Incidental Mutation 'R7553:Dlk1'
| ID |
584569 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dlk1
|
| Ensembl Gene |
ENSMUSG00000040856 |
| Gene Name |
delta like non-canonical Notch ligand 1 |
| Synonyms |
SCP1, pref-1, pG2, Peg9, ZOG, DlkI, FA1 |
| MMRRC Submission |
045622-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.657)
|
| Stock # |
R7553 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
12 |
| Chromosomal Location |
109418749-109429262 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 109420889 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 15
(V15I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133530
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056110]
[ENSMUST00000109841]
[ENSMUST00000109842]
[ENSMUST00000109843]
[ENSMUST00000109844]
[ENSMUST00000109846]
[ENSMUST00000124293]
[ENSMUST00000173539]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000056110
|
| SMART Domains |
Protein: ENSMUSP00000063104
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
EGF
|
213 |
247 |
4.06e-6 |
SMART |
|
transmembrane domain
|
307 |
329 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109841
|
| SMART Domains |
Protein: ENSMUSP00000105467
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
transmembrane domain
|
214 |
236 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109842
|
| SMART Domains |
Protein: ENSMUSP00000105468
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
transmembrane domain
|
234 |
256 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109843
|
| SMART Domains |
Protein: ENSMUSP00000105469
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
transmembrane domain
|
212 |
234 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109844
|
| SMART Domains |
Protein: ENSMUSP00000105470
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
EGF
|
213 |
247 |
4.06e-6 |
SMART |
|
transmembrane domain
|
307 |
329 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109846
|
| SMART Domains |
Protein: ENSMUSP00000105472
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
transmembrane domain
|
256 |
278 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000124293
AA Change: V15I
|
| SMART Domains |
Protein: ENSMUSP00000133530
Gene: ENSMUSG00000040856
AA Change: V15I
| Domain | Start | End | E-Value | Type |
|---|
|
EGF
|
24 |
54 |
1.43e-1 |
SMART |
|
EGF
|
55 |
85 |
1.26e-2 |
SMART |
|
EGF_CA
|
87 |
124 |
1.77e-6 |
SMART |
|
EGF
|
129 |
167 |
8.71e-6 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173539
|
| SMART Domains |
Protein: ENSMUSP00000133430
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
|
EGF
|
25 |
55 |
1.43e-1 |
SMART |
|
EGF
|
56 |
86 |
1.26e-2 |
SMART |
|
EGF_CA
|
88 |
125 |
1.77e-6 |
SMART |
|
EGF
|
130 |
168 |
8.71e-6 |
SMART |
|
EGF
|
175 |
208 |
1.41e-5 |
SMART |
|
transmembrane domain
|
232 |
254 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173812
|
| SMART Domains |
Protein: ENSMUSP00000134308
Gene: ENSMUSG00000040856
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1eqga2
|
2 |
15 |
4e-3 |
SMART |
|
transmembrane domain
|
44 |
66 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
98% (62/63) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transmembrane protein that contains multiple epidermal growth factor repeats that functions as a regulator of cell growth. The encoded protein is involved in the differentiation of several cell types including adipocytes. This gene is located in a region of chromosome 14 frequently showing unparental disomy, and is imprinted and expressed from the paternal allele. A single nucleotide variant in this gene is associated with child and adolescent obesity and shows polar overdominance, where heterozygotes carrying an active paternal allele express the phenotype, while mutant homozygotes are normal. [provided by RefSeq, Nov 2015]
PHENOTYPE: Homozygote null mice have reduced fetal growth and 50% lethality 2 days after birth. Survivors are small but have enlarged fat pad masses. Homozygotes for another null allele have abnormal B cell development. Paternally-inherited null alleles phenocopy homozygotes due to maternal imprinting. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 66 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc6 |
A |
G |
7: 45,648,545 (GRCm39) |
L649P |
probably damaging |
Het |
| Acad10 |
T |
C |
5: 121,777,318 (GRCm39) |
Y371C |
probably damaging |
Het |
| Avp |
A |
G |
2: 130,423,098 (GRCm39) |
V71A |
probably damaging |
Het |
| Bhmt |
C |
T |
13: 93,756,589 (GRCm39) |
|
probably null |
Het |
| Capn15 |
T |
C |
17: 26,179,738 (GRCm39) |
E874G |
probably damaging |
Het |
| Capn5 |
A |
G |
7: 97,773,231 (GRCm39) |
F591S |
probably damaging |
Het |
| Ccne2 |
A |
T |
4: 11,201,348 (GRCm39) |
Q292L |
probably benign |
Het |
| Cd96 |
T |
G |
16: 45,872,384 (GRCm39) |
T406P |
probably damaging |
Het |
| Csnk1e |
G |
A |
15: 79,310,566 (GRCm39) |
A153V |
probably damaging |
Het |
| Dmbt1 |
A |
G |
7: 130,706,597 (GRCm39) |
N1372S |
unknown |
Het |
| Dntt |
A |
T |
19: 41,017,926 (GRCm39) |
R17W |
probably damaging |
Het |
| Erich3 |
G |
T |
3: 154,439,137 (GRCm39) |
A260S |
probably benign |
Het |
| Foxp2 |
C |
T |
6: 15,437,881 (GRCm39) |
S669L |
unknown |
Het |
| Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
| Grid2 |
A |
G |
6: 64,053,925 (GRCm39) |
K375E |
possibly damaging |
Het |
| Grin2b |
C |
T |
6: 135,749,394 (GRCm39) |
G603S |
possibly damaging |
Het |
| Hexb |
C |
T |
13: 97,334,681 (GRCm39) |
R30Q |
probably benign |
Het |
| Homer3 |
A |
T |
8: 70,742,774 (GRCm39) |
T162S |
probably benign |
Het |
| L3mbtl1 |
A |
G |
2: 162,790,151 (GRCm39) |
E15G |
probably benign |
Het |
| Manea |
A |
T |
4: 26,327,986 (GRCm39) |
F352I |
probably damaging |
Het |
| Mcf2l |
T |
A |
8: 13,047,268 (GRCm39) |
M210K |
probably benign |
Het |
| Morc3 |
T |
C |
16: 93,667,824 (GRCm39) |
L734P |
probably damaging |
Het |
| Mybpc2 |
A |
G |
7: 44,155,571 (GRCm39) |
V894A |
possibly damaging |
Het |
| Myh4 |
T |
A |
11: 67,147,221 (GRCm39) |
M1622K |
probably damaging |
Het |
| Myrf |
A |
G |
19: 10,206,240 (GRCm39) |
F59L |
probably benign |
Het |
| Ndst3 |
G |
T |
3: 123,350,709 (GRCm39) |
|
probably null |
Het |
| Nln |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
13: 104,186,924 (GRCm39) |
|
probably null |
Het |
| Nos3 |
A |
T |
5: 24,586,715 (GRCm39) |
D986V |
possibly damaging |
Het |
| Nrp1 |
G |
A |
8: 129,158,468 (GRCm39) |
A252T |
probably damaging |
Het |
| Nup205 |
G |
T |
6: 35,178,934 (GRCm39) |
R668L |
probably damaging |
Het |
| Or51aa2 |
T |
C |
7: 103,188,363 (GRCm39) |
Y26C |
probably damaging |
Het |
| Or5af2 |
T |
A |
11: 58,707,886 (GRCm39) |
D17E |
probably benign |
Het |
| Or5p56 |
G |
A |
7: 107,589,682 (GRCm39) |
V37I |
probably benign |
Het |
| Pcdhga1 |
T |
A |
18: 37,882,735 (GRCm39) |
|
probably null |
Het |
| Pck1 |
A |
G |
2: 172,998,860 (GRCm39) |
I373V |
probably benign |
Het |
| Pde8b |
T |
C |
13: 95,223,258 (GRCm39) |
N227S |
probably benign |
Het |
| Pianp |
T |
G |
6: 124,976,214 (GRCm39) |
S8A |
unknown |
Het |
| Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
| Pla2r1 |
A |
T |
2: 60,353,243 (GRCm39) |
N239K |
possibly damaging |
Het |
| Pls1 |
T |
A |
9: 95,669,140 (GRCm39) |
N27I |
probably damaging |
Het |
| Prep |
T |
C |
10: 45,034,620 (GRCm39) |
*711Q |
probably null |
Het |
| Prkag3 |
A |
G |
1: 74,783,894 (GRCm39) |
F330L |
probably damaging |
Het |
| Prss56 |
A |
G |
1: 87,111,261 (GRCm39) |
D16G |
probably benign |
Het |
| Rad17 |
A |
T |
13: 100,769,794 (GRCm39) |
F255Y |
probably damaging |
Het |
| Rap1gap2 |
T |
C |
11: 74,326,548 (GRCm39) |
E173G |
probably damaging |
Het |
| Retreg3 |
C |
T |
11: 100,997,216 (GRCm39) |
R88H |
possibly damaging |
Het |
| Rhag |
G |
A |
17: 41,139,286 (GRCm39) |
G74R |
probably damaging |
Het |
| Rybp |
A |
G |
6: 100,209,220 (GRCm39) |
S201P |
possibly damaging |
Het |
| S100a10 |
G |
A |
3: 93,471,602 (GRCm39) |
C62Y |
probably benign |
Het |
| Scgb2b3 |
T |
A |
7: 31,059,673 (GRCm39) |
S34C |
possibly damaging |
Het |
| Serpind1 |
A |
G |
16: 17,154,539 (GRCm39) |
D122G |
probably benign |
Het |
| Setdb1 |
A |
G |
3: 95,254,076 (GRCm39) |
L242P |
probably damaging |
Het |
| Slc14a2 |
T |
A |
18: 78,198,803 (GRCm39) |
I776F |
probably damaging |
Het |
| Slc9a1 |
A |
G |
4: 133,139,580 (GRCm39) |
E266G |
probably damaging |
Het |
| Stard9 |
A |
T |
2: 120,524,289 (GRCm39) |
|
probably null |
Het |
| Stpg2 |
A |
G |
3: 138,924,098 (GRCm39) |
Y167C |
probably damaging |
Het |
| Tex264 |
T |
C |
9: 106,536,335 (GRCm39) |
E274G |
probably damaging |
Het |
| Tigd2 |
G |
A |
6: 59,188,564 (GRCm39) |
S477N |
probably benign |
Het |
| Urb1 |
A |
G |
16: 90,589,752 (GRCm39) |
L343P |
probably damaging |
Het |
| Vars2 |
A |
T |
17: 35,975,680 (GRCm39) |
C246S |
possibly damaging |
Het |
| Vil1 |
G |
A |
1: 74,465,891 (GRCm39) |
|
probably null |
Het |
| Vmn2r61 |
C |
G |
7: 41,916,205 (GRCm39) |
L273V |
not run |
Het |
| Vmn2r-ps158 |
T |
G |
7: 42,697,447 (GRCm39) |
C835G |
probably damaging |
Het |
| Zfp37 |
C |
A |
4: 62,110,236 (GRCm39) |
G317V |
probably damaging |
Het |
| Zfp760 |
A |
G |
17: 21,941,872 (GRCm39) |
K349R |
possibly damaging |
Het |
| Zyx |
A |
T |
6: 42,327,408 (GRCm39) |
E69V |
probably null |
Het |
|
| Other mutations in Dlk1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0041:Dlk1
|
UTSW |
12 |
109,421,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0379:Dlk1
|
UTSW |
12 |
109,420,985 (GRCm39) |
unclassified |
probably benign |
|
|
R1250:Dlk1
|
UTSW |
12 |
109,425,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1363:Dlk1
|
UTSW |
12 |
109,421,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1757:Dlk1
|
UTSW |
12 |
109,425,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1763:Dlk1
|
UTSW |
12 |
109,424,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1772:Dlk1
|
UTSW |
12 |
109,425,685 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2189:Dlk1
|
UTSW |
12 |
109,420,975 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2334:Dlk1
|
UTSW |
12 |
109,419,614 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3751:Dlk1
|
UTSW |
12 |
109,426,239 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5256:Dlk1
|
UTSW |
12 |
109,425,697 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5268:Dlk1
|
UTSW |
12 |
109,425,764 (GRCm39) |
missense |
probably benign |
0.34 |
|
R5356:Dlk1
|
UTSW |
12 |
109,421,447 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5669:Dlk1
|
UTSW |
12 |
109,425,964 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5748:Dlk1
|
UTSW |
12 |
109,425,898 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5992:Dlk1
|
UTSW |
12 |
109,421,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6076:Dlk1
|
UTSW |
12 |
109,425,895 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6539:Dlk1
|
UTSW |
12 |
109,426,245 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6638:Dlk1
|
UTSW |
12 |
109,426,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7480:Dlk1
|
UTSW |
12 |
109,421,540 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7602:Dlk1
|
UTSW |
12 |
109,421,551 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8531:Dlk1
|
UTSW |
12 |
109,424,066 (GRCm39) |
missense |
probably null |
0.06 |
|
R9120:Dlk1
|
UTSW |
12 |
109,424,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9554:Dlk1
|
UTSW |
12 |
109,420,889 (GRCm39) |
missense |
unknown |
|
|
X0020:Dlk1
|
UTSW |
12 |
109,425,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0053:Dlk1
|
UTSW |
12 |
109,426,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAAGGTGTCTGCTTTGCACTTG -3'
(R):5'- TTTTATTTGGCAAAGCACCCC -3'
Sequencing Primer
(F):5'- CTGCTTTGCACTTGGAGAATCAG -3'
(R):5'- CCCTCCCTTTCAGCCTGG -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation