Incidental Mutation 'R9606:Rb1'
| ID |
723896 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rb1
|
| Ensembl Gene |
ENSMUSG00000022105 |
| Gene Name |
RB transcriptional corepressor 1 |
| Synonyms |
Rb-1, retinoblastoma 1, Rb, pRb |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9606 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
14 |
| Chromosomal Location |
73430298-73563446 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 73517573 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 278
(N278D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000022701
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022701]
[ENSMUST00000164624]
|
| AlphaFold |
P13405 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000022701
AA Change: N278D
PolyPhen 2
Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000022701
Gene: ENSMUSG00000022105
AA Change: N278D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
28 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
53 |
N/A |
INTRINSIC |
|
DUF3452
|
97 |
223 |
4.59e-25 |
SMART |
|
RB_A
|
367 |
567 |
5.53e-92 |
SMART |
|
CYCLIN
|
653 |
740 |
1.62e-5 |
SMART |
|
Rb_C
|
761 |
920 |
1.28e-96 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164624
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted mutations exhibit abnormalities of the neuronal and hematopoietic systems and die in utero. Heterozygotes may develop pituitary tumors associated with loss of the normal allele. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 6430548M08Rik |
A |
G |
8: 120,880,706 (GRCm39) |
Y286C |
probably damaging |
Het |
| Cacna1c |
T |
C |
6: 118,587,455 (GRCm39) |
T1657A |
|
Het |
| Ccs |
A |
T |
19: 4,882,897 (GRCm39) |
D151E |
probably benign |
Het |
| Cfap74 |
A |
G |
4: 155,509,133 (GRCm39) |
T295A |
|
Het |
| Chmp4c |
A |
T |
3: 10,432,222 (GRCm39) |
E44V |
probably damaging |
Het |
| Crybg2 |
A |
T |
4: 133,801,383 (GRCm39) |
K539* |
probably null |
Het |
| Dgkg |
T |
C |
16: 22,441,011 (GRCm39) |
M1V |
probably null |
Het |
| E2f2 |
T |
A |
4: 135,911,743 (GRCm39) |
Y251* |
probably null |
Het |
| Fat2 |
T |
C |
11: 55,180,093 (GRCm39) |
Y1416C |
probably damaging |
Het |
| Fgl2 |
T |
C |
5: 21,577,991 (GRCm39) |
S93P |
possibly damaging |
Het |
| Hivep3 |
C |
T |
4: 119,989,786 (GRCm39) |
T2079I |
probably damaging |
Het |
| Igfl3 |
A |
C |
7: 17,913,920 (GRCm39) |
K90T |
possibly damaging |
Het |
| Lsamp |
A |
G |
16: 41,709,292 (GRCm39) |
D74G |
probably benign |
Het |
| Mmrn2 |
C |
A |
14: 34,119,654 (GRCm39) |
T211K |
possibly damaging |
Het |
| Mov10 |
A |
T |
3: 104,707,664 (GRCm39) |
V570D |
probably benign |
Het |
| Mrc1 |
A |
T |
2: 14,313,517 (GRCm39) |
Y916F |
probably benign |
Het |
| Myo10 |
CAGGTATAAAG |
CAG |
15: 25,776,401 (GRCm39) |
|
probably null |
Het |
| Ndc1 |
T |
A |
4: 107,246,686 (GRCm39) |
C370S |
probably damaging |
Het |
| Nln |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
13: 104,186,924 (GRCm39) |
|
probably null |
Het |
| Nrcam |
A |
T |
12: 44,609,240 (GRCm39) |
N455I |
probably damaging |
Het |
| Nrp1 |
G |
A |
8: 129,229,029 (GRCm39) |
E836K |
probably benign |
Het |
| Or2t29 |
C |
T |
11: 58,433,753 (GRCm39) |
C196Y |
probably damaging |
Het |
| Or5b120 |
A |
T |
19: 13,479,943 (GRCm39) |
K79* |
probably null |
Het |
| Or6c216 |
A |
T |
10: 129,678,625 (GRCm39) |
C95* |
probably null |
Het |
| Or8b1d |
A |
G |
9: 38,558,620 (GRCm39) |
S67P |
probably damaging |
Het |
| Pcca |
T |
C |
14: 122,901,717 (GRCm39) |
S287P |
probably damaging |
Het |
| Pitpnm3 |
T |
A |
11: 71,955,069 (GRCm39) |
T482S |
probably benign |
Het |
| Pld2 |
C |
T |
11: 70,445,893 (GRCm39) |
R676* |
probably null |
Het |
| Ppm1k |
T |
C |
6: 57,491,057 (GRCm39) |
Y286C |
possibly damaging |
Het |
| Sema3g |
T |
C |
14: 30,943,783 (GRCm39) |
L221P |
probably damaging |
Het |
| Skint2 |
C |
T |
4: 112,483,147 (GRCm39) |
T184I |
probably benign |
Het |
| Slc38a2 |
A |
G |
15: 96,591,172 (GRCm39) |
F232S |
probably damaging |
Het |
| Snx6 |
T |
C |
12: 54,814,811 (GRCm39) |
N170S |
probably benign |
Het |
| Sox9 |
T |
A |
11: 112,673,416 (GRCm39) |
N2K |
probably damaging |
Het |
| Sp140l1 |
G |
C |
1: 85,075,344 (GRCm39) |
|
probably null |
Het |
| Srpk2 |
T |
C |
5: 23,729,604 (GRCm39) |
E345G |
probably benign |
Het |
| Tbc1d21 |
T |
C |
9: 58,268,487 (GRCm39) |
M291V |
possibly damaging |
Het |
| Tekt2 |
T |
C |
4: 126,218,693 (GRCm39) |
N20S |
probably benign |
Het |
| Tnxb |
T |
G |
17: 34,914,578 (GRCm39) |
I1888S |
possibly damaging |
Het |
| Tsnaxip1 |
G |
A |
8: 106,566,685 (GRCm39) |
E174K |
probably damaging |
Het |
| Ttc28 |
G |
A |
5: 111,433,140 (GRCm39) |
R2058Q |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
| Ttyh2 |
T |
A |
11: 114,601,667 (GRCm39) |
D430E |
probably benign |
Het |
| Ubr2 |
C |
T |
17: 47,245,020 (GRCm39) |
G1669R |
probably damaging |
Het |
| Vcan |
A |
T |
13: 89,853,491 (GRCm39) |
S490T |
probably damaging |
Het |
| Vmn1r86 |
T |
A |
7: 12,836,741 (GRCm39) |
D45V |
probably damaging |
Het |
| Wdr12 |
A |
G |
1: 60,127,226 (GRCm39) |
V143A |
possibly damaging |
Het |
| Zbtb18 |
T |
A |
1: 177,274,989 (GRCm39) |
Y116* |
probably null |
Het |
| Zdbf2 |
C |
T |
1: 63,342,536 (GRCm39) |
T305I |
possibly damaging |
Het |
| Zfp384 |
T |
A |
6: 125,007,802 (GRCm39) |
M244K |
possibly damaging |
Het |
| Zfp423 |
A |
T |
8: 88,414,595 (GRCm39) |
V1241D |
probably damaging |
Het |
| Zfp574 |
A |
G |
7: 24,780,640 (GRCm39) |
Y554C |
probably damaging |
Het |
| Zfp616 |
T |
C |
11: 73,976,220 (GRCm39) |
S830P |
probably damaging |
Het |
| Zfp839 |
A |
G |
12: 110,834,776 (GRCm39) |
Y677C |
probably benign |
Het |
|
| Other mutations in Rb1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00497:Rb1
|
APN |
14 |
73,502,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00951:Rb1
|
APN |
14 |
73,559,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01152:Rb1
|
APN |
14 |
73,443,310 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01339:Rb1
|
APN |
14 |
73,501,811 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01349:Rb1
|
APN |
14 |
73,506,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01390:Rb1
|
APN |
14 |
73,532,439 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02066:Rb1
|
APN |
14 |
73,435,974 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02207:Rb1
|
APN |
14 |
73,443,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02860:Rb1
|
APN |
14 |
73,443,452 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03370:Rb1
|
APN |
14 |
73,520,306 (GRCm39) |
critical splice donor site |
probably null |
|
|
rubidium
|
UTSW |
14 |
73,436,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0028:Rb1
|
UTSW |
14 |
73,502,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0553:Rb1
|
UTSW |
14 |
73,449,152 (GRCm39) |
nonsense |
probably null |
|
|
R0563:Rb1
|
UTSW |
14 |
73,454,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0586:Rb1
|
UTSW |
14 |
73,525,124 (GRCm39) |
intron |
probably benign |
|
|
R0595:Rb1
|
UTSW |
14 |
73,511,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0755:Rb1
|
UTSW |
14 |
73,434,653 (GRCm39) |
makesense |
probably null |
|
|
R1480:Rb1
|
UTSW |
14 |
73,500,042 (GRCm39) |
missense |
probably benign |
|
|
R1513:Rb1
|
UTSW |
14 |
73,559,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1752:Rb1
|
UTSW |
14 |
73,525,064 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1919:Rb1
|
UTSW |
14 |
73,450,430 (GRCm39) |
nonsense |
probably null |
|
|
R2010:Rb1
|
UTSW |
14 |
73,532,433 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2087:Rb1
|
UTSW |
14 |
73,517,692 (GRCm39) |
missense |
probably benign |
0.09 |
|
R2152:Rb1
|
UTSW |
14 |
73,526,165 (GRCm39) |
missense |
probably benign |
|
|
R2167:Rb1
|
UTSW |
14 |
73,449,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3950:Rb1
|
UTSW |
14 |
73,500,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4183:Rb1
|
UTSW |
14 |
73,435,966 (GRCm39) |
splice site |
probably null |
|
|
R4225:Rb1
|
UTSW |
14 |
73,506,631 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R4306:Rb1
|
UTSW |
14 |
73,500,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4464:Rb1
|
UTSW |
14 |
73,436,638 (GRCm39) |
splice site |
probably null |
|
|
R4609:Rb1
|
UTSW |
14 |
73,499,954 (GRCm39) |
splice site |
probably benign |
|
|
R4671:Rb1
|
UTSW |
14 |
73,511,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4916:Rb1
|
UTSW |
14 |
73,454,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5160:Rb1
|
UTSW |
14 |
73,501,895 (GRCm39) |
synonymous |
silent |
|
|
R5210:Rb1
|
UTSW |
14 |
73,436,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5320:Rb1
|
UTSW |
14 |
73,450,566 (GRCm39) |
nonsense |
probably null |
|
|
R5436:Rb1
|
UTSW |
14 |
73,450,580 (GRCm39) |
splice site |
probably null |
|
|
R5467:Rb1
|
UTSW |
14 |
73,449,060 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5592:Rb1
|
UTSW |
14 |
73,449,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6326:Rb1
|
UTSW |
14 |
73,435,974 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6363:Rb1
|
UTSW |
14 |
73,525,081 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6395:Rb1
|
UTSW |
14 |
73,436,636 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6414:Rb1
|
UTSW |
14 |
73,520,414 (GRCm39) |
missense |
unknown |
|
|
R6460:Rb1
|
UTSW |
14 |
73,515,894 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6503:Rb1
|
UTSW |
14 |
73,443,320 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6519:Rb1
|
UTSW |
14 |
73,535,503 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6671:Rb1
|
UTSW |
14 |
73,434,706 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7026:Rb1
|
UTSW |
14 |
73,535,539 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7103:Rb1
|
UTSW |
14 |
73,500,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7263:Rb1
|
UTSW |
14 |
73,520,363 (GRCm39) |
nonsense |
probably null |
|
|
R7478:Rb1
|
UTSW |
14 |
73,506,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7519:Rb1
|
UTSW |
14 |
73,502,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7817:Rb1
|
UTSW |
14 |
73,435,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8323:Rb1
|
UTSW |
14 |
73,503,023 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8809:Rb1
|
UTSW |
14 |
73,503,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8813:Rb1
|
UTSW |
14 |
73,500,027 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8849:Rb1
|
UTSW |
14 |
73,434,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9272:Rb1
|
UTSW |
14 |
73,517,602 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9482:Rb1
|
UTSW |
14 |
73,443,493 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGACAGAAGGGAGCTATTCTC -3'
(R):5'- CTACCAGGATTATTTCAGACATCTTAG -3'
Sequencing Primer
(F):5'- GGGAGCTATTCTCTTTAAAAGCAAAG -3'
(R):5'- ATGAACCCAGGGTTTCATGC -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation