Incidental Mutation 'R0242:Golgb1'
| ID |
66292 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Golgb1
|
| Ensembl Gene |
ENSMUSG00000034243 |
| Gene Name |
golgin B1 |
| Synonyms |
C130074L01Rik, Gm6840, F730017E11Rik, Giantin, 6330407A06Rik |
| MMRRC Submission |
038480-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.918)
|
| Stock # |
R0242 (G1)
|
| Quality Score |
100 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
36695502-36753447 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 36695992 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 164
(Q164*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000023534
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023534]
[ENSMUST00000023535]
[ENSMUST00000075946]
[ENSMUST00000114812]
[ENSMUST00000114819]
[ENSMUST00000134616]
[ENSMUST00000135406]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000023534
AA Change: Q164*
|
| SMART Domains |
Protein: ENSMUSP00000023534
Gene: ENSMUSG00000034243
AA Change: Q164*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
55 |
99 |
N/A |
INTRINSIC |
|
low complexity region
|
109 |
126 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000023535
|
| SMART Domains |
Protein: ENSMUSP00000023535
Gene: ENSMUSG00000022837
| Domain | Start | End | E-Value | Type |
|---|
|
IQ
|
293 |
315 |
5.92e-4 |
SMART |
|
low complexity region
|
341 |
358 |
N/A |
INTRINSIC |
|
IQ
|
386 |
408 |
2.66e-6 |
SMART |
|
low complexity region
|
428 |
442 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000075946
|
| SMART Domains |
Protein: ENSMUSP00000075331
Gene: ENSMUSG00000022838
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
44 |
71 |
N/A |
INTRINSIC |
|
low complexity region
|
117 |
132 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114812
|
| SMART Domains |
Protein: ENSMUSP00000110460
Gene: ENSMUSG00000034243
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_2
|
24 |
61 |
6.71e-6 |
PROSPERO |
|
low complexity region
|
87 |
107 |
N/A |
INTRINSIC |
|
low complexity region
|
120 |
134 |
N/A |
INTRINSIC |
|
low complexity region
|
143 |
154 |
N/A |
INTRINSIC |
|
low complexity region
|
200 |
219 |
N/A |
INTRINSIC |
|
low complexity region
|
450 |
471 |
N/A |
INTRINSIC |
|
internal_repeat_3
|
478 |
517 |
6.71e-6 |
PROSPERO |
|
coiled coil region
|
522 |
553 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
586 |
620 |
3.05e-5 |
PROSPERO |
|
coiled coil region
|
638 |
1080 |
N/A |
INTRINSIC |
|
coiled coil region
|
1112 |
1199 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
1212 |
1247 |
3.05e-5 |
PROSPERO |
|
low complexity region
|
1259 |
1273 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1280 |
1311 |
3.14e-6 |
PROSPERO |
|
low complexity region
|
1316 |
1328 |
N/A |
INTRINSIC |
|
coiled coil region
|
1361 |
1714 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
1719 |
1757 |
6.71e-6 |
PROSPERO |
|
internal_repeat_3
|
1720 |
1763 |
6.71e-6 |
PROSPERO |
|
coiled coil region
|
1777 |
1993 |
N/A |
INTRINSIC |
|
low complexity region
|
2250 |
2265 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
2310 |
2341 |
3.14e-6 |
PROSPERO |
|
low complexity region
|
2359 |
2377 |
N/A |
INTRINSIC |
|
low complexity region
|
2497 |
2508 |
N/A |
INTRINSIC |
|
coiled coil region
|
2734 |
2786 |
N/A |
INTRINSIC |
|
coiled coil region
|
2813 |
2902 |
N/A |
INTRINSIC |
|
low complexity region
|
2923 |
2935 |
N/A |
INTRINSIC |
|
coiled coil region
|
2966 |
3016 |
N/A |
INTRINSIC |
|
coiled coil region
|
3076 |
3122 |
N/A |
INTRINSIC |
|
transmembrane domain
|
3174 |
3196 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114819
|
| SMART Domains |
Protein: ENSMUSP00000110467
Gene: ENSMUSG00000022837
| Domain | Start | End | E-Value | Type |
|---|
|
IQ
|
293 |
315 |
5.92e-4 |
SMART |
|
low complexity region
|
341 |
358 |
N/A |
INTRINSIC |
|
IQ
|
386 |
408 |
2.66e-6 |
SMART |
|
low complexity region
|
428 |
442 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134556
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000134616
|
| SMART Domains |
Protein: ENSMUSP00000116503
Gene: ENSMUSG00000034243
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
42 |
107 |
N/A |
INTRINSIC |
|
low complexity region
|
120 |
134 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135800
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138660
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153572
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000157072
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135406
|
| SMART Domains |
Protein: ENSMUSP00000115848
Gene: ENSMUSG00000034243
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
42 |
107 |
N/A |
INTRINSIC |
|
low complexity region
|
120 |
134 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.2%
- 10x: 90.8%
- 20x: 69.4%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Homozygous knockout affects glycosylation of glycoproteins in the extra-cellular matrix of the palatal shelves, resulting in their failure to elevate and fuse, leading to cleft palate. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(7) : Targeted, other(2) Gene trapped(5)
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700029H14Rik |
T |
C |
8: 13,601,676 (GRCm39) |
D230G |
probably benign |
Het |
| Abhd13 |
A |
G |
8: 10,037,561 (GRCm39) |
I53V |
probably benign |
Het |
| Adgrl2 |
A |
C |
3: 148,544,821 (GRCm39) |
|
probably null |
Het |
| Aldh16a1 |
G |
A |
7: 44,794,088 (GRCm39) |
A596V |
probably damaging |
Het |
| Aldh3b2 |
T |
A |
19: 4,029,414 (GRCm39) |
Y262* |
probably null |
Het |
| Ambn |
A |
G |
5: 88,615,831 (GRCm39) |
Q420R |
possibly damaging |
Het |
| Arhgap9 |
C |
A |
10: 127,165,407 (GRCm39) |
H430Q |
probably benign |
Het |
| Arhgef25 |
C |
T |
10: 127,019,933 (GRCm39) |
G435E |
probably damaging |
Het |
| Armc12 |
A |
T |
17: 28,751,366 (GRCm39) |
D120V |
possibly damaging |
Het |
| Asxl3 |
G |
A |
18: 22,649,738 (GRCm39) |
E576K |
possibly damaging |
Het |
| Bcdin3d |
T |
C |
15: 99,368,776 (GRCm39) |
E141G |
probably benign |
Het |
| Bmpr1b |
G |
A |
3: 141,546,437 (GRCm39) |
T483M |
probably damaging |
Het |
| Caprin2 |
C |
T |
6: 148,744,452 (GRCm39) |
S991N |
probably damaging |
Het |
| Cd96 |
T |
C |
16: 45,892,129 (GRCm39) |
I286M |
possibly damaging |
Het |
| Cdcp1 |
G |
T |
9: 123,009,237 (GRCm39) |
F480L |
probably benign |
Het |
| Celf5 |
T |
C |
10: 81,300,243 (GRCm39) |
T258A |
probably benign |
Het |
| Clca3b |
A |
G |
3: 144,547,226 (GRCm39) |
S304P |
probably benign |
Het |
| Cmya5 |
A |
T |
13: 93,232,108 (GRCm39) |
H993Q |
probably benign |
Het |
| Cnbp |
A |
T |
6: 87,822,746 (GRCm39) |
C6S |
probably damaging |
Het |
| Col14a1 |
C |
T |
15: 55,360,907 (GRCm39) |
R1605W |
probably damaging |
Het |
| Cops7a |
T |
C |
6: 124,941,817 (GRCm39) |
N11S |
probably benign |
Het |
| Cpvl |
T |
C |
6: 53,909,485 (GRCm39) |
H217R |
possibly damaging |
Het |
| Cyp2c66 |
A |
G |
19: 39,130,369 (GRCm39) |
Y68C |
probably damaging |
Het |
| Dicer1 |
G |
A |
12: 104,668,710 (GRCm39) |
T1324M |
probably benign |
Het |
| Dlgap2 |
A |
G |
8: 14,777,562 (GRCm39) |
D268G |
probably benign |
Het |
| Dnm1 |
T |
A |
2: 32,207,001 (GRCm39) |
M535L |
possibly damaging |
Het |
| Dock7 |
A |
T |
4: 98,850,517 (GRCm39) |
F1575Y |
probably benign |
Het |
| Dpp10 |
T |
A |
1: 123,326,275 (GRCm39) |
H403L |
possibly damaging |
Het |
| Dync1h1 |
A |
G |
12: 110,616,285 (GRCm39) |
D3112G |
possibly damaging |
Het |
| Eno3 |
A |
G |
11: 70,548,761 (GRCm39) |
E21G |
probably null |
Het |
| Fam120b |
T |
A |
17: 15,643,186 (GRCm39) |
V655D |
probably damaging |
Het |
| Fkbp5 |
A |
T |
17: 28,647,426 (GRCm39) |
D136E |
probably benign |
Het |
| Gfer |
A |
G |
17: 24,913,277 (GRCm39) |
W192R |
probably damaging |
Het |
| Gpnmb |
A |
G |
6: 49,024,276 (GRCm39) |
N197S |
probably damaging |
Het |
| Gtf2f1 |
G |
A |
17: 57,310,802 (GRCm39) |
T414M |
probably benign |
Het |
| Helz2 |
C |
T |
2: 180,872,223 (GRCm39) |
R2539Q |
probably damaging |
Het |
| Hsd17b12 |
T |
A |
2: 93,988,160 (GRCm39) |
I19F |
probably benign |
Het |
| Incenp |
T |
C |
19: 9,871,114 (GRCm39) |
T172A |
unknown |
Het |
| Jmy |
A |
G |
13: 93,578,126 (GRCm39) |
Y681H |
probably benign |
Het |
| Kbtbd11 |
A |
G |
8: 15,077,508 (GRCm39) |
T36A |
probably benign |
Het |
| Kcnh4 |
T |
C |
11: 100,646,525 (GRCm39) |
D267G |
probably damaging |
Het |
| Krt40 |
T |
A |
11: 99,429,568 (GRCm39) |
E335D |
probably damaging |
Het |
| Krt86 |
T |
A |
15: 101,374,454 (GRCm39) |
Y282* |
probably null |
Het |
| Lgi3 |
C |
T |
14: 70,772,255 (GRCm39) |
R267* |
probably null |
Het |
| Lrp1b |
T |
A |
2: 40,888,195 (GRCm39) |
H2355L |
probably benign |
Het |
| Lrrc8e |
G |
A |
8: 4,285,401 (GRCm39) |
R542H |
probably benign |
Het |
| Mast4 |
G |
A |
13: 102,990,350 (GRCm39) |
S57F |
probably damaging |
Het |
| Mia2 |
T |
C |
12: 59,155,642 (GRCm39) |
Y452H |
probably damaging |
Het |
| Mmachc |
C |
T |
4: 116,561,738 (GRCm39) |
R132Q |
probably damaging |
Het |
| Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
| Mtbp |
T |
A |
15: 55,440,882 (GRCm39) |
N356K |
possibly damaging |
Het |
| Myo5b |
A |
G |
18: 74,794,787 (GRCm39) |
H552R |
possibly damaging |
Het |
| Niban1 |
A |
G |
1: 151,593,967 (GRCm39) |
D884G |
probably benign |
Het |
| Noxred1 |
A |
G |
12: 87,273,753 (GRCm39) |
V96A |
probably benign |
Het |
| Nr1d2 |
T |
A |
14: 18,211,933 (GRCm38) |
D390V |
possibly damaging |
Het |
| Odad2 |
A |
T |
18: 7,211,516 (GRCm39) |
V786D |
probably damaging |
Het |
| Or1r1 |
T |
C |
11: 73,874,538 (GRCm39) |
S299G |
probably benign |
Het |
| Or6c1b |
T |
A |
10: 129,273,217 (GRCm39) |
Y179N |
probably damaging |
Het |
| Otog |
G |
T |
7: 45,916,805 (GRCm39) |
C914F |
probably damaging |
Het |
| Pank2 |
G |
T |
2: 131,122,117 (GRCm39) |
C214F |
probably damaging |
Het |
| Pcdhb1 |
T |
A |
18: 37,399,788 (GRCm39) |
S580T |
probably benign |
Het |
| Pdia3 |
T |
C |
2: 121,244,592 (GRCm39) |
S2P |
probably damaging |
Het |
| Peli1 |
G |
T |
11: 21,092,602 (GRCm39) |
R83L |
probably damaging |
Het |
| Pla2g3 |
T |
A |
11: 3,441,935 (GRCm39) |
C366* |
probably null |
Het |
| Pon3 |
T |
A |
6: 5,240,860 (GRCm39) |
D107V |
probably benign |
Het |
| Ppip5k2 |
A |
G |
1: 97,668,816 (GRCm39) |
C532R |
probably damaging |
Het |
| Psd3 |
A |
G |
8: 68,210,738 (GRCm39) |
M270T |
probably damaging |
Het |
| Pus1 |
A |
T |
5: 110,927,664 (GRCm39) |
H30Q |
probably benign |
Het |
| Pwwp3a |
T |
C |
10: 80,070,092 (GRCm39) |
S354P |
probably benign |
Het |
| Rab7 |
A |
T |
6: 87,982,114 (GRCm39) |
V87E |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,147,595 (GRCm39) |
|
probably null |
Het |
| S1pr3 |
A |
G |
13: 51,572,938 (GRCm39) |
T40A |
probably benign |
Het |
| Senp7 |
T |
A |
16: 55,999,884 (GRCm39) |
I853N |
probably damaging |
Het |
| Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
| Shroom1 |
T |
G |
11: 53,356,312 (GRCm39) |
|
probably null |
Het |
| Slc24a3 |
T |
C |
2: 145,448,584 (GRCm39) |
I376T |
probably benign |
Het |
| Slc46a1 |
T |
C |
11: 78,359,493 (GRCm39) |
I375T |
possibly damaging |
Het |
| Slc4a9 |
T |
C |
18: 36,666,733 (GRCm39) |
F527S |
probably damaging |
Het |
| Slc4a9 |
T |
A |
18: 36,674,286 (GRCm39) |
I924N |
probably damaging |
Het |
| Slx4 |
T |
A |
16: 3,804,816 (GRCm39) |
E666V |
probably damaging |
Het |
| Sorcs1 |
C |
T |
19: 50,216,659 (GRCm39) |
G640E |
probably damaging |
Het |
| Spmap2l |
G |
T |
5: 77,164,152 (GRCm39) |
E52* |
probably null |
Het |
| Sptan1 |
A |
T |
2: 29,908,413 (GRCm39) |
M1725L |
probably benign |
Het |
| Sync |
G |
A |
4: 129,187,514 (GRCm39) |
R182K |
probably damaging |
Het |
| Syne2 |
G |
A |
12: 76,144,808 (GRCm39) |
G1586S |
probably damaging |
Het |
| Sytl1 |
G |
T |
4: 132,980,768 (GRCm39) |
T522K |
probably damaging |
Het |
| Tex2 |
T |
A |
11: 106,410,781 (GRCm39) |
K414* |
probably null |
Het |
| Thsd7a |
G |
A |
6: 12,503,915 (GRCm39) |
T413I |
probably benign |
Het |
| Tm9sf1 |
C |
T |
14: 55,875,392 (GRCm39) |
A451T |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,656,496 (GRCm39) |
|
probably benign |
Het |
| Uba2 |
T |
C |
7: 33,854,054 (GRCm39) |
I140V |
possibly damaging |
Het |
| Ushbp1 |
C |
A |
8: 71,842,762 (GRCm39) |
G361* |
probably null |
Het |
| Wbp2nl |
C |
T |
15: 82,197,988 (GRCm39) |
A175V |
probably benign |
Het |
| Zc3h12d |
A |
G |
10: 7,738,330 (GRCm39) |
E212G |
probably damaging |
Het |
|
| Other mutations in Golgb1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01394:Golgb1
|
APN |
16 |
36,751,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01717:Golgb1
|
APN |
16 |
36,735,864 (GRCm39) |
nonsense |
probably null |
|
|
IGL01965:Golgb1
|
APN |
16 |
36,738,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02128:Golgb1
|
APN |
16 |
36,736,666 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02268:Golgb1
|
APN |
16 |
36,733,490 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02383:Golgb1
|
APN |
16 |
36,706,562 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02444:Golgb1
|
APN |
16 |
36,728,178 (GRCm39) |
splice site |
probably benign |
|
|
IGL02635:Golgb1
|
APN |
16 |
36,735,375 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02655:Golgb1
|
APN |
16 |
36,738,442 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02887:Golgb1
|
APN |
16 |
36,746,211 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02937:Golgb1
|
APN |
16 |
36,736,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02973:Golgb1
|
APN |
16 |
36,732,442 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02982:Golgb1
|
APN |
16 |
36,746,172 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03065:Golgb1
|
APN |
16 |
36,733,228 (GRCm39) |
missense |
probably benign |
0.11 |
|
IGL03109:Golgb1
|
APN |
16 |
36,735,973 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL03323:Golgb1
|
APN |
16 |
36,733,815 (GRCm39) |
nonsense |
probably null |
|
|
I2288:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
|
I2289:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0071:Golgb1
|
UTSW |
16 |
36,735,865 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0071:Golgb1
|
UTSW |
16 |
36,735,865 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0080:Golgb1
|
UTSW |
16 |
36,718,973 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0102:Golgb1
|
UTSW |
16 |
36,695,830 (GRCm39) |
intron |
probably benign |
|
|
R0242:Golgb1
|
UTSW |
16 |
36,695,992 (GRCm39) |
nonsense |
probably null |
|
|
R0276:Golgb1
|
UTSW |
16 |
36,734,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0394:Golgb1
|
UTSW |
16 |
36,695,941 (GRCm39) |
intron |
probably benign |
|
|
R0469:Golgb1
|
UTSW |
16 |
36,751,997 (GRCm39) |
missense |
probably benign |
0.41 |
|
R0522:Golgb1
|
UTSW |
16 |
36,735,567 (GRCm39) |
frame shift |
probably null |
|
|
R0575:Golgb1
|
UTSW |
16 |
36,739,171 (GRCm39) |
missense |
probably benign |
|
|
R0600:Golgb1
|
UTSW |
16 |
36,736,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0608:Golgb1
|
UTSW |
16 |
36,736,692 (GRCm39) |
nonsense |
probably null |
|
|
R0711:Golgb1
|
UTSW |
16 |
36,739,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0785:Golgb1
|
UTSW |
16 |
36,719,152 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0893:Golgb1
|
UTSW |
16 |
36,732,639 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R1163:Golgb1
|
UTSW |
16 |
36,736,488 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R1208:Golgb1
|
UTSW |
16 |
36,735,567 (GRCm39) |
frame shift |
probably null |
|
|
R1315:Golgb1
|
UTSW |
16 |
36,735,262 (GRCm39) |
missense |
probably benign |
0.40 |
|
R1429:Golgb1
|
UTSW |
16 |
36,720,925 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1505:Golgb1
|
UTSW |
16 |
36,740,005 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1537:Golgb1
|
UTSW |
16 |
36,719,150 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1610:Golgb1
|
UTSW |
16 |
36,746,463 (GRCm39) |
missense |
probably benign |
0.25 |
|
R1659:Golgb1
|
UTSW |
16 |
36,707,979 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1769:Golgb1
|
UTSW |
16 |
36,736,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2105:Golgb1
|
UTSW |
16 |
36,735,026 (GRCm39) |
missense |
probably benign |
|
|
R2212:Golgb1
|
UTSW |
16 |
36,707,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2261:Golgb1
|
UTSW |
16 |
36,713,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2352:Golgb1
|
UTSW |
16 |
36,718,921 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2357:Golgb1
|
UTSW |
16 |
36,732,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2400:Golgb1
|
UTSW |
16 |
36,738,828 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R2513:Golgb1
|
UTSW |
16 |
36,735,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R3103:Golgb1
|
UTSW |
16 |
36,715,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3413:Golgb1
|
UTSW |
16 |
36,707,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3748:Golgb1
|
UTSW |
16 |
36,739,274 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3847:Golgb1
|
UTSW |
16 |
36,719,095 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3850:Golgb1
|
UTSW |
16 |
36,719,095 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3936:Golgb1
|
UTSW |
16 |
36,734,418 (GRCm39) |
nonsense |
probably null |
|
|
R3975:Golgb1
|
UTSW |
16 |
36,738,933 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4025:Golgb1
|
UTSW |
16 |
36,735,706 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4369:Golgb1
|
UTSW |
16 |
36,737,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4518:Golgb1
|
UTSW |
16 |
36,749,625 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4600:Golgb1
|
UTSW |
16 |
36,738,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4610:Golgb1
|
UTSW |
16 |
36,738,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4660:Golgb1
|
UTSW |
16 |
36,707,980 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4811:Golgb1
|
UTSW |
16 |
36,711,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4815:Golgb1
|
UTSW |
16 |
36,733,477 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R4835:Golgb1
|
UTSW |
16 |
36,711,769 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4904:Golgb1
|
UTSW |
16 |
36,713,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4916:Golgb1
|
UTSW |
16 |
36,736,480 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5121:Golgb1
|
UTSW |
16 |
36,739,620 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5133:Golgb1
|
UTSW |
16 |
36,711,819 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R5143:Golgb1
|
UTSW |
16 |
36,719,051 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5185:Golgb1
|
UTSW |
16 |
36,695,503 (GRCm39) |
unclassified |
probably benign |
|
|
R5188:Golgb1
|
UTSW |
16 |
36,738,827 (GRCm39) |
missense |
probably benign |
0.13 |
|
R5260:Golgb1
|
UTSW |
16 |
36,733,503 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5297:Golgb1
|
UTSW |
16 |
36,695,978 (GRCm39) |
intron |
probably benign |
|
|
R5386:Golgb1
|
UTSW |
16 |
36,732,677 (GRCm39) |
nonsense |
probably null |
|
|
R5438:Golgb1
|
UTSW |
16 |
36,720,870 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5439:Golgb1
|
UTSW |
16 |
36,720,870 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5494:Golgb1
|
UTSW |
16 |
36,749,045 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5592:Golgb1
|
UTSW |
16 |
36,746,125 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5740:Golgb1
|
UTSW |
16 |
36,739,362 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5862:Golgb1
|
UTSW |
16 |
36,746,453 (GRCm39) |
splice site |
silent |
|
|
R5928:Golgb1
|
UTSW |
16 |
36,732,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6009:Golgb1
|
UTSW |
16 |
36,735,321 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6062:Golgb1
|
UTSW |
16 |
36,735,033 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6102:Golgb1
|
UTSW |
16 |
36,733,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6198:Golgb1
|
UTSW |
16 |
36,713,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6253:Golgb1
|
UTSW |
16 |
36,735,984 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6254:Golgb1
|
UTSW |
16 |
36,734,340 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6321:Golgb1
|
UTSW |
16 |
36,738,559 (GRCm39) |
nonsense |
probably null |
|
|
R6700:Golgb1
|
UTSW |
16 |
36,695,946 (GRCm39) |
intron |
probably benign |
|
|
R6870:Golgb1
|
UTSW |
16 |
36,738,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6882:Golgb1
|
UTSW |
16 |
36,734,352 (GRCm39) |
missense |
probably benign |
|
|
R6944:Golgb1
|
UTSW |
16 |
36,732,475 (GRCm39) |
missense |
probably benign |
|
|
R7108:Golgb1
|
UTSW |
16 |
36,734,083 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7124:Golgb1
|
UTSW |
16 |
36,734,035 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7125:Golgb1
|
UTSW |
16 |
36,738,325 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7187:Golgb1
|
UTSW |
16 |
36,736,512 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7205:Golgb1
|
UTSW |
16 |
36,695,663 (GRCm39) |
missense |
unknown |
|
|
R7206:Golgb1
|
UTSW |
16 |
36,734,111 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7233:Golgb1
|
UTSW |
16 |
36,735,120 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7320:Golgb1
|
UTSW |
16 |
36,736,313 (GRCm39) |
nonsense |
probably null |
|
|
R7367:Golgb1
|
UTSW |
16 |
36,718,908 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7408:Golgb1
|
UTSW |
16 |
36,718,909 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7419:Golgb1
|
UTSW |
16 |
36,733,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7556:Golgb1
|
UTSW |
16 |
36,736,155 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7599:Golgb1
|
UTSW |
16 |
36,695,758 (GRCm39) |
missense |
unknown |
|
|
R7673:Golgb1
|
UTSW |
16 |
36,734,031 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7789:Golgb1
|
UTSW |
16 |
36,695,761 (GRCm39) |
missense |
unknown |
|
|
R7792:Golgb1
|
UTSW |
16 |
36,739,092 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7830:Golgb1
|
UTSW |
16 |
36,719,083 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7847:Golgb1
|
UTSW |
16 |
36,752,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7905:Golgb1
|
UTSW |
16 |
36,734,047 (GRCm39) |
missense |
probably benign |
|
|
R7944:Golgb1
|
UTSW |
16 |
36,734,466 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7945:Golgb1
|
UTSW |
16 |
36,734,466 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7950:Golgb1
|
UTSW |
16 |
36,735,786 (GRCm39) |
missense |
probably benign |
0.13 |
|
R8040:Golgb1
|
UTSW |
16 |
36,733,841 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8077:Golgb1
|
UTSW |
16 |
36,738,995 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8181:Golgb1
|
UTSW |
16 |
36,737,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8370:Golgb1
|
UTSW |
16 |
36,732,679 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8684:Golgb1
|
UTSW |
16 |
36,734,764 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8725:Golgb1
|
UTSW |
16 |
36,739,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8727:Golgb1
|
UTSW |
16 |
36,739,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8738:Golgb1
|
UTSW |
16 |
36,736,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8785:Golgb1
|
UTSW |
16 |
36,740,106 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8824:Golgb1
|
UTSW |
16 |
36,736,051 (GRCm39) |
missense |
probably benign |
|
|
R8825:Golgb1
|
UTSW |
16 |
36,739,809 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8940:Golgb1
|
UTSW |
16 |
36,736,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8962:Golgb1
|
UTSW |
16 |
36,733,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9245:Golgb1
|
UTSW |
16 |
36,739,181 (GRCm39) |
nonsense |
probably null |
|
|
R9365:Golgb1
|
UTSW |
16 |
36,736,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9612:Golgb1
|
UTSW |
16 |
36,739,967 (GRCm39) |
missense |
probably benign |
0.41 |
|
R9620:Golgb1
|
UTSW |
16 |
36,739,811 (GRCm39) |
missense |
probably benign |
|
|
R9691:Golgb1
|
UTSW |
16 |
36,718,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9747:Golgb1
|
UTSW |
16 |
36,713,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
V1662:Golgb1
|
UTSW |
16 |
36,718,904 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0067:Golgb1
|
UTSW |
16 |
36,734,665 (GRCm39) |
nonsense |
probably null |
|
|
Z1088:Golgb1
|
UTSW |
16 |
36,740,104 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
|
| Posted On |
2013-08-19 |
Incidental Mutation