ZMP

b4galt7

Ensembl ID:

ENSDARG00000021899

ZFIN ID:

ZDB-GENE-040727-3

Description:

beta-1,4-galactosyltransferase 7 [Source:RefSeq peptide;Acc:NP_001003417]

Human Orthologue:

B4GALT7

Human Description:

xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I) [Source:HGNC

Mouse Orthologue:

B4galt7

Mouse Description:

xylosylprotein beta1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I) Gene [Source:M

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39001	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa22486	Essential Splice Site	Available for shipment	Available now
sa35695	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa39001

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
ENSDART00000037999	Essential Splice Site	203	317	3	6

Genomic Location (Zv9):

Chromosome 14 (position 27394538)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26087335
GRCz11	14	26385440

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACGTATGTTGGAGGAATCCTGCTGCTCACTAAGAAACATTATCTGGCGG[T/C]AAGAAACCCAAAGTCTTTGGAACATTCTGGGATTTTCCGAATTTGTTTGT

Long Flanking Sequence:

GGTGAGTATTATTAACAACACTGTTTGTTTGTTTGTTTGTTTGCTAGTTATAGTTTTTGTGCTATTGTTACCTGAGATCTATCATACACTAACATTTAAAAATCATATCTAATTATTGTTTTCAGTTGTTTGTGTTTTTTAATTTTTTAAAAATGTTTTCCCCATGAAAATAGCTCTTGTTGCTGACATGGCACTAAATAAATATACTTGCTATGATACCAGTTGTTTATTGGAAGCACACATTATGATTTTGTTTTCTAACTCTTGTCTCAGGTTCAATCGTGCCTCTCTTATTAACGTTGGCTTCATGGAAAGTGGGAATGACACAGACTACATTGCAATGCATGATGTGGACTTGTTGCCTCAAAACGAGGATCTGAACTATGGGTTTCCAGTAGACGGGCCCTTCCACGTGGCCTCACCAGAGCTTCATCCTTTATATCACTATAAGACGTATGTTGGAGGAATCCTGCTGCTCACTAAGAAACATTATCTGGCGG[T/C]AAGAAACCCAAAGTCTTTGGAACATTCTGGGATTTTCCGAATTTGTTTGTAAATTACAATTGCTTGTGATTTCTGCCTAAAGTGCAACGGGATGTCAAACCGCTTTTGGGGATGGGGAAGAGAAGATGACGAGTTTTTCAGGAGACTGAAAGCAGCTAATCTTGAGGTACATGATATAATCTAATCTAATCTAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAAACAATTGTCAATGTATATTTGCAGCTTTTTAGACCAACAGGTATTACTACAGGAACTAAAACATTTAGACACATCCATGATCCAGCCTGGAGAAAAAGAGACCAGAAGCGGATCGCTGCACAAAAACAGGTAATATTCATTAATATTTAAAAAGCTTTTTGACAAAAATATGTTGCTTATTAAGGCTGCATTTATTTAATTTTAAATAAAATAAAAACATTAATGTTGTAAAATATTAGAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22486

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037999	Essential Splice Site	231	317	4	6

Genomic Location (Zv9):

Chromosome 14 (position 27394370)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26087167
GRCz11	14	26385272

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGAGAAGATGACGAGTTTTTCAGGAGACTGAAAGCAGCTAATCTTGAGG[T/G]ACATGATATAATCTAATCTAATCTAATATAATATAATATAATATAATATA

Long Flanking Sequence:

AATAGCTCTTGTTGCTGACATGGCACTAAATAAATATACTTGCTATGATACCAGTTGTTTATTGGAAGCACACATTATGATTTTGTTTTCTAACTCTTGTCTCAGGTTCAATCGTGCCTCTCTTATTAACGTTGGCTTCATGGAAAGTGGGAATGACACAGACTACATTGCAATGCATGATGTGGACTTGTTGCCTCAAAACGAGGATCTGAACTATGGGTTTCCAGTAGACGGGCCCTTCCACGTGGCCTCACCAGAGCTTCATCCTTTATATCACTATAAGACGTATGTTGGAGGAATCCTGCTGCTCACTAAGAAACATTATCTGGCGGTAAGAAACCCAAAGTCTTTGGAACATTCTGGGATTTTCCGAATTTGTTTGTAAATTACAATTGCTTGTGATTTCTGCCTAAAGTGCAACGGGATGTCAAACCGCTTTTGGGGATGGGGAAGAGAAGATGACGAGTTTTTCAGGAGACTGAAAGCAGCTAATCTTGAGG[T/G]ACATGATATAATCTAATCTAATCTAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAAACAATTGTCAATGTATATTTGCAGCTTTTTAGACCAACAGGTATTACTACAGGAACTAAAACATTTAGACACATCCATGATCCAGCCTGGAGAAAAAGAGACCAGAAGCGGATCGCTGCACAAAAACAGGTAATATTCATTAATATTTAAAAAGCTTTTTGACAAAAATATGTTGCTTATTAAGGCTGCATTTATTTAATTTTAAATAAAATAAAAACATTAATGTTGTAAAATATTAGAACAATATAAAAGGGCTGTTTGTGTTTATTGCTATTATTTATTTATTACTTTTTGAATGTTCCTCAGCTGTTACTCGAGGCTTAAGTTTCATATGTTTCTTCTGAAATCATATGATAATCTGATCCTCTAGAATCATTTGTTATATTATCATTGTTAAATATGAGCTGCCTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35695

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
ENSDART00000037999	Nonsense	274	317	6	6

Genomic Location (Zv9):

Chromosome 14 (position 27391305)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26084102
GRCz11	14	26382207

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGTTTCAGCTTCTGTCTGCTTTTGGCAGGAGCAGTTTAAGGTGGACCCT[G/T]AGGGTGGCCTGAGTAACCTTCGCTACAAGGTGGAGTCCAGAAAAGAAGTG

Long Flanking Sequence:

ACATCATATGTATCGCTAAAAATCCTGAACTTATTTTAATGGTATTTGTTTTAGCAATTTCATCAAATAGCCATACCTTCCTGATGTGGCAATAAATGAACAAACGACAGCAGTGAGGAATCGTTTCTTCACTGTTGTTGCAATCATTTTTCAATTGCAGAATGGGAATTGACTCATTTCATTTTTAAAGATCGTTGATTAGATATTGAATGGTTATAGAATGATTGAATACATTTCCGTCAACACATTTGGATTGTTCACTTCAATAAAAATTTTTCAAATAGCCATTAAAATAGAGACTTTCTGTGATTTCACCGATTTTGAAGTGTCACACAGTATGACACAAATTAGATTTAGCCAAATTAGCAGTGTCATTATATAAACTTGGCCCCATTTACACCTGGCAACTGACAAACAGATGTTGATATTAGGTTGTAAACAAGGCCAACTGTGTTTCAGCTTCTGTCTGCTTTTGGCAGGAGCAGTTTAAGGTGGACCCT[G/T]AGGGTGGCCTGAGTAACCTTCGCTACAAGGTGGAGTCCAGAAAAGAAGTGTCTATCAGTGGAGCTCCATGTACTGTGATCAACACCTTTGTGGAGTGTGACCTCAACCAGACCCCATGGTGCCAGTTCAGCTAATAATAGTTGATAATGCATAATTCACTTAATGCTTGAACAGGACCTGGGAAGCCAGAATGATACGGATTCTCCTTCTGTGGTGCAAGGAAAGCTTTCACAGATTATCAGTGCCAGTCACACTTGAAAAAAAAAAAAACAGATCGTCGAACCAAAAGGACTTGAATGTGTGACTGGTGGAAAAGGAGGCTTTATTTTTCTATGACAAGTGTTTTTGACTTCATCCCCGATGAAGCTTTGCCTCGTATTTGAAGAGAATTATGGACCATTAACAGGTACAGCACTGAGTTTGCATCAGCGACACTGCAAGCATCAAAATGTCTGATTTTTAACGATGAGTTTTATAATATTTTTAGCTGTAGCCGTGGC

Associated Phenotype:

Not determined