Incidental Mutation 'R6413:Sh2b3'
| ID |
514810 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Sh2b3
|
| Ensembl Gene |
ENSMUSG00000042594 |
| Gene Name |
SH2B adaptor protein 3 |
| Synonyms |
Lnk |
| MMRRC Submission |
044555-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.532)
|
| Stock # |
R6413 (G1)
|
| Quality Score |
97.0078 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
121953551-121975709 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 121966986 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 43
(Y43H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142666
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040308]
[ENSMUST00000086310]
[ENSMUST00000118580]
[ENSMUST00000122426]
[ENSMUST00000136960]
[ENSMUST00000137682]
[ENSMUST00000197892]
|
| AlphaFold |
O09039 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000040308
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000041611
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
23 |
76 |
1.1e-20 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
PH
|
168 |
281 |
1.2e-2 |
SMART |
|
SH2
|
334 |
419 |
3.53e-19 |
SMART |
|
low complexity region
|
512 |
525 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000086310
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000083490
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
2e-22 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
PH
|
168 |
281 |
1.2e-2 |
SMART |
|
SH2
|
334 |
419 |
3.53e-19 |
SMART |
|
low complexity region
|
512 |
525 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000118580
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000113808
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
4.1e-23 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
PH
|
168 |
281 |
1.2e-2 |
SMART |
|
SH2
|
324 |
409 |
3.53e-19 |
SMART |
|
low complexity region
|
502 |
515 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000122426
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000113926
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
2e-22 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
PH
|
168 |
281 |
1.2e-2 |
SMART |
|
SH2
|
334 |
419 |
3.53e-19 |
SMART |
|
low complexity region
|
512 |
525 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000136960
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000119086
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
2.4e-23 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
PH
|
168 |
281 |
1.2e-2 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000137682
AA Change: Y43H
PolyPhen 2
Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000118523
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
2e-23 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000197892
AA Change: Y43H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000142666
Gene: ENSMUSG00000042594
AA Change: Y43H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
21 |
N/A |
INTRINSIC |
|
Pfam:Phe_ZIP
|
22 |
77 |
6.3e-20 |
PFAM |
|
low complexity region
|
114 |
128 |
N/A |
INTRINSIC |
|
Blast:PH
|
168 |
250 |
3e-53 |
BLAST |
|
PDB:1V5M|A
|
171 |
250 |
1e-12 |
PDB |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000198161
|
| Meta Mutation Damage Score |
0.4400 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 98.1%
|
| Validation Efficiency |
100% (37/37) |
| MGI Phenotype |
FUNCTION: This gene encodes a member of the SH2B family of adapter proteins that play an important role in T cell receptor signaling. This gene is preferentially expressed in hematopoietic stem cells, hematopoietic progenitors, pre and immature B cells, as well as megakaryocytes and mastocytes. In hematopoietic stem cells, the encoded protein is a key regulator of self-renewal, proliferation and apoptosis. Mice lacking the encoded protein exhibit pre and immature B cell expansion in spleen and the bone marrow. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit severe perturbations in hematopoiesis, splenomegaly, and abnormal lymphoid and myeloid homeostasis. Mice homozygous for a different knock-out allele display altered mobility of hematopoietic stem/progenitor cells. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3110070M22Rik |
C |
A |
13: 119,624,647 (GRCm39) |
|
probably benign |
Het |
| Agtpbp1 |
A |
G |
13: 59,647,834 (GRCm39) |
V662A |
possibly damaging |
Het |
| Ambra1 |
T |
G |
2: 91,599,429 (GRCm39) |
V183G |
possibly damaging |
Het |
| Amdhd2 |
A |
G |
17: 24,377,290 (GRCm39) |
S208P |
probably damaging |
Het |
| Ankdd1a |
C |
T |
9: 65,417,654 (GRCm39) |
V133I |
probably benign |
Het |
| Ankrd35 |
A |
G |
3: 96,592,129 (GRCm39) |
K805R |
probably damaging |
Het |
| Arhgap28 |
T |
C |
17: 68,182,583 (GRCm39) |
Q270R |
probably benign |
Het |
| Cabp2 |
G |
A |
19: 4,135,698 (GRCm39) |
|
probably null |
Het |
| Ccnt1 |
A |
G |
15: 98,441,850 (GRCm39) |
S473P |
probably benign |
Het |
| Cenpt |
G |
A |
8: 106,572,973 (GRCm39) |
P373S |
possibly damaging |
Het |
| Cyp3a44 |
T |
A |
5: 145,731,254 (GRCm39) |
D182V |
probably damaging |
Het |
| Ddx54 |
A |
G |
5: 120,765,127 (GRCm39) |
T799A |
probably benign |
Het |
| Dtna |
T |
A |
18: 23,755,071 (GRCm39) |
D464E |
probably damaging |
Het |
| E030025P04Rik |
T |
C |
11: 109,030,425 (GRCm39) |
Y154C |
unknown |
Het |
| Ephb2 |
C |
A |
4: 136,498,433 (GRCm39) |
E215D |
probably benign |
Het |
| Eya4 |
T |
C |
10: 22,992,724 (GRCm39) |
D445G |
probably damaging |
Het |
| Flg2 |
A |
T |
3: 93,127,683 (GRCm39) |
L2198F |
unknown |
Het |
| Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
| Klhl22 |
T |
C |
16: 17,607,181 (GRCm39) |
F496L |
probably benign |
Het |
| Numa1 |
A |
T |
7: 101,639,778 (GRCm39) |
|
probably null |
Het |
| Papola |
T |
C |
12: 105,772,763 (GRCm39) |
|
probably benign |
Het |
| Phldb1 |
T |
C |
9: 44,607,440 (GRCm39) |
E1255G |
probably damaging |
Het |
| Rgs8 |
A |
T |
1: 153,568,619 (GRCm39) |
D168V |
probably damaging |
Het |
| Rlf |
A |
G |
4: 121,004,522 (GRCm39) |
V1486A |
probably damaging |
Het |
| Rpa2 |
G |
T |
4: 132,501,156 (GRCm39) |
A118S |
probably benign |
Het |
| Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
| Serpina1f |
T |
A |
12: 103,659,953 (GRCm39) |
I110F |
probably damaging |
Het |
| Serpini2 |
T |
C |
3: 75,166,921 (GRCm39) |
Y112C |
probably damaging |
Het |
| Shank2 |
A |
G |
7: 143,963,955 (GRCm39) |
E514G |
probably damaging |
Het |
| Slc44a5 |
T |
C |
3: 153,963,387 (GRCm39) |
F388S |
probably benign |
Het |
| Spmip6 |
A |
T |
4: 41,505,135 (GRCm39) |
V196D |
possibly damaging |
Het |
| Tmem176b |
T |
C |
6: 48,815,266 (GRCm39) |
N9S |
possibly damaging |
Het |
| Trip11 |
T |
A |
12: 101,851,790 (GRCm39) |
Q758L |
probably benign |
Het |
| Trrap |
T |
A |
5: 144,720,856 (GRCm39) |
I231N |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,730,397 (GRCm39) |
|
probably benign |
Het |
| Vmn2r68 |
T |
C |
7: 84,870,973 (GRCm39) |
N770S |
probably damaging |
Het |
| Vmn2r73 |
A |
T |
7: 85,519,544 (GRCm39) |
Y471* |
probably null |
Het |
| Vmn2r8 |
T |
G |
5: 108,949,589 (GRCm39) |
E419D |
probably benign |
Het |
| Wdfy4 |
C |
A |
14: 32,689,604 (GRCm39) |
L2818F |
probably damaging |
Het |
| Zfhx4 |
A |
T |
3: 5,308,205 (GRCm39) |
Y477F |
probably damaging |
Het |
|
| Other mutations in Sh2b3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02283:Sh2b3
|
APN |
5 |
121,956,718 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02328:Sh2b3
|
APN |
5 |
121,955,922 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4449001:Sh2b3
|
UTSW |
5 |
121,966,742 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0164:Sh2b3
|
UTSW |
5 |
121,967,100 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0164:Sh2b3
|
UTSW |
5 |
121,967,100 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2898:Sh2b3
|
UTSW |
5 |
121,967,111 (GRCm39) |
start codon destroyed |
probably null |
0.93 |
|
R4374:Sh2b3
|
UTSW |
5 |
121,966,549 (GRCm39) |
unclassified |
probably benign |
|
|
R4688:Sh2b3
|
UTSW |
5 |
121,956,697 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4822:Sh2b3
|
UTSW |
5 |
121,966,618 (GRCm39) |
unclassified |
probably benign |
|
|
R5743:Sh2b3
|
UTSW |
5 |
121,966,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5888:Sh2b3
|
UTSW |
5 |
121,967,084 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6130:Sh2b3
|
UTSW |
5 |
121,953,626 (GRCm39) |
splice site |
probably null |
|
|
R6167:Sh2b3
|
UTSW |
5 |
121,966,418 (GRCm39) |
splice site |
probably null |
|
|
R7499:Sh2b3
|
UTSW |
5 |
121,956,536 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7615:Sh2b3
|
UTSW |
5 |
121,956,763 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7672:Sh2b3
|
UTSW |
5 |
121,956,822 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9748:Sh2b3
|
UTSW |
5 |
121,955,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATTGGTGTCACTGGTAGCCC -3'
(R):5'- TCTGACTTGTCTTACAGCCCGG -3'
Sequencing Primer
(F):5'- GTCCTCGGAGCTGCGTG -3'
(R):5'- GCTCTCCACCATGAACG -3'
|
| Posted On |
2018-05-04 |
Incidental Mutation