Incidental Mutation 'IGL02341:Hlcs'
| ID |
289074 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Hlcs
|
| Ensembl Gene |
ENSMUSG00000040820 |
| Gene Name |
holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) |
| Synonyms |
D16Jhu34, 410I21.SP6 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02341
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
16 |
| Chromosomal Location |
93929741-94114430 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 94031969 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 612
(I612F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153773
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099512]
[ENSMUST00000163193]
[ENSMUST00000227141]
[ENSMUST00000228910]
|
| AlphaFold |
Q920N2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099512
AA Change: I465F
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000097112
Gene: ENSMUSG00000040820
AA Change: I465F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
38 |
55 |
N/A |
INTRINSIC |
|
low complexity region
|
377 |
391 |
N/A |
INTRINSIC |
|
Pfam:BPL_LplA_LipB
|
467 |
599 |
1.9e-21 |
PFAM |
|
Pfam:BPL_C
|
665 |
714 |
3.7e-12 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000163193
AA Change: I465F
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000130981
Gene: ENSMUSG00000040820
AA Change: I465F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
38 |
55 |
N/A |
INTRINSIC |
|
low complexity region
|
377 |
391 |
N/A |
INTRINSIC |
|
Pfam:BPL_LplA_LipB
|
467 |
599 |
3.6e-30 |
PFAM |
|
Pfam:BPL_C
|
665 |
714 |
4.9e-13 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226776
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000227141
AA Change: I612F
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000228910
AA Change: I70F
PolyPhen 2
Score 0.912 (Sensitivity: 0.81; Specificity: 0.94)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an enzyme that catalyzes the binding of biotin to carboxylases and histones. The protein plays an important role in gluconeogenesis, fatty acid synthesis and branched chain amino acid catabolism. Defects in this gene are the cause of holocarboxylase synthetase deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jun 2011]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 56 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arid2 |
C |
T |
15: 96,270,066 (GRCm39) |
S1393L |
probably benign |
Het |
| Bahcc1 |
T |
A |
11: 120,163,346 (GRCm39) |
I548N |
probably damaging |
Het |
| Baiap3 |
A |
T |
17: 25,467,290 (GRCm39) |
L405Q |
possibly damaging |
Het |
| Cacna1g |
T |
G |
11: 94,352,978 (GRCm39) |
Q349P |
probably damaging |
Het |
| Ccdc30 |
T |
C |
4: 119,213,978 (GRCm39) |
T184A |
possibly damaging |
Het |
| Ccdc63 |
A |
G |
5: 122,251,261 (GRCm39) |
I383T |
probably benign |
Het |
| Ccnk |
A |
G |
12: 108,161,989 (GRCm39) |
E298G |
unknown |
Het |
| Ccnt1 |
T |
C |
15: 98,444,664 (GRCm39) |
E223G |
possibly damaging |
Het |
| Clcc1 |
T |
A |
3: 108,580,699 (GRCm39) |
L333I |
possibly damaging |
Het |
| Cyp2b10 |
G |
A |
7: 25,610,667 (GRCm39) |
R59Q |
probably benign |
Het |
| Cyp3a41b |
T |
A |
5: 145,510,461 (GRCm39) |
T138S |
probably benign |
Het |
| Dennd4a |
C |
T |
9: 64,749,843 (GRCm39) |
R145* |
probably null |
Het |
| Dnah8 |
A |
T |
17: 30,966,231 (GRCm39) |
I2474F |
probably damaging |
Het |
| Dok1 |
T |
C |
6: 83,010,035 (GRCm39) |
T25A |
probably damaging |
Het |
| Ears2 |
G |
A |
7: 121,638,987 (GRCm39) |
A479V |
probably benign |
Het |
| Erc1 |
T |
A |
6: 119,571,934 (GRCm39) |
I981F |
possibly damaging |
Het |
| Gm8730 |
A |
G |
8: 103,591,775 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9962 |
C |
T |
7: 57,037,042 (GRCm39) |
|
probably benign |
Het |
| Has3 |
A |
T |
8: 107,600,637 (GRCm39) |
Y33F |
probably damaging |
Het |
| Hk1 |
A |
G |
10: 62,120,159 (GRCm39) |
S607P |
possibly damaging |
Het |
| Llgl2 |
T |
A |
11: 115,741,946 (GRCm39) |
S663T |
possibly damaging |
Het |
| Lrriq1 |
T |
C |
10: 103,060,802 (GRCm39) |
H100R |
probably benign |
Het |
| Lypd8l |
T |
C |
11: 58,503,656 (GRCm39) |
S17G |
possibly damaging |
Het |
| Magi2 |
T |
A |
5: 20,671,201 (GRCm39) |
I678N |
probably damaging |
Het |
| Megf11 |
G |
A |
9: 64,451,902 (GRCm39) |
G109S |
probably damaging |
Het |
| Morc2b |
A |
T |
17: 33,356,281 (GRCm39) |
I497K |
probably damaging |
Het |
| Mybpc2 |
A |
C |
7: 44,164,354 (GRCm39) |
S404A |
probably benign |
Het |
| Mylip |
A |
G |
13: 45,544,752 (GRCm39) |
R59G |
probably damaging |
Het |
| Mylk3 |
A |
T |
8: 86,078,601 (GRCm39) |
I501N |
probably damaging |
Het |
| Myo19 |
A |
G |
11: 84,778,871 (GRCm39) |
|
probably benign |
Het |
| Nat2 |
A |
G |
8: 67,954,370 (GRCm39) |
Y160C |
possibly damaging |
Het |
| Nf1 |
C |
T |
11: 79,455,752 (GRCm39) |
A2554V |
probably benign |
Het |
| Niban3 |
A |
T |
8: 72,056,443 (GRCm39) |
N381I |
possibly damaging |
Het |
| Ninl |
A |
T |
2: 150,786,525 (GRCm39) |
C153* |
probably null |
Het |
| Nlrp5 |
C |
T |
7: 23,103,577 (GRCm39) |
R15C |
probably benign |
Het |
| Nphp4 |
A |
T |
4: 152,639,926 (GRCm39) |
|
probably benign |
Het |
| Obscn |
C |
A |
11: 59,026,651 (GRCm39) |
R184L |
probably benign |
Het |
| Or6c202 |
T |
A |
10: 128,996,302 (GRCm39) |
I184F |
probably benign |
Het |
| Or6c6c |
A |
T |
10: 129,541,358 (GRCm39) |
T204S |
probably damaging |
Het |
| Or6c8 |
A |
T |
10: 128,915,330 (GRCm39) |
C167* |
probably null |
Het |
| Phip |
A |
T |
9: 82,814,936 (GRCm39) |
V262D |
probably damaging |
Het |
| Ptprg |
T |
A |
14: 12,154,360 (GRCm38) |
S694T |
probably benign |
Het |
| Reck |
T |
A |
4: 43,925,160 (GRCm39) |
D466E |
probably damaging |
Het |
| Rimbp2 |
G |
T |
5: 128,878,025 (GRCm39) |
Y213* |
probably null |
Het |
| Scn2a |
C |
T |
2: 65,518,721 (GRCm39) |
T365M |
probably damaging |
Het |
| Scpep1 |
T |
A |
11: 88,835,314 (GRCm39) |
T120S |
probably benign |
Het |
| Sp7 |
T |
A |
15: 102,267,657 (GRCm39) |
T50S |
possibly damaging |
Het |
| Tbc1d1 |
A |
G |
5: 64,432,750 (GRCm39) |
R304G |
probably damaging |
Het |
| Tiam1 |
A |
G |
16: 89,695,257 (GRCm39) |
S67P |
probably damaging |
Het |
| Tjp1 |
G |
A |
7: 64,962,382 (GRCm39) |
T1185I |
probably damaging |
Het |
| Tspan2 |
T |
A |
3: 102,672,529 (GRCm39) |
I178N |
probably damaging |
Het |
| Tusc2 |
T |
A |
9: 107,442,109 (GRCm39) |
*103R |
probably null |
Het |
| Uggt1 |
A |
T |
1: 36,203,600 (GRCm39) |
*47R |
probably null |
Het |
| Unc13c |
T |
A |
9: 73,840,492 (GRCm39) |
I120F |
possibly damaging |
Het |
| Vcpip1 |
T |
A |
1: 9,795,175 (GRCm39) |
K1065N |
possibly damaging |
Het |
| Zfp532 |
C |
A |
18: 65,757,849 (GRCm39) |
P594Q |
probably damaging |
Het |
|
| Other mutations in Hlcs |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01078:Hlcs
|
APN |
16 |
93,934,019 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02026:Hlcs
|
APN |
16 |
93,935,564 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03075:Hlcs
|
APN |
16 |
93,939,706 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4515001:Hlcs
|
UTSW |
16 |
94,068,275 (GRCm39) |
missense |
probably benign |
0.45 |
|
R0372:Hlcs
|
UTSW |
16 |
93,939,766 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0664:Hlcs
|
UTSW |
16 |
94,032,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0731:Hlcs
|
UTSW |
16 |
93,932,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1465:Hlcs
|
UTSW |
16 |
94,069,151 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1465:Hlcs
|
UTSW |
16 |
94,069,151 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1761:Hlcs
|
UTSW |
16 |
94,068,866 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2013:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2014:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2015:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2204:Hlcs
|
UTSW |
16 |
94,032,011 (GRCm39) |
missense |
probably benign |
0.30 |
|
R2371:Hlcs
|
UTSW |
16 |
94,068,926 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3816:Hlcs
|
UTSW |
16 |
93,933,947 (GRCm39) |
missense |
probably benign |
0.11 |
|
R3822:Hlcs
|
UTSW |
16 |
94,068,840 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4422:Hlcs
|
UTSW |
16 |
93,939,819 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R4657:Hlcs
|
UTSW |
16 |
94,063,557 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4783:Hlcs
|
UTSW |
16 |
94,069,398 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5347:Hlcs
|
UTSW |
16 |
94,068,383 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5808:Hlcs
|
UTSW |
16 |
94,063,491 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5940:Hlcs
|
UTSW |
16 |
93,935,571 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6341:Hlcs
|
UTSW |
16 |
94,032,022 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6943:Hlcs
|
UTSW |
16 |
93,942,261 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7053:Hlcs
|
UTSW |
16 |
94,068,874 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7157:Hlcs
|
UTSW |
16 |
94,069,023 (GRCm39) |
nonsense |
probably null |
|
|
R7166:Hlcs
|
UTSW |
16 |
94,063,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7313:Hlcs
|
UTSW |
16 |
94,068,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7427:Hlcs
|
UTSW |
16 |
94,068,758 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7428:Hlcs
|
UTSW |
16 |
94,068,758 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7547:Hlcs
|
UTSW |
16 |
94,032,031 (GRCm39) |
nonsense |
probably null |
|
|
R7548:Hlcs
|
UTSW |
16 |
93,933,876 (GRCm39) |
nonsense |
probably null |
|
|
R8172:Hlcs
|
UTSW |
16 |
94,068,485 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8241:Hlcs
|
UTSW |
16 |
94,068,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8500:Hlcs
|
UTSW |
16 |
94,063,617 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8940:Hlcs
|
UTSW |
16 |
94,032,085 (GRCm39) |
missense |
probably benign |
|
|
R9274:Hlcs
|
UTSW |
16 |
94,088,785 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9360:Hlcs
|
UTSW |
16 |
93,932,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9361:Hlcs
|
UTSW |
16 |
93,939,799 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9564:Hlcs
|
UTSW |
16 |
93,935,580 (GRCm39) |
missense |
probably benign |
0.01 |
|
X0065:Hlcs
|
UTSW |
16 |
93,934,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Hlcs
|
UTSW |
16 |
94,063,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation