Incidental Mutation 'IGL01792:Khdrbs2'
| ID |
155241 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Khdrbs2
|
| Ensembl Gene |
ENSMUSG00000026058 |
| Gene Name |
KH domain containing, RNA binding, signal transduction associated 2 |
| Synonyms |
SLM-1, 6330586C16Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.219)
|
| Stock # |
IGL01792
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
32211795-32697649 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 32696548 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Cysteine
at position 326
(R326C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027226
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027226]
|
| AlphaFold |
Q9WU01 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000027226
AA Change: R326C
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000027226
Gene: ENSMUSG00000026058
AA Change: R326C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
41 |
48 |
N/A |
INTRINSIC |
|
KH
|
58 |
156 |
4.93e-7 |
SMART |
|
low complexity region
|
185 |
197 |
N/A |
INTRINSIC |
|
low complexity region
|
204 |
231 |
N/A |
INTRINSIC |
|
Pfam:Sam68-YY
|
267 |
321 |
1.3e-22 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: The protein encoded by this gene is similar to the src associated in mitosis, 68 kDa protein, which is an RNA-binding protein and a substrate for Src-family tyrosine kinases during mitosis. This protein has a KH RNA-binding motif and proline-rich motifs which may be SH2 and SH3 domain binding sites. A similar rat protein is an RNA-binding protein which is tyrosine phosphorylated by Src during mitosis. These studies also suggest that the rat protein may function as an adaptor protein for Src by binding the SH2 and SH3 domains of various other proteins. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant animals display smaller brain size and reduced weight in the cerebellum. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 23 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9830107B12Rik |
G |
T |
17: 48,452,680 (GRCm39) |
F86L |
probably damaging |
Het |
| A2ml1 |
T |
C |
6: 128,537,642 (GRCm39) |
T690A |
probably benign |
Het |
| Adam3 |
T |
C |
8: 25,187,219 (GRCm39) |
N424S |
probably benign |
Het |
| Adarb2 |
T |
C |
13: 8,620,185 (GRCm39) |
F224L |
probably damaging |
Het |
| Clcn3 |
T |
C |
8: 61,382,356 (GRCm39) |
T438A |
probably damaging |
Het |
| Cyp2c55 |
A |
G |
19: 39,030,631 (GRCm39) |
I488V |
probably benign |
Het |
| Dennd1a |
A |
G |
2: 38,016,592 (GRCm39) |
F84S |
probably damaging |
Het |
| Dennd4b |
A |
G |
3: 90,187,152 (GRCm39) |
R1475G |
probably damaging |
Het |
| Ift172 |
G |
A |
5: 31,434,215 (GRCm39) |
R508W |
probably damaging |
Het |
| Krt78 |
T |
G |
15: 101,855,085 (GRCm39) |
M909L |
probably benign |
Het |
| Ncapg2 |
T |
A |
12: 116,389,438 (GRCm39) |
F353I |
probably damaging |
Het |
| Or10d4c |
A |
T |
9: 39,558,955 (GRCm39) |
N311I |
probably benign |
Het |
| Pigb |
A |
T |
9: 72,925,268 (GRCm39) |
H396Q |
probably damaging |
Het |
| Rev3l |
C |
T |
10: 39,699,336 (GRCm39) |
P1278S |
probably benign |
Het |
| Setd1b |
T |
A |
5: 123,295,209 (GRCm39) |
V955D |
unknown |
Het |
| Slc22a16 |
T |
A |
10: 40,449,928 (GRCm39) |
H121Q |
possibly damaging |
Het |
| Slc22a29 |
A |
T |
19: 8,195,893 (GRCm39) |
C49S |
probably damaging |
Het |
| Smad1 |
T |
C |
8: 80,098,752 (GRCm39) |
K21E |
probably damaging |
Het |
| Speer4c2 |
C |
A |
5: 15,861,884 (GRCm39) |
|
probably benign |
Het |
| Spic |
A |
G |
10: 88,515,807 (GRCm39) |
I5T |
possibly damaging |
Het |
| Srpk1 |
G |
A |
17: 28,818,441 (GRCm39) |
|
probably benign |
Het |
| Tubgcp6 |
T |
C |
15: 88,985,484 (GRCm39) |
D1559G |
probably damaging |
Het |
| Unc13b |
T |
C |
4: 43,250,218 (GRCm39) |
F992L |
probably damaging |
Het |
|
| Other mutations in Khdrbs2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00848:Khdrbs2
|
APN |
1 |
32,511,833 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01326:Khdrbs2
|
APN |
1 |
32,696,558 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL01767:Khdrbs2
|
APN |
1 |
32,658,257 (GRCm39) |
nonsense |
probably null |
|
|
IGL01839:Khdrbs2
|
APN |
1 |
32,453,943 (GRCm39) |
splice site |
probably benign |
|
|
R0046:Khdrbs2
|
UTSW |
1 |
32,658,283 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R0079:Khdrbs2
|
UTSW |
1 |
32,558,996 (GRCm39) |
splice site |
probably null |
|
|
R0396:Khdrbs2
|
UTSW |
1 |
32,559,054 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0613:Khdrbs2
|
UTSW |
1 |
32,696,603 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0616:Khdrbs2
|
UTSW |
1 |
32,506,856 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R1034:Khdrbs2
|
UTSW |
1 |
32,506,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1055:Khdrbs2
|
UTSW |
1 |
32,683,238 (GRCm39) |
splice site |
probably benign |
|
|
R1156:Khdrbs2
|
UTSW |
1 |
32,506,956 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1456:Khdrbs2
|
UTSW |
1 |
32,559,777 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R2007:Khdrbs2
|
UTSW |
1 |
32,559,629 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2079:Khdrbs2
|
UTSW |
1 |
32,506,955 (GRCm39) |
missense |
probably benign |
|
|
R2384:Khdrbs2
|
UTSW |
1 |
32,558,976 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3123:Khdrbs2
|
UTSW |
1 |
32,558,858 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3124:Khdrbs2
|
UTSW |
1 |
32,558,858 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3772:Khdrbs2
|
UTSW |
1 |
32,283,157 (GRCm39) |
nonsense |
probably null |
|
|
R4078:Khdrbs2
|
UTSW |
1 |
32,558,895 (GRCm39) |
intron |
probably benign |
|
|
R4088:Khdrbs2
|
UTSW |
1 |
32,372,605 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4955:Khdrbs2
|
UTSW |
1 |
32,559,158 (GRCm39) |
intron |
probably benign |
|
|
R5465:Khdrbs2
|
UTSW |
1 |
32,658,255 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5668:Khdrbs2
|
UTSW |
1 |
32,506,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5792:Khdrbs2
|
UTSW |
1 |
32,511,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6639:Khdrbs2
|
UTSW |
1 |
32,506,943 (GRCm39) |
nonsense |
probably null |
|
|
R7027:Khdrbs2
|
UTSW |
1 |
32,453,997 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7380:Khdrbs2
|
UTSW |
1 |
32,372,685 (GRCm39) |
missense |
unknown |
|
|
R7381:Khdrbs2
|
UTSW |
1 |
32,372,883 (GRCm39) |
missense |
not run |
|
|
R7939:Khdrbs2
|
UTSW |
1 |
32,212,056 (GRCm39) |
missense |
probably benign |
0.27 |
|
R8087:Khdrbs2
|
UTSW |
1 |
32,454,057 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9347:Khdrbs2
|
UTSW |
1 |
32,511,828 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0020:Khdrbs2
|
UTSW |
1 |
32,454,055 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Khdrbs2
|
UTSW |
1 |
32,283,136 (GRCm39) |
intron |
probably benign |
|
|
Z1176:Khdrbs2
|
UTSW |
1 |
32,372,743 (GRCm39) |
missense |
unknown |
|
|
Z1177:Khdrbs2
|
UTSW |
1 |
32,283,048 (GRCm39) |
missense |
probably benign |
0.30 |
|
| Posted On |
2014-02-04 |
Incidental Mutation