ZMP

si:ch211-13f8.2

Ensembl ID:

ENSDARG00000078299

ZFIN ID:

ZDB-GENE-070705-32

Description:

Novel protein similar to vertebrate glycosyltransferase 25 domain containing 1 (GLT25D1) [Source:Uni

Human Orthologue:

GLT25D2

Human Description:

glycosyltransferase 25 domain containing 2 [Source:HGNC Symbol;Acc:16790]

Mouse Orthologue:

Glt25d2

Mouse Description:

glycosyltransferase 25 domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2138232]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39768	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available
sa18548	Essential Splice Site	Available for shipment	Available now
sa6826	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39768

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110689	Splice Site, Nonsense	121	521	3	11
ENSDART00000146547	Splice Site, Nonsense	198	598	4	12

Genomic Location (Zv9):

Chromosome 2 (position 6924061)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	7347631
GRCz11	2	7219237

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTCGACTCAAGAACGCTCTATTCAAACTTCTGGTGTGGCATGACCTCA[C/T]AGGTACAATACGCCTTTTCATCTTTCATTACAAAGACTTCCATTCATATT

Long Flanking Sequence:

GGGTTGCTAAATTGAACCTCAGCTTAGTTAGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCATTCGGGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCAGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGTGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGAAAAAACGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTAGCGACCTCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGATTTCTGATTGATTTGTATGATTGTTTGCATGTTTTTCCCCCTTAGTTCACAGACAGTGATAACCTGCTTACAAACACACAAGTGCTGAATCAACTGATTTCTGAAAATCGGACGCTGGTGGCTCCAATGCTCGACTCAAGAACGCTCTATTCAAACTTCTGGTGTGGCATGACCTCA[C/T]AGGTACAATACGCCTTTTCATCTTTCATTACAAAGACTTCCATTCATATTTACGGAACTAGCATAGTGAACACCAGATCTCAGTCATTATATGGTCTCATTGGAGCAACAGAAGTCTATTTTCAAACTTTTTTACCAAATTTATTCCAACAGGTTATAGACTCTAACATTATTTAGGCAGTTGGCTAATCTTTGGCTATAGAGATCCATTTTGGTAGCTAATATCTAAACTTTTCTGATTTTGATTGTAATTTTTTAATGTGTGAAAATTGTTAAGTATTGTGAAAAGCGCTTTACAAATAAACTTGAATTGAATCATTCTGAATGCGACTGATAAATGACCTGACGTGAAAACAAGTGAAGATTATTTCAGTCATGCACATCCAGTGAACTCTTTGTTGAATAATAATAATAAACTTTATATGGATAGTTCACCGAAAAATGACATTATTTCTCTTGAACACAAAAGAAGATATTTTGAAAAATGTTAGAAACTGGTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa18548

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
Order Allele From EZRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110689	Essential Splice Site	122	521	4	11
ENSDART00000146547	Essential Splice Site	199	598	5	12

Genomic Location (Zv9):

Chromosome 2 (position 6926559)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	7350129
GRCz11	2	7221735

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCTGCACCACGTGTTGRTAATCTCGAAAATATCTGATTYTTCTTTCWGC[A/T]GGGCTATTATAAGYGAACACCACATTATGTACCCATTCGAACCTGGAAGC

Long Flanking Sequence:

TACTATTTAAAGCATGAAATATTTAGCTTTATCAGTTTTTAAAATCCATACAACCAATCTATGGGTCTGGTAAGAGCACTTTTAGCTTAGCTTAGCATAAATTACTCAATCAGATTAGACCATTAGCATCTCTTTCAAAAAAACAAACAAACAAACAAAAAAAAAAAACGGGTTTTTGTCATATTTCTATTAAAATCCGGACTCTTTAATAGTTCCATTGTGTGCTAGGACCAACAGAAAATTAAAAGTTCCTATTTTCATTATGGCTAGGCACTACACTCTCATTCAGGTGTTATAATCAATGCTGCCGCATACATTTTTTTGCAGTAACAGAAGTGAGGTTAAAGGTATGCCAGTACTTCAGTAGTCATATGTAATAGTTAGAATAGCTGTATTATGTATTATTCATTGTTTCTCATTTTGTCTGCACAATTTTTTGAGGGTTAGTTTTTCTGCACCACGTGTTGGTAATCTCGAAAATATCTGATTCTTCTTTCTGC[A/T]GGGCTATTATAAGCGAACACCACATTATGTACCCATTCGAACCTGGAAGCGAACCGGTTGTCACCCGGTTCCCATGATTCACTCCACAATGTTGATAGACCTGCGCCGCAGAGCTAGTGAATTGCTGGCCTTTTACCCCGTGCACCATCACTATCTTTGGGCCCTCGATGATATCATGGCATTTGCTTTTTCTGCAAGACAAACAGGTAATGATATAACATTTGATATAACATGATTAACATAATGATATAACAGTCAAGTGGAGGTCAAAACCAGGGAACAGCTTACAATTTCCTAAATTTCCCAAAAGAGGAGTTAGAGAGCTCTTTATTATTAAGGGATTGGGATTGGGGTCAAATACCAGCATACACAACAACAGATATAATCCACAAGCATAATCTGTAAAACAGGCGAAGGGGTTGAGATGGACGGCAAACAATCAGAAGAGAAAGCCGGCACAGGAAGGCAAAAAAAGTAAAAACGCCTGGCAATGATAGCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6826

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110689	Essential Splice Site	290	521	8	11
ENSDART00000146547	Essential Splice Site	367	598	9	12

Genomic Location (Zv9):

Chromosome 2 (position 6932623)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	7356193
GRCz11	2	7227799

KASP Assay ID:

554-5008.1 (used for ordering genotyping assays)

KASP Sequence:

CAGTKACACAACATGCCGCTGTCAAAAATGACTTCTTTCTGTTTCTYCTC[A/C]GAGCCATGAATTCAACTCAGCTYAGGACTTTAGGAATTGAGATGCTTCCT

Long Flanking Sequence:

ACTATTGTATGATGTCATATCTCTTATGAATATCTTTCTGCCAGAAAAAAATATTTCATTTGTGGTTAAAAGAGAAATAATCTGAAGTTCATCTTTCCACAGTTGACTTTAAAATGGAAACTTCACAGTATCTGCACATTGTCTCCAAACCCAAAGACACCATGGCTTTCAATCAGGTATAGATGCAGACAATTGCAATAGAATGTTGTCACATATTCAGTTTTTGTGTTAATACTCACATTAAATGAATTTTTTTGTGTCATATCCGTTCCTCCTTTAAGGTCTACCTGATCAATCTGAAGCGTCGGGAAGATCGTAGAGATCGTATGCTGCGCTCGCTGGAAGTCCTGGGCATAGACGTCACCCTTACCGATGCGGTGGATGGCAAGTATGATATTATAACCCACTCTTCTTCATTTAATTTGTATATTGAATATTAATTATATCTTACAGTTACACAACATGCCGCTGTCAAAAATGACTTCTTTCTGTTTCTCCTC[A/C]GAGCCATGAATTCAACTCAGCTCAGGACTTTAGGAATTGAGATGCTTCCTGGTTTTAAAGATCCGTACTCTGACCGAGTGCTGACTAAGGGGGAAATTGGCTGCTTCCTTAGTCATTATAACATCTGGAAAAAGGTACAAAGGAAAGAGGAATGCATTACAATCAGCTTCTACAAAAACTCTACATTTTAACCACATATTTGTGGGTCAATTTAAAAAAAAATTCACATTTTTGGTTCACCCAAAAATGAACATTTTGCCATGATTTTCACACCTTTTACTTTTACCCTTTACCTTTTACACAAAAGCTGGAGAAAGCTGGAAACCTGTAACAATTGATAGTATTTCCATACTTTTGTTTTTTCTACTATGGAAGTCAATGGCTACAGGTTTTCAGCTTTCCTCAAAATGTCTTCTTTAGTGTTCAATAGGGTGAAAAAACAAGTACGTTTTTATTTTGAACATCTCTTTAAGAGAACAAAAATGTCATTAAAGTGTCAA

Associated Phenotype:

Not determined