Incidental Mutation 'IGL02980:Recql5'
| ID |
406522 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Recql5
|
| Ensembl Gene |
ENSMUSG00000020752 |
| Gene Name |
RecQ protein-like 5 |
| Synonyms |
Recql5b, Recq5b |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.355)
|
| Stock # |
IGL02980 (G1)
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
115783421-115824303 bp(-) (GRCm39) |
| Type of Mutation |
splice site (3 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 115784770 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000021097
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021097]
[ENSMUST00000093911]
[ENSMUST00000131578]
[ENSMUST00000140174]
[ENSMUST00000222123]
[ENSMUST00000167507]
|
| AlphaFold |
Q8VID5 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000021097
|
| SMART Domains |
Protein: ENSMUSP00000021097
Gene: ENSMUSG00000020752
| Domain | Start | End | E-Value | Type |
|---|
|
DEXDc
|
25 |
230 |
1.13e-29 |
SMART |
|
HELICc
|
274 |
355 |
8.68e-22 |
SMART |
|
Pfam:RecQ_Zn_bind
|
366 |
436 |
1.8e-12 |
PFAM |
|
low complexity region
|
472 |
499 |
N/A |
INTRINSIC |
|
PDB:4BK0|B
|
516 |
621 |
2e-51 |
PDB |
|
Pfam:RecQ5
|
626 |
818 |
3.1e-97 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000093911
|
| SMART Domains |
Protein: ENSMUSP00000091439
Gene: ENSMUSG00000034427
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
1 |
640 |
2.4e-134 |
SMART |
|
IQ
|
660 |
682 |
1.03e1 |
SMART |
|
Pfam:MyTH4
|
837 |
945 |
2.1e-23 |
PFAM |
|
low complexity region
|
1050 |
1068 |
N/A |
INTRINSIC |
|
low complexity region
|
1136 |
1170 |
N/A |
INTRINSIC |
|
low complexity region
|
1207 |
1246 |
N/A |
INTRINSIC |
|
low complexity region
|
1302 |
1327 |
N/A |
INTRINSIC |
|
low complexity region
|
1454 |
1468 |
N/A |
INTRINSIC |
|
low complexity region
|
1489 |
1509 |
N/A |
INTRINSIC |
|
SH3
|
1735 |
1792 |
1.15e-7 |
SMART |
|
Pfam:MyTH4
|
1928 |
2029 |
8.3e-25 |
PFAM |
|
B41
|
2032 |
2235 |
6.99e-4 |
SMART |
|
low complexity region
|
2243 |
2253 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131578
|
| SMART Domains |
Protein: ENSMUSP00000136178
Gene: ENSMUSG00000020752
| Domain | Start | End | E-Value | Type |
|---|
|
HELICc
|
1 |
82 |
8.68e-22 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132447
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136774
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140174
|
| SMART Domains |
Protein: ENSMUSP00000136506
Gene: ENSMUSG00000020752
| Domain | Start | End | E-Value | Type |
|---|
|
DEXDc
|
25 |
230 |
1.13e-29 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141947
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000147172
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144824
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000222123
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000167507
|
| SMART Domains |
Protein: ENSMUSP00000129226
Gene: ENSMUSG00000034427
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MyTH4
|
100 |
205 |
3.1e-24 |
PFAM |
|
B41
|
207 |
410 |
6.99e-4 |
SMART |
|
low complexity region
|
418 |
428 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 0.0%
- 3x: 0.0%
- 10x: 0.0%
- 20x: 0.0%
|
| Validation Efficiency |
97% (35/36) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a helicase that is important for genome stability. The encoded protein also prevents aberrant homologous recombination by displacing RAD51 from ssDNA. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]
PHENOTYPE: Mice homozygous for disruptions in this gene express elevated levels of sister chromatid exchange due to a failure to suppress crossovers. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acvr1b |
A |
G |
15: 101,100,959 (GRCm39) |
R374G |
probably damaging |
Het |
| Adam28 |
A |
T |
14: 68,857,255 (GRCm39) |
S584T |
probably benign |
Het |
| Akap1 |
A |
T |
11: 88,735,990 (GRCm39) |
I224N |
probably benign |
Het |
| Ankdd1b |
C |
T |
13: 96,572,448 (GRCm39) |
R214Q |
probably benign |
Het |
| Armt1 |
A |
G |
10: 4,400,643 (GRCm39) |
|
probably benign |
Het |
| C1rl |
T |
C |
6: 124,485,487 (GRCm39) |
I286T |
probably benign |
Het |
| Cdh23 |
T |
C |
10: 60,150,399 (GRCm39) |
T2528A |
probably damaging |
Het |
| Col4a4 |
A |
G |
1: 82,447,198 (GRCm39) |
|
probably null |
Het |
| Dag1 |
A |
G |
9: 108,095,237 (GRCm39) |
I85T |
probably benign |
Het |
| Elf2 |
A |
G |
3: 51,172,379 (GRCm39) |
V86A |
possibly damaging |
Het |
| Emsy |
T |
C |
7: 98,268,587 (GRCm39) |
T485A |
probably damaging |
Het |
| Fam169a |
T |
C |
13: 97,250,188 (GRCm39) |
|
probably null |
Het |
| Hsd17b4 |
A |
G |
18: 50,279,585 (GRCm39) |
H188R |
probably benign |
Het |
| Ighv9-2 |
C |
T |
12: 114,072,839 (GRCm39) |
V45M |
probably damaging |
Het |
| Kifbp |
A |
C |
10: 62,394,947 (GRCm39) |
L565W |
probably damaging |
Het |
| Lama3 |
C |
T |
18: 12,686,288 (GRCm39) |
L2784F |
probably benign |
Het |
| Ms4a4c |
G |
T |
19: 11,393,747 (GRCm39) |
A64S |
probably benign |
Het |
| Nudt22 |
A |
G |
19: 6,970,500 (GRCm39) |
L280P |
probably damaging |
Het |
| Oscar |
T |
C |
7: 3,614,062 (GRCm39) |
|
probably benign |
Het |
| Paics |
A |
G |
5: 77,114,102 (GRCm39) |
I321V |
probably benign |
Het |
| Pappa |
A |
T |
4: 65,226,011 (GRCm39) |
H1288L |
probably benign |
Het |
| Pla2r1 |
T |
C |
2: 60,345,390 (GRCm39) |
E322G |
possibly damaging |
Het |
| Poldip2 |
T |
A |
11: 78,412,054 (GRCm39) |
M330K |
probably damaging |
Het |
| Potefam1 |
G |
A |
2: 110,994,818 (GRCm39) |
H232Y |
unknown |
Het |
| Rnf145 |
A |
G |
11: 44,452,484 (GRCm39) |
M488V |
probably benign |
Het |
| Rrp1b |
T |
A |
17: 32,269,013 (GRCm39) |
D170E |
possibly damaging |
Het |
| Slamf7 |
T |
C |
1: 171,468,566 (GRCm39) |
S109G |
possibly damaging |
Het |
| Slf1 |
A |
G |
13: 77,192,123 (GRCm39) |
S904P |
possibly damaging |
Het |
| St7 |
C |
A |
6: 17,749,545 (GRCm39) |
|
probably benign |
Het |
| Stk25 |
A |
G |
1: 93,555,390 (GRCm39) |
S102P |
probably damaging |
Het |
| Supt6 |
C |
T |
11: 78,116,548 (GRCm39) |
A659T |
probably damaging |
Het |
| Tdrp |
A |
C |
8: 14,003,918 (GRCm39) |
S140A |
probably damaging |
Het |
| Thbs3 |
A |
G |
3: 89,130,451 (GRCm39) |
N527D |
probably benign |
Het |
| Tsnaxip1 |
G |
T |
8: 106,568,842 (GRCm39) |
V444L |
probably damaging |
Het |
| U2af2 |
A |
G |
7: 5,071,042 (GRCm39) |
I116V |
probably benign |
Het |
| Zfp931 |
C |
A |
2: 177,711,409 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Recql5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01108:Recql5
|
APN |
11 |
115,788,007 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL01589:Recql5
|
APN |
11 |
115,785,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02040:Recql5
|
APN |
11 |
115,823,623 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02131:Recql5
|
APN |
11 |
115,814,068 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02198:Recql5
|
APN |
11 |
115,785,499 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02236:Recql5
|
APN |
11 |
115,784,856 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02501:Recql5
|
APN |
11 |
115,785,917 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL03028:Recql5
|
APN |
11 |
115,785,257 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
PIT4581001:Recql5
|
UTSW |
11 |
115,823,682 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R0152:Recql5
|
UTSW |
11 |
115,785,499 (GRCm39) |
missense |
probably benign |
|
|
R0269:Recql5
|
UTSW |
11 |
115,819,050 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0317:Recql5
|
UTSW |
11 |
115,785,499 (GRCm39) |
missense |
probably benign |
|
|
R0511:Recql5
|
UTSW |
11 |
115,819,209 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0786:Recql5
|
UTSW |
11 |
115,786,628 (GRCm39) |
missense |
probably benign |
|
|
R0975:Recql5
|
UTSW |
11 |
115,814,082 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1170:Recql5
|
UTSW |
11 |
115,788,060 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1208:Recql5
|
UTSW |
11 |
115,783,982 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1208:Recql5
|
UTSW |
11 |
115,783,982 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1807:Recql5
|
UTSW |
11 |
115,785,941 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R1872:Recql5
|
UTSW |
11 |
115,814,135 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1878:Recql5
|
UTSW |
11 |
115,785,927 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1935:Recql5
|
UTSW |
11 |
115,788,017 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1936:Recql5
|
UTSW |
11 |
115,788,017 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1945:Recql5
|
UTSW |
11 |
115,819,123 (GRCm39) |
nonsense |
probably null |
|
|
R2011:Recql5
|
UTSW |
11 |
115,787,923 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2012:Recql5
|
UTSW |
11 |
115,787,923 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2023:Recql5
|
UTSW |
11 |
115,784,466 (GRCm39) |
missense |
probably benign |
|
|
R2183:Recql5
|
UTSW |
11 |
115,787,613 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3881:Recql5
|
UTSW |
11 |
115,784,781 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3881:Recql5
|
UTSW |
11 |
115,784,780 (GRCm39) |
missense |
probably benign |
|
|
R4093:Recql5
|
UTSW |
11 |
115,795,714 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4857:Recql5
|
UTSW |
11 |
115,819,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5245:Recql5
|
UTSW |
11 |
115,784,385 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5323:Recql5
|
UTSW |
11 |
115,818,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5796:Recql5
|
UTSW |
11 |
115,818,691 (GRCm39) |
intron |
probably benign |
|
|
R6160:Recql5
|
UTSW |
11 |
115,823,613 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6229:Recql5
|
UTSW |
11 |
115,821,540 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6824:Recql5
|
UTSW |
11 |
115,814,038 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7013:Recql5
|
UTSW |
11 |
115,785,402 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7043:Recql5
|
UTSW |
11 |
115,821,502 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7135:Recql5
|
UTSW |
11 |
115,821,498 (GRCm39) |
splice site |
probably null |
|
|
R7354:Recql5
|
UTSW |
11 |
115,819,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7373:Recql5
|
UTSW |
11 |
115,819,198 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7503:Recql5
|
UTSW |
11 |
115,785,881 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7574:Recql5
|
UTSW |
11 |
115,819,248 (GRCm39) |
missense |
probably benign |
|
|
R7597:Recql5
|
UTSW |
11 |
115,819,207 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7658:Recql5
|
UTSW |
11 |
115,814,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8025:Recql5
|
UTSW |
11 |
115,818,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8038:Recql5
|
UTSW |
11 |
115,818,178 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8316:Recql5
|
UTSW |
11 |
115,784,861 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8463:Recql5
|
UTSW |
11 |
115,787,619 (GRCm39) |
nonsense |
probably null |
|
|
R8770:Recql5
|
UTSW |
11 |
115,787,943 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8788:Recql5
|
UTSW |
11 |
115,786,628 (GRCm39) |
missense |
probably benign |
|
|
R9083:Recql5
|
UTSW |
11 |
115,785,475 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R9653:Recql5
|
UTSW |
11 |
115,788,032 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9711:Recql5
|
UTSW |
11 |
115,784,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0026:Recql5
|
UTSW |
11 |
115,814,087 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0028:Recql5
|
UTSW |
11 |
115,785,432 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation