Incidental Mutation 'R0036:Slf1'
ID |
18601 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Slf1
|
Ensembl Gene |
ENSMUSG00000021597 |
Gene Name |
SMC5-SMC6 complex localization factor 1 |
Synonyms |
2700017A04Rik, Brctx, Brctd1, C730024G01Rik, Ankrd32 |
MMRRC Submission |
038330-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0036 (G1)
|
Quality Score |
|
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
77043088-77135473 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 77100951 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Lysine
at position 373
(Q373K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118312
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000151524]
[ENSMUST00000159300]
[ENSMUST00000159462]
[ENSMUST00000162921]
[ENSMUST00000162944]
|
AlphaFold |
Q8R3P9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000151524
AA Change: Q373K
PolyPhen 2
Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)
|
SMART Domains |
Protein: ENSMUSP00000118312 Gene: ENSMUSG00000021597 AA Change: Q373K
Domain | Start | End | E-Value | Type |
BRCT
|
2 |
80 |
1.37e-2 |
SMART |
BRCT
|
121 |
199 |
2.12e1 |
SMART |
low complexity region
|
260 |
273 |
N/A |
INTRINSIC |
low complexity region
|
527 |
541 |
N/A |
INTRINSIC |
low complexity region
|
765 |
785 |
N/A |
INTRINSIC |
ANK
|
802 |
832 |
1.52e0 |
SMART |
ANK
|
836 |
865 |
4.32e-5 |
SMART |
ANK
|
870 |
900 |
2.07e-2 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159300
|
SMART Domains |
Protein: ENSMUSP00000124865 Gene: ENSMUSG00000021597
Domain | Start | End | E-Value | Type |
BRCT
|
2 |
80 |
1.37e-2 |
SMART |
BRCT
|
121 |
199 |
2.12e1 |
SMART |
low complexity region
|
260 |
273 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159462
|
SMART Domains |
Protein: ENSMUSP00000124543 Gene: ENSMUSG00000021597
Domain | Start | End | E-Value | Type |
BRCT
|
8 |
86 |
1.37e-2 |
SMART |
BRCT
|
127 |
205 |
2.12e1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162320
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162921
|
SMART Domains |
Protein: ENSMUSP00000124946 Gene: ENSMUSG00000021597
Domain | Start | End | E-Value | Type |
BRCT
|
2 |
80 |
1.37e-2 |
SMART |
Blast:BRCT
|
121 |
173 |
1e-8 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162944
|
SMART Domains |
Protein: ENSMUSP00000123982 Gene: ENSMUSG00000021597
Domain | Start | End | E-Value | Type |
BRCT
|
2 |
80 |
1.37e-2 |
SMART |
Blast:BRCT
|
121 |
173 |
1e-8 |
BLAST |
|
Meta Mutation Damage Score |
0.0898  |
Coding Region Coverage |
- 1x: 79.1%
- 3x: 69.3%
- 10x: 43.3%
- 20x: 23.5%
|
Validation Efficiency |
91% (49/54) |
MGI Phenotype |
PHENOTYPE: Homozygous null mice are developmentally normal and fertile with no pathological abnormalities or defects in T-cell development and genomic stability. Mutant MEFs grow at a normal rate and are not more sensitive to DNA-damaging agents while thymocytes donot show any major cell cycle defects. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 17 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028P14Rik |
A |
T |
19: 23,616,568 |
|
probably benign |
Het |
Cfap44 |
A |
G |
16: 44,439,069 |
E1098G |
possibly damaging |
Het |
Ctsq |
C |
T |
13: 61,037,671 |
|
probably null |
Het |
Dock9 |
C |
T |
14: 121,622,853 |
V886M |
probably damaging |
Het |
Eaf2 |
T |
C |
16: 36,800,658 |
Y224C |
probably benign |
Het |
Eif5b |
T |
A |
1: 38,019,111 |
S165T |
probably benign |
Het |
Eln |
A |
G |
5: 134,711,060 |
|
probably null |
Het |
Jakmip1 |
A |
G |
5: 37,134,304 |
K514R |
probably null |
Het |
Myo1e |
T |
A |
9: 70,341,308 |
W435R |
probably damaging |
Het |
Nadsyn1 |
T |
C |
7: 143,811,291 |
I226V |
probably benign |
Het |
Nedd4l |
T |
C |
18: 65,051,123 |
|
probably benign |
Het |
Phrf1 |
T |
C |
7: 141,261,780 |
M1435T |
probably damaging |
Het |
Ppic |
A |
T |
18: 53,409,192 |
I148N |
probably damaging |
Het |
Sdr16c6 |
C |
A |
4: 4,063,335 |
|
probably benign |
Het |
Sgo2a |
T |
C |
1: 58,015,628 |
S324P |
probably benign |
Het |
Tfg |
G |
T |
16: 56,690,995 |
Q324K |
probably benign |
Het |
Wdr64 |
G |
T |
1: 175,728,930 |
G248* |
probably null |
Het |
|
Other mutations in Slf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00942:Slf1
|
APN |
13 |
77043947 |
missense |
possibly damaging |
0.95 |
IGL01105:Slf1
|
APN |
13 |
77100912 |
unclassified |
probably benign |
|
IGL01108:Slf1
|
APN |
13 |
77125475 |
splice site |
probably benign |
|
IGL01149:Slf1
|
APN |
13 |
77112648 |
missense |
probably damaging |
0.99 |
IGL01642:Slf1
|
APN |
13 |
77049915 |
missense |
probably benign |
0.00 |
IGL01757:Slf1
|
APN |
13 |
77084440 |
missense |
probably benign |
|
IGL01887:Slf1
|
APN |
13 |
77100982 |
missense |
probably benign |
0.02 |
IGL02323:Slf1
|
APN |
13 |
77051294 |
missense |
possibly damaging |
0.87 |
IGL02861:Slf1
|
APN |
13 |
77126359 |
splice site |
probably benign |
|
IGL02971:Slf1
|
APN |
13 |
77047104 |
splice site |
probably benign |
|
IGL03088:Slf1
|
APN |
13 |
77084435 |
missense |
probably damaging |
1.00 |
IGL03215:Slf1
|
APN |
13 |
77049977 |
missense |
probably benign |
0.00 |
IGL02980:Slf1
|
UTSW |
13 |
77044004 |
missense |
possibly damaging |
0.92 |
PIT1430001:Slf1
|
UTSW |
13 |
77050050 |
splice site |
probably benign |
|
R0036:Slf1
|
UTSW |
13 |
77100951 |
missense |
probably benign |
0.02 |
R0125:Slf1
|
UTSW |
13 |
77043745 |
missense |
probably benign |
0.02 |
R0230:Slf1
|
UTSW |
13 |
77112748 |
intron |
probably benign |
|
R0244:Slf1
|
UTSW |
13 |
77126632 |
nonsense |
probably null |
|
R0395:Slf1
|
UTSW |
13 |
77105969 |
splice site |
probably benign |
|
R0614:Slf1
|
UTSW |
13 |
77049114 |
missense |
probably benign |
0.10 |
R0661:Slf1
|
UTSW |
13 |
77083596 |
missense |
probably benign |
0.31 |
R0837:Slf1
|
UTSW |
13 |
77100948 |
splice site |
probably null |
|
R0945:Slf1
|
UTSW |
13 |
77103471 |
unclassified |
probably benign |
|
R1282:Slf1
|
UTSW |
13 |
77043840 |
missense |
probably damaging |
0.97 |
R1365:Slf1
|
UTSW |
13 |
77126371 |
missense |
probably damaging |
1.00 |
R1449:Slf1
|
UTSW |
13 |
77083449 |
missense |
probably damaging |
1.00 |
R1646:Slf1
|
UTSW |
13 |
77066648 |
nonsense |
probably null |
|
R2071:Slf1
|
UTSW |
13 |
77104624 |
missense |
probably benign |
0.02 |
R2141:Slf1
|
UTSW |
13 |
77049219 |
critical splice acceptor site |
probably null |
|
R2217:Slf1
|
UTSW |
13 |
77046706 |
critical splice acceptor site |
probably null |
|
R2397:Slf1
|
UTSW |
13 |
77103583 |
nonsense |
probably null |
|
R2520:Slf1
|
UTSW |
13 |
77051265 |
missense |
probably damaging |
1.00 |
R3108:Slf1
|
UTSW |
13 |
77126721 |
splice site |
probably benign |
|
R4178:Slf1
|
UTSW |
13 |
77043569 |
missense |
probably damaging |
1.00 |
R4663:Slf1
|
UTSW |
13 |
77126604 |
missense |
probably damaging |
1.00 |
R4730:Slf1
|
UTSW |
13 |
77046632 |
missense |
probably damaging |
1.00 |
R4910:Slf1
|
UTSW |
13 |
77043880 |
missense |
probably benign |
0.14 |
R4912:Slf1
|
UTSW |
13 |
77051294 |
missense |
probably damaging |
1.00 |
R5122:Slf1
|
UTSW |
13 |
77049987 |
missense |
probably benign |
0.01 |
R5269:Slf1
|
UTSW |
13 |
77104581 |
missense |
probably benign |
0.33 |
R5336:Slf1
|
UTSW |
13 |
77106010 |
makesense |
probably null |
|
R5346:Slf1
|
UTSW |
13 |
77092371 |
missense |
probably benign |
0.00 |
R5445:Slf1
|
UTSW |
13 |
77091204 |
missense |
probably benign |
0.10 |
R5568:Slf1
|
UTSW |
13 |
77046704 |
missense |
probably damaging |
1.00 |
R5622:Slf1
|
UTSW |
13 |
77049971 |
missense |
probably benign |
0.14 |
R5685:Slf1
|
UTSW |
13 |
77083479 |
missense |
possibly damaging |
0.88 |
R5792:Slf1
|
UTSW |
13 |
77066737 |
missense |
probably benign |
0.03 |
R5856:Slf1
|
UTSW |
13 |
77106087 |
missense |
possibly damaging |
0.63 |
R6109:Slf1
|
UTSW |
13 |
77126680 |
missense |
probably damaging |
0.99 |
R6245:Slf1
|
UTSW |
13 |
77084383 |
missense |
probably damaging |
1.00 |
R6338:Slf1
|
UTSW |
13 |
77084462 |
critical splice acceptor site |
probably null |
|
R6438:Slf1
|
UTSW |
13 |
77066606 |
missense |
probably damaging |
1.00 |
R6487:Slf1
|
UTSW |
13 |
77066617 |
missense |
probably damaging |
1.00 |
R6597:Slf1
|
UTSW |
13 |
77049129 |
missense |
probably benign |
0.01 |
R6600:Slf1
|
UTSW |
13 |
77083536 |
missense |
probably benign |
0.00 |
R6661:Slf1
|
UTSW |
13 |
77043845 |
missense |
probably damaging |
1.00 |
R7268:Slf1
|
UTSW |
13 |
77066707 |
missense |
probably damaging |
1.00 |
R7308:Slf1
|
UTSW |
13 |
77051168 |
missense |
probably benign |
0.19 |
R7355:Slf1
|
UTSW |
13 |
77091303 |
missense |
probably damaging |
1.00 |
R7546:Slf1
|
UTSW |
13 |
77049192 |
missense |
probably benign |
|
R7807:Slf1
|
UTSW |
13 |
77046704 |
missense |
probably damaging |
1.00 |
R8175:Slf1
|
UTSW |
13 |
77112671 |
missense |
probably damaging |
1.00 |
R8385:Slf1
|
UTSW |
13 |
77105990 |
missense |
probably benign |
|
R8698:Slf1
|
UTSW |
13 |
77049165 |
missense |
possibly damaging |
0.78 |
R8770:Slf1
|
UTSW |
13 |
77046647 |
missense |
probably damaging |
1.00 |
R8786:Slf1
|
UTSW |
13 |
77126687 |
missense |
possibly damaging |
0.93 |
R8796:Slf1
|
UTSW |
13 |
77066665 |
missense |
probably benign |
0.00 |
R8932:Slf1
|
UTSW |
13 |
77046574 |
missense |
probably damaging |
1.00 |
R9132:Slf1
|
UTSW |
13 |
77100954 |
missense |
probably benign |
0.24 |
R9243:Slf1
|
UTSW |
13 |
77125456 |
missense |
possibly damaging |
0.95 |
R9274:Slf1
|
UTSW |
13 |
77043550 |
makesense |
probably null |
|
R9286:Slf1
|
UTSW |
13 |
77043813 |
missense |
probably damaging |
0.99 |
R9416:Slf1
|
UTSW |
13 |
77046537 |
missense |
|
|
R9612:Slf1
|
UTSW |
13 |
77049085 |
critical splice donor site |
probably null |
|
X0018:Slf1
|
UTSW |
13 |
77051238 |
missense |
probably damaging |
1.00 |
|
Posted On |
2013-03-25 |