Busch Lab

ZMP

NRG3

Ensembl ID:
ENSDARG00000089766
Description:
neuregulin 3 [Source:HGNC Symbol;Acc:7999]
Human Orthologue:
NRG3
Human Description:
neuregulin 3 [Source:HGNC Symbol;Acc:7999]
Mouse Orthologue:
Nrg3
Mouse Description:
neuregulin 3 Gene [Source:MGI Symbol;Acc:MGI:1097165]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa22123 Nonsense Available for shipment Available now
sa35314 Nonsense Mutation detected in F1 DNA Not yet available
sa42055 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22123
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126744 Nonsense 125 764 1 9
Genomic Location (Zv9):
Chromosome 12 (position 31172427)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 29509364
GRCz11 12 29624266
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCATCTACCACTTCCACCACTCCCTCAGCAGCTCCAGGTTCTGCAACT[C/T]GAGCAGCTGAGGGCACAGGTACAGTGCAAAGAACTCGAATTGGGCAGTCC
Long Flanking Sequence:
GTATTGCATGTATCTGTAGCTGTGGAAGAGTGTTAAATGAATATTAATGAGATGCCCAGTTTTGGCTCCCTCCCCAGCCCCCTCCACTGCTTGCACTACTTCCTGGCTGGGCCCTGAACCCCAGAAGCATGAGTGAGAGAACAGCACTAGGGGCCACCATGGAGACCATGACCCTGGAGGAGCCCGGGGGTGAACAAGCCTCTCCCCGGGCCCCAGGGCCCCTCCGCTGTGGCCCCTGTGCAGTCTGGCCACGCCAGCAGACCTGGCTTTGTGTTGTGCCCTTGCTGATGGGCTTTGTGGGCCTGGGCCTCAGCCTGATGCTTCTAAAATGGATTGTGGTGGGCTCAGTGCAGGATTACGTCCCAACTGATCTGGTGGACGCCAATCGCATTGGACAGGACCCGATTTTCCTATCTAAACCCAGTTCCCTGCCTAAGGGTTCTGATGCTTCAGCATCTACCACTTCCACCACTCCCTCAGCAGCTCCAGGTTCTGCAACT[C/T]GAGCAGCTGAGGGCACAGGTACAGTGCAAAGAACTCGAATTGGGCAGTCCTCAAACCACACGGCCAGTAGCAGTAGCAGCAGTGGAGGTGGCGGTGGGGGGTTAGGGGGAGGCTCAGGAAACAGAGCTCCACACCTGCATAACAGAGTGGGAACGCGAGTGACCAACATCACAACCACAACCCGGGCCACCAATCCTGCTCCACCAGGAGGAAAGGAGGTTACTCCACGCAGCACCACTGTCCGAAAGCCCAACGGTGAGGGCGGGAGTCGAAGCGCATCACCTTCTGCACGAGCTGGGCCACCGAGTCCGACCACCACTAGCACGACAACCACTACGATTACAACGAGCACTACCACCACCCAAGCTGCCCAACCGACCTCTACCCCTGCATCGCCCTCCAAGCCTGGTCAACGCTGGAACCATGGGCGCTCCTCCAAGGGGCCTTCCACCAAACCTACTCGCCCACACCATCGCTTCAGGACACGTAAGTGTGATCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35314
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126744 Nonsense 328 764 2 9
Genomic Location (Zv9):
Chromosome 12 (position 30998936)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 29335873
GRCz11 12 29450775
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGAATGAGGGCGAGTGCTTCATCATTGAAACTGTGGCAGGGGTGCAC[A/T]GACACTGCAGGTGAGTCTACCTTTATGTGTGTGTCATGTCAAATAAAAGT
Long Flanking Sequence:
AAAATGGTGAAAAATCCCAGTTACAGCTTATTAAATGAGCTTTATTATCTCTGATAGCCTGTGTCATTAAACCCCCATACCCTATATAAGCTCCATAATAGACTCTAGAACATATTCTCCATCCTCACATGGGCTCATTTGTAATCAGTGAAGTGGTTGTGAAACCATCATACTTGAACGTGTGATTCAATTAACAGCATTCATGTCATAATATTGAGAAATCACTCAGATGTAATTTTATCATCGGAATGGACGTTATGGAAATGGATGGATTATTAGTGTTTGATTCATTTGATTAAACTGATGTAATCTTGATTAATCTCTTTCTGTCCCCCTTCCTCTTTTTTTGCACCCTCCTCCTGTCTCTTTCACACACAGTTGCTCCCACAACCTCCACGGTGCGTTCGGAGTTCTTCAAGCCCTGCCAGGACAGTCAGGAGATGGCCTTCTGTTTGAATGAGGGCGAGTGCTTCATCATTGAAACTGTGGCAGGGGTGCAC[A/T]GACACTGCAGGTGAGTCTACCTTTATGTGTGTGTCATGTCAAATAAAAGTGGATTTCCATCTTTACCTTTTCTTCAGTGACAATATCAAACTCCAAATGATTTTTATGGTTGTTACCCTATGAAATCTATTTTTATGTTGTTGTACTGTTTTTTTTTTTTTTTTTTTTTTTTGGCTTTCTCTTTTTTAGGGGGAACTTTATTAACATTTTAACACTTCAATTTAAAAAATGTAGTTAATTATTTTACAATAGTTCAAATGAATTAAAAACTAAAGTTAACATTTAAAGAGCTTGCAAAATTAACACTTAATTAATTTAACAACAATCAATTGAGTTTAATAATATTAAAACATCACAAACCCTACAAAACCACTTATTTTCTCAAGTTAAATTCAGTTGTTGTTGTTGTTGTTGTTTTTATCCATTTTTTGAAACTTTATTTTAATCATTATTTTTAAGTATGTCTTGTTAATTATACTTGGTAAAGCTAAGCTAAAAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42055
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126744 Nonsense 435 764 6 9
Genomic Location (Zv9):
Chromosome 12 (position 30916832)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 29253769
GRCz11 12 29368671
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTACTGTCAACGCCTCTGGTCTCATGTCTAAATCAAGCCCCAGACTC[G/T]AGAGCAGCCTCCAGCTTCAAAAGGTGATGTTTGTTTACATCTCAGACAGC
Long Flanking Sequence:
GAGTATTAGCAGACTGTCTGCTTAATATTTGGTGATACTGCTCCTTCAACAGACATTTAACTGACTAAAGGAAACTTTGCAAGTACATGTCAACTTACACTAACCCTAACCCCAACCTAAGAGTCTACTTATAGTCTAATGATAATTAGTTGGCATGTAGATGCAATGTAACTTAAATTCAACAAACAGACCATCAAAATATAGTGTGACCAATGTTAGTTGTGGGTCATTAAAATAACCTGGAAAATGCTGTTTACTATAGATACTACTAGTATACTAGCAGTATCTAAAAGTACTACATACTTTTTAATAATAAGAAACCAGCATGTCATTGACCTGAATGTCATTGCACAAAATGAAATCTTGTGGTTTCAAAAAATGTACCGACACTTTTCAGGAGACAAAGAGAGAAGCATCGAGCGCATCTGACCGAAATTCGCAACTTGAGGGACTGTACTGTCAACGCCTCTGGTCTCATGTCTAAATCAAGCCCCAGACTC[G/T]AGAGCAGCCTCCAGCTTCAAAAGGTGATGTTTGTTTACATCTCAGACAGCAAATCTGCATGATGTCCATATTTATGCTGACAGTGCACATGATGATCACTTGTTCCAAAAAAAAGCCTCCATCTCCACACTCATACGTCTACCACATATACAGAAGCACAGTCTGATTTCAAGCCACCCACATGTGCTGTTATGAAAATTCGAATAAAGTCCCCTGCGCATAACAGTCACCAGTAATGAATACAATTGGCCAGCAGGCAACTGGAGGAATGATGCCCTCCACGGCTTTACTGCTTTCCCACCTGCCCCGCAGATCCCTCAAGCTGACAGAAATAACACTGCATGCAGCTCGGGGAGCAAACACTGCATCTATCTGATGCAACAACAGTCAAAGGCAGCCAGCACCTAGCTGATGAAGAACTGGATGAATCGAGCCGCATTATCCAAACAGAAAGATCAGTCTCTCTTTCTCTGCTGCCACATGGCGGCTCATTTACACCC
Associated Phenotype:
Not determined