Incidental Mutation 'R9457:Tnrc6a'
| ID |
714651 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tnrc6a
|
| Ensembl Gene |
ENSMUSG00000052707 |
| Gene Name |
trinucleotide repeat containing 6a |
| Synonyms |
3110054G10Rik, 2010321I05Rik, Tnrc6, CAGH26, D130023A07Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.879)
|
| Stock # |
R9457 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
122723108-122794519 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 122778958 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glutamine
at position 1223
(R1223Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000091595
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094053]
[ENSMUST00000205514]
[ENSMUST00000206014]
[ENSMUST00000206888]
|
| AlphaFold |
Q3UHK8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094053
AA Change: R1223Q
PolyPhen 2
Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000091595
Gene: ENSMUSG00000052707
AA Change: R1223Q
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
5 |
54 |
N/A |
INTRINSIC |
|
low complexity region
|
69 |
92 |
N/A |
INTRINSIC |
|
low complexity region
|
93 |
113 |
N/A |
INTRINSIC |
|
low complexity region
|
281 |
294 |
N/A |
INTRINSIC |
|
low complexity region
|
430 |
443 |
N/A |
INTRINSIC |
|
low complexity region
|
568 |
590 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
690 |
853 |
3.51e-6 |
PROSPERO |
|
low complexity region
|
858 |
871 |
N/A |
INTRINSIC |
|
Pfam:Ago_hook
|
1028 |
1190 |
1.2e-29 |
PFAM |
|
low complexity region
|
1284 |
1296 |
N/A |
INTRINSIC |
|
low complexity region
|
1301 |
1316 |
N/A |
INTRINSIC |
|
low complexity region
|
1337 |
1376 |
N/A |
INTRINSIC |
|
low complexity region
|
1386 |
1392 |
N/A |
INTRINSIC |
|
Pfam:TNRC6-PABC_bdg
|
1439 |
1714 |
1.5e-126 |
PFAM |
|
RRM
|
1717 |
1784 |
4.95e-2 |
SMART |
|
low complexity region
|
1808 |
1820 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205514
|
| Predicted Effect |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000206014
AA Change: R86Q
PolyPhen 2
Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000206888
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the trinucleotide repeat containing 6 protein family. The protein is highly similar to a human protein that functions in post-transcriptional gene silencing through the RNA interference (RNAi) and microRNA pathways. The human protein associates with messenger RNAs and argonaute proteins in cytoplasmic bodies known as GW-bodies or P-bodies, and inhibiting its expression delocalizes other GW-body proteins and impairs RNAi and microRNA-induced gene silencing. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit partial embryonic lethality during organogenesis associated with impaired hematopoiesis. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(21) : Gene trapped(21) |
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A930009A15Rik |
T |
C |
10: 115,414,236 (GRCm39) |
L54P |
unknown |
Het |
| Ablim3 |
A |
G |
18: 61,978,920 (GRCm39) |
S204P |
probably benign |
Het |
| Acadl |
A |
G |
1: 66,892,400 (GRCm39) |
V141A |
probably benign |
Het |
| Ace3 |
A |
G |
11: 105,885,687 (GRCm39) |
D31G |
probably benign |
Het |
| Acte1 |
T |
C |
7: 143,437,713 (GRCm39) |
V137A |
possibly damaging |
Het |
| Adam11 |
T |
G |
11: 102,660,724 (GRCm39) |
V85G |
probably benign |
Het |
| Adarb1 |
A |
T |
10: 77,157,982 (GRCm39) |
M155K |
possibly damaging |
Het |
| Arhgap10 |
G |
A |
8: 78,111,415 (GRCm39) |
T376M |
probably benign |
Het |
| Bod1l |
G |
T |
5: 41,979,310 (GRCm39) |
T668K |
probably damaging |
Het |
| Ccdc87 |
A |
G |
19: 4,891,659 (GRCm39) |
E717G |
probably damaging |
Het |
| Cdh17 |
T |
A |
4: 11,771,329 (GRCm39) |
I37N |
probably damaging |
Het |
| Cfap99 |
T |
G |
5: 34,458,741 (GRCm39) |
F45L |
probably benign |
Het |
| Chsy1 |
C |
A |
7: 65,822,148 (GRCm39) |
H794Q |
probably benign |
Het |
| Clec4a3 |
G |
A |
6: 122,931,045 (GRCm39) |
V45I |
probably benign |
Het |
| Clic3 |
G |
A |
2: 25,347,730 (GRCm39) |
V32I |
probably benign |
Het |
| Clip2 |
A |
T |
5: 134,531,584 (GRCm39) |
D740E |
probably benign |
Het |
| Col5a2 |
C |
T |
1: 45,426,004 (GRCm39) |
V1062I |
probably benign |
Het |
| Col5a2 |
A |
G |
1: 45,431,973 (GRCm39) |
|
probably null |
Het |
| Cyp2j11 |
C |
T |
4: 96,195,596 (GRCm39) |
V367I |
probably damaging |
Het |
| Ddr1 |
C |
T |
17: 35,993,650 (GRCm39) |
A821T |
possibly damaging |
Het |
| Dna2 |
G |
A |
10: 62,786,572 (GRCm39) |
E107K |
probably benign |
Het |
| Eif3d |
A |
G |
15: 77,843,894 (GRCm39) |
V484A |
probably benign |
Het |
| Fgfr4 |
A |
G |
13: 55,308,940 (GRCm39) |
T354A |
probably benign |
Het |
| Fkbp6 |
T |
C |
5: 135,378,486 (GRCm39) |
D54G |
probably benign |
Het |
| Gm4787 |
T |
A |
12: 81,426,020 (GRCm39) |
E46V |
probably damaging |
Het |
| Gm47995 |
A |
G |
1: 151,074,226 (GRCm39) |
T10A |
possibly damaging |
Het |
| Gnb1l |
T |
A |
16: 18,359,745 (GRCm39) |
I50N |
probably damaging |
Het |
| Gphb5 |
A |
T |
12: 75,462,523 (GRCm39) |
V22D |
probably damaging |
Het |
| Gstt4 |
C |
T |
10: 75,650,959 (GRCm39) |
C221Y |
probably benign |
Het |
| Hmces |
T |
C |
6: 87,910,256 (GRCm39) |
V222A |
possibly damaging |
Het |
| Kat14 |
T |
A |
2: 144,215,702 (GRCm39) |
D62E |
probably benign |
Het |
| Kcnmb2 |
T |
A |
3: 32,236,018 (GRCm39) |
V89E |
probably benign |
Het |
| Kif23 |
T |
A |
9: 61,851,507 (GRCm39) |
N63I |
probably benign |
Het |
| Lamc2 |
T |
C |
1: 153,015,600 (GRCm39) |
M578V |
probably benign |
Het |
| Ltbp2 |
A |
T |
12: 84,835,927 (GRCm39) |
C1335S |
probably benign |
Het |
| Lyst |
A |
G |
13: 13,862,330 (GRCm39) |
E2622G |
possibly damaging |
Het |
| Mctp1 |
A |
T |
13: 76,532,793 (GRCm39) |
H47L |
probably benign |
Het |
| Mical2 |
A |
G |
7: 112,010,665 (GRCm39) |
K618R |
probably damaging |
Het |
| Mllt6 |
T |
C |
11: 97,556,586 (GRCm39) |
I92T |
probably benign |
Het |
| Morc2a |
A |
G |
11: 3,626,184 (GRCm39) |
I223V |
probably benign |
Het |
| Msh3 |
A |
T |
13: 92,481,594 (GRCm39) |
I306N |
probably benign |
Het |
| Myo3b |
T |
A |
2: 69,925,553 (GRCm39) |
S35T |
probably benign |
Het |
| Nfkbiz |
A |
T |
16: 55,634,347 (GRCm39) |
V700E |
probably damaging |
Het |
| Oit3 |
T |
A |
10: 59,277,505 (GRCm39) |
M1L |
unknown |
Het |
| Or4c1 |
A |
T |
2: 89,133,075 (GRCm39) |
I287N |
probably damaging |
Het |
| Or51l14 |
T |
A |
7: 103,100,618 (GRCm39) |
F25I |
probably benign |
Het |
| Or8k17 |
A |
T |
2: 86,066,816 (GRCm39) |
I114K |
probably damaging |
Het |
| Peg3 |
T |
G |
7: 6,710,998 (GRCm39) |
D1408A |
probably damaging |
Het |
| Plaa |
A |
C |
4: 94,475,120 (GRCm39) |
S201R |
possibly damaging |
Het |
| Potefam1 |
A |
T |
2: 111,000,631 (GRCm39) |
M196K |
unknown |
Het |
| Psmd5 |
A |
G |
2: 34,744,338 (GRCm39) |
S395P |
probably benign |
Het |
| Ralgapa2 |
T |
C |
2: 146,176,474 (GRCm39) |
I1701V |
probably damaging |
Het |
| Rmc1 |
A |
G |
18: 12,312,303 (GRCm39) |
H181R |
probably benign |
Het |
| Rnf32 |
G |
A |
5: 29,411,184 (GRCm39) |
A157T |
probably damaging |
Het |
| Rrad |
T |
A |
8: 105,356,359 (GRCm39) |
|
probably null |
Het |
| Samm50 |
T |
A |
15: 84,092,042 (GRCm39) |
L339Q |
probably damaging |
Het |
| Scin |
T |
C |
12: 40,154,957 (GRCm39) |
E212G |
possibly damaging |
Het |
| Scrib |
T |
C |
15: 75,939,148 (GRCm39) |
D146G |
probably damaging |
Het |
| Slc19a1 |
G |
A |
10: 76,885,605 (GRCm39) |
D502N |
probably benign |
Het |
| Slc4a4 |
T |
C |
5: 89,362,432 (GRCm39) |
S839P |
probably damaging |
Het |
| Slc4a8 |
A |
G |
15: 100,704,141 (GRCm39) |
D764G |
probably damaging |
Het |
| Slc6a19 |
G |
A |
13: 73,829,884 (GRCm39) |
A590V |
probably damaging |
Het |
| Slfn8 |
G |
T |
11: 82,908,532 (GRCm39) |
H4N |
probably benign |
Het |
| Smad9 |
T |
A |
3: 54,696,756 (GRCm39) |
F274I |
possibly damaging |
Het |
| Snx4 |
A |
G |
16: 33,106,380 (GRCm39) |
E271G |
probably benign |
Het |
| Spata31h1 |
A |
G |
10: 82,122,573 (GRCm39) |
V3479A |
probably benign |
Het |
| Tektip1 |
C |
A |
10: 81,201,611 (GRCm39) |
V4L |
probably benign |
Het |
| Thap4 |
G |
A |
1: 93,678,028 (GRCm39) |
R253* |
probably null |
Het |
| Tmem65 |
T |
A |
15: 58,662,028 (GRCm39) |
I144F |
|
Het |
| Traf7 |
CA |
CAA |
17: 24,746,737 (GRCm39) |
|
probably benign |
Het |
| Trpm2 |
T |
C |
10: 77,747,226 (GRCm39) |
Y1424C |
possibly damaging |
Het |
| Trrap |
T |
A |
5: 144,763,478 (GRCm39) |
Y2457N |
probably damaging |
Het |
| Vmn1r7 |
A |
G |
6: 57,001,508 (GRCm39) |
S251P |
probably damaging |
Het |
| Vmn2r89 |
A |
T |
14: 51,693,469 (GRCm39) |
E273V |
probably damaging |
Het |
| Vps52 |
A |
G |
17: 34,181,156 (GRCm39) |
D466G |
probably damaging |
Het |
| Xirp2 |
T |
C |
2: 67,345,976 (GRCm39) |
V2739A |
probably benign |
Het |
| Zc3h4 |
C |
T |
7: 16,168,675 (GRCm39) |
S1003F |
unknown |
Het |
| Zyg11a |
A |
T |
4: 108,075,102 (GRCm39) |
H6Q |
probably damaging |
Het |
|
| Other mutations in Tnrc6a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00335:Tnrc6a
|
APN |
7 |
122,770,003 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL00580:Tnrc6a
|
APN |
7 |
122,773,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01309:Tnrc6a
|
APN |
7 |
122,770,717 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02004:Tnrc6a
|
APN |
7 |
122,780,589 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
IGL02142:Tnrc6a
|
APN |
7 |
122,751,414 (GRCm39) |
intron |
probably benign |
|
|
IGL02220:Tnrc6a
|
APN |
7 |
122,769,679 (GRCm39) |
missense |
probably benign |
|
|
IGL02436:Tnrc6a
|
APN |
7 |
122,783,438 (GRCm39) |
nonsense |
probably null |
|
|
IGL02670:Tnrc6a
|
APN |
7 |
122,770,535 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02743:Tnrc6a
|
APN |
7 |
122,770,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
0152:Tnrc6a
|
UTSW |
7 |
122,779,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0008:Tnrc6a
|
UTSW |
7 |
122,769,617 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0008:Tnrc6a
|
UTSW |
7 |
122,769,617 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0369:Tnrc6a
|
UTSW |
7 |
122,770,083 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0512:Tnrc6a
|
UTSW |
7 |
122,785,951 (GRCm39) |
splice site |
probably benign |
|
|
R0566:Tnrc6a
|
UTSW |
7 |
122,770,136 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0600:Tnrc6a
|
UTSW |
7 |
122,771,039 (GRCm39) |
missense |
probably benign |
0.14 |
|
R0751:Tnrc6a
|
UTSW |
7 |
122,769,563 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R1184:Tnrc6a
|
UTSW |
7 |
122,769,563 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R1319:Tnrc6a
|
UTSW |
7 |
122,783,474 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1405:Tnrc6a
|
UTSW |
7 |
122,770,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1405:Tnrc6a
|
UTSW |
7 |
122,770,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1585:Tnrc6a
|
UTSW |
7 |
122,776,098 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1709:Tnrc6a
|
UTSW |
7 |
122,769,205 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1776:Tnrc6a
|
UTSW |
7 |
122,770,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1791:Tnrc6a
|
UTSW |
7 |
122,792,140 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R1807:Tnrc6a
|
UTSW |
7 |
122,761,669 (GRCm39) |
splice site |
probably benign |
|
|
R1876:Tnrc6a
|
UTSW |
7 |
122,761,669 (GRCm39) |
splice site |
probably benign |
|
|
R2010:Tnrc6a
|
UTSW |
7 |
122,770,269 (GRCm39) |
missense |
probably benign |
0.26 |
|
R2086:Tnrc6a
|
UTSW |
7 |
122,761,669 (GRCm39) |
splice site |
probably benign |
|
|
R2089:Tnrc6a
|
UTSW |
7 |
122,771,343 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2091:Tnrc6a
|
UTSW |
7 |
122,771,343 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2091:Tnrc6a
|
UTSW |
7 |
122,771,343 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2511:Tnrc6a
|
UTSW |
7 |
122,770,315 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2830:Tnrc6a
|
UTSW |
7 |
122,792,172 (GRCm39) |
makesense |
probably null |
|
|
R2850:Tnrc6a
|
UTSW |
7 |
122,779,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3916:Tnrc6a
|
UTSW |
7 |
122,780,607 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4028:Tnrc6a
|
UTSW |
7 |
122,769,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4235:Tnrc6a
|
UTSW |
7 |
122,770,903 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4439:Tnrc6a
|
UTSW |
7 |
122,751,405 (GRCm39) |
nonsense |
probably null |
|
|
R4525:Tnrc6a
|
UTSW |
7 |
122,779,005 (GRCm39) |
missense |
probably benign |
|
|
R4578:Tnrc6a
|
UTSW |
7 |
122,783,444 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4613:Tnrc6a
|
UTSW |
7 |
122,783,512 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4711:Tnrc6a
|
UTSW |
7 |
122,770,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4722:Tnrc6a
|
UTSW |
7 |
122,791,313 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4746:Tnrc6a
|
UTSW |
7 |
122,789,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4892:Tnrc6a
|
UTSW |
7 |
122,769,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4942:Tnrc6a
|
UTSW |
7 |
122,791,836 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4967:Tnrc6a
|
UTSW |
7 |
122,789,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5064:Tnrc6a
|
UTSW |
7 |
122,785,946 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5239:Tnrc6a
|
UTSW |
7 |
122,785,842 (GRCm39) |
missense |
probably benign |
|
|
R5604:Tnrc6a
|
UTSW |
7 |
122,773,459 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5805:Tnrc6a
|
UTSW |
7 |
122,769,299 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5942:Tnrc6a
|
UTSW |
7 |
122,785,888 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5988:Tnrc6a
|
UTSW |
7 |
122,781,603 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6212:Tnrc6a
|
UTSW |
7 |
122,742,965 (GRCm39) |
splice site |
probably null |
|
|
R6284:Tnrc6a
|
UTSW |
7 |
122,770,558 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6417:Tnrc6a
|
UTSW |
7 |
122,770,297 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6420:Tnrc6a
|
UTSW |
7 |
122,770,297 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6575:Tnrc6a
|
UTSW |
7 |
122,769,133 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6760:Tnrc6a
|
UTSW |
7 |
122,771,222 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6886:Tnrc6a
|
UTSW |
7 |
122,786,668 (GRCm39) |
missense |
probably benign |
0.17 |
|
R6968:Tnrc6a
|
UTSW |
7 |
122,781,650 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7216:Tnrc6a
|
UTSW |
7 |
122,770,718 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7260:Tnrc6a
|
UTSW |
7 |
122,785,813 (GRCm39) |
missense |
probably benign |
0.36 |
|
R7299:Tnrc6a
|
UTSW |
7 |
122,770,136 (GRCm39) |
missense |
probably benign |
|
|
R7322:Tnrc6a
|
UTSW |
7 |
122,770,731 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7500:Tnrc6a
|
UTSW |
7 |
122,772,673 (GRCm39) |
splice site |
probably null |
|
|
R7872:Tnrc6a
|
UTSW |
7 |
122,779,057 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8270:Tnrc6a
|
UTSW |
7 |
122,769,294 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8313:Tnrc6a
|
UTSW |
7 |
122,769,936 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8348:Tnrc6a
|
UTSW |
7 |
122,791,346 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8390:Tnrc6a
|
UTSW |
7 |
122,761,794 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8448:Tnrc6a
|
UTSW |
7 |
122,791,346 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8514:Tnrc6a
|
UTSW |
7 |
122,783,438 (GRCm39) |
nonsense |
probably null |
|
|
R8552:Tnrc6a
|
UTSW |
7 |
122,761,669 (GRCm39) |
splice site |
probably benign |
|
|
R8767:Tnrc6a
|
UTSW |
7 |
122,783,133 (GRCm39) |
unclassified |
probably benign |
|
|
R9047:Tnrc6a
|
UTSW |
7 |
122,778,946 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9147:Tnrc6a
|
UTSW |
7 |
122,785,667 (GRCm39) |
intron |
probably benign |
|
|
R9153:Tnrc6a
|
UTSW |
7 |
122,773,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9166:Tnrc6a
|
UTSW |
7 |
122,786,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9179:Tnrc6a
|
UTSW |
7 |
122,791,881 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9192:Tnrc6a
|
UTSW |
7 |
122,789,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9778:Tnrc6a
|
UTSW |
7 |
122,769,635 (GRCm39) |
missense |
probably benign |
0.43 |
|
X0064:Tnrc6a
|
UTSW |
7 |
122,769,021 (GRCm39) |
missense |
probably benign |
0.28 |
|
Z1176:Tnrc6a
|
UTSW |
7 |
122,761,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACCAGGTGTGTGGACCTTG -3'
(R):5'- AAGGGTATGGTTGATTATGCTCAGATC -3'
Sequencing Primer
(F):5'- GTGATGACCAAGTACTTACATGTC -3'
(R):5'- CTTTGGAAATCTGAGGCC -3'
|
| Posted On |
2022-06-15 |
Incidental Mutation