Incidental Mutation 'RF020:Cluh'
| ID |
603826 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cluh
|
| Ensembl Gene |
ENSMUSG00000020741 |
| Gene Name |
clustered mitochondria homolog |
| Synonyms |
1300001I01Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.227)
|
| Stock # |
RF020 (G1)
|
| Quality Score |
201.873 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
74540321-74561673 bp(+) (GRCm39) |
| Type of Mutation |
small insertion (2 aa in frame mutation) |
| DNA Base Change (assembly) |
G to GCCAGAT
at 74560364 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113371
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021091]
[ENSMUST00000092915]
[ENSMUST00000102520]
[ENSMUST00000117818]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021091
|
| SMART Domains |
Protein: ENSMUSP00000021091
Gene: ENSMUSG00000020745
| Domain | Start | End | E-Value | Type |
|---|
|
LisH
|
7 |
39 |
6.12e-7 |
SMART |
|
WD40
|
97 |
136 |
2.1e-7 |
SMART |
|
WD40
|
139 |
178 |
9.73e-12 |
SMART |
|
WD40
|
181 |
220 |
1.1e-10 |
SMART |
|
WD40
|
223 |
262 |
9.3e-9 |
SMART |
|
WD40
|
265 |
324 |
4.65e-9 |
SMART |
|
WD40
|
327 |
366 |
4.11e-10 |
SMART |
|
WD40
|
369 |
408 |
8.81e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092915
|
| SMART Domains |
Protein: ENSMUSP00000090593
Gene: ENSMUSG00000020741
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CLU_N
|
104 |
177 |
3.1e-28 |
PFAM |
|
Pfam:CLU
|
394 |
614 |
3.4e-89 |
PFAM |
|
Pfam:eIF3_p135
|
806 |
988 |
1.3e-58 |
PFAM |
|
Pfam:TPR_10
|
1059 |
1100 |
2.9e-7 |
PFAM |
|
low complexity region
|
1114 |
1125 |
N/A |
INTRINSIC |
|
Pfam:TPR_12
|
1140 |
1218 |
1.7e-10 |
PFAM |
|
low complexity region
|
1316 |
1334 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102520
|
| SMART Domains |
Protein: ENSMUSP00000099578
Gene: ENSMUSG00000020745
| Domain | Start | End | E-Value | Type |
|---|
|
LisH
|
7 |
39 |
6.12e-7 |
SMART |
|
WD40
|
97 |
136 |
2.1e-7 |
SMART |
|
WD40
|
139 |
178 |
9.73e-12 |
SMART |
|
WD40
|
181 |
220 |
1.1e-10 |
SMART |
|
WD40
|
223 |
262 |
9.3e-9 |
SMART |
|
WD40
|
265 |
324 |
4.65e-9 |
SMART |
|
WD40
|
327 |
366 |
4.11e-10 |
SMART |
|
WD40
|
369 |
408 |
8.81e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000117818
|
| SMART Domains |
Protein: ENSMUSP00000113371
Gene: ENSMUSG00000020741
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CLU_N
|
102 |
177 |
9.8e-30 |
PFAM |
|
Pfam:CLU
|
394 |
615 |
5.3e-92 |
PFAM |
|
Pfam:eIF3_p135
|
796 |
938 |
2.9e-38 |
PFAM |
|
Pfam:TPR_10
|
1008 |
1049 |
9.5e-7 |
PFAM |
|
low complexity region
|
1063 |
1074 |
N/A |
INTRINSIC |
|
Pfam:TPR_12
|
1089 |
1167 |
1.1e-9 |
PFAM |
|
low complexity region
|
1265 |
1283 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.3%
- 20x: 98.5%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Constitutive homozygous KO affects liver mitochondrial function and leads to neonatal lethality. Conditional homozygous KO in the adult liver affects cellular respiration under energy stress conditions. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca16 |
A |
G |
7: 120,132,880 (GRCm39) |
K1270E |
possibly damaging |
Het |
| Adgrb2 |
T |
C |
4: 129,903,877 (GRCm39) |
S668P |
probably damaging |
Het |
| Ahdc1 |
T |
G |
4: 132,791,588 (GRCm39) |
L943R |
possibly damaging |
Het |
| Ank2 |
T |
C |
3: 126,739,125 (GRCm39) |
K2253R |
unknown |
Het |
| Arhgap23 |
T |
C |
11: 97,354,387 (GRCm39) |
S767P |
probably damaging |
Het |
| Arhgef12 |
A |
G |
9: 42,901,285 (GRCm39) |
I839T |
possibly damaging |
Het |
| Begain |
CGCCGC |
CGCCGCGGCCGC |
12: 108,999,350 (GRCm39) |
|
probably benign |
Het |
| Btbd19 |
A |
T |
4: 116,979,472 (GRCm39) |
C116S |
probably damaging |
Het |
| Cbr1 |
C |
T |
16: 93,407,067 (GRCm39) |
A261V |
probably benign |
Het |
| Ccdc137 |
A |
G |
11: 120,349,022 (GRCm39) |
R18G |
probably benign |
Het |
| Cdsn |
AG |
AGACAGGAAGTAGTAGCTCTCAG |
17: 35,865,876 (GRCm39) |
|
probably benign |
Het |
| Celsr3 |
C |
T |
9: 108,726,256 (GRCm39) |
R3162C |
probably benign |
Het |
| Cep350 |
A |
T |
1: 155,791,224 (GRCm39) |
V1300E |
probably benign |
Het |
| Cmya5 |
G |
T |
13: 93,205,799 (GRCm39) |
Q3357K |
possibly damaging |
Het |
| Col6a2 |
T |
G |
10: 76,442,043 (GRCm39) |
|
probably null |
Het |
| Cyp2j9 |
T |
A |
4: 96,465,889 (GRCm39) |
T315S |
probably damaging |
Het |
| Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
| Dnah6 |
T |
A |
6: 73,095,040 (GRCm39) |
Y2181F |
probably benign |
Het |
| Dnah7b |
A |
G |
1: 46,412,421 (GRCm39) |
D4010G |
possibly damaging |
Het |
| E4f1 |
CCG |
CCGACG |
17: 24,674,169 (GRCm39) |
|
probably benign |
Het |
| Ep300 |
A |
T |
15: 81,470,772 (GRCm39) |
|
probably benign |
Het |
| Fam234a |
A |
G |
17: 26,437,725 (GRCm39) |
V90A |
probably benign |
Het |
| Gab3 |
TCT |
TCTGCT |
X: 74,043,623 (GRCm39) |
|
probably benign |
Het |
| Gal3st1 |
A |
G |
11: 3,948,153 (GRCm39) |
Y120C |
possibly damaging |
Het |
| Garin5a |
GGA |
GGAAGGGTGGATCCTGGATACCTGGGTCTGAGGGAAGA |
7: 44,149,959 (GRCm39) |
|
probably null |
Het |
| Gm5475 |
GTGGAAGGAAAGGT |
G |
15: 100,325,030 (GRCm39) |
|
probably null |
Het |
| Gm6665 |
T |
TC |
18: 31,953,430 (GRCm39) |
|
probably null |
Het |
| Hdlbp |
T |
C |
1: 93,368,456 (GRCm39) |
T8A |
probably benign |
Het |
| Hnrnpa2b1 |
T |
A |
6: 51,443,674 (GRCm39) |
K92N |
probably damaging |
Het |
| Hsdl2 |
GGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
GGAGCAGCCACAGCTGCAGGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
4: 59,610,640 (GRCm39) |
|
probably benign |
Het |
| Klhl10 |
C |
G |
11: 100,332,896 (GRCm39) |
Q14E |
probably benign |
Het |
| Klra2 |
GAAAGAAATCCA |
GAAAGAAATCCAAAGAAATCCA |
6: 131,198,801 (GRCm39) |
|
probably null |
Het |
| Kmt2b |
CC |
CCTCCTGC |
7: 30,285,807 (GRCm39) |
|
probably benign |
Het |
| Krt1c |
A |
G |
15: 101,726,403 (GRCm39) |
I45T |
unknown |
Het |
| Ksr2 |
T |
C |
5: 117,693,283 (GRCm39) |
S244P |
probably benign |
Het |
| Lama5 |
A |
T |
2: 179,837,971 (GRCm39) |
M915K |
probably benign |
Het |
| Lrp1b |
A |
C |
2: 41,660,858 (GRCm39) |
H197Q |
|
Het |
| Lrrc1 |
T |
C |
9: 77,359,913 (GRCm39) |
E293G |
probably damaging |
Het |
| Med12l |
AACA |
AACAACA |
3: 59,183,379 (GRCm39) |
|
probably benign |
Het |
| Mgam |
T |
A |
6: 40,662,243 (GRCm39) |
Y1179N |
probably damaging |
Het |
| Mgat4c |
A |
G |
10: 102,224,928 (GRCm39) |
I381V |
probably benign |
Het |
| Mrgprx1 |
A |
AGAC |
7: 47,671,259 (GRCm39) |
|
probably benign |
Het |
| Myc |
A |
T |
15: 61,857,672 (GRCm39) |
|
probably benign |
Het |
| Nipbl |
A |
G |
15: 8,388,418 (GRCm39) |
S401P |
probably damaging |
Het |
| Nlrp9c |
A |
T |
7: 26,084,649 (GRCm39) |
I310N |
probably benign |
Het |
| Nwd2 |
C |
A |
5: 63,963,066 (GRCm39) |
Y883* |
probably null |
Het |
| Oas1e |
T |
A |
5: 120,932,383 (GRCm39) |
T87S |
possibly damaging |
Het |
| Or10n7-ps1 |
GA |
GATACA |
9: 39,598,049 (GRCm39) |
|
probably null |
Het |
| Or51a5 |
A |
T |
7: 102,771,098 (GRCm39) |
C294S |
probably benign |
Het |
| Or52d3 |
A |
G |
7: 104,229,497 (GRCm39) |
M215V |
probably benign |
Het |
| Or8b38 |
G |
A |
9: 37,972,620 (GRCm39) |
M1I |
probably null |
Het |
| Pappa |
T |
G |
4: 65,123,282 (GRCm39) |
S872R |
possibly damaging |
Het |
| Parp4 |
T |
C |
14: 56,884,806 (GRCm39) |
L1295P |
unknown |
Het |
| Pcdh15 |
A |
T |
10: 74,021,242 (GRCm39) |
Y152F |
probably damaging |
Het |
| Pdk1 |
A |
T |
2: 71,714,240 (GRCm39) |
I217L |
possibly damaging |
Het |
| Phldb1 |
A |
C |
9: 44,609,243 (GRCm39) |
C450W |
probably damaging |
Het |
| Pnma8a |
C |
CCATGATGCACCTGCTTCAACATCA |
7: 16,695,376 (GRCm39) |
|
probably benign |
Het |
| Prl2c5 |
G |
A |
13: 13,360,497 (GRCm39) |
G55S |
probably benign |
Het |
| Psme2b |
A |
T |
11: 48,836,397 (GRCm39) |
H183Q |
probably damaging |
Het |
| Ptms |
CCTCCTC |
CCTCCTCCTC |
6: 124,891,412 (GRCm39) |
|
probably benign |
Het |
| Rln3 |
T |
C |
8: 84,769,931 (GRCm39) |
T73A |
probably benign |
Het |
| Rprd1a |
T |
A |
18: 24,663,062 (GRCm39) |
Q21L |
probably damaging |
Het |
| Septin3 |
A |
T |
15: 82,168,662 (GRCm39) |
D155V |
probably damaging |
Het |
| Sh3rf3 |
T |
A |
10: 58,649,590 (GRCm39) |
V65E |
probably damaging |
Het |
| Shank3 |
A |
G |
15: 89,384,593 (GRCm39) |
N155S |
probably benign |
Het |
| Shox2 |
G |
T |
3: 66,881,146 (GRCm39) |
P278Q |
probably damaging |
Het |
| Slc1a1 |
T |
C |
19: 28,856,555 (GRCm39) |
|
probably null |
Het |
| Slc39a10 |
A |
T |
1: 46,849,175 (GRCm39) |
F814I |
probably damaging |
Het |
| Slc5a1 |
T |
C |
5: 33,290,773 (GRCm39) |
I119T |
probably damaging |
Het |
| Slc6a13 |
T |
C |
6: 121,301,310 (GRCm39) |
|
probably null |
Het |
| Spmap2l |
CAGCGATCCTCCCCAGTCCCGCAAGGC |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAGCGATCCTCCCCAGTCCCGCAAGGC |
5: 77,164,247 (GRCm39) |
|
probably benign |
Het |
| Spta1 |
A |
G |
1: 174,041,010 (GRCm39) |
D1270G |
probably benign |
Het |
| Spta1 |
T |
A |
1: 174,045,469 (GRCm39) |
F1542L |
probably damaging |
Het |
| Tacc3 |
T |
A |
5: 33,818,568 (GRCm39) |
M1K |
probably null |
Het |
| Tax1bp1 |
T |
C |
6: 52,698,339 (GRCm39) |
V17A |
probably damaging |
Het |
| Tmem156 |
T |
A |
5: 65,248,890 (GRCm39) |
E3D |
probably benign |
Het |
| Tmem209 |
T |
A |
6: 30,487,417 (GRCm39) |
M530L |
probably benign |
Het |
| Trpc2 |
A |
G |
7: 101,745,433 (GRCm39) |
D883G |
unknown |
Het |
| Tsen34 |
GGAGCCAAAAT |
G |
7: 3,698,795 (GRCm39) |
|
probably null |
Het |
| Uhrf2 |
T |
C |
19: 30,063,791 (GRCm39) |
Y585H |
probably damaging |
Het |
| Vmn1r26 |
T |
A |
6: 57,985,705 (GRCm39) |
K161N |
probably benign |
Het |
| Vmn1r29 |
A |
G |
6: 58,284,528 (GRCm39) |
S83G |
probably benign |
Het |
| Vps13b |
G |
T |
15: 35,925,552 (GRCm39) |
W3829L |
probably null |
Het |
| Vwce |
G |
A |
19: 10,630,449 (GRCm39) |
G503R |
probably damaging |
Het |
| Zc3h11a |
T |
C |
1: 133,554,735 (GRCm39) |
E415G |
possibly damaging |
Het |
| Zc3h14 |
T |
A |
12: 98,746,541 (GRCm39) |
|
probably null |
Het |
| Zfp119b |
A |
T |
17: 56,246,499 (GRCm39) |
M229K |
probably benign |
Het |
| Zfp384 |
CCAAGCTCAAGC |
CCAAGC |
6: 125,013,418 (GRCm39) |
|
probably benign |
Het |
| Zfp384 |
GGCCCAGGC |
GGCCCAGGCCCACGCCCAGGC |
6: 125,013,451 (GRCm39) |
|
probably benign |
Het |
| Zyx |
T |
A |
6: 42,334,330 (GRCm39) |
L518Q |
probably damaging |
Het |
|
| Other mutations in Cluh |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00095:Cluh
|
APN |
11 |
74,554,890 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL00858:Cluh
|
APN |
11 |
74,550,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL01380:Cluh
|
APN |
11 |
74,556,772 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02402:Cluh
|
APN |
11 |
74,547,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02620:Cluh
|
APN |
11 |
74,555,893 (GRCm39) |
nonsense |
probably null |
|
|
IGL02990:Cluh
|
APN |
11 |
74,558,591 (GRCm39) |
splice site |
probably null |
|
|
IGL03163:Cluh
|
APN |
11 |
74,556,894 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03208:Cluh
|
APN |
11 |
74,560,332 (GRCm39) |
splice site |
probably null |
|
|
IGL03293:Cluh
|
APN |
11 |
74,556,578 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03408:Cluh
|
APN |
11 |
74,556,779 (GRCm39) |
missense |
probably benign |
0.06 |
|
spent
|
UTSW |
11 |
74,551,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4342:Cluh
|
UTSW |
11 |
74,560,352 (GRCm39) |
small insertion |
probably benign |
|
|
FR4342:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
FR4449:Cluh
|
UTSW |
11 |
74,560,358 (GRCm39) |
small insertion |
probably benign |
|
|
FR4589:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,345 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,359 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Cluh
|
UTSW |
11 |
74,560,346 (GRCm39) |
small insertion |
probably benign |
|
|
R0147:Cluh
|
UTSW |
11 |
74,556,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0153:Cluh
|
UTSW |
11 |
74,548,176 (GRCm39) |
splice site |
probably benign |
|
|
R0506:Cluh
|
UTSW |
11 |
74,555,720 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0526:Cluh
|
UTSW |
11 |
74,556,812 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0834:Cluh
|
UTSW |
11 |
74,554,631 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1873:Cluh
|
UTSW |
11 |
74,552,902 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R1991:Cluh
|
UTSW |
11 |
74,550,355 (GRCm39) |
nonsense |
probably null |
|
|
R1992:Cluh
|
UTSW |
11 |
74,550,828 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2095:Cluh
|
UTSW |
11 |
74,552,550 (GRCm39) |
nonsense |
probably null |
|
|
R2101:Cluh
|
UTSW |
11 |
74,551,328 (GRCm39) |
splice site |
probably benign |
|
|
R2103:Cluh
|
UTSW |
11 |
74,550,355 (GRCm39) |
nonsense |
probably null |
|
|
R2220:Cluh
|
UTSW |
11 |
74,557,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3702:Cluh
|
UTSW |
11 |
74,556,182 (GRCm39) |
missense |
probably benign |
|
|
R3853:Cluh
|
UTSW |
11 |
74,547,279 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3900:Cluh
|
UTSW |
11 |
74,557,930 (GRCm39) |
missense |
probably benign |
0.29 |
|
R4891:Cluh
|
UTSW |
11 |
74,555,885 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R4895:Cluh
|
UTSW |
11 |
74,558,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5056:Cluh
|
UTSW |
11 |
74,552,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5089:Cluh
|
UTSW |
11 |
74,551,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5217:Cluh
|
UTSW |
11 |
74,550,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5346:Cluh
|
UTSW |
11 |
74,556,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5382:Cluh
|
UTSW |
11 |
74,555,935 (GRCm39) |
intron |
probably benign |
|
|
R5516:Cluh
|
UTSW |
11 |
74,551,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5809:Cluh
|
UTSW |
11 |
74,552,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6146:Cluh
|
UTSW |
11 |
74,558,054 (GRCm39) |
splice site |
probably null |
|
|
R6326:Cluh
|
UTSW |
11 |
74,557,068 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6541:Cluh
|
UTSW |
11 |
74,548,040 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6674:Cluh
|
UTSW |
11 |
74,557,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6870:Cluh
|
UTSW |
11 |
74,556,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6875:Cluh
|
UTSW |
11 |
74,552,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7086:Cluh
|
UTSW |
11 |
74,558,166 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7225:Cluh
|
UTSW |
11 |
74,557,232 (GRCm39) |
splice site |
probably null |
|
|
R7310:Cluh
|
UTSW |
11 |
74,560,285 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7317:Cluh
|
UTSW |
11 |
74,556,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7674:Cluh
|
UTSW |
11 |
74,558,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7941:Cluh
|
UTSW |
11 |
74,550,583 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9061:Cluh
|
UTSW |
11 |
74,551,192 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9326:Cluh
|
UTSW |
11 |
74,554,902 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9489:Cluh
|
UTSW |
11 |
74,558,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9605:Cluh
|
UTSW |
11 |
74,558,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
RF032:Cluh
|
UTSW |
11 |
74,560,341 (GRCm39) |
small insertion |
probably benign |
|
|
X0028:Cluh
|
UTSW |
11 |
74,554,292 (GRCm39) |
missense |
probably benign |
0.26 |
|
Z1177:Cluh
|
UTSW |
11 |
74,558,580 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
Z1186:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
Z1186:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,342 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,346 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,347 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,355 (GRCm39) |
small insertion |
probably benign |
|
|
Z1188:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
nonsense |
probably null |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,355 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,349 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,345 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,344 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,358 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,349 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,352 (GRCm39) |
small insertion |
probably benign |
|
|
Z1192:Cluh
|
UTSW |
11 |
74,560,351 (GRCm39) |
small insertion |
probably benign |
|
|
Z1192:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AGTGTCCTGAAAGCTGCAGG -3'
(R):5'- CTTTTAGGGGCAGGCAAACC -3'
Sequencing Primer
(F):5'- TGAAAGCTGCAGGGTGCC -3'
(R):5'- GGTATAAAGTTGAGGACTAGCTTCC -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation