Incidental Mutation 'IGL00832:Ltk'
| ID |
11872 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ltk
|
| Ensembl Gene |
ENSMUSG00000027297 |
| Gene Name |
leukocyte tyrosine kinase |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00832
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
119581807-119590912 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to T
at 119586086 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000138201
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028758]
[ENSMUST00000028759]
[ENSMUST00000082130]
[ENSMUST00000140224]
[ENSMUST00000182203]
|
| AlphaFold |
P08923 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028758
|
| SMART Domains |
Protein: ENSMUSP00000028758
Gene: ENSMUSG00000027296
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
40 |
64 |
N/A |
INTRINSIC |
|
low complexity region
|
116 |
149 |
N/A |
INTRINSIC |
|
Pfam:IPK
|
243 |
454 |
1.3e-43 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028759
|
| SMART Domains |
Protein: ENSMUSP00000028759
Gene: ENSMUSG00000027297
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
Pfam:Gly_rich
|
111 |
381 |
2.4e-21 |
PFAM |
|
transmembrane domain
|
423 |
445 |
N/A |
INTRINSIC |
|
TyrKc
|
506 |
773 |
2.61e-127 |
SMART |
|
low complexity region
|
824 |
841 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000082130
|
| SMART Domains |
Protein: ENSMUSP00000080774
Gene: ENSMUSG00000027297
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
Pfam:Gly_rich
|
109 |
294 |
6.1e-16 |
PFAM |
|
transmembrane domain
|
362 |
384 |
N/A |
INTRINSIC |
|
TyrKc
|
445 |
712 |
2.61e-127 |
SMART |
|
low complexity region
|
763 |
780 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127470
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134295
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140224
|
| SMART Domains |
Protein: ENSMUSP00000123020
Gene: ENSMUSG00000027297
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
|
transmembrane domain
|
111 |
133 |
N/A |
INTRINSIC |
|
TyrKc
|
194 |
461 |
1.2e-129 |
SMART |
|
low complexity region
|
512 |
529 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000182203
|
| SMART Domains |
Protein: ENSMUSP00000138201
Gene: ENSMUSG00000027297
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
|
transmembrane domain
|
111 |
133 |
N/A |
INTRINSIC |
|
TyrKc
|
194 |
461 |
2.61e-127 |
SMART |
|
low complexity region
|
512 |
529 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: The protein encoded by this gene is a member of the ros/insulin receptor family of tyrosine kinases. Tyrosine-specific phosphorylation of proteins is a key to the control of diverse pathways leading to cell growth and differentiation. Four alternatively spliced transcript variants encoding different isoforms have been described for this gene. These transcripts are expressed in a tissue-specific manner in lymphocytes, brain and neuroblastoma cells, and the encoded isoforms exhibit different subcellular localization. The lymphocyte and brain specific variants initiate translation at non-AUG (CUG) start codons. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700030K09Rik |
A |
G |
8: 73,209,193 (GRCm39) |
Y407C |
probably damaging |
Het |
| Amtn |
T |
G |
5: 88,532,908 (GRCm39) |
H174Q |
possibly damaging |
Het |
| Cdon |
T |
A |
9: 35,389,412 (GRCm39) |
I839N |
probably damaging |
Het |
| Ces2g |
A |
G |
8: 105,694,471 (GRCm39) |
|
probably benign |
Het |
| Cgas |
A |
T |
9: 78,341,599 (GRCm39) |
C393S |
probably damaging |
Het |
| Colq |
G |
T |
14: 31,250,303 (GRCm39) |
C367* |
probably null |
Het |
| Dop1b |
T |
C |
16: 93,560,289 (GRCm39) |
V745A |
probably benign |
Het |
| E2f8 |
C |
T |
7: 48,517,951 (GRCm39) |
G657D |
probably damaging |
Het |
| Gpcpd1 |
G |
A |
2: 132,388,770 (GRCm39) |
T334M |
probably damaging |
Het |
| Gria2 |
T |
C |
3: 80,614,558 (GRCm39) |
D494G |
probably damaging |
Het |
| Gtf3c1 |
T |
C |
7: 125,253,632 (GRCm39) |
|
probably benign |
Het |
| Gtf3c2 |
G |
A |
5: 31,330,349 (GRCm39) |
|
probably benign |
Het |
| Hnf4g |
G |
A |
3: 3,706,336 (GRCm39) |
C77Y |
probably damaging |
Het |
| Ido1 |
G |
A |
8: 25,074,575 (GRCm39) |
T265I |
possibly damaging |
Het |
| Ifih1 |
A |
G |
2: 62,475,814 (GRCm39) |
|
probably benign |
Het |
| Itga6 |
A |
G |
2: 71,668,606 (GRCm39) |
|
probably null |
Het |
| Kctd10 |
C |
A |
5: 114,506,997 (GRCm39) |
|
probably null |
Het |
| Luc7l3 |
T |
C |
11: 94,194,768 (GRCm39) |
D84G |
probably benign |
Het |
| Mc3r |
A |
T |
2: 172,090,948 (GRCm39) |
I57F |
possibly damaging |
Het |
| Mmp1b |
T |
A |
9: 7,387,023 (GRCm39) |
Q63L |
possibly damaging |
Het |
| Ncr1 |
C |
A |
7: 4,344,287 (GRCm39) |
T225N |
possibly damaging |
Het |
| Nf2 |
T |
C |
11: 4,741,123 (GRCm39) |
K364E |
probably benign |
Het |
| Ppl |
A |
T |
16: 4,906,839 (GRCm39) |
L1152H |
probably damaging |
Het |
| Primpol |
A |
G |
8: 47,034,632 (GRCm39) |
V432A |
probably damaging |
Het |
| Rbl2 |
A |
G |
8: 91,812,073 (GRCm39) |
D214G |
probably damaging |
Het |
| Rxfp2 |
A |
T |
5: 149,989,893 (GRCm39) |
M425L |
probably benign |
Het |
| Slc5a3 |
T |
C |
16: 91,874,519 (GRCm39) |
M192T |
probably damaging |
Het |
| Tbx18 |
T |
A |
9: 87,587,714 (GRCm39) |
S468C |
probably damaging |
Het |
| Tex10 |
T |
C |
4: 48,468,864 (GRCm39) |
T104A |
probably benign |
Het |
| Unc13b |
T |
G |
4: 43,258,921 (GRCm39) |
V4153G |
probably damaging |
Het |
| Vmn1r188 |
A |
G |
13: 22,272,351 (GRCm39) |
T102A |
probably damaging |
Het |
|
| Other mutations in Ltk |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01287:Ltk
|
APN |
2 |
119,586,186 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01339:Ltk
|
APN |
2 |
119,583,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01614:Ltk
|
APN |
2 |
119,583,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01827:Ltk
|
APN |
2 |
119,583,219 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02229:Ltk
|
APN |
2 |
119,589,054 (GRCm39) |
missense |
probably benign |
0.01 |
|
Envy
|
UTSW |
2 |
119,583,516 (GRCm39) |
splice site |
probably null |
|
|
R2105:Ltk
|
UTSW |
2 |
119,582,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3763:Ltk
|
UTSW |
2 |
119,582,318 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4119:Ltk
|
UTSW |
2 |
119,588,429 (GRCm39) |
intron |
probably benign |
|
|
R4120:Ltk
|
UTSW |
2 |
119,588,429 (GRCm39) |
intron |
probably benign |
|
|
R4257:Ltk
|
UTSW |
2 |
119,583,485 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R4460:Ltk
|
UTSW |
2 |
119,586,094 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4888:Ltk
|
UTSW |
2 |
119,583,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5121:Ltk
|
UTSW |
2 |
119,583,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5696:Ltk
|
UTSW |
2 |
119,590,080 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5784:Ltk
|
UTSW |
2 |
119,584,840 (GRCm39) |
nonsense |
probably null |
|
|
R6301:Ltk
|
UTSW |
2 |
119,582,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6470:Ltk
|
UTSW |
2 |
119,583,516 (GRCm39) |
splice site |
probably null |
|
|
R6860:Ltk
|
UTSW |
2 |
119,585,075 (GRCm39) |
nonsense |
probably null |
|
|
R7083:Ltk
|
UTSW |
2 |
119,582,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8537:Ltk
|
UTSW |
2 |
119,588,588 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8861:Ltk
|
UTSW |
2 |
119,590,094 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9266:Ltk
|
UTSW |
2 |
119,585,121 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9299:Ltk
|
UTSW |
2 |
119,584,721 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R9319:Ltk
|
UTSW |
2 |
119,590,096 (GRCm39) |
missense |
probably benign |
|
|
R9662:Ltk
|
UTSW |
2 |
119,582,330 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2012-12-06 |
Incidental Mutation