ZMP

slc22a7a

Ensembl ID:

ENSDARG00000056028

ZFIN ID:

ZDB-GENE-050506-52

Description:

solute carrier family 22 member 7 [Source:RefSeq peptide;Acc:NP_001077330]

Human Orthologue:

SLC22A7

Human Description:

solute carrier family 22 (organic anion transporter), member 7 [Source:HGNC Symbol;Acc:10971]

Mouse Orthologue:

Slc22a7

Mouse Description:

solute carrier family 22 (organic anion transporter), member 7 Gene [Source:MGI Symbol;Acc:MGI:18595

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41871	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35119	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41871

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103270	Essential Splice Site	427	560	8	10

Genomic Location (Zv9):

Chromosome 11 (position 31615400)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	30492762
GRCz11	11	30739946

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTAAGAAAGAAAATAACACATTGTTTTTGTTGTGGCTCTTTCATCCAC[A/T]GAGTTTGCTGCTGTTCGTACAGGAATTGCAGTTATTGGGAAGGGTTTCTC

Long Flanking Sequence:

CCAGAAGTTTAGAACCAAATGTGTCCATAACTCGTACTCTTTGAAATCATTAATTTCGAAGAGTCCTTTGAAGTTTTGGCGTGGAGTGATATGGCGAAGTGTCCTTCAAATAGGATTAAACCAGTTAGAACAGCAGCATTTATTTGAATGTCAGCTTGGACAATAAAATTCAAAGCACAGGGTCAATTATTTTACATTACTTCAGTTAGCAAGCAGTCTCTCTTGTGAAGGACTGTGTTCTCATTTTTATCACAGTATCTAATTTATTTTATTGCTTTGTTGGTGTGGGTTTGTGGGTTTTGGTTCCTTTGCTGTTGTAGCCTGTAAGGACAAACTAAAATAATTTGTGATATGGACGTATAATGTGGTCTGGAACTACTTCAACTGTGCATTTACTGGAAAATTGAATGTTTGCCAGCCAATCTGAGTGGAGCATTCAGTAGCCTCATAGTCTAAGAAAGAAAATAACACATTGTTTTTGTTGTGGCTCTTTCATCCAC[A/T]GAGTTTGCTGCTGTTCGTACAGGAATTGCAGTTATTGGGAAGGGTTTCTCAGAGGCGGCGTTTACCATTGCCTTTCTGTACACATCTGAGCTTTACCCTACTGTACTCCGGTAATTTATAAAACATATAAAATATATAAGCTATACACTTAAAAATAGGCTCCAAAAGCTGGTGGTGCCATTCTAAAAGCTACACATTTGAATCGAATTGGTCCATATTGGTACCATTGGTCCCTGTGATATCAAATGAAAGGTTTTTAGATGTTAGTATCAGTATGTTAGTCTTAGGGATATCTATAAGGTAGTGTTCTCCCTAAAAAAAAGCATTAAGAAGATCAAAACATCTAAAACTTATACATTACAAAATATCTGCCAACATTTGTCTCTGAAATTCCGGGAGAGGGTGGGGTGTTATTATTGTCTGAATAATACAGCTCAGAACCAGGTTAGTAACTAGTGTTGTGGTGTTAGTAACAATTGCACTATGGACTGAGTTTCAGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35119

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103270	Splice Site, Nonsense	464	560	9	10

Genomic Location (Zv9):

Chromosome 11 (position 31616744)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	30494106
GRCz11	11	30741290

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGTTTTTGGATTGAAGCATGCCTCTTTTCTTCTCTGTGACTTTTTACAGG[C/T]AGTGCGGCTTAGGCTACACCTCTTTTATAGCCCGTATTGGAGGTTCTCTG

Long Flanking Sequence:

TGATGCGCTAGAGATAAACCACTCTCACTGGCAGAGCTGTGATAAAAATTAAACATTTTTTTTGTTTTGTTCTTTTTTAAAGGACCCCCGCCTCCCAGTCTTAATGTTTCAGTTTAAATTATGTCACATATTGGAAAAAAATCACACATTTCAAATTACTTCATGAGACGTTTACCTTTAAGGCAGGGATTTCTTAATCTCGGTCCTGGAGGTCTGGTTTCCTGCAGATTTTACTGTAGCTCCAAATGAAATCAGACACACCTGGGCTAGCTAATCAAACTTCTACTAGGCTTACTAGAAACATCCTTGCAGGTGTGTTGGAATTAAAATCTGCAGGACACCAGCCTTCCAAGTTTGAGAACCCCTGTTTTTAGGTATCAATATGTTTAGAAAAAAGTAAACTCTTGTACCTTTATTTCTGTGAGTGCATTAATCCATAAATCTGACTCTCGTTTTTGGATTGAAGCATGCCTCTTTTCTTCTCTGTGACTTTTTACAGG[C/T]AGTGCGGCTTAGGCTACACCTCTTTTATAGCCCGTATTGGAGGTTCTCTGGCCCCGATGGTCATCCTGTTTGAGGATATTTGGCACTATGGTCCACCGGTAGTGTTTTCAGCCACTGCAGTTTTCAGTGGATGTGTCGTTTTCCTGCTGCCCGAGACCACCAATGTCCAGCTTCCAGAGAACATTCTGGATGTTGAGGAGGGGAGGTACAGTATCATAACATATCAGATAACAAAATAGCTTTCTGCTGAAGTCACACAAAATACCAGATCACGAGTATTAAATAAGCTGATACAATAAATGTAAAACACTGTTTCTTTGTCCACTAGTCAATTTTGAGATTTGGAGCTTTTGACTTTTCACAATGTGTTTTTTAGACTAATATAAAGAAAAAATCAAATATACTCTTTTTAAATATTTCTTTCATAGCACTGTATTAATTTTACCTGCATATTTCAATTGCAATGCATATTTTTTAAACGTTTAAAACAAATCTCATAG

Associated Phenotype:

Not determined