ZMP

slc7a14b

Ensembl ID:

ENSDARG00000079231

ZFIN ID:

ZDB-GENE-091113-47

Human Orthologue:

SLC7A14

Human Description:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 [Source:HGNC Symbol;

Mouse Orthologue:

Slc7a14

Mouse Description:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 Gene [Source:MGI Sym

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44156	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39456	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44156

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078628	Essential Splice Site	370	756	5	7

Genomic Location (Zv9):

Chromosome 24 (position 27249103)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	26307460
GRCz11	24	26452501

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAATGCCAAGAGTCATCTACGCCATGGCCGGAGATGGTCTGCTTTTCAG[G/A]TATACAAGTCATTTTAAGGATAGTCAGTTCATTGACAGCCATGATATTTG

Long Flanking Sequence:

GGACTGTAATTTATTCAAGCCCAATCCTGATCCCTAGAGCTGAAGACCTCTGCTTATCCTCCAATATTAATCTGAAAGTGATTTTCCTTTTACTCTCCAGAGGCAGATTAAATACAGTACGATATCAATTTTCTTAATGTACAGTGGAATCGGGTGAATCATCCTACAGCATCCATTCACAACCACACCTAGAAATGAGAATGTTGTTTAATGGTTATTTCAGGCAATGTATTAAAAATAATTCTTACAAACTGTTAAAAAAATAACCCATTTGATCTGTTTGTGTCTCAGGTGAGTGTGATTCTGACATTGCTGGTACCCTATAACCTGATTGATGGCGATGCCCCGCTCATGGAGATGTTTGCAGATCATGGCTTCCTGGCAGGGAAGTATATAGTAGCTGTGGGTGCAGTCGCAGGACTCACCGTCAGCCTGCTTGGATCTCTGTTTCCAATGCCAAGAGTCATCTACGCCATGGCCGGAGATGGTCTGCTTTTCAG[G/A]TATACAAGTCATTTTAAGGATAGTCAGTTCATTGACAGCCATGATATTTGCAATGGTTTTTGGCCAAGCAAAACTAAGTCCAATCCTAAATTGAATGGGGCAATACAAACATTAAATTTAAAATCTGCTTATACATTTTAACGTATAAAGGCATCCTAAAATGAACATTTACTCATTATTTACTGACCCTCAAGTACTTTCAAACTATTTTGTGTTAGAAAACGGAAACTATTGACTTAAAAAACAAATATTGTGGAAGTCAATGGCTACCAGTTTTCAGGATTTTTCAAAATGACTTCGTGTTCATTGTGACTCAAACAGGTTTGTGGCAAGGGAAGGGTGAGTAAATGATGACAGAATCTTCAGTTTAAGATGAACCATCCCTTTAAAAAACAAATAAATAGCAAACAGTTCCTGCTTATAGCACCACCGAAGTTATCCAGATAAGAATTGGACTATTGGGGAACATACCCCAGAATGCTGCAAGTTGCAACTGACCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39456

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078628	Nonsense	746	756	7	7

Genomic Location (Zv9):

Chromosome 24 (position 27242958)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	26301315
GRCz11	24	26446356

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGAACAGAGTCACAATTACAGAAGCAAAGGCAGGACCAATAAAGGCTTC[G/T]AGGAGCTGGACAATGAAGAGTATTCCCCTGAGTGAGCATTACCCACTGGA

Long Flanking Sequence:

CTGTGACATACTATACACAATAAAACAAGTTTCTTGGATCCCAGGACAACAATGCAAAAAATGTAGTGTGAATAAAGTCCATTAGACTGAAAGTTTCATTCATCCACAATAAAATTAACAGCAATATTGATCCCATGTGGTATATTATGATCTTGGCTGTACTTGCTAGTTATTGTCCTTCATGTGAACTGGCCAGAGCTGACCCCGTCTCTCTTCATCCCACAGGTGTGCTGATCTATTTCAGCTATGGGATGTGGAACAGCTCTCTGGAGCTCAGCGCTAGAGAAGAAGCGGCTCACGCTAGCTCCTACCAGAGATACGATACCGAGGTGGACGACAGCTTCAATGTCGAAGAAGAACTTCCCCCTGAGGAGAACGAAGAGGATGGACAATACCAGGGCTGGGCGGCGGAGGAGCGCGGCTATCACTACCAGAAGCAGTACCAGGACGAGGAACAGAGTCACAATTACAGAAGCAAAGGCAGGACCAATAAAGGCTTC[G/T]AGGAGCTGGACAATGAAGAGTATTCCCCTGAGTGAGCATTACCCACTGGATTTGAGTGCATGTCATTTTGCAGAGTAGATTATGTTCCTGGATCAGCGATATTTAGAAAAATCACGTGAATATTAAAAGAGAGTCATGATGACAATATATATGACCCTTGAACACAAAACTAGTTTTAAAGGTCCTTTACAATTAAAATTAAACATTTAGGCCACATTTACACTGCACTGATTAACTGGCTCAATTCCGATTTCTTTTCTCCAATGTGGCACAGATCAGAAATGACCCATGTACGTGCAAGCAGGAACAAATCACATGGATTCCGATTTACTCAAATCAAATTCAGGCCTTGTTCATATCTGGAAATTTATCCGATATGAACGGATCGCTCGTGTCTGCAGTGTAAGCAGGTAGATCGGTTTTCCCATCAATGCGAGTTGCGCGTCTTTAAAAACCATAGCGAATGATGTCAAGTCTGACACTTTCATTTCAGAACAGAC

Associated Phenotype:

Not determined