Incidental Mutation 'IGL01375:Dyrk2'
| ID |
78679 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Dyrk2
|
| Ensembl Gene |
ENSMUSG00000028630 |
| Gene Name |
dual-specificity tyrosine phosphorylation regulated kinase 2 |
| Synonyms |
1810038L18Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.572)
|
| Stock # |
IGL01375
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
118691508-118706114 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 118696592 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 222
(V222A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000004281
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004281]
|
| AlphaFold |
Q5U4C9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000004281
AA Change: V222A
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000004281
Gene: ENSMUSG00000028630
AA Change: V222A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
220 |
533 |
1.16e-92 |
SMART |
|
low complexity region
|
560 |
574 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000191892
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218477
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218692
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] DYRK2 belongs to a family of protein kinases whose members are presumed to be involved in cellular growth and/or development. The family is defined by structural similarity of their kinase domains and their capability to autophosphorylate on tyrosine residues. DYRK2 has demonstrated tyrosine autophosphorylation and catalyzed phosphorylation of histones H3 and H2B in vitro. Two isoforms of DYRK2 have been isolated. The predominant isoform, isoform 1, lacks a 5' terminal insert. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Anxa2 |
C |
T |
9: 69,390,301 (GRCm39) |
R68* |
probably null |
Het |
| Apc |
C |
T |
18: 34,446,707 (GRCm39) |
S1167L |
probably damaging |
Het |
| Aqp2 |
A |
G |
15: 99,479,983 (GRCm39) |
T149A |
possibly damaging |
Het |
| Asb8 |
T |
C |
15: 98,039,190 (GRCm39) |
E70G |
probably damaging |
Het |
| Carmil1 |
T |
C |
13: 24,278,454 (GRCm39) |
I172V |
possibly damaging |
Het |
| Cd38 |
A |
G |
5: 44,060,939 (GRCm39) |
M172V |
probably benign |
Het |
| Dync2i1 |
G |
T |
12: 116,193,296 (GRCm39) |
A552E |
possibly damaging |
Het |
| Ephb6 |
T |
A |
6: 41,592,845 (GRCm39) |
|
probably benign |
Het |
| Fbxo15 |
T |
C |
18: 84,976,404 (GRCm39) |
S48P |
possibly damaging |
Het |
| Gsdma3 |
T |
C |
11: 98,520,767 (GRCm39) |
|
probably null |
Het |
| H2bl1 |
A |
G |
13: 99,120,650 (GRCm39) |
|
probably benign |
Het |
| Htr1d |
A |
G |
4: 136,170,484 (GRCm39) |
T238A |
probably benign |
Het |
| Kcnh3 |
G |
A |
15: 99,124,874 (GRCm39) |
W108* |
probably null |
Het |
| Kdsr |
A |
T |
1: 106,655,424 (GRCm39) |
Y272N |
probably benign |
Het |
| Lrp2 |
A |
G |
2: 69,308,910 (GRCm39) |
|
probably benign |
Het |
| Nup210l |
G |
A |
3: 90,067,200 (GRCm39) |
V747M |
probably damaging |
Het |
| Or10g3 |
A |
G |
14: 52,609,865 (GRCm39) |
I215T |
probably damaging |
Het |
| Or4a67 |
A |
G |
2: 88,597,810 (GRCm39) |
V283A |
probably benign |
Het |
| Pfn3 |
T |
A |
13: 55,562,641 (GRCm39) |
R113S |
possibly damaging |
Het |
| Pik3r4 |
T |
C |
9: 105,521,803 (GRCm39) |
I123T |
possibly damaging |
Het |
| Plec |
A |
T |
15: 76,060,640 (GRCm39) |
I3121N |
probably damaging |
Het |
| Prepl |
C |
T |
17: 85,379,419 (GRCm39) |
G336D |
possibly damaging |
Het |
| Prpf8 |
C |
A |
11: 75,385,121 (GRCm39) |
A794D |
possibly damaging |
Het |
| Prps1l1 |
A |
G |
12: 35,035,631 (GRCm39) |
T249A |
possibly damaging |
Het |
| Rptor |
T |
A |
11: 119,787,262 (GRCm39) |
F1276I |
possibly damaging |
Het |
| Serpina3f |
G |
A |
12: 104,186,735 (GRCm39) |
V434I |
unknown |
Het |
| Slc25a12 |
T |
C |
2: 71,138,394 (GRCm39) |
|
probably benign |
Het |
| Slc4a4 |
T |
C |
5: 89,327,593 (GRCm39) |
C642R |
probably damaging |
Het |
| Slit2 |
C |
T |
5: 48,439,056 (GRCm39) |
|
probably benign |
Het |
| Tasor |
A |
G |
14: 27,162,120 (GRCm39) |
R159G |
probably damaging |
Het |
| Tgfbr3 |
A |
G |
5: 107,284,837 (GRCm39) |
V604A |
probably benign |
Het |
| Tnfrsf1b |
T |
C |
4: 144,951,986 (GRCm39) |
Y126C |
probably damaging |
Het |
| Traf4 |
T |
C |
11: 78,050,908 (GRCm39) |
N416S |
probably benign |
Het |
| Trappc10 |
A |
G |
10: 78,024,733 (GRCm39) |
I1132T |
possibly damaging |
Het |
| Vps8 |
T |
A |
16: 21,378,122 (GRCm39) |
Y642* |
probably null |
Het |
|
| Other mutations in Dyrk2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00392:Dyrk2
|
APN |
10 |
118,695,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00536:Dyrk2
|
APN |
10 |
118,696,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01288:Dyrk2
|
APN |
10 |
118,696,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01637:Dyrk2
|
APN |
10 |
118,696,412 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02052:Dyrk2
|
APN |
10 |
118,696,448 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0452:Dyrk2
|
UTSW |
10 |
118,704,668 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0833:Dyrk2
|
UTSW |
10 |
118,697,027 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0836:Dyrk2
|
UTSW |
10 |
118,697,027 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1346:Dyrk2
|
UTSW |
10 |
118,695,624 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1610:Dyrk2
|
UTSW |
10 |
118,695,830 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2397:Dyrk2
|
UTSW |
10 |
118,697,273 (GRCm39) |
intron |
probably benign |
|
|
R2409:Dyrk2
|
UTSW |
10 |
118,696,532 (GRCm39) |
missense |
probably benign |
|
|
R2965:Dyrk2
|
UTSW |
10 |
118,696,242 (GRCm39) |
nonsense |
probably null |
|
|
R2966:Dyrk2
|
UTSW |
10 |
118,696,242 (GRCm39) |
nonsense |
probably null |
|
|
R4700:Dyrk2
|
UTSW |
10 |
118,704,191 (GRCm39) |
missense |
probably benign |
|
|
R4896:Dyrk2
|
UTSW |
10 |
118,704,153 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4978:Dyrk2
|
UTSW |
10 |
118,696,252 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5393:Dyrk2
|
UTSW |
10 |
118,695,753 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5442:Dyrk2
|
UTSW |
10 |
118,696,643 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R5496:Dyrk2
|
UTSW |
10 |
118,695,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5810:Dyrk2
|
UTSW |
10 |
118,696,245 (GRCm39) |
missense |
probably benign |
0.16 |
|
R5875:Dyrk2
|
UTSW |
10 |
118,696,602 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5930:Dyrk2
|
UTSW |
10 |
118,696,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6877:Dyrk2
|
UTSW |
10 |
118,696,328 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7234:Dyrk2
|
UTSW |
10 |
118,696,136 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R7442:Dyrk2
|
UTSW |
10 |
118,695,786 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7741:Dyrk2
|
UTSW |
10 |
118,695,594 (GRCm39) |
missense |
probably benign |
|
|
R8108:Dyrk2
|
UTSW |
10 |
118,695,734 (GRCm39) |
missense |
probably benign |
0.27 |
|
R8137:Dyrk2
|
UTSW |
10 |
118,695,789 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8347:Dyrk2
|
UTSW |
10 |
118,695,888 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8507:Dyrk2
|
UTSW |
10 |
118,696,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8517:Dyrk2
|
UTSW |
10 |
118,696,926 (GRCm39) |
missense |
probably benign |
|
|
R8695:Dyrk2
|
UTSW |
10 |
118,696,922 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9018:Dyrk2
|
UTSW |
10 |
118,696,014 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9619:Dyrk2
|
UTSW |
10 |
118,696,292 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-11-05 |
Incidental Mutation