ZMP

glud1b

Ensembl ID:

ENSDARG00000002414

ZFIN ID:

ZDB-GENE-030828-1

Description:

glutamate dehydrogenase 1b [Source:RefSeq peptide;Acc:NP_955839]

Human Orthologues:

GLUD1, GLUD2

Human Descriptions:

glutamate dehydrogenase 1 [Source:HGNC Symbol;Acc:4335]
glutamate dehydrogenase 2 [Source:HGNC Symbol;Acc:4336]

Mouse Orthologues:

AC160930.1, Glud1

Mouse Descriptions:

glutamate dehydrogenase 1 Gene [Source:MGI Symbol;Acc:MGI:95753]
glutamate dehydrogenase 1, mitochondrial precursor [Source:RefSeq peptide;Acc:NP_032159]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa27954	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa2641	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa27954

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026657	Essential Splice Site	337	542	7	13
ENSDART00000101042	Essential Splice Site	337	542	7	13
ENSDART00000145078	None	None	410	None	12

Genomic Location (Zv9):

Chromosome 12 (position 27400394)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	25781382
GRCz11	12	25872742

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGGAACCCCAACGGCATGGACCCCAAAGAGCTGGAAGACTACAAACTGG[T/C]CTGTTAAAGCTCCATGTACAATCACTTTTCTGAAATGTCCCTCTGTACTT

Long Flanking Sequence:

TACAAACCTGTTGGAGTTTCTTTCTTCTGTTGAACAGAAAACAAAAAAACACCCGAAAACCTGTAACCACAGACTTCTATAGTGTTTATTTTTCCTATTATGGAGTATGATTATAAGTCAAGTCAGAGTTTCTAACAATTTTCTAAATTACATTAAAAATATAGTCATAAAACTAAAAAAGTTTGAAACCATTTAGAGGTGAATAAATATTAAGTAAATTTAGATTTTTAGGAGAACTTTCCCTGTAACCACTAATTAGGAGCCAATGCCGATTCAAACCACACGGTGGCGGCACCTCCTCATAAAAAAAGCCATTCTTAAAATTTTTTTGTCACAACCTGTCCTTTCTCCTATGCTTCAGGGCTTTGGTAATGTGGGTCTGCATTCCATGCGTTATCTTCACCGTTATGGAGCCAAGTGTGTAGGAATTGCTGAAATCGATGGCAGCATCTGGAACCCCAACGGCATGGACCCCAAAGAGCTGGAAGACTACAAACTGG[T/C]CTGTTAAAGCTCCATGTACAATCACTTTTCTGAAATGTCCCTCTGTACTTGCTTTTTTAAAACACCTTTATTTATGCTTTCTTTTTAGCAACATGGCACCATTGTGGGCTTCCCCAACTCTCAGCCATATGAAGGAAACATTCTGGAAGCTCAGTGTGATATTCTCATCCCTGCAGCTGGAGAGAAACAGCTGACCAGGAAAAATGCACACAATATCAAAGCTAAGGTCTGACAGCAGTGCCAACATCCAACTGAGCTTGTTATGCTTAAATTCCACTCATCGATTTTAACAGTTTCTTACTTTTTAAATTGATGTAGATTATTGCTGAAGGTGCTAATGGTCCCACAACACCCGATGCTGACAAAATCTTCATTGAGAGGAACGTCATGGTCATTCCAGTAAGTCCATTTAAGTGGTACTCTCTTGTTTGGGCTTCAGGAAGAAACTAATTGGAGTATTAATGTACATTTTAATGTGTAGGACATGTACCTGAATGCCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa2641

Status:

F2 line generated
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
ENSDART00000026657	Nonsense	371	542	8	13
ENSDART00000101042	Nonsense	371	542	8	13
ENSDART00000145078	None	None	410	None	12

Genomic Location (Zv9):

Chromosome 12 (position 27400582)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	25781570
GRCz11	12	25872930

KASP Assay ID:

554-2842.1 (used for ordering genotyping assays)

KASP Sequence:

ACATTCTGGAAGCTCAGTGTGATATTCTCATCCCTGCAGCTGGAGAGAAA[C/T]AGCTGACCAGGAAAAAKKCACACAATATCAAAGCTAAGGTCTGACAGCAG

Long Flanking Sequence:

CCATTTAGAGGTGAATAAATATTAAGTAAATTTAGATTTTTAGGAGAACTTTCCCTGTAACCACTAATTAGGAGCCAATGCCGATTCAAACCACACGGTGGCGGCACCTCCTCATAAAAAAAGCCATTCTTAAAATTTTTTTGTCACAACCTGTCCTTTCTCCTATGCTTCAGGGCTTTGGTAATGTGGGTCTGCATTCCATGCGTTATCTTCACCGTTATGGAGCCAAGTGTGTAGGAATTGCTGAAATCGATGGCAGCATCTGGAACCCCAACGGCATGGACCCCAAAGAGCTGGAAGACTACAAACTGGTCTGTTAAAGCTCCATGTACAATCACTTTTCTGAAATGTCCCTCTGTACTTGCTTTTTTAAAACACCTTTATTTATGCTTTCTTTTTAGCAACATGGCACCATTGTGGGCTTCCCCAACTCTCAGCCATATGAAGGAAACATTCTGGAAGCTCAGTGTGATATTCTCATCCCTGCAGCTGGAGAGAAA[C/T]AGCTGACCAGGAAAAATGCACACAATATCAAAGCTAAGGTCTGACAGCAGTGCCAACATCCAACTGAGCTTGTTATGCTTAAATTCCACTCATCGATTTTAACAGTTTCTTACTTTTTAAATTGATGTAGATTATTGCTGAAGGTGCTAATGGTCCCACAACACCCGATGCTGACAAAATCTTCATTGAGAGGAACGTCATGGTCATTCCAGTAAGTCCATTTAAGTGGTACTCTCTTGTTTGGGCTTCAGGAAGAAACTAATTGGAGTATTAATGTACATTTTAATGTGTAGGACATGTACCTGAATGCCGGAGGTGTCACAGTCTCTTACTTTGAGTGGCTGAAGAACCTGAACCACGTCAGCTATGGTCGCCTGACCTTCAAGTATGAGAGGGACTCCAACTACCACCTGCTGAGTATGTTTTACACTTCCTCCAACTACCTTGTGTCAAAACCCCCCCTTGCACCTTTTGCCAATATGATTACAAGTGGATGATGC

Associated Phenotype:

Not determined