ZMP

si:ch211-251b21.1

Ensembl ID:

ENSDARG00000007275

ZFIN ID:

ZDB-GENE-060809-5

Description:

si:ch211-251b21.1 [Source:RefSeq peptide;Acc:NP_001138274]

Human Orthologues:

GRID1, GRID2, GRIN3A, GRIN3B

Human Descriptions:

glutamate receptor, ionotropic, N-methyl-D-aspartate 3A [Source:HGNC Symbol;Acc:16767]
glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Source:HGNC Symbol;Acc:16768]
glutamate receptor, ionotropic, delta 1 [Source:HGNC Symbol;Acc:4575]
glutamate receptor, ionotropic, delta 2 [Source:HGNC Symbol;Acc:4576]

Mouse Orthologues:

Grid1, Grid2, Grin3a, Grin3b

Mouse Descriptions:

glutamate receptor ionotropic, NMDA3A Gene [Source:MGI Symbol;Acc:MGI:1933206]
glutamate receptor, ionotropic, NMDA3B Gene [Source:MGI Symbol;Acc:MGI:2150393]
glutamate receptor, ionotropic, delta 1 Gene [Source:MGI Symbol;Acc:MGI:95812]
glutamate receptor, ionotropic, delta 2 Gene [Source:MGI Symbol;Acc:MGI:95813]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa45338	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45338

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
ENSDART00000008778	Nonsense	175	458	5	9
ENSDART00000139096	Nonsense	175	458	6	10

Genomic Location (Zv9):

Chromosome 8 (position 49810621)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	47662598
GRCz11	8	47651590

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAATCATGACTTAAGTTCTGTTTTCCAGGATCAGCCCCTGTGAGTGGGAG[C/T]AACCAGAGAAAGACAACAATTCCTTCACGCTCTCACACAGTTTTTGGTAT

Long Flanking Sequence:

CCTCACAGTCCAAAAATATGCATCTTAAGTCAATTGACTAATCCAAATCAACACTATAGACGTGCACCTTGTAAGTAGTTATCTCTTAAGAGCAATCACAATCTGTTCATTAGCAACTACAGTAGGGGGGGTTCTCGAGTTCTACCTTAGCTCAAACTTCCCTCTTGCCTTGCAATGGGAGGGAGCCCCGGGCTCGATGATCTTTTGAGCTAAGGGCTCTCTCCTGGGACAACATGCTAAACAAGTTTCATAATCAATCATCAGCTAAGTGTGAACTCTTGAAACACACTTGATCATACTATTCGAGTCCTTCAGGCTTGTTTGAATCCTACGGGAAAGTGTGTTAAAGCAGGATTGGAACTAAACTGAGCTGCGGCCCTCCAGGAACTGAGTCTGAAACCCCTGAGCTATGGTTATTATTTAAAACAATTAAATACCCCAAAAATGGCAAAATCATGACTTAAGTTCTGTTTTCCAGGATCAGCCCCTGTGAGTGGGAG[C/T]AACCAGAGAAAGACAACAATTCCTTCACGCTCTCACACAGTTTTTGGTATACTGTTGGAGCACTGACACTTCAAGGTAGCGTAGCTTGGATAAGTATGGTTATACCATTATAACATCTCATTTTAGGTTGTTTTAAGCTGTGTTTTCTTGGATTTGTTTATCAAGTTATGTGTTTAAATGCCAGGCTATAGAAATTGCTGTTAAGTGAATTGGGTATCACTTCATTTTGATGGGCCATTTTAACACATTTAGTTGATTTTAAGTTACATTGCAACTACATGCCAACTCATTATAGTTCTCAATGTCTCATTCCCTACCAATCGACTTTGAAGTCGTTCAGTAAGAAAACAGAGTACTAGCAAGAGCAATATGCATACATGTAGGGTAAGATGGCGTCATGCATCAAATTATTTCGGCAGAGACAGTGGCCATAGAGTTGTGGCTATCAGGACACAACATGGTATCTGTTCCCTACATTAAGAAATGAGCAACCCGGGCTC

Associated Phenotype:

Not determined