Incidental Mutation 'RF042:Anapc2'
| ID |
604855 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Anapc2
|
| Ensembl Gene |
ENSMUSG00000026965 |
| Gene Name |
anaphase promoting complex subunit 2 |
| Synonyms |
Emi4, expressed during mesenchymal induction 4, 9230107K09Rik, Imi4, APC2 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
RF042 (G1)
|
| Quality Score |
214.458 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
25162490-25175927 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
GCGGCGGCGGCGAC to GC
at 25162573 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000115177
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028341]
[ENSMUST00000028342]
[ENSMUST00000114336]
[ENSMUST00000129300]
|
| AlphaFold |
Q8BZQ7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028341
|
| SMART Domains |
Protein: ENSMUSP00000028341
Gene: ENSMUSG00000026965
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
123 |
133 |
N/A |
INTRINSIC |
|
low complexity region
|
153 |
164 |
N/A |
INTRINSIC |
|
low complexity region
|
221 |
229 |
N/A |
INTRINSIC |
|
low complexity region
|
456 |
467 |
N/A |
INTRINSIC |
|
CULLIN
|
515 |
663 |
6.72e-9 |
SMART |
|
APC2
|
772 |
832 |
3.67e-27 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028342
|
| SMART Domains |
Protein: ENSMUSP00000028342
Gene: ENSMUSG00000026966
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
13 |
70 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114336
|
| SMART Domains |
Protein: ENSMUSP00000109975
Gene: ENSMUSG00000048707
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Phostensin_N
|
8 |
89 |
8.3e-38 |
PFAM |
|
low complexity region
|
105 |
117 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
149 |
273 |
1.71e-5 |
PROSPERO |
|
low complexity region
|
290 |
322 |
N/A |
INTRINSIC |
|
low complexity region
|
401 |
410 |
N/A |
INTRINSIC |
|
Pfam:Phostensin
|
506 |
645 |
1.8e-65 |
PFAM |
|
low complexity region
|
647 |
665 |
N/A |
INTRINSIC |
|
low complexity region
|
684 |
697 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000129300
|
| SMART Domains |
Protein: ENSMUSP00000115177
Gene: ENSMUSG00000026965
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
170 |
181 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.4%
- 20x: 98.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle by ubiquitinating its specific substrates, such as mitotic cyclins and anaphase inhibitor, for subsequent degradation by the proteasome. [provided by RefSeq, Oct 2009]
PHENOTYPE: Homozygous mutation of this gene results in embryonic lethality before E6.5. Conditional ablation in the liver results in liver failure and premature death. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 5430401F13Rik |
AAAGGAAAAGGTGGCCAG |
AAAGGAAAAGGTGGCCAGCAAAAACAGGAAGGAAAAGGTGGCCAG |
6: 131,529,849 (GRCm39) |
|
probably benign |
Het |
| A030005L19Rik |
GCTGCTG |
GCTGCTGTGACTGCTG |
1: 82,891,305 (GRCm39) |
|
probably benign |
Het |
| AI837181 |
CG |
CGGTG |
19: 5,475,265 (GRCm39) |
|
probably benign |
Het |
| AI837181 |
GGC |
GGCTGC |
19: 5,475,245 (GRCm39) |
|
probably benign |
Het |
| Cgnl1 |
AGCG |
AGCGGCG |
9: 71,631,997 (GRCm39) |
|
probably benign |
Het |
| Cntnap1 |
TTT |
TTTTGTT |
11: 101,071,131 (GRCm39) |
|
probably benign |
Het |
| Cul9 |
TTCTC |
TTC |
17: 46,851,541 (GRCm39) |
|
probably null |
Het |
| Dnmt1 |
GGGGCGGAGCACAGTTCCTACCTCGTT |
GGGGCGGAGCACAGTTCCTACCTCGTTTTGTGGGCGGAGCACAGTTCCTACCTCGTT |
9: 20,821,415 (GRCm39) |
|
probably null |
Het |
| Frem3 |
GATC |
GATCATC |
8: 81,341,867 (GRCm39) |
|
probably benign |
Het |
| Gab3 |
TCT |
TCTACT |
X: 74,043,611 (GRCm39) |
|
probably benign |
Het |
| Gab3 |
TTC |
TTCGTC |
X: 74,043,628 (GRCm39) |
|
probably benign |
Het |
| Gabre |
GGCTCC |
GGCTCCTGCTCC |
X: 71,313,653 (GRCm39) |
|
probably benign |
Het |
| Gm8369 |
TGTG |
TGTGAGTG |
19: 11,489,137 (GRCm39) |
|
probably null |
Het |
| Gm8369 |
GTGTGT |
GTGTGTTTGTGT |
19: 11,489,142 (GRCm39) |
|
probably benign |
Het |
| Gykl1 |
G |
A |
18: 52,827,488 (GRCm39) |
R232Q |
probably benign |
Het |
| Igkv12-89 |
G |
GCAACGCCAT |
6: 68,812,270 (GRCm39) |
|
probably benign |
Het |
| Iqcf4 |
TCCTTTTCCTTTTCCTTTT |
TCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTGCCTTTTCCTTTTCCTTTT |
9: 106,447,804 (GRCm39) |
|
probably benign |
Het |
| Kmt2e |
TTT |
TTTTCTT |
5: 23,683,507 (GRCm39) |
|
probably benign |
Het |
| Krtap28-10 |
CCACAG |
CCACAGACACAG |
1: 83,019,846 (GRCm39) |
|
probably benign |
Het |
| Las1l |
CTTCCT |
CTTCCTTTTCCT |
X: 94,984,226 (GRCm39) |
|
probably benign |
Het |
| Lca5l |
GCCCTGGCCCTGGCCCC |
GCCC |
16: 95,960,497 (GRCm39) |
|
probably null |
Het |
| Lce1m |
CACTGCTGCTGC |
CACTGCTGCTGCAACTGCTGCTGC |
3: 92,925,446 (GRCm39) |
|
probably benign |
Het |
| Lypd8 |
CA |
CAGTTCCCTCGCCTCTGTTACCCCACAAATCACCAATA |
11: 58,281,069 (GRCm39) |
|
probably benign |
Het |
| Mamld1 |
GCAACA |
GCAACAACA |
X: 70,162,418 (GRCm39) |
|
probably benign |
Het |
| Mamld1 |
A |
AGCC |
X: 70,162,459 (GRCm39) |
|
probably benign |
Het |
| Map1a |
T |
TTGCTCCACCTCCAGCTCCAGCTCCAGCTCC |
2: 121,136,768 (GRCm39) |
|
probably benign |
Het |
| Med12l |
CAG |
CAGAAG |
3: 59,183,402 (GRCm39) |
|
probably benign |
Het |
| Med12l |
GC |
GCATC |
3: 59,183,416 (GRCm39) |
|
probably benign |
Het |
| Med12l |
GCAACA |
GCAACAACA |
3: 59,183,377 (GRCm39) |
|
probably benign |
Het |
| Med12l |
AGC |
AGCGGC |
3: 59,183,388 (GRCm39) |
|
probably benign |
Het |
| Morn4 |
GCAGTGAG |
GCAGTGAGTCAGTCAGTGAG |
19: 42,064,550 (GRCm39) |
|
probably null |
Het |
| Nusap1 |
GAGA |
GAGATACACGTTAGCAGTGAGGAGCAAGCTTAGA |
2: 119,458,088 (GRCm39) |
|
probably null |
Het |
| Opa3 |
GCGGGC |
GCGGGCGGAGCTGCGGGCGGAGCTGCGGGCGGAGCTACGGGC |
7: 18,989,594 (GRCm39) |
|
probably benign |
Het |
| Pdia4 |
CTCTTCCTCCT |
C |
6: 47,785,240 (GRCm39) |
|
probably null |
Het |
| Reep1 |
CGCCA |
CGCCAGCCA |
6: 71,684,950 (GRCm39) |
|
probably null |
Het |
| Sbp |
AAGA |
AAGACGCTGACAACAGAGA |
17: 24,164,358 (GRCm39) |
|
probably benign |
Het |
| Sfswap |
CTCGGCCCA |
CTCGGCCCAGTCGGCCCA |
5: 129,646,807 (GRCm39) |
|
probably benign |
Het |
| Slc39a4 |
TC |
TCATCATGATCACCATGGTCACCATGATCACTGTGGCC |
15: 76,499,071 (GRCm39) |
|
probably benign |
Het |
| Srpk2 |
ATCCT |
AT |
5: 23,730,573 (GRCm39) |
|
probably benign |
Het |
| Tfeb |
GCA |
GCACCA |
17: 48,097,022 (GRCm39) |
|
probably benign |
Het |
| Tgoln1 |
T |
TCACCTCCCGTGGGCTTGCCAGAAG |
6: 72,593,057 (GRCm39) |
|
probably benign |
Het |
| Tob1 |
CACA |
CACAACA |
11: 94,105,277 (GRCm39) |
|
probably benign |
Het |
| Trappc9 |
A |
AGCTGCTGCTGCTGCT |
15: 72,673,132 (GRCm39) |
|
probably benign |
Het |
| Tsen2 |
GGA |
GGATGA |
6: 115,537,028 (GRCm39) |
|
probably benign |
Het |
| Zfhx3 |
GC |
GCCACAGCAAC |
8: 109,682,720 (GRCm39) |
|
probably benign |
Het |
| Zfhx3 |
CAGCAGCA |
CAGCAGCAAAAGCAGCA |
8: 109,682,730 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Anapc2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01367:Anapc2
|
APN |
2 |
25,164,794 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL01575:Anapc2
|
APN |
2 |
25,175,188 (GRCm39) |
splice site |
probably benign |
|
|
IGL01993:Anapc2
|
APN |
2 |
25,164,725 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02586:Anapc2
|
APN |
2 |
25,175,108 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL02721:Anapc2
|
APN |
2 |
25,164,680 (GRCm39) |
nonsense |
probably null |
|
|
FR4976:Anapc2
|
UTSW |
2 |
25,162,544 (GRCm39) |
unclassified |
probably benign |
|
|
R0415:Anapc2
|
UTSW |
2 |
25,168,337 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1539:Anapc2
|
UTSW |
2 |
25,163,075 (GRCm39) |
missense |
probably benign |
|
|
R1675:Anapc2
|
UTSW |
2 |
25,162,651 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1720:Anapc2
|
UTSW |
2 |
25,164,724 (GRCm39) |
missense |
probably benign |
0.13 |
|
R2150:Anapc2
|
UTSW |
2 |
25,162,682 (GRCm39) |
missense |
probably benign |
0.27 |
|
R2173:Anapc2
|
UTSW |
2 |
25,163,288 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4028:Anapc2
|
UTSW |
2 |
25,167,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4254:Anapc2
|
UTSW |
2 |
25,163,357 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4643:Anapc2
|
UTSW |
2 |
25,166,406 (GRCm39) |
missense |
probably benign |
|
|
R4742:Anapc2
|
UTSW |
2 |
25,163,555 (GRCm39) |
splice site |
probably null |
|
|
R4824:Anapc2
|
UTSW |
2 |
25,167,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5039:Anapc2
|
UTSW |
2 |
25,164,808 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R5530:Anapc2
|
UTSW |
2 |
25,174,595 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6456:Anapc2
|
UTSW |
2 |
25,170,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6479:Anapc2
|
UTSW |
2 |
25,175,407 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6587:Anapc2
|
UTSW |
2 |
25,162,550 (GRCm39) |
unclassified |
probably benign |
|
|
R7164:Anapc2
|
UTSW |
2 |
25,175,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7494:Anapc2
|
UTSW |
2 |
25,166,376 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7829:Anapc2
|
UTSW |
2 |
25,167,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7954:Anapc2
|
UTSW |
2 |
25,164,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7970:Anapc2
|
UTSW |
2 |
25,163,299 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8015:Anapc2
|
UTSW |
2 |
25,174,688 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8064:Anapc2
|
UTSW |
2 |
25,166,418 (GRCm39) |
missense |
probably benign |
|
|
R8838:Anapc2
|
UTSW |
2 |
25,163,546 (GRCm39) |
missense |
probably benign |
0.11 |
|
R8954:Anapc2
|
UTSW |
2 |
25,170,490 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9180:Anapc2
|
UTSW |
2 |
25,163,303 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9468:Anapc2
|
UTSW |
2 |
25,163,132 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9525:Anapc2
|
UTSW |
2 |
25,166,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9750:Anapc2
|
UTSW |
2 |
25,174,982 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
RF043:Anapc2
|
UTSW |
2 |
25,162,573 (GRCm39) |
unclassified |
probably benign |
|
|
RF062:Anapc2
|
UTSW |
2 |
25,162,549 (GRCm39) |
frame shift |
probably null |
|
|
X0025:Anapc2
|
UTSW |
2 |
25,169,290 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1088:Anapc2
|
UTSW |
2 |
25,163,380 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGTTGTAGTTCTGCAGCGCC -3'
(R):5'- CAAAGTCGCGGGAAATCTGC -3'
Sequencing Primer
(F):5'- TGGGTCATGGTCTGCACC -3'
(R):5'- CGGGAAATCTGCACAGGC -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation