ZMP

zgc:91960

Ensembl ID:

ENSDARG00000059365

ZFIN ID:

ZDB-GENE-040718-412

Description:

magnesium transporter NIPA4 [Source:RefSeq peptide;Acc:NP_001002664]

Human Orthologue:

NIPAL4

Human Description:

NIPA-like domain containing 4 [Source:HGNC Symbol;Acc:28018]

Mouse Orthologue:

Nipal4

Mouse Description:

NIPA-like domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:2444671]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11592	Nonsense	Available for shipment	Available now
sa9713	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa11592

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082469	Nonsense	115	407	3	6
ENSDART00000139320	Nonsense	119	411	3	6

Genomic Location (Zv9):

Chromosome 21 (position 25502237)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	26072055
GRCz11	21	26108750

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTCTGTTTAGCCGAGGGAGGTCATGGGTACCTGAAAGACTGGCTATGGT[G/A]GGGAGGCCTTTTGACAAGTAAGTGCAATGCAAAGCAATTGTAAATAACCT

Long Flanking Sequence:

CATAGAAGTCAGTCAAAAAACTTGTTTAAACTACTTATTTAAAATGAATTGAAACAACACAATTCTTAAGGTTTTTTTGGGGACAAATTTATTGTTTAATGTTCAGTCCATGTAAATTTGTATAAACAATCAAGTTAACTAAATCGATTTGTGTTGGGACAACATGAAGGAATTGTGTGAAACACAGCATATTTTACACTGTCCGCTACATGAAAAGTCCTGGATTGGAATGTTTTCCTTAAAAGCCTTAATTTCATTTCAGCTGGAAGTGAATTAATACTTAAATTGTTAGAGAAACTTGTCATATGGGGGTATGTAATGTTTATTTTTTTTTACTTGACTGAATAGCAATTGCAAAATTGGTTGAAACTGGTTTCTTTGTTTGCTTAACTAATACTGACAGAATACTGAGTCAAGTGTTCTTTAATGCGCTAAATTACTGGAAATGTTTGTCTGTTTAGCCGAGGGAGGTCATGGGTACCTGAAAGACTGGCTATGGT[G/A]GGGAGGCCTTTTGACAAGTAAGTGCAATGCAAAGCAATTGTAAATAACCTTTTGATGACTCTGATAACATCTTCTAATGTTCTGGCAGTGGGCGGAGGTGAAGCAGCAAATTTCGCAGCCTACATGTTTGCTCCAGCCACAGTGGTGACCCCGCTAGGAGCTCTCAGTGTTCTTATTAGGTAATGGCACGCCTTTATTTACACTCGCCAATGGTCTGATCCACACTGTGCTGTGTAAACTTTACAAGCCTGTGAGTGAGAGGACCAATGTGTTTTGAAATATATACCAAATGACTAAAATGTTCAACATGCCAAACTTGTTTTGTGCTATTATTGTGGAACTTTGGTGTCAAGTATGTTTAATGTATTATTTTACATTTTCAGGAATATATATTAACTTTTTCTACACTCAAAAAAAGAAAAGATTTTTGCTGTTTGTTCAAACTATTCAAATAGTGCTGAAACACAATCCTTGAATTCAATTTTTTTTGGGGGGGGGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9713

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082469	Essential Splice Site	205	407	5	6
ENSDART00000139320	Essential Splice Site	209	411	5	6

Genomic Location (Zv9):

Chromosome 21 (position 25493410)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	26063228
GRCz11	21	26099923

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAAGAGGTGACCACACTTAAAGAAATGGCCGAGAAACTCCTTGATCCTGG[T/C]TAGTGTTAAAATTCCTTTAAWTTTTGAACTCCAAAAGCAGTTGCTATGGA

Long Flanking Sequence:

GCCAGGACATTGGAATACATTCATTTCAAATAGAAAGTCTCAACAGAGCTCTATATGATGTCATTTTAACTTAAACTGATTTGCCCAAAAAGCCTGTCAATTGATTATTTCAATAATTATAATCAGTTCATTATGATTATTTTTTTATTTATATTTTAGAATATTATAAGCATATGCTAAGTATATTGAAGTGCATGCATTATAGCTGAATCCTTTGCACATTACTTACTCTTTATGAAAACGTTGAATTCCTGTAATAGCCTTTATGTTTCTTTCTGGTGTTTTCATTAGAGCTAAATGGAAAGGTAGTAGTGTTAATGTTTATTTACTCTCTTCAGCGCGGTGCTGTCCTCCCACTTGTTCAGAGAAACAATGAATCTGCTTGGAAAATTGGGCTGCATGCTCAGCGTACTGGGAAGCACTTTAATGGTTATACATGCACCTGAAGAAGAAGAGGTGACCACACTTAAAGAAATGGCCGAGAAACTCCTTGATCCTGG[T/C]TAGTGTTAAAATTCCTTTAATTTTTGAACTCCAAAAGCAGTTGCTATGGATAACAACAGGTTTTTATGCTTCTCCTGCAAGGTTTTCTGGTGTTTGCCAGCATCCTGTTGGTCACTTGTTTAATCCTGATCTTCTACGTCTCTCCTCGATTTGGTCAGTCTAATATATTGGTATACATCAGCATCTGCTCTCTGCTCGGATCCTTTACTGTGTCCTCTGTCAAGGGTCTTGGCATTGCCATCCGCACCATGTTCACAGACACTTCAGTGGTCCGTAATCCTCTCATGTGGATTCTTTTGCTGACCTTAATTGGATCCATCATCATTCAGGTCAACTATCTGAACAAATCCCTGGATACTTTCAATACTCTTTTGGTTTACCCCATCTACTACGTCTTCTTCACCACAGTGGTCCTGAGCACGTCTGTGATCCTTTTTAAGGAATGGGGTGCCATGTCAGGAGTGGATGTGGTGGGCACCATTGGGGCATTTTTGGTGATT

Associated Phenotype:

Not determined