ZMP

grin3b

Ensembl ID:

ENSDARG00000005364

ZFIN ID:

ZDB-GENE-070912-354

Human Orthologue:

GRIN3B

Human Description:

glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Source:HGNC Symbol;Acc:16768]

Mouse Orthologue:

Grin3b

Mouse Description:

glutamate receptor, ionotropic, NMDA3B Gene [Source:MGI Symbol;Acc:MGI:2150393]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25813	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38334	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25813

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058111	Nonsense	126	1118	1	9
ENSDART00000147354	Nonsense	94	912	1	8

Genomic Location (Zv9):

Chromosome 2 (position 26209185)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26405381
GRCz11	2	26061015

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGGAGTCTCGGCTGTGCTCGCGTTCCCCCAGAGCCACGAGGAGCTCATA[C/T]AAGTGGAGTTCATGTCCTCGTTTTTGGAAATACCCTTCATCAGCATCATT

Long Flanking Sequence:

CGCTTGCATTTCAACCGTGGCTGCATCCGCGCGCGCGTAAAACCATTAAGGACAAGAACAACTGGACAAAAATAGAGCGATGCCATCTTGTGACGAAACCTCAATCCAGTTGCGAAAGGAGCAGGATGAATTTAGTGCTCTTCAGATTCTTGGCATACCTTCACGTTGGGCTCCAGGTCGCTCTCCAGATGTTTATTTACCCTTGTCATCTGCATCCCCAGCCCTGTCACATCCTGGCACGCATTGGGCACACCGTGCGCTTGGGTGCGCTCCTGCCGACCCGCCAGCAGTCCAGGATACAGGGCGCCCTCAACCGCGCCCTGGTCCACCTCCGGCAAAGTGGGAACAACTTCTTGCCCTACAACCTGAGCTTGGAAGTATTGTCCCGAGAACCGCTCAATGGAGACCCGGAGTCCATGTTCAGGTGCGTGTGCCAGGATATCGTTGTTCAGGGAGTCTCGGCTGTGCTCGCGTTCCCCCAGAGCCACGAGGAGCTCATA[C/T]AAGTGGAGTTCATGTCCTCGTTTTTGGAAATACCCTTCATCAGCATCATTGAACAGGGTGAACCTCTTAAGACACAGGTGAGCAGCAAACTCGTTTCCTTTACTTTTATCCAAATCGCTCGGCTGGTTTTCAGGAACATTCCGGCAAACTTGTTAAAGAACTGGCGTGGGTCTTGAGAAAGTCGTTGTCTTTTCTCTCAGTTACAACTGTCACGTTTAATTGAGACATATTCAACATAATCCAAAAGCGCGCGACGCCGCGAAGTGTTTGTTTCGCGTCTGAAACTCGGCGTTTTTTACTTTGTGTGTCAAACTATTAAATAACATTAAAGGAATAAGAATTACTCAAAGTTGTTCGAAATCTACAACGTATCCCTAAAATACGCAAATCAATGTCAAGGCTGCAGAGTATTGATCTTTGGGGTATTAAACACCAACTAACAACGTGAATTAATTGAAACTTTAAAATTAAAATAATCACATTTATTGTTTTGAATTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38334

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058111	Essential Splice Site	816	1118	5	9
ENSDART00000147354	Essential Splice Site	784	912	5	8

Genomic Location (Zv9):

Chromosome 2 (position 26275296)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26471492
GRCz11	2	26127126

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACGCAGACTGCAAACTCCTGACTGTAGGAAAACCGTTTGCTATTGAAGG[T/G]AAGGTCCGCTGTGCCACTGAAACATATTGCTAACACCTCAGGCTATGCCT

Long Flanking Sequence:

TGACGCAATTCATGCTGGGTTTTTATAATTGGCTTCATTACACACTATTATTAGTCAGTTCCTCTGCTGTTTCTTTGCCACCCATGTAATAGGCTACACTATAAACCTCTTTGAAAACAATCATTTGCAATGTAGGCTTCTATAAAGAAACAAAACACAAAAAAGCGAGCTCAATGATTGAAAAAAATCACACGCATACTACACAAAAACACTTTCTATTCAGTAAATCTGGCTAAATCCTGACAGTTTAAGCAGTTTATTGCAACAGGCTTTAGCATTCAAGCTTATTGTAATCAAGTTTTAAAGTCAGAGGCAATTAGCATAAATTTGGCTAGCTGTGTTTGTTGTGATTGGCTCTGACTATCGTTCTCTGTGTGTTGAAGGACAGATCCCCCTCAGCTTGACGCCTTCATCATGGATAAAGCTTTGCTGGACTACGAGGTATCCATAGACGCAGACTGCAAACTCCTGACTGTAGGAAAACCGTTTGCTATTGAAGG[T/G]AAGGTCCGCTGTGCCACTGAAACATATTGCTAACACCTCAGGCTATGCCTGTAGAATTAAAGTACCTTACAAAAACCTGTGAAGTTCTTCTTTTTTGAAGGTGCTCAAGGTGCTTCTTAAACAAGTATGCTATTAAAATTCTACCCCACATTAAGAGCCGTCCATGAATTTCCCTCAAGGATGTTGTAATTACCCTCCCAAATCTGAGCAAGTCAAGTTTGACACATGTCATTTCTTAAGCGAAGGCTATTACGGGGTGTAGATGGGTTTGATGGCAGTCACCCAGGCGTATCCGCACCTCTCATCCGGATGTTATCTCCGGCTGCATGCATAGGAATTTTCCCTGTTATCTGCCAAAAGCCTCCCCTCACGCCTTTTGAGCCAGGTTTTATTAGATGGATGATCAAGACTGAACCATCGCTATCACGTCCGCTAGCCTGAAAATGGACAGCTCCGTCAGGGTCTGTAGAACCTGTAAATAGCACGGTGCATAATCCAGC

Associated Phenotype:

Not determined