ZMP

slco3a1

Ensembl ID:

ENSDARG00000018726

ZFIN ID:

ZDB-GENE-030131-8662

Description:

solute carrier organic anion transporter family, member 3A1 [Source:RefSeq peptide;Acc:NP_001038653

Human Orthologue:

SLCO3A1

Human Description:

solute carrier organic anion transporter family, member 3A1 [Source:HGNC Symbol;Acc:10952]

Mouse Orthologue:

Slco3a1

Mouse Description:

solute carrier organic anion transporter family, member 3a1 Gene [Source:MGI Symbol;Acc:MGI:1351867]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43116	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43115	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43116

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
ENSDART00000013363	Nonsense	131	701	2	10

Genomic Location (Zv9):

Chromosome 18 (position 24940854)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25170627
GRCz11	18	25157159

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGAATTCCTCGCCAGTCAATACAAGATCACAGACACTTGGAGCAAAGAT[C/T]AGGGCCGAGATGTTTGCTCCAACACCTCAAAAGCTGATGAACCATGTGGA

Long Flanking Sequence:

AGTGGTTTTAAATGTAAGTACCCCAAATTGCAAGTGCAACCTATCATTTGAAACACTATTTTGTATAGAAAAGGGTGGATATAAAGCTGCAGAATGACATACGTTTACTTTTTTACTTTATTACACTCTGCCTTCAATCTTCGAACTTCAATCTGTCCTTAATAGAACTACTGTCTTTCTCAAATTGCGCAATGGAACAAATGATGACTGTACATTACACATTAACATACAATCTTCTCATTTGTTTATTCCAGGTAAGTGTGTTGACCACGTTGGAGCGGCGCTTCAATCTTCAGAGCGCTGATGTTGGTGTCATCGCAAGCAGCTTTGAGATCGGCAACCTGGCCCTCATTCTCTTCGTTAGTTATTTTGGTGCTAAAGCCCACCGTCCTCGTTTAATTGGCTGCGGAGGCATTGTCATGGCTTTGGGAGCCTTGCTTTCTGCATTACCAGAATTCCTCGCCAGTCAATACAAGATCACAGACACTTGGAGCAAAGAT[C/T]AGGGCCGAGATGTTTGCTCCAACACCTCAAAAGCTGATGAACCATGTGGAAACAGAGCAAACACCAACATGATGTACCTGCTTCTGATTGGAGCACAGGTGTTGCTGGGAATCGGCGCGACACCCGTTCAGCCCCTGGGTGTTTCCTACATAGACGATCACGTGCGGAAGAAAGATTCTTCGCTCTATATCGGTATGTAAGAGATGGTTTCTAATTCATTTAGCAGCAATGCGGTGACTTTTTTACTGTCTCATTCTGTTTGTTGTAGGAATGTCCTAATACAACATTTTAACTTCCAATATAATACAGATATTGCAGCCTTCAGTACTAACCGATACAAATCCGATACAATAATCAGCACAAATCATGAATACTTTACTTTTACCTATTTCGTTGAGTGGAATGTATGAACGGCTAGATCAAACCAAGAACAAAAGTCAGCAACAGTCAGTAAAGAAAACAACGACCAATGTATTTACTATTAGTTGCATAAATGTGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43115

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
ENSDART00000013363	Nonsense	219	701	3	10

Genomic Location (Zv9):

Chromosome 18 (position 24880452)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25110225
GRCz11	18	25096757

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGGACCTGCATGTGGTTTCATCCTGGGATCTGTCTGTACCAACTTTTA[T/A]GTGGATGCTTTGTTCATCGACACAAGTGAGTTTCTCTTTATCCTCTGCAC

Long Flanking Sequence:

GGATGGGAGACCAGCCACAATTAATCATATTACATGCTCCTCTCGAAATTAAGCTGCGGTCAAACTAGAGTTTTAACATGCAATATTCTCTCGTATGGCGCTGCATACTGTACAGAGAGGTCATGTTTTGATCCTTGATTGGTCTCACGTAGTCAAGTGATGCAATTTCGCAGGTCAGAGTCCACAAAACTAGAACTTTGCAATGCAGCGAAATTGAAAAACTTGTTGCACGAGCTTGCATTTTTGATCTGACGCATTTGCGTACGTATGAATGGAAGTCTATGGGGAGAAAAGTGCAGTGCAGTGTAAAGTAAAGCGTTCCCTTTGACTTCACATTTTTTCACTTTAACTTCAATTTATGCATGCTCGATTTATCATTGTGAAACTGAAATAAGATTTCTGATGATTTTTTATCATTGCATTTCAGGTATCCTCTTTTCCACATTGGTGTTTGGACCTGCATGTGGTTTCATCCTGGGATCTGTCTGTACCAACTTTTA[T/A]GTGGATGCTTTGTTCATCGACACAAGTGAGTTTCTCTTTATCCTCTGCACTCCAAATCCAAATACAACACAAACACTCAGAACAACAGAAAATGCTGCTAGGCATTTTGTTTCTTACCACCACGGCTCTTGTGTCTTTTGAATAATTGAAAGCACAAGGCCTCAAATTCTGGCTCACTGTCACAATCAATAATCAGCAAGTGAATCTGAAATAGAAGAAAAATTTGGCATTCATTTCAGCCACGCTTGGAATCCACATTCCTGCTTGCTGATACACTATGTTGGCATCTCTATAATAGACACATTGCATTAAATAAAACAAGAAAACTCTTTAGATACATATTTTTGTAGAATAAAATACACCAAGTGGATCAGTGACTTAGTTTTGATGTTAGATTTCTGCGAGTTTCGTCATGTAGAGATTTGTTGTCATTGTTGTTTTAGAAGCTTTTCTCAAATGTCAGCAAAATGATATTTTATTTACAGATGTTTTTCCATTCC

Associated Phenotype:

Not determined