ZMP

slc30a9

Ensembl ID:

ENSDARG00000057272

ZFIN ID:

ZDB-GENE-040724-254

Description:

Zinc transporter 9 [Source:UniProtKB/Swiss-Prot;Acc:Q5PQZ3]

Human Orthologue:

SLC30A9

Human Description:

solute carrier family 30 (zinc transporter), member 9 [Source:HGNC Symbol;Acc:1329]

Mouse Orthologue:

Slc30a9

Mouse Description:

solute carrier family 30 (zinc transporter), member 9 Gene [Source:MGI Symbol;Acc:MGI:1923690]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24966	Nonsense	Mutation detected in F1 DNA	Not yet available
sa42441	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24966

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
ENSDART00000079860	Nonsense	129	336	7	12
ENSDART00000079866	Nonsense	366	573	14	19
ENSDART00000138897	None	None	89	None	4

Genomic Location (Zv9):

Chromosome 14 (position 47037638)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	44354765
GRCz11	14	44816077

KASP Assay ID:

554-7637.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACACATCACTAACATCATCTGTCTGCTGATTTACTTAAAGCTACACTGT[T/A]AGTGGCCATTAATGAGATCAAGAAGAGTGCACGTACACAAGGCTTGTCCT

Long Flanking Sequence:

CTCTTTTAAATAGTTTTTTTTTCTTGCCATTACTTTAGTTTTCAGTGTCTCGTGATTCTCCATTAAGTTATTCTAATATACTAATTTGGTGCTCAATAAATATTTGTTCTTTATAATCACTGTGTTGTTGCTGTGAAGGTATATTTTTATACTTTATTACGTTTTGTTTTTTTAGATTTCTTTGTTCATTAGACATTTCAAAAGAACTGCAACTTTTCATACTATAGTTTTTTTTTTAATTATAAATAAATTTGCTGTAACTTTTGACCAATTTAATACATTACTTCTGAATTAAAGTTACAACATCTTTAAAAAACAATCCTTGTGTATTTATTAGATGTGTATATATTATTTTTCAGGCATATTGTATTTTAGCAGGATCTCTGGTATCTGAAGGAGGTGAGATTTGTTTTTTCTTCCGAATTTTCATTAGCATTCACAAATGTGTCTGACACATCACTAACATCATCTGTCTGCTGATTTACTTAAAGCTACACTGT[T/A]AGTGGCCATTAATGAGATCAAGAAGAGTGCACGTACACAAGGCTTGTCCTTTTACGAGTACGGTAAGTACCTTCTATCAGCCTATACTGTTACAGTATTTGATTGTAATTGTAGTTTGGAGACGACCAGTTGATCATGCTTGCTTGTTTGTATGTGACAGTAATGCAAAGTCGAGACCCCAGCACTAATGTGGTCCTGTTGGAGGACGCTGCTGCTGTGCTTGGGGTGGTGTTGGCAGCTGGATGTATGGGACTCACATCTCTTACAGGTATTGCATTTTTATTATACCATGTTTCTTTTTAAAGGAACACGCCACTTTTTTTTTGAAAATAGGCTAATTTTCCAATTTCCCTAGAGTTAAACATTTAAGTTTTACCATTTTTAAGTCCATTAAGCCAATCTCTGGGCCTTGCTGGAGCACTTTTAGCTTAGCTTAGCATAAATCATTGAATTGGATCAGACCATTAGCAATTAAAAAAGAGCTTTAATAATATTTATGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42441

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079860	Essential Splice Site	150	336	8	12
ENSDART00000079866	Essential Splice Site	387	573	15	19
ENSDART00000138897	None	None	89	None	4

Genomic Location (Zv9):

Chromosome 14 (position 47037798)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	44354925
GRCz11	14	44816237

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTAGTTTGGAGACGACCAGTTGATCATGCTTGCTTGTTTGTATGTGACA[G/T]TAATGCAAAGTCGAGACCCCAGCACTAATGTGGTCCTGTTGGAGGACGCT

Long Flanking Sequence:

GTTTTGTTTTTTTAGATTTCTTTGTTCATTAGACATTTCAAAAGAACTGCAACTTTTCATACTATAGTTTTTTTTTTAATTATAAATAAATTTGCTGTAACTTTTGACCAATTTAATACATTACTTCTGAATTAAAGTTACAACATCTTTAAAAAACAATCCTTGTGTATTTATTAGATGTGTATATATTATTTTTCAGGCATATTGTATTTTAGCAGGATCTCTGGTATCTGAAGGAGGTGAGATTTGTTTTTTCTTCCGAATTTTCATTAGCATTCACAAATGTGTCTGACACATCACTAACATCATCTGTCTGCTGATTTACTTAAAGCTACACTGTTAGTGGCCATTAATGAGATCAAGAAGAGTGCACGTACACAAGGCTTGTCCTTTTACGAGTACGGTAAGTACCTTCTATCAGCCTATACTGTTACAGTATTTGATTGTAATTGTAGTTTGGAGACGACCAGTTGATCATGCTTGCTTGTTTGTATGTGACA[G/T]TAATGCAAAGTCGAGACCCCAGCACTAATGTGGTCCTGTTGGAGGACGCTGCTGCTGTGCTTGGGGTGGTGTTGGCAGCTGGATGTATGGGACTCACATCTCTTACAGGTATTGCATTTTTATTATACCATGTTTCTTTTTAAAGGAACACGCCACTTTTTTTTTGAAAATAGGCTAATTTTCCAATTTCCCTAGAGTTAAACATTTAAGTTTTACCATTTTTAAGTCCATTAAGCCAATCTCTGGGCCTTGCTGGAGCACTTTTAGCTTAGCTTAGCATAAATCATTGAATTGGATCAGACCATTAGCAATTAAAAAAGAGCTTTAATAATATTTATGTTTAAAACTTGACTCTTCTGTAGTTACATTGTGTACTAAAATCAACAGAAAATTGAATGGTTTTTTAAGGTCTATATGGCTAGGTTTTTATGAGGTCTATATGGCTAGGAACTATACTCTCATTCTGTGTTCACACCAGACGCGGAACGTGCGTAAATAGC

Associated Phenotype:

Not determined