ZMP

fam171a1

Ensembl ID:

ENSDARG00000079788

ZFIN ID:

ZDB-GENE-061208-1

Human Orthologue:

FAM171A1

Human Description:

family with sequence similarity 171, member A1 [Source:HGNC Symbol;Acc:23522]

Mouse Orthologue:

Fam171a1

Mouse Description:

family with sequence similarity 171, member A1 Gene [Source:MGI Symbol;Acc:MGI:2442917]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15232	Nonsense	Available for shipment	Available now
sa42738	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15232

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
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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109450	Nonsense	337	888	8	9

Genomic Location (Zv9):

Chromosome 16 (position 30801372)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	28638510
GRCz11	16	28573133

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTNAATTCAGTAGTCAAMTTGAACAATGCTTCTGTGTTTCAGGAGGAAGTG[T/A]ACCCGTTTGCGGCCTGCTCACCGGAAGTTCACATTATCCTCAGCTTTGGA

Long Flanking Sequence:

GTTGCAATGACAGTAAAAAATATCCTGGTTATCTAAGTGATTAAGTGTGAAAAGGGTGGAAGATGACATGATCGTTTTCGAGTTTCATGGAATGTAGACATAAGTTAAGCGTTTCGAAGACTAAATGGACTGCTGCAAATTATAGTGCCACATATCAGTGAAACTAAGAAAAGAACACAACGCATTAGACAAAGGTAGCAGGTAAATTTGGTTAATATTGGTATTCTGTATCTGCTTGTTCAGTAGTGTAGTGCTTTGAAATACTTATCTGGTGTTTCATATCGCATTCAATCACCCAGTTAATGTACAGTCACACATGCATCTCTTATTGTGCTTGATTAAAAAGGAGTTTCTCTAAATAAAATTCTTTCCTAGTTTCTGCAATACGAACGAGCTAAAAAGTGGGTACTTTTGCAATCAGTTTTTTGAACAATGCAAAAGTTCCTTTTTTTAATTCAGTAGTCAAATTGAACAATGCTTCTGTGTTTCAGGAGGAAGTG[T/A]ACCCGTTTGCGGCCTGCTCACCGGAAGTTCACATTATCCTCAGCTTTGGATGGCTCTAAACGAGACCAGGCTACTTCCATGTCCCACCTTAACCTCATCAATGAGACTCACCTTGACCAGAACGGGGCAGAGCCGGACATGCACACACCTATGCTTAAACCCACTCCCTACGACTCCTCCACCAATGAGCTTGCGACTTCGCGTGGCGAGCTTCACAGCCGAGGATCCAACCACTACAAACACTCAGTTGAAATATTTCCTCTCAAATCGGCTTGCTCAAACAATCCCTCTGAAGGTTATGATTCCGCTGCTGGACGAGGGGAATACCGACGGAGCTATACGTCCATTACGACTTCGTCCGTCCATCCCCTCCACATGTCTGTCTCCTCCTCTTCGCCTCATACCTTGCATCACACCACCTCTGCAGGACGTCTCTCTTCGGAGAGTAAATCAAGCTTGCGGGATCAACGTCTGTCTCCTGTTTCGGCCGCAAGTCCTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42738

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
ENSDART00000109450	Nonsense	358	888	8	9

Genomic Location (Zv9):

Chromosome 16 (position 30801433)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	28638571
GRCz11	16	28573194

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCCTGCTCACCGGAAGTTCACATTATCCTCAGCTTTGGATGGCTCTAAA[C/T]GAGACCAGGCTACTTCCATGTCCCACCTTAACCTCATCAATGAGACTCAC

Long Flanking Sequence:

GATGACATGATCGTTTTCGAGTTTCATGGAATGTAGACATAAGTTAAGCGTTTCGAAGACTAAATGGACTGCTGCAAATTATAGTGCCACATATCAGTGAAACTAAGAAAAGAACACAACGCATTAGACAAAGGTAGCAGGTAAATTTGGTTAATATTGGTATTCTGTATCTGCTTGTTCAGTAGTGTAGTGCTTTGAAATACTTATCTGGTGTTTCATATCGCATTCAATCACCCAGTTAATGTACAGTCACACATGCATCTCTTATTGTGCTTGATTAAAAAGGAGTTTCTCTAAATAAAATTCTTTCCTAGTTTCTGCAATACGAACGAGCTAAAAAGTGGGTACTTTTGCAATCAGTTTTTTGAACAATGCAAAAGTTCCTTTTTTTAATTCAGTAGTCAAATTGAACAATGCTTCTGTGTTTCAGGAGGAAGTGTACCCGTTTGCGGCCTGCTCACCGGAAGTTCACATTATCCTCAGCTTTGGATGGCTCTAAA[C/T]GAGACCAGGCTACTTCCATGTCCCACCTTAACCTCATCAATGAGACTCACCTTGACCAGAACGGGGCAGAGCCGGACATGCACACACCTATGCTTAAACCCACTCCCTACGACTCCTCCACCAATGAGCTTGCGACTTCGCGTGGCGAGCTTCACAGCCGAGGATCCAACCACTACAAACACTCAGTTGAAATATTTCCTCTCAAATCGGCTTGCTCAAACAATCCCTCTGAAGGTTATGATTCCGCTGCTGGACGAGGGGAATACCGACGGAGCTATACGTCCATTACGACTTCGTCCGTCCATCCCCTCCACATGTCTGTCTCCTCCTCTTCGCCTCATACCTTGCATCACACCACCTCTGCAGGACGTCTCTCTTCGGAGAGTAAATCAAGCTTGCGGGATCAACGTCTGTCTCCTGTTTCGGCCGCAAGTCCTGCCGGATCTCCAGAACGGGAGCAAGGAATTGAGCGACGGACAACTGATTACTTGTTGTCCCGC

Associated Phenotype:

Not determined