ZMP

C14orf148

Ensembl ID:

ENSDARG00000027538

Description:

chromosome 14 open reading frame 148 [Source:HGNC Symbol;Acc:20487]

Human Orthologue:

C14orf148

Human Description:

chromosome 14 open reading frame 148 [Source:HGNC Symbol;Acc:20487]

Mouse Orthologue:

4933437F05Rik

Mouse Description:

RIKEN cDNA 4933437F05 gene Gene [Source:MGI Symbol;Acc:MGI:1918525]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42997	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15278	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa42997

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
ENSDART00000036442	Nonsense	241	340	6	7
ENSDART00000062109	Nonsense	230	332	5	6
ENSDART00000062111	Nonsense	240	335	6	7

Genomic Location (Zv9):

Chromosome 17 (position 45322214)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	45041396
GRCz11	17	45155161

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATTAAGTAAACTGGCAGTGTTTACTGAAGGTGGGCTCTTCCTGGATCGA[C/T]GATGGACGTCTGCTGTGCTCTACGCTCTCCTCAACATGTGCACAGCAGAA

Long Flanking Sequence:

CCGAAAATAAAATGAATGATTGAATAAATGATATTAAATGTTTACTTTAGTCATGTGTGATAGTGAAAATGCAACATCAAATCAACAACCAATAAACAGACAATTCCGGTCCTTGATTCTGATTGGTTGACAAGGTTGCAAAATACACTATAACACACATGTGAGTTGCATGGCAGCCATTCCATTCCATCAGTTCTGAGTCAAATAAATAATTTAATTTGCTTTGCTTCCTTTTGTGAATAACCGCTATTTAAAAACAGAGCAAAACCATGGTTTACTGTGATTTTACAACAGCTAAGGCGCTCAATGCTTTATTTTAGGTGTACCAATATTCTTTTGGTAACTTCACAGTTTTTTCACATCAAAATAAATCTTTTATGAGTGTTCAGAATGTATCCACATTCGTCTGTCATGTGAAGTGAGTATAGTGTAGTGTTTTATATGGTGTGCTATTAAGTAAACTGGCAGTGTTTACTGAAGGTGGGCTCTTCCTGGATCGA[C/T]GATGGACGTCTGCTGTGCTCTACGCTCTCCTCAACATGTGCACAGCAGAAAAGCTGGACTCCGGAAACACTCTTCAGCTGCTAAATGGACTGTTTGAGACTGGTGTTTCAACAGAGACGTTCACTTATCACAGTTTTGTCAATTCACCCAATGCCACCTCTGATGTCCATAAACCAGACGAGTGAGTTCGAGGCAGTTTTGCATACTAGTTTTTTCATATTCAAAATGATGTGTACGAAAATTGAATGATGACTATTTAATAATTATGCCTCTGTTGTTTTACAGACTTTTTCCATGGATCAGTTTGGTCAATGCACAAACTAAAGACACTCCACTGACTGACCTGCTGTCAAGGAATTCAGGTTTGCGAGACTGTATTTCATGCATGTACTACAATGTTTTTGCAAACTTAGCTGAAGGATAGTATTTTTGTTGTTGGTGATTAGATCTGATACACACGACTATTGAATTGTGTAATGTACATTGTGTGCACTCATGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15278

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036442	Nonsense	254	340	6	7
ENSDART00000062109	Nonsense	243	332	5	6
ENSDART00000062111	Nonsense	253	335	6	7

Genomic Location (Zv9):

Chromosome 17 (position 45322173)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	45041355
GRCz11	17	45155120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

NNNNNNNNNNNATCGACGATGGACGTCTGCTGTGYTYTACGCTCTCCTCAACATGTG[C/A]ACAGCAGAAAAGCTGGACTCSGGAAACACTCTTCWGCTGCYAAATRGACT

Long Flanking Sequence:

TTACTTTAGTCATGTGTGATAGTGAAAATGCAACATCAAATCAACAACCAATAAACAGACAATTCCGGTCCTTGATTCTGATTGGTTGACAAGGTTGCAAAATACACTATAACACACATGTGAGTTGCATGGCAGCCATTCCATTCCATCAGTTCTGAGTCAAATAAATAATTTAATTTGCTTTGCTTCCTTTTGTGAATAACCGCTATTTAAAAACAGAGCAAAACCATGGTTTACTGTGATTTTACAACAGCTAAGGCGCTCAATGCTTTATTTTAGGTGTACCAATATTCTTTTGGTAACTTCACAGTTTTTTCACATCAAAATAAATCTTTTATGAGTGTTCAGAATGTATCCACATTCGTCTGTCATGTGAAGTGAGTATAGTGTAGTGTTTTATATGGTGTGCTATTAAGTAAACTGGCAGTGTTTACTGAAGGTGGGCTCTTCCTGGATCGACGATGGACGTCTGCTGTGCTCTACGCTCTCCTCAACATGTG[C/A]ACAGCAGAAAAGCTGGACTCCGGAAACACTCTTCAGCTGCTAAATGGACTGTTTGAGACTGGTGTTTCAACAGAGACGTTCACTTATCACAGTTTTGTCAATTCACCCAATGCCACCTCTGATGTCCATAAACCAGACGAGTGAGTTCGAGGCAGTTTTGCATACTAGTTTTTTCATATTCAAAATGATGTGTACGAAAATTGAATGATGACTATTTAATAATTATGCCTCTGTTGTTTTACAGACTTTTTCCATGGATCAGTTTGGTCAATGCACAAACTAAAGACACTCCACTGACTGACCTGCTGTCAAGGAATTCAGGTTTGCGAGACTGTATTTCATGCATGTACTACAATGTTTTTGCAAACTTAGCTGAAGGATAGTATTTTTGTTGTTGGTGATTAGATCTGATACACACGACTATTGAATTGTGTAATGTACATTGTGTGCACTCATGTTAAGTCTGTTTATCGTCAGTCATATGTGAAGGTGTTTGTGAT

Associated Phenotype:

Not determined