ZMP

si:ch211-32g22.2

Ensembl ID:

ENSDARG00000004177

ZFIN ID:

ZDB-GENE-091118-95

Description:

LOC553309 protein [Source:UniProtKB/TrEMBL;Acc:Q5CZM1]

Human Orthologue:

FAM169A

Human Description:

family with sequence similarity 169, member A [Source:HGNC Symbol;Acc:29138]

Mouse Orthologue:

Fam169a

Mouse Description:

family with sequence similarity 169, member A Gene [Source:MGI Symbol;Acc:MGI:2444268]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39324	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11663	Nonsense	Available for shipment	Available now
sa37263	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39324

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
ENSDART00000023640	Nonsense	14	364	2	11
ENSDART00000122015	Nonsense	14	508	2	13
ENSDART00000124807	Nonsense	14	826	1	12

Genomic Location (Zv9):

Chromosome 21 (position 14086653)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	15787608
GRCz11	21	15883585

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGTATAGGGATGGAGTTCCCTGTAGATGTTCTGGTGTCTGGCCGACAT[G/T]AAGACCTTGAAAGTTCAGCCCAAAGCTACATGAACAAACTTCTTTACAGC

Long Flanking Sequence:

TATTCTCTTCTAAACAGATATTAAAATCATATACAGATGTTTTGTAAATTACTCTAAATACAATTCCTGTGAAATAAAAGCACATGAGGATGTTTTATTTTTGTATGGTGATAATATTAAAAGATGTGTGATCATGGAAAAATAACAAAATGTCAGATTTGCTGTTGCTTTATTTTTTAGTAAGTTCCTTAAAAAAAATGTCAAGAACTCCCTGTGTTCACGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAAGTCCAAAGACATGTGTTATGAATGAATGAATGAATGAATGAAATGGCAAGAATTTCATGTTTTTGCTATTATTTTTGGAATGTTGTTTATTTGCAAAGCATTTTGAAAGTAAGTAGTTAGTGACGAGTTCTGATTAAAAATAAAGTAAGCGATTATAAGAAACCAAATGATGATGTTTGTGTGATCTGTGATCTCTGTATAGGGATGGAGTTCCCTGTAGATGTTCTGGTGTCTGGCCGACAT[G/T]AAGACCTTGAAAGTTCAGCCCAAAGCTACATGAACAAACTTCTTTACAGCAACCCAGATAACGCAGAATACCTTACCTTGTCCAACACAAGAAAGGTAACGCACCACAGAGAATATCTGATCATTTTAAAATGCGTAAAGCCAGTATGCGTTCACACGTTAGGCTTGATTAAAATGAACTCTAATGCGATTGCTTTGCTGGTGTAGTTCAGTAAAGAAGTGTGAACATGGTCATCTTTTTTTTAACTTTCTTTTAAAGAGCTTGAATATTTAAAGGGCACCCAATTTACCCCTTTTAAATAAGCCTTTGGTGTCTGCAAAACGTGTCTGTAAAGTTTCATCTCAGAATGCCCATTAGATAATTTATTATAGCCTCCAGAATCTGCCCATTTTGGTGTCTGAATACATTGTAGCTGTGACTTTAAATGCAAATGAACTGCTTCTCACCGCCCACCGCTCCCACGTGCGTGTCTGCTTCTTATCATGCGTTGCGTCAGATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11663

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000023640	Nonsense	109	364	5	11
ENSDART00000122015	Nonsense	109	508	5	13
ENSDART00000124807	Nonsense	109	826	4	12

Genomic Location (Zv9):

Chromosome 21 (position 14093064)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	15794019
GRCz11	21	15889996

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TAATGTTTCTAAAACACAAGTTTTTCTTYATGATTATATTTCGGCAGGTA[C/T]GATCTGTKGGCGAGAGGATAGTCTTATATGTACTGAACCGCATTATTTAC

Long Flanking Sequence:

CAATCGTGACACACCAACCTATCTGGCCCAGTTCAGGCCCAGTTATGAGTTATTAACTTGGCTGAGACTTGGCCCAGATATGGTCTGTGTTTGGCCCTTGTCTGGAAGCCAGATTTGGTCCAGTCATGTACCATAATTCACTGCGGCATGTGGGCCAAGCAAAACCTGATTGTGTGGGCCAGAGCTGGGCCAGAGAAATTTTGCTATGTGGGTAACGTTGCATTTTATGGATCACCACAGTGCACAGTTCCATCTATTTATCTTGAGTGCCTTTCATATCAGATGGATAAAAGAAATGTTCATGTTTGGGTGAATTTAAGACCCATTCTTTTATCTAATCTACAAATGATTGATATTAGCACTTGTTTTCCTTTTCACAATCCACATGAAATGATCTGTTGTTACTTCTCTTACATAGTGACTTGAAACCCTGGGAAATCACTATCAAATTAATGTTTCTAAAACACAAGTTTTTCTTCATGATTATATTTCGGCAGGTA[C/T]GATCTGTTGGCGAGAGGATAGTCTTATATGTACTGAACCGCATTATTTACCGGACGATGGAAATGGGCACTAATGAGGTGCCTTTCCTCTGCCATGAAGAAGACGTCTTTGCCAAAATCCTCTGGAAGAATGGAGAGGCAGTGGGCTTCTACTCGGTCAAATGTAAAGGTCAGTCCTTCTCCCAGCAGAGTCTGGTATTGCTCATTCTGCCTTCTGTGTGAGATATTTATAAAGCAATCTACAGTGTCTTCATTAAAGGATGAGCGAGATATGAAGCTAGGCCTTGTCTTGCTTGTAAGATGTGGCCTAGAAATACAGATCTTGGTTAGTACGATTACACATTCATTAGCAGACTCTTTTATCCAAAGTGACTTGCAGATGAGAGATTGCAGGGTTGCAATGGGCTATATGCACATCTAGTGTTTTTCAGCCAATGATGAACTTCCAGTGAAAGCTTTGTGACAATTTTTAATTTCACAAGGTTCTTTTTACAGCATCGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37263

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
ENSDART00000023640	Essential Splice Site	165	364	5	11
ENSDART00000122015	Essential Splice Site	165	508	5	13
ENSDART00000124807	Essential Splice Site	165	826	4	12

Genomic Location (Zv9):

Chromosome 21 (position 14093234)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	15794189
GRCz11	21	15890166

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTGGAAGAATGGAGAGGCAGTGGGCTTCTACTCGGTCAAATGTAAAGG[T/G]CAGTCCTTCTCCCAGCAGAGTCTGGTATTGCTCATTCTGCCTTCTGTGTG

Long Flanking Sequence:

TGTGTGGGCCAGAGCTGGGCCAGAGAAATTTTGCTATGTGGGTAACGTTGCATTTTATGGATCACCACAGTGCACAGTTCCATCTATTTATCTTGAGTGCCTTTCATATCAGATGGATAAAAGAAATGTTCATGTTTGGGTGAATTTAAGACCCATTCTTTTATCTAATCTACAAATGATTGATATTAGCACTTGTTTTCCTTTTCACAATCCACATGAAATGATCTGTTGTTACTTCTCTTACATAGTGACTTGAAACCCTGGGAAATCACTATCAAATTAATGTTTCTAAAACACAAGTTTTTCTTCATGATTATATTTCGGCAGGTACGATCTGTTGGCGAGAGGATAGTCTTATATGTACTGAACCGCATTATTTACCGGACGATGGAAATGGGCACTAATGAGGTGCCTTTCCTCTGCCATGAAGAAGACGTCTTTGCCAAAATCCTCTGGAAGAATGGAGAGGCAGTGGGCTTCTACTCGGTCAAATGTAAAGG[T/G]CAGTCCTTCTCCCAGCAGAGTCTGGTATTGCTCATTCTGCCTTCTGTGTGAGATATTTATAAAGCAATCTACAGTGTCTTCATTAAAGGATGAGCGAGATATGAAGCTAGGCCTTGTCTTGCTTGTAAGATGTGGCCTAGAAATACAGATCTTGGTTAGTACGATTACACATTCATTAGCAGACTCTTTTATCCAAAGTGACTTGCAGATGAGAGATTGCAGGGTTGCAATGGGCTATATGCACATCTAGTGTTTTTCAGCCAATGATGAACTTCCAGTGAAAGCTTTGTGACAATTTTTAATTTCACAAGGTTCTTTTTACAGCATCGATGTTGTAATGTAATTCAAATATAGTCAGATGAACAGACTTAAGCATTCATTTGGTTGTTAAAGTGCAAAAAGAGACGAAAGACCATTTAAATGCAGGCGCCACCATTAGCAGCAGGCTAACACTGAAATTCCATTGAAAATACTGGGGTAAAACTAATTTCCATATTTTA

Associated Phenotype:

Not determined