Incidental Mutation 'R7751:Resf1'
| ID |
597227 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Resf1
|
| Ensembl Gene |
ENSMUSG00000032712 |
| Gene Name |
retroelement silencing factor 1 |
| Synonyms |
2810474O19Rik, GET |
| MMRRC Submission |
045807-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7751 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
149210912-149237161 bp(+) (GRCm39) |
| Type of Mutation |
start gained |
| DNA Base Change (assembly) |
A to G
at 149226936 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139624
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046689]
[ENSMUST00000100765]
[ENSMUST00000127680]
[ENSMUST00000130664]
[ENSMUST00000185930]
[ENSMUST00000187881]
[ENSMUST00000189837]
[ENSMUST00000189932]
[ENSMUST00000190785]
|
| AlphaFold |
Q5DTW7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000046689
|
| SMART Domains |
Protein: ENSMUSP00000041180
Gene: ENSMUSG00000032712
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000100765
|
| SMART Domains |
Protein: ENSMUSP00000098328
Gene: ENSMUSG00000032712
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127680
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000130664
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000185930
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187881
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000189837
|
| SMART Domains |
Protein: ENSMUSP00000139660
Gene: ENSMUSG00000032712
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1511 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000189932
|
| SMART Domains |
Protein: ENSMUSP00000140026
Gene: ENSMUSG00000032712
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000190785
|
| SMART Domains |
Protein: ENSMUSP00000139624
Gene: ENSMUSG00000032712
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1173 |
9.4e-255 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
98% (82/84) |
| Allele List at MGI |
All alleles(126) : Targeted, knock-out(1) Gene trapped(125) |
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca15 |
A |
T |
7: 119,965,044 (GRCm39) |
I769F |
possibly damaging |
Het |
| Ackr1 |
A |
C |
1: 173,159,779 (GRCm39) |
W247G |
probably damaging |
Het |
| Adgrl4 |
G |
A |
3: 151,197,946 (GRCm39) |
G69S |
probably damaging |
Het |
| Agrn |
C |
T |
4: 156,260,886 (GRCm39) |
S710N |
probably damaging |
Het |
| Aox3 |
A |
G |
1: 58,218,494 (GRCm39) |
M1103V |
probably benign |
Het |
| Asb18 |
G |
A |
1: 89,896,206 (GRCm39) |
A278V |
probably benign |
Het |
| B3gat2 |
A |
G |
1: 23,801,945 (GRCm39) |
E77G |
probably benign |
Het |
| Camta1 |
T |
C |
4: 151,232,863 (GRCm39) |
|
probably null |
Het |
| Cbll1 |
A |
T |
12: 31,537,579 (GRCm39) |
I392N |
probably damaging |
Het |
| Ccdc113 |
A |
G |
8: 96,264,829 (GRCm39) |
D113G |
possibly damaging |
Het |
| Cd79a |
T |
C |
7: 24,599,092 (GRCm39) |
F148L |
probably benign |
Het |
| Chad |
T |
A |
11: 94,455,999 (GRCm39) |
C26S |
probably damaging |
Het |
| Cog4 |
T |
C |
8: 111,607,600 (GRCm39) |
F696L |
probably damaging |
Het |
| Csf2rb |
T |
G |
15: 78,225,839 (GRCm39) |
S303R |
probably damaging |
Het |
| Cstpp1 |
A |
T |
2: 91,214,118 (GRCm39) |
L79H |
probably damaging |
Het |
| Cubn |
C |
T |
2: 13,365,176 (GRCm39) |
G1621R |
probably damaging |
Het |
| Dennd4c |
T |
A |
4: 86,747,179 (GRCm39) |
N1454K |
probably benign |
Het |
| Dennd5b |
T |
C |
6: 148,918,604 (GRCm39) |
I853V |
probably benign |
Het |
| Dnaaf11 |
T |
C |
15: 66,321,412 (GRCm39) |
E243G |
probably benign |
Het |
| Dop1a |
A |
T |
9: 86,389,783 (GRCm39) |
D561V |
probably benign |
Het |
| Dpysl4 |
A |
G |
7: 138,669,456 (GRCm39) |
I45V |
probably benign |
Het |
| Ect2l |
A |
C |
10: 18,045,153 (GRCm39) |
S301A |
possibly damaging |
Het |
| Elf2 |
A |
G |
3: 51,165,035 (GRCm39) |
V323A |
probably damaging |
Het |
| Epcam |
C |
T |
17: 87,947,904 (GRCm39) |
R125* |
probably null |
Het |
| Ephb4 |
T |
C |
5: 137,363,937 (GRCm39) |
V612A |
probably damaging |
Het |
| Erich3 |
C |
T |
3: 154,469,426 (GRCm39) |
R1293C |
unknown |
Het |
| F830045P16Rik |
C |
A |
2: 129,302,367 (GRCm39) |
L408F |
probably damaging |
Het |
| Gask1a |
G |
A |
9: 121,793,887 (GRCm39) |
V14I |
probably benign |
Het |
| Gm13102 |
T |
C |
4: 143,835,787 (GRCm39) |
I485T |
probably benign |
Het |
| Gm16494 |
A |
T |
17: 47,327,800 (GRCm39) |
L28* |
probably null |
Het |
| Grin2c |
A |
G |
11: 115,144,696 (GRCm39) |
V610A |
probably damaging |
Het |
| Hacd2 |
T |
A |
16: 34,922,434 (GRCm39) |
Y208N |
probably damaging |
Het |
| Hlf |
A |
T |
11: 90,278,821 (GRCm39) |
F81Y |
probably damaging |
Het |
| Igfbp7 |
G |
A |
5: 77,499,134 (GRCm39) |
A257V |
probably damaging |
Het |
| Il12a |
A |
T |
3: 68,605,235 (GRCm39) |
N167I |
probably damaging |
Het |
| Il1r2 |
G |
A |
1: 40,162,371 (GRCm39) |
C338Y |
probably damaging |
Het |
| Irf2bpl |
G |
T |
12: 86,930,489 (GRCm39) |
H61Q |
probably damaging |
Het |
| Kansl1 |
A |
G |
11: 104,314,890 (GRCm39) |
F383L |
probably benign |
Het |
| Kcnh8 |
A |
G |
17: 53,268,871 (GRCm39) |
T863A |
probably damaging |
Het |
| Klhl36 |
C |
A |
8: 120,596,397 (GRCm39) |
Q33K |
probably benign |
Het |
| Lrig2 |
A |
T |
3: 104,401,985 (GRCm39) |
Y113* |
probably null |
Het |
| Lrrc36 |
T |
A |
8: 106,178,667 (GRCm39) |
S287R |
possibly damaging |
Het |
| Mr1 |
A |
T |
1: 155,005,054 (GRCm39) |
Y329N |
probably damaging |
Het |
| Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
| Nectin4 |
G |
A |
1: 171,211,326 (GRCm39) |
|
probably null |
Het |
| Nsrp1 |
A |
G |
11: 76,940,097 (GRCm39) |
|
probably null |
Het |
| Or1e21 |
A |
T |
11: 73,344,372 (GRCm39) |
I222N |
possibly damaging |
Het |
| Or9g3 |
A |
G |
2: 85,583,836 (GRCm39) |
T44A |
probably benign |
Het |
| Pcdh8 |
A |
T |
14: 80,008,143 (GRCm39) |
I140N |
probably damaging |
Het |
| Pdzd8 |
A |
G |
19: 59,333,208 (GRCm39) |
V271A |
probably damaging |
Het |
| Pex3 |
T |
A |
10: 13,403,550 (GRCm39) |
I324L |
possibly damaging |
Het |
| Pira12 |
T |
A |
7: 3,898,603 (GRCm39) |
I282F |
probably damaging |
Het |
| Pitpnm1 |
T |
A |
19: 4,153,470 (GRCm39) |
F209I |
probably benign |
Het |
| Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
| Pkhd1 |
T |
A |
1: 20,271,149 (GRCm39) |
T3135S |
probably damaging |
Het |
| Pramel32 |
T |
C |
4: 88,547,356 (GRCm39) |
D192G |
probably benign |
Het |
| Prdm16 |
T |
C |
4: 154,412,756 (GRCm39) |
N1082S |
probably damaging |
Het |
| Psmd12 |
A |
T |
11: 107,370,439 (GRCm39) |
I13F |
possibly damaging |
Het |
| Ptgs2 |
A |
T |
1: 149,980,258 (GRCm39) |
I399F |
probably benign |
Het |
| Rasa3 |
A |
T |
8: 13,618,708 (GRCm39) |
S830T |
probably benign |
Het |
| Rasgef1c |
A |
T |
11: 49,861,120 (GRCm39) |
R362W |
probably damaging |
Het |
| Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
| Rnf217 |
C |
A |
10: 31,393,415 (GRCm39) |
G389W |
probably damaging |
Het |
| Sec16b |
A |
T |
1: 157,385,630 (GRCm39) |
D675V |
probably damaging |
Het |
| Serpinb12 |
A |
G |
1: 106,877,401 (GRCm39) |
Y137C |
probably damaging |
Het |
| Slc2a5 |
T |
A |
4: 150,227,591 (GRCm39) |
I470N |
probably damaging |
Het |
| Slc5a1 |
T |
C |
5: 33,290,761 (GRCm39) |
I115T |
possibly damaging |
Het |
| Slco1a4 |
A |
T |
6: 141,780,413 (GRCm39) |
S126T |
possibly damaging |
Het |
| St6galnac2 |
T |
C |
11: 116,568,410 (GRCm39) |
D351G |
probably damaging |
Het |
| Stat4 |
G |
A |
1: 52,121,711 (GRCm39) |
V357M |
possibly damaging |
Het |
| Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
| Tdrd9 |
T |
A |
12: 111,958,982 (GRCm39) |
C139S |
probably benign |
Het |
| Tmed9 |
G |
A |
13: 55,741,054 (GRCm39) |
R23Q |
not run |
Het |
| Tmem150a |
A |
C |
6: 72,336,028 (GRCm39) |
H205P |
probably damaging |
Het |
| Tns2 |
C |
A |
15: 102,018,163 (GRCm39) |
L350I |
probably benign |
Het |
| Tpr |
A |
G |
1: 150,295,646 (GRCm39) |
T964A |
probably benign |
Het |
| Traf3ip1 |
G |
T |
1: 91,422,479 (GRCm39) |
|
probably benign |
Het |
| Trem2 |
G |
T |
17: 48,653,567 (GRCm39) |
|
probably benign |
Het |
| Ttc14 |
G |
A |
3: 33,863,590 (GRCm39) |
G666D |
unknown |
Het |
| Ulk1 |
T |
C |
5: 110,957,078 (GRCm39) |
D40G |
probably damaging |
Het |
| Vmn1r30 |
A |
G |
6: 58,412,397 (GRCm39) |
V145A |
probably benign |
Het |
| Vmn1r79 |
C |
T |
7: 11,910,762 (GRCm39) |
Q215* |
probably null |
Het |
| Wnk2 |
G |
A |
13: 49,231,493 (GRCm39) |
T16I |
unknown |
Het |
| Yme1l1 |
T |
C |
2: 23,077,856 (GRCm39) |
|
probably null |
Het |
| Zbtb16 |
T |
A |
9: 48,654,769 (GRCm39) |
H454L |
probably damaging |
Het |
| Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably damaging |
Het |
| Zrsr2-ps1 |
A |
G |
11: 22,923,595 (GRCm39) |
Q123R |
possibly damaging |
Het |
|
| Other mutations in Resf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00767:Resf1
|
APN |
6 |
149,236,248 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL01401:Resf1
|
APN |
6 |
149,228,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01461:Resf1
|
APN |
6 |
149,233,013 (GRCm39) |
unclassified |
probably benign |
|
|
IGL01610:Resf1
|
APN |
6 |
149,230,449 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02873:Resf1
|
APN |
6 |
149,228,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03202:Resf1
|
APN |
6 |
149,227,937 (GRCm39) |
missense |
probably benign |
0.08 |
|
grand_junction
|
UTSW |
6 |
149,229,376 (GRCm39) |
missense |
probably damaging |
0.98 |
|
grand_marais
|
UTSW |
6 |
149,227,958 (GRCm39) |
nonsense |
probably null |
|
|
3-1:Resf1
|
UTSW |
6 |
149,229,227 (GRCm39) |
missense |
probably damaging |
0.98 |
|
B6584:Resf1
|
UTSW |
6 |
149,230,844 (GRCm39) |
missense |
probably damaging |
0.96 |
|
PIT4280001:Resf1
|
UTSW |
6 |
149,227,023 (GRCm39) |
missense |
probably benign |
0.23 |
|
R0053:Resf1
|
UTSW |
6 |
149,229,088 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0053:Resf1
|
UTSW |
6 |
149,229,088 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0243:Resf1
|
UTSW |
6 |
149,227,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0620:Resf1
|
UTSW |
6 |
149,229,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0633:Resf1
|
UTSW |
6 |
149,227,199 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0727:Resf1
|
UTSW |
6 |
149,227,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0904:Resf1
|
UTSW |
6 |
149,229,767 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1221:Resf1
|
UTSW |
6 |
149,227,719 (GRCm39) |
missense |
probably benign |
0.24 |
|
R1282:Resf1
|
UTSW |
6 |
149,230,670 (GRCm39) |
nonsense |
probably null |
|
|
R1435:Resf1
|
UTSW |
6 |
149,227,580 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1452:Resf1
|
UTSW |
6 |
149,228,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1587:Resf1
|
UTSW |
6 |
149,228,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1912:Resf1
|
UTSW |
6 |
149,230,342 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R1926:Resf1
|
UTSW |
6 |
149,230,902 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1978:Resf1
|
UTSW |
6 |
149,227,930 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2035:Resf1
|
UTSW |
6 |
149,230,724 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2136:Resf1
|
UTSW |
6 |
149,230,320 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2333:Resf1
|
UTSW |
6 |
149,229,009 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2360:Resf1
|
UTSW |
6 |
149,236,145 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3027:Resf1
|
UTSW |
6 |
149,230,533 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3121:Resf1
|
UTSW |
6 |
149,230,741 (GRCm39) |
nonsense |
probably null |
|
|
R3707:Resf1
|
UTSW |
6 |
149,230,611 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4204:Resf1
|
UTSW |
6 |
149,231,042 (GRCm39) |
nonsense |
probably null |
|
|
R4247:Resf1
|
UTSW |
6 |
149,227,041 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4249:Resf1
|
UTSW |
6 |
149,227,041 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4304:Resf1
|
UTSW |
6 |
149,227,736 (GRCm39) |
nonsense |
probably null |
|
|
R4385:Resf1
|
UTSW |
6 |
149,227,706 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4702:Resf1
|
UTSW |
6 |
149,230,901 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4747:Resf1
|
UTSW |
6 |
149,228,392 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4912:Resf1
|
UTSW |
6 |
149,230,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4913:Resf1
|
UTSW |
6 |
149,230,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4965:Resf1
|
UTSW |
6 |
149,229,896 (GRCm39) |
nonsense |
probably null |
|
|
R4971:Resf1
|
UTSW |
6 |
149,227,097 (GRCm39) |
unclassified |
probably benign |
|
|
R5077:Resf1
|
UTSW |
6 |
149,227,528 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5213:Resf1
|
UTSW |
6 |
149,227,551 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R5382:Resf1
|
UTSW |
6 |
149,227,958 (GRCm39) |
nonsense |
probably null |
|
|
R5418:Resf1
|
UTSW |
6 |
149,227,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5452:Resf1
|
UTSW |
6 |
149,230,611 (GRCm39) |
nonsense |
probably null |
|
|
R5498:Resf1
|
UTSW |
6 |
149,229,738 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5673:Resf1
|
UTSW |
6 |
149,229,491 (GRCm39) |
nonsense |
probably null |
|
|
R5690:Resf1
|
UTSW |
6 |
149,229,735 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5916:Resf1
|
UTSW |
6 |
149,228,076 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5917:Resf1
|
UTSW |
6 |
149,236,179 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6160:Resf1
|
UTSW |
6 |
149,233,005 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6280:Resf1
|
UTSW |
6 |
149,228,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6326:Resf1
|
UTSW |
6 |
149,230,493 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6396:Resf1
|
UTSW |
6 |
149,229,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6702:Resf1
|
UTSW |
6 |
149,229,376 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6972:Resf1
|
UTSW |
6 |
149,227,607 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7127:Resf1
|
UTSW |
6 |
149,229,443 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7168:Resf1
|
UTSW |
6 |
149,229,341 (GRCm39) |
missense |
probably benign |
|
|
R7316:Resf1
|
UTSW |
6 |
149,228,136 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7586:Resf1
|
UTSW |
6 |
149,228,291 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7719:Resf1
|
UTSW |
6 |
149,228,853 (GRCm39) |
missense |
probably benign |
|
|
R8013:Resf1
|
UTSW |
6 |
149,230,368 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8358:Resf1
|
UTSW |
6 |
149,228,076 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8393:Resf1
|
UTSW |
6 |
149,229,998 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R8968:Resf1
|
UTSW |
6 |
149,228,664 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8977:Resf1
|
UTSW |
6 |
149,229,906 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8981:Resf1
|
UTSW |
6 |
149,227,997 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9106:Resf1
|
UTSW |
6 |
149,230,368 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9208:Resf1
|
UTSW |
6 |
149,228,027 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9294:Resf1
|
UTSW |
6 |
149,227,930 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9352:Resf1
|
UTSW |
6 |
149,236,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9361:Resf1
|
UTSW |
6 |
149,228,132 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R9513:Resf1
|
UTSW |
6 |
149,229,793 (GRCm39) |
nonsense |
probably null |
|
|
R9566:Resf1
|
UTSW |
6 |
149,227,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9623:Resf1
|
UTSW |
6 |
149,226,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9689:Resf1
|
UTSW |
6 |
149,229,766 (GRCm39) |
nonsense |
probably null |
|
|
R9752:Resf1
|
UTSW |
6 |
149,228,068 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9794:Resf1
|
UTSW |
6 |
149,228,239 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGAGGTCCTTCTTTAGTTACCATAGAC -3'
(R):5'- ACATGCATGCTTCTTGGTTATG -3'
Sequencing Primer
(F):5'- TTTTTCCAAATTTTGTCTAGGCAGTG -3'
(R):5'- ATGCTTCTTGGTTATGGAGAGAATAG -3'
|
| Posted On |
2019-11-26 |
Incidental Mutation