,823,587 (GRCm39) |
missense |
probably damaging |
0.96 |
R1766:Chd6
|
UTSW |
2 |
160,808,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Chd6
|
UTSW |
2 |
160,832,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Chd6
|
UTSW |
2 |
160,808,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R2200:Chd6
|
UTSW |
2 |
160,825,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R2340:Chd6
|
UTSW |
2 |
160,807,679 (GRCm39) |
frame shift |
probably null |
|
R2341:Chd6
|
UTSW |
2 |
160,807,679 (GRCm39) |
frame shift |
probably null |
|
R2519:Chd6
|
UTSW |
2 |
160,871,796 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2919:Chd6
|
UTSW |
2 |
160,809,800 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3025:Chd6
|
UTSW |
2 |
160,808,472 (GRCm39) |
small deletion |
probably benign |
|
R3426:Chd6
|
UTSW |
2 |
160,832,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R3427:Chd6
|
UTSW |
2 |
160,832,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Chd6
|
UTSW |
2 |
160,830,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Chd6
|
UTSW |
2 |
160,803,211 (GRCm39) |
missense |
probably benign |
0.04 |
R4360:Chd6
|
UTSW |
2 |
160,791,776 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4399:Chd6
|
UTSW |
2 |
160,807,238 (GRCm39) |
missense |
probably benign |
|
R4458:Chd6
|
UTSW |
2 |
160,871,796 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4583:Chd6
|
UTSW |
2 |
160,856,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Chd6
|
UTSW |
2 |
160,811,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R4740:Chd6
|
UTSW |
2 |
160,812,103 (GRCm39) |
missense |
probably benign |
|
R4765:Chd6
|
UTSW |
2 |
160,808,164 (GRCm39) |
nonsense |
probably null |
|
R4779:Chd6
|
UTSW |
2 |
160,791,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Chd6
|
UTSW |
2 |
160,871,219 (GRCm39) |
splice site |
probably benign |
|
R5068:Chd6
|
UTSW |
2 |
160,808,289 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5215:Chd6
|
UTSW |
2 |
160,791,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5275:Chd6
|
UTSW |
2 |
160,811,283 (GRCm39) |
missense |
probably benign |
|
R5405:Chd6
|
UTSW |
2 |
160,807,310 (GRCm39) |
missense |
probably benign |
|
R5598:Chd6
|
UTSW |
2 |
160,856,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Chd6
|
UTSW |
2 |
160,807,185 (GRCm39) |
missense |
probably benign |
|
R5697:Chd6
|
UTSW |
2 |
160,859,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Chd6
|
UTSW |
2 |
160,791,798 (GRCm39) |
missense |
probably benign |
0.00 |
R5759:Chd6
|
UTSW |
2 |
160,825,682 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5761:Chd6
|
UTSW |
2 |
160,798,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5761:Chd6
|
UTSW |
2 |
160,798,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5954:Chd6
|
UTSW |
2 |
160,807,747 (GRCm39) |
missense |
probably benign |
0.00 |
R6025:Chd6
|
UTSW |
2 |
160,807,502 (GRCm39) |
missense |
probably benign |
|
R6104:Chd6
|
UTSW |
2 |
160,856,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Chd6
|
UTSW |
2 |
160,791,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Chd6
|
UTSW |
2 |
160,821,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6452:Chd6
|
UTSW |
2 |
160,807,418 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6468:Chd6
|
UTSW |
2 |
160,854,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Chd6
|
UTSW |
2 |
160,808,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6803:Chd6
|
UTSW |
2 |
160,802,279 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6869:Chd6
|
UTSW |
2 |
160,807,650 (GRCm39) |
missense |
probably benign |
|
R6895:Chd6
|
UTSW |
2 |
160,830,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6925:Chd6
|
UTSW |
2 |
160,855,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R7061:Chd6
|
UTSW |
2 |
160,867,885 (GRCm39) |
nonsense |
probably null |
|
R7064:Chd6
|
UTSW |
2 |
160,791,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Chd6
|
UTSW |
2 |
160,803,199 (GRCm39) |
nonsense |
probably null |
|
R7287:Chd6
|
UTSW |
2 |
160,850,312 (GRCm39) |
missense |
probably benign |
0.07 |
R7431:Chd6
|
UTSW |
2 |
160,868,248 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7486:Chd6
|
UTSW |
2 |
160,791,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Chd6
|
UTSW |
2 |
160,855,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Chd6
|
UTSW |
2 |
160,867,863 (GRCm39) |
missense |
probably benign |
0.13 |
R7748:Chd6
|
UTSW |
2 |
160,808,539 (GRCm39) |
missense |
probably benign |
0.37 |
R7785:Chd6
|
UTSW |
2 |
160,812,095 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8002:Chd6
|
UTSW |
2 |
160,832,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Chd6
|
UTSW |
2 |
160,799,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Chd6
|
UTSW |
2 |
160,832,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8388:Chd6
|
UTSW |
2 |
160,861,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Chd6
|
UTSW |
2 |
160,862,989 (GRCm39) |
missense |
probably benign |
0.10 |
R8867:Chd6
|
UTSW |
2 |
160,862,989 (GRCm39) |
missense |
probably benign |
0.10 |
R8996:Chd6
|
UTSW |
2 |
160,823,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Chd6
|
UTSW |
2 |
160,871,793 (GRCm39) |
nonsense |
probably null |
|
R9270:Chd6
|
UTSW |
2 |
160,871,793 (GRCm39) |
nonsense |
probably null |
|
R9310:Chd6
|
UTSW |
2 |
160,881,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Chd6
|
UTSW |
2 |
160,871,784 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9438:Chd6
|
UTSW |
2 |
160,799,078 (GRCm39) |
missense |
probably benign |
0.01 |
R9756:Chd6
|
UTSW |
2 |
160,802,259 (GRCm39) |
missense |
probably benign |
|
Z1088:Chd6
|
UTSW |
2 |
160,808,408 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCATCTTTCCATGCGGGGAG -3'
(R):5'- CATCGTCATGAGGGAAAGGC -3'
Sequencing Primer
(F):5'- GGGGAGACGACACACATTCC -3'
(R):5'- CCCCTCTTTGGAAGCAGATGTAAG -3'
|
Posted On |
2014-07-14 |