Incidental Mutation 'R8719:Ahdc1'
ID |
670000 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ahdc1
|
Ensembl Gene |
ENSMUSG00000037692 |
Gene Name |
AT hook, DNA binding motif, containing 1 |
Synonyms |
D030015G18Rik |
MMRRC Submission |
068614-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.189)
|
Stock # |
R8719 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
132738797-132805421 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 132791533 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 925
(Y925N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000047113
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044521]
[ENSMUST00000105914]
[ENSMUST00000105915]
[ENSMUST00000105916]
|
AlphaFold |
Q6PAL7 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044521
AA Change: Y925N
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000047113 Gene: ENSMUSG00000037692 AA Change: Y925N
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: Y925N
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000101534 Gene: ENSMUSG00000037692 AA Change: Y925N
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: Y925N
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000101535 Gene: ENSMUSG00000037692 AA Change: Y925N
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: Y925N
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000101536 Gene: ENSMUSG00000037692 AA Change: Y925N
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 |
|
Meta Mutation Damage Score |
0.0737 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
100% (61/61) |
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 |
Acsl1 |
T |
C |
8: 46,966,700 (GRCm39) |
I224T |
probably benign |
Het |
Adamts20 |
C |
G |
15: 94,241,903 (GRCm39) |
A702P |
probably damaging |
Het |
Anapc1 |
T |
C |
2: 128,483,369 (GRCm39) |
E1242G |
probably damaging |
Het |
Angptl2 |
A |
G |
2: 33,133,914 (GRCm39) |
N412S |
possibly damaging |
Het |
Aox3 |
T |
C |
1: 58,158,696 (GRCm39) |
V89A |
probably damaging |
Het |
Atxn1l |
A |
T |
8: 110,459,861 (GRCm39) |
S134T |
possibly damaging |
Het |
Brf1 |
C |
A |
12: 112,943,304 (GRCm39) |
|
probably benign |
Het |
Cab39l |
A |
T |
14: 59,734,314 (GRCm39) |
H11L |
probably benign |
Het |
Cabcoco1 |
A |
G |
10: 68,272,671 (GRCm39) |
|
probably benign |
Het |
Ccdc150 |
C |
A |
1: 54,302,668 (GRCm39) |
P96Q |
probably benign |
Het |
Chek2 |
T |
C |
5: 111,014,908 (GRCm39) |
V459A |
probably damaging |
Het |
Cntnap2 |
A |
T |
6: 45,978,161 (GRCm39) |
D272V |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,160,516 (GRCm39) |
S572P |
possibly damaging |
Het |
Cysltr2 |
T |
C |
14: 73,267,111 (GRCm39) |
T200A |
possibly damaging |
Het |
Dglucy |
T |
C |
12: 100,804,821 (GRCm39) |
L104P |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,960,289 (GRCm39) |
M2222K |
probably damaging |
Het |
Dync2h1 |
C |
A |
9: 7,041,641 (GRCm39) |
V3334F |
probably benign |
Het |
Ear2 |
A |
T |
14: 44,340,734 (GRCm39) |
T131S |
possibly damaging |
Het |
Eef1akmt2 |
A |
T |
7: 132,452,340 (GRCm39) |
V92D |
probably damaging |
Het |
Fam83c |
T |
A |
2: 155,671,128 (GRCm39) |
Q769L |
probably benign |
Het |
Fanca |
A |
T |
8: 124,014,867 (GRCm39) |
C812S |
probably benign |
Het |
Gm21663 |
T |
G |
5: 26,146,162 (GRCm39) |
R50S |
probably damaging |
Het |
Gm5591 |
T |
G |
7: 38,221,614 (GRCm39) |
S152R |
probably benign |
Het |
Gm6370 |
T |
G |
5: 146,430,626 (GRCm39) |
D270E |
probably damaging |
Het |
H2-T22 |
T |
C |
17: 36,352,835 (GRCm39) |
I91V |
probably benign |
Het |
Hdac5 |
T |
C |
11: 102,097,963 (GRCm39) |
M61V |
probably benign |
Het |
Hsd17b6 |
A |
G |
10: 127,829,492 (GRCm39) |
S237P |
possibly damaging |
Het |
Khk |
T |
A |
5: 31,088,374 (GRCm39) |
F294I |
possibly damaging |
Het |
Klc1 |
G |
A |
12: 111,772,509 (GRCm39) |
|
probably benign |
Het |
Lamb3 |
T |
C |
1: 193,006,099 (GRCm39) |
W143R |
probably damaging |
Het |
Lmo2 |
T |
C |
2: 103,811,264 (GRCm39) |
I171T |
probably damaging |
Het |
Meis1 |
A |
G |
11: 18,835,587 (GRCm39) |
S344P |
probably benign |
Het |
Nf1 |
C |
A |
11: 79,281,119 (GRCm39) |
R125S |
possibly damaging |
Het |
Nrcam |
A |
G |
12: 44,586,325 (GRCm39) |
E105G |
probably benign |
Het |
Nudt22 |
T |
C |
19: 6,972,638 (GRCm39) |
D150G |
possibly damaging |
Het |
Or14j8 |
T |
C |
17: 38,263,895 (GRCm39) |
T7A |
probably damaging |
Het |
Or5an1 |
A |
G |
19: 12,260,792 (GRCm39) |
I127V |
probably benign |
Het |
Or5b109 |
A |
G |
19: 13,211,836 (GRCm39) |
Y74C |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,763,778 (GRCm39) |
R799* |
probably null |
Het |
Pelp1 |
T |
C |
11: 70,292,789 (GRCm39) |
N175S |
probably damaging |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,302,525 (GRCm39) |
|
probably benign |
Het |
Pik3r4 |
C |
A |
9: 105,559,394 (GRCm39) |
S1162R |
probably benign |
Het |
Pkd1l3 |
A |
T |
8: 110,341,255 (GRCm39) |
N36I |
unknown |
Het |
Pomk |
T |
A |
8: 26,473,503 (GRCm39) |
Y150F |
possibly damaging |
Het |
Rdh11 |
T |
A |
12: 79,229,574 (GRCm39) |
H233L |
probably benign |
Het |
Rln1 |
A |
T |
19: 29,309,281 (GRCm39) |
M166K |
probably benign |
Het |
Rnf40 |
T |
A |
7: 127,191,834 (GRCm39) |
L356Q |
probably damaging |
Het |
Sin3b |
G |
T |
8: 73,450,139 (GRCm39) |
G19W |
unknown |
Het |
Slc6a15 |
A |
G |
10: 103,240,176 (GRCm39) |
R300G |
probably damaging |
Het |
Sncaip |
A |
T |
18: 53,027,910 (GRCm39) |
K433M |
probably damaging |
Het |
Tead2 |
A |
T |
7: 44,882,316 (GRCm39) |
|
probably benign |
Het |
Tespa1 |
A |
G |
10: 130,184,108 (GRCm39) |
D63G |
probably benign |
Het |
Tmem117 |
T |
C |
15: 94,992,248 (GRCm39) |
F303L |
probably damaging |
Het |
Tmem270 |
T |
G |
5: 134,930,650 (GRCm39) |
T204P |
probably damaging |
Het |
Trip12 |
A |
G |
1: 84,722,790 (GRCm39) |
V1320A |
probably damaging |
Het |
Ttc7b |
A |
G |
12: 100,267,812 (GRCm39) |
L843P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,543,041 (GRCm39) |
Y33315C |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,607,146 (GRCm39) |
V17959A |
possibly damaging |
Het |
Vmn2r73 |
A |
G |
7: 85,521,095 (GRCm39) |
V291A |
probably damaging |
Het |
Ywhag |
T |
A |
5: 135,939,998 (GRCm39) |
T199S |
probably benign |
Het |
Zfp810 |
T |
C |
9: 22,190,571 (GRCm39) |
T77A |
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 |
R6271:Ahdc1
|
UTSW |
4 |
132,792,035 (GRCm39) |
missense |
possibly damaging |
0.73 |
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 |
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'- GGTCCCTGCTTGATTCAGATG -3'
(R):5'- ACAGTCCTGGCCTGAAAAG -3'
Sequencing Primer
(F):5'- GATTCAGATGACTCCTCTGACC -3'
(R):5'- GCCTGAAAAGGGCTTTGC -3'
|
Posted On |
2021-04-30 |