SRRM4
Serine/arginine repetitive matrix protein 4
Also known as: KIAA1853, nSR100, SRRM4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A7MD48
- Gene
- SRRM4
- Ensembl
- ENSG00000139767
- Chromosome
- 12
- Canonical length
- 611 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
SRRM4 promotes alternative splicing and inclusion of neural-specific exons in target mRNAs (Calarco et al., 2009 [PubMed 19737518]).[supplied by OMIM, Oct 2009]
Canonical amino-acid sequenceUniProt
611 residues, UniProt reviewed canonical sequence.
>A7MD48|SRRM4
1 MASVQQGEKQ LFEKFWRGTF KAVATPRPES IIVASITARK PLPRTEPQNN PVVPAQDGPS
61 EKLGQHLATE PLGTNSWERD KTCRELGATR GHSASHDKDL TPPPSSRGKK KKKKSTRKKR
121 RRSSSYSPSP VKKKKKKSSK KHKRRRSFSK KRRHSSSSPK SKRRDEKRHK KQSRSRPRKS
181 HRHRHHRCPS RSQSSESRPS SCESRHRGRS PEEGQKSRRR HSRRCSKTLC KDSPEAQSSR
241 PPSQPLQMLG YLSARGVITG SGSAADLFTK TASPLTTSRG RSQEYDSGND TSSPPSTQTS
301 SARSRGQEKG SPSGGLSKSR ELNSGNTSDS GNSFTTSSPQ NKGAMLENLS PTSRGRESRG
361 FQSPCLECAE VKKSSLVPST ARSSPMKGCS RSSSYASTRS SSHSSRSPNP RASPRYTQSR
421 STSSEKRSYS RSPSYSSKSG KRSPPSRSSR SRRSPSYSRY SPSRERDPKY SEKDSQQRER
481 ERARRRRRSY SPMRKRRRDS PSHLEARRIT SARKRPIPYY RPSPSSSGSL SSTSSWYSSS
541 SSRSASRSYS RSRSRSRSRR RSRTRTSSSS SSRSPSPGSR SRSRSRSRSR SRSRSQSRSY
601 SSADSYSSTR RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SRRM4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.71
- Highest tissue expression
- 44 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 44 nTPM
- retina: 27 nTPM
- cerebral cortex: 14 nTPM
- hypothalamus: 4.9 nTPM
- hippocampal formation: 4.3 nTPM
- amygdala: 4.1 nTPM
Single-cell type
- cone photoreceptor cells: 1,052 nCPM
- retinal amacrine cells: 957 nCPM
- rod photoreceptor cells: 775 nCPM
- retinal bipolar cells: 700 nCPM
- brain excitatory neurons: 330 nCPM
- retinal ganglion cells: 232 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 66 nTPM
- cerebellum: 60 nTPM
- basal ganglia: 44 nTPM
- white matter: 40 nTPM
- thalamus: 25 nTPM
- hippocampal formation: 23 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.41
- gnomAD pLI
- 0.46
- gnomAD missense Z
- 1.39
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- mRNA processing
- nervous system development
- neuron maturation
- regulation of alternative mRNA splicing, via spliceosome
- regulation of RNA splicing
- RNA splicing
- sensory perception of sound
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SRRM4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SRRM4 as an antibody target. Whether an autoantibody or antibody against SRRM4 could matter depends on whether native SRRM4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SRRM4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SRRM4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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