ZMP

zgc:174356

Ensembl ID:

ENSDARG00000088263

ZFIN ID:

ZDB-GENE-080215-21

Description:

zgc:174356 (zgc:174356), mRNA [Source:RefSeq DNA;Acc:NM_001114717]

Human Orthologues:

SLC46A1, SLC46A2, SLC46A3

Human Descriptions:

solute carrier family 46 (folate transporter), member 1 [Source:HGNC Symbol;Acc:30521]
solute carrier family 46, member 2 [Source:HGNC Symbol;Acc:16055]
solute carrier family 46, member 3 [Source:HGNC Symbol;Acc:27501]

Mouse Orthologues:

Slc46a1, Slc46a2, Slc46a3

Mouse Descriptions:

solute carrier family 46, member 1 Gene [Source:MGI Symbol;Acc:MGI:1098733]
solute carrier family 46, member 2 Gene [Source:MGI Symbol;Acc:MGI:1353616]
solute carrier family 46, member 3 Gene [Source:MGI Symbol;Acc:MGI:1918956]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa36486	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36486

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
ENSDART00000128863	Nonsense	92	464	2	7

Genomic Location (Zv9):

Chromosome 17 (position 39414541)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	39299438
GRCz11	17	39247023

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCCATCCTCAGCCTGGTCTCCATCCCTCCTGCCATCATGCTGGGCTCGT[G/A]GTCAGATAGCGCTGGCCGTCGATCAGTCATGGCTCTGCCGTCAGTTCTGT

Long Flanking Sequence:

CTCCACCCTATAATAGTATTAATTGGTTTGGTTTTATCAGAGCTGTTTCCTCATGTAAAATACGTCCAAATACAGTTGAAGTCAGAATTATTAGCCCCTCTTTAAAGTGTTTTTTTTTTAATATTTCCAAAATTATGTTTAACAGAGGAAGGACATTTTTATAGTATGTCTGATAATATTTTTTCTTCTGAAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCATTTAAAAAACATTTTAAGGTCGAAATTATTAGCCCCTTTGATATAGTGTTTAATCTGTATTCATGTGGCGTCTCATCTATGTATAATATGACATATTGAATCCATTTTCCAGGTATGTCAAGACGTGCTGAAAAACGTCAGTATCTGCAGTGACCCTGAGCACCACAAAGAGTATGAGCATGTTCAGACTACATCCTCCTACATCTTTCTTCAGTTCAATGCCATCCTCAGCCTGGTCTCCATCCCTCCTGCCATCATGCTGGGCTCGT[G/A]GTCAGATAGCGCTGGCCGTCGATCAGTCATGGCTCTGCCGTCAGTTCTGTCTCTGCTGAGTGGAGGCTTGCTCTTGGCTGTATCTCTTCTGGACAACATCAGTGTTTACTGGACTCTGATGGCTGCCGCTTTAATGGGCCTGACAGGCGGCCATGTTTCCATATTCCTCAGCTCTTTCAGCTACCTGGCCGACTTGACCATGGGCTCCAGTTCCACTCGCACTTTGCGTATGGCAGTGGCCGAGTCCATGATTTTTGTAGGAGGCACGATTGGCTTCCTACTTGGCGGATTCCTGGAGCAAGAATTCGGGCTTCAGGCTGCATTTGGGGCTTACATTGGCTGTCATGTTCTGGTGTTGCTTTATATTGTGCTTTGGCTGAGAGACCCCTCGGTGGGGAAAAACACACGTTTAGTTCTCTGCAAAGAGGAGACGGCTGAAAGCGGATCTCAGGAAGATCAGTCTCGGCTGTTTATCCTAAAGTATGCCAAGATGTCTTTCA

Associated Phenotype:

Not determined