ZMP

flrt1b

Ensembl ID:

ENSDARG00000075597

ZFIN ID:

ZDB-GENE-080327-6

Description:

cDNA, clone cssl:d0318 [Source:UniProtKB/TrEMBL;Acc:A8BAV0]

Human Orthologue:

FLRT1

Human Description:

fibronectin leucine rich transmembrane protein 1 [Source:HGNC Symbol;Acc:3760]

Mouse Orthologue:

Flrt1

Mouse Description:

fibronectin leucine rich transmembrane protein 1 Gene [Source:MGI Symbol;Acc:MGI:3026647]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
hu3283	Nonsense	Confirmed mutation in F2 line	Not yet available
sa35756	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

hu3283

Status:

Confirmed mutation in F2 line
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
ENSDART00000114790	Nonsense	83	696	2	2

Genomic Location (Zv9):

Chromosome 14 (position 48861162)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	46938821
GRCz11	14	45926113

KASP Assay ID:

554-0140.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCAAAACAACCGCATAGACAATGCTGGGCTACCGACATCTTTAGAGCGA[C/T]GACTGACTGTGAGAGTAGTTTACCTCTATGATAATGAACTTGACGATTTT

Long Flanking Sequence:

AGGAGTCTAACACAAATGTAACCTCGGTGTTTTGAAAAATTCTCATCCCAAAAATCTTTTCTATATTTCCCACAGGGCTTGTGATTGGAAGCAAAGAAAGCAAAGAAAGAGCTGTGCACCCGGACCAAGAATATTGACTTCTGAGACATTAAGTTGCATTAACTCTGCAGAGAGAGTGGGGTACACTGCCTGGAATTATGGCCACGGAGAGCCTTGTTGAACTCCGCGACTGGTTGTTTCTACTTCTCCTATGCCTGACGTTACTTGTTGAAGTGCTGGAGTTTGCTGCAGCTACAGCCGCCGCGGCTGAAGCAGCTCTCGGGGAAGCGGAGCTACAGGGAGAAGTGCCATGTCCGTCTGCTTGCAGGTGCGACGATGGATTCATTTACTGCAATGACCGTGGCTTGACTCTCATCCCTCCATTACCATTAACAGCAGCTGTGCTCTATCTCCAAAACAACCGCATAGACAATGCTGGGCTACCGACATCTTTAGAGCGA[C/T]GACTGACTGTGAGAGTAGTTTACCTCTATGATAATGAACTTGACGATTTTCCGACACACCTGCCTCCGTCGTTACGAGAACTTCACCTACAGGACAACAACATACGAACTTTACCGCGTTCTGCCCTTGCACGGCTCCCCCTGCTGGAGAAGCTTCACATGGATGACAATTCAATTTCCACTGTGAGCATAGAAGACAAAGCCTTCACCAACAATCCGAGGCTGCGTCTTCTTTTCTTGTCCCGCAACCACCTCTCGAGTATACCATCGGGATTGCCTGCATCCCTGGAGGAACTCCGTTTAGATGACAATCGCATTTCAACCATTCCGACGCATGCTTTTCGAGGTCTCTCCTCTCTAAGGCGTCTCTTCCTGGACGGAAATCTGCTGGCAAATCAACGAATTGCAGACGACACATTCTCGCGGCTGTCCAATCTCACAGAGCTTTCTCTGGTGCGTAACTCATTACAGGCACCACCGTTAAACCTTCCAAGTTTGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35756

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
ENSDART00000114790	Nonsense	216	696	2	2

Genomic Location (Zv9):

Chromosome 14 (position 48861561)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	46939220
GRCz11	14	45926512

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTCCTCTCTAAGGCGTCTCTTCCTGGACGGAAATCTGCTGGCAAATCAA[C/T]GAATTGCAGACGACACATTCTCGCGGCTGTCCAATCTCACAGAGCTTTCT

Long Flanking Sequence:

GTGGCTTGACTCTCATCCCTCCATTACCATTAACAGCAGCTGTGCTCTATCTCCAAAACAACCGCATAGACAATGCTGGGCTACCGACATCTTTAGAGCGACGACTGACTGTGAGAGTAGTTTACCTCTATGATAATGAACTTGACGATTTTCCGACACACCTGCCTCCGTCGTTACGAGAACTTCACCTACAGGACAACAACATACGAACTTTACCGCGTTCTGCCCTTGCACGGCTCCCCCTGCTGGAGAAGCTTCACATGGATGACAATTCAATTTCCACTGTGAGCATAGAAGACAAAGCCTTCACCAACAATCCGAGGCTGCGTCTTCTTTTCTTGTCCCGCAACCACCTCTCGAGTATACCATCGGGATTGCCTGCATCCCTGGAGGAACTCCGTTTAGATGACAATCGCATTTCAACCATTCCGACGCATGCTTTTCGAGGTCTCTCCTCTCTAAGGCGTCTCTTCCTGGACGGAAATCTGCTGGCAAATCAA[C/T]GAATTGCAGACGACACATTCTCGCGGCTGTCCAATCTCACAGAGCTTTCTCTGGTGCGTAACTCATTACAGGCACCACCGTTAAACCTTCCAAGTTTGCATCTCCTTAGACTCTATCTGCAGGACAATGCTATAGCCCACATGCCTCGAGGCTCCCTAGATGGCATGCGGAGGCTACAGAAACTAGACATATCTGGTAATAACCTAACGACTCTTCCGAGAGGTTTGTTTAAAGATTTAGACAGCCTTTCACAATTACTTGTCCGAGGAAACCCATGGTACTGTGGCTGCAACCTCCGCTGGCTTCACGACTGGCTGCATGAGCGAGGTTCATCTGTGACTGTAAGAGGTTTAACGTGCCATGCACCAGAGAGACTAAGAGGCATGGCACTAAGGGACCTTAGCAGTCAACTGGAAGACTGCGAGGTCACTGTCGACGCCGCTGGAGGAATGGTTGGAAATGAGGTCGCCAAAAAGGAGAAGGGTTATTTTCCAACCCAA

Associated Phenotype:

Not determined