Incidental Mutation 'R6271:Ahdc1'
ID |
507322 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ahdc1
|
Ensembl Gene |
ENSMUSG00000037692 |
Gene Name |
AT hook, DNA binding motif, containing 1 |
Synonyms |
D030015G18Rik |
MMRRC Submission |
044379-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.189)
|
Stock # |
R6271 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
132738797-132805421 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 132792035 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Phenylalanine
at position 1092
(C1092F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101536
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044521]
[ENSMUST00000105914]
[ENSMUST00000105915]
[ENSMUST00000105916]
|
AlphaFold |
Q6PAL7 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044521
AA Change: C1092F
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000047113 Gene: ENSMUSG00000037692 AA Change: C1092F
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105914
AA Change: C1092F
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101534 Gene: ENSMUSG00000037692 AA Change: C1092F
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
Pfam:DUF4683
|
559 |
639 |
6.4e-15 |
PFAM |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105915
AA Change: C1092F
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101535 Gene: ENSMUSG00000037692 AA Change: C1092F
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105916
AA Change: C1092F
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101536 Gene: ENSMUSG00000037692 AA Change: C1092F
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135548
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142524
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156677
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148518
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154646
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154482
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.1%
- 20x: 94.4%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing two AT-hooks, which likely function in DNA binding. Mutations in this gene were found in individuals with Xia-Gibbs syndrome. [provided by RefSeq, Jun 2014]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aplf |
T |
C |
6: 87,623,230 (GRCm39) |
E304G |
possibly damaging |
Het |
Atp12a |
A |
G |
14: 56,615,879 (GRCm39) |
D547G |
probably benign |
Het |
B3gat2 |
T |
C |
1: 23,854,342 (GRCm39) |
L212P |
probably damaging |
Het |
Babam2 |
G |
T |
5: 32,158,706 (GRCm39) |
A219S |
probably damaging |
Het |
Ccdc18 |
A |
C |
5: 108,322,753 (GRCm39) |
S618R |
possibly damaging |
Het |
Ces2c |
G |
A |
8: 105,578,748 (GRCm39) |
G342D |
probably damaging |
Het |
Cfap57 |
A |
C |
4: 118,452,956 (GRCm39) |
D582E |
probably benign |
Het |
Cisd2 |
T |
C |
3: 135,114,627 (GRCm39) |
N115D |
possibly damaging |
Het |
Cyp17a1 |
A |
G |
19: 46,661,159 (GRCm39) |
F42L |
probably benign |
Het |
Fam234a |
T |
C |
17: 26,437,211 (GRCm39) |
D156G |
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,513,767 (GRCm39) |
I1554K |
probably benign |
Het |
Fv1 |
A |
G |
4: 147,954,474 (GRCm39) |
T347A |
possibly damaging |
Het |
Gm5134 |
T |
A |
10: 75,831,643 (GRCm39) |
C361S |
probably benign |
Het |
Grin3a |
T |
C |
4: 49,792,516 (GRCm39) |
I406V |
probably benign |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Ifna13 |
A |
C |
4: 88,562,082 (GRCm39) |
L181V |
possibly damaging |
Het |
Irx4 |
A |
G |
13: 73,414,713 (GRCm39) |
|
probably null |
Het |
Kcna3 |
T |
A |
3: 106,944,922 (GRCm39) |
M395K |
probably damaging |
Het |
Kcnma1 |
A |
T |
14: 23,559,957 (GRCm39) |
V347D |
probably damaging |
Het |
Kng2 |
A |
T |
16: 22,822,698 (GRCm39) |
V218E |
probably benign |
Het |
Krt36 |
G |
A |
11: 99,995,298 (GRCm39) |
Q167* |
probably null |
Het |
Lama2 |
T |
C |
10: 26,899,325 (GRCm39) |
D2457G |
possibly damaging |
Het |
Ldah |
G |
A |
12: 8,318,599 (GRCm39) |
|
probably null |
Het |
Lhfpl3 |
G |
T |
5: 22,951,242 (GRCm39) |
A18S |
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,956,851 (GRCm39) |
|
probably null |
Het |
Ltv1 |
T |
C |
10: 13,055,445 (GRCm39) |
Y352C |
probably damaging |
Het |
Lyst |
G |
T |
13: 13,833,339 (GRCm39) |
M1720I |
probably benign |
Het |
Mkx |
A |
T |
18: 6,937,059 (GRCm39) |
|
probably null |
Het |
Myo18a |
A |
G |
11: 77,711,635 (GRCm39) |
H626R |
probably damaging |
Het |
Nop9 |
A |
C |
14: 55,991,198 (GRCm39) |
Q618H |
probably damaging |
Het |
Or12k5 |
T |
C |
2: 36,895,554 (GRCm39) |
Q24R |
probably damaging |
Het |
Or4c12b |
T |
C |
2: 89,646,906 (GRCm39) |
S73P |
probably damaging |
Het |
Or7g32 |
A |
G |
9: 19,389,337 (GRCm39) |
S67P |
probably damaging |
Het |
Or8c9 |
T |
C |
9: 38,241,578 (GRCm39) |
S232P |
probably benign |
Het |
Otog |
C |
A |
7: 45,901,464 (GRCm39) |
Q388K |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Oxct2b |
T |
G |
4: 123,011,508 (GRCm39) |
V476G |
probably damaging |
Het |
Parp10 |
T |
C |
15: 76,126,202 (GRCm39) |
T329A |
probably benign |
Het |
Pcdhga5 |
T |
C |
18: 37,829,735 (GRCm39) |
S728P |
probably benign |
Het |
Piezo1 |
G |
T |
8: 123,221,671 (GRCm39) |
H574Q |
probably damaging |
Het |
Pnpla1 |
G |
A |
17: 29,100,342 (GRCm39) |
G403E |
probably benign |
Het |
Preb |
C |
A |
5: 31,115,395 (GRCm39) |
V255F |
probably damaging |
Het |
Prmt9 |
A |
G |
8: 78,304,092 (GRCm39) |
N725S |
probably damaging |
Het |
Ric1 |
A |
T |
19: 29,544,765 (GRCm39) |
|
probably null |
Het |
Semp2l1 |
T |
A |
1: 32,584,572 (GRCm39) |
D446V |
probably damaging |
Het |
Serinc3 |
G |
C |
2: 163,472,896 (GRCm39) |
L245V |
probably benign |
Het |
Sgce |
T |
C |
6: 4,730,015 (GRCm39) |
K70E |
possibly damaging |
Het |
Simc1 |
T |
G |
13: 54,687,537 (GRCm39) |
V102G |
probably damaging |
Het |
Slc66a3 |
T |
C |
12: 17,047,704 (GRCm39) |
D76G |
probably damaging |
Het |
Smyd2 |
A |
G |
1: 189,616,049 (GRCm39) |
Y362H |
probably damaging |
Het |
Sptbn1 |
G |
T |
11: 30,050,660 (GRCm39) |
H2310N |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,184,652 (GRCm39) |
Y4077C |
probably damaging |
Het |
Syne2 |
C |
A |
12: 75,937,155 (GRCm39) |
A251E |
probably damaging |
Het |
Taok1 |
A |
T |
11: 77,464,609 (GRCm39) |
L159Q |
probably damaging |
Het |
Tasor2 |
C |
T |
13: 3,631,891 (GRCm39) |
R870H |
possibly damaging |
Het |
Timeless |
T |
C |
10: 128,086,593 (GRCm39) |
L1043P |
probably damaging |
Het |
Tmprss3 |
T |
C |
17: 31,405,536 (GRCm39) |
E352G |
probably damaging |
Het |
Trav6-4 |
A |
T |
14: 53,692,039 (GRCm39) |
T46S |
probably benign |
Het |
Ubiad1 |
A |
T |
4: 148,521,083 (GRCm39) |
Y180* |
probably null |
Het |
Usp47 |
A |
G |
7: 111,686,263 (GRCm39) |
E627G |
probably damaging |
Het |
Vmn2r124 |
A |
G |
17: 18,283,145 (GRCm39) |
T280A |
probably benign |
Het |
|
Other mutations in Ahdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Ahdc1
|
APN |
4 |
132,790,373 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02293:Ahdc1
|
APN |
4 |
132,792,929 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02338:Ahdc1
|
APN |
4 |
132,789,860 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02828:Ahdc1
|
APN |
4 |
132,790,232 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02859:Ahdc1
|
APN |
4 |
132,790,004 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02859:Ahdc1
|
APN |
4 |
132,790,003 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02901:Ahdc1
|
APN |
4 |
132,792,245 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03323:Ahdc1
|
APN |
4 |
132,792,739 (GRCm39) |
missense |
probably benign |
|
FR4304:Ahdc1
|
UTSW |
4 |
132,790,070 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ahdc1
|
UTSW |
4 |
132,790,071 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ahdc1
|
UTSW |
4 |
132,790,068 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Ahdc1
|
UTSW |
4 |
132,790,070 (GRCm39) |
small insertion |
probably benign |
|
R0325:Ahdc1
|
UTSW |
4 |
132,790,030 (GRCm39) |
missense |
unknown |
|
R0550:Ahdc1
|
UTSW |
4 |
132,790,348 (GRCm39) |
missense |
probably benign |
0.33 |
R0681:Ahdc1
|
UTSW |
4 |
132,792,827 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0683:Ahdc1
|
UTSW |
4 |
132,792,827 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0731:Ahdc1
|
UTSW |
4 |
132,790,262 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0751:Ahdc1
|
UTSW |
4 |
132,792,707 (GRCm39) |
missense |
probably benign |
0.02 |
R1137:Ahdc1
|
UTSW |
4 |
132,789,424 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1184:Ahdc1
|
UTSW |
4 |
132,792,707 (GRCm39) |
missense |
probably benign |
0.02 |
R1331:Ahdc1
|
UTSW |
4 |
132,791,002 (GRCm39) |
missense |
probably benign |
0.18 |
R1599:Ahdc1
|
UTSW |
4 |
132,792,247 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2202:Ahdc1
|
UTSW |
4 |
132,793,220 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2205:Ahdc1
|
UTSW |
4 |
132,793,220 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2261:Ahdc1
|
UTSW |
4 |
132,790,474 (GRCm39) |
missense |
unknown |
|
R2262:Ahdc1
|
UTSW |
4 |
132,790,474 (GRCm39) |
missense |
unknown |
|
R3683:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3684:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3685:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3713:Ahdc1
|
UTSW |
4 |
132,793,297 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4027:Ahdc1
|
UTSW |
4 |
132,791,476 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4807:Ahdc1
|
UTSW |
4 |
132,791,624 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4987:Ahdc1
|
UTSW |
4 |
132,791,631 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5126:Ahdc1
|
UTSW |
4 |
132,790,833 (GRCm39) |
missense |
probably benign |
0.18 |
R5276:Ahdc1
|
UTSW |
4 |
132,790,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5680:Ahdc1
|
UTSW |
4 |
132,792,907 (GRCm39) |
missense |
probably benign |
|
R5997:Ahdc1
|
UTSW |
4 |
132,791,206 (GRCm39) |
missense |
probably benign |
0.05 |
R6050:Ahdc1
|
UTSW |
4 |
132,793,202 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6410:Ahdc1
|
UTSW |
4 |
132,790,210 (GRCm39) |
missense |
probably damaging |
0.97 |
R6519:Ahdc1
|
UTSW |
4 |
132,792,079 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6970:Ahdc1
|
UTSW |
4 |
132,789,656 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7199:Ahdc1
|
UTSW |
4 |
132,791,935 (GRCm39) |
missense |
probably benign |
0.33 |
R7202:Ahdc1
|
UTSW |
4 |
132,789,198 (GRCm39) |
nonsense |
probably null |
|
R7576:Ahdc1
|
UTSW |
4 |
132,792,313 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7614:Ahdc1
|
UTSW |
4 |
132,790,825 (GRCm39) |
missense |
probably benign |
0.18 |
R7794:Ahdc1
|
UTSW |
4 |
132,791,289 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7875:Ahdc1
|
UTSW |
4 |
132,791,161 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8016:Ahdc1
|
UTSW |
4 |
132,790,226 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8295:Ahdc1
|
UTSW |
4 |
132,788,762 (GRCm39) |
start codon destroyed |
probably null |
0.53 |
R8332:Ahdc1
|
UTSW |
4 |
132,791,282 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8719:Ahdc1
|
UTSW |
4 |
132,791,533 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8725:Ahdc1
|
UTSW |
4 |
132,792,743 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8862:Ahdc1
|
UTSW |
4 |
132,791,129 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9158:Ahdc1
|
UTSW |
4 |
132,792,505 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9179:Ahdc1
|
UTSW |
4 |
132,788,929 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9362:Ahdc1
|
UTSW |
4 |
132,790,348 (GRCm39) |
missense |
probably benign |
0.33 |
R9428:Ahdc1
|
UTSW |
4 |
132,791,773 (GRCm39) |
missense |
possibly damaging |
0.93 |
RF017:Ahdc1
|
UTSW |
4 |
132,790,062 (GRCm39) |
small insertion |
probably benign |
|
RF020:Ahdc1
|
UTSW |
4 |
132,791,588 (GRCm39) |
missense |
possibly damaging |
0.96 |
T0722:Ahdc1
|
UTSW |
4 |
132,790,065 (GRCm39) |
small insertion |
probably benign |
|
T0975:Ahdc1
|
UTSW |
4 |
132,790,065 (GRCm39) |
small insertion |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- TCCTTCTTCAACAGCTCTGAGG -3'
(R):5'- TGACTGAACTGGGTGCTGTC -3'
Sequencing Primer
(F):5'- GGGGGCCCCTTCTCTGG -3'
(R):5'- TGACTCGGAGAAGGTCTCG -3'
|
Posted On |
2018-03-15 |