Incidental Mutation 'IGL00328:Ltn1'
ID |
3949 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Ltn1
|
Ensembl Gene |
ENSMUSG00000052299 |
Gene Name |
listerin E3 ubiquitin protein ligase 1 |
Synonyms |
4930528H02Rik, Rnf160, Zfp294, Listerin |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL00328
|
Quality Score |
|
Status
|
|
Chromosome |
16 |
Chromosomal Location |
87376651-87432612 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 87418490 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 419
(I419T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000156299
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039449]
[ENSMUST00000232095]
|
AlphaFold |
Q6A009 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000039449
AA Change: I419T
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000038775 Gene: ENSMUSG00000052299 AA Change: I419T
Domain | Start | End | E-Value | Type |
low complexity region
|
160 |
176 |
N/A |
INTRINSIC |
low complexity region
|
400 |
410 |
N/A |
INTRINSIC |
low complexity region
|
509 |
522 |
N/A |
INTRINSIC |
low complexity region
|
553 |
569 |
N/A |
INTRINSIC |
low complexity region
|
815 |
832 |
N/A |
INTRINSIC |
low complexity region
|
1380 |
1392 |
N/A |
INTRINSIC |
low complexity region
|
1427 |
1451 |
N/A |
INTRINSIC |
RING
|
1716 |
1762 |
1.05e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083713
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000232095
AA Change: I419T
PolyPhen 2
Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Like most RING finger proteins, LTN1 functions as an E3 ubiquitin ligase (Chu et al., 2009 [PubMed 19196968]).[supplied by OMIM, Nov 2010] PHENOTYPE: Mice homozygous for a gene trap allele display embryonic lethality. Mice homozygous for a point mutation display progressive neuron degeneration and age dependent motor deficits. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 13 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
C |
T |
15: 102,339,374 |
V378I |
possibly damaging |
Het |
Acad12 |
C |
T |
5: 121,604,253 |
|
probably benign |
Het |
Bap1 |
T |
G |
14: 31,253,569 |
S123R |
probably damaging |
Het |
Cers2 |
A |
T |
3: 95,320,686 |
K73I |
probably benign |
Het |
Dab1 |
T |
C |
4: 104,688,438 |
V240A |
possibly damaging |
Het |
Fry |
C |
T |
5: 150,340,404 |
R171* |
probably null |
Het |
Krtap5-3 |
G |
T |
7: 142,201,875 |
|
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,004,816 |
R540G |
probably damaging |
Het |
Mki67 |
A |
C |
7: 135,696,695 |
S2203R |
probably benign |
Het |
Ptrh1 |
G |
T |
2: 32,776,341 |
|
probably null |
Het |
Tnfaip8 |
A |
G |
18: 50,090,326 |
E67G |
probably damaging |
Het |
Vmn1r2 |
T |
A |
4: 3,172,807 |
L242Q |
probably damaging |
Het |
Vmn2r52 |
A |
G |
7: 10,171,417 |
L165P |
probably benign |
Het |
|
Other mutations in Ltn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01139:Ltn1
|
APN |
16 |
87416009 |
missense |
probably benign |
0.04 |
IGL01359:Ltn1
|
APN |
16 |
87405693 |
splice site |
probably benign |
|
IGL01503:Ltn1
|
APN |
16 |
87420807 |
critical splice donor site |
probably benign |
|
IGL01529:Ltn1
|
APN |
16 |
87381471 |
missense |
probably benign |
0.00 |
IGL02437:Ltn1
|
APN |
16 |
87398001 |
missense |
probably benign |
0.04 |
IGL02658:Ltn1
|
APN |
16 |
87415774 |
missense |
probably damaging |
1.00 |
IGL02890:Ltn1
|
APN |
16 |
87409297 |
splice site |
probably null |
|
IGL02899:Ltn1
|
APN |
16 |
87382659 |
missense |
probably benign |
0.34 |
IGL02902:Ltn1
|
APN |
16 |
87379805 |
missense |
possibly damaging |
0.70 |
IGL03128:Ltn1
|
APN |
16 |
87415944 |
missense |
probably benign |
0.00 |
IGL03392:Ltn1
|
APN |
16 |
87425611 |
missense |
probably damaging |
1.00 |
IGL03046:Ltn1
|
UTSW |
16 |
87405621 |
missense |
probably benign |
0.10 |
PIT4305001:Ltn1
|
UTSW |
16 |
87420323 |
missense |
probably damaging |
1.00 |
PIT4366001:Ltn1
|
UTSW |
16 |
87380840 |
nonsense |
probably null |
|
R0126:Ltn1
|
UTSW |
16 |
87425640 |
missense |
probably benign |
0.00 |
R0164:Ltn1
|
UTSW |
16 |
87405519 |
splice site |
probably benign |
|
R0165:Ltn1
|
UTSW |
16 |
87405519 |
splice site |
probably benign |
|
R0280:Ltn1
|
UTSW |
16 |
87397838 |
missense |
probably damaging |
1.00 |
R0565:Ltn1
|
UTSW |
16 |
87416010 |
missense |
probably benign |
0.01 |
R0733:Ltn1
|
UTSW |
16 |
87412507 |
missense |
probably benign |
0.01 |
R1034:Ltn1
|
UTSW |
16 |
87397137 |
splice site |
probably null |
|
R1252:Ltn1
|
UTSW |
16 |
87416030 |
missense |
probably benign |
0.00 |
R1524:Ltn1
|
UTSW |
16 |
87381556 |
missense |
probably damaging |
1.00 |
R1746:Ltn1
|
UTSW |
16 |
87411781 |
missense |
possibly damaging |
0.86 |
R1826:Ltn1
|
UTSW |
16 |
87415616 |
missense |
probably damaging |
1.00 |
R1831:Ltn1
|
UTSW |
16 |
87400146 |
missense |
possibly damaging |
0.94 |
R1839:Ltn1
|
UTSW |
16 |
87416264 |
nonsense |
probably null |
|
R1860:Ltn1
|
UTSW |
16 |
87416343 |
missense |
probably benign |
0.06 |
R1997:Ltn1
|
UTSW |
16 |
87381637 |
missense |
probably damaging |
1.00 |
R2109:Ltn1
|
UTSW |
16 |
87415642 |
missense |
probably benign |
0.03 |
R2134:Ltn1
|
UTSW |
16 |
87382713 |
missense |
probably damaging |
1.00 |
R2135:Ltn1
|
UTSW |
16 |
87382713 |
missense |
probably damaging |
1.00 |
R2193:Ltn1
|
UTSW |
16 |
87427647 |
missense |
probably damaging |
1.00 |
R2307:Ltn1
|
UTSW |
16 |
87432424 |
critical splice donor site |
probably null |
|
R2376:Ltn1
|
UTSW |
16 |
87420807 |
critical splice donor site |
probably null |
|
R3054:Ltn1
|
UTSW |
16 |
87404073 |
missense |
probably benign |
0.32 |
R3404:Ltn1
|
UTSW |
16 |
87416215 |
missense |
probably damaging |
0.98 |
R3405:Ltn1
|
UTSW |
16 |
87416215 |
missense |
probably damaging |
0.98 |
R3618:Ltn1
|
UTSW |
16 |
87420899 |
missense |
probably damaging |
1.00 |
R4065:Ltn1
|
UTSW |
16 |
87416230 |
missense |
possibly damaging |
0.84 |
R4066:Ltn1
|
UTSW |
16 |
87416230 |
missense |
possibly damaging |
0.84 |
R4067:Ltn1
|
UTSW |
16 |
87416230 |
missense |
possibly damaging |
0.84 |
R4288:Ltn1
|
UTSW |
16 |
87397988 |
missense |
possibly damaging |
0.57 |
R4436:Ltn1
|
UTSW |
16 |
87405614 |
missense |
probably benign |
0.17 |
R4535:Ltn1
|
UTSW |
16 |
87426286 |
missense |
probably damaging |
1.00 |
R4581:Ltn1
|
UTSW |
16 |
87402024 |
critical splice donor site |
probably null |
|
R4669:Ltn1
|
UTSW |
16 |
87418487 |
missense |
possibly damaging |
0.90 |
R4715:Ltn1
|
UTSW |
16 |
87418494 |
missense |
probably damaging |
0.98 |
R4830:Ltn1
|
UTSW |
16 |
87379694 |
missense |
probably damaging |
1.00 |
R4887:Ltn1
|
UTSW |
16 |
87398809 |
nonsense |
probably null |
|
R4961:Ltn1
|
UTSW |
16 |
87397791 |
missense |
probably benign |
|
R4992:Ltn1
|
UTSW |
16 |
87405587 |
missense |
possibly damaging |
0.70 |
R5073:Ltn1
|
UTSW |
16 |
87427740 |
missense |
probably damaging |
0.99 |
R5288:Ltn1
|
UTSW |
16 |
87416011 |
missense |
possibly damaging |
0.80 |
R5802:Ltn1
|
UTSW |
16 |
87415681 |
missense |
probably benign |
0.17 |
R5907:Ltn1
|
UTSW |
16 |
87381503 |
missense |
possibly damaging |
0.94 |
R6180:Ltn1
|
UTSW |
16 |
87427789 |
missense |
probably damaging |
1.00 |
R6194:Ltn1
|
UTSW |
16 |
87415810 |
missense |
probably damaging |
1.00 |
R6257:Ltn1
|
UTSW |
16 |
87411774 |
missense |
possibly damaging |
0.74 |
R6301:Ltn1
|
UTSW |
16 |
87420306 |
missense |
probably benign |
|
R6481:Ltn1
|
UTSW |
16 |
87378980 |
missense |
probably damaging |
1.00 |
R6525:Ltn1
|
UTSW |
16 |
87420186 |
missense |
probably damaging |
1.00 |
R6958:Ltn1
|
UTSW |
16 |
87397791 |
missense |
probably benign |
|
R6969:Ltn1
|
UTSW |
16 |
87415690 |
missense |
probably damaging |
1.00 |
R7002:Ltn1
|
UTSW |
16 |
87423473 |
missense |
probably benign |
|
R7038:Ltn1
|
UTSW |
16 |
87424871 |
missense |
probably damaging |
1.00 |
R7062:Ltn1
|
UTSW |
16 |
87427603 |
missense |
probably damaging |
0.98 |
R7152:Ltn1
|
UTSW |
16 |
87427641 |
missense |
probably damaging |
1.00 |
R7180:Ltn1
|
UTSW |
16 |
87418494 |
missense |
probably damaging |
0.98 |
R7247:Ltn1
|
UTSW |
16 |
87409387 |
missense |
probably benign |
0.00 |
R7454:Ltn1
|
UTSW |
16 |
87397812 |
missense |
probably benign |
0.03 |
R7471:Ltn1
|
UTSW |
16 |
87397899 |
missense |
probably benign |
|
R7511:Ltn1
|
UTSW |
16 |
87408828 |
missense |
possibly damaging |
0.63 |
R7691:Ltn1
|
UTSW |
16 |
87398686 |
missense |
probably damaging |
0.99 |
R7702:Ltn1
|
UTSW |
16 |
87426278 |
missense |
probably damaging |
1.00 |
R7761:Ltn1
|
UTSW |
16 |
87411793 |
missense |
probably benign |
|
R8002:Ltn1
|
UTSW |
16 |
87415947 |
missense |
probably benign |
0.17 |
R8101:Ltn1
|
UTSW |
16 |
87418497 |
missense |
probably damaging |
1.00 |
R8142:Ltn1
|
UTSW |
16 |
87381641 |
missense |
probably benign |
0.21 |
R8214:Ltn1
|
UTSW |
16 |
87380803 |
missense |
probably benign |
0.02 |
R8674:Ltn1
|
UTSW |
16 |
87398785 |
missense |
probably benign |
|
R8783:Ltn1
|
UTSW |
16 |
87410359 |
missense |
probably benign |
0.30 |
R8839:Ltn1
|
UTSW |
16 |
87418502 |
missense |
probably damaging |
1.00 |
R8885:Ltn1
|
UTSW |
16 |
87381545 |
missense |
probably damaging |
1.00 |
R8889:Ltn1
|
UTSW |
16 |
87432342 |
intron |
probably benign |
|
R8892:Ltn1
|
UTSW |
16 |
87432342 |
intron |
probably benign |
|
R8919:Ltn1
|
UTSW |
16 |
87381493 |
missense |
probably damaging |
0.98 |
R8970:Ltn1
|
UTSW |
16 |
87416038 |
missense |
probably benign |
|
R9113:Ltn1
|
UTSW |
16 |
87427644 |
missense |
probably damaging |
1.00 |
R9206:Ltn1
|
UTSW |
16 |
87400410 |
missense |
probably benign |
0.00 |
R9208:Ltn1
|
UTSW |
16 |
87400410 |
missense |
probably benign |
0.00 |
R9234:Ltn1
|
UTSW |
16 |
87397201 |
missense |
probably damaging |
0.98 |
R9421:Ltn1
|
UTSW |
16 |
87418487 |
missense |
possibly damaging |
0.90 |
R9558:Ltn1
|
UTSW |
16 |
87423407 |
missense |
probably benign |
0.05 |
R9654:Ltn1
|
UTSW |
16 |
87410339 |
missense |
probably benign |
0.00 |
R9738:Ltn1
|
UTSW |
16 |
87425636 |
missense |
probably damaging |
1.00 |
X0028:Ltn1
|
UTSW |
16 |
87402134 |
missense |
probably benign |
0.01 |
Z1177:Ltn1
|
UTSW |
16 |
87402037 |
missense |
probably benign |
|
|
Posted On |
2012-04-20 |