ZMP

fancm

Ensembl ID:

ENSDARG00000077800

ZFIN ID:

ZDB-GENE-090929-1

Description:

Fanconi anemia, complementation group M [Source:RefSeq peptide;Acc:NP_001107132]

Human Orthologue:

FANCM

Human Description:

Fanconi anemia, complementation group M [Source:HGNC Symbol;Acc:23168]

Mouse Orthologue:

Fancm

Mouse Description:

Fanconi anemia, complementation group M Gene [Source:MGI Symbol;Acc:MGI:2442306]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24767	Nonsense	Available for shipment	Available now
sa44432	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24767

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
ENSDART00000052772	Nonsense	274	693	7	15

Genomic Location (Zv9):

Chromosome Zv9_NA92 (position 5934)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	1465335
GRCz11	17	691561

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAAGATGGAGATGTTTCCTCAGATGAAGATGATGGAGACGAGCAGAAC[C/T]AATCACTGCAGGGCTTCGTGGTCAACAACACACAGTGCTCGCAGGGGCTC

Long Flanking Sequence:

TGTTTGTGGTTGGTTGTTGTTGTTTGTTTGTGGTTGTTGTTTTGGTTGTTGTTGGTTGATGTTGTTTGTGCTTGTTGTTTTGGTTGTTGTTGTTGTTTGTTTTGGTTGTTGTTTTGGTTGTTGTTGGTTGTTGTTTTGGTTGTTGTTGTTTGTGGTTGGTTGTTGTTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTCACACACTCTCACTAACATACTCAGATATGCTGACACGCACTCTCACACACACTTGCACATATGCACACACACACACACACACGGTGATCATCGTCTTCTGCGTCTCCTCTGTGTGTTCTAGAAGTTTCCCCGTGGCGCGGCTCGTCAGTTTCTGGATGAGGAGGCCGAACTCTCTGAGGATGAAGATGGAGATGTTTCCTCAGATGAAGATGATGGAGACGAGCAGAAC[C/T]AATCACTGCAGGGCTTCGTGGTCAACAACACACAGTGCTCGCAGGGGCTCAACGGTGAGACACACACACACACACACACACACACACACACACACAGTCATACACTACGGTCAGTTTAGTTGATCAATTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGTGCACCTGGAGAAAACCCACACCAACAGGGGGGAGAACATGCAAACTCCACACAGAAACACACACTGACCCAGCCGAGACTCAAACCAGCGACCTTCTTGCTGTGAGGCCACAGTGCAACACCACTGAGACTTTGTGACGCCAGCTCAAATATACATTAAGAATATTTTCTTTTCCTTTAATTGTACTGTTGTAATCTTCCAGGTTCAGTCTCAATAACATCTGCATCATAAGTAATGTAAATGTGATGTCAGTGTAGTGTGCTGTGCTGACAGGCCGGTCTCAGATGCACTGTTATTACACTGAACTGTGCTCAGATCAGGTTTGATGTCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44432

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
ENSDART00000052772	Essential Splice Site	459	693	9	15

Genomic Location (Zv9):

Chromosome Zv9_NA92 (position 11662)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	1471063
GRCz11	17	697289

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATCAGGCAGAGCTGTCAGAAGAGCTGGACTTCCAGACCCACAAACAGG[T/G]GAGGACTTTTAATGCCATAACAGAGTTGACGGTAGCGGAGTTGCAATAGG

Long Flanking Sequence:

TTAATGACACAAAGACCCTTACATTAAATACAGTGAGTTGAAAAGCAGATGTTTAGGGGGTGTGTGTAGTTTCACACAGTTTTTCCGACTCTGCAATTGTCAGGTGCCAGAACAGGACGAGTCGTATGCCGAGGACAGTTTTGTGGTTGATGGAAGCGAGGAGGAGGATGAAGTGTCTGCTGATGAGGAGTCTGTGGAGCTGATCCCTGAAGACTCCTTCATCGATGGGAGGAGGCAGTACGCCACGCGCCGCAGGGCTCGGATACGGCAGATACGTGCGGCAAACCCTGCCACAGATCAGCAGCATAAAAACAAACGCTCCCGCATCATTCGCCCACAGGATTCTAGCGATGAGGACGAGGACCAACCTCAGACCCACAGTGTGTTTAAAGTCCCGCAGAGTGTCTGCCGTCGGCCCGAGCCGGAGATCCAGAAGAGGCAGAGACTTGAAGATCAGGCAGAGCTGTCAGAAGAGCTGGACTTCCAGACCCACAAACAGG[T/G]GAGGACTTTTAATGCCATAACAGAGTTGACGGTAGCGGAGTTGCAATAGGGGAGTTCACTGTAGCCGTGTTGATGGTAGCGGAGTTGACGATAACAGTATATCAGAGTTGACGGTAGCAGAGAATACGATAGCAGAGTTGACGGTAACAGTATATCAGAGTTGAAGGTGGCAGAGTTAACGATGGCGGAGTTGACGGTAGAGAGTTGACAGTAGCAGAGTTGACTGTAGTGGAGTGGACGATAACAGTATATCAGAGTTGACGGTAGCGGAGTTGACAGTAGCAGAGTTGACTGTAGCGGAGTTGACGATAACAGTATATCAGAGTTGACTGTAGTGGAGTTGACGATAACAGTATATCGGAATTGACTGTAGCAGAGTTGACAGTAGCAGTGTTGACTATTGCAGAGTTGATGGTAACAGAGTTGACTGTAGCGGAGTTGACGATAACAGTATATCAGAGTTGACTGTAGTGGAGTTGACGATAATAGTATATCGGAAT

Associated Phenotype:

Not determined