ZMP

glt25d1

Ensembl ID:

ENSDARG00000073974

ZFIN ID:

ZDB-GENE-070720-6

Human Orthologue:

GLT25D1

Human Description:

glycosyltransferase 25 domain containing 1 [Source:HGNC Symbol;Acc:26182]

Mouse Orthologue:

Glt25d1

Mouse Description:

glycosyltransferase 25 domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1924348]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25261	Nonsense	Mutation detected in F1 DNA	Not yet available
sa33311	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25261

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114521	Nonsense	413	623	9	12

Genomic Location (Zv9):

Chromosome 3 (position 53363418)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	52470733
GRCz11	3	52725396

KASP Assay ID:

554-7725.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACAGTGACCCTTATCACGGCAGACCTCTCACTAAAGGAGAGCTGGGCTG[C/A]TTCCTGTCCCACTATAACATCTGGAAAGAGGTCTGGCACACATCCCTGTT

Long Flanking Sequence:

CATTAGAAGCTGGTTATAGTCAAAGACTGTTCCCACAAAACTGTGTTTAAACCCCTTATTAAAGTGATTTTTGCATAATAGGTCCCTTTTAACATCAAAAATGGAGTCTTATGATTGGTTTTCTGGTCTATTGCCACATTTTAGCATCGGTGCTGTTGATGTGTTTATCAAATGTGCTGTGTGTGTGGTTAAAGGTGTTTATAATCAACCTGAAGCGACGAGGTGACAGGCGTGAGCGCATGCTGAGGGCATTGACAGAGCAAGAGATTGAATGTAAGATTATCGCTGCTGTTGATGGCAAGTGAGTCTGCTTGTGTTATCTTCAAACAAACGAGACCTTCTTTATCAGGTCAAAACACTCACTCACAGCTTGTCTTTTTTGTTTTTTTTAAACCTAGAGCTATGAACGTCAGTGAGATCCATGCTTTAGGAATACACATGCTGCCTGGCTACAGTGACCCTTATCACGGCAGACCTCTCACTAAAGGAGAGCTGGGCTG[C/A]TTCCTGTCCCACTATAACATCTGGAAAGAGGTCTGGCACACATCCCTGTTTGTTGTTTGGCTACAAAATCGCTGCATTAGAGTCAACTGCTTGAGAAAAGTACCATTCAAAAGCCTAGGGAAATTTTTTTATAAACTGATCTGTTCTCAGAATAATGCAGGAATTAAATTGTGAAATCAAACAGTAGAGTATTTCTCTACAAAGCCTTGCTATATTGTTGTATTAAGGGCGACAGGAAAGATGCAAGTGTCTTTGCTAGTTTCAGCAGGGTGCTGGTATCTTTTTCACATCTTGCACCTTACAGATTGTTGACCTGATTCCATTTAAATTCTTAGATCATTTTAGGACCATGATGACAAGCTGTACAATGATTTCTCAAACAGTTTATGTATTACTGATCAACAAAATTGTTGACATGTTGCTAAAATTTAAGCCTGTATTTCTGCATTTCTTTGGTAAATCTGCAGCATTACTCTCAGTGTTGGGCACATTCCTTTAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33311

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
ENSDART00000114521	Nonsense	418	623	9	12

Genomic Location (Zv9):

Chromosome 3 (position 53363433)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	52470748
GRCz11	3	52725411

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACGGCAGACCTCTCACTAAAGGAGAGCTGGGCTGCTTCCTGTCCCACTA[T/A]AACATCTGGAAAGAGGTCTGGCACACATCCCTGTTTGTTGTTTGGCTACA

Long Flanking Sequence:

ATAGTCAAAGACTGTTCCCACAAAACTGTGTTTAAACCCCTTATTAAAGTGATTTTTGCATAATAGGTCCCTTTTAACATCAAAAATGGAGTCTTATGATTGGTTTTCTGGTCTATTGCCACATTTTAGCATCGGTGCTGTTGATGTGTTTATCAAATGTGCTGTGTGTGTGGTTAAAGGTGTTTATAATCAACCTGAAGCGACGAGGTGACAGGCGTGAGCGCATGCTGAGGGCATTGACAGAGCAAGAGATTGAATGTAAGATTATCGCTGCTGTTGATGGCAAGTGAGTCTGCTTGTGTTATCTTCAAACAAACGAGACCTTCTTTATCAGGTCAAAACACTCACTCACAGCTTGTCTTTTTTGTTTTTTTTAAACCTAGAGCTATGAACGTCAGTGAGATCCATGCTTTAGGAATACACATGCTGCCTGGCTACAGTGACCCTTATCACGGCAGACCTCTCACTAAAGGAGAGCTGGGCTGCTTCCTGTCCCACTA[T/A]AACATCTGGAAAGAGGTCTGGCACACATCCCTGTTTGTTGTTTGGCTACAAAATCGCTGCATTAGAGTCAACTGCTTGAGAAAAGTACCATTCAAAAGCCTAGGGAAATTTTTTTATAAACTGATCTGTTCTCAGAATAATGCAGGAATTAAATTGTGAAATCAAACAGTAGAGTATTTCTCTACAAAGCCTTGCTATATTGTTGTATTAAGGGCGACAGGAAAGATGCAAGTGTCTTTGCTAGTTTCAGCAGGGTGCTGGTATCTTTTTCACATCTTGCACCTTACAGATTGTTGACCTGATTCCATTTAAATTCTTAGATCATTTTAGGACCATGATGACAAGCTGTACAATGATTTCTCAAACAGTTTATGTATTACTGATCAACAAAATTGTTGACATGTTGCTAAAATTTAAGCCTGTATTTCTGCATTTCTTTGGTAAATCTGCAGCATTACTCTCAGTGTTGGGCACATTCCTTTAAAAGAGTAATCAGTTAT

Associated Phenotype:

Not determined