Incidental Mutation 'IGL00530:Prdm2'
ID |
332451 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Prdm2
|
Ensembl Gene |
ENSMUSG00000057637 |
Gene Name |
PR domain containing 2, with ZNF domain |
Synonyms |
KMT8, LOC381568, E330024L24Rik, Riz1, Riz, 4833427P12Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL00530
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
143107391-143212995 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 143133759 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Histidine
at position 987
(P987H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101404
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000105778]
|
AlphaFold |
A2A7B5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105778
AA Change: P987H
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000101404 Gene: ENSMUSG00000057637 AA Change: P987H
Domain | Start | End | E-Value | Type |
SET
|
29 |
146 |
2.79e-21 |
SMART |
coiled coil region
|
254 |
293 |
N/A |
INTRINSIC |
low complexity region
|
333 |
346 |
N/A |
INTRINSIC |
ZnF_C2H2
|
356 |
378 |
2.95e-3 |
SMART |
ZnF_C2H2
|
386 |
408 |
4.79e-3 |
SMART |
ZnF_C2H2
|
477 |
500 |
4.17e-3 |
SMART |
low complexity region
|
517 |
528 |
N/A |
INTRINSIC |
low complexity region
|
653 |
669 |
N/A |
INTRINSIC |
low complexity region
|
682 |
697 |
N/A |
INTRINSIC |
low complexity region
|
726 |
744 |
N/A |
INTRINSIC |
low complexity region
|
868 |
877 |
N/A |
INTRINSIC |
low complexity region
|
931 |
951 |
N/A |
INTRINSIC |
low complexity region
|
954 |
992 |
N/A |
INTRINSIC |
low complexity region
|
1011 |
1032 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1080 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1126 |
1148 |
3.52e-1 |
SMART |
ZnF_C2H2
|
1154 |
1177 |
7.55e-1 |
SMART |
ZnF_C2H2
|
1183 |
1206 |
4.72e-2 |
SMART |
low complexity region
|
1239 |
1253 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1324 |
1344 |
5.12e1 |
SMART |
low complexity region
|
1406 |
1423 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1446 |
1466 |
1.86e1 |
SMART |
low complexity region
|
1475 |
1507 |
N/A |
INTRINSIC |
low complexity region
|
1551 |
1568 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197026
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This tumor suppressor gene is a member of a nuclear histone/protein methyltransferase superfamily. It encodes a zinc finger protein that can bind to retinoblastoma protein, estrogen receptor, and the TPA-responsive element (MTE) of the heme-oxygenase-1 gene. Although the functions of this protein have not been fully characterized, it may (1) play a role in transcriptional regulation during neuronal differentiation and pathogenesis of retinoblastoma, (2) act as a transcriptional activator of the heme-oxygenase-1 gene, and (3) be a specific effector of estrogen action. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008] PHENOTYPE: Homozygous null mice have shortened life spans, becoming moribund due to increased incidence of tumors. Mice had a broad spectrum of unusual tumors in multiple organs, with a high incidence of diffuse large B cell lymphomas. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 8 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Champ1 |
C |
T |
8: 13,879,522 |
S560L |
possibly damaging |
Het |
Hecw2 |
C |
T |
1: 53,853,280 |
R1186H |
probably damaging |
Het |
Hivep1 |
T |
C |
13: 42,154,649 |
S122P |
probably benign |
Het |
Pcdhb15 |
T |
C |
18: 37,475,154 |
S480P |
probably damaging |
Het |
Tada2b |
A |
T |
5: 36,476,073 |
I312N |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,825,444 |
I34V |
possibly damaging |
Het |
Zfp616 |
A |
T |
11: 74,083,613 |
D236V |
probably damaging |
Het |
Zhx3 |
T |
A |
2: 160,780,841 |
N469Y |
probably damaging |
Het |
|
Other mutations in Prdm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00843:Prdm2
|
APN |
4 |
143134314 |
missense |
probably damaging |
1.00 |
IGL01419:Prdm2
|
APN |
4 |
143133648 |
missense |
probably damaging |
0.99 |
IGL01662:Prdm2
|
APN |
4 |
143133568 |
missense |
possibly damaging |
0.73 |
IGL01892:Prdm2
|
APN |
4 |
143134404 |
missense |
probably damaging |
1.00 |
IGL02104:Prdm2
|
APN |
4 |
143133427 |
missense |
probably benign |
0.01 |
IGL02208:Prdm2
|
APN |
4 |
143135743 |
missense |
probably benign |
0.01 |
IGL02260:Prdm2
|
APN |
4 |
143134587 |
missense |
probably damaging |
1.00 |
IGL02479:Prdm2
|
APN |
4 |
143134929 |
missense |
probably damaging |
1.00 |
IGL02943:Prdm2
|
APN |
4 |
143131972 |
missense |
probably benign |
|
IGL02972:Prdm2
|
APN |
4 |
143132166 |
missense |
probably benign |
|
IGL03038:Prdm2
|
APN |
4 |
143134001 |
missense |
probably damaging |
1.00 |
IGL03399:Prdm2
|
APN |
4 |
143135088 |
missense |
probably benign |
0.07 |
G1patch:Prdm2
|
UTSW |
4 |
143132901 |
missense |
possibly damaging |
0.96 |
PIT4677001:Prdm2
|
UTSW |
4 |
143135078 |
missense |
probably damaging |
1.00 |
R0088:Prdm2
|
UTSW |
4 |
143134954 |
missense |
possibly damaging |
0.86 |
R0153:Prdm2
|
UTSW |
4 |
143133768 |
missense |
possibly damaging |
0.93 |
R0320:Prdm2
|
UTSW |
4 |
143179351 |
missense |
probably damaging |
1.00 |
R0384:Prdm2
|
UTSW |
4 |
143135688 |
missense |
probably benign |
0.01 |
R0400:Prdm2
|
UTSW |
4 |
143111670 |
missense |
probably benign |
|
R0658:Prdm2
|
UTSW |
4 |
143135265 |
missense |
probably damaging |
1.00 |
R0850:Prdm2
|
UTSW |
4 |
143132203 |
missense |
possibly damaging |
0.53 |
R1118:Prdm2
|
UTSW |
4 |
143132383 |
missense |
possibly damaging |
0.52 |
R1355:Prdm2
|
UTSW |
4 |
143131963 |
missense |
probably benign |
0.33 |
R1519:Prdm2
|
UTSW |
4 |
143135583 |
missense |
probably damaging |
1.00 |
R1936:Prdm2
|
UTSW |
4 |
143134462 |
missense |
probably benign |
0.00 |
R1987:Prdm2
|
UTSW |
4 |
143132509 |
missense |
possibly damaging |
0.73 |
R2006:Prdm2
|
UTSW |
4 |
143131877 |
missense |
possibly damaging |
0.73 |
R2008:Prdm2
|
UTSW |
4 |
143134947 |
missense |
probably damaging |
1.00 |
R2030:Prdm2
|
UTSW |
4 |
143132764 |
missense |
possibly damaging |
0.53 |
R2112:Prdm2
|
UTSW |
4 |
143131936 |
missense |
probably benign |
|
R2221:Prdm2
|
UTSW |
4 |
143134899 |
missense |
possibly damaging |
0.58 |
R2223:Prdm2
|
UTSW |
4 |
143134899 |
missense |
possibly damaging |
0.58 |
R2426:Prdm2
|
UTSW |
4 |
143111750 |
nonsense |
probably null |
|
R2430:Prdm2
|
UTSW |
4 |
143133163 |
missense |
possibly damaging |
0.73 |
R2484:Prdm2
|
UTSW |
4 |
143135206 |
missense |
probably damaging |
1.00 |
R3735:Prdm2
|
UTSW |
4 |
143134359 |
missense |
probably damaging |
1.00 |
R3944:Prdm2
|
UTSW |
4 |
143131815 |
missense |
possibly damaging |
0.53 |
R4209:Prdm2
|
UTSW |
4 |
143134437 |
missense |
probably damaging |
1.00 |
R4411:Prdm2
|
UTSW |
4 |
143133670 |
missense |
probably benign |
0.18 |
R4647:Prdm2
|
UTSW |
4 |
143132955 |
missense |
possibly damaging |
0.85 |
R4898:Prdm2
|
UTSW |
4 |
143134191 |
missense |
probably damaging |
1.00 |
R5032:Prdm2
|
UTSW |
4 |
143179367 |
nonsense |
probably null |
|
R5181:Prdm2
|
UTSW |
4 |
143134966 |
missense |
probably benign |
0.35 |
R5513:Prdm2
|
UTSW |
4 |
143135893 |
small deletion |
probably benign |
|
R5539:Prdm2
|
UTSW |
4 |
143132694 |
missense |
possibly damaging |
0.53 |
R5563:Prdm2
|
UTSW |
4 |
143134630 |
missense |
probably benign |
0.09 |
R5618:Prdm2
|
UTSW |
4 |
143133537 |
missense |
probably benign |
0.00 |
R5900:Prdm2
|
UTSW |
4 |
143134720 |
missense |
probably damaging |
1.00 |
R5990:Prdm2
|
UTSW |
4 |
143170113 |
missense |
probably damaging |
1.00 |
R6148:Prdm2
|
UTSW |
4 |
143132907 |
missense |
probably benign |
0.33 |
R6166:Prdm2
|
UTSW |
4 |
143134736 |
missense |
probably damaging |
0.99 |
R6223:Prdm2
|
UTSW |
4 |
143142207 |
missense |
probably benign |
0.41 |
R6530:Prdm2
|
UTSW |
4 |
143134047 |
missense |
probably benign |
0.05 |
R6631:Prdm2
|
UTSW |
4 |
143134884 |
missense |
probably benign |
0.05 |
R6725:Prdm2
|
UTSW |
4 |
143132901 |
missense |
possibly damaging |
0.96 |
R6847:Prdm2
|
UTSW |
4 |
143132950 |
missense |
probably benign |
0.18 |
R7193:Prdm2
|
UTSW |
4 |
143180894 |
missense |
probably damaging |
1.00 |
R7238:Prdm2
|
UTSW |
4 |
143135821 |
missense |
probably benign |
0.35 |
R7292:Prdm2
|
UTSW |
4 |
143132901 |
missense |
possibly damaging |
0.96 |
R7417:Prdm2
|
UTSW |
4 |
143179299 |
missense |
probably damaging |
1.00 |
R7748:Prdm2
|
UTSW |
4 |
143135889 |
missense |
possibly damaging |
0.89 |
R7885:Prdm2
|
UTSW |
4 |
143134570 |
missense |
probably benign |
0.41 |
R7936:Prdm2
|
UTSW |
4 |
143135864 |
missense |
probably damaging |
0.99 |
R7976:Prdm2
|
UTSW |
4 |
143133242 |
nonsense |
probably null |
|
R8124:Prdm2
|
UTSW |
4 |
143135265 |
missense |
probably damaging |
1.00 |
R8150:Prdm2
|
UTSW |
4 |
143132733 |
missense |
possibly damaging |
0.73 |
R8156:Prdm2
|
UTSW |
4 |
143134768 |
missense |
probably benign |
0.01 |
R8178:Prdm2
|
UTSW |
4 |
143132448 |
missense |
probably benign |
0.33 |
R8235:Prdm2
|
UTSW |
4 |
143132467 |
nonsense |
probably null |
|
R8404:Prdm2
|
UTSW |
4 |
143135014 |
missense |
probably damaging |
0.98 |
R8498:Prdm2
|
UTSW |
4 |
143180897 |
missense |
probably damaging |
1.00 |
R8502:Prdm2
|
UTSW |
4 |
143135014 |
missense |
probably damaging |
0.98 |
R8688:Prdm2
|
UTSW |
4 |
143111740 |
missense |
probably benign |
|
R8732:Prdm2
|
UTSW |
4 |
143136010 |
missense |
probably benign |
0.00 |
R8796:Prdm2
|
UTSW |
4 |
143133447 |
missense |
probably benign |
0.33 |
R8874:Prdm2
|
UTSW |
4 |
143133215 |
missense |
possibly damaging |
0.70 |
R8887:Prdm2
|
UTSW |
4 |
143134201 |
missense |
probably damaging |
1.00 |
R9119:Prdm2
|
UTSW |
4 |
143131879 |
nonsense |
probably null |
|
R9139:Prdm2
|
UTSW |
4 |
143132182 |
missense |
probably benign |
0.03 |
R9165:Prdm2
|
UTSW |
4 |
143132104 |
missense |
possibly damaging |
0.73 |
R9342:Prdm2
|
UTSW |
4 |
143134908 |
missense |
probably damaging |
1.00 |
R9518:Prdm2
|
UTSW |
4 |
143134009 |
missense |
possibly damaging |
0.94 |
R9546:Prdm2
|
UTSW |
4 |
143134991 |
missense |
probably damaging |
1.00 |
R9547:Prdm2
|
UTSW |
4 |
143134991 |
missense |
probably damaging |
1.00 |
R9680:Prdm2
|
UTSW |
4 |
143132509 |
missense |
possibly damaging |
0.73 |
R9730:Prdm2
|
UTSW |
4 |
143132089 |
missense |
possibly damaging |
0.73 |
X0017:Prdm2
|
UTSW |
4 |
143134707 |
missense |
probably benign |
|
|
Posted On |
2015-08-05 |