Incidental Mutation 'IGL00921:Dnttip2'
ID |
27091 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Dnttip2
|
Ensembl Gene |
ENSMUSG00000039756 |
Gene Name |
deoxynucleotidyltransferase, terminal, interacting protein 2 |
Synonyms |
4930588M11Rik |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.969)
|
Stock # |
IGL00921
|
Quality Score |
|
Status
|
|
Chromosome |
3 |
Chromosomal Location |
122068045-122078920 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 122068939 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Asparagine
at position 51
(K51N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000045043
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029769]
[ENSMUST00000035776]
|
AlphaFold |
Q8R2M2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000029769
|
SMART Domains |
Protein: ENSMUSP00000029769 Gene: ENSMUSG00000028124
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
16 |
N/A |
INTRINSIC |
Pfam:Aldo_ket_red
|
70 |
237 |
2.6e-8 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000035776
AA Change: K51N
PolyPhen 2
Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000045043 Gene: ENSMUSG00000039756 AA Change: K51N
Domain | Start | End | E-Value | Type |
low complexity region
|
125 |
143 |
N/A |
INTRINSIC |
low complexity region
|
447 |
458 |
N/A |
INTRINSIC |
coiled coil region
|
513 |
541 |
N/A |
INTRINSIC |
low complexity region
|
550 |
565 |
N/A |
INTRINSIC |
Pfam:Fcf2
|
639 |
733 |
3.4e-41 |
PFAM |
low complexity region
|
748 |
756 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000072769
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197215
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199449
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199627
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is thought to be involved in chromatin remodeling and gene transcription. The encoded nuclear protein binds to and enhances the transcriptional activity of the estrogen receptor alpha, and also interacts with terminal deoxynucleotidyltransferase. The expression profile of this gene is a potential biomarker for chronic obstructive pulmonary disease. [provided by RefSeq, Dec 2010]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,324,888 (GRCm39) |
I1530T |
probably damaging |
Het |
Actb |
T |
C |
5: 142,890,191 (GRCm39) |
E237G |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,690,585 (GRCm39) |
E931G |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,185,387 (GRCm39) |
T375A |
probably benign |
Het |
D1Pas1 |
A |
G |
1: 186,700,983 (GRCm39) |
D304G |
probably benign |
Het |
Ddx49 |
G |
A |
8: 70,747,406 (GRCm39) |
Q345* |
probably null |
Het |
Fxr2 |
A |
G |
11: 69,543,066 (GRCm39) |
E621G |
probably damaging |
Het |
Grhpr |
A |
G |
4: 44,988,991 (GRCm39) |
D216G |
probably damaging |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Hook2 |
T |
C |
8: 85,729,126 (GRCm39) |
|
probably benign |
Het |
Hspbp1 |
A |
G |
7: 4,667,750 (GRCm39) |
S248P |
probably damaging |
Het |
Kat6a |
C |
T |
8: 23,430,279 (GRCm39) |
P1878L |
unknown |
Het |
Klrg1 |
A |
T |
6: 122,259,711 (GRCm39) |
D20E |
probably benign |
Het |
Layn |
G |
A |
9: 50,968,708 (GRCm39) |
T345I |
probably damaging |
Het |
Mpi |
G |
A |
9: 57,459,549 (GRCm39) |
L9F |
probably damaging |
Het |
Nbn |
T |
C |
4: 15,963,833 (GRCm39) |
V78A |
possibly damaging |
Het |
Pkdrej |
A |
G |
15: 85,701,427 (GRCm39) |
I1503T |
probably damaging |
Het |
Pou2f2 |
C |
A |
7: 24,792,125 (GRCm39) |
E577* |
probably null |
Het |
Prim2 |
G |
T |
1: 33,551,241 (GRCm39) |
H292Q |
probably damaging |
Het |
Tg |
A |
G |
15: 66,636,302 (GRCm39) |
N630D |
probably benign |
Het |
Trim80 |
A |
G |
11: 115,338,490 (GRCm39) |
N440S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,766,746 (GRCm39) |
S3111G |
probably damaging |
Het |
Ubash3a |
A |
G |
17: 31,447,160 (GRCm39) |
T339A |
probably benign |
Het |
Zbtb21 |
A |
C |
16: 97,753,222 (GRCm39) |
S354A |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,736,696 (GRCm39) |
T980A |
possibly damaging |
Het |
|
Other mutations in Dnttip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00535:Dnttip2
|
APN |
3 |
122,078,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01120:Dnttip2
|
APN |
3 |
122,072,386 (GRCm39) |
splice site |
probably benign |
|
IGL01341:Dnttip2
|
APN |
3 |
122,070,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01636:Dnttip2
|
APN |
3 |
122,076,123 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01988:Dnttip2
|
APN |
3 |
122,069,944 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02096:Dnttip2
|
APN |
3 |
122,078,062 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02216:Dnttip2
|
APN |
3 |
122,069,910 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03234:Dnttip2
|
APN |
3 |
122,076,087 (GRCm39) |
missense |
probably damaging |
1.00 |
Abyss
|
UTSW |
3 |
122,069,870 (GRCm39) |
missense |
probably damaging |
0.99 |
Chasm
|
UTSW |
3 |
122,069,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Dnttip2
|
UTSW |
3 |
122,069,111 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0102:Dnttip2
|
UTSW |
3 |
122,069,452 (GRCm39) |
missense |
probably benign |
0.00 |
R0102:Dnttip2
|
UTSW |
3 |
122,069,452 (GRCm39) |
missense |
probably benign |
0.00 |
R0195:Dnttip2
|
UTSW |
3 |
122,069,810 (GRCm39) |
missense |
probably benign |
0.02 |
R1103:Dnttip2
|
UTSW |
3 |
122,070,071 (GRCm39) |
missense |
probably benign |
0.02 |
R1733:Dnttip2
|
UTSW |
3 |
122,070,397 (GRCm39) |
missense |
probably benign |
0.25 |
R1759:Dnttip2
|
UTSW |
3 |
122,069,798 (GRCm39) |
missense |
probably benign |
0.21 |
R2019:Dnttip2
|
UTSW |
3 |
122,074,393 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2022:Dnttip2
|
UTSW |
3 |
122,069,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R2415:Dnttip2
|
UTSW |
3 |
122,070,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Dnttip2
|
UTSW |
3 |
122,069,040 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4194:Dnttip2
|
UTSW |
3 |
122,074,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Dnttip2
|
UTSW |
3 |
122,070,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Dnttip2
|
UTSW |
3 |
122,078,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Dnttip2
|
UTSW |
3 |
122,070,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R5082:Dnttip2
|
UTSW |
3 |
122,069,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R5436:Dnttip2
|
UTSW |
3 |
122,072,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R5483:Dnttip2
|
UTSW |
3 |
122,070,446 (GRCm39) |
missense |
probably damaging |
0.97 |
R5933:Dnttip2
|
UTSW |
3 |
122,069,217 (GRCm39) |
missense |
probably benign |
0.07 |
R5966:Dnttip2
|
UTSW |
3 |
122,078,817 (GRCm39) |
utr 3 prime |
probably benign |
|
R6171:Dnttip2
|
UTSW |
3 |
122,072,511 (GRCm39) |
missense |
probably damaging |
0.99 |
R6251:Dnttip2
|
UTSW |
3 |
122,068,905 (GRCm39) |
missense |
probably benign |
0.14 |
R6286:Dnttip2
|
UTSW |
3 |
122,078,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6512:Dnttip2
|
UTSW |
3 |
122,069,172 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6519:Dnttip2
|
UTSW |
3 |
122,069,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6670:Dnttip2
|
UTSW |
3 |
122,069,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R6833:Dnttip2
|
UTSW |
3 |
122,070,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R6870:Dnttip2
|
UTSW |
3 |
122,069,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Dnttip2
|
UTSW |
3 |
122,076,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Dnttip2
|
UTSW |
3 |
122,070,181 (GRCm39) |
nonsense |
probably null |
|
R7233:Dnttip2
|
UTSW |
3 |
122,070,039 (GRCm39) |
missense |
probably benign |
0.26 |
R7423:Dnttip2
|
UTSW |
3 |
122,069,175 (GRCm39) |
missense |
probably benign |
|
R7591:Dnttip2
|
UTSW |
3 |
122,070,117 (GRCm39) |
nonsense |
probably null |
|
R7765:Dnttip2
|
UTSW |
3 |
122,069,594 (GRCm39) |
missense |
probably benign |
0.09 |
R7842:Dnttip2
|
UTSW |
3 |
122,069,990 (GRCm39) |
missense |
probably benign |
0.03 |
R7899:Dnttip2
|
UTSW |
3 |
122,076,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Dnttip2
|
UTSW |
3 |
122,070,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R8753:Dnttip2
|
UTSW |
3 |
122,074,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R9165:Dnttip2
|
UTSW |
3 |
122,070,355 (GRCm39) |
missense |
probably benign |
|
Z1189:Dnttip2
|
UTSW |
3 |
122,070,305 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Posted On |
2013-04-17 |