ZMP

slc26a6l

Ensembl ID:

ENSDARG00000054127

ZFIN ID:

ZDB-GENE-080220-10

Description:

solute carrier family 26, member 6 [Source:RefSeq peptide;Acc:NP_001107889]

Human Orthologue:

SLC26A6

Human Description:

solute carrier family 26, member 6 [Source:HGNC Symbol;Acc:14472]

Mouse Orthologue:

Slc26a6

Mouse Description:

solute carrier family 26, member 6 Gene [Source:MGI Symbol;Acc:MGI:2159728]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9249	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38573	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9249

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
ENSDART00000103833	Nonsense	210	808	5	19

Genomic Location (Zv9):

Chromosome 6 (position 40655587)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	40727187
GRCz11	6	40724723

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGTTTGGATTTGTTGGTACGTATCTCTCAGAGCCTCTGGTYAGAGGTTA[T/A]ACCACAGCTGCCTCTGCTCATGCCGTAGTGGCCCAGTTGAAGTACATWCT

Long Flanking Sequence:

AATGTAAAAATGGACTTTAATATTCACTTTAAATGCATTTGTGTGTGTGTTTCAATGTACAGGCACATTTACTATCCTCAGTATTATGATTGGTAGTGTGACTGAGAGACTGGCCCCTGATACAGATTTTCTCATTTACAATGGGACTAATGTGACTGGGGAGGTGGATATTGCATCTAGAGATTTGTACAGGGTACAAGTTGCAGCTGCTGCCACTGTACTGGGAGGTCTCATTCAGGTGATGAAAAACAAACATACAAAATGTGCATATGCATACCTAAATCCATGGTTAAACCATTTGAATGTATGTAATAAGCAGAATCTCATATTCCATTTGGACACAAATATATTATTTATTTTCATTATAGTCTGAAAAACAAGTTCTCAATATTACAGGTGGAATTAACTAGAATCTTGTATTGTGATCCTTAGGTTGTATTAGGCTTGGTGCAGTTTGGATTTGTTGGTACGTATCTCTCAGAGCCTCTGGTTAGAGGTTA[T/A]ACCACAGCTGCCTCTGCTCATGCCGTAGTGGCCCAGTTGAAGTACATACTTGGAGTCTCACCCAAGCGCTTCAATGGACCTCTGTCTATTGTCTACGTGAGTACAATCACAGCACATAACTGAAAGAAACATGTTAAAGTTATGTTATTAAACATTACTCTGTTGTTTTTCTTTGCAGACTCTTGTAGACTTATTCACACTCTTGCCAGAAACTCACCTCCCAACTCTTGTGGCCAGTGTTGTGTCCATCGTGGTTCTTATCACAGCCAAGGAGCTTAACAATGCACTTAAGAAAAAAATGATTATACCCATACCAGTGGAGCTCTGCACTGTATGTAACCAAGGAGGAAAATTCAGTCCTACCAATATGCTGTTTTAGTATTACATTTATTGTATTAGATTTGTTAAATCCTTAACAGAGTTTCTCTGTCTTTGGTTGTTTATCAGTACATCCTGTCCTCTCTGTTTATTAATCTGTTTAGTCAGCATTTCGACTCTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38573

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103833	Nonsense	603	808	16	19

Genomic Location (Zv9):

Chromosome 6 (position 40660833)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	40732433
GRCz11	6	40729969

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTGTCATTTCATTCTTTACAGAAAAAAGCTTTCAGAGAAGCCTCTCAG[C/T]GATCCAAACATGCTGTATTCTCAGTGGAAGAGGAGGCAGGGCAGTTGAGT

Long Flanking Sequence:

ATATATCTTCCACTATAGGAAAGAATCCCTTTCCAAGTATCTTTAGCTATATCATTATTAAAATCTATTTGCCAAATTAATTTTACATTTTTTAGTTTTTATCATTAATTTTTGAACTACATTTGTAATTACTTCTTTTTTAACCCTTTGTTCGCATAAGTACAAAATCTTTTTTGTATATTTTTGCAGAATTTGGCATTTCCATCACTTGTTTCACATGCAATACTTTTTAATGTGCATTAAAACAGGGTGATGGAAACCCAGCTACTCTGTCATTAAGCTAATATCAATTGTTTACAGTGCAGAAGGTTTATAGTCCCTTATAAAAGTAATTTCATGATGATTATAATTAAGCAGCAAGCAAGGCATCATGTCTGCGATCGAACACTTGCAGCTTCCATAATAGGCCTTTAGTGAACTCCTAATAAATTGATCTACTACAGATCTGAAAACTGTCATTTCATTCTTTACAGAAAAAAGCTTTCAGAGAAGCCTCTCAG[C/T]GATCCAAACATGCTGTATTCTCAGTGGAAGAGGAGGCAGGGCAGTTGAGTGATATGAATGGAGACTTACACAGAGAGGCAGAGATAGGTTGGAAAGAGCGGGAAAACAATACAGTGTTCGTAATACCTGAGACAGCACGGACATCTGATGGCCAGCACACCTGGATGTACCTTAAAGGCACTGACCCTGACACAGCCACCCTGGGATCAGTGTCCGATCTGCATGACGCCGATGTTACCACCATTGACTCCAGCAGTGAGGACACTTTAAGCCGAGACCTGGAGAGAGTCTCTCTGGGATCTCTGGGCAAGTGGACATGGGACATTCATTCCATCATCTTAGATTTGTCCACCGCCAACTTTATTGATACCGTGGCCATTAAGACATTGAGGAATGTAGGTGATGCAAAACTATTTTCTATGGAACAAAAATGTTACTGTGTTGCAACTGAGTTTACGCTAACACTTTCATTATTGCCTCTTATTGCAGATATTTCATGA

Associated Phenotype:

Not determined