ZMP

nrg2b

Ensembl ID:

ENSDARG00000086585

ZFIN ID:

ZDB-GENE-090205-2

Description:

neuregulin 2b [Source:RefSeq peptide;Acc:NP_001138563]

Human Orthologue:

NRG2

Human Description:

neuregulin 2 [Source:HGNC Symbol;Acc:7998]

Mouse Orthologue:

Nrg2

Mouse Description:

neuregulin 2 Gene [Source:MGI Symbol;Acc:MGI:1098246]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35635	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11366	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa35635

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127494	Nonsense	155	599	4	11
ENSDART00000129055	Nonsense	261	697	4	10

Genomic Location (Zv9):

Chromosome 14 (position 8358739)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	8082529
GRCz11	14	8388643

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGTGCAATGAAACTGAGAAGACATACTGCATCAACGGTGGAGACTGTTA[T/A]TTCATACATGGTATAAATCAGCTGTCCTGCAAGTAAGTTACACATTGTCA

Long Flanking Sequence:

TTTAGTTAAAAATGAAAAAACACTGCATATTGTTGTCTTCGCTGCAGTGTACTATCCCTTTTGCGTACTGTAAACTAAATTTTACATCTTTCTGACAATATTTGATCGCACTGCCGGAAAGATTCATTTAAAAAAAAGTATTTGTCATCTATGTTCTTAATCCGCATGCCCCTTCAATGACTTAAAAACAATAGTGCCACCATGTGAAAACAATGTAGCATAATAAATTGCTGAATTGCTTACCACTGGATTCTACTGCATTCTGTTTCACACGGACACTCTGTTTGCTGACAATTTGTAGACAGTATATAGTATTACTGTGACTGACACATTTTTCACAATGTCACTAATGTCTGCTGCTCATCTCTCTCTCTCTTTCTCTGCGTGTGTGTGCGTGTGTGTGTTTCTATAGTAACCACCACATTGTCTCCGGGCTCAAGTCATGCCAGGAAGTGCAATGAAACTGAGAAGACATACTGCATCAACGGTGGAGACTGTTA[T/A]TTCATACATGGTATAAATCAGCTGTCCTGCAAGTAAGTTACACATTGTCAAAACACATGCATTTACCCTAATTTCACATTGACAATCCTTTAACCAAATGTTGTTTTCATTAGACTGTTTATGGGCTTGATTTTAACACACTAGAGAGTGTTTGTTGAAATGCTAGTTTGACATTGCCTTTCATTGCTTGTTTAATTAGTTAATAAAAAATAAATTATGATTATTGCTATTAAAAATATTGCAACAAATGTCTGTTTGCAGTTCTGAATGCCATAAACCATGCATAGATTCCTTATTAGTAAACCATGTTATTTGATTACTGCTACTATACTTTAATTTATTGCTAATATTTAGATTTTTTCCTTCATTTTAATTCTAGTGCAGATTCAAGTAATTTTGTTTTGTGTTTTTGTATTTTTGTTAGTTTGTTTTAAAATATTTGTTGCTTTTTATAGAGCTGTGGCAAAAAAAAAAAGTTTTGATTCTGCGTTGATTCTAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11366

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
Order Allele From EZRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127494	Essential Splice Site	270	599	9	11
ENSDART00000129055	Essential Splice Site	368	697	8	10

Genomic Location (Zv9):

Chromosome 14 (position 8399147)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	8122391
GRCz11	14	8428505

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGTCTGAATAGNTTTTGATTTGTCATCAAGCKTTTTTSNTTTTTATTGC[A/T]GTATATATCTAAGAATGTCCCGGCAACTGAACGAGTAGTACGACATGGAA

Long Flanking Sequence:

ACTCAGTTTTTTTAAGTCCAATTTATATAGACTGTAGCCAGTGTCTAAATTATACAATGACTATCGGATGAAAAAAGTCTGTAATATTAGTTTGTGCAATGCATTTGCAAATTTATTTATTTAATTCCATTACATATTAAATAACCAAATGTATTTAAGTTTTCAATGTTTTGAGGGTTAGTGAGTGTAATATCTGACCTACAGCAACCTTTGATTGACTGTTTCAGCAGATGTGTGATGATCAAACACAAATGTATTTTTGACATAAAACAAACGGTTACAAATTAATATTCCTGCACCAATAAATGAATGTAGTATTAATATGTATGTATGTACTGATAAAATTTGTCACAAGATGAAGTTTTGACACTGTTTATCTCTGAATTTGTCATATTTTATTACCATTTTCTAAACTGTTGAATAAACTGTGATATAATGTGAGAAATGTTGCTGTCTGAATAGTTTTTGATTTGTCATCAAGCGTTTTTGTTTTTTATTGC[A/T]GTATATATCTAAGAATGTCCCGGCAACTGAACGAGTAGTACGACATGGAACTGAAACATCAGGCAATTTCTCGGGCAGCCGAATGTCGTCACGGTCCCACCACACCTCCACAGCGTCTCACACTTCCAGCCACCGGTACTGACCTCTGTCAATATATCCAGAAATATATCCGTCTCCTACTGCACTGTATATCCTCCTCTCATCTGTCTCTTTAGATGCTCATTTGCCAACTCAACTAACTTAATGTATATCTATCCATCCGTTGATGTATTTTGTTTGTTTAAAGGAAATATATAGTATATATAAAAGAATTTATCATCTTACAAAACTGCTGTTTTTACTGCATCTTTATTAAATGAGCATGAGGGACTATTAAGAGGCTGCACTCATCAAAAAAACAGTAAAAAGAGTTATATTGTGGGGGGAAATACAGCAATTTAGTATCATTGATTTACTAGTGAATAGTTAATATTTTAATACAATTGTACTACCTTAAGTTT

Associated Phenotype:

Not determined