ZMP

zgc:110528

Ensembl ID:

ENSDARG00000012051

ZFIN ID:

ZDB-GENE-050320-145

Description:

Protein FAM119A [Source:UniProtKB/Swiss-Prot;Acc:Q5BLD8]

Human Orthologue:

FAM119A

Human Description:

family with sequence similarity 119, member A [Source:HGNC Symbol;Acc:30476]

Mouse Orthologue:

Fam119a

Mouse Description:

family with sequence similarity 119, member A Gene [Source:MGI Symbol;Acc:MGI:1914349]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16102	Essential Splice Site	Available for shipment	Available now
sa6698	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16102

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025198	Essential Splice Site	49	218	2	4

Genomic Location (Zv9):

Chromosome 22 (position 11771219)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	11631387
GRCz11	22	11661069

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TYAGTCAGGACTGGAAGCGATTGGGTGTCGCTGCWGTGGTTTGGGACGCT[G/T]TAAGTTCACACTACCCCAACTTTAANTCCGGATCCAGTTTYGTTTTWAAAT

Long Flanking Sequence:

TATGCCTAAAAGCATACGACATTAGATATCAGAGAGGAAATTGCATATTAGTAAGGAAAGTGGAGACCAAAAACTCAACTATTTAGTCTCCACTTTCCTTACTAATATGCAATTCCCTCTCTGACTCCTCCACTAACTACAAAAAAACTAATGTTTTGCTTCTTACACTTTCTTTACATACCTGAAACTTGCCTACAGCACTCATTGTTGCTCTTATAGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCACTTTGGATAAAAGCGTCTGCTGAATGACTAAATGTAAATACGATTTTAATTGTAATGAACAATGTGTTGGTCTTTTCAGACATTTTATCAGCTCGAGATGGCTTTGGTTCCTTATGATGAGAATGTTCTTCCTGCTCTGTCAAAACTGCATCAGTCTTCAGCTGAATTCACTCTGGCCAATCACAGGATCAGACTCAGTCAGGACTGGAAGCGATTGGGTGTCGCTGCAGTGGTTTGGGACGCT[G/T]TAAGTTCACACTACCCCAACTTTAATCCGGATCCAGTTTTGTTTTTAAATGCTTTCTGTTAACAGAGAAAGAGAAGTTTTAAAGCATGTCCACTCTGAAATATCTGCAAACATACATTATTCTGTATGTATTAAATGTAGACCGGGGCTCTGAAACTGAAATTGGCAGGGGGCCATTGCAGTGACTGAAGATTCTTTGGCCATTTTAACATTTAAGCACAAGAAAAATGAGGAAACCTGACGTTATTGATGCATCTTAGAACAACCATCACACAGCTGCTGAAATGCATCCGTGGCTGTTGTGTGCCGAGTGTTATGGTGCGTTCACAACAGGCGCAAATGAAGTGTCAAATGCGAGTGATTTATATGTTAAATCAAGGCAAAGATGCGAATAGACATCCTATGCCGCAGTTTGCATGAATGACACAACACTATGTTTTACACAGCGGATGCCCTTCCAGCTGCAACGCATCACAGGGAAACATCCATACACTCTTGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6698

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025198	Nonsense	95	218	4	4

Genomic Location (Zv9):

Chromosome 22 (position 11767901)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	11628069
GRCz11	22	11657751

KASP Assay ID:

554-5005.1 (used for ordering genotyping assays)

KASP Sequence:

TTKTATCAATAAATATATTTTCTGCAGGAGCCAATGTTACMATCACAGAC[C/T]GWGAGCCTGCGCTGGAATTTCTGACMGCCAATGTACATGAAAACATTCCT

Long Flanking Sequence:

GGGATTACGGATTATTAGAGATTACATTTACGTTTTGGTGTCGCCTGAACATCAATGTTGATTGATGATTCGTTTTTTATAGTGTTATTTTAAATTGCTGTCATGCAAACATTGTGTTTAACTGTAGATGAAGCCTCAATTTCATAATCTGATCTGGGGTTTTAATGGTTACAGATCTGGATGGGTTAAAGAGAGGTTGCCAGTTCGAATCGTAATGTGATTTAATCCGTTAACGATCACAACTTTATACATTTTAGTCTCAAATCTGAAGCCTATCCCTGTTTATTGTCCAGGCAGTAGTTCTCTGCATGTTCCTGGAGATGGGAAAAGTGGATCTGAAAGGAAAGAGGGTTATCGAGCTGGGAGCAGGCACTGGTTTGGTGGGCATCGTAGCAGCTCTGCTGGGTAAGAAAGAATGATATTTCAACACTTTTCATATTTCAGCATCATTTTTATCAATAAATATATTTTCTGCAGGAGCCAATGTTACAATCACAGAC[C/T]GAGAGCCTGCGCTGGAATTTCTGACAGCCAATGTACATGAAAACATTCCTCAAGGCCGGCAAAAGGCAGTACAGGTATCTGAACTGACCTGGGGGGAGAATCTAGATCTGTATCCTCAAGGCGGCTATGATTTAATTCTGGGAGCCGATATAGTTTACCTGGAGGAGACGTTTCCTGCACTTTTGCAGACTCTCGAACACCTGAGTTCAGGAGATACTGTGGTGTTGTTGTCCTGCAGGATTCGATATGAGCGAGACGAGCGTTTTCTGACGGAGCTCCGGCAGAGGTTTTCTGTGCAGGAAGTCCATTATGACTCTCAGAGGGACATTCATGTTTACAGAGCCGTGAAGAACAAGAGCAACACTGAACTGTAAGAGGAAACATTGAGGAAACGTTGGGTAGAGCTGTTTTTATTTTTAATGAAGTTTGTTTTGGTTTTGTTAAATATATTGAAGGTGATTAAATTACAGTATTTAACAGGACTATGGTGGTGGTTTTGG

Associated Phenotype:

Not determined