Incidental Mutation 'IGL02227:Hk1'
| ID |
285635 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Hk1
|
| Ensembl Gene |
ENSMUSG00000037012 |
| Gene Name |
hexokinase 1 |
| Synonyms |
mHk1-s, Hk1-s, Hk-1 |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.430)
|
| Stock # |
IGL02227
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
62104634-62215687 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 62116919 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118601
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072357]
[ENSMUST00000099691]
[ENSMUST00000116238]
[ENSMUST00000130422]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000072357
|
| SMART Domains |
Protein: ENSMUSP00000072195
Gene: ENSMUSG00000037012
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hexokinase_1
|
25 |
224 |
1.2e-70 |
PFAM |
|
Pfam:Hexokinase_2
|
229 |
486 |
8e-79 |
PFAM |
|
Pfam:Hexokinase_1
|
496 |
695 |
7e-76 |
PFAM |
|
Pfam:Hexokinase_2
|
700 |
934 |
4.2e-85 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099691
|
| SMART Domains |
Protein: ENSMUSP00000097282
Gene: ENSMUSG00000037012
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hexokinase_1
|
16 |
221 |
1.9e-86 |
PFAM |
|
Pfam:Hexokinase_2
|
223 |
462 |
1e-102 |
PFAM |
|
Pfam:Hexokinase_1
|
464 |
669 |
1.1e-90 |
PFAM |
|
Pfam:Hexokinase_2
|
671 |
910 |
2.2e-109 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000116238
|
| SMART Domains |
Protein: ENSMUSP00000111946
Gene: ENSMUSG00000037012
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hexokinase_1
|
21 |
225 |
1.3e-85 |
PFAM |
|
Pfam:Hexokinase_2
|
227 |
357 |
3.6e-56 |
PFAM |
|
Pfam:Hexokinase_2
|
362 |
489 |
9.3e-41 |
PFAM |
|
Pfam:Hexokinase_1
|
491 |
696 |
2e-90 |
PFAM |
|
Pfam:Hexokinase_2
|
698 |
937 |
3.8e-109 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000130422
|
| SMART Domains |
Protein: ENSMUSP00000118601
Gene: ENSMUSG00000037012
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hexokinase_1
|
16 |
220 |
1.4e-85 |
PFAM |
|
Pfam:Hexokinase_2
|
222 |
461 |
1e-102 |
PFAM |
|
Pfam:Hexokinase_1
|
463 |
668 |
1.1e-90 |
PFAM |
|
Pfam:Hexokinase_2
|
670 |
909 |
2.2e-109 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161160
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue-specific. [provided by RefSeq, Apr 2016]
PHENOTYPE: Homozygous mutant mice exhibit hemolytic anemia with extensive tissue iron deposition and reticulocytosis and female infertility. [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 |
|---|
| Acsl1 |
A |
G |
8: 46,987,402 (GRCm39) |
E662G |
probably benign |
Het |
| Acss3 |
A |
G |
10: 106,881,196 (GRCm39) |
S262P |
probably benign |
Het |
| Agap1 |
T |
C |
1: 89,591,497 (GRCm39) |
V263A |
probably damaging |
Het |
| Ap3b2 |
A |
G |
7: 81,123,152 (GRCm39) |
L454P |
probably damaging |
Het |
| Arrdc1 |
A |
T |
2: 24,816,164 (GRCm39) |
F280I |
possibly damaging |
Het |
| Atp8b1 |
G |
T |
18: 64,695,261 (GRCm39) |
H485N |
probably benign |
Het |
| Atrip |
A |
G |
9: 108,890,732 (GRCm39) |
S91P |
possibly damaging |
Het |
| Bcorl1 |
T |
C |
X: 47,458,237 (GRCm39) |
V590A |
probably benign |
Het |
| Brf1 |
C |
A |
12: 112,925,394 (GRCm39) |
R590S |
probably damaging |
Het |
| Ccdc18 |
A |
T |
5: 108,296,788 (GRCm39) |
D197V |
possibly damaging |
Het |
| Ccr6 |
T |
C |
17: 8,475,284 (GRCm39) |
V163A |
probably damaging |
Het |
| Cct6b |
T |
C |
11: 82,632,217 (GRCm39) |
E257G |
probably damaging |
Het |
| Cdc42bpa |
A |
G |
1: 179,921,989 (GRCm39) |
D564G |
possibly damaging |
Het |
| Cdh2 |
C |
T |
18: 16,762,643 (GRCm39) |
V434I |
probably benign |
Het |
| Cfap410 |
A |
G |
10: 77,818,784 (GRCm39) |
N152D |
possibly damaging |
Het |
| Cltc |
C |
T |
11: 86,588,166 (GRCm39) |
V1610M |
possibly damaging |
Het |
| Cnot4 |
A |
G |
6: 35,028,198 (GRCm39) |
F473L |
probably benign |
Het |
| Dock3 |
T |
C |
9: 106,939,254 (GRCm39) |
K165E |
probably damaging |
Het |
| Duox2 |
A |
T |
2: 122,115,634 (GRCm39) |
|
probably benign |
Het |
| Epha7 |
A |
G |
4: 28,821,587 (GRCm39) |
S251G |
possibly damaging |
Het |
| Epn1 |
T |
A |
7: 5,098,035 (GRCm39) |
V282E |
probably benign |
Het |
| Fat1 |
T |
C |
8: 45,476,696 (GRCm39) |
L1914P |
probably damaging |
Het |
| Fbln2 |
T |
C |
6: 91,233,349 (GRCm39) |
I611T |
possibly damaging |
Het |
| Fgd6 |
G |
T |
10: 93,969,946 (GRCm39) |
M1198I |
probably damaging |
Het |
| Frmpd4 |
T |
A |
X: 166,275,931 (GRCm39) |
I379F |
probably damaging |
Het |
| Grk4 |
T |
A |
5: 34,852,126 (GRCm39) |
D123E |
probably benign |
Het |
| Hc |
T |
G |
2: 34,899,923 (GRCm39) |
|
probably benign |
Het |
| Hephl1 |
T |
C |
9: 14,981,089 (GRCm39) |
Y781C |
probably damaging |
Het |
| Hfe |
T |
C |
13: 23,890,926 (GRCm39) |
E71G |
probably benign |
Het |
| Ifnk |
G |
A |
4: 35,152,642 (GRCm39) |
|
probably benign |
Het |
| Kcnv1 |
C |
A |
15: 44,977,670 (GRCm39) |
G123C |
probably damaging |
Het |
| Klhl38 |
A |
T |
15: 58,186,633 (GRCm39) |
I32N |
possibly damaging |
Het |
| Lpl |
T |
C |
8: 69,348,452 (GRCm39) |
V227A |
probably damaging |
Het |
| Lurap1l |
A |
T |
4: 80,872,094 (GRCm39) |
S196C |
probably damaging |
Het |
| Mta1 |
T |
C |
12: 113,084,528 (GRCm39) |
L91P |
possibly damaging |
Het |
| Nelfe |
C |
A |
17: 35,073,330 (GRCm39) |
D288E |
probably benign |
Het |
| Or5p1 |
T |
A |
7: 107,916,408 (GRCm39) |
C102* |
probably null |
Het |
| Otof |
T |
C |
5: 30,528,128 (GRCm39) |
E1905G |
probably damaging |
Het |
| Pck2 |
T |
C |
14: 55,781,323 (GRCm39) |
I148T |
probably benign |
Het |
| Plcl2 |
G |
T |
17: 50,913,425 (GRCm39) |
V145F |
probably damaging |
Het |
| Plec |
A |
G |
15: 76,056,474 (GRCm39) |
S4510P |
probably damaging |
Het |
| Plxna2 |
A |
G |
1: 194,434,397 (GRCm39) |
E641G |
probably damaging |
Het |
| Poglut3 |
T |
C |
9: 53,299,779 (GRCm39) |
L96S |
probably damaging |
Het |
| Ppp1r12a |
C |
T |
10: 108,105,185 (GRCm39) |
T434M |
probably damaging |
Het |
| Ppp6r3 |
A |
T |
19: 3,568,245 (GRCm39) |
N184K |
possibly damaging |
Het |
| Prkar1a |
G |
A |
11: 109,551,001 (GRCm39) |
|
probably benign |
Het |
| Psmb1 |
A |
T |
17: 15,710,546 (GRCm39) |
M1K |
probably null |
Het |
| Pwwp2a |
T |
C |
11: 43,596,448 (GRCm39) |
S538P |
possibly damaging |
Het |
| Rbm25 |
C |
T |
12: 83,719,527 (GRCm39) |
R516W |
probably damaging |
Het |
| Rnf103 |
A |
G |
6: 71,487,172 (GRCm39) |
D601G |
probably benign |
Het |
| Senp3 |
A |
G |
11: 69,565,356 (GRCm39) |
V467A |
possibly damaging |
Het |
| Slc8a3 |
T |
G |
12: 81,362,457 (GRCm39) |
T121P |
probably damaging |
Het |
| Slco1a8 |
A |
T |
6: 141,939,401 (GRCm39) |
C197* |
probably null |
Het |
| Srrt |
G |
A |
5: 137,294,536 (GRCm39) |
T790M |
probably damaging |
Het |
| Ssc5d |
T |
C |
7: 4,936,453 (GRCm39) |
|
probably null |
Het |
| Tas2r129 |
G |
A |
6: 132,928,357 (GRCm39) |
W98* |
probably null |
Het |
| Thoc5 |
A |
C |
11: 4,876,217 (GRCm39) |
M609L |
probably benign |
Het |
| Tnip1 |
G |
A |
11: 54,827,297 (GRCm39) |
T155M |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,618,672 (GRCm39) |
V14458A |
probably benign |
Het |
| Unc5cl |
A |
G |
17: 48,766,809 (GRCm39) |
E61G |
probably benign |
Het |
| Usp32 |
T |
C |
11: 84,877,307 (GRCm39) |
K151E |
probably damaging |
Het |
| Vmn2r121 |
T |
C |
X: 123,042,378 (GRCm39) |
M260V |
probably benign |
Het |
| Vwa7 |
G |
T |
17: 35,239,060 (GRCm39) |
R345L |
probably damaging |
Het |
| Zfp366 |
G |
T |
13: 99,370,696 (GRCm39) |
R472L |
possibly damaging |
Het |
| Zfp811 |
A |
T |
17: 33,017,616 (GRCm39) |
Y141* |
probably null |
Het |
| Zpbp |
C |
T |
11: 11,365,248 (GRCm39) |
E200K |
probably benign |
Het |
|
| Other mutations in Hk1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00493:Hk1
|
APN |
10 |
62,122,127 (GRCm39) |
nonsense |
probably null |
|
|
IGL01108:Hk1
|
APN |
10 |
62,132,487 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01810:Hk1
|
APN |
10 |
62,188,884 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL01950:Hk1
|
APN |
10 |
62,151,173 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02165:Hk1
|
APN |
10 |
62,117,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02257:Hk1
|
APN |
10 |
62,107,422 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL02341:Hk1
|
APN |
10 |
62,120,159 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
IGL02553:Hk1
|
APN |
10 |
62,131,552 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
IGL02623:Hk1
|
APN |
10 |
62,128,138 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL02700:Hk1
|
APN |
10 |
62,120,590 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02863:Hk1
|
APN |
10 |
62,131,534 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL03002:Hk1
|
APN |
10 |
62,107,578 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB009:Hk1
|
UTSW |
10 |
62,151,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB019:Hk1
|
UTSW |
10 |
62,151,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0029:Hk1
|
UTSW |
10 |
62,151,173 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0436:Hk1
|
UTSW |
10 |
62,135,054 (GRCm39) |
splice site |
probably benign |
|
|
R0853:Hk1
|
UTSW |
10 |
62,107,495 (GRCm39) |
nonsense |
probably null |
|
|
R1422:Hk1
|
UTSW |
10 |
62,131,873 (GRCm39) |
missense |
probably null |
0.98 |
|
R1531:Hk1
|
UTSW |
10 |
62,120,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1760:Hk1
|
UTSW |
10 |
62,117,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2064:Hk1
|
UTSW |
10 |
62,122,315 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3236:Hk1
|
UTSW |
10 |
62,131,798 (GRCm39) |
splice site |
probably null |
|
|
R3788:Hk1
|
UTSW |
10 |
62,111,467 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R3977:Hk1
|
UTSW |
10 |
62,126,098 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4373:Hk1
|
UTSW |
10 |
62,151,319 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4374:Hk1
|
UTSW |
10 |
62,151,319 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4377:Hk1
|
UTSW |
10 |
62,151,319 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4435:Hk1
|
UTSW |
10 |
62,111,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4609:Hk1
|
UTSW |
10 |
62,194,194 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R4648:Hk1
|
UTSW |
10 |
62,140,558 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4864:Hk1
|
UTSW |
10 |
62,178,318 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4934:Hk1
|
UTSW |
10 |
62,194,165 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R5110:Hk1
|
UTSW |
10 |
62,122,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5352:Hk1
|
UTSW |
10 |
62,140,549 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5569:Hk1
|
UTSW |
10 |
62,122,220 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5609:Hk1
|
UTSW |
10 |
62,178,330 (GRCm39) |
missense |
probably benign |
0.30 |
|
R5647:Hk1
|
UTSW |
10 |
62,111,523 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5750:Hk1
|
UTSW |
10 |
62,110,245 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R5770:Hk1
|
UTSW |
10 |
62,122,228 (GRCm39) |
missense |
probably benign |
|
|
R5832:Hk1
|
UTSW |
10 |
62,128,144 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5905:Hk1
|
UTSW |
10 |
62,188,837 (GRCm39) |
missense |
probably null |
0.82 |
|
R5933:Hk1
|
UTSW |
10 |
62,105,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6028:Hk1
|
UTSW |
10 |
62,188,837 (GRCm39) |
missense |
probably null |
0.82 |
|
R6196:Hk1
|
UTSW |
10 |
62,135,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6314:Hk1
|
UTSW |
10 |
62,128,223 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6372:Hk1
|
UTSW |
10 |
62,127,757 (GRCm39) |
missense |
probably benign |
|
|
R6801:Hk1
|
UTSW |
10 |
62,116,910 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6838:Hk1
|
UTSW |
10 |
62,107,437 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7045:Hk1
|
UTSW |
10 |
62,122,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7420:Hk1
|
UTSW |
10 |
62,105,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7491:Hk1
|
UTSW |
10 |
62,131,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7527:Hk1
|
UTSW |
10 |
62,140,561 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7561:Hk1
|
UTSW |
10 |
62,116,807 (GRCm39) |
splice site |
probably null |
|
|
R7932:Hk1
|
UTSW |
10 |
62,151,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8031:Hk1
|
UTSW |
10 |
62,132,478 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8128:Hk1
|
UTSW |
10 |
62,117,622 (GRCm39) |
missense |
probably benign |
|
|
R8204:Hk1
|
UTSW |
10 |
62,132,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8294:Hk1
|
UTSW |
10 |
62,131,624 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8685:Hk1
|
UTSW |
10 |
62,132,453 (GRCm39) |
splice site |
probably benign |
|
|
R8865:Hk1
|
UTSW |
10 |
62,151,294 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9015:Hk1
|
UTSW |
10 |
62,128,118 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9022:Hk1
|
UTSW |
10 |
62,105,768 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9063:Hk1
|
UTSW |
10 |
62,122,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9404:Hk1
|
UTSW |
10 |
62,131,859 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
X0018:Hk1
|
UTSW |
10 |
62,111,485 (GRCm39) |
missense |
probably benign |
0.02 |
|
X0063:Hk1
|
UTSW |
10 |
62,111,483 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation