ZMP

zgc:56429

Ensembl ID:

ENSDARG00000021383

ZFIN ID:

ZDB-GENE-040426-1025

Description:

hypothetical protein LOC393247 [Source:RefSeq peptide;Acc:NP_956571]

Human Orthologues:

FOLH1, NAALAD2

Human Descriptions:

N-acetylated alpha-linked acidic dipeptidase 2 [Source:HGNC Symbol;Acc:14526]
folate hydrolase (prostate-specific membrane antigen) 1 [Source:HGNC Symbol;Acc:3788]

Mouse Orthologues:

Folh1, Naalad2

Mouse Descriptions:

N-acetylated alpha-linked acidic dipeptidase 2 Gene [Source:MGI Symbol;Acc:MGI:1919810]
folate hydrolase Gene [Source:MGI Symbol;Acc:MGI:1858193]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6399	Nonsense	Mutation detected in F1 DNA	Not yet available
sa42624	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6399

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
ENSDART00000010881	Nonsense	251	745	6	19

Genomic Location (Zv9):

Chromosome 15 (position 42721056)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	43900378
GRCz11	15	43923821

KASP Assay ID:

554-5423.1 (used for ordering genotyping assays)

KASP Sequence:

GGAATCTGCCCGGTGGAGGCGCTCARAGGGGGAACGTGCTGAATCTGAAT[G/T]GAGCCGGAGACCCTCTYACACCAGGATACCCTGCTAAAGNNNNNNNNNNNNNNNNN

Long Flanking Sequence:

TTTATGCTAATGAGGGAGAGATAGTCACTTGTGGGCGGGGCTTTCCCCCTCTGATGACACGTACAAAGGGAGAATGTCAATCAAAGTGTTTCTGCAGACTCTTTTTATCAAGTGTGATTATAAAAAAATACAATTAATGCATTTTTACTATAAGGAGCTGCTTATAGTCACACTCTGCTGCCACACAACTGTGTAAACCCCCTTATAAAGATTTTTCGCAATTATTTTGCGTAATAGGTCCCCTTTAAGATGTCAAATAATTGTATTTTACCTAGACCGTGCAGTGTAATTTCAGTTACAATAATGTCGATAGATAACTTTGGTAAAATTTTTGGGTAAACTGTCCTTTTCAGGTGAAGAATGCGGTGCTAGCGGGCGCTAAAGGGATCATACTGTTCTCGGACCCTGCGGATTACTGGGCGGAGGATGTAGAGCCATACCCTAAAGGCTGGAATCTGCCCGGTGGAGGCGCTCAAAGGGGGAACGTGCTGAATCTGAAT[G/T]GAGCCGGAGACCCTCTCACACCAGGATACCCTGCTAAAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGAGAGAGAGATTCTGCATCAATGATCGGTGTTGACCAGTGTGTCTCCTCAATGTCCAGAATACACATACAGGTCCAGTCTGGAGGATGCAGTGGGCCTTCCCAAAATTCCTGTGCATCCCATCGGATTTCATGATGCAGTTCATTTGCTGCAGTGAGTACAACACACTCCCTTAGAGAAGACAAAAGTATTAGTATTACTATTAGTAAAAAAAATAACATTTTATTTCAAGAGTTCACACTTGCGTATTTGGCATGCTGTCCCGGAAGAGAGCCCTGAGCTCGTAATATCCTCGAGCCCGGGGTTCCCTCCCGTTAGAAGGTCGAGAGGGGAGTTCGAGCTCAGGTTGGTCTCGACAACTCCTCTGCTGTTGCCGTGTGAGAAGTGTAAACTTTGGTTATAATTTGGTTTAGTCGATTGGCCATTGTGTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42624

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
ENSDART00000010881	Essential Splice Site	327	745	9	19

Genomic Location (Zv9):

Chromosome 15 (position 42726078)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	43905400
GRCz11	15	43928843

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGCACTGTGTTTGTGTATTATTAATATTAATTTTTTCCCTTCATTTTA[G/A]AAAAGTGCGTATGAACATCCACACTAACAATCAGGTGACCCGTATCTACA

Long Flanking Sequence:

CCTGTGATCCTGATTGTAATGAAGTGTAACTTAAACTTTACACTTTGCATAATCAGCTTGTACACACACACACACACACACATACATTCATACGCTCCTGCTAATCTTCAACTCGTTTTTATGCATGATGTCAGCAGTACAGAGAGATCTGTGTGTTCATCAGTCACACACATTTGTTCCCACCACACACACACACACACACATTTGTGACCCTGTTGTTTTTCAGTAATGAACTCTGGAGGTCTGCCAATTTCACACAATGGCCTTGTGTTTGGAGTCTCTGCAGACTATAAATACCATAATGAAGCGTTAATTTACATGTATGCATATTTGGAAATGCTTTTATCTAAAGCAACTTACAGTTTATGAACTACCTAGGAATTCAACTGTTGATTTAATCGAACATATCAGTGTATATACTGGTTATTTACTGGATTGTATAATCATGATAAAGCACTGTGTTTGTGTATTATTAATATTAATTTTTTCCCTTCATTTTA[G/A]AAAAGTGCGTATGAACATCCACACTAACAATCAGGTGACCCGTATCTACAATGTGATTGGCTGGATCAGAGGAGCAGTCGAGCCAGGTGATGTTACTCTAGAGTCTAAAGCCTGGTTTATACTTCTGCGTCAAGTGATCAGCGTGACCCGCATGCAACGCATGTAGCTGTGCATTTATACTTCTGAACGCTGTTTCTGTTGCTCAGCAATAACATTTCCGAAACGCTAGTTGGCAGTGAGGAGTTTATGTTCCTCTGTGTCGAGTTTCTTCACTGGTGTTTTGTTTTTTCTGAACGCTTCCTTAATCTACAAGTGGTTCAAACTCGCTCATCTTGAGGCAGGAACCGGCGGATGTGCAACAACTTTAACCATGAGGTAAACAAAAAAACAAAACTTTCCATCTGGAGCTCCTTCACGGGACTCCACACTTGTAAACAATCATTCTATCGGGCTTGCACGGCTCTCAATCCCGCCCACACTCGTCAGCGCTACCAAGCCGA

Associated Phenotype:

Not determined