Incidental Mutation 'R2016:Mylk'
| ID |
223101 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mylk
|
| Ensembl Gene |
ENSMUSG00000022836 |
| Gene Name |
myosin, light polypeptide kinase |
| Synonyms |
Mlck, telokin, nmMlck, 9530072E15Rik, A930019C19Rik, MLCK108, MLCK210 |
| MMRRC Submission |
040025-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R2016 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
34565580-34822790 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 34817187 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 61
(V61M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000156149
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023538]
[ENSMUST00000231589]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000023538
AA Change: V1852M
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000023538
Gene: ENSMUSG00000022836
AA Change: V1852M
| Domain | Start | End | E-Value | Type |
|---|
|
IGc2
|
54 |
122 |
9.05e-11 |
SMART |
|
IGc2
|
177 |
244 |
3.94e-11 |
SMART |
|
Pfam:23ISL
|
255 |
409 |
3.6e-60 |
PFAM |
|
IGc2
|
423 |
491 |
1.55e-9 |
SMART |
|
IGc2
|
523 |
587 |
3.32e-18 |
SMART |
|
IGc2
|
632 |
699 |
6.02e-7 |
SMART |
|
IGc2
|
730 |
798 |
1.36e-5 |
SMART |
|
low complexity region
|
827 |
844 |
N/A |
INTRINSIC |
|
IGc2
|
1141 |
1208 |
2.42e-11 |
SMART |
|
low complexity region
|
1251 |
1269 |
N/A |
INTRINSIC |
|
IG
|
1275 |
1359 |
4.56e-7 |
SMART |
|
FN3
|
1362 |
1444 |
2.33e-11 |
SMART |
|
low complexity region
|
1457 |
1479 |
N/A |
INTRINSIC |
|
S_TKc
|
1495 |
1750 |
4.23e-95 |
SMART |
|
IGc2
|
1852 |
1920 |
5.92e-15 |
SMART |
|
low complexity region
|
1934 |
1950 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000231589
AA Change: V61M
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232296
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232477
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232548
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232649
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.5%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene, a muscle member of the immunoglobulin gene superfamily, encodes myosin light chain kinase which is a calcium/calmodulin dependent enzyme. This kinase phosphorylates myosin regulatory light chains to facilitate myosin interaction with actin filaments to produce contractile activity. This gene encodes both smooth muscle and nonmuscle isoforms. In addition, using a separate promoter in an intron in the 3' region, it encodes telokin, a small protein identical in sequence to the C-terminus of myosin light chain kinase, that is independently expressed in smooth muscle and functions to stabilize unphosphorylated myosin filaments. A pseudogene is located on the p arm of chromosome 3. Four transcript variants that produce four isoforms of the calcium/calmodulin dependent enzyme have been identified as well as two transcripts that produce two isoforms of telokin. Additional variants have been identified but lack full length transcripts. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice that lack the isoform abundant in endothelial cells show a reduced susceptibility to acute lung injury. Mice lacking the smooth muscle isoform exhibit partial pre- or neonatal lethality, short small intestine and impaired smooth muscle contraction in the colon. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700025C18Rik |
T |
C |
2: 164,920,946 (GRCm39) |
D29G |
unknown |
Het |
| Abca13 |
A |
T |
11: 9,240,619 (GRCm39) |
L827F |
probably damaging |
Het |
| Abca8a |
A |
G |
11: 109,961,213 (GRCm39) |
F570L |
probably damaging |
Het |
| Adck1 |
T |
A |
12: 88,427,862 (GRCm39) |
I493N |
probably damaging |
Het |
| Adra2c |
T |
C |
5: 35,437,656 (GRCm39) |
C143R |
probably damaging |
Het |
| Afg2a |
T |
C |
3: 37,632,911 (GRCm39) |
V839A |
possibly damaging |
Het |
| Akap13 |
C |
T |
7: 75,354,279 (GRCm39) |
T1800M |
probably damaging |
Het |
| Angpt2 |
T |
C |
8: 18,755,747 (GRCm39) |
N240S |
probably damaging |
Het |
| Apob |
G |
A |
12: 8,057,751 (GRCm39) |
D2078N |
possibly damaging |
Het |
| Atp8b1 |
T |
C |
18: 64,673,405 (GRCm39) |
N989S |
probably damaging |
Het |
| B3gnt2 |
T |
C |
11: 22,786,621 (GRCm39) |
D189G |
probably damaging |
Het |
| Bcam |
G |
A |
7: 19,494,274 (GRCm39) |
T374M |
probably benign |
Het |
| Blm |
T |
C |
7: 80,155,674 (GRCm39) |
D335G |
probably benign |
Het |
| Cbfa2t2 |
T |
C |
2: 154,359,727 (GRCm39) |
L264P |
probably damaging |
Het |
| Col4a2 |
T |
C |
8: 11,495,086 (GRCm39) |
F1515L |
probably benign |
Het |
| Csf2ra |
T |
G |
19: 61,215,331 (GRCm39) |
M95L |
probably benign |
Het |
| Cyp2c70 |
T |
A |
19: 40,152,856 (GRCm39) |
T300S |
possibly damaging |
Het |
| Cyp4f15 |
A |
T |
17: 32,921,133 (GRCm39) |
H440L |
probably damaging |
Het |
| Dcaf1 |
T |
A |
9: 106,716,287 (GRCm39) |
D360E |
probably benign |
Het |
| Ddr2 |
T |
C |
1: 169,812,537 (GRCm39) |
M652V |
probably damaging |
Het |
| Dnah2 |
T |
A |
11: 69,327,896 (GRCm39) |
I3370F |
probably damaging |
Het |
| Dpysl5 |
G |
A |
5: 30,948,941 (GRCm39) |
D399N |
probably damaging |
Het |
| Efemp1 |
G |
T |
11: 28,871,613 (GRCm39) |
R376L |
probably damaging |
Het |
| Efl1 |
A |
C |
7: 82,402,917 (GRCm39) |
D673A |
probably damaging |
Het |
| Eid1 |
A |
G |
2: 125,515,121 (GRCm39) |
M4V |
probably benign |
Het |
| Emc10 |
G |
A |
7: 44,142,616 (GRCm39) |
R109W |
probably damaging |
Het |
| Emilin3 |
G |
A |
2: 160,751,530 (GRCm39) |
R170C |
possibly damaging |
Het |
| Erap1 |
T |
C |
13: 74,812,270 (GRCm39) |
W362R |
probably damaging |
Het |
| Fam234a |
A |
G |
17: 26,437,290 (GRCm39) |
F91L |
probably benign |
Het |
| Flnc |
G |
A |
6: 29,443,796 (GRCm39) |
|
probably null |
Het |
| Fsip2 |
A |
G |
2: 82,813,076 (GRCm39) |
K3132E |
possibly damaging |
Het |
| Garin5b |
A |
T |
7: 4,762,397 (GRCm39) |
I244N |
probably damaging |
Het |
| Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
| Gnl3 |
A |
G |
14: 30,738,326 (GRCm39) |
|
probably null |
Het |
| Has1 |
A |
T |
17: 18,068,532 (GRCm39) |
I274N |
probably damaging |
Het |
| Ift70a1 |
A |
G |
2: 75,811,801 (GRCm39) |
L94P |
probably benign |
Het |
| Itsn1 |
T |
C |
16: 91,702,389 (GRCm39) |
|
probably null |
Het |
| Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
| Kif13a |
T |
C |
13: 46,964,275 (GRCm39) |
D475G |
probably benign |
Het |
| Klhl20 |
A |
T |
1: 160,930,608 (GRCm39) |
M298K |
probably damaging |
Het |
| Kynu |
G |
T |
2: 43,494,289 (GRCm39) |
G241* |
probably null |
Het |
| Lrif1 |
G |
T |
3: 106,639,522 (GRCm39) |
L202F |
possibly damaging |
Het |
| Lrp5 |
T |
C |
19: 3,660,056 (GRCm39) |
K1003E |
probably benign |
Het |
| Mamdc2 |
T |
C |
19: 23,311,393 (GRCm39) |
D487G |
probably damaging |
Het |
| Mapk8ip1 |
A |
G |
2: 92,221,379 (GRCm39) |
|
probably null |
Het |
| Mettl25 |
T |
A |
10: 105,633,167 (GRCm39) |
E425D |
probably benign |
Het |
| Midn |
G |
T |
10: 79,985,949 (GRCm39) |
R13L |
possibly damaging |
Het |
| Mtmr9 |
T |
C |
14: 63,777,713 (GRCm39) |
Y136C |
possibly damaging |
Het |
| Nalcn |
T |
C |
14: 123,831,993 (GRCm39) |
|
probably null |
Het |
| Nle1 |
G |
T |
11: 82,796,373 (GRCm39) |
P166Q |
probably damaging |
Het |
| Nr4a3 |
G |
A |
4: 48,083,252 (GRCm39) |
C595Y |
probably damaging |
Het |
| Or10d4 |
A |
G |
9: 39,580,851 (GRCm39) |
Y166C |
probably damaging |
Het |
| Or4g7 |
G |
T |
2: 111,309,532 (GRCm39) |
M134I |
probably benign |
Het |
| Or4l15 |
A |
G |
14: 50,197,959 (GRCm39) |
I190T |
probably benign |
Het |
| Or5w1b |
C |
T |
2: 87,476,396 (GRCm39) |
V24M |
probably benign |
Het |
| Or8b1 |
A |
T |
9: 38,399,309 (GRCm39) |
|
probably null |
Het |
| Pds5a |
T |
A |
5: 65,805,350 (GRCm39) |
|
probably null |
Het |
| Pitpnm1 |
T |
C |
19: 4,161,873 (GRCm39) |
V955A |
probably benign |
Het |
| Plcb1 |
T |
A |
2: 135,204,340 (GRCm39) |
I898N |
possibly damaging |
Het |
| Plcl2 |
G |
A |
17: 50,913,722 (GRCm39) |
V244M |
probably damaging |
Het |
| Plk1 |
A |
G |
7: 121,761,663 (GRCm39) |
K257R |
probably damaging |
Het |
| Prkcg |
A |
T |
7: 3,372,066 (GRCm39) |
T460S |
probably damaging |
Het |
| Prl7d1 |
G |
A |
13: 27,894,156 (GRCm39) |
H138Y |
probably damaging |
Het |
| Prss35 |
A |
G |
9: 86,637,565 (GRCm39) |
S112G |
probably benign |
Het |
| Ptprj |
C |
T |
2: 90,294,958 (GRCm39) |
V417M |
probably damaging |
Het |
| Pwwp2b |
A |
T |
7: 138,836,067 (GRCm39) |
I503F |
possibly damaging |
Het |
| Rasgrp2 |
T |
C |
19: 6,463,195 (GRCm39) |
V498A |
probably benign |
Het |
| Sall1 |
A |
G |
8: 89,755,037 (GRCm39) |
V1314A |
probably benign |
Het |
| Sema6c |
A |
G |
3: 95,078,545 (GRCm39) |
I549V |
probably benign |
Het |
| Slc17a1 |
A |
G |
13: 24,062,522 (GRCm39) |
S230G |
probably benign |
Het |
| Slc5a4a |
T |
G |
10: 75,989,414 (GRCm39) |
F106V |
probably benign |
Het |
| Stat6 |
T |
C |
10: 127,486,665 (GRCm39) |
L147P |
probably damaging |
Het |
| Taar7d |
T |
A |
10: 23,903,642 (GRCm39) |
S175T |
probably benign |
Het |
| Tasor2 |
A |
T |
13: 3,626,770 (GRCm39) |
I1060K |
probably benign |
Het |
| Tmem132b |
A |
G |
5: 125,700,080 (GRCm39) |
Q206R |
probably benign |
Het |
| Tmem229a |
T |
C |
6: 24,955,061 (GRCm39) |
D231G |
probably benign |
Het |
| Trim66 |
A |
G |
7: 109,071,439 (GRCm39) |
|
probably null |
Het |
| Ttll9 |
A |
T |
2: 152,844,214 (GRCm39) |
E374V |
probably damaging |
Het |
| Vmn2r69 |
A |
T |
7: 85,056,493 (GRCm39) |
D548E |
probably damaging |
Het |
| Zcchc2 |
T |
A |
1: 105,931,851 (GRCm39) |
|
probably null |
Het |
| Zfp282 |
T |
A |
6: 47,874,721 (GRCm39) |
|
probably null |
Het |
| Zfp352 |
A |
G |
4: 90,113,408 (GRCm39) |
E516G |
probably benign |
Het |
|
| Other mutations in Mylk |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01384:Mylk
|
APN |
16 |
34,759,322 (GRCm39) |
missense |
probably benign |
0.36 |
|
IGL01386:Mylk
|
APN |
16 |
34,791,610 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01684:Mylk
|
APN |
16 |
34,792,310 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
IGL01884:Mylk
|
APN |
16 |
34,809,247 (GRCm39) |
splice site |
probably benign |
|
|
IGL02079:Mylk
|
APN |
16 |
34,681,001 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02104:Mylk
|
APN |
16 |
34,635,805 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02624:Mylk
|
APN |
16 |
34,750,266 (GRCm39) |
missense |
probably benign |
0.29 |
|
IGL02756:Mylk
|
APN |
16 |
34,784,016 (GRCm39) |
missense |
probably benign |
0.42 |
|
IGL02794:Mylk
|
APN |
16 |
34,806,911 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL02833:Mylk
|
APN |
16 |
34,735,270 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02946:Mylk
|
APN |
16 |
34,742,158 (GRCm39) |
missense |
probably benign |
0.10 |
|
IGL03012:Mylk
|
APN |
16 |
34,773,151 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03093:Mylk
|
APN |
16 |
34,732,562 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL03272:Mylk
|
APN |
16 |
34,799,559 (GRCm39) |
missense |
probably benign |
0.09 |
|
billy
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
|
brutus
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
|
Club
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
|
popeye
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
|
F5770:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
|
P4717OSA:Mylk
|
UTSW |
16 |
34,797,483 (GRCm39) |
splice site |
probably benign |
|
|
PIT4382001:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0131:Mylk
|
UTSW |
16 |
34,695,874 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0309:Mylk
|
UTSW |
16 |
34,732,667 (GRCm39) |
splice site |
probably benign |
|
|
R0358:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0381:Mylk
|
UTSW |
16 |
34,605,344 (GRCm39) |
splice site |
probably null |
|
|
R0390:Mylk
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0413:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0536:Mylk
|
UTSW |
16 |
34,820,757 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0544:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0545:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0546:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0547:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0548:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0627:Mylk
|
UTSW |
16 |
34,820,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0726:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0755:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0782:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0783:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0784:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1136:Mylk
|
UTSW |
16 |
34,820,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1170:Mylk
|
UTSW |
16 |
34,694,409 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1222:Mylk
|
UTSW |
16 |
34,681,022 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1445:Mylk
|
UTSW |
16 |
34,635,835 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R1583:Mylk
|
UTSW |
16 |
34,695,956 (GRCm39) |
missense |
probably benign |
0.29 |
|
R1618:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1643:Mylk
|
UTSW |
16 |
34,696,005 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1702:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1776:Mylk
|
UTSW |
16 |
34,773,152 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1865:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1975:Mylk
|
UTSW |
16 |
34,700,673 (GRCm39) |
splice site |
probably null |
|
|
R2045:Mylk
|
UTSW |
16 |
34,774,023 (GRCm39) |
missense |
probably benign |
0.29 |
|
R2134:Mylk
|
UTSW |
16 |
34,806,846 (GRCm39) |
missense |
probably benign |
0.13 |
|
R3547:Mylk
|
UTSW |
16 |
34,700,538 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R3844:Mylk
|
UTSW |
16 |
34,742,247 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4003:Mylk
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
|
R4396:Mylk
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
|
R4470:Mylk
|
UTSW |
16 |
34,732,522 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4507:Mylk
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4700:Mylk
|
UTSW |
16 |
34,742,805 (GRCm39) |
missense |
probably benign |
0.16 |
|
R4751:Mylk
|
UTSW |
16 |
34,699,539 (GRCm39) |
missense |
probably benign |
0.29 |
|
R4815:Mylk
|
UTSW |
16 |
34,715,295 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4832:Mylk
|
UTSW |
16 |
34,742,737 (GRCm39) |
missense |
probably benign |
0.36 |
|
R4872:Mylk
|
UTSW |
16 |
34,735,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4953:Mylk
|
UTSW |
16 |
34,809,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4969:Mylk
|
UTSW |
16 |
34,791,810 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5009:Mylk
|
UTSW |
16 |
34,719,877 (GRCm39) |
missense |
probably benign |
0.39 |
|
R5130:Mylk
|
UTSW |
16 |
34,809,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5173:Mylk
|
UTSW |
16 |
34,797,383 (GRCm39) |
missense |
probably benign |
0.40 |
|
R5195:Mylk
|
UTSW |
16 |
34,799,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5209:Mylk
|
UTSW |
16 |
34,742,995 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R5311:Mylk
|
UTSW |
16 |
34,742,127 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5418:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5481:Mylk
|
UTSW |
16 |
34,741,974 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5590:Mylk
|
UTSW |
16 |
34,699,722 (GRCm39) |
missense |
probably benign |
0.29 |
|
R5603:Mylk
|
UTSW |
16 |
34,776,862 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5823:Mylk
|
UTSW |
16 |
34,715,317 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6290:Mylk
|
UTSW |
16 |
34,715,213 (GRCm39) |
missense |
probably benign |
0.39 |
|
R6351:Mylk
|
UTSW |
16 |
34,742,341 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6365:Mylk
|
UTSW |
16 |
34,680,961 (GRCm39) |
missense |
probably benign |
0.12 |
|
R6490:Mylk
|
UTSW |
16 |
34,750,237 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R6723:Mylk
|
UTSW |
16 |
34,750,258 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R6864:Mylk
|
UTSW |
16 |
34,694,520 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6908:Mylk
|
UTSW |
16 |
34,700,643 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6949:Mylk
|
UTSW |
16 |
34,820,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7018:Mylk
|
UTSW |
16 |
34,820,796 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7035:Mylk
|
UTSW |
16 |
34,797,352 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7162:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7236:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7269:Mylk
|
UTSW |
16 |
34,605,381 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7475:Mylk
|
UTSW |
16 |
34,734,446 (GRCm39) |
splice site |
probably null |
|
|
R7525:Mylk
|
UTSW |
16 |
34,809,357 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7587:Mylk
|
UTSW |
16 |
34,742,887 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7607:Mylk
|
UTSW |
16 |
34,715,184 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7616:Mylk
|
UTSW |
16 |
34,699,927 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7647:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7648:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7764:Mylk
|
UTSW |
16 |
34,742,553 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7890:Mylk
|
UTSW |
16 |
34,784,018 (GRCm39) |
nonsense |
probably null |
|
|
R7892:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7893:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
|
R8065:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8067:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8143:Mylk
|
UTSW |
16 |
34,734,525 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R8210:Mylk
|
UTSW |
16 |
34,820,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8271:Mylk
|
UTSW |
16 |
34,742,949 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8540:Mylk
|
UTSW |
16 |
34,750,257 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R8721:Mylk
|
UTSW |
16 |
34,817,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8743:Mylk
|
UTSW |
16 |
34,741,427 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8798:Mylk
|
UTSW |
16 |
34,719,772 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8956:Mylk
|
UTSW |
16 |
34,791,779 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9131:Mylk
|
UTSW |
16 |
34,776,835 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9403:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
nonsense |
probably null |
|
|
R9624:Mylk
|
UTSW |
16 |
34,699,677 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9735:Mylk
|
UTSW |
16 |
34,735,179 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9756:Mylk
|
UTSW |
16 |
34,734,387 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9763:Mylk
|
UTSW |
16 |
34,699,482 (GRCm39) |
nonsense |
probably null |
|
|
RF001:Mylk
|
UTSW |
16 |
34,699,741 (GRCm39) |
missense |
probably benign |
0.03 |
|
V7580:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
|
V7583:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0065:Mylk
|
UTSW |
16 |
34,820,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Mylk
|
UTSW |
16 |
34,743,021 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCACTTCCCTAAGCAGCACTATT -3'
(R):5'- AAGGTAAAGGGGCCCAGTGT -3'
Sequencing Primer
(F):5'- TTATAGAAACTTTAAGGGGGAGGG -3'
(R):5'- GGCCCAGTGTCCCTTTG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation