Varaico: Literature-Extracted Genetic Variants

Gene:ZNF513
Variant:p.P145S

ZNF513

98 papers

RefSeq Summary

The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcrip...

Pfam Domains

zf-C2H2aa 178–200UCSCZinc finger, C2H2 type
zf-C2H2aa 178–200UCSCZinc finger, C2H2 type
zf-C2H2aa 206–228UCSCZinc finger, C2H2 type
zf-C2H2aa 206–228UCSCZinc finger, C2H2 type
zf-C2H2aa 388–410UCSCZinc finger, C2H2 type
zf-C2H2aa 416–438UCSCZinc finger, C2H2 type

Gene Aliases

HGNC Name

zinc finger protein 513

HGNC Alias Symbols

FLJ32203; RP58; Zfp513

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_144631.6
p.P145S
c.433C>T
Surrounding Variants
1 paper
NM_144631.6
p.P142del1
c.424_425delGGG
1 paper
NM_144631.6
p.G141_P142del1
c.423_425delGGC
1 paper
NM_144631.6
p.G141insFs
c.423dupG
1 paper
NM_144631.6
p.P142fs
c.424_425fs
1 paper
NM_144631.6
p.C123*
c.369T>A
1 paper
NM_144631.6
p.Q121fs
c.361_362fs
1 paper
NM_144631.6
p.Q121insFs
c.361_362ins26
1 paper
NM_144631.6
p.Q170*
c.508C>T
1 paper
NM_144631.6
p.P118_A119insFs
c.354_355ins37
1 paper
NM_144631.6
p.P116_P118del0
c.346_354del9
1 paper
NM_144631.6
p.R106_A111del6
c.316_332del18
3 papers
NM_144631.6
p.C183C
c.549C>T
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