Incidental Mutation 'R5223:Acin1'
ID |
402455 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Acin1
|
Ensembl Gene |
ENSMUSG00000022185 |
Gene Name |
apoptotic chromatin condensation inducer 1 |
Synonyms |
2610036I19Rik, 2610510L13Rik, Acinus |
MMRRC Submission |
042796-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.940)
|
Stock # |
R5223 (G1)
|
Quality Score |
217 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
54879618-54924388 bp(-) (GRCm39) |
Type of Mutation |
frame shift |
DNA Base Change (assembly) |
CCGC to CC
at 54880398 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125776
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022793]
[ENSMUST00000022794]
[ENSMUST00000067784]
[ENSMUST00000111484]
[ENSMUST00000123875]
[ENSMUST00000126166]
[ENSMUST00000141453]
[ENSMUST00000148754]
[ENSMUST00000150371]
[ENSMUST00000167015]
[ENSMUST00000169818]
|
AlphaFold |
Q9JIX8 |
Predicted Effect |
probably null
Transcript: ENSMUST00000022793
|
SMART Domains |
Protein: ENSMUSP00000022793 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
SAP
|
72 |
106 |
1.29e-8 |
SMART |
coiled coil region
|
138 |
175 |
N/A |
INTRINSIC |
low complexity region
|
205 |
220 |
N/A |
INTRINSIC |
coiled coil region
|
259 |
300 |
N/A |
INTRINSIC |
low complexity region
|
378 |
396 |
N/A |
INTRINSIC |
low complexity region
|
414 |
423 |
N/A |
INTRINSIC |
low complexity region
|
573 |
603 |
N/A |
INTRINSIC |
low complexity region
|
631 |
662 |
N/A |
INTRINSIC |
low complexity region
|
734 |
743 |
N/A |
INTRINSIC |
low complexity region
|
760 |
773 |
N/A |
INTRINSIC |
low complexity region
|
778 |
792 |
N/A |
INTRINSIC |
low complexity region
|
803 |
813 |
N/A |
INTRINSIC |
internal_repeat_1
|
817 |
892 |
1.63e-6 |
PROSPERO |
low complexity region
|
927 |
952 |
N/A |
INTRINSIC |
RRM
|
1012 |
1081 |
8.3e-2 |
SMART |
Pfam:RSB_motif
|
1139 |
1246 |
5.7e-30 |
PFAM |
low complexity region
|
1275 |
1329 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000022794
|
SMART Domains |
Protein: ENSMUSP00000022794 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
169 |
194 |
N/A |
INTRINSIC |
RRM
|
254 |
323 |
8.3e-2 |
SMART |
low complexity region
|
355 |
405 |
N/A |
INTRINSIC |
low complexity region
|
412 |
450 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
451 |
475 |
4e-6 |
PDB |
low complexity region
|
477 |
512 |
N/A |
INTRINSIC |
low complexity region
|
517 |
571 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000067784
|
SMART Domains |
Protein: ENSMUSP00000066005 Gene: ENSMUSG00000059674
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CA
|
67 |
148 |
7.85e-18 |
SMART |
CA
|
172 |
257 |
3.23e-28 |
SMART |
CA
|
281 |
369 |
4.24e-14 |
SMART |
CA
|
396 |
477 |
1.48e-22 |
SMART |
Blast:CA
|
500 |
581 |
3e-31 |
BLAST |
transmembrane domain
|
602 |
624 |
N/A |
INTRINSIC |
Pfam:Cadherin_C
|
627 |
775 |
2e-48 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000111484
|
SMART Domains |
Protein: ENSMUSP00000107109 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
SAP
|
72 |
106 |
1.29e-8 |
SMART |
coiled coil region
|
138 |
172 |
N/A |
INTRINSIC |
coiled coil region
|
219 |
260 |
N/A |
INTRINSIC |
low complexity region
|
338 |
356 |
N/A |
INTRINSIC |
low complexity region
|
374 |
383 |
N/A |
INTRINSIC |
low complexity region
|
533 |
563 |
N/A |
INTRINSIC |
low complexity region
|
591 |
622 |
N/A |
INTRINSIC |
low complexity region
|
694 |
703 |
N/A |
INTRINSIC |
low complexity region
|
720 |
733 |
N/A |
INTRINSIC |
low complexity region
|
738 |
752 |
N/A |
INTRINSIC |
low complexity region
|
763 |
773 |
N/A |
INTRINSIC |
internal_repeat_1
|
777 |
852 |
1.21e-6 |
PROSPERO |
low complexity region
|
887 |
912 |
N/A |
INTRINSIC |
RRM
|
972 |
1041 |
8.3e-2 |
SMART |
low complexity region
|
1073 |
1123 |
N/A |
INTRINSIC |
low complexity region
|
1130 |
1168 |
N/A |
INTRINSIC |
coiled coil region
|
1188 |
1253 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123875
|
SMART Domains |
Protein: ENSMUSP00000117210 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
35 |
N/A |
INTRINSIC |
low complexity region
|
87 |
101 |
N/A |
INTRINSIC |
low complexity region
|
112 |
122 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124271
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125767
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152773
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126166
|
SMART Domains |
Protein: ENSMUSP00000114546 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
low complexity region
|
30 |
40 |
N/A |
INTRINSIC |
low complexity region
|
154 |
179 |
N/A |
INTRINSIC |
RRM
|
239 |
308 |
8.3e-2 |
SMART |
low complexity region
|
340 |
390 |
N/A |
INTRINSIC |
low complexity region
|
397 |
435 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
436 |
460 |
4e-6 |
PDB |
low complexity region
|
462 |
497 |
N/A |
INTRINSIC |
low complexity region
|
502 |
556 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000141453
|
SMART Domains |
Protein: ENSMUSP00000116664 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
low complexity region
|
30 |
40 |
N/A |
INTRINSIC |
low complexity region
|
141 |
166 |
N/A |
INTRINSIC |
RRM
|
226 |
295 |
8.3e-2 |
SMART |
low complexity region
|
327 |
377 |
N/A |
INTRINSIC |
low complexity region
|
384 |
422 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
423 |
447 |
4e-6 |
PDB |
low complexity region
|
449 |
484 |
N/A |
INTRINSIC |
low complexity region
|
489 |
543 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000147714
|
SMART Domains |
Protein: ENSMUSP00000119080 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
SAP
|
18 |
52 |
1.29e-8 |
SMART |
coiled coil region
|
83 |
120 |
N/A |
INTRINSIC |
low complexity region
|
151 |
166 |
N/A |
INTRINSIC |
coiled coil region
|
204 |
245 |
N/A |
INTRINSIC |
low complexity region
|
324 |
342 |
N/A |
INTRINSIC |
low complexity region
|
360 |
369 |
N/A |
INTRINSIC |
low complexity region
|
519 |
549 |
N/A |
INTRINSIC |
low complexity region
|
577 |
608 |
N/A |
INTRINSIC |
low complexity region
|
680 |
689 |
N/A |
INTRINSIC |
low complexity region
|
706 |
719 |
N/A |
INTRINSIC |
low complexity region
|
724 |
738 |
N/A |
INTRINSIC |
low complexity region
|
749 |
759 |
N/A |
INTRINSIC |
low complexity region
|
861 |
886 |
N/A |
INTRINSIC |
RRM
|
946 |
1015 |
8.3e-2 |
SMART |
Pfam:RSB_motif
|
1065 |
1180 |
1.1e-29 |
PFAM |
low complexity region
|
1209 |
1263 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000148754
|
SMART Domains |
Protein: ENSMUSP00000122003 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
170 |
195 |
N/A |
INTRINSIC |
RRM
|
255 |
324 |
8.3e-2 |
SMART |
low complexity region
|
356 |
406 |
N/A |
INTRINSIC |
low complexity region
|
413 |
451 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
452 |
476 |
4e-6 |
PDB |
low complexity region
|
478 |
513 |
N/A |
INTRINSIC |
low complexity region
|
518 |
572 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000150371
|
SMART Domains |
Protein: ENSMUSP00000118069 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
35 |
N/A |
INTRINSIC |
low complexity region
|
74 |
88 |
N/A |
INTRINSIC |
low complexity region
|
99 |
109 |
N/A |
INTRINSIC |
low complexity region
|
223 |
248 |
N/A |
INTRINSIC |
RRM
|
308 |
377 |
8.3e-2 |
SMART |
low complexity region
|
409 |
459 |
N/A |
INTRINSIC |
low complexity region
|
466 |
504 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
505 |
529 |
3e-6 |
PDB |
low complexity region
|
531 |
566 |
N/A |
INTRINSIC |
low complexity region
|
571 |
625 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000167015
|
SMART Domains |
Protein: ENSMUSP00000125776 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
170 |
195 |
N/A |
INTRINSIC |
RRM
|
255 |
324 |
8.3e-2 |
SMART |
low complexity region
|
356 |
406 |
N/A |
INTRINSIC |
low complexity region
|
413 |
451 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
452 |
476 |
4e-6 |
PDB |
low complexity region
|
478 |
513 |
N/A |
INTRINSIC |
low complexity region
|
518 |
572 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151487
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170299
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000196776
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133706
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000167495
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000169818
|
SMART Domains |
Protein: ENSMUSP00000131860 Gene: ENSMUSG00000091306
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
61 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000138321
|
SMART Domains |
Protein: ENSMUSP00000119326 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
Pfam:RSB_motif
|
20 |
128 |
4.7e-23 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Apoptosis is defined by several morphologic nuclear changes, including chromatin condensation and nuclear fragmentation. This gene encodes a nuclear protein that induces apoptotic chromatin condensation after activation by caspase-3, without inducing DNA fragmentation. This protein has also been shown to be a component of a splicing-dependent multiprotein exon junction complex (EJC) that is deposited at splice junctions on mRNAs, as a consequence of pre-mRNA splicing. It may thus be involved in mRNA metabolism associated with splicing. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
C |
T |
11: 119,904,278 (GRCm39) |
V273M |
possibly damaging |
Het |
Acvr1b |
T |
A |
15: 101,091,857 (GRCm39) |
C46S |
probably damaging |
Het |
Ahi1 |
A |
T |
10: 20,846,818 (GRCm39) |
H416L |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,406,072 (GRCm39) |
L1653Q |
probably damaging |
Het |
Cacna1a |
G |
A |
8: 85,313,824 (GRCm39) |
V1533M |
possibly damaging |
Het |
Ccdc33 |
C |
T |
9: 57,940,267 (GRCm39) |
E502K |
possibly damaging |
Het |
Ctnnd1 |
C |
T |
2: 84,447,133 (GRCm39) |
V371M |
probably damaging |
Het |
Cyp2a12 |
A |
T |
7: 26,735,888 (GRCm39) |
|
probably null |
Het |
Dnai4 |
T |
A |
4: 102,906,600 (GRCm39) |
S738C |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,816,496 (GRCm39) |
V2675A |
probably damaging |
Het |
Foxh1 |
T |
A |
15: 76,552,929 (GRCm39) |
|
probably null |
Het |
Gad1-ps |
G |
A |
10: 99,281,009 (GRCm39) |
|
noncoding transcript |
Het |
Gpnmb |
C |
T |
6: 49,033,139 (GRCm39) |
T539M |
probably benign |
Het |
Hdac1-ps |
A |
G |
17: 78,799,867 (GRCm39) |
E286G |
probably benign |
Het |
Hspa9 |
A |
G |
18: 35,085,724 (GRCm39) |
|
probably null |
Het |
Hspg2 |
T |
C |
4: 137,271,225 (GRCm39) |
L2454P |
probably damaging |
Het |
Ift140 |
T |
A |
17: 25,254,786 (GRCm39) |
I422N |
probably benign |
Het |
Igkv6-32 |
T |
C |
6: 70,051,207 (GRCm39) |
S50G |
probably benign |
Het |
Il23r |
T |
A |
6: 67,463,154 (GRCm39) |
Y113F |
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,793,434 (GRCm39) |
D636G |
probably benign |
Het |
Klhl41 |
G |
A |
2: 69,510,171 (GRCm39) |
W569* |
probably null |
Het |
Klra4 |
T |
A |
6: 130,039,110 (GRCm39) |
D94V |
probably damaging |
Het |
Lca5 |
T |
A |
9: 83,280,666 (GRCm39) |
H378L |
probably benign |
Het |
Lhx8 |
T |
A |
3: 154,027,281 (GRCm39) |
T254S |
probably damaging |
Het |
Lrch3 |
C |
T |
16: 32,734,767 (GRCm39) |
R86W |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,354,397 (GRCm39) |
N477I |
probably damaging |
Het |
Man2a1 |
T |
A |
17: 65,019,266 (GRCm39) |
I710K |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,229,826 (GRCm39) |
Y881N |
probably damaging |
Het |
Nhsl1 |
T |
A |
10: 18,402,074 (GRCm39) |
V1100E |
probably damaging |
Het |
Oprk1 |
T |
C |
1: 5,659,519 (GRCm39) |
V83A |
probably benign |
Het |
Or4p8 |
T |
C |
2: 88,727,678 (GRCm39) |
T88A |
probably benign |
Het |
Or5p62 |
A |
G |
7: 107,771,915 (GRCm39) |
V12A |
probably benign |
Het |
Or7g35 |
T |
C |
9: 19,496,322 (GRCm39) |
V163A |
probably benign |
Het |
Pacs1 |
C |
T |
19: 5,195,169 (GRCm39) |
V472I |
probably benign |
Het |
Pard3b |
T |
C |
1: 62,383,272 (GRCm39) |
Y789H |
probably damaging |
Het |
Pcdha2 |
T |
C |
18: 37,073,844 (GRCm39) |
Y492H |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,216,106 (GRCm39) |
N2261D |
probably damaging |
Het |
Pex5l |
A |
T |
3: 33,012,945 (GRCm39) |
S15T |
probably damaging |
Het |
Plekhg4 |
A |
G |
8: 106,105,581 (GRCm39) |
N682S |
probably benign |
Het |
Poc5 |
A |
T |
13: 96,539,463 (GRCm39) |
M335L |
probably benign |
Het |
Polr1a |
C |
T |
6: 71,944,891 (GRCm39) |
R1316W |
possibly damaging |
Het |
Pp2d1 |
T |
C |
17: 53,814,873 (GRCm39) |
H617R |
probably benign |
Het |
Pramel24 |
T |
A |
4: 143,454,591 (GRCm39) |
S296R |
probably benign |
Het |
Prpsap1 |
T |
C |
11: 116,378,974 (GRCm39) |
K65E |
probably benign |
Het |
Ptgfrn |
T |
C |
3: 100,952,909 (GRCm39) |
E775G |
probably benign |
Het |
Ptprc |
T |
A |
1: 138,045,600 (GRCm39) |
I87F |
probably benign |
Het |
Rbbp8 |
C |
A |
18: 11,854,747 (GRCm39) |
A324E |
probably benign |
Het |
Rfx6 |
G |
T |
10: 51,554,092 (GRCm39) |
G63* |
probably null |
Het |
Rpl37a |
T |
C |
1: 72,751,308 (GRCm39) |
M47T |
probably benign |
Het |
Samm50 |
T |
G |
15: 84,084,831 (GRCm39) |
N187K |
probably benign |
Het |
Skic2 |
A |
G |
17: 35,064,142 (GRCm39) |
|
probably null |
Het |
Slamf9 |
T |
C |
1: 172,303,799 (GRCm39) |
I48T |
possibly damaging |
Het |
Slc2a12 |
A |
G |
10: 22,577,931 (GRCm39) |
K576E |
probably damaging |
Het |
Slc4a10 |
G |
A |
2: 62,083,710 (GRCm39) |
G388S |
probably damaging |
Het |
Smtn |
G |
T |
11: 3,479,530 (GRCm39) |
N512K |
probably benign |
Het |
Sntb1 |
C |
G |
15: 55,506,191 (GRCm39) |
G461R |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,455,258 (GRCm39) |
Y3040C |
probably damaging |
Het |
Stat1 |
T |
A |
1: 52,183,401 (GRCm39) |
V389E |
probably damaging |
Het |
Sult5a1 |
A |
T |
8: 123,872,161 (GRCm39) |
M227K |
probably damaging |
Het |
Thsd4 |
T |
C |
9: 59,964,325 (GRCm39) |
D389G |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,923,052 (GRCm39) |
V2545A |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,142,589 (GRCm39) |
I712F |
probably damaging |
Het |
Trim62 |
T |
C |
4: 128,803,204 (GRCm39) |
V418A |
probably damaging |
Het |
Uqcrc1 |
C |
A |
9: 108,771,224 (GRCm39) |
H95N |
probably damaging |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vmn2r66 |
T |
C |
7: 84,657,093 (GRCm39) |
D104G |
probably benign |
Het |
Wdr26 |
T |
C |
1: 181,015,251 (GRCm39) |
I371V |
probably benign |
Het |
Zfp273 |
T |
G |
13: 67,974,298 (GRCm39) |
C475W |
probably damaging |
Het |
Zfp738 |
G |
T |
13: 67,821,182 (GRCm39) |
T55K |
probably damaging |
Het |
Zmym2 |
A |
G |
14: 57,183,971 (GRCm39) |
I978V |
probably benign |
Het |
|
Other mutations in Acin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00988:Acin1
|
APN |
14 |
54,884,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Acin1
|
APN |
14 |
54,881,443 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02396:Acin1
|
APN |
14 |
54,882,256 (GRCm39) |
intron |
probably benign |
|
IGL02967:Acin1
|
APN |
14 |
54,880,210 (GRCm39) |
missense |
possibly damaging |
0.80 |
Protuberant
|
UTSW |
14 |
54,882,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Acin1
|
UTSW |
14 |
54,884,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Acin1
|
UTSW |
14 |
54,902,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R0755:Acin1
|
UTSW |
14 |
54,889,292 (GRCm39) |
start codon destroyed |
probably null |
0.93 |
R0784:Acin1
|
UTSW |
14 |
54,890,985 (GRCm39) |
unclassified |
probably benign |
|
R1600:Acin1
|
UTSW |
14 |
54,881,174 (GRCm39) |
intron |
probably benign |
|
R1682:Acin1
|
UTSW |
14 |
54,901,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Acin1
|
UTSW |
14 |
54,901,995 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Acin1
|
UTSW |
14 |
54,902,661 (GRCm39) |
missense |
probably benign |
0.30 |
R1867:Acin1
|
UTSW |
14 |
54,881,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Acin1
|
UTSW |
14 |
54,884,156 (GRCm39) |
splice site |
probably null |
|
R2067:Acin1
|
UTSW |
14 |
54,902,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R3947:Acin1
|
UTSW |
14 |
54,916,790 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4374:Acin1
|
UTSW |
14 |
54,891,351 (GRCm39) |
unclassified |
probably benign |
|
R4476:Acin1
|
UTSW |
14 |
54,882,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4501:Acin1
|
UTSW |
14 |
54,924,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4547:Acin1
|
UTSW |
14 |
54,883,124 (GRCm39) |
missense |
probably benign |
0.01 |
R4621:Acin1
|
UTSW |
14 |
54,890,900 (GRCm39) |
unclassified |
probably benign |
|
R4657:Acin1
|
UTSW |
14 |
54,880,504 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4680:Acin1
|
UTSW |
14 |
54,924,215 (GRCm39) |
missense |
probably benign |
0.00 |
R4696:Acin1
|
UTSW |
14 |
54,880,474 (GRCm39) |
intron |
probably benign |
|
R4806:Acin1
|
UTSW |
14 |
54,916,685 (GRCm39) |
splice site |
probably benign |
|
R4826:Acin1
|
UTSW |
14 |
54,902,074 (GRCm39) |
missense |
probably damaging |
0.97 |
R5096:Acin1
|
UTSW |
14 |
54,916,679 (GRCm39) |
intron |
probably benign |
|
R5153:Acin1
|
UTSW |
14 |
54,883,070 (GRCm39) |
missense |
probably benign |
0.25 |
R5260:Acin1
|
UTSW |
14 |
54,880,279 (GRCm39) |
intron |
probably benign |
|
R5525:Acin1
|
UTSW |
14 |
54,901,848 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5575:Acin1
|
UTSW |
14 |
54,916,195 (GRCm39) |
splice site |
probably null |
|
R5902:Acin1
|
UTSW |
14 |
54,901,130 (GRCm39) |
missense |
probably benign |
0.01 |
R6211:Acin1
|
UTSW |
14 |
54,881,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Acin1
|
UTSW |
14 |
54,882,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Acin1
|
UTSW |
14 |
54,916,290 (GRCm39) |
missense |
probably benign |
0.24 |
R6916:Acin1
|
UTSW |
14 |
54,902,873 (GRCm39) |
missense |
probably benign |
0.27 |
R7201:Acin1
|
UTSW |
14 |
54,902,356 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7833:Acin1
|
UTSW |
14 |
54,902,059 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8096:Acin1
|
UTSW |
14 |
54,882,726 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8167:Acin1
|
UTSW |
14 |
54,902,337 (GRCm39) |
missense |
probably benign |
0.01 |
R8421:Acin1
|
UTSW |
14 |
54,880,486 (GRCm39) |
missense |
unknown |
|
R8771:Acin1
|
UTSW |
14 |
54,880,496 (GRCm39) |
missense |
unknown |
|
R8862:Acin1
|
UTSW |
14 |
54,901,172 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Acin1
|
UTSW |
14 |
54,901,913 (GRCm39) |
missense |
probably benign |
0.16 |
R9755:Acin1
|
UTSW |
14 |
54,889,292 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Acin1
|
UTSW |
14 |
54,904,558 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Acin1
|
UTSW |
14 |
54,880,207 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TACAGGTGTGCTTCGACTCC -3'
(R):5'- CTGTTAATAGAAACTGACAGTGACCC -3'
Sequencing Primer
(F):5'- GACTCCGGCTTCTGCTGTG -3'
(R):5'- AAGCACAGCCTGGGATCAGTTC -3'
|
Posted On |
2016-07-22 |