Gene
hnrnph1l
- ID
- ZDB-GENE-030131-275
- Name
- heterogeneous nuclear ribonucleoprotein H1, like
- Symbol
- hnrnph1l Nomenclature History
- Previous Names
-
- fb19a06
- wu:fb19a06
- zgc:55399
- zgc:85960 (1)
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to have RNA binding activity. Human ortholog(s) of this gene implicated in Sjogren's syndrome and syndromic X-linked intellectual disability. Orthologous to several human genes including HNRNPH1 (heterogeneous nuclear ribonucleoprotein H1) and HNRNPH2 (heterogeneous nuclear ribonucleoprotein H2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:55399 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Domain | IPR000504 | RNA recognition motif domain |
| Domain | IPR012996 | Zinc finger, CHHC-type |
| Family | IPR050666 | Epithelial Splicing Regulatory |
| Homologous_superfamily | IPR012677 | Nucleotide-binding alpha-beta plait domain superfamily |
| Homologous_superfamily | IPR035979 | RNA-binding domain superfamily |
Domain Details Per Protein
| Protein | Length | Epithelial Splicing Regulatory | Nucleotide-binding alpha-beta plait domain superfamily | RNA-binding domain superfamily | RNA recognition motif domain | Zinc finger, CHHC-type |
|---|---|---|---|---|---|---|
|
UniProtKB:F1QFJ8
|
407 | |||||
|
UniProtKB:A0A8M9PCG7
|
210 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
hnrnph1l-201
(1)
|
Ensembl | 1,830 nt | ||
| mRNA |
hnrnph1l-203
(1)
|
Ensembl | 1,255 nt | ||
| ncRNA |
hnrnph1l-002
(1)
|
Ensembl | 771 nt |
Interactions and Pathways
No data available
Plasmids
No data available