Incidental Mutation 'R9741:H1f10'
ID 731830
Institutional Source Beutler Lab
Gene Symbol H1f10
Ensembl Gene ENSMUSG00000044927
Gene Name H1.10 linker histone
Synonyms H1X, H1-10, H1fx, LOC243529
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9741 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 87957403-87958464 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 87958200 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 47 (Y47H)
Ref Sequence ENSEMBL: ENSMUSP00000060761 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056403]
AlphaFold Q80ZM5
Predicted Effect probably damaging
Transcript: ENSMUST00000056403
AA Change: Y47H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000060761
Gene: ENSMUSG00000044927
AA Change: Y47H

DomainStartEndE-ValueType
H15 40 107 1.74e-9 SMART
low complexity region 124 153 N/A INTRINSIC
low complexity region 159 185 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.5%
  • 20x: 99.0%
Validation Efficiency
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. This gene encodes a replication-independent histone that is a member of the histone H1 family. [provided by RefSeq, Nov 2015]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd6 T A 4: 32,860,339 (GRCm39) K35* probably null Het
Apoc3 G T 9: 46,145,998 (GRCm39) T5K unknown Het
Arhgap20 T A 9: 51,760,730 (GRCm39) Y860* probably null Het
Arhgef11 T C 3: 87,595,156 (GRCm39) S123P probably benign Het
Armh4 A G 14: 50,008,081 (GRCm39) I464T probably benign Het
Axdnd1 T A 1: 156,169,385 (GRCm39) Y827F probably benign Het
Bbs5 A G 2: 69,484,695 (GRCm39) T122A probably benign Het
Btbd6 T A 12: 112,940,923 (GRCm39) D173E probably benign Het
Cblb T C 16: 51,932,490 (GRCm39) I149T probably damaging Het
Cyp2ab1 G A 16: 20,132,953 (GRCm39) R214C probably damaging Het
Dbn1 C T 13: 55,624,114 (GRCm39) S372N possibly damaging Het
Dlg1 T A 16: 31,676,735 (GRCm39) Y776* probably null Het
Dock9 A T 14: 121,877,516 (GRCm39) I409N probably damaging Het
Ect2 A T 3: 27,156,607 (GRCm39) N815K probably benign Het
Fbxw11 G T 11: 32,685,358 (GRCm39) V398L probably damaging Het
Gcsam T C 16: 45,436,319 (GRCm39) F34S possibly damaging Het
Ghsr G A 3: 27,428,898 (GRCm39) V308I possibly damaging Het
Gm40460 ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG 7: 141,794,450 (GRCm39) probably benign Het
Hspg2 T C 4: 137,239,962 (GRCm39) F510S probably damaging Het
Htr1a T C 13: 105,581,861 (GRCm39) V367A possibly damaging Het
Iars1 T G 13: 49,844,978 (GRCm39) F163C probably damaging Het
Igfn1 T C 1: 135,895,383 (GRCm39) T1728A probably benign Het
Ighv7-3 C T 12: 114,116,995 (GRCm39) V56I probably benign Het
Lrp1b A T 2: 41,002,300 (GRCm39) I2133N Het
Lrrc37 T C 11: 103,504,255 (GRCm39) E2571G possibly damaging Het
Or2d2 A G 7: 106,728,366 (GRCm39) V78A possibly damaging Het
Or52z1 G T 7: 103,436,941 (GRCm39) P181H probably benign Het
Pkd1l1 T C 11: 8,897,224 (GRCm39) T562A Het
Ppp1r10 G A 17: 36,237,331 (GRCm39) R167Q possibly damaging Het
Ppp1r13l C T 7: 19,103,725 (GRCm39) R69W probably damaging Het
Proser2 G A 2: 6,105,580 (GRCm39) A328V probably benign Het
Rhou A G 8: 124,380,914 (GRCm39) Y77C possibly damaging Het
Rprml T A 11: 103,540,857 (GRCm39) L84Q probably damaging Het
Ryr3 C T 2: 112,477,271 (GRCm39) C4515Y probably benign Het
Slc9a3 T A 13: 74,306,994 (GRCm39) I373N possibly damaging Het
Snx21 C T 2: 164,634,231 (GRCm39) A339V probably benign Het
Srpk1 G A 17: 28,818,652 (GRCm39) P395S probably benign Het
Syt14 A T 1: 192,666,449 (GRCm39) S152T unknown Het
Urb2 G T 8: 124,755,751 (GRCm39) R486L probably damaging Het
Utrn T A 10: 12,702,564 (GRCm39) M7L probably benign Het
Vmn2r59 T A 7: 41,708,209 (GRCm39) D66V probably damaging Het
Znrf2 T C 6: 54,855,370 (GRCm39) I197T probably damaging Het
Other mutations in H1f10
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1370:H1f10 UTSW 6 87,958,133 (GRCm39) missense probably damaging 1.00
R1535:H1f10 UTSW 6 87,958,130 (GRCm39) missense probably damaging 1.00
R2312:H1f10 UTSW 6 87,958,130 (GRCm39) missense probably damaging 1.00
R6823:H1f10 UTSW 6 87,958,284 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- CAGTAGCGTATCGTTCTGCAC -3'
(R):5'- GTTGTTCTCAACGTGGTCCG -3'

Sequencing Primer
(F):5'- GTATCGTTCTGCACCAGCG -3'
(R):5'- CCGCCACGGGGAAATAAAAGC -3'
Posted On 2022-11-14