ZMP

LOC565514

Ensembl ID:

ENSDARG00000030472

Human Orthologue:

SLC16A5

Human Description:

solute carrier family 16, member 5 (monocarboxylic acid transporter 6) [Source:HGNC Symbol;Acc:10926

Mouse Orthologue:

Slc16a5

Mouse Description:

solute carrier family 16 (monocarboxylic acid transporters), member 5 Gene [Source:MGI Symbol;Acc:MG

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38896	Nonsense	Mutation detected in F1 DNA	Not yet available
sa27955	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38896

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
ENSDART00000045186	Nonsense	393	506	3	4

Genomic Location (Zv9):

Chromosome 12 (position 28143119)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	26480728
GRCz11	12	26572088

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACCTACGGACTGTCCATGAGTGTGGTTGGCTCGCTGATGTTCACCGTTT[T/A]GATGGACACAGTGGAAATGAGTCGATTTCCTTCTGCTCTCGGCCTGCTGT

Long Flanking Sequence:

ACCAATCAGACCTCGCAAGCCCAGAAAGACCAATGAGATCAACAACAGCCCCAAAACCTCAGACAAAAAGGGTTGCATGCTGGGGATCTGTCAAAGTTTAGCGTCATCCCTCAGACAACAAATGGCCTTTGACCTCTTCTGTAGCAACACAAGATTTCGGGTGTTTTCATTGGGCATCACTTGGATGATGCTGGGTTTTGTGGTGCCACTGATTTACCTCGTCCCGTATGCATCGGCTGATGATATGGATCCAAGCCGGGCTGCCTTGCTCCTCTCCATTCTGGGATTTGTTAACATCTTTGTTCGGCCTCCTGTCGGAGTCCTCTTTAGCCTTCCCTGGTTCAAAGGTCGCCACATTTACGTTTTTTCAGCCGCGCTCCTAATAAACGGACTCAGTAATAGCATTTGCTGCATTTCTGCAAGTTTTCCTGTGCTGTTAGTTTACGTGTTGACCTACGGACTGTCCATGAGTGTGGTTGGCTCGCTGATGTTCACCGTTT[T/A]GATGGACACAGTGGAAATGAGTCGATTTCCTTCTGCTCTCGGCCTGCTGTCTATCATGGAGAGCGTCACATTGCTGATTGGACCTCCACTCGCAGGTAACTTGAAAACCTTGTGTGTTTTGAATTGTATGTTAGGAAGGCACAATGCACAATGTCACAATGCCATTAAATGTATTTTATTTATTTTTTTATTTTTTTTGGCCTTTTTGCCTATATTAGATAGGACAGTATTTAGACAAGAAGCGAAGTTGGAGAGAGAGAGGGTAGAGTAGGGAAATGTCCTTAAGCCTGGATTCGAACACGGGACACCCTGACATACTACTGCACCATATGTCGACACGCTAACCACTAGGCTATTGCACCGACTCTGCCATTAAATGTAGTGGAAATCAAATGTGAGAGAACACTTGATTTTAATACTACTACTAATAATAATAATCAATAAGTAATCTTAATTGTTCAAAATTTGAAAGAGTTTAAGATTTCACTATGCTATGCCTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27955

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045186	Nonsense	457	506	4	4

Genomic Location (Zv9):

Chromosome 12 (position 28137766)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	26475375
GRCz11	12	26566735

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCACCATCATAGTGGTCTTATCAGCTCTGTTCCTCATGTTCACCTTTTA[C/G]TGGCTGGACTCCCGTGATGCAGCTAAAAAGGATTCTCCAGCCAAACCTGC

Long Flanking Sequence:

ATTAACGTCTTATGACGTTGTGTGCCTGCTAGGCAATAACTAAATGCACTACAGAATGTTACGTTTACAGACATCCACAAGTTACATGTAAACCAGCTTTTCACAGCGTAATGCTCATTACTCACTACTCTTAAATACTTTTAGGGCTACTTTTTACTCATACTTTGAGTCATATTTACAACAGATACCTTTACTCCACTGAAATAGATTTTAGGCAAGCAATGGTACTTTTACTTGAGTATGATTTTTCAGTACTCTTTCCACCACTGGTCAAGAAGACACACGGTTGCATTTTATTTTTTTTTCTATTTATATAAAATCACTTTAGAGAATTGAGACATGTCTAGCCTTTGACCTAGATGCAAATAAACTTTTAAATGTAACCATATGGGTTGTGTTACAGGATTCCTTGTGGACCGTACCCAGCTGTACACATATGTGTTCATGGCCTGCACCATCATAGTGGTCTTATCAGCTCTGTTCCTCATGTTCACCTTTTA[C/G]TGGCTGGACTCCCGTGATGCAGCTAAAAAGGATTCTCCAGCCAAACCTGCAATCAATATCTCCACAGACTGTCAATACAGCAGTGTGCCTATAGATGGAGACAAGACCAATAAACCATCATCAGAAACAGAAAACACCACCTGCGTATGAGACCTGGATCTTGGTTTATTTACATTATTTCTTTGTAATTGTGATCCAGATCAGGTATATAAAATGTGCTGTTTAGAATTGTATAATTTCACATTCATTTTTTGAGTGTCAAACCCTGGTTGTTTTATAGAGTGCAGATGTATTTTTTCCATTTATTTTCCTATAGTGATAAAAAAAAAAAGATATATATATTTGTTAAAAGGTTATAAGCCATAAACCAAACCAATCAGCTATTAGGTGAATCACAACATTACAAATCTAAAGCAAAGAAATATATGAAAATCAGACAAAAAGTACAAGAATTAGTACTTGACGGCATTAATGAGAAAAATAACTGCAAACACAATTGT

Associated Phenotype:

Not determined