ZMP

zgc:152990

Ensembl ID:

ENSDARG00000060796

ZFIN IDs:

ZDB-GENE-060929-828, ZDB-GENE-060929-828

Description:

sodium-dependent phosphate transporter 2 [Source:RefSeq peptide;Acc:NP_001071014]

Human Orthologue:

SLC20A2

Human Description:

solute carrier family 20 (phosphate transporter), member 2 [Source:HGNC Symbol;Acc:10947]

Mouse Orthologue:

Slc20a2

Mouse Description:

solute carrier family 20, member 2 Gene [Source:MGI Symbol;Acc:MGI:97851]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21321	Nonsense	Available for shipment	Available now
sa34429	Essential Splice Site, Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21321

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086044	Nonsense	79	496	2	12
ENSDART00000086047	Nonsense	79	496	2	11

Genomic Location (Zv9):

Chromosome 8 (position 30667321)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	29810047
GRCz11	8	29819279

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGTGCCAAGGTCGGGGAAACCATCCGGAAGGGAATTATAGACGTCAGTT[T/A]GTACAATGACACAGTGCCCATACTGATGGCGGGAGAGGTCAGCGCCATGG

Long Flanking Sequence:

GACGGGACACTTTGAGGGCCAAACAATGGAATGCTCTCTCCTGCCTTCACCGCACTGCACTCAACAGACTGAGGTTAAACGCTTTAGTTAGCAGTGTGCCTCTTCCCAAAAAACTCTCTTTAGCTAGGGGAAAGTTGGGAGAAATAAAACAAAAAACACACAAGTGAAGGAAAACGACCTTCATAGTACAGCACCTTATTCCACTTCTTTGTAGTTCGAGTTTGTCTTGGATTCTTTCAGAAGCTTTACGTGCACAAACACCAAGATGGATTTGGAATCGTATCTGTGGATGGTGGTGATTGGCTTCATTATAGCCTTCATCCTGGCATTTTCGGTGGGAGCCAATGACGTGGCCAACTCATTTGGGACGGCGGTGGGGTCAGGAGTGGTGACGCTACGTCAGGCCTGCATTCTGGCATCCATATTTGAGACCCTGGGCTCCATGCTCCTTGGTGCCAAGGTCGGGGAAACCATCCGGAAGGGAATTATAGACGTCAGTT[T/A]GTACAATGACACAGTGCCCATACTGATGGCGGGAGAGGTCAGCGCCATGGTCGGTAAGTGATGGCTCATTTAAAGTTGAAAGCTCAATGTGTCATTGCGAAGATTAACGATGGAGAAGCTTACTGAGGCATTTGTTTGTTCAATGTTGGCTGCCGGATTCTGGTAGTTGTAACCACTGTGAAAAAAAAAGTTGTTGCTGCTTTTACATTTTGAAGTTGAAGCAATTTAACTTTACAAGTTATTTAATGTTGCATTGAAACTTGATTAACTTATTTAAATGAATTCTATTACATGTTACTACATGTAATTACATAGCTTTATACTACTACAAACTACATGTAACTGCTTTTGATGACATTTTTGATCATATACTTTTTATTAATGCCGAGTTTTTAAGAAATCACTTCCAAAAAATTTATCACACTTTATTTTAAGGTTTCAGTCTCGAAATTAAACTGTGCATCAGCCACAGCCATGTCACCCTGCAGCCCAAGACCGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34429

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:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086044	Missense	361	496	8	12
ENSDART00000086047	Essential Splice Site	360	496	None	11

Genomic Location (Zv9):

Chromosome 8 (position 30647544)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	29790270
GRCz11	8	29799502

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAGGTTTACCATACCGTCCACAAAGACTCTGGTCTCTACAAAGACCTCC[T/A]GCACAAAATCCACAAGGGCCGCCTGGAGGATGAGCGCCACGGCTCCCGTC

Long Flanking Sequence:

TTTACCTTTTTTAAACAACCAACTATTTACAGCTTTTACTCAAAGCAAAAATCTAAAATTACACCTGAAAGATATATAGACCTTTAACTTTTATTGTGATAAATATCAATGTCAATTGACAATTTGTGAATTTAATTTAAAAATGTTGTGTTTATTTTTTATTATTATTATTATTATTTATTTTATTTTATATTTTATATATTTAAAAAAATATATATATTTATTTAAAAATAATTACATTTAATTTAATTTTATTTTGGGGACATATTAGCCAGCCCATAACTACCTTTTGACAAAAATGTCCTCTGCTAAGCTAAGATATATTTGTTTCATTTAATGTTTGTTTGTTTTGTTTTCATCAGGTCGCACCAACTCCATGACCAATGGCTGCCTGAAATCTCCCGTTTCCAATGGAGGCTTCAGCTTCGACGGCCACATGCGCAGCGATGGCCAGGTTTACCATACCGTCCACAAAGACTCTGGTCTCTACAAAGACCTCC[T/A]GCACAAAATCCACAAGGGCCGCCTGGAGGATGAGCGCCACGGCTCCCGTCCCGACAACAACTACCGTCACCTCCGCCGCAACAACAGCTACACCTGCTACACTGCGGCCATTTGTGGGATGCCTGTACAGCCGCTCTTGCGCTCTGAATCCAGTGCGCCTCCGCCAGAGGACAGCGAGAAGCTTGTAGGCGACACCGTTTTCTACTCCAAGAAGCGTCTGCGCTACGACAGCTACTCCAGTTACTGTAATGCCGTGGCGGAGGCTGAGATTGAAGCGGAGGAGGGCGATGTGGATGTGAATCTGGCGGCAGATAAAAGGGAGCCACGGGTTCCGGCTGAAGGGGTGTTAGAGGACTGTGTTGATGAGGACAAGGCGGAGAAAGACAATTCTCAGGTCTTCCTGCTCTTCCACTTTCTGCAGATCCTCACAGCCTGCTTCGGCTCTTTCGCACATGGGGGGAATGATGTCAGGTAAGAGGACACTCAATGTGTTGGTTAAT

Associated Phenotype:

Not determined