ZMP

A7MC17_DANRE

Ensembl ID:

ENSDARG00000062182

Description:

LOC100001772 protein [Source:UniProtKB/TrEMBL;Acc:A7MC17]

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42917	Nonsense	Mutation detected in F1 DNA	Not yet available
sa8561	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16596	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa42917

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
ENSDART00000078873	Nonsense	300	555	5	10

Genomic Location (Zv9):

Chromosome 17 (position 21819226)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	21969375
GRCz11	17	21989211

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGCTCGATGGCTGATAGCCAATGGAGACGTGGAAAAAGCTCATTATTA[T/A]CTGCATAAATGTGCCGTCATGAACCGTAAAGCTGAAGTTACATCAAGAAT

Long Flanking Sequence:

TTCCTTCACCATGTTCGCAGTGCTGAGATTCTTCAGTGGATTCACTATTACTGGCATTGTTATTGTCTCTTCTGTCCTCAGTAAGAATCTCTTGGCTTCTCAGATTATGGCTGAGTGTCAGTATGAAGCAAAGTAAAAGAGTCAGATGGATTGCTAATGCATGTGTTCCTCCAGATCTGGAGTGGGTGGACATTGAGCACAGGAGACTAGTGAGTATCATTGACAGTATGGCATGGGCTGTTGGGAGCACCTCGTTGGCTCTGATTGCATACTTTATTCGAGACTGGAGATGGCTGACAGTGGCTGTCACTTCACCTTTAGTGCTGTGCACTATCCTTTGGTGGTAATAGCTCTGATTTGTTCTGTCAAATTAAAAACATAATGAGTAAGTTCAGCCTAAAGGTTTTTCTACAGCAAATGTTTCTGGTGTACTGTAGGTGGGTTCCAGAGTCTGCTCGATGGCTGATAGCCAATGGAGACGTGGAAAAAGCTCATTATTA[T/A]CTGCATAAATGTGCCGTCATGAACCGTAAAGCTGAAGTTACATCAAGAATCAAACCTGAGGTGGGAAAATGGTCTAGGTTGACAAACTTTTCAAAAACATGCTTGTTAGTAACCCAGGTAGCAAAGAATTCTGGCACAGATTTGGCATAAAGCTGGCAAAGCAGGCATTCATCTGGCTTTAAGGCAGCACACAAGATTTGAGCCAGACGTAAAATGTAGTATTTGGCCCAGATGTTAAATATTGATTTATGGGCCACTTAAGTTTGGCCTGTCTTGACCCACATTTAAAATATATTTAAAAAAATTTTGAGTAAAGTTCTACCAATCAGGTCGCTTTGGGAAAAAGCACGCCCATAGTGTGCTAAAAGCGCAAGGCTTCATAGTTTTATCAATTTCATTGCAATCTTGACACACCGACCTATCTGGCACAGTTCAGGCCCAGTTATGAGTTATTAACCTGGCTGTGACTTGACGTAGATCCATGTTTGGCCCTTGTCTGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8561

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078873	Essential Splice Site	428	555	7	10

Genomic Location (Zv9):

Chromosome 17 (position 21817762)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	21967911
GRCz11	17	21987747

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAACTATTTGCAGGAATCAGCCTCATGATTAACATATTCATACCCAAAGG[T/G]GAGTGTGGAAATGTTAATTCTACATTTCAAACCAACCGGTTTGCAGTGYA

Long Flanking Sequence:

ATTTTGTATGTGTTCAACATGAAGAAAAAAAGGAATGGAACCATTTAAGGGCGAGTAAATAATGAGTAAACATTTAATTTTTTGGAGAACTATCCCTCTAAGAGTTAAACTGGCTACATGTTCAAGTCAGAAACTCTTGCTATTTGGTGACATCGCTGGTCAATAACTAAACTGCACTTAACAGCTTATTTCTTACACACATATCATATGTTAATCTTCAGTAGTAATATATTGAAAAACATGGTATAGTAAATAATGTAATAATGGCTTTTGGCCTCTTGCAGGTTTTGTGTCGCCACTATGACCTATGGTATAAGCCTCAATATCACAGGCTTTGGATTAAATATGTACCTCACTCAGTTTGTTTATGGAGCCATTGAGGTTCCATCTAAACTGATTGTATATTATCTTCTGGAGAAAATTGGCAGGCGGAAGACTGAAGCAGGAGCTCAACTATTTGCAGGAATCAGCCTCATGATTAACATATTCATACCCAAAGG[T/G]GAGTGTGGAAATGTTAATTCTACATTTCAAACCAACCGGTTTGCAGTGCATTTGAGCAAAAGAGCTGATGTTCTCTAATATCTTGGATAAACAGTATAACTGTTTTAAAGGGCACCTATGATGAAAATCATCTTTTGAAAGCTATTTAGACAAAACTGTGTGTAGGTGTAGTGTCTCCACAGTAATATTGGAGTGACATAAACACAATAAGTCTCTTTTTTTAAATTTCCTTGCGTTAAAATAGAATCCAAATCCCTCTTATTTTGAGGCCCACTGCAACGTGACGTGGGGATGTGGTTTCCCCGCCCACCGAATTGTTTGACAGCCGCATATAAATGCGTATAATCATATCAACAAGACAGGACGTGCGCAGGGGCTGCACGGGGCACAGTGGGTAGCACATTCATCTCACAGGAAGAAGGTCACTGGTTTGAGCCTCGGCTGGGTCAGTTCACATTTCTGTGTGGAGTTTGCATGTTCTCTCCGTGTTTGCATGTGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16596

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
Order Allele From EZRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078873	Essential Splice Site	464	555	9	10

Genomic Location (Zv9):

Chromosome 17 (position 21814919)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	21965068
GRCz11	17	21984904

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATCTGTAATTGCACACTACACGCTAAATAAACACTTTGATTGGATCCKCT[A/T]GGCAAAATGGCATGGGCTATAATTCCTTCCTGGCTCGTCTGGGTGTTTCT

Long Flanking Sequence:

AAACCAGAGAAATTGGAGGAAACCCACGTGAACATGGGAAGAACATGCAAACTCCACGCAGAAATGCCAACTGACCCAGCCGGGACTCAAACCAGTGACTTTCTTGCTGTAAGGTGACAGCGCTACCCACTACGCCACCATGTCACAACTAACTTTTCATTAACTTTAAATATGTTGAATTGGCAAACTACCCATCTCATAATGGCTAAAAGAGGGTGAGTTTCACTTGTTTATTCAGTCAGTTAAACATGGTTCAATATCTTCTCTCTCTCTATCTTATTCAGATCAGTGGATTGGTCGTACTGTGGTTGCTGTTCTGGGTAAAGGCTTCGCAGTTGCTGCCTTTTGCACAATTGTATTATATAGCTCTGAGCTTTACCCGACTGTTCTCAGGTAACATTGACCTCCTGCCTTTTGTTTCCTTCGAGTTAATTTGCAACTTGACATAAAATCTGTAATTGCACACTACACGCTAAATAAACACTTTGATTGGATCCTCT[A/T]GGCAAAATGGCATGGGCTATAATTCCTTCCTGGCTCGTCTGGGTGTTTCTGTGGCTCCTTTAGTCCTGCTATTGGACACTTTCTGGGGTCAGTTCTCTCAGACCATCTTGTGCTCGGTGGCATTAATTGCTTCTGTGGTGGCTTGGAATTTACCAGAGACTCGAGACAGGTGTCTACCAGAGACTATAGAGGATGTTGAGGGCACTGGGTAAGTCTTAACATTCAGTACAACATCATTCTGAACACTTAAAGTGACAGTACTCCCAAAATGAAAATTTCCTCACTATTTCCTCACACTAAAGTGCATCTAAACTTTAATGAATTTTTTTTTTCTTCTGTTGATCACAAAACAAGATAAACTGTTTGTCATTAGATACATTTTTGGAACAAAAATATGGAAGTCAACGGCTGTTTTTAATCCACACAGTATATCTTTCTTTGTGTTTAACAGAATGAATAAATGATGAAAAGTTTAACAGAATGAAAAGTTTCATTGATAA

Associated Phenotype:

Not determined