ZMP

galnt14

Ensembl ID:

ENSDARG00000023448

ZFIN ID:

ZDB-GENE-041014-351

Description:

polypeptide N-acetylgalactosaminyltransferase 14 [Source:RefSeq peptide;Acc:NP_001038460]

Human Orthologue:

GALNT14

Human Description:

UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 (GalNAc-T14) [So

Mouse Orthologue:

Galnt14

Mouse Description:

UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 Gene [Source:MGI

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37118	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37119	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa29422	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37118

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
ENSDART00000032161	Nonsense	47	554	2	15

Genomic Location (Zv9):

Chromosome 20 (position 38070512)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	38142924
GRCz11	20	38045803

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATACATGTAAAACCAATCTGACCGCAGTGTTTTCATTATGTTGTAGATCT[C/A]AGATACTGAGTGGGATGACCTGCTGGAAGAGTTTGAAGAGAAAAGCTACC

Long Flanking Sequence:

TTAATTACTGTTTAGAGTAATTAACTAATGTTGACAAATGGAGCCTTGTTGTAGGTGTTTATGAACAATAGATCTATAAAAAAACAGAACTATTTTATAAATATCTCTGGCATGTCGTAACTCAGATTAACACATGGAAATGTATATGTTAAAAATAAATGGCCAATTATGTGTTCAATCATCTGGTGCATTGATGAAAATCACTGTGAATAAAACAATCAGAATATTCTTTAAAAGCTTTTGAAGTGGTTAAATGCCCACAATAAAAACAATATCATGCATGTTCTTATCACAATATTATTTAATATCAGCTCATGTCTCTAAGCATGTTTTGAGTTATTGTTTATGCTGAAATTCTACTTAATATTCAAACATACATTTAACCCGATGTGCCTTTGACACCTAGTATTTCTATCAAAGGAGACCGTGTGAATAGAATGAATAGGCTTAATACATGTAAAACCAATCTGACCGCAGTGTTTTCATTATGTTGTAGATCT[C/A]AGATACTGAGTGGGATGACCTGCTGGAAGAGTTTGAAGAGAAAAGCTACCTCAGTGCTCACAGATGGAAACCGGGCCAGGACCCATACAGTCTGTATGCCTTCAATCAAAGAGAGAGCGAACGAATCCCCAGCAACAGAGCACTTAGAGACACCCGACATTACAGGTGTGTGTGTGTGTGTGTGATCTATATGTAATGCCCACACGCTTCATATTAAATTAATGAAGGTACATCTGTGAGTTCTTGAAAACTTTAAGAAACTGATGAAAGGTTTGCTGTGGTAAGAGGAGTTGGGATTAACATTGGCATTTTTATATATGGTTTAAAGCAGTGTAGTGAATAAGGTATCTATGTTTTGAAGTATTTTAAATATATGTAATATATAATAATTCTCCAGGTGCTTCTGTTTCCCACACAGTCCAAAGACATGCGGTATAGGTGAATTGAATAAGCTAAATTGGCCACTGTGTATTTGTGTTAATGAGAGTGTATGGGTGTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37119

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
ENSDART00000032161	Essential Splice Site	220	554	6	15

Genomic Location (Zv9):

Chromosome 20 (position 38108298)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	38180710
GRCz11	20	38083589

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAGGTCAACAAAGATTGGCTGCCTCCACTGCTGCAGAGGGTCAAAGAGG[T/C]ACCATTTTATATTCAGTTTTGTTGTGTTCAAAGTCTGCTAAGAAATTCTG

Long Flanking Sequence:

AAAAAACTAAAAGTATCCATGTTTTACTATGTGTGTATATTCATTTTTGCACAGCACAATTCTAATGTAATAACTTCAGATTAGTTTAGAAATTTTAATTTTGTGAAATAACCCAGATTTTAGGTTACAGGAAAAGAAAACATTTCTGATTCTGATCAAATGTTATTTTTTGTAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAACCAAAAGACTTTATTTTGAATTTGGAAAAAATGTTATCAGATCTGTATTAAATAAAACAGATACTAACATTTGAATCAAACCTACGCCTAAAAAATACTGGGAATTTGAAAGAATTTTATAGCTTATGTGTCTGTCTGTGTGTCAATATTTGTTTGTGTGTGTGTTTTTTCAGGATTGATCCGCTCTCGTGTTCGAGGGGCTGACGCTGCAGGAGCCCAGATCCTGACTTTTTTGGACAGTCACTGTGAGGTCAACAAAGATTGGCTGCCTCCACTGCTGCAGAGGGTCAAAGAGG[T/C]ACCATTTTATATTCAGTTTTGTTGTGTTCAAAGTCTGCTAAGAAATTCTGCCTGCATGATATGCTATTTTTTCCATCTTTTAGTGTCCTCTTTCAATTCGTTTTCTGTGGAGAAGGGTCAGCGGTTAGTAAATGTAACATTTCTTGTCAAGCACAACAAAATAACGCCACTTTGTTCTGCTTAAATGTTAGCAGCACTGCTATTTGACTTTTGACCAGCAGACTTCCACAAAACTAATGCTGTCAATGTGTTAAACATTCAATACACCAGCAGTGATGTTCAACTTTTTATTTACTTTGTTTACAGTTCATTTCACAACCATGAAATTATGATTTTTTTCACAACAAATCAGCATTTAGCTGACACCTGTTGTTCAGACACAATTTGTTAATGAACAAGCCAAAACATTTTAGTTATGTTACATCACAAACATATGTTGTCGCTTGTCACATTAAAGATTATAGTACATTATGAATGAAATCAGTATGTTTGATTAAAGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29422

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
ENSDART00000032161	Nonsense	432	554	13	15

Genomic Location (Zv9):

Chromosome 20 (position 38128779)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	38201191
GRCz11	20	38104070

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTGATGATTCTGATGCCAAGTCTGGTGTGATCCGGCAGAGACAGAACTG[T/A]CTAGAGTCTCGAGTAGTCGAAGGCCAGGATCTCCCAGTGCTCACACTCGC

Long Flanking Sequence:

ATAGAATTTGAGGTGCACTCAAAAATTCAATGAATCTTATGAAATGTGCTGCTTACCTTTGGAATTTTCATTGGACGATTGAGTTAAAGGTAAAAAGGTAATTGAAAGATGTACTTGGATGAATAATTCAGGTATGTTCAACTTAAGAACTTACAAAACAAATGCATTTTATTTAAATGTTCATTTCACGTTGATATTTTCATGGGCTATTTATAGCTTTTTGTGGCTGAATTTTCATAAAAATCTTTATGTTGAGTTTTCATATAAATACAGGCTCTTTGGTCACTCTGTGTATGTATATGACATACAGTGAGGTATTGAGTATTATAGCAACCGCTCTAAATACAATATCCTTTAGGAGCAAGAATTGAGACCTCATTTAAGTGTACCCTTTATTCTGTATATTTGTTATTATAATACTATTGTGCTTAATTCCCTCGATCCAGAGTACCTGATGATTCTGATGCCAAGTCTGGTGTGATCCGGCAGAGACAGAACTG[T/A]CTAGAGTCTCGAGTAGTCGAAGGCCAGGATCTCCCAGTGCTCACACTCGCACCCTGCATCATCACCAAAGAGACACCAGCAGCCAATCAGGTACAAGACTCCATGACATAATATCAGAAGGAGCATGCATTAATTATTAAATAAGCAGCTTTCTTTTTCTATATCAATAAATACTTCTATCGTTCACTCTTTAAAATAAAGATTTCAAAATTAGGTTTTAACACAAATGCAATAGAAGAGTCATTTTGAGTTCCTCAAAGAACATTTTAAGAAGCCTTAAGAAGTTTTTCTCCATAAAGAACCTTTTGTTGAAAGGAAAGGTTCTATGGATGCTATATTTCCTTCATGGAACCATCAATAGAGTGGATGAACTATGACGTCACCTTGTAGACCAATCGGCTGTTAGCATAAAACTGGTTCCCTCGTCAAAATCCCCATAGGATTTTCCCATAGTGTTTTTGAAGATTGCAAGTAATAAGCTGTATGTTCAAACAGTTCAT

Associated Phenotype:

Not determined