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Table 4 Mouse histone variants with poor annotation status in the UniProtKB database

From: MS_HistoneDB, a manually curated resource for proteomic analysis of human and mouse histones

Names

Accession number

Protein status

Method of detection

References

This study (number of identified peptides)

Other MS-based studies

Not MS-based studies

H1.0 (H1°)

P10922

Transcript

Yes (5)

Yes

RT-PCR; WB

[128]

TS H1.7 (H1T2, HANP1)

Q8CJI4

Transcript

Yes (6)

 

NB; WB

[55]

OO H1.8 (H1oo)

Q8VIK3

Transcript

  

WB

[59, 60, 129]

H1.11

F7DCP6

Inferred

    

Macro-H2A.3

Q9D3V6

Transcript

    

H2A.L.1 gene: H2al1b

A0A087WP11

Inferred

Yes (1)

   

H2A.L.1 gene: H2al1j

A2BFR3

Inferred

    

H2A.L.1 gene: H2al1 k

J3QP08

Inferred

    

H2A.L.1 gene: H2al1 m

Q9DAD9

Transcript

    

H2A.L.1 gene: H2al1n

Q497L1

Transcript

Yes (2)

   

H2A.L.1 gene: H2al1o

L7MU04

Inferred

    

H2A.L.2 (H2A.B1,H2A.Lap3)

Q9CQ70

Transcript

Yes (3)

Yes

RT-PCR; NB; WB

[38, 39, 125]

Y-chr H2A.L.3

A9Z055

Transcript

  

RT-PCR

[98]

H2A.P (H2A.L3,H2A.Lap4,)

Q9CR04

Inferred

  

RT-PCR

[38, 39]

H2A.B.2

S4R1M3

Inferred

  

RT-PCR; WB

[40, 99]

H2A.B.3 gene: H2afb3

S4R1G7

Inferred

  

RT-PCR; WB

[40, 99]

H2A.B.3 (H2A.Lap1) gene: GM14920

S4R1E0

Inferred

  

RT-PCR; WB

[39, 40, 99]

H2B.L.2

Q9DAB5

Transcript

Yes (4)

Yes

RT-PCR; WB

[38]

H3.3 gene: GM6421

EDL18362.1

Predicted

Yes (1)

Yes

RT-PCR

[103]

H3.3 gene: GM10257

XP_003084990.1

Record removed

Yes (1)

 

RT-PCR

[103]

CENPA-cenH3

O35216

Transcript

 

Yes

qPCR; WB

[126, 127]

H3.5

P02301

Inferred

  

RT-PCR

 

TS H3.4 (H3t)

NP_001304932.1

Predicted

 

Yes

RT-PCR

[103]

  1. The “protein status” was retrieved from UniProtKB: “Evidence at transcript level” (noted “Transcript”) or “Inferred from homology” (noted “Inferred”, update of July 2016). Three variants are predicted in NCBI database and are absent in UniProtKB. Information about the detection of some variants at the mRNA level (e.g. by RT-PCR) or at the protein level (e.g. by WB or MS) was further completed with publications and compared to the MS identification results obtained in the present study
  2. NB northern blot, WB western blot, MS mass spectrometry