Incidental Mutation 'R1756:Heatr1'
ID |
194886 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Heatr1
|
Ensembl Gene |
ENSMUSG00000050244 |
Gene Name |
HEAT repeat containing 1 |
Synonyms |
B130016L12Rik |
MMRRC Submission |
039788-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.965)
|
Stock # |
R1756 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
12410256-12453774 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 12411341 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Serine
at position 61
(A61S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000152410
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059270]
[ENSMUST00000221046]
[ENSMUST00000223324]
|
AlphaFold |
G3X9B1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000059270
AA Change: A61S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000054084 Gene: ENSMUSG00000050244 AA Change: A61S
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
15 |
N/A |
INTRINSIC |
Pfam:U3snoRNP10
|
238 |
354 |
7e-30 |
PFAM |
SCOP:d1qbkb_
|
919 |
1795 |
3e-8 |
SMART |
low complexity region
|
1805 |
1814 |
N/A |
INTRINSIC |
BP28CT
|
1856 |
2009 |
2.25e-77 |
SMART |
Blast:BP28CT
|
2015 |
2061 |
2e-15 |
BLAST |
coiled coil region
|
2109 |
2137 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000221046
AA Change: A61S
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000222817
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000223324
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.5%
- 20x: 93.0%
|
Validation Efficiency |
100% (96/96) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330008L17Rik |
C |
A |
8: 100,148,514 (GRCm39) |
|
noncoding transcript |
Het |
Acin1 |
A |
G |
14: 54,902,661 (GRCm39) |
V377A |
probably benign |
Het |
Adam39 |
A |
T |
8: 41,278,361 (GRCm39) |
I251F |
probably damaging |
Het |
Adnp2 |
A |
T |
18: 80,170,912 (GRCm39) |
*1166K |
probably null |
Het |
Akap12 |
T |
A |
10: 4,307,574 (GRCm39) |
D1461E |
probably benign |
Het |
Aopep |
T |
A |
13: 63,215,875 (GRCm39) |
H382Q |
possibly damaging |
Het |
Apba1 |
A |
G |
19: 23,871,056 (GRCm39) |
D296G |
possibly damaging |
Het |
Apol7a |
G |
T |
15: 77,277,671 (GRCm39) |
L26M |
possibly damaging |
Het |
Bcl2 |
C |
T |
1: 106,640,122 (GRCm39) |
M163I |
probably damaging |
Het |
Cap2 |
T |
G |
13: 46,684,489 (GRCm39) |
I53R |
probably benign |
Het |
Ccdc74a |
T |
C |
16: 17,468,332 (GRCm39) |
V318A |
possibly damaging |
Het |
Ccnb2 |
A |
G |
9: 70,318,070 (GRCm39) |
V234A |
probably benign |
Het |
Cd207 |
C |
T |
6: 83,652,579 (GRCm39) |
V184I |
probably benign |
Het |
Cdk12 |
C |
A |
11: 98,132,587 (GRCm39) |
C1005* |
probably null |
Het |
Cep83 |
T |
C |
10: 94,586,129 (GRCm39) |
S344P |
probably damaging |
Het |
Ces1g |
A |
T |
8: 94,033,582 (GRCm39) |
Y447N |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,883,923 (GRCm39) |
L277Q |
probably damaging |
Het |
Cfh |
A |
G |
1: 140,028,615 (GRCm39) |
Y1027H |
probably damaging |
Het |
Clcnkb |
T |
A |
4: 141,142,525 (GRCm39) |
I28F |
possibly damaging |
Het |
Clec4d |
A |
G |
6: 123,244,068 (GRCm39) |
D59G |
probably damaging |
Het |
Colq |
G |
A |
14: 31,269,409 (GRCm39) |
P153S |
probably damaging |
Het |
Crybg1 |
T |
A |
10: 43,862,275 (GRCm39) |
T1500S |
probably damaging |
Het |
Cyp2d34 |
T |
A |
15: 82,501,725 (GRCm39) |
R262W |
probably damaging |
Het |
Dennd4b |
C |
G |
3: 90,178,912 (GRCm39) |
L559V |
probably damaging |
Het |
Dhrs1 |
A |
G |
14: 55,976,766 (GRCm39) |
V306A |
probably benign |
Het |
Diaph1 |
A |
T |
18: 37,987,626 (GRCm39) |
D1043E |
possibly damaging |
Het |
Dis3 |
G |
T |
14: 99,323,539 (GRCm39) |
D538E |
probably damaging |
Het |
Dnai2 |
T |
G |
11: 114,641,206 (GRCm39) |
S344A |
probably benign |
Het |
Dner |
C |
T |
1: 84,423,311 (GRCm39) |
V431M |
probably damaging |
Het |
Dnm1l |
A |
G |
16: 16,160,559 (GRCm39) |
|
probably null |
Het |
Eps15 |
T |
G |
4: 109,170,115 (GRCm39) |
L139* |
probably null |
Het |
Fam193a |
T |
A |
5: 34,623,636 (GRCm39) |
I55N |
possibly damaging |
Het |
Gm10308 |
T |
A |
17: 91,396,385 (GRCm39) |
Y102* |
probably null |
Het |
Gm10509 |
A |
G |
17: 21,909,762 (GRCm39) |
K30E |
possibly damaging |
Het |
Gpr155 |
T |
C |
2: 73,197,921 (GRCm39) |
M400V |
probably benign |
Het |
H2-M10.2 |
T |
C |
17: 36,597,015 (GRCm39) |
|
probably benign |
Het |
Helb |
G |
T |
10: 119,930,147 (GRCm39) |
T744K |
probably damaging |
Het |
Hmcn1 |
C |
A |
1: 150,474,781 (GRCm39) |
W4702L |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,286,132 (GRCm39) |
R2095W |
probably damaging |
Het |
Igfbp3 |
G |
C |
11: 7,158,461 (GRCm39) |
D267E |
probably damaging |
Het |
Ighmbp2 |
T |
A |
19: 3,318,669 (GRCm39) |
H469L |
probably damaging |
Het |
Kcnj3 |
A |
C |
2: 55,327,232 (GRCm39) |
K7T |
probably damaging |
Het |
Krtap5-5 |
T |
G |
7: 141,783,358 (GRCm39) |
K97N |
unknown |
Het |
Lcor |
T |
C |
19: 41,547,705 (GRCm39) |
S430P |
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,588,541 (GRCm39) |
V883A |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,000,837 (GRCm39) |
Y2243C |
probably damaging |
Het |
Lrrc46 |
G |
A |
11: 96,925,556 (GRCm39) |
|
probably benign |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mpdz |
C |
T |
4: 81,225,114 (GRCm39) |
V1438M |
possibly damaging |
Het |
Muc21 |
A |
T |
17: 35,930,131 (GRCm39) |
|
probably benign |
Het |
Ncbp1 |
T |
A |
4: 46,169,131 (GRCm39) |
L635* |
probably null |
Het |
Nipbl |
T |
C |
15: 8,368,035 (GRCm39) |
N1202D |
possibly damaging |
Het |
Nphs1 |
A |
G |
7: 30,160,959 (GRCm39) |
D196G |
probably benign |
Het |
Nup58 |
A |
T |
14: 60,482,119 (GRCm39) |
|
probably benign |
Het |
Or2b2b |
A |
G |
13: 21,858,865 (GRCm39) |
I83T |
probably benign |
Het |
Or8b42 |
A |
T |
9: 38,342,291 (GRCm39) |
I238F |
probably benign |
Het |
Or8k16 |
A |
G |
2: 85,520,427 (GRCm39) |
Y218C |
probably damaging |
Het |
Pax8 |
A |
T |
2: 24,325,833 (GRCm39) |
N350K |
probably damaging |
Het |
Pik3cd |
T |
C |
4: 149,743,207 (GRCm39) |
K298E |
probably benign |
Het |
Pkd1 |
C |
T |
17: 24,813,459 (GRCm39) |
R4000C |
probably damaging |
Het |
Pkn2 |
A |
T |
3: 142,516,488 (GRCm39) |
V546D |
possibly damaging |
Het |
Plcg2 |
A |
G |
8: 118,319,447 (GRCm39) |
K673E |
probably benign |
Het |
Pld4 |
T |
G |
12: 112,729,826 (GRCm39) |
|
probably null |
Het |
Plek |
A |
T |
11: 16,942,901 (GRCm39) |
N130K |
probably damaging |
Het |
Prune2 |
G |
A |
19: 17,101,068 (GRCm39) |
D2191N |
probably benign |
Het |
Ptgis |
T |
C |
2: 167,048,723 (GRCm39) |
Y431C |
probably damaging |
Het |
Rhbdf2 |
T |
C |
11: 116,498,092 (GRCm39) |
S36G |
probably benign |
Het |
Rtn4ip1 |
C |
T |
10: 43,786,826 (GRCm39) |
A178V |
probably damaging |
Het |
Rxfp1 |
A |
G |
3: 79,578,188 (GRCm39) |
S168P |
probably benign |
Het |
Sec24a |
A |
G |
11: 51,624,590 (GRCm39) |
|
probably benign |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Slitrk6 |
C |
T |
14: 110,987,984 (GRCm39) |
M574I |
probably benign |
Het |
Slk |
T |
C |
19: 47,611,116 (GRCm39) |
F861L |
probably damaging |
Het |
Smpd3 |
C |
A |
8: 106,991,603 (GRCm39) |
A317S |
probably benign |
Het |
Spopfm1 |
A |
T |
3: 94,173,525 (GRCm39) |
M174L |
probably benign |
Het |
Spz1 |
T |
A |
13: 92,711,633 (GRCm39) |
Q281L |
probably damaging |
Het |
Syde1 |
T |
A |
10: 78,422,814 (GRCm39) |
R519S |
probably benign |
Het |
Taf4 |
T |
C |
2: 179,618,324 (GRCm39) |
H39R |
unknown |
Het |
Tbx5 |
A |
T |
5: 119,983,178 (GRCm39) |
|
probably null |
Het |
Tektl1 |
T |
A |
10: 78,583,031 (GRCm39) |
K451M |
probably damaging |
Het |
Tenm2 |
C |
T |
11: 35,954,004 (GRCm39) |
G1236R |
possibly damaging |
Het |
Th |
G |
A |
7: 142,451,903 (GRCm39) |
Q19* |
probably null |
Het |
Tmprss11a |
T |
A |
5: 86,568,038 (GRCm39) |
I230F |
probably damaging |
Het |
Tnfrsf14 |
T |
A |
4: 155,009,779 (GRCm39) |
H50L |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,885 (GRCm39) |
|
probably null |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Trim2 |
A |
G |
3: 84,098,107 (GRCm39) |
I398T |
possibly damaging |
Het |
Trpc5 |
A |
T |
X: 143,264,222 (GRCm39) |
S212T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,617,678 (GRCm39) |
|
probably benign |
Het |
Unc80 |
A |
G |
1: 66,678,407 (GRCm39) |
T2063A |
possibly damaging |
Het |
Usp37 |
A |
T |
1: 74,518,814 (GRCm39) |
S260T |
probably benign |
Het |
Vcan |
A |
G |
13: 89,839,800 (GRCm39) |
S1915P |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,282 (GRCm39) |
I91F |
possibly damaging |
Het |
Zfp422 |
T |
C |
6: 116,603,385 (GRCm39) |
T205A |
probably benign |
Het |
|
Other mutations in Heatr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00666:Heatr1
|
APN |
13 |
12,425,331 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00863:Heatr1
|
APN |
13 |
12,450,009 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00899:Heatr1
|
APN |
13 |
12,450,057 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01147:Heatr1
|
APN |
13 |
12,452,793 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01317:Heatr1
|
APN |
13 |
12,413,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01323:Heatr1
|
APN |
13 |
12,413,819 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01625:Heatr1
|
APN |
13 |
12,428,409 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01973:Heatr1
|
APN |
13 |
12,444,680 (GRCm39) |
missense |
probably benign |
|
IGL02803:Heatr1
|
APN |
13 |
12,448,867 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02830:Heatr1
|
APN |
13 |
12,441,093 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02956:Heatr1
|
APN |
13 |
12,430,940 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03000:Heatr1
|
APN |
13 |
12,449,292 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03024:Heatr1
|
APN |
13 |
12,422,390 (GRCm39) |
unclassified |
probably benign |
|
IGL03035:Heatr1
|
APN |
13 |
12,428,100 (GRCm39) |
splice site |
probably benign |
|
IGL03301:Heatr1
|
APN |
13 |
12,449,086 (GRCm39) |
missense |
probably damaging |
1.00 |
hasan
|
UTSW |
13 |
12,432,328 (GRCm39) |
splice site |
probably benign |
|
H8562:Heatr1
|
UTSW |
13 |
12,423,594 (GRCm39) |
missense |
probably benign |
0.13 |
R0226:Heatr1
|
UTSW |
13 |
12,425,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R0571:Heatr1
|
UTSW |
13 |
12,445,121 (GRCm39) |
missense |
probably damaging |
0.98 |
R0722:Heatr1
|
UTSW |
13 |
12,420,918 (GRCm39) |
missense |
probably benign |
0.14 |
R1264:Heatr1
|
UTSW |
13 |
12,439,491 (GRCm39) |
unclassified |
probably benign |
|
R1371:Heatr1
|
UTSW |
13 |
12,432,513 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1388:Heatr1
|
UTSW |
13 |
12,432,328 (GRCm39) |
splice site |
probably benign |
|
R1396:Heatr1
|
UTSW |
13 |
12,420,927 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1519:Heatr1
|
UTSW |
13 |
12,427,040 (GRCm39) |
missense |
probably benign |
|
R1689:Heatr1
|
UTSW |
13 |
12,439,506 (GRCm39) |
missense |
probably benign |
0.00 |
R1696:Heatr1
|
UTSW |
13 |
12,438,602 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1859:Heatr1
|
UTSW |
13 |
12,418,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Heatr1
|
UTSW |
13 |
12,450,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Heatr1
|
UTSW |
13 |
12,411,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Heatr1
|
UTSW |
13 |
12,429,359 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2106:Heatr1
|
UTSW |
13 |
12,426,939 (GRCm39) |
missense |
probably benign |
0.03 |
R2119:Heatr1
|
UTSW |
13 |
12,447,527 (GRCm39) |
missense |
probably null |
1.00 |
R2121:Heatr1
|
UTSW |
13 |
12,418,145 (GRCm39) |
missense |
probably benign |
0.10 |
R2122:Heatr1
|
UTSW |
13 |
12,418,145 (GRCm39) |
missense |
probably benign |
0.10 |
R2367:Heatr1
|
UTSW |
13 |
12,448,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Heatr1
|
UTSW |
13 |
12,428,229 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3783:Heatr1
|
UTSW |
13 |
12,449,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Heatr1
|
UTSW |
13 |
12,449,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R3786:Heatr1
|
UTSW |
13 |
12,449,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Heatr1
|
UTSW |
13 |
12,449,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R3843:Heatr1
|
UTSW |
13 |
12,450,002 (GRCm39) |
missense |
probably benign |
0.00 |
R4533:Heatr1
|
UTSW |
13 |
12,449,392 (GRCm39) |
missense |
probably benign |
0.05 |
R4725:Heatr1
|
UTSW |
13 |
12,439,543 (GRCm39) |
nonsense |
probably null |
|
R4763:Heatr1
|
UTSW |
13 |
12,445,811 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4793:Heatr1
|
UTSW |
13 |
12,446,718 (GRCm39) |
missense |
probably benign |
0.00 |
R4797:Heatr1
|
UTSW |
13 |
12,426,929 (GRCm39) |
missense |
probably benign |
0.36 |
R4798:Heatr1
|
UTSW |
13 |
12,426,929 (GRCm39) |
missense |
probably benign |
0.36 |
R4942:Heatr1
|
UTSW |
13 |
12,428,391 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4952:Heatr1
|
UTSW |
13 |
12,425,480 (GRCm39) |
missense |
probably benign |
0.38 |
R4954:Heatr1
|
UTSW |
13 |
12,422,397 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5370:Heatr1
|
UTSW |
13 |
12,416,403 (GRCm39) |
missense |
probably benign |
0.02 |
R5464:Heatr1
|
UTSW |
13 |
12,448,524 (GRCm39) |
missense |
probably benign |
0.00 |
R5483:Heatr1
|
UTSW |
13 |
12,413,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Heatr1
|
UTSW |
13 |
12,435,945 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5504:Heatr1
|
UTSW |
13 |
12,421,500 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5527:Heatr1
|
UTSW |
13 |
12,419,829 (GRCm39) |
missense |
probably benign |
|
R5527:Heatr1
|
UTSW |
13 |
12,417,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Heatr1
|
UTSW |
13 |
12,423,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R5916:Heatr1
|
UTSW |
13 |
12,449,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R6018:Heatr1
|
UTSW |
13 |
12,420,939 (GRCm39) |
missense |
probably benign |
0.26 |
R6018:Heatr1
|
UTSW |
13 |
12,419,828 (GRCm39) |
missense |
probably benign |
|
R6216:Heatr1
|
UTSW |
13 |
12,447,545 (GRCm39) |
missense |
probably benign |
0.16 |
R6396:Heatr1
|
UTSW |
13 |
12,420,978 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6472:Heatr1
|
UTSW |
13 |
12,449,111 (GRCm39) |
missense |
probably benign |
0.29 |
R6922:Heatr1
|
UTSW |
13 |
12,449,956 (GRCm39) |
missense |
probably benign |
0.00 |
R7077:Heatr1
|
UTSW |
13 |
12,433,045 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7297:Heatr1
|
UTSW |
13 |
12,435,941 (GRCm39) |
nonsense |
probably null |
|
R7445:Heatr1
|
UTSW |
13 |
12,445,919 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7669:Heatr1
|
UTSW |
13 |
12,426,143 (GRCm39) |
missense |
probably benign |
0.33 |
R7672:Heatr1
|
UTSW |
13 |
12,453,545 (GRCm39) |
missense |
probably damaging |
0.96 |
R7772:Heatr1
|
UTSW |
13 |
12,432,522 (GRCm39) |
missense |
probably benign |
0.03 |
R8205:Heatr1
|
UTSW |
13 |
12,430,928 (GRCm39) |
missense |
probably benign |
|
R8518:Heatr1
|
UTSW |
13 |
12,425,415 (GRCm39) |
missense |
probably benign |
|
R8754:Heatr1
|
UTSW |
13 |
12,428,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R8874:Heatr1
|
UTSW |
13 |
12,445,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Heatr1
|
UTSW |
13 |
12,415,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R9045:Heatr1
|
UTSW |
13 |
12,428,233 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Heatr1
|
UTSW |
13 |
12,428,247 (GRCm39) |
missense |
probably benign |
|
R9183:Heatr1
|
UTSW |
13 |
12,436,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R9186:Heatr1
|
UTSW |
13 |
12,436,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Heatr1
|
UTSW |
13 |
12,419,802 (GRCm39) |
missense |
probably benign |
0.00 |
R9242:Heatr1
|
UTSW |
13 |
12,448,806 (GRCm39) |
missense |
probably benign |
|
R9267:Heatr1
|
UTSW |
13 |
12,421,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Heatr1
|
UTSW |
13 |
12,447,608 (GRCm39) |
missense |
probably benign |
0.13 |
R9310:Heatr1
|
UTSW |
13 |
12,453,491 (GRCm39) |
missense |
probably benign |
|
R9312:Heatr1
|
UTSW |
13 |
12,446,565 (GRCm39) |
missense |
probably benign |
|
R9358:Heatr1
|
UTSW |
13 |
12,433,087 (GRCm39) |
missense |
probably benign |
0.09 |
R9385:Heatr1
|
UTSW |
13 |
12,421,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Heatr1
|
UTSW |
13 |
12,439,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Heatr1
|
UTSW |
13 |
12,429,306 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9647:Heatr1
|
UTSW |
13 |
12,441,679 (GRCm39) |
missense |
probably benign |
0.00 |
R9683:Heatr1
|
UTSW |
13 |
12,449,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9695:Heatr1
|
UTSW |
13 |
12,438,624 (GRCm39) |
missense |
probably damaging |
1.00 |
RF011:Heatr1
|
UTSW |
13 |
12,422,425 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Heatr1
|
UTSW |
13 |
12,413,889 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
Predicted Primers |
PCR Primer
(F):5'- GCCACCTTTCACTTAGCAAAGCTCC -3'
(R):5'- AGCCATTCCAGACACTTCTGCG -3'
Sequencing Primer
(F):5'- CAGCAATACTGCTAGATGTGTG -3'
(R):5'- ACTTCTGCGCTGGCTTG -3'
|
Posted On |
2014-05-23 |