ZMP

slc25a16

Ensembl ID:

ENSDARG00000057287

ZFIN ID:

ZDB-GENE-030131-3299

Description:

solute carrier family 25, member 16 [Source:RefSeq peptide;Acc:NP_991112]

Human Orthologue:

SLC25A16

Human Description:

solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 [Source:HGNC

Mouse Orthologue:

Slc25a16

Mouse Description:

solute carrier family 25 (mitochondrial carrier, Graves disease autoantigen), member 16 Gene [Source

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42171	Nonsense	Mutation detected in F1 DNA	Not yet available
sa22264	Essential Splice Site	Available for shipment	Available now
sa28091	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42171

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
ENSDART00000079902	Nonsense	95	321	4	10

Genomic Location (Zv9):

Chromosome 13 (position 18241413)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18061448
GRCz11	13	18192440

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGGACTCTATAAAGGAAATGGAGCTATGATGATCAGGATTTTCCCATA[T/A]GGGGCCATACAGTTCATGGCTTTTGATAACTACAAAAAGGTGCCTTTAGT

Long Flanking Sequence:

TTTATTTATTATTATTATTATTAGTAGCAGTATTATTATTATTATTTTAGTAGTAGTCGTAGTAATTGTTGTTGTTGTTGTTGTAGTAGTAGTAGTAGTAGTAGAAGTATTAGTATTATTTTTATTTTTATTATTATTGCTTTGATTTAAAAATTGATTGTAAATTTATAATTTTTTTTATCACAAAGGTGTTGCGGGATGCTGTGCCAAATCCACTATAGCGCCTCTTGATAGAGTGAAAATTTTGCTACAGGCTCAAAATCCTCATTACAAACACCTTGGTAAGTTAAGGTCCCAATATTTGCAGGTATTTTGCATAACTTGATTATTAGAGAACCTAAGGACTAGATAAAAGTTATTTTAAAAAAAAGTTATTGATGATCATATACATTGCATGTTTCTGCAGGAGTGTTTGCCACACTTAAGGCTGTGCCGAAAAAAGAGGGTTTCCTTGGACTCTATAAAGGAAATGGAGCTATGATGATCAGGATTTTCCCATA[T/A]GGGGCCATACAGTTCATGGCTTTTGATAACTACAAAAAGGTGCCTTTAGTCATCATTTACTTACTCTTTTTTGGGAATAAGAAACTAAATGTGTACAATTTTAGTAGTGTGACAGTTGTTCAAATACTGTTGTTTTTCCAGTCCCACTTTAGCAGTTAGTCACATTGTATGGCACAAAATAATAAAAATAGGCAGTAATCGTTCACAATCTCCTAAAATCGTCTCAAGAGAAACACTAGTCATTTTCGAGATTTCATTTATTCTGCTAATTTATTTCAGTAAGCCAGTTTACAAGACTATTAAACAATGATTGTACTGGTCGTTTTAGGTGTTATTTTGGTATAAAAATCAGATGACCGTTGTTCAAAAACCATAACTTTGGCCATAAATAGACATTATTCAAAGACTGTGATCTAAACCGTTCTTTGAAGTTAAATACTTGGCTAAATTATTTTGGAGGTTTTGTCTATTCTGAAAATGTTTTAAATAAATGTATTTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22264

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079902	Essential Splice Site	108	321	4	10

Genomic Location (Zv9):

Chromosome 13 (position 18241373)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18061408
GRCz11	13	18192400

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTCCCATATGGGGCCATACAGTTCATGGCTTTTGATAACTACAAAAAG[G/A]TGCCTTTAGTCATCATTTACTTACTCTTTTTTGGGAATAAGAAACTAAAT

Long Flanking Sequence:

ATTATTTTAGTAGTAGTCGTAGTAATTGTTGTTGTTGTTGTTGTAGTAGTAGTAGTAGTAGTAGAAGTATTAGTATTATTTTTATTTTTATTATTATTGCTTTGATTTAAAAATTGATTGTAAATTTATAATTTTTTTTATCACAAAGGTGTTGCGGGATGCTGTGCCAAATCCACTATAGCGCCTCTTGATAGAGTGAAAATTTTGCTACAGGCTCAAAATCCTCATTACAAACACCTTGGTAAGTTAAGGTCCCAATATTTGCAGGTATTTTGCATAACTTGATTATTAGAGAACCTAAGGACTAGATAAAAGTTATTTTAAAAAAAAGTTATTGATGATCATATACATTGCATGTTTCTGCAGGAGTGTTTGCCACACTTAAGGCTGTGCCGAAAAAAGAGGGTTTCCTTGGACTCTATAAAGGAAATGGAGCTATGATGATCAGGATTTTCCCATATGGGGCCATACAGTTCATGGCTTTTGATAACTACAAAAAG[G/A]TGCCTTTAGTCATCATTTACTTACTCTTTTTTGGGAATAAGAAACTAAATGTGTACAATTTTAGTAGTGTGACAGTTGTTCAAATACTGTTGTTTTTCCAGTCCCACTTTAGCAGTTAGTCACATTGTATGGCACAAAATAATAAAAATAGGCAGTAATCGTTCACAATCTCCTAAAATCGTCTCAAGAGAAACACTAGTCATTTTCGAGATTTCATTTATTCTGCTAATTTATTTCAGTAAGCCAGTTTACAAGACTATTAAACAATGATTGTACTGGTCGTTTTAGGTGTTATTTTGGTATAAAAATCAGATGACCGTTGTTCAAAAACCATAACTTTGGCCATAAATAGACATTATTCAAAGACTGTGATCTAAACCGTTCTTTGAAGTTAAATACTTGGCTAAATTATTTTGGAGGTTTTGTCTATTCTGAAAATGTTTTAAATAAATGTATTTAATCATGCTAGAATCATGCTAACAATATGCTATTTTATGTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28091

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079902	Essential Splice Site	170	321	6	10

Genomic Location (Zv9):

Chromosome 13 (position 18235016)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18055051
GRCz11	13	18186043

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCATCGGTACACCGGCATAAGACATGCCTTTCAGACAATTTACCATAAG[G/A]TATTAGGGATACAAACGAGTATAATTAAGAAAAAATCTGAGAATTCTTTG

Long Flanking Sequence:

AGTAGTAAACTTTATTGTCCTTTACAGGAAACTTGCTATGGGCATCACCATACTGCTGCAGACATTCCATAAGAACAAGCAATAAAAACAATACAAAATACAGCAGTTACGAAATTTATAATGCTGATTAAGATAGACTCTTGTTAAATAAACCTACTGAAATGGGTACAAAGGATTTCTTATAACAGTTTAACATACACTTTGGGACTTTGTATCTTCTACCAGAGGGAAGCAGTTCATAATGTGAAAACAAAAAATGGGTTTGATCCTTCACAATCCTTTCCACCTGATTGAGGACACAATTCTCATATAAATCTTGAGGATTAAAATAATTATAATTATTATATTAAAAATATCTGCTTTCTATTTCCTCTCCAGGGATGACTGCGGTTATTTGCACCTATCCACTGGATGTTATCCGAGCTCGCTTGGCATTTCAGGTGACAGGACACCATCGGTACACCGGCATAAGACATGCCTTTCAGACAATTTACCATAAG[G/A]TATTAGGGATACAAACGAGTATAATTAAGAAAAAATCTGAGAATTCTTTGCTTTTAATGACAGTGTTTTTAATCCTTAAAGGAAGGAGGAATCTCTGGTTTTTACCGTGGTCTGATACCCACAATCATTGGCATGGCTCCATATGCAGGTAACTTTCTTGTATGCGATTTTCTAGTATAAACATTTGCTTCACTGTAAAAAATGCTGGGTTTCACATAATAAATTTGTGTTGGGACAACATAAAAAAATTAAGTTAACTTATTAGTTTTTACTAATTTAAATGGATTGAACATAAAACAATTAAGCTGTCCCCTCAAAAACTCAAGAATGGTGGGTTTTAAATCAGGATTCCACACAATTCATTCATGTTGTCCCAACACAAATCAATTCAATTAACTTAACACATTTAAATAGATTGAACATAAAACAATTCATGTGTAACAAACATAATCTCAATAATTGAGTTTTTCAGCTCATTTTAAACAAGAAGTTTGAACAAG

Associated Phenotype:

Not determined