ZMP

si:dkey-204f11.59

Ensembl ID:

ENSDARG00000024708

ZFIN ID:

ZDB-GENE-040724-220

Description:

solute carrier family 25, member 23 [Source:RefSeq peptide;Acc:NP_001038417]

Human Orthologues:

SLC25A23, SLC25A41

Human Descriptions:

solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 [Source:HGNC Symbol;A
solute carrier family 25, member 41 [Source:HGNC Symbol;Acc:28533]

Mouse Orthologues:

Slc25a23, Slc25a41

Mouse Descriptions:

solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 Gene [Source:MGI Symb
solute carrier family 25, member 41 Gene [Source:MGI Symbol;Acc:MGI:2144215]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20065	Nonsense	Available for shipment	Available now
sa40107	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20065

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
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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000030530	Nonsense	324	478	9	11
ENSDART00000145859	Nonsense	327	481	8	10

Genomic Location (Zv9):

Chromosome 3 (position 34312933)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	34098129
GRCz11	3	34227637

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCTTTCTGTTTCTCAGGTGTTGAAGACCCGTTTGACCCTTCGGAAGACT[G/T]GACAGTATTCTGGCATGGCAGACTGTGCCAAGCAGATACTGCGTAAAGAA

Long Flanking Sequence:

AATGAGAATCAGACCTGGCACATTTCTTTACTGATCTGACTCACATAATGTCTGTCTGAAAAGGTATCTGTCATCTCAAGTCGTGTGTAGTGTTCACAGATTTCAAACACCAGAGAATCATGTAACAGAGGAAGCTGTTAAACAAAGTTGTTCCTAATTTGTTTGCTTGTTAATTTATGCTATTCTAAATGCTCAAAGAGCCTGAAAATAAGCCGGGTCTGACTGTGAACATCTTCGATTGTCTACTCCTGGTAGGCTTCAATGCAAAAAACAAGCTTCTTTTCTGTCTTCGATTATTTATTCATTGAGCAGATCGGATTTTTAGAAGCCAAACACTTCATTTATTTATTTAAAGCACTTGATTAGACATGCTGAACAGAGCTGCTGATACTTACAGTTTCCTTGCAGGACCTCTAAGCTTTCTCTATATTTTCTGTATTGTTACTCTGTTCCTTTCTGTTTCTCAGGTGTTGAAGACCCGTTTGACCCTTCGGAAGACT[G/T]GACAGTATTCTGGCATGGCAGACTGTGCCAAGCAGATACTGCGTAAAGAAGGAGTGCGTGCGTTCTATAAGGGCTATGTGCCCAACACACTTGGCATCATCCCTTATGCTGGCATTGATCTGGCTGTCTATGAGGTATGGCTCTGTGTGTGTGTGTGTGTGTGTATGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTTTTACACATTAAAGTGTTTGTGAATGCTTTATGCCATTGACAAGCTCTGGGAATTCATCATTCTGAGTTGCTATGGTTTGTTAAACGATGTTATGTATTTACGTTGCTGTGTTCTGTCGTCTCTTCCCAACAACTCACAGATTATTTTTCAGCTGAACTCTATTAACCCCTTGTCATTCTTTACTTGGTGCCAAAAAACATCTTTTATTCAGCCAAGCATGCAATAAACTGATTAAAATTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40107

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000030530	Nonsense	374	478	10	11
ENSDART00000145859	Nonsense	377	481	9	10

Genomic Location (Zv9):

Chromosome 3 (position 34315416)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	34100612
GRCz11	3	34230120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTAAAAGTATATCTATAACCCTGTTCTCTCAGACACTGAAGAACGCTTG[G/A]CTCCAGCGGTACTGTATGGGCTCGGCTGATCCAGGAGTTCTGGTGCTGCT

Long Flanking Sequence:

GGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAACAGATGCTGGATAAGTTGGCGGTTCATTCCACTGTGGCAACCCCAGATTAATAAAATGAATGAATGAATGAATATATTTTGTGGCGATGGTGCAGTGGGTAGCGCTCTCGCCTCACAACAAGAAGGTCGCTGGTTCGAGCCTTGGCAGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCTTGTGTTTGCATGGGTTTCCCATGGTATAGGTGAATTGGGTAAGCTGAATTGTCCTTAGTGTATGTGTGTGAATAAGTGTGTAGGGATGTTTCCCAGTGATGGGATTGCATTTGCTGCATAAACATATGCTGGATAAGTTGATGGTTTATTCCGCTGTGGCGACCCCTGATTAATAAAGTGACTAAGCCGAAAATAAAATAAAAAATTATAGATTTTTTTGTACATATATTTAAAAGTATATCTATAACCCTGTTCTCTCAGACACTGAAGAACGCTTG[G/A]CTCCAGCGGTACTGTATGGGCTCGGCTGATCCAGGAGTTCTGGTGCTGCTGGCATGTGGCACTGTGTCCAGCACATGTGGACAGCTGGCTAGTTACCCACTCGCTTTAATCCGAACCCGCATGCAGGCTCAGGGTGAGCCAGATCTAATTCAATCACATAATTCTCTAGTCATATTACTCCGCTTCCCTTGCAGTTCTTTATGAGACCAAATATGTTCGCAAGCACAATAATATTCTTTCATTTCTCCCTTTGTTCTTGACAGCCTCAGCAGAAGGCGCTCCTCAGCTGTCGATGGTTGGTCAGTTCAAGCACATTGTGTCCCATGAGGGCGTTCCAGGACTGTACCGTGGCATCGCCCCCAATTTCCTCAAAGTCATTCCTGCTGTGAGCATCTCTTATGTGGTTTATGAGCATATGAAGAAAGCACTGGGAGTGGGATCTTAAATGAAGACGCAGGGTCCAAGAGAAGAACCCGTAGTTAAAGAGGACAATGTAACTT

Associated Phenotype:

Not determined