Incidental Mutation 'R7853:Fhad1'
ID |
607050 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Fhad1
|
Ensembl Gene |
ENSMUSG00000051435 |
Gene Name |
forkhead-associated phosphopeptide binding domain 1 |
Synonyms |
2900090M10Rik |
MMRRC Submission |
045906-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
R7853 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
141617749-141742393 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 141637134 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 1111
(S1111P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101405
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000105779]
[ENSMUST00000105780]
|
AlphaFold |
A6PWD2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105779
AA Change: S1111P
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000101405 Gene: ENSMUSG00000051435 AA Change: S1111P
Domain | Start | End | E-Value | Type |
FHA
|
17 |
69 |
8.41e-8 |
SMART |
low complexity region
|
111 |
124 |
N/A |
INTRINSIC |
coiled coil region
|
307 |
434 |
N/A |
INTRINSIC |
coiled coil region
|
640 |
915 |
N/A |
INTRINSIC |
low complexity region
|
1091 |
1102 |
N/A |
INTRINSIC |
coiled coil region
|
1111 |
1140 |
N/A |
INTRINSIC |
coiled coil region
|
1255 |
1339 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105780
AA Change: S1111P
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000101406 Gene: ENSMUSG00000051435 AA Change: S1111P
Domain | Start | End | E-Value | Type |
FHA
|
17 |
69 |
8.41e-8 |
SMART |
low complexity region
|
111 |
124 |
N/A |
INTRINSIC |
coiled coil region
|
307 |
434 |
N/A |
INTRINSIC |
coiled coil region
|
640 |
915 |
N/A |
INTRINSIC |
low complexity region
|
1091 |
1102 |
N/A |
INTRINSIC |
coiled coil region
|
1111 |
1140 |
N/A |
INTRINSIC |
coiled coil region
|
1255 |
1339 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,315,600 (GRCm39) |
I26T |
probably damaging |
Het |
Aadacl4 |
G |
T |
4: 144,344,592 (GRCm39) |
A123S |
probably benign |
Het |
Adamts20 |
A |
C |
15: 94,243,871 (GRCm39) |
C619G |
probably damaging |
Het |
Ahcyl1 |
C |
A |
3: 107,575,604 (GRCm39) |
V394L |
probably benign |
Het |
Ankrd17 |
A |
C |
5: 90,386,825 (GRCm39) |
L2378V |
possibly damaging |
Het |
B3gnt3 |
T |
C |
8: 72,145,357 (GRCm39) |
Y337C |
probably damaging |
Het |
Bcl10 |
A |
G |
3: 145,630,266 (GRCm39) |
K18R |
possibly damaging |
Het |
Calcr |
G |
A |
6: 3,707,499 (GRCm39) |
A267V |
probably benign |
Het |
Ces1d |
C |
T |
8: 93,901,695 (GRCm39) |
G425S |
probably benign |
Het |
Col1a1 |
G |
T |
11: 94,838,505 (GRCm39) |
R899L |
unknown |
Het |
Commd1 |
C |
T |
11: 22,906,532 (GRCm39) |
R168H |
possibly damaging |
Het |
Cps1 |
T |
C |
1: 67,213,640 (GRCm39) |
S791P |
possibly damaging |
Het |
Ctsj |
T |
A |
13: 61,151,884 (GRCm39) |
I58F |
probably damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,529,656 (GRCm39) |
K238N |
probably benign |
Het |
Dlgap4 |
A |
G |
2: 156,547,802 (GRCm39) |
D423G |
probably benign |
Het |
Eef1ece2 |
T |
A |
16: 20,463,010 (GRCm39) |
|
probably null |
Het |
Egln1 |
T |
C |
8: 125,675,256 (GRCm39) |
N180D |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,327,225 (GRCm39) |
F74S |
probably damaging |
Het |
Ext1 |
G |
A |
15: 52,970,881 (GRCm39) |
A350V |
probably damaging |
Het |
Fam186b |
T |
A |
15: 99,178,628 (GRCm39) |
I233F |
probably damaging |
Het |
Fam193a |
T |
G |
5: 34,597,473 (GRCm39) |
N91K |
probably benign |
Het |
Far1 |
T |
A |
7: 113,153,355 (GRCm39) |
N329K |
probably damaging |
Het |
Fhl2 |
A |
G |
1: 43,180,984 (GRCm39) |
S69P |
probably damaging |
Het |
Flg2 |
C |
A |
3: 93,128,054 (GRCm39) |
P2322Q |
unknown |
Het |
Flvcr1 |
A |
G |
1: 190,757,843 (GRCm39) |
Y108H |
probably damaging |
Het |
Fos |
T |
A |
12: 85,522,792 (GRCm39) |
S235T |
probably benign |
Het |
Foxf1 |
T |
A |
8: 121,811,438 (GRCm39) |
S101T |
probably damaging |
Het |
Gfer |
C |
A |
17: 24,913,259 (GRCm39) |
D198Y |
probably damaging |
Het |
Ggps1 |
T |
C |
13: 14,229,034 (GRCm39) |
I50V |
probably benign |
Het |
Gkn2 |
A |
G |
6: 87,355,255 (GRCm39) |
T155A |
probably benign |
Het |
Gna12 |
C |
T |
5: 140,746,449 (GRCm39) |
C332Y |
probably damaging |
Het |
Hc |
T |
A |
2: 34,900,045 (GRCm39) |
Y1096F |
probably damaging |
Het |
Hoxa3 |
G |
A |
6: 52,147,267 (GRCm39) |
|
probably benign |
Het |
Hsd17b8 |
T |
G |
17: 34,246,411 (GRCm39) |
D117A |
probably benign |
Het |
Ifi206 |
A |
T |
1: 173,299,100 (GRCm39) |
Y835* |
probably null |
Het |
Ighv13-2 |
T |
G |
12: 114,321,544 (GRCm39) |
E65A |
probably damaging |
Het |
Kif5a |
A |
T |
10: 127,071,537 (GRCm39) |
Y770* |
probably null |
Het |
Lfng |
A |
G |
5: 140,593,384 (GRCm39) |
S72G |
probably benign |
Het |
Lipo2 |
C |
T |
19: 33,737,344 (GRCm39) |
|
probably benign |
Het |
Lnpep |
C |
T |
17: 17,783,109 (GRCm39) |
S564N |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,025 (GRCm39) |
L500* |
probably null |
Het |
Mllt6 |
G |
A |
11: 97,561,142 (GRCm39) |
V277I |
probably benign |
Het |
Mroh5 |
C |
T |
15: 73,663,189 (GRCm39) |
D192N |
probably benign |
Het |
Myo1f |
T |
A |
17: 33,795,672 (GRCm39) |
V106D |
probably damaging |
Het |
Mypn |
T |
A |
10: 62,981,652 (GRCm39) |
I643F |
probably benign |
Het |
Nup188 |
A |
G |
2: 30,213,575 (GRCm39) |
N669D |
possibly damaging |
Het |
Or14j5 |
C |
G |
17: 38,161,714 (GRCm39) |
T77R |
probably damaging |
Het |
Or2r11 |
A |
T |
6: 42,437,573 (GRCm39) |
C127S |
probably damaging |
Het |
Or5g26 |
T |
C |
2: 85,494,689 (GRCm39) |
T30A |
probably benign |
Het |
Or8s8 |
T |
C |
15: 98,354,866 (GRCm39) |
V225A |
probably benign |
Het |
Osbpl10 |
A |
G |
9: 115,036,726 (GRCm39) |
T241A |
probably damaging |
Het |
Peg3 |
C |
T |
7: 6,711,839 (GRCm39) |
E1128K |
possibly damaging |
Het |
Plch1 |
C |
A |
3: 63,681,068 (GRCm39) |
M186I |
probably benign |
Het |
Pon3 |
A |
C |
6: 5,236,911 (GRCm39) |
L152R |
probably damaging |
Het |
Prr36 |
G |
A |
8: 4,263,905 (GRCm39) |
P587L |
unknown |
Het |
Psma2 |
T |
A |
13: 14,799,832 (GRCm39) |
I192N |
probably damaging |
Het |
Rbm11 |
T |
C |
16: 75,389,923 (GRCm39) |
F30L |
probably damaging |
Het |
Rpap3 |
G |
A |
15: 97,576,299 (GRCm39) |
A622V |
possibly damaging |
Het |
Scgb2b11 |
T |
A |
7: 31,908,807 (GRCm39) |
N98Y |
probably damaging |
Het |
Siglec1 |
A |
G |
2: 130,923,212 (GRCm39) |
L511P |
probably damaging |
Het |
Sirpb1c |
C |
T |
3: 15,887,156 (GRCm39) |
V228M |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,460,605 (GRCm39) |
Y804N |
probably damaging |
Het |
Sult6b2 |
T |
C |
6: 142,747,524 (GRCm39) |
D75G |
not run |
Het |
Sycp3 |
A |
C |
10: 88,302,368 (GRCm39) |
K119N |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,078,278 (GRCm39) |
L4703P |
probably damaging |
Het |
Tex12 |
C |
G |
9: 50,470,523 (GRCm39) |
L20F |
possibly damaging |
Het |
Them5 |
T |
A |
3: 94,250,603 (GRCm39) |
Y55* |
probably null |
Het |
Tmem43 |
A |
T |
6: 91,458,968 (GRCm39) |
D213V |
probably benign |
Het |
Tnfrsf10b |
A |
C |
14: 70,005,239 (GRCm39) |
Q44P |
unknown |
Het |
Trbv2 |
A |
T |
6: 41,024,836 (GRCm39) |
Q84L |
probably benign |
Het |
Trim2 |
C |
T |
3: 84,212,537 (GRCm39) |
|
probably benign |
Het |
Trim36 |
A |
G |
18: 46,305,558 (GRCm39) |
V475A |
probably benign |
Het |
Ttbk1 |
C |
A |
17: 46,758,269 (GRCm39) |
E788D |
probably benign |
Het |
Ttn |
T |
C |
2: 76,543,626 (GRCm39) |
D33120G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,576,256 (GRCm39) |
N24879I |
probably damaging |
Het |
Ube4a |
T |
A |
9: 44,864,308 (GRCm39) |
Q76L |
probably benign |
Het |
Vmn2r27 |
T |
A |
6: 124,168,980 (GRCm39) |
I717F |
probably damaging |
Het |
Vmn2r45 |
T |
C |
7: 8,485,987 (GRCm39) |
K434E |
possibly damaging |
Het |
Vta1 |
T |
C |
10: 14,531,461 (GRCm39) |
T305A |
probably damaging |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Fhad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Fhad1
|
APN |
4 |
141,632,923 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01478:Fhad1
|
APN |
4 |
141,678,949 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01752:Fhad1
|
APN |
4 |
141,700,210 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01788:Fhad1
|
APN |
4 |
141,660,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01919:Fhad1
|
APN |
4 |
141,691,906 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02489:Fhad1
|
APN |
4 |
141,684,931 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02568:Fhad1
|
APN |
4 |
141,660,105 (GRCm39) |
missense |
probably null |
1.00 |
IGL02583:Fhad1
|
APN |
4 |
141,738,955 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02716:Fhad1
|
APN |
4 |
141,645,642 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02819:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02820:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03038:Fhad1
|
APN |
4 |
141,729,805 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03167:Fhad1
|
APN |
4 |
141,700,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03255:Fhad1
|
APN |
4 |
141,700,191 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4466_Fhad1_343
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831_Fhad1_494
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R5504_Fhad1_818
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
BB002:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
BB012:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT1430001:Fhad1
|
UTSW |
4 |
141,637,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R0014:Fhad1
|
UTSW |
4 |
141,655,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Fhad1
|
UTSW |
4 |
141,667,406 (GRCm39) |
missense |
probably benign |
0.06 |
R0143:Fhad1
|
UTSW |
4 |
141,656,957 (GRCm39) |
splice site |
probably benign |
|
R0178:Fhad1
|
UTSW |
4 |
141,682,651 (GRCm39) |
missense |
probably benign |
0.31 |
R0308:Fhad1
|
UTSW |
4 |
141,712,904 (GRCm39) |
splice site |
probably benign |
|
R0384:Fhad1
|
UTSW |
4 |
141,729,737 (GRCm39) |
missense |
probably benign |
|
R0583:Fhad1
|
UTSW |
4 |
141,631,301 (GRCm39) |
missense |
probably benign |
0.37 |
R1501:Fhad1
|
UTSW |
4 |
141,691,936 (GRCm39) |
missense |
probably benign |
|
R1584:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.22 |
R1615:Fhad1
|
UTSW |
4 |
141,649,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R1991:Fhad1
|
UTSW |
4 |
141,709,473 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2060:Fhad1
|
UTSW |
4 |
141,626,560 (GRCm39) |
missense |
probably benign |
0.08 |
R2079:Fhad1
|
UTSW |
4 |
141,718,513 (GRCm39) |
nonsense |
probably null |
|
R2133:Fhad1
|
UTSW |
4 |
141,655,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2337:Fhad1
|
UTSW |
4 |
141,649,655 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2843:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2844:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2845:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2846:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2866:Fhad1
|
UTSW |
4 |
141,648,099 (GRCm39) |
missense |
probably benign |
0.00 |
R3119:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
frame shift |
probably null |
|
R3760:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Fhad1
|
UTSW |
4 |
141,712,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4466:Fhad1
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Fhad1
|
UTSW |
4 |
141,623,779 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4680:Fhad1
|
UTSW |
4 |
141,738,858 (GRCm39) |
nonsense |
probably null |
|
R4725:Fhad1
|
UTSW |
4 |
141,655,689 (GRCm39) |
critical splice donor site |
probably null |
|
R4755:Fhad1
|
UTSW |
4 |
141,655,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Fhad1
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R4909:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.01 |
R4968:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fhad1
|
UTSW |
4 |
141,729,910 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5036:Fhad1
|
UTSW |
4 |
141,648,052 (GRCm39) |
missense |
probably benign |
0.03 |
R5048:Fhad1
|
UTSW |
4 |
141,691,987 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5416:Fhad1
|
UTSW |
4 |
141,646,113 (GRCm39) |
missense |
probably benign |
0.39 |
R5504:Fhad1
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
R5586:Fhad1
|
UTSW |
4 |
141,632,442 (GRCm39) |
missense |
probably benign |
0.44 |
R5692:Fhad1
|
UTSW |
4 |
141,690,768 (GRCm39) |
missense |
probably benign |
0.00 |
R5706:Fhad1
|
UTSW |
4 |
141,681,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Fhad1
|
UTSW |
4 |
141,656,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R5823:Fhad1
|
UTSW |
4 |
141,682,617 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5833:Fhad1
|
UTSW |
4 |
141,729,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Fhad1
|
UTSW |
4 |
141,618,263 (GRCm39) |
nonsense |
probably null |
|
R6286:Fhad1
|
UTSW |
4 |
141,648,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Fhad1
|
UTSW |
4 |
141,643,707 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6755:Fhad1
|
UTSW |
4 |
141,691,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7008:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7012:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7014:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7058:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7059:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7060:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7159:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Fhad1
|
UTSW |
4 |
141,691,937 (GRCm39) |
missense |
probably benign |
|
R7670:Fhad1
|
UTSW |
4 |
141,678,802 (GRCm39) |
missense |
probably benign |
0.01 |
R7694:Fhad1
|
UTSW |
4 |
141,632,375 (GRCm39) |
missense |
probably benign |
0.41 |
R7745:Fhad1
|
UTSW |
4 |
141,618,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7848:Fhad1
|
UTSW |
4 |
141,632,913 (GRCm39) |
missense |
probably benign |
0.29 |
R7867:Fhad1
|
UTSW |
4 |
141,632,902 (GRCm39) |
missense |
probably benign |
0.00 |
R7925:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
R8089:Fhad1
|
UTSW |
4 |
141,684,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Fhad1
|
UTSW |
4 |
141,712,836 (GRCm39) |
missense |
probably benign |
0.02 |
R8711:Fhad1
|
UTSW |
4 |
141,684,924 (GRCm39) |
missense |
probably benign |
0.25 |
R8751:Fhad1
|
UTSW |
4 |
141,646,134 (GRCm39) |
missense |
probably benign |
0.04 |
R8783:Fhad1
|
UTSW |
4 |
141,636,403 (GRCm39) |
missense |
probably benign |
0.02 |
R8858:Fhad1
|
UTSW |
4 |
141,666,339 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8867:Fhad1
|
UTSW |
4 |
141,656,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R8890:Fhad1
|
UTSW |
4 |
141,656,902 (GRCm39) |
missense |
probably benign |
0.01 |
R8982:Fhad1
|
UTSW |
4 |
141,729,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Fhad1
|
UTSW |
4 |
141,649,735 (GRCm39) |
splice site |
probably benign |
|
R9021:Fhad1
|
UTSW |
4 |
141,709,620 (GRCm39) |
missense |
probably damaging |
0.97 |
R9190:Fhad1
|
UTSW |
4 |
141,646,058 (GRCm39) |
critical splice donor site |
probably null |
|
R9237:Fhad1
|
UTSW |
4 |
141,632,483 (GRCm39) |
missense |
probably benign |
0.11 |
R9614:Fhad1
|
UTSW |
4 |
141,678,882 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9744:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
PCR Primer
(F):5'- TTGGCCGACTAGCTGATCTC -3'
(R):5'- TCCTCCCACCTAAGACTTGATATCAG -3'
Sequencing Primer
(F):5'- TAGCTGATCTCCAAGGTGCAC -3'
(R):5'- ACCTGCTGAAGCTCTCGTGATG -3'
|
Posted On |
2019-12-20 |