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Query results
Results for
NRG1
Expand for information on NRG1
NRG1
Description
neuregulin 1
Aliases
ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF-IT2, SMDF, NRG1
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001159995.3; NM_001159996.2; NM_001159999.3; NM_001160001.3; NM_001160002.2; NM_001160004.3; NM_001160005.1; NM_001160007.2; NM_001160008.2; NM_001322197.2; NM_001322201.2; NM_001322202.2; NM_001322205.2; NM_001322206.2; NM_001322207.2; NM_004495.4; NM_013956.5; NM_013957.5; NM_013958.3; NM_013959.3; NM_013960.5; NM_013962.2; NM_013964.5; XM_005273486.3; XM_005273487.3; XM_006716335.3; XM_011544512.2; XM_017013365.2; XM_017013366.2; XM_017013367.1; XM_017013368.2; XM_017013369.2; XM_017013370.1; XM_017013371.2; XM_017013372.2; XM_024447143.1
Protein Identifiers
RefSeq (protein)
NP_001153467.1; NP_001153468.1; NP_001153471.1; NP_001153473.1; NP_001153474.1; NP_001153476.1; NP_001153477.1; NP_001153479.1; NP_001153480.1; NP_001309126.1; NP_001309130.1; NP_001309131.1; NP_001309134.1; NP_001309135.1; NP_001309136.1; NP_004486.2; NP_039250.2; NP_039251.2; NP_039252.2; NP_039253.1; NP_039254.1; NP_039256.2; NP_039258.1; XP_005273543.1; XP_005273544.1; XP_006716398.1; XP_011542814.1; XP_016868854.1; XP_016868855.1; XP_016868856.1; XP_016868857.1; XP_016868858.1; XP_016868859.1; XP_016868860.1; XP_016868861.1; XP_024302911.1
Uniprot ID
A6MW56; E3SFM9; Q02297; F6RJN6; B7Z1D7; E3SFM9; A6MW55; Q02297; E3SFM9; Q02297; B0FYA7; B0FYA9; B0FWZ3; Q02297; B0FYA8; Q6PK61; Q02297; B7Z1E3; E3SFM9; A5YAK6; A5YAK8; E3SFM9; Q02297; A6MW54; Q02297; Q02297; Q7RTW5; Q6PK61; Q02297; Q7RTW3; Q6PK61; Q02297; A0A024QY88; Q02297; Q02297; Q02297; Q6PK61; Q02297; Q02297; Q6PK61
Ensembl protein ID
ENSP00000499008.1; ENSP00000439276.2; ENSP00000499045.1; ENSP00000429582.1; ENSP00000498583.1; ENSP00000498833.1; ENSP00000430120.1; ENSP00000498646.1; ENSP00000498590.1; ENSP00000498946.1; -; ENSP00000287842.4; ENSP00000349275.6; ENSP00000498811.1; ENSP00000433289.1; ENSP00000428828.1; ENSP00000434640.1; ENSP00000384620.2; ENSP00000429067.1
Protein Architecture
SMART
Disease Mapping
Druggability
- Fewer loss of function mutations
- Fewer damaging SNVs/indels
- Fewer structural variants