Incidental Mutation 'R9469:Myocd'
| ID |
715372 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myocd
|
| Ensembl Gene |
ENSMUSG00000020542 |
| Gene Name |
myocardin |
| Synonyms |
Srfcp |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9469 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
65067387-65160815 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 65087220 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 236
(S236P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104335
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000101042]
[ENSMUST00000102635]
[ENSMUST00000108695]
|
| AlphaFold |
Q8VIM5 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000101042
AA Change: S108P
PolyPhen 2
Score 0.497 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000098603
Gene: ENSMUSG00000020542
AA Change: S108P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
32 |
N/A |
INTRINSIC |
|
low complexity region
|
119 |
132 |
N/A |
INTRINSIC |
|
SCOP:d1lsha3
|
140 |
221 |
4e-3 |
SMART |
|
SAP
|
252 |
286 |
1.29e-8 |
SMART |
|
low complexity region
|
326 |
343 |
N/A |
INTRINSIC |
|
low complexity region
|
371 |
383 |
N/A |
INTRINSIC |
|
coiled coil region
|
396 |
435 |
N/A |
INTRINSIC |
|
low complexity region
|
557 |
573 |
N/A |
INTRINSIC |
|
low complexity region
|
615 |
629 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000102635
AA Change: S236P
PolyPhen 2
Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000099695
Gene: ENSMUSG00000020542
AA Change: S236P
| Domain | Start | End | E-Value | Type |
|---|
|
RPEL
|
18 |
43 |
4e-1 |
SMART |
|
RPEL
|
62 |
87 |
9.26e0 |
SMART |
|
RPEL
|
106 |
131 |
1.15e-6 |
SMART |
|
low complexity region
|
147 |
160 |
N/A |
INTRINSIC |
|
low complexity region
|
247 |
260 |
N/A |
INTRINSIC |
|
SCOP:d1lsha3
|
268 |
349 |
4e-3 |
SMART |
|
SAP
|
380 |
414 |
1.29e-8 |
SMART |
|
low complexity region
|
454 |
471 |
N/A |
INTRINSIC |
|
low complexity region
|
499 |
511 |
N/A |
INTRINSIC |
|
coiled coil region
|
524 |
563 |
N/A |
INTRINSIC |
|
low complexity region
|
695 |
709 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108695
AA Change: S236P
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000104335
Gene: ENSMUSG00000020542
AA Change: S236P
| Domain | Start | End | E-Value | Type |
|---|
|
RPEL
|
18 |
43 |
4e-1 |
SMART |
|
RPEL
|
62 |
87 |
9.26e0 |
SMART |
|
RPEL
|
106 |
131 |
1.15e-6 |
SMART |
|
low complexity region
|
147 |
160 |
N/A |
INTRINSIC |
|
low complexity region
|
247 |
260 |
N/A |
INTRINSIC |
|
SCOP:d1lsha3
|
268 |
349 |
5e-3 |
SMART |
|
SAP
|
380 |
414 |
1.29e-8 |
SMART |
|
low complexity region
|
454 |
471 |
N/A |
INTRINSIC |
|
low complexity region
|
499 |
511 |
N/A |
INTRINSIC |
|
coiled coil region
|
524 |
563 |
N/A |
INTRINSIC |
|
low complexity region
|
685 |
701 |
N/A |
INTRINSIC |
|
low complexity region
|
743 |
757 |
N/A |
INTRINSIC |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000115572
Gene: ENSMUSG00000020542
AA Change: S110P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
22 |
35 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
135 |
N/A |
INTRINSIC |
|
low complexity region
|
160 |
195 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.0955 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear protein, which is expressed in heart, aorta, and in smooth muscle cell-containing tissues. It functions as a transcriptional co-activator of serum response factor (SRF) and modulates expression of cardiac and smooth muscle-specific SRF-target genes, and thus may play a crucial role in cardiogenesis and differentiation of the smooth muscle cell lineage. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
PHENOTYPE: Mice homozygous for a null mutation exhibit embryonic lethality and fail to form vascular smooth muscle. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acsbg3 |
A |
T |
17: 57,183,283 (GRCm39) |
D8V |
probably benign |
Het |
| Ada |
T |
A |
2: 163,574,192 (GRCm39) |
M155L |
probably benign |
Het |
| Adam23 |
A |
G |
1: 63,584,671 (GRCm39) |
I360V |
probably benign |
Het |
| Ahnak |
G |
A |
19: 8,988,225 (GRCm39) |
G3170R |
probably damaging |
Het |
| Alb |
G |
A |
5: 90,610,659 (GRCm39) |
D80N |
probably benign |
Het |
| Amph |
G |
T |
13: 19,270,769 (GRCm39) |
G126V |
probably damaging |
Het |
| Anks1b |
A |
T |
10: 90,733,205 (GRCm39) |
M994L |
possibly damaging |
Het |
| Atp8a2 |
A |
G |
14: 60,028,668 (GRCm39) |
L933P |
probably benign |
Het |
| Bcas1 |
T |
C |
2: 170,191,292 (GRCm39) |
D546G |
possibly damaging |
Het |
| Bmpr2 |
A |
C |
1: 59,881,928 (GRCm39) |
M186L |
probably benign |
Het |
| Clca3a2 |
T |
C |
3: 144,507,938 (GRCm39) |
I711V |
probably damaging |
Het |
| Cobll1 |
G |
A |
2: 64,966,774 (GRCm39) |
T128I |
probably damaging |
Het |
| Cog4 |
T |
C |
8: 111,608,804 (GRCm39) |
W165R |
unknown |
Het |
| Cyp2j5 |
G |
A |
4: 96,517,731 (GRCm39) |
R494* |
probably null |
Het |
| Dnah2 |
G |
A |
11: 69,321,896 (GRCm39) |
A3808V |
probably damaging |
Het |
| Dnah5 |
A |
T |
15: 28,421,146 (GRCm39) |
T3828S |
probably benign |
Het |
| Dsg1c |
T |
C |
18: 20,400,947 (GRCm39) |
I150T |
probably damaging |
Het |
| Ehd2 |
A |
T |
7: 15,684,332 (GRCm39) |
I489N |
probably damaging |
Het |
| Fam24a |
C |
A |
7: 130,938,392 (GRCm39) |
T94K |
probably damaging |
Het |
| Gata2 |
A |
G |
6: 88,182,301 (GRCm39) |
E423G |
possibly damaging |
Het |
| Gm8947 |
A |
G |
1: 151,069,063 (GRCm39) |
I299V |
unknown |
Het |
| Gpr161 |
A |
G |
1: 165,133,896 (GRCm39) |
I53V |
possibly damaging |
Het |
| Guca2b |
G |
A |
4: 119,515,817 (GRCm39) |
Q15* |
probably null |
Het |
| Hus1 |
A |
G |
11: 8,948,744 (GRCm39) |
V219A |
probably benign |
Het |
| Il5 |
T |
C |
11: 53,614,824 (GRCm39) |
W129R |
probably damaging |
Het |
| Ipmk |
A |
G |
10: 71,201,843 (GRCm39) |
Y77C |
probably damaging |
Het |
| Kcnip3 |
A |
G |
2: 127,307,322 (GRCm39) |
L136P |
probably benign |
Het |
| Klhl2 |
G |
A |
8: 65,196,069 (GRCm39) |
A558V |
probably benign |
Het |
| Klra5 |
C |
A |
6: 129,883,686 (GRCm39) |
W147L |
possibly damaging |
Het |
| Lig3 |
G |
A |
11: 82,686,199 (GRCm39) |
C613Y |
probably benign |
Het |
| Lrriq1 |
A |
G |
10: 103,050,761 (GRCm39) |
S664P |
probably benign |
Het |
| Megf6 |
A |
G |
4: 154,335,369 (GRCm39) |
Y276C |
probably damaging |
Het |
| Mlph |
A |
G |
1: 90,856,068 (GRCm39) |
E119G |
probably damaging |
Het |
| Mrpl39 |
T |
G |
16: 84,517,170 (GRCm39) |
R316S |
probably damaging |
Het |
| Myo18b |
T |
C |
5: 112,994,247 (GRCm39) |
D902G |
probably benign |
Het |
| Myom1 |
G |
T |
17: 71,368,122 (GRCm39) |
A482S |
possibly damaging |
Het |
| Nol4 |
A |
G |
18: 23,085,318 (GRCm39) |
V32A |
probably damaging |
Het |
| Nrp2 |
T |
C |
1: 62,804,030 (GRCm39) |
Y555H |
probably damaging |
Het |
| Or12d12 |
T |
C |
17: 37,610,956 (GRCm39) |
D119G |
probably damaging |
Het |
| Or4d10c |
G |
A |
19: 12,065,434 (GRCm39) |
H241Y |
probably benign |
Het |
| Or52l1 |
A |
T |
7: 104,829,967 (GRCm39) |
H199Q |
probably damaging |
Het |
| Or8k27 |
C |
A |
2: 86,275,787 (GRCm39) |
D180Y |
probably damaging |
Het |
| Papss1 |
A |
G |
3: 131,288,959 (GRCm39) |
K175E |
possibly damaging |
Het |
| Pdcd5 |
T |
C |
7: 35,343,827 (GRCm39) |
M39V |
probably benign |
Het |
| Plcl2 |
G |
A |
17: 50,913,953 (GRCm39) |
D321N |
probably benign |
Het |
| Plxna4 |
G |
A |
6: 32,494,526 (GRCm39) |
P30L |
probably benign |
Het |
| Pou2f1 |
G |
A |
1: 165,740,830 (GRCm39) |
T113I |
probably benign |
Het |
| Ptpn2 |
T |
A |
18: 67,808,907 (GRCm39) |
H303L |
probably benign |
Het |
| R3hdm1 |
T |
A |
1: 128,106,921 (GRCm39) |
|
probably null |
Het |
| Rdx |
T |
C |
9: 51,977,069 (GRCm39) |
V106A |
probably damaging |
Het |
| Ripk2 |
T |
C |
4: 16,138,181 (GRCm39) |
D249G |
possibly damaging |
Het |
| Rnf169 |
A |
T |
7: 99,575,567 (GRCm39) |
S343T |
possibly damaging |
Het |
| Rnf40 |
T |
A |
7: 127,195,769 (GRCm39) |
L671Q |
probably damaging |
Het |
| Scube3 |
C |
A |
17: 28,386,138 (GRCm39) |
S793* |
probably null |
Het |
| Sipa1l3 |
A |
T |
7: 29,028,481 (GRCm39) |
M1633K |
possibly damaging |
Het |
| Slc16a14 |
A |
T |
1: 84,900,612 (GRCm39) |
N124K |
probably benign |
Het |
| Smarcd2 |
G |
A |
11: 106,163,332 (GRCm39) |
A68V |
probably benign |
Het |
| Smg1 |
T |
C |
7: 117,739,774 (GRCm39) |
E3391G |
possibly damaging |
Het |
| Spata32 |
T |
C |
11: 103,099,741 (GRCm39) |
M255V |
possibly damaging |
Het |
| Sstr5 |
T |
A |
17: 25,710,941 (GRCm39) |
Q96L |
probably damaging |
Het |
| Tcaf3 |
A |
G |
6: 42,573,828 (GRCm39) |
I128T |
probably benign |
Het |
| Tfdp1 |
C |
T |
8: 13,422,965 (GRCm39) |
T290M |
probably benign |
Het |
| Ticrr |
C |
T |
7: 79,344,511 (GRCm39) |
H1459Y |
probably benign |
Het |
| Tmed4 |
T |
A |
11: 6,223,763 (GRCm39) |
Q171L |
probably benign |
Het |
| Tmem40 |
G |
A |
6: 115,719,321 (GRCm39) |
S48F |
possibly damaging |
Het |
| Tnfaip1 |
A |
G |
11: 78,419,075 (GRCm39) |
|
probably null |
Het |
| Top1mt |
A |
G |
15: 75,539,742 (GRCm39) |
Y290H |
probably damaging |
Het |
| Topaz1 |
A |
T |
9: 122,577,585 (GRCm39) |
D165V |
probably damaging |
Het |
| Trim44 |
T |
C |
2: 102,230,651 (GRCm39) |
S127G |
unknown |
Het |
| Ubac1 |
G |
A |
2: 25,897,763 (GRCm39) |
R286C |
probably damaging |
Het |
| Ube2u |
A |
G |
4: 100,406,958 (GRCm39) |
E273G |
possibly damaging |
Het |
| Vmn1r213 |
G |
A |
13: 23,196,101 (GRCm39) |
S228N |
probably benign |
Het |
| Vmn2r28 |
A |
T |
7: 5,487,118 (GRCm39) |
V515E |
probably damaging |
Het |
| Vps13d |
A |
G |
4: 144,780,691 (GRCm39) |
L4011P |
|
Het |
| Ythdc2 |
T |
C |
18: 45,019,383 (GRCm39) |
F1384S |
probably damaging |
Het |
| Zfp423 |
T |
A |
8: 88,509,519 (GRCm39) |
Y275F |
probably damaging |
Het |
| Zfp493 |
A |
G |
13: 67,934,325 (GRCm39) |
K93E |
probably benign |
Het |
| Zfp980 |
G |
T |
4: 145,427,687 (GRCm39) |
G139W |
probably benign |
Het |
|
| Other mutations in Myocd |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00092:Myocd
|
APN |
11 |
65,071,770 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL00481:Myocd
|
APN |
11 |
65,077,980 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00857:Myocd
|
APN |
11 |
65,069,662 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01012:Myocd
|
APN |
11 |
65,075,451 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
IGL01570:Myocd
|
APN |
11 |
65,091,633 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01865:Myocd
|
APN |
11 |
65,091,723 (GRCm39) |
missense |
probably benign |
0.30 |
|
IGL01938:Myocd
|
APN |
11 |
65,077,914 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02324:Myocd
|
APN |
11 |
65,069,484 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02598:Myocd
|
APN |
11 |
65,074,296 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL02886:Myocd
|
APN |
11 |
65,069,569 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03008:Myocd
|
APN |
11 |
65,078,392 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03034:Myocd
|
APN |
11 |
65,109,511 (GRCm39) |
missense |
probably benign |
0.00 |
|
harvey
|
UTSW |
11 |
65,069,856 (GRCm39) |
splice site |
probably null |
|
|
irma
|
UTSW |
11 |
65,087,220 (GRCm39) |
missense |
probably benign |
0.02 |
|
myra
|
UTSW |
11 |
65,069,685 (GRCm39) |
missense |
probably benign |
0.10 |
|
Nate
|
UTSW |
11 |
65,123,914 (GRCm39) |
splice site |
probably null |
|
|
R0838_Myocd_053
|
UTSW |
11 |
65,069,758 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0078:Myocd
|
UTSW |
11 |
65,078,290 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R0097:Myocd
|
UTSW |
11 |
65,069,840 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R0097:Myocd
|
UTSW |
11 |
65,069,840 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R0234:Myocd
|
UTSW |
11 |
65,078,066 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0234:Myocd
|
UTSW |
11 |
65,078,066 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0453:Myocd
|
UTSW |
11 |
65,087,051 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0523:Myocd
|
UTSW |
11 |
65,071,728 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0838:Myocd
|
UTSW |
11 |
65,069,758 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0899:Myocd
|
UTSW |
11 |
65,086,018 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R1167:Myocd
|
UTSW |
11 |
65,087,203 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1472:Myocd
|
UTSW |
11 |
65,078,330 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1508:Myocd
|
UTSW |
11 |
65,075,342 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1620:Myocd
|
UTSW |
11 |
65,087,220 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1630:Myocd
|
UTSW |
11 |
65,087,220 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1731:Myocd
|
UTSW |
11 |
65,091,714 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1740:Myocd
|
UTSW |
11 |
65,109,347 (GRCm39) |
splice site |
probably benign |
|
|
R1769:Myocd
|
UTSW |
11 |
65,069,527 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1823:Myocd
|
UTSW |
11 |
65,069,496 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1968:Myocd
|
UTSW |
11 |
65,091,733 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1997:Myocd
|
UTSW |
11 |
65,095,147 (GRCm39) |
nonsense |
probably null |
|
|
R2018:Myocd
|
UTSW |
11 |
65,077,854 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2105:Myocd
|
UTSW |
11 |
65,109,484 (GRCm39) |
nonsense |
probably null |
|
|
R2314:Myocd
|
UTSW |
11 |
65,091,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4330:Myocd
|
UTSW |
11 |
65,114,590 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4331:Myocd
|
UTSW |
11 |
65,114,590 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4603:Myocd
|
UTSW |
11 |
65,078,571 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4619:Myocd
|
UTSW |
11 |
65,069,254 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4631:Myocd
|
UTSW |
11 |
65,069,685 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4865:Myocd
|
UTSW |
11 |
65,069,856 (GRCm39) |
splice site |
probably null |
|
|
R4974:Myocd
|
UTSW |
11 |
65,074,299 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4976:Myocd
|
UTSW |
11 |
65,112,876 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5478:Myocd
|
UTSW |
11 |
65,123,914 (GRCm39) |
splice site |
probably null |
|
|
R5499:Myocd
|
UTSW |
11 |
65,069,575 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R6052:Myocd
|
UTSW |
11 |
65,087,082 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6356:Myocd
|
UTSW |
11 |
65,109,396 (GRCm39) |
splice site |
probably null |
|
|
R7144:Myocd
|
UTSW |
11 |
65,109,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7261:Myocd
|
UTSW |
11 |
65,078,422 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7354:Myocd
|
UTSW |
11 |
65,078,319 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7461:Myocd
|
UTSW |
11 |
65,109,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7613:Myocd
|
UTSW |
11 |
65,109,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7718:Myocd
|
UTSW |
11 |
65,109,452 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7956:Myocd
|
UTSW |
11 |
65,160,494 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8345:Myocd
|
UTSW |
11 |
65,077,958 (GRCm39) |
nonsense |
probably null |
|
|
R8975:Myocd
|
UTSW |
11 |
65,069,287 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9051:Myocd
|
UTSW |
11 |
65,077,795 (GRCm39) |
missense |
probably benign |
|
|
R9400:Myocd
|
UTSW |
11 |
65,086,934 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9565:Myocd
|
UTSW |
11 |
65,078,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9567:Myocd
|
UTSW |
11 |
65,078,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9585:Myocd
|
UTSW |
11 |
65,095,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9710:Myocd
|
UTSW |
11 |
65,087,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9768:Myocd
|
UTSW |
11 |
65,078,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0057:Myocd
|
UTSW |
11 |
65,074,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
Z1186:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1189:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Myocd
|
UTSW |
11 |
65,075,418 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GCAGGAATAGCTGCTGTTGC -3'
(R):5'- TTGAAGTGCTTGCTTACATACACTC -3'
Sequencing Primer
(F):5'- AATAGCTGCTGTTGCTGGAGC -3'
(R):5'- CACCAGAGTGCTAAGATATCTATAGG -3'
|
| Posted On |
2022-06-15 |
Incidental Mutation