Incidental Mutation 'R3831:Hkdc1'
| ID |
274007 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hkdc1
|
| Ensembl Gene |
ENSMUSG00000020080 |
| Gene Name |
hexokinase domain containing 1 |
| Synonyms |
|
| MMRRC Submission |
040777-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.130)
|
| Stock # |
R3831 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
62218916-62258270 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 62235991 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 517
(Y517C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000020277
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020277]
|
| AlphaFold |
Q91W97 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000020277
AA Change: Y517C
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000020277
Gene: ENSMUSG00000020080
AA Change: Y517C
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hexokinase_1
|
21 |
220 |
3.3e-71 |
PFAM |
|
Pfam:Hexokinase_2
|
225 |
459 |
5.6e-79 |
PFAM |
|
Pfam:Hexokinase_1
|
469 |
665 |
9.5e-76 |
PFAM |
|
Pfam:Hexokinase_2
|
670 |
904 |
5.1e-84 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159493
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.7%
- 20x: 96.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the hexokinase protein family. The encoded protein is involved in glucose metabolism, and reduced expression may be associated with gestational diabetes mellitus. High expression of this gene may also be associated with poor prognosis in hepatocarcinoma. [provided by RefSeq, Sep 2016]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit lethality prior to genotyping. Mice heterozygous for a knock-out allele exhibit impaired glucose tolerance and female-specific increased in hepatic triglyceride levels. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930563M21Rik |
T |
C |
9: 55,880,992 (GRCm39) |
T527A |
unknown |
Het |
| Bcat1 |
T |
A |
6: 144,955,834 (GRCm39) |
D349V |
probably damaging |
Het |
| Cacna1c |
A |
G |
6: 118,581,424 (GRCm39) |
S1727P |
probably benign |
Het |
| Cacnb2 |
A |
T |
2: 14,986,236 (GRCm39) |
I338F |
probably damaging |
Het |
| Cemip2 |
T |
G |
19: 21,825,315 (GRCm39) |
S1204R |
probably damaging |
Het |
| Cibar2 |
T |
A |
8: 120,901,633 (GRCm39) |
Y24F |
probably damaging |
Het |
| Cyb5d2 |
G |
T |
11: 72,686,349 (GRCm39) |
S80R |
possibly damaging |
Het |
| Cyfip2 |
T |
C |
11: 46,152,333 (GRCm39) |
D485G |
probably benign |
Het |
| Cyp27b1 |
G |
T |
10: 126,886,929 (GRCm39) |
V382L |
probably damaging |
Het |
| Dpp9 |
A |
T |
17: 56,506,113 (GRCm39) |
F429I |
possibly damaging |
Het |
| Frmd4b |
T |
A |
6: 97,389,486 (GRCm39) |
K73* |
probably null |
Het |
| Hao1 |
A |
T |
2: 134,364,925 (GRCm39) |
V234D |
probably damaging |
Het |
| Iglv2 |
A |
T |
16: 19,079,593 (GRCm39) |
M1K |
probably null |
Het |
| Inpp5j |
T |
C |
11: 3,450,229 (GRCm39) |
D228G |
probably damaging |
Het |
| Itih5 |
A |
G |
2: 10,256,081 (GRCm39) |
D849G |
possibly damaging |
Het |
| Itpkb |
T |
C |
1: 180,161,260 (GRCm39) |
V462A |
probably benign |
Het |
| Kif26b |
GAAA |
GAA |
1: 178,744,181 (GRCm39) |
|
probably null |
Het |
| Kremen1 |
G |
GGGC |
11: 5,151,794 (GRCm39) |
|
probably benign |
Het |
| Lzic |
G |
C |
4: 149,573,185 (GRCm39) |
E112D |
probably null |
Het |
| Mageh1 |
A |
T |
X: 151,820,004 (GRCm39) |
W111R |
probably damaging |
Het |
| Mapk7 |
A |
G |
11: 61,380,680 (GRCm39) |
S641P |
possibly damaging |
Het |
| Mapt |
A |
T |
11: 104,177,961 (GRCm39) |
Q38L |
possibly damaging |
Het |
| Med12 |
C |
A |
X: 100,339,498 (GRCm39) |
P2037Q |
possibly damaging |
Het |
| Med22 |
A |
G |
2: 26,800,379 (GRCm39) |
S17P |
probably damaging |
Het |
| Melk |
C |
A |
4: 44,345,021 (GRCm39) |
Q384K |
probably benign |
Het |
| Morc2b |
C |
T |
17: 33,356,233 (GRCm39) |
S513N |
probably benign |
Het |
| Nap1l3 |
A |
G |
X: 121,305,995 (GRCm39) |
V241A |
possibly damaging |
Het |
| Or2t45 |
T |
A |
11: 58,669,571 (GRCm39) |
|
probably null |
Het |
| Or56a4 |
A |
G |
7: 104,806,589 (GRCm39) |
F100S |
probably damaging |
Het |
| Or9e1 |
T |
G |
11: 58,732,686 (GRCm39) |
F249V |
probably damaging |
Het |
| Pdgfd |
T |
C |
9: 6,359,762 (GRCm39) |
S278P |
probably damaging |
Het |
| Pgc |
C |
A |
17: 48,040,236 (GRCm39) |
F93L |
probably null |
Het |
| Phf14 |
A |
G |
6: 11,933,873 (GRCm39) |
|
probably null |
Het |
| Pja2 |
T |
C |
17: 64,616,397 (GRCm39) |
D166G |
probably benign |
Het |
| Rgs5 |
A |
G |
1: 169,504,470 (GRCm39) |
Y40C |
probably benign |
Het |
| Rsad1 |
A |
G |
11: 94,434,130 (GRCm39) |
V366A |
probably benign |
Het |
| S100a10 |
T |
C |
3: 93,471,680 (GRCm39) |
V88A |
probably damaging |
Het |
| Scarf1 |
T |
C |
11: 75,406,078 (GRCm39) |
C121R |
probably damaging |
Het |
| Scn7a |
A |
G |
2: 66,528,028 (GRCm39) |
S821P |
probably damaging |
Het |
| Sco1 |
T |
C |
11: 66,944,605 (GRCm39) |
V76A |
probably damaging |
Het |
| Selp |
T |
A |
1: 163,959,849 (GRCm39) |
C368* |
probably null |
Het |
| Sema3e |
T |
A |
5: 14,276,496 (GRCm39) |
C294S |
probably damaging |
Het |
| Slit3 |
A |
T |
11: 35,579,509 (GRCm39) |
S1229C |
probably null |
Het |
| Smarca5 |
A |
T |
8: 81,455,123 (GRCm39) |
N199K |
probably damaging |
Het |
| Sorbs2 |
A |
T |
8: 46,248,132 (GRCm39) |
D442V |
probably damaging |
Het |
| Specc1 |
T |
A |
11: 62,008,793 (GRCm39) |
I183N |
probably damaging |
Het |
| Tcerg1 |
G |
T |
18: 42,701,554 (GRCm39) |
R872L |
probably damaging |
Het |
| Tekt1 |
T |
C |
11: 72,245,645 (GRCm39) |
N170S |
probably benign |
Het |
| Thsd1 |
T |
G |
8: 22,733,132 (GRCm39) |
S60A |
possibly damaging |
Het |
| Usp24 |
T |
C |
4: 106,219,209 (GRCm39) |
|
probably null |
Het |
| Usp28 |
A |
G |
9: 48,946,938 (GRCm39) |
T505A |
probably benign |
Het |
| Zcchc17 |
T |
C |
4: 130,232,317 (GRCm39) |
D62G |
probably benign |
Het |
| Zfp445 |
T |
G |
9: 122,681,541 (GRCm39) |
E800A |
probably damaging |
Het |
| Zranb1 |
C |
T |
7: 132,584,505 (GRCm39) |
A591V |
probably damaging |
Het |
|
| Other mutations in Hkdc1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00094:Hkdc1
|
APN |
10 |
62,229,568 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01300:Hkdc1
|
APN |
10 |
62,231,040 (GRCm39) |
splice site |
probably benign |
|
|
IGL01415:Hkdc1
|
APN |
10 |
62,229,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01935:Hkdc1
|
APN |
10 |
62,236,165 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02903:Hkdc1
|
APN |
10 |
62,235,970 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03100:Hkdc1
|
APN |
10 |
62,253,608 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03154:Hkdc1
|
APN |
10 |
62,221,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0368:Hkdc1
|
UTSW |
10 |
62,247,486 (GRCm39) |
missense |
probably null |
0.04 |
|
R0549:Hkdc1
|
UTSW |
10 |
62,236,019 (GRCm39) |
missense |
probably benign |
|
|
R0667:Hkdc1
|
UTSW |
10 |
62,247,644 (GRCm39) |
splice site |
probably benign |
|
|
R0751:Hkdc1
|
UTSW |
10 |
62,234,452 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1779:Hkdc1
|
UTSW |
10 |
62,227,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1929:Hkdc1
|
UTSW |
10 |
62,253,677 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2271:Hkdc1
|
UTSW |
10 |
62,253,677 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4480:Hkdc1
|
UTSW |
10 |
62,227,151 (GRCm39) |
missense |
probably benign |
|
|
R4561:Hkdc1
|
UTSW |
10 |
62,245,618 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4576:Hkdc1
|
UTSW |
10 |
62,221,622 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R4655:Hkdc1
|
UTSW |
10 |
62,236,242 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4723:Hkdc1
|
UTSW |
10 |
62,236,133 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4810:Hkdc1
|
UTSW |
10 |
62,247,304 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5086:Hkdc1
|
UTSW |
10 |
62,231,053 (GRCm39) |
intron |
probably benign |
|
|
R5138:Hkdc1
|
UTSW |
10 |
62,234,470 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5781:Hkdc1
|
UTSW |
10 |
62,253,712 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5900:Hkdc1
|
UTSW |
10 |
62,244,445 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5982:Hkdc1
|
UTSW |
10 |
62,229,589 (GRCm39) |
missense |
probably benign |
|
|
R6418:Hkdc1
|
UTSW |
10 |
62,219,583 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6463:Hkdc1
|
UTSW |
10 |
62,229,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6612:Hkdc1
|
UTSW |
10 |
62,231,220 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R6673:Hkdc1
|
UTSW |
10 |
62,239,385 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6761:Hkdc1
|
UTSW |
10 |
62,244,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6915:Hkdc1
|
UTSW |
10 |
62,237,711 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7114:Hkdc1
|
UTSW |
10 |
62,229,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7395:Hkdc1
|
UTSW |
10 |
62,221,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8498:Hkdc1
|
UTSW |
10 |
62,221,662 (GRCm39) |
missense |
probably benign |
|
|
R8777:Hkdc1
|
UTSW |
10 |
62,234,612 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8777-TAIL:Hkdc1
|
UTSW |
10 |
62,234,612 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8894:Hkdc1
|
UTSW |
10 |
62,244,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8989:Hkdc1
|
UTSW |
10 |
62,229,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9331:Hkdc1
|
UTSW |
10 |
62,236,114 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GACACAGATACACGCACACATTTT -3'
(R):5'- TCCTCCTGTCAGAGAGTGGA -3'
Sequencing Primer
(F):5'- GCACACATTTTAACCAAGTCATG -3'
(R):5'- CTCCTGTCAGAGAGTGGAAGCAC -3'
|
| Posted On |
2015-04-02 |
Incidental Mutation