Incidental Mutation 'R7276:Rb1cc1'
ID |
565551 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rb1cc1
|
Ensembl Gene |
ENSMUSG00000025907 |
Gene Name |
RB1-inducible coiled-coil 1 |
Synonyms |
Fip200, 2900055E04Rik, 5930404L04Rik, Cc1, LaXp180 |
MMRRC Submission |
045359-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7276 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
6284858-6346599 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 6319416 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 945
(C945Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000027040
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027040]
[ENSMUST00000162795]
|
AlphaFold |
Q9ESK9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000027040
AA Change: C945Y
PolyPhen 2
Score 0.129 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000027040 Gene: ENSMUSG00000025907 AA Change: C945Y
Domain | Start | End | E-Value | Type |
SCOP:d1euvb_
|
1 |
51 |
7e-4 |
SMART |
Blast:UBQ
|
3 |
76 |
8e-12 |
BLAST |
low complexity region
|
471 |
486 |
N/A |
INTRINSIC |
low complexity region
|
643 |
653 |
N/A |
INTRINSIC |
low complexity region
|
658 |
674 |
N/A |
INTRINSIC |
coiled coil region
|
859 |
921 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1045 |
N/A |
INTRINSIC |
low complexity region
|
1055 |
1066 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
1159 |
1305 |
1e-3 |
SMART |
low complexity region
|
1374 |
1388 |
N/A |
INTRINSIC |
Pfam:ATG11
|
1447 |
1583 |
5.6e-28 |
PFAM |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000125348 Gene: ENSMUSG00000025907 AA Change: C824Y
Domain | Start | End | E-Value | Type |
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
low complexity region
|
523 |
533 |
N/A |
INTRINSIC |
low complexity region
|
538 |
554 |
N/A |
INTRINSIC |
coiled coil region
|
738 |
800 |
N/A |
INTRINSIC |
low complexity region
|
913 |
925 |
N/A |
INTRINSIC |
low complexity region
|
935 |
946 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
1039 |
1174 |
3e-3 |
SMART |
low complexity region
|
1254 |
1268 |
N/A |
INTRINSIC |
Pfam:ATG11
|
1327 |
1463 |
6.7e-28 |
PFAM |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000125334 Gene: ENSMUSG00000025907 AA Change: C35Y
Domain | Start | End | E-Value | Type |
coiled coil region
|
33 |
331 |
N/A |
INTRINSIC |
low complexity region
|
335 |
355 |
N/A |
INTRINSIC |
coiled coil region
|
363 |
483 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162795
|
SMART Domains |
Protein: ENSMUSP00000124676 Gene: ENSMUSG00000025907
Domain | Start | End | E-Value | Type |
SCOP:d1euvb_
|
1 |
51 |
2e-4 |
SMART |
Blast:UBQ
|
3 |
76 |
4e-12 |
BLAST |
low complexity region
|
454 |
469 |
N/A |
INTRINSIC |
low complexity region
|
626 |
636 |
N/A |
INTRINSIC |
low complexity region
|
641 |
657 |
N/A |
INTRINSIC |
coiled coil region
|
842 |
865 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (74/74) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene interacts with signaling pathways to coordinately regulate cell growth, cell proliferation, apoptosis, autophagy, and cell migration. This tumor suppressor also enhances retinoblastoma 1 gene expression in cancer cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009] PHENOTYPE: Homozygous mutation of this gene results in embryonic lethality at mid/late gestation associated with heart failure and liver degeneration. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930455H04Rik |
T |
C |
3: 116,762,227 (GRCm39) |
V26A |
unknown |
Het |
4930546C10Rik |
C |
T |
18: 69,083,093 (GRCm39) |
W40* |
probably null |
Het |
Abcc5 |
T |
C |
16: 20,195,258 (GRCm39) |
|
probably null |
Het |
Adamts18 |
T |
A |
8: 114,501,896 (GRCm39) |
M322L |
probably damaging |
Het |
Ankrd44 |
T |
A |
1: 54,774,239 (GRCm39) |
N406I |
probably benign |
Het |
Arhgap35 |
T |
G |
7: 16,298,493 (GRCm39) |
T191P |
probably damaging |
Het |
Atg3 |
G |
A |
16: 44,982,805 (GRCm39) |
E37K |
possibly damaging |
Het |
Bbs1 |
A |
T |
19: 4,947,738 (GRCm39) |
|
probably null |
Het |
BC048562 |
A |
G |
9: 108,322,435 (GRCm39) |
N60D |
probably damaging |
Het |
Btnl9 |
T |
A |
11: 49,066,617 (GRCm39) |
I335F |
probably benign |
Het |
C7 |
A |
T |
15: 5,041,449 (GRCm39) |
C486S |
probably damaging |
Het |
Cchcr1 |
C |
A |
17: 35,840,031 (GRCm39) |
Q634K |
possibly damaging |
Het |
Cd93 |
A |
T |
2: 148,283,660 (GRCm39) |
V562E |
probably damaging |
Het |
Cemip2 |
A |
G |
19: 21,812,824 (GRCm39) |
I1010V |
probably benign |
Het |
Cript |
T |
A |
17: 87,341,696 (GRCm39) |
Y50* |
probably null |
Het |
Dnah14 |
T |
A |
1: 181,513,372 (GRCm39) |
F1908L |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,367,984 (GRCm39) |
N2790D |
probably damaging |
Het |
Eif3h |
C |
A |
15: 51,728,717 (GRCm39) |
|
probably null |
Het |
Ffar3 |
C |
G |
7: 30,555,273 (GRCm39) |
V16L |
possibly damaging |
Het |
Gcn1 |
C |
T |
5: 115,749,119 (GRCm39) |
R1884W |
probably damaging |
Het |
Gpatch1 |
T |
A |
7: 34,996,921 (GRCm39) |
M426L |
probably benign |
Het |
Hcn2 |
T |
A |
10: 79,564,934 (GRCm39) |
Y449N |
possibly damaging |
Het |
Hdac10 |
T |
C |
15: 89,012,488 (GRCm39) |
T32A |
probably benign |
Het |
Hykk |
T |
C |
9: 54,853,502 (GRCm39) |
Y275H |
probably damaging |
Het |
Igfn1 |
G |
C |
1: 135,926,376 (GRCm39) |
P25A |
possibly damaging |
Het |
Jph1 |
T |
C |
1: 17,162,266 (GRCm39) |
Q132R |
probably damaging |
Het |
Kat2b |
T |
A |
17: 53,931,450 (GRCm39) |
D149E |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,902,167 (GRCm39) |
K1289N |
probably damaging |
Het |
Lrrc37a |
G |
A |
11: 103,347,572 (GRCm39) |
S3041L |
unknown |
Het |
Mtrex |
A |
T |
13: 113,050,973 (GRCm39) |
Y201N |
probably benign |
Het |
Mtus2 |
C |
T |
5: 148,013,368 (GRCm39) |
R54C |
probably benign |
Het |
Myo1d |
A |
T |
11: 80,583,898 (GRCm39) |
I38N |
probably damaging |
Het |
Nasp |
A |
G |
4: 116,471,546 (GRCm39) |
S94P |
probably damaging |
Het |
Nfat5 |
C |
A |
8: 108,093,731 (GRCm39) |
N657K |
probably benign |
Het |
Ngfr |
A |
G |
11: 95,465,170 (GRCm39) |
L226P |
probably benign |
Het |
Nos1 |
T |
C |
5: 118,048,303 (GRCm39) |
S703P |
probably damaging |
Het |
Nsun7 |
A |
G |
5: 66,434,484 (GRCm39) |
D275G |
probably benign |
Het |
Oas1d |
A |
G |
5: 121,054,944 (GRCm39) |
N172S |
possibly damaging |
Het |
Or11h4 |
A |
G |
14: 50,974,187 (GRCm39) |
V144A |
possibly damaging |
Het |
Or2y17 |
T |
A |
11: 49,231,821 (GRCm39) |
M154K |
probably benign |
Het |
Or4c11b |
T |
A |
2: 88,625,025 (GRCm39) |
F100I |
probably damaging |
Het |
Or52e8 |
T |
A |
7: 104,624,857 (GRCm39) |
M116L |
possibly damaging |
Het |
Papss1 |
A |
G |
3: 131,324,995 (GRCm39) |
E484G |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,160,224 (GRCm39) |
D447G |
probably benign |
Het |
Phkg2 |
A |
G |
7: 127,181,558 (GRCm39) |
E247G |
possibly damaging |
Het |
Pramel30 |
A |
G |
4: 144,059,216 (GRCm39) |
E309G |
possibly damaging |
Het |
Prelid2 |
T |
C |
18: 42,045,487 (GRCm39) |
N141S |
possibly damaging |
Het |
Psg18 |
T |
C |
7: 18,079,909 (GRCm39) |
M431V |
probably damaging |
Het |
Psmd12 |
A |
T |
11: 107,394,471 (GRCm39) |
R397* |
probably null |
Het |
Ralgds |
G |
A |
2: 28,435,884 (GRCm39) |
R503Q |
probably damaging |
Het |
Rgs12 |
A |
G |
5: 35,183,715 (GRCm39) |
D1026G |
probably benign |
Het |
Scn7a |
G |
A |
2: 66,587,506 (GRCm39) |
P66S |
probably damaging |
Het |
Supt16 |
T |
C |
14: 52,414,458 (GRCm39) |
E448G |
probably benign |
Het |
Syt16 |
C |
T |
12: 74,313,483 (GRCm39) |
R470C |
probably damaging |
Het |
Tas2r114 |
T |
C |
6: 131,666,310 (GRCm39) |
I239M |
probably damaging |
Het |
Tecpr1 |
C |
T |
5: 144,153,838 (GRCm39) |
W138* |
probably null |
Het |
Tex101 |
T |
C |
7: 24,369,829 (GRCm39) |
N45S |
probably damaging |
Het |
Tmx1 |
C |
A |
12: 70,512,917 (GRCm39) |
T275K |
possibly damaging |
Het |
Trappc8 |
T |
G |
18: 20,951,148 (GRCm39) |
I1434L |
probably damaging |
Het |
Trappc9 |
G |
T |
15: 72,924,119 (GRCm39) |
H208N |
probably damaging |
Het |
Trcg1 |
T |
A |
9: 57,149,862 (GRCm39) |
L478Q |
probably damaging |
Het |
Trim42 |
G |
T |
9: 97,251,625 (GRCm39) |
Y91* |
probably null |
Het |
Vmn2r114 |
A |
G |
17: 23,509,934 (GRCm39) |
S849P |
probably damaging |
Het |
Vmn2r120 |
T |
C |
17: 57,831,881 (GRCm39) |
T303A |
probably benign |
Het |
Vmn2r13 |
A |
G |
5: 109,321,645 (GRCm39) |
W351R |
probably damaging |
Het |
Vmn2r53 |
T |
C |
7: 12,340,359 (GRCm39) |
D38G |
probably damaging |
Het |
Vsig8 |
C |
A |
1: 172,390,850 (GRCm39) |
C411* |
probably null |
Het |
Vwce |
A |
T |
19: 10,641,538 (GRCm39) |
T755S |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,611,782 (GRCm39) |
S897G |
probably damaging |
Het |
Zfp111 |
C |
A |
7: 23,898,978 (GRCm39) |
C212F |
probably damaging |
Het |
Zfp385b |
G |
T |
2: 77,280,624 (GRCm39) |
H193N |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,755 (GRCm39) |
E95G |
probably benign |
Het |
|
Other mutations in Rb1cc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Rb1cc1
|
APN |
1 |
6,319,730 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00590:Rb1cc1
|
APN |
1 |
6,308,520 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00678:Rb1cc1
|
APN |
1 |
6,304,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00705:Rb1cc1
|
APN |
1 |
6,314,357 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00957:Rb1cc1
|
APN |
1 |
6,319,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01363:Rb1cc1
|
APN |
1 |
6,320,333 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01599:Rb1cc1
|
APN |
1 |
6,318,995 (GRCm39) |
nonsense |
probably null |
|
IGL01610:Rb1cc1
|
APN |
1 |
6,318,705 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01929:Rb1cc1
|
APN |
1 |
6,310,383 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01978:Rb1cc1
|
APN |
1 |
6,308,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Rb1cc1
|
APN |
1 |
6,335,847 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02471:Rb1cc1
|
APN |
1 |
6,310,275 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02677:Rb1cc1
|
APN |
1 |
6,319,643 (GRCm39) |
missense |
probably benign |
|
IGL02702:Rb1cc1
|
APN |
1 |
6,310,247 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02816:Rb1cc1
|
APN |
1 |
6,333,052 (GRCm39) |
splice site |
probably benign |
|
IGL02899:Rb1cc1
|
APN |
1 |
6,334,807 (GRCm39) |
missense |
probably damaging |
1.00 |
fingerling
|
UTSW |
1 |
6,331,256 (GRCm39) |
missense |
probably damaging |
1.00 |
tots
|
UTSW |
1 |
6,315,861 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02988:Rb1cc1
|
UTSW |
1 |
6,318,035 (GRCm39) |
critical splice donor site |
probably null |
|
R0020:Rb1cc1
|
UTSW |
1 |
6,334,772 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0254:Rb1cc1
|
UTSW |
1 |
6,333,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Rb1cc1
|
UTSW |
1 |
6,318,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0466:Rb1cc1
|
UTSW |
1 |
6,333,491 (GRCm39) |
splice site |
probably null |
|
R0482:Rb1cc1
|
UTSW |
1 |
6,310,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Rb1cc1
|
UTSW |
1 |
6,319,395 (GRCm39) |
missense |
probably benign |
0.00 |
R0512:Rb1cc1
|
UTSW |
1 |
6,318,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Rb1cc1
|
UTSW |
1 |
6,314,486 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0617:Rb1cc1
|
UTSW |
1 |
6,319,014 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0837:Rb1cc1
|
UTSW |
1 |
6,304,495 (GRCm39) |
splice site |
probably null |
|
R1399:Rb1cc1
|
UTSW |
1 |
6,320,042 (GRCm39) |
missense |
probably benign |
0.00 |
R1532:Rb1cc1
|
UTSW |
1 |
6,319,958 (GRCm39) |
missense |
probably benign |
0.00 |
R1542:Rb1cc1
|
UTSW |
1 |
6,314,473 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1746:Rb1cc1
|
UTSW |
1 |
6,333,237 (GRCm39) |
splice site |
probably null |
|
R1764:Rb1cc1
|
UTSW |
1 |
6,284,904 (GRCm39) |
intron |
probably benign |
|
R1968:Rb1cc1
|
UTSW |
1 |
6,318,419 (GRCm39) |
splice site |
probably null |
|
R2025:Rb1cc1
|
UTSW |
1 |
6,315,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Rb1cc1
|
UTSW |
1 |
6,320,262 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2101:Rb1cc1
|
UTSW |
1 |
6,319,559 (GRCm39) |
missense |
probably benign |
|
R2249:Rb1cc1
|
UTSW |
1 |
6,342,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Rb1cc1
|
UTSW |
1 |
6,319,590 (GRCm39) |
missense |
probably benign |
|
R3276:Rb1cc1
|
UTSW |
1 |
6,319,590 (GRCm39) |
missense |
probably benign |
|
R3716:Rb1cc1
|
UTSW |
1 |
6,340,914 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3747:Rb1cc1
|
UTSW |
1 |
6,318,966 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3850:Rb1cc1
|
UTSW |
1 |
6,320,337 (GRCm39) |
missense |
probably benign |
0.22 |
R3967:Rb1cc1
|
UTSW |
1 |
6,318,494 (GRCm39) |
splice site |
probably benign |
|
R3969:Rb1cc1
|
UTSW |
1 |
6,318,494 (GRCm39) |
splice site |
probably benign |
|
R3972:Rb1cc1
|
UTSW |
1 |
6,319,224 (GRCm39) |
missense |
probably benign |
0.00 |
R4166:Rb1cc1
|
UTSW |
1 |
6,335,887 (GRCm39) |
intron |
probably benign |
|
R4168:Rb1cc1
|
UTSW |
1 |
6,300,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4358:Rb1cc1
|
UTSW |
1 |
6,315,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R4370:Rb1cc1
|
UTSW |
1 |
6,318,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Rb1cc1
|
UTSW |
1 |
6,285,245 (GRCm39) |
intron |
probably benign |
|
R4945:Rb1cc1
|
UTSW |
1 |
6,319,851 (GRCm39) |
missense |
probably benign |
0.24 |
R5111:Rb1cc1
|
UTSW |
1 |
6,284,858 (GRCm39) |
intron |
probably benign |
|
R5175:Rb1cc1
|
UTSW |
1 |
6,318,545 (GRCm39) |
missense |
probably benign |
|
R5196:Rb1cc1
|
UTSW |
1 |
6,304,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R5271:Rb1cc1
|
UTSW |
1 |
6,319,417 (GRCm39) |
nonsense |
probably null |
|
R5341:Rb1cc1
|
UTSW |
1 |
6,285,266 (GRCm39) |
intron |
probably benign |
|
R5952:Rb1cc1
|
UTSW |
1 |
6,318,406 (GRCm39) |
missense |
probably benign |
|
R5992:Rb1cc1
|
UTSW |
1 |
6,304,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Rb1cc1
|
UTSW |
1 |
6,320,058 (GRCm39) |
missense |
probably benign |
0.01 |
R6064:Rb1cc1
|
UTSW |
1 |
6,319,958 (GRCm39) |
missense |
probably benign |
0.00 |
R6313:Rb1cc1
|
UTSW |
1 |
6,314,357 (GRCm39) |
missense |
probably benign |
0.00 |
R6345:Rb1cc1
|
UTSW |
1 |
6,333,481 (GRCm39) |
missense |
probably benign |
0.00 |
R6488:Rb1cc1
|
UTSW |
1 |
6,340,951 (GRCm39) |
missense |
probably damaging |
0.97 |
R6566:Rb1cc1
|
UTSW |
1 |
6,319,316 (GRCm39) |
missense |
probably benign |
0.15 |
R6739:Rb1cc1
|
UTSW |
1 |
6,304,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R6829:Rb1cc1
|
UTSW |
1 |
6,319,488 (GRCm39) |
missense |
probably benign |
0.04 |
R6945:Rb1cc1
|
UTSW |
1 |
6,331,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R6976:Rb1cc1
|
UTSW |
1 |
6,333,126 (GRCm39) |
missense |
probably benign |
0.01 |
R7031:Rb1cc1
|
UTSW |
1 |
6,308,690 (GRCm39) |
critical splice donor site |
probably null |
|
R7066:Rb1cc1
|
UTSW |
1 |
6,320,229 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7185:Rb1cc1
|
UTSW |
1 |
6,308,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Rb1cc1
|
UTSW |
1 |
6,315,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7463:Rb1cc1
|
UTSW |
1 |
6,319,404 (GRCm39) |
missense |
probably benign |
|
R7484:Rb1cc1
|
UTSW |
1 |
6,344,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7496:Rb1cc1
|
UTSW |
1 |
6,318,415 (GRCm39) |
missense |
probably null |
0.02 |
R7618:Rb1cc1
|
UTSW |
1 |
6,335,782 (GRCm39) |
splice site |
probably null |
|
R7681:Rb1cc1
|
UTSW |
1 |
6,310,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7774:Rb1cc1
|
UTSW |
1 |
6,318,309 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7780:Rb1cc1
|
UTSW |
1 |
6,319,138 (GRCm39) |
nonsense |
probably null |
|
R7947:Rb1cc1
|
UTSW |
1 |
6,318,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Rb1cc1
|
UTSW |
1 |
6,315,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Rb1cc1
|
UTSW |
1 |
6,333,448 (GRCm39) |
nonsense |
probably null |
|
R8527:Rb1cc1
|
UTSW |
1 |
6,315,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R8758:Rb1cc1
|
UTSW |
1 |
6,310,451 (GRCm39) |
missense |
probably benign |
0.10 |
R8843:Rb1cc1
|
UTSW |
1 |
6,315,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Rb1cc1
|
UTSW |
1 |
6,319,194 (GRCm39) |
missense |
probably benign |
|
R8937:Rb1cc1
|
UTSW |
1 |
6,333,441 (GRCm39) |
missense |
probably benign |
|
R9018:Rb1cc1
|
UTSW |
1 |
6,319,490 (GRCm39) |
missense |
probably benign |
|
R9106:Rb1cc1
|
UTSW |
1 |
6,319,109 (GRCm39) |
missense |
|
|
R9127:Rb1cc1
|
UTSW |
1 |
6,333,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9130:Rb1cc1
|
UTSW |
1 |
6,315,109 (GRCm39) |
missense |
probably damaging |
0.99 |
R9311:Rb1cc1
|
UTSW |
1 |
6,310,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R9365:Rb1cc1
|
UTSW |
1 |
6,315,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Rb1cc1
|
UTSW |
1 |
6,314,339 (GRCm39) |
missense |
probably benign |
|
R9598:Rb1cc1
|
UTSW |
1 |
6,310,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Rb1cc1
|
UTSW |
1 |
6,318,528 (GRCm39) |
missense |
probably benign |
0.02 |
R9659:Rb1cc1
|
UTSW |
1 |
6,318,673 (GRCm39) |
missense |
probably benign |
0.33 |
R9799:Rb1cc1
|
UTSW |
1 |
6,315,126 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Rb1cc1
|
UTSW |
1 |
6,319,242 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- CTTGATGCTCTAGTAAAAGACAGTG -3'
(R):5'- CCAAAGACATATTGTGGTCTGTC -3'
Sequencing Primer
(F):5'- GTATCCCTTGAAGAGGCT -3'
(R):5'- GTGGTCTGTCATAACTTTCTCAAAC -3'
|
Posted On |
2019-06-26 |