ZMP

gpd1

Ensembl ID:

ENSDARG00000036942

ZFIN ID:

ZDB-GENE-040426-2576

Description:

glycerol-3-phosphate dehydrogenase 1 (soluble) [Source:RefSeq peptide;Acc:NP_999918]

Human Orthologue:

GPD1L

Human Description:

glycerol-3-phosphate dehydrogenase 1-like [Source:HGNC Symbol;Acc:28956]

Mouse Orthologue:

Gpd1l

Mouse Description:

glycerol-3-phosphate dehydrogenase 1-like Gene [Source:MGI Symbol;Acc:MGI:1289257]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23400	Nonsense	Available for shipment	Available now
sa36742	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23400

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053639	Nonsense	33	349	2	10
ENSDART00000134266	Nonsense	33	349	2	8

The following transcripts of ENSDARG00000036942 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 334293)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	324224
GRCz11	19	324431

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCCATCGCTAAGATCGTGGGCCACAATGTGAAGTCTTCCAACCGCTTC[G/T]AGCCGCTGGTGAAGATGTGGGTCTACGAGGAGATGATCGACGGACGCAAA

Long Flanking Sequence:

AATCTGTCCTAATAACAAGATGAATAATGAGATGATTGATGATAATGATCATATATAAACATGCTGCCTTGTTTCTTTATGCTCCTCCTGTGCTTGATTTAGTCAGATCTGCAGAATCTCTGTCTCTTTACTGTTGCTTCTGTTCTGTAGAGTTCATCACTGAGCAGTTTTCAGTGTCTCGCTCATTCAGATCTGCAGTGACTGTAGCAGAGGTGTCCAGCCCTGCTCCAGGAGATCTGCAGAGTTCAGCTGCAGCCTTGATCCAATGCTCCTGTCTTTATCACCAAGTGCTCCTGCAGATCCTGCTTAGTTGGTTTATTTGTGTTGGAGCTAAACTCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGAGCACCACTGCTGTGGAGGATATGTGTGTCTGTGTGTGTTTGATGTGTGTGTGTGTGTTTAATGTGTGTGTTCAGGGGTTCAGCCATCGCTAAGATCGTGGGCCACAATGTGAAGTCTTCCAACCGCTTC[G/T]AGCCGCTGGTGAAGATGTGGGTCTACGAGGAGATGATCGACGGACGCAAACTCACCGAGATCATCAACACCGAACACGAGAACGTCAAATACCTGCCCGGACACAAGCTGCCCAAAACTGTGGTGCGTCTTCATCATTATAATATCCTCATCATCGTTATAATTATTACTACTATCATCTTCATCCTCATCCTCATCACTCTGAGCTGTTATCAGACACACACTGATGATCAAACACATGAACTCTGATCAGATCACCTTCAACACACTGCTGCAGGATTACACAGGATTATAACACAGACAACACAACACAACACAACACAACACATCACAACATATCAAAACAACTCTAAACCCTAACACAACACATCATATCACAACACATAACAACACACACACACACACACACACACACACACACACACACACACAACACTGCACTACACATCACAACATATTAAAACAACTCTAAACCCTAACACAACGCATCATACCACAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36742

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053639	Essential Splice Site	121	349	None	10
ENSDART00000134266	Essential Splice Site	121	349	None	8

The following transcripts of ENSDARG00000036942 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 329980)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	319911
GRCz11	19	320118

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACCGTGTTACCCACACACAAAGCACATATACACATGTTTGTGTGTGTTC[A/T]GGGTATTGACGAGGGTCCGGACGGCCTGACTCTGATCTCTGACATCATCA

Long Flanking Sequence:

GAGCCATCGGCATCTCTCTCATTAAAGTACAGCACACACACACACACACACACACACACATACACACACACACACACACACACACACACACACACACACACACACACACACACAGACAACATTCATTCATTCATTTTCTCTTTTGGCTTAGTTCTTTTATTCATCAGGGATCGCCACAGTGGAATGAACCACCAATTATTCCATCATATGTTTTACACAGCGAATGCCCTTCTAGCTGCAACCCAGTACTGGGAAACACACACACACACTCATACACTACGGCCAGTTTAGTTGATCAGTTCCCCTATAGCACATGTGTTTGGACTGTGAAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCCGGGACTCAAACCAGAGACCTTCTTGCTGTGAGGCCACAGTGCGACACCACTGAGCCACCGTGTTACCCACACACAAAGCACATATACACATGTTTGTGTGTGTTC[A/T]GGGTATTGACGAGGGTCCGGACGGCCTGACTCTGATCTCTGACATCATCAGGGCGAAGCTGGAGATCGAGGTGTGTGTTCTGATGGGCGCCAACATCGCCAGCGAGGTGGCCGACGAGAAGTTCTGCGAGACCACCATCGGTCAGTGACATCACTTCCTGTCTGAACCTGCAGGCTGAGCGCTGGAGCTCATGTGCTAATCACTGCATGTGTGTGTGTGTGTGTGCATGCATGTGTGTATTTGTGTGTGCATTTGTGTGGATATGTGTATGCATGTGTGTGTGTGTGTGCATGTGCATGTTTTTGTGTGTGCATGCATGTGTGTTTGTGACTGTGTATGTATGCATATCTGTGTGTGTGTGTTCATGCATGGTCTGTGTGAATGTGTGTGAGCATGCATGTCCATGTGTGTATGCGTTCTTGCTTGTGTGTGTGTGTGTGTGTGTGTTCATGCATGTGTGTGCATGTGTGTTTACGTGCATGTGTATGTGCATGTGTGTT

Associated Phenotype:

Not determined