Incidental Mutation 'R7082:Ahctf1'
| ID |
549577 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahctf1
|
| Ensembl Gene |
ENSMUSG00000026491 |
| Gene Name |
AT hook containing transcription factor 1 |
| Synonyms |
Elys, 6230412P20Rik |
| MMRRC Submission |
045176-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7082 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
179572459-179631245 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 179602898 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 887
(R887G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027768
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027768]
[ENSMUST00000145968]
|
| AlphaFold |
Q8CJF7 |
| PDB Structure |
Nucleoporin ELYS (aa1-494), Mus musculus [X-RAY DIFFRACTION]
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000027768
AA Change: R887G
PolyPhen 2
Score 0.151 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000027768
Gene: ENSMUSG00000026491
AA Change: R887G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ELYS-bb
|
1 |
489 |
1.6e-307 |
PFAM |
|
Pfam:ELYS
|
722 |
955 |
2.5e-58 |
PFAM |
|
low complexity region
|
1138 |
1155 |
N/A |
INTRINSIC |
|
low complexity region
|
1180 |
1192 |
N/A |
INTRINSIC |
|
low complexity region
|
1352 |
1366 |
N/A |
INTRINSIC |
|
low complexity region
|
1597 |
1610 |
N/A |
INTRINSIC |
|
low complexity region
|
1684 |
1694 |
N/A |
INTRINSIC |
|
low complexity region
|
1834 |
1841 |
N/A |
INTRINSIC |
|
low complexity region
|
1918 |
1935 |
N/A |
INTRINSIC |
|
AT_hook
|
1955 |
1967 |
3.35e-1 |
SMART |
|
low complexity region
|
2060 |
2066 |
N/A |
INTRINSIC |
|
low complexity region
|
2073 |
2084 |
N/A |
INTRINSIC |
|
low complexity region
|
2096 |
2108 |
N/A |
INTRINSIC |
|
Blast:KISc
|
2164 |
2217 |
2e-12 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000145968
|
| Meta Mutation Damage Score |
0.0723 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
100% (88/88) |
| MGI Phenotype |
PHENOTYPE: Homozygous null mice die between E3.5 and E5.5. The inner cell mass cells exhibit impaired proliferation and apoptosis when grown in culture. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 5730596B20Rik |
A |
T |
6: 52,156,260 (GRCm39) |
N109Y |
unknown |
Het |
| A430005L14Rik |
C |
T |
4: 154,044,221 (GRCm39) |
R11W |
probably damaging |
Het |
| Aadacl2 |
T |
A |
3: 59,932,306 (GRCm39) |
S274T |
probably damaging |
Het |
| Aox4 |
G |
T |
1: 58,263,352 (GRCm39) |
R158L |
possibly damaging |
Het |
| Atp10a |
T |
C |
7: 58,308,567 (GRCm39) |
I122T |
probably damaging |
Het |
| Batf2 |
G |
T |
19: 6,221,405 (GRCm39) |
A72S |
possibly damaging |
Het |
| Bltp3a |
G |
T |
17: 28,109,039 (GRCm39) |
R1086L |
probably damaging |
Het |
| Bptf |
T |
C |
11: 106,977,573 (GRCm39) |
D749G |
probably benign |
Het |
| Cacybp |
A |
G |
1: 160,031,229 (GRCm39) |
Y200H |
probably damaging |
Het |
| Cdc40 |
A |
T |
10: 40,743,869 (GRCm39) |
V76D |
probably benign |
Het |
| Cdc42ep4 |
T |
C |
11: 113,619,944 (GRCm39) |
D149G |
probably benign |
Het |
| Chtop |
A |
G |
3: 90,414,891 (GRCm39) |
V9A |
probably benign |
Het |
| Cnot9 |
A |
G |
1: 74,566,165 (GRCm39) |
I185M |
probably damaging |
Het |
| Col6a5 |
A |
G |
9: 105,808,438 (GRCm39) |
I870T |
unknown |
Het |
| Cr1l |
A |
G |
1: 194,806,006 (GRCm39) |
I159T |
probably benign |
Het |
| Cthrc1 |
T |
C |
15: 38,940,495 (GRCm39) |
S33P |
probably benign |
Het |
| Dlg2 |
T |
A |
7: 90,381,192 (GRCm39) |
W44R |
probably benign |
Het |
| Dlgap4 |
T |
C |
2: 156,590,342 (GRCm39) |
|
probably null |
Het |
| Dna2 |
A |
G |
10: 62,790,096 (GRCm39) |
H193R |
possibly damaging |
Het |
| Espnl |
T |
A |
1: 91,262,521 (GRCm39) |
F322Y |
probably benign |
Het |
| Fam171a1 |
G |
A |
2: 3,224,512 (GRCm39) |
V293I |
probably benign |
Het |
| Fam76b |
A |
G |
9: 13,744,308 (GRCm39) |
Y135C |
probably damaging |
Het |
| Flvcr2 |
A |
T |
12: 85,793,728 (GRCm39) |
I35F |
probably benign |
Het |
| Gm9195 |
T |
A |
14: 72,680,152 (GRCm39) |
Q2219L |
probably benign |
Het |
| Gnptg |
T |
C |
17: 25,453,694 (GRCm39) |
T283A |
probably benign |
Het |
| Grap2 |
G |
A |
15: 80,532,699 (GRCm39) |
V289M |
probably benign |
Het |
| Hk3 |
T |
C |
13: 55,154,710 (GRCm39) |
T767A |
probably benign |
Het |
| Hs3st5 |
A |
G |
10: 36,708,833 (GRCm39) |
I123V |
probably benign |
Het |
| Il6st |
A |
G |
13: 112,640,566 (GRCm39) |
T781A |
probably damaging |
Het |
| Inpp5d |
T |
A |
1: 87,623,102 (GRCm39) |
H398Q |
probably damaging |
Het |
| Kcnk1 |
A |
G |
8: 126,722,287 (GRCm39) |
Y30C |
probably damaging |
Het |
| Klhl6 |
T |
C |
16: 19,801,633 (GRCm39) |
T41A |
probably benign |
Het |
| Krt14 |
G |
A |
11: 100,094,167 (GRCm39) |
H476Y |
possibly damaging |
Het |
| Lingo3 |
G |
C |
10: 80,671,625 (GRCm39) |
R102G |
probably benign |
Het |
| Map3k9 |
G |
A |
12: 81,771,476 (GRCm39) |
T704M |
probably damaging |
Het |
| Mdn1 |
C |
A |
4: 32,762,341 (GRCm39) |
N5088K |
probably benign |
Het |
| Mmp9 |
T |
A |
2: 164,790,812 (GRCm39) |
S67T |
probably benign |
Het |
| Mrps18c |
A |
G |
5: 100,952,270 (GRCm39) |
E143G |
probably damaging |
Het |
| Msantd5f9 |
G |
T |
4: 73,835,808 (GRCm39) |
L219M |
probably benign |
Het |
| Muc21 |
A |
T |
17: 35,932,093 (GRCm39) |
S698T |
unknown |
Het |
| Nags |
C |
A |
11: 102,038,298 (GRCm39) |
R335S |
possibly damaging |
Het |
| Nars1 |
A |
G |
18: 64,637,425 (GRCm39) |
V385A |
possibly damaging |
Het |
| Nipal2 |
A |
C |
15: 34,584,809 (GRCm39) |
V253G |
possibly damaging |
Het |
| Nos2 |
C |
A |
11: 78,819,405 (GRCm39) |
T39K |
probably benign |
Het |
| Or10p1 |
T |
A |
10: 129,443,416 (GRCm39) |
*311Y |
probably null |
Het |
| Or10p1 |
T |
A |
10: 129,443,417 (GRCm39) |
*311L |
probably null |
Het |
| Or51t4 |
T |
C |
7: 102,598,455 (GRCm39) |
V261A |
probably damaging |
Het |
| Or52s19 |
C |
A |
7: 103,007,495 (GRCm39) |
R302L |
possibly damaging |
Het |
| Or6c66 |
C |
T |
10: 129,461,634 (GRCm39) |
V99M |
probably benign |
Het |
| Or9s15 |
G |
A |
1: 92,524,140 (GRCm39) |
|
probably benign |
Het |
| Panx3 |
G |
A |
9: 37,577,913 (GRCm39) |
P106S |
probably benign |
Het |
| Pappa2 |
G |
A |
1: 158,590,689 (GRCm39) |
T1655I |
possibly damaging |
Het |
| Pcdhb1 |
A |
G |
18: 37,400,044 (GRCm39) |
D665G |
probably damaging |
Het |
| Pde2a |
T |
C |
7: 101,157,303 (GRCm39) |
L676P |
probably damaging |
Het |
| Pf4 |
A |
G |
5: 90,920,851 (GRCm39) |
T60A |
possibly damaging |
Het |
| Pira12 |
C |
T |
7: 3,898,510 (GRCm39) |
V313M |
probably damaging |
Het |
| Pld5 |
A |
T |
1: 175,917,442 (GRCm39) |
C164S |
probably benign |
Het |
| Psd3 |
A |
T |
8: 68,356,800 (GRCm39) |
M640K |
probably benign |
Het |
| Ptf1a |
A |
G |
2: 19,450,676 (GRCm39) |
D2G |
possibly damaging |
Het |
| Ptprq |
C |
T |
10: 107,544,591 (GRCm39) |
C313Y |
probably benign |
Het |
| Ranbp10 |
A |
G |
8: 106,500,578 (GRCm39) |
S467P |
probably damaging |
Het |
| Rap1gap |
C |
T |
4: 137,446,247 (GRCm39) |
T333M |
probably damaging |
Het |
| Rfpl4 |
A |
G |
7: 5,118,558 (GRCm39) |
L4P |
probably benign |
Het |
| Rgs12 |
A |
G |
5: 35,124,050 (GRCm39) |
N611S |
probably benign |
Het |
| Sacs |
C |
A |
14: 61,447,966 (GRCm39) |
N3337K |
possibly damaging |
Het |
| Sbno2 |
A |
T |
10: 79,895,924 (GRCm39) |
|
probably null |
Het |
| Scrn2 |
T |
A |
11: 96,923,908 (GRCm39) |
V264E |
possibly damaging |
Het |
| Serpinb9c |
T |
A |
13: 33,338,390 (GRCm39) |
I198L |
probably benign |
Het |
| Shank2 |
T |
C |
7: 143,964,096 (GRCm39) |
F568S |
probably damaging |
Het |
| Slc47a1 |
C |
T |
11: 61,268,767 (GRCm39) |
R36Q |
probably benign |
Het |
| Slc4a8 |
A |
C |
15: 100,688,908 (GRCm39) |
E406A |
probably damaging |
Het |
| Speg |
C |
T |
1: 75,388,091 (GRCm39) |
T1483I |
probably damaging |
Het |
| Srbd1 |
A |
G |
17: 86,365,160 (GRCm39) |
V632A |
probably damaging |
Het |
| Srd5a2 |
A |
T |
17: 74,328,515 (GRCm39) |
Y188N |
probably damaging |
Het |
| Sspo |
A |
T |
6: 48,455,543 (GRCm39) |
|
probably null |
Het |
| Ssx2ip |
A |
T |
3: 146,136,703 (GRCm39) |
D317V |
probably benign |
Het |
| Tmco3 |
G |
T |
8: 13,370,847 (GRCm39) |
E172* |
probably null |
Het |
| Trpc4 |
G |
A |
3: 54,206,519 (GRCm39) |
W573* |
probably null |
Het |
| Ttn |
T |
C |
2: 76,580,340 (GRCm39) |
I23518V |
probably benign |
Het |
| Tubal3 |
A |
G |
13: 3,983,050 (GRCm39) |
T277A |
possibly damaging |
Het |
| Unc5b |
A |
T |
10: 60,610,867 (GRCm39) |
L391H |
probably damaging |
Het |
| Vmn2r76 |
A |
G |
7: 85,874,440 (GRCm39) |
F846L |
probably benign |
Het |
| Vps13c |
T |
A |
9: 67,790,735 (GRCm39) |
Y338N |
probably damaging |
Het |
| Zc3hav1 |
G |
T |
6: 38,309,328 (GRCm39) |
S498* |
probably null |
Het |
| Zfand4 |
T |
A |
6: 116,305,337 (GRCm39) |
|
probably null |
Het |
| Zfp451 |
A |
T |
1: 33,811,972 (GRCm39) |
|
probably null |
Het |
| Zfp607a |
A |
T |
7: 27,578,183 (GRCm39) |
I418F |
probably damaging |
Het |
| Zfp612 |
A |
G |
8: 110,816,337 (GRCm39) |
T515A |
probably damaging |
Het |
| Zfp708 |
G |
T |
13: 67,219,200 (GRCm39) |
L208I |
possibly damaging |
Het |
|
| Other mutations in Ahctf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00757:Ahctf1
|
APN |
1 |
179,596,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01714:Ahctf1
|
APN |
1 |
179,623,442 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01787:Ahctf1
|
APN |
1 |
179,580,887 (GRCm39) |
missense |
probably benign |
|
|
IGL01997:Ahctf1
|
APN |
1 |
179,583,027 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02035:Ahctf1
|
APN |
1 |
179,593,579 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02158:Ahctf1
|
APN |
1 |
179,607,217 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL02182:Ahctf1
|
APN |
1 |
179,580,643 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02298:Ahctf1
|
APN |
1 |
179,580,044 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02325:Ahctf1
|
APN |
1 |
179,603,580 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02619:Ahctf1
|
APN |
1 |
179,620,016 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02858:Ahctf1
|
APN |
1 |
179,596,599 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02893:Ahctf1
|
APN |
1 |
179,603,576 (GRCm39) |
nonsense |
probably null |
|
|
IGL02895:Ahctf1
|
APN |
1 |
179,621,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03180:Ahctf1
|
APN |
1 |
179,602,895 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03220:Ahctf1
|
APN |
1 |
179,615,767 (GRCm39) |
missense |
probably benign |
0.01 |
|
cerebro
|
UTSW |
1 |
179,596,979 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0003:Ahctf1
|
UTSW |
1 |
179,591,038 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0024:Ahctf1
|
UTSW |
1 |
179,580,001 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0030:Ahctf1
|
UTSW |
1 |
179,580,001 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0432:Ahctf1
|
UTSW |
1 |
179,611,726 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0481:Ahctf1
|
UTSW |
1 |
179,587,836 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0600:Ahctf1
|
UTSW |
1 |
179,591,033 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0613:Ahctf1
|
UTSW |
1 |
179,596,979 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0814:Ahctf1
|
UTSW |
1 |
179,590,473 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1055:Ahctf1
|
UTSW |
1 |
179,591,051 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R1473:Ahctf1
|
UTSW |
1 |
179,626,844 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1473:Ahctf1
|
UTSW |
1 |
179,603,673 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1689:Ahctf1
|
UTSW |
1 |
179,595,948 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1778:Ahctf1
|
UTSW |
1 |
179,580,580 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R1878:Ahctf1
|
UTSW |
1 |
179,603,074 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R1925:Ahctf1
|
UTSW |
1 |
179,598,218 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2118:Ahctf1
|
UTSW |
1 |
179,597,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2122:Ahctf1
|
UTSW |
1 |
179,597,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2124:Ahctf1
|
UTSW |
1 |
179,597,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2373:Ahctf1
|
UTSW |
1 |
179,623,361 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2509:Ahctf1
|
UTSW |
1 |
179,598,258 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R2697:Ahctf1
|
UTSW |
1 |
179,580,097 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3035:Ahctf1
|
UTSW |
1 |
179,581,435 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3155:Ahctf1
|
UTSW |
1 |
179,583,148 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3899:Ahctf1
|
UTSW |
1 |
179,605,345 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4036:Ahctf1
|
UTSW |
1 |
179,590,181 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R4681:Ahctf1
|
UTSW |
1 |
179,580,361 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4695:Ahctf1
|
UTSW |
1 |
179,580,619 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4735:Ahctf1
|
UTSW |
1 |
179,580,964 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4857:Ahctf1
|
UTSW |
1 |
179,626,922 (GRCm39) |
unclassified |
probably benign |
|
|
R4898:Ahctf1
|
UTSW |
1 |
179,583,077 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4905:Ahctf1
|
UTSW |
1 |
179,576,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5011:Ahctf1
|
UTSW |
1 |
179,611,675 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5013:Ahctf1
|
UTSW |
1 |
179,611,675 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5053:Ahctf1
|
UTSW |
1 |
179,614,349 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5207:Ahctf1
|
UTSW |
1 |
179,621,159 (GRCm39) |
intron |
probably benign |
|
|
R5319:Ahctf1
|
UTSW |
1 |
179,596,615 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5343:Ahctf1
|
UTSW |
1 |
179,598,199 (GRCm39) |
nonsense |
probably null |
|
|
R5546:Ahctf1
|
UTSW |
1 |
179,581,633 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5718:Ahctf1
|
UTSW |
1 |
179,596,904 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R5862:Ahctf1
|
UTSW |
1 |
179,615,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5958:Ahctf1
|
UTSW |
1 |
179,574,107 (GRCm39) |
unclassified |
probably benign |
|
|
R6010:Ahctf1
|
UTSW |
1 |
179,623,378 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6081:Ahctf1
|
UTSW |
1 |
179,609,237 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6093:Ahctf1
|
UTSW |
1 |
179,590,517 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6207:Ahctf1
|
UTSW |
1 |
179,604,955 (GRCm39) |
splice site |
probably null |
|
|
R6268:Ahctf1
|
UTSW |
1 |
179,591,048 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6656:Ahctf1
|
UTSW |
1 |
179,581,078 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6668:Ahctf1
|
UTSW |
1 |
179,579,972 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6788:Ahctf1
|
UTSW |
1 |
179,580,199 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6860:Ahctf1
|
UTSW |
1 |
179,580,853 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6998:Ahctf1
|
UTSW |
1 |
179,598,480 (GRCm39) |
nonsense |
probably null |
|
|
R7385:Ahctf1
|
UTSW |
1 |
179,580,946 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7414:Ahctf1
|
UTSW |
1 |
179,611,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7663:Ahctf1
|
UTSW |
1 |
179,617,879 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7673:Ahctf1
|
UTSW |
1 |
179,590,411 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7715:Ahctf1
|
UTSW |
1 |
179,598,413 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7819:Ahctf1
|
UTSW |
1 |
179,595,880 (GRCm39) |
missense |
probably benign |
|
|
R7846:Ahctf1
|
UTSW |
1 |
179,614,638 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7912:Ahctf1
|
UTSW |
1 |
179,580,656 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7942:Ahctf1
|
UTSW |
1 |
179,613,660 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8282:Ahctf1
|
UTSW |
1 |
179,605,371 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8376:Ahctf1
|
UTSW |
1 |
179,610,520 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8439:Ahctf1
|
UTSW |
1 |
179,590,175 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8482:Ahctf1
|
UTSW |
1 |
179,591,107 (GRCm39) |
unclassified |
probably benign |
|
|
R8683:Ahctf1
|
UTSW |
1 |
179,623,321 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8734:Ahctf1
|
UTSW |
1 |
179,608,430 (GRCm39) |
nonsense |
probably null |
|
|
R8855:Ahctf1
|
UTSW |
1 |
179,614,341 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8928:Ahctf1
|
UTSW |
1 |
179,596,626 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R9009:Ahctf1
|
UTSW |
1 |
179,581,171 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9106:Ahctf1
|
UTSW |
1 |
179,614,601 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9228:Ahctf1
|
UTSW |
1 |
179,611,685 (GRCm39) |
missense |
probably benign |
0.28 |
|
R9408:Ahctf1
|
UTSW |
1 |
179,603,638 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R9800:Ahctf1
|
UTSW |
1 |
179,581,433 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
X0067:Ahctf1
|
UTSW |
1 |
179,605,269 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Ahctf1
|
UTSW |
1 |
179,621,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGTAGTCATGTCTCAGCCAAGC -3'
(R):5'- AGACCTTCTGTTTCACCCAG -3'
Sequencing Primer
(F):5'- CACTGTTTACTTGGTGAAAGGCAC -3'
(R):5'- GTTTCACCCAGTTACTGCAAAG -3'
|
| Posted On |
2019-05-15 |
Incidental Mutation