Incidental Mutation 'R0559:H1f8'
| ID |
45790 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
H1f8
|
| Ensembl Gene |
ENSMUSG00000042279 |
| Gene Name |
H1.8 linker histone |
| Synonyms |
H1foo, H1-8, H1oo |
| MMRRC Submission |
038751-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0559 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
115921899-115927197 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 115924760 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 89
(Y89H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000125701
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037831]
[ENSMUST00000161617]
[ENSMUST00000161969]
[ENSMUST00000162084]
[ENSMUST00000205177]
|
| AlphaFold |
Q8VIK3 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000037831
AA Change: Y89H
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000036951
Gene: ENSMUSG00000042279
AA Change: Y89H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
H15
|
43 |
110 |
8.84e-11 |
SMART |
|
low complexity region
|
123 |
146 |
N/A |
INTRINSIC |
|
low complexity region
|
182 |
197 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000161617
AA Change: Y89H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000125701
Gene: ENSMUSG00000042279
AA Change: Y89H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
H15
|
43 |
110 |
8.84e-11 |
SMART |
|
low complexity region
|
123 |
146 |
N/A |
INTRINSIC |
|
low complexity region
|
182 |
197 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000161969
AA Change: Y89H
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000123797
Gene: ENSMUSG00000042279
AA Change: Y89H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
H15
|
43 |
110 |
8.84e-11 |
SMART |
|
low complexity region
|
123 |
146 |
N/A |
INTRINSIC |
|
low complexity region
|
182 |
197 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000162084
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205177
|
| SMART Domains |
Protein: ENSMUSP00000144958
Gene: ENSMUSG00000042279
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
26 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1020 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.5%
|
| Validation Efficiency |
97% (34/35) |
| MGI Phenotype |
FUNCTION: Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. The protein encoded is a replication-independent histone that is a member of the histone H1 family. This gene contains introns, unlike most histone genes and the encoded protein is expressed only in oocytes. [provided by RefSeq, Oct 2015]
PHENOTYPE: Mice homozygous for a targeted mutation exhibit no detectable abnormalities. Oocytes develop normally and no defects in fertility or litter sizes are observed. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1a |
A |
T |
5: 8,748,535 (GRCm39) |
I289F |
probably benign |
Het |
| Adam15 |
G |
A |
3: 89,251,085 (GRCm39) |
A540V |
probably damaging |
Het |
| Adat1 |
T |
C |
8: 112,709,062 (GRCm39) |
T254A |
probably damaging |
Het |
| Agtpbp1 |
A |
G |
13: 59,644,814 (GRCm39) |
V684A |
probably benign |
Het |
| Ahi1 |
A |
G |
10: 20,876,618 (GRCm39) |
|
probably benign |
Het |
| Arl5b |
T |
C |
2: 15,077,998 (GRCm39) |
Y108H |
probably damaging |
Het |
| Cep85l |
A |
G |
10: 53,224,597 (GRCm39) |
F331L |
probably benign |
Het |
| Ctnna2 |
T |
C |
6: 76,892,833 (GRCm39) |
K785E |
probably damaging |
Het |
| Dgkd |
T |
A |
1: 87,842,826 (GRCm39) |
I118N |
probably damaging |
Het |
| Dicer1 |
G |
A |
12: 104,672,560 (GRCm39) |
R896W |
probably damaging |
Het |
| Eif1ad19 |
T |
A |
12: 87,740,223 (GRCm39) |
H112L |
probably benign |
Het |
| Fbxl19 |
G |
T |
7: 127,349,390 (GRCm39) |
W160L |
possibly damaging |
Het |
| Ipo5 |
T |
C |
14: 121,176,053 (GRCm39) |
V626A |
probably damaging |
Het |
| Isx |
A |
G |
8: 75,600,369 (GRCm39) |
K34R |
probably benign |
Het |
| Myh6 |
T |
C |
14: 55,196,011 (GRCm39) |
E596G |
probably benign |
Het |
| Olfml2a |
T |
C |
2: 38,849,832 (GRCm39) |
I516T |
probably damaging |
Het |
| Or14j5 |
C |
T |
17: 38,161,746 (GRCm39) |
R88* |
probably null |
Het |
| Or5w12 |
T |
G |
2: 87,502,244 (GRCm39) |
T156P |
possibly damaging |
Het |
| Or8b37 |
G |
T |
9: 37,959,123 (GRCm39) |
V202L |
probably benign |
Het |
| Parp9 |
T |
C |
16: 35,768,362 (GRCm39) |
F181L |
probably benign |
Het |
| Pkdcc |
G |
A |
17: 83,523,454 (GRCm39) |
G187D |
probably benign |
Het |
| Plekhh3 |
C |
T |
11: 101,055,592 (GRCm39) |
E483K |
possibly damaging |
Het |
| Ptx4 |
C |
T |
17: 25,342,082 (GRCm39) |
Q186* |
probably null |
Het |
| Qsox2 |
T |
A |
2: 26,104,169 (GRCm39) |
H287L |
probably benign |
Het |
| Rev3l |
G |
A |
10: 39,700,483 (GRCm39) |
G1660D |
probably damaging |
Het |
| Scamp1 |
G |
T |
13: 94,344,690 (GRCm39) |
A217E |
possibly damaging |
Het |
| Slc5a9 |
T |
C |
4: 111,742,779 (GRCm39) |
I438V |
probably benign |
Het |
| Sort1 |
T |
C |
3: 108,263,895 (GRCm39) |
F818S |
probably damaging |
Het |
| Srl |
G |
A |
16: 4,314,842 (GRCm39) |
P267S |
probably benign |
Het |
| Tbc1d1 |
T |
C |
5: 64,331,136 (GRCm39) |
I105T |
probably damaging |
Het |
| Tifab |
A |
G |
13: 56,324,060 (GRCm39) |
Y128H |
probably benign |
Het |
| Trp53bp1 |
A |
T |
2: 121,058,282 (GRCm39) |
S907T |
probably damaging |
Het |
| Ubr1 |
G |
A |
2: 120,778,364 (GRCm39) |
R225* |
probably null |
Het |
| Upk3bl |
A |
G |
5: 136,086,330 (GRCm39) |
T89A |
probably benign |
Het |
| Vars1 |
T |
A |
17: 35,233,034 (GRCm39) |
C916* |
probably null |
Het |
| Ywhaz |
T |
C |
15: 36,791,208 (GRCm39) |
E5G |
possibly damaging |
Het |
| Zfp91 |
T |
C |
19: 12,747,419 (GRCm39) |
D568G |
probably damaging |
Het |
| Zgpat |
T |
C |
2: 181,021,985 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in H1f8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00334:H1f8
|
APN |
6 |
115,924,588 (GRCm39) |
unclassified |
probably benign |
|
|
IGL00864:H1f8
|
APN |
6 |
115,925,587 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0050:H1f8
|
UTSW |
6 |
115,924,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0050:H1f8
|
UTSW |
6 |
115,924,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0056:H1f8
|
UTSW |
6 |
115,923,934 (GRCm39) |
unclassified |
probably benign |
|
|
R0081:H1f8
|
UTSW |
6 |
115,926,942 (GRCm39) |
missense |
probably benign |
|
|
R1302:H1f8
|
UTSW |
6 |
115,924,610 (GRCm39) |
nonsense |
probably null |
|
|
R1476:H1f8
|
UTSW |
6 |
115,924,701 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1824:H1f8
|
UTSW |
6 |
115,925,719 (GRCm39) |
missense |
probably null |
0.97 |
|
R3778:H1f8
|
UTSW |
6 |
115,926,708 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3928:H1f8
|
UTSW |
6 |
115,925,757 (GRCm39) |
missense |
probably benign |
0.12 |
|
R3929:H1f8
|
UTSW |
6 |
115,925,757 (GRCm39) |
missense |
probably benign |
0.12 |
|
R6316:H1f8
|
UTSW |
6 |
115,925,876 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8356:H1f8
|
UTSW |
6 |
115,925,745 (GRCm39) |
missense |
probably benign |
|
|
R8456:H1f8
|
UTSW |
6 |
115,925,745 (GRCm39) |
missense |
probably benign |
|
|
R8869:H1f8
|
UTSW |
6 |
115,926,911 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9628:H1f8
|
UTSW |
6 |
115,924,700 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCAAGTTGCCGCAGAATCCAAG -3'
(R):5'- ACATGAGGCTAGTAGAGACTGCCC -3'
Sequencing Primer
(F):5'- TCCAAGCAGGCCAAAGG -3'
(R):5'- TAGTAGAGACTGCCCCAGTG -3'
|
| Posted On |
2013-06-11 |
Incidental Mutation