ZMP

LOC100330824

Ensembl ID:

ENSDARG00000073728

Human Orthologue:

GAL3ST3

Human Description:

galactose-3-O-sulfotransferase 3 [Source:HGNC Symbol;Acc:24144]

Mouse Orthologue:

Gal3st3

Mouse Description:

galactose-3-O-sulfotransferase 3 Gene [Source:MGI Symbol;Acc:MGI:3617843]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13055	Essential Splice Site	Available for shipment	Available now
sa25352	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13055

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109485	Essential Splice Site	28	429	1	2

Genomic Location (Zv9):

Chromosome 7 (position 8066822)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	7005496
GRCz11	7	7238875

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCARTCAGCACTGTCAGCTTTCTTCTRCACCATGGGGGTCACTTGAACTT[G/T]TAAGAGCCTTTGAAAAATKATCCTTTCATTCAGTCCACACCCTCAWACCC

Long Flanking Sequence:

AGATGAAGAATCTTGATTGGGTTTAAAAGTTATAAACATAAGTGAAACTTTGGACAAGCGGTGGCGCTAGAGACTTCCAATTTGTTGTGGCTGAAGATCATACTGTCCTCTATCAGTGTGCCAAAGCTTGCACGAATGGTTCATAGGGCTGCCATAGTGGAAGCAGAAGAAGCCGAAGAAATTATAATAATAAGAACCAGAACGGATGCAATAGGTGCCACGATGCAATTTGAGATCCAGTTTGCAAGAAAACACTCTAAATCTACACAAATATTCAGCATGATATTTAAACCAATTCTTGTGCTCAGGAACTTGCGTGTGAGAGAGGGCTTGTGTCCTGGATGTGTGTCGAACACAGGAGTAAGCTACACCTTTGTAATGTTTGCTTCTTGTCTTTTGCAGTGAAAGAAGCTGGAGATGTCTCAGAAGAAGATATTCCTAGTATTGATTGCAATCAGCACTGTCAGCTTTCTTCTGCACCATGGGGGTCACTTGAACTT[G/T]TAAGAGCCTTTGAAAAATGATCCTTTCATTCAGTCCACACCCTCATACCCAAACGTATACTTCCTGATCTTATCCAGTATGGGTCAAAGAAGTAGGCAGCACTGACTCAGCAAAAATGTGTTGCTGCGGTCAATTATTGTACAGTTCTTTTGCTGTTTTGACCAAATTATCCCACTTTCCAAACTTTCTAAGTATCGTAACTCATTCCTCATTTTTTTTTTTTTTTTGGATTATTCAATTGCCTCGTACTTTGCCTTGCATTAAAGATGACCCAGAATCGGTCACCACGCTGGTCTTCACTGGTTTAGATAAACCTCCATTCAGATTACACAATTTTGTCCTGATTTCAGCATGAATTGCTTGTCATAGGGTGTCATGGGGATTCGTAAATGACAAATGGCTGTCAAGACTAGTGATGTCCCGATCAGTTTTTTTCACCCTAGAGTCAGAGTCCTTTGATTTTGAGTATCTACCGAAACCTGATCCGATACTTTTATAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25352

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
ENSDART00000109485	Nonsense	396	429	2	2

Genomic Location (Zv9):

Chromosome 7 (position 8069987)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	7008661
GRCz11	7	7242040

KASP Assay ID:

554-7895.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAATGCCAGAAGTGCAATACACAAAGCTGTTGCTTCGTTCAGAATCTGTA[C/T]GATATCGAAAGCGGCTTCCAATACGGAGCCGCCAGCAGACTGCACGGTCC

Long Flanking Sequence:

TGATTGCAGAATACTTTGATGAATCCTTGGTGCTGTTACGCCGCTTGTTGGCTTGGGATCTCGATGATGTTCTTTACGTCAGTCTCAACATGCGCACAGCCGACTCCAAAAGCAGCCTTTCTAGTGATAATACGGAGAAAATCAGAGACTGGAATGCTATAGATTCAGCTCTCTACGATCATTTCAATGCCTCGCTATGGCGGCAGCTGAGAGCATTGGGACTAGCATGTGTTGAGCGGGAAGTCCAGCTGTTGCGGCAGTCTAGAGACCGACTTGTTCGCAGCTGTTTCGGGGGAAGTTTACCACCGCTTCGCTCTGCTGCACAAATCACGAATAAAGAGTTGCGGCCGTGGCAGCCCAGTGCCAAAGTGACAATCGTTGGGTACGACTTACCAGTTAATATATCAAAGAAAGGCCCCATCCCTCCTCGAGATGAGTGTCTAAAGATGATAATGCCAGAAGTGCAATACACAAAGCTGTTGCTTCGTTCAGAATCTGTA[C/T]GATATCGAAAGCGGCTTCCAATACGGAGCCGCCAGCAGACTGCACGGTCCGTCGGACAACCTCGGGTTCACAAAGAGTCTTCATCTCAGAGTTTGGTACCATGACCTTCGGAGACTATGGTTCGAAGCACTAGAGTTATTCTCCCAATTTTAAAAAAGTGTGAAAGCATAGTTTTTTCTTATTTCCTAGTTGATCTAGACTGCATCTTTTAACGTTTATGACATGTTGGAATTATTTAAAAGCTTGAGGTTATACCTCTTTTATACTGAATGTGAGCACGACCACATGCACGCTCACAACCCTTGATCAATTAGTAAAGGAAACCATTCAAGTCCAAAAACTTTGACATCGGGAATGCTTCTCAATCTCTCAAGGACAATCTCTCCACATATATACCATCATTCACTGTTTGCATTTAAGCCATCTTTACCCGGCAGGAAGATCCTGATTGATCTGCTTCAGGTGGTACCCGCTTTACACTGTTCCTAGCTAGTTGAAGC

Associated Phenotype:

Not determined